Podcasts about Lyme disease

Could Lyme disease and other chronic inflammatory triggers play a role in Alzheimer's disease—and could addressing those underlying factors change measurable Alzheimer's biomarkers? In this episode of the Tick Boot Camp Podcast, Dr. Richard Horowitz returns to discuss a provocative new case report he published exploring the relationship between Lyme disease, neuroinflammation, Alzheimer's disease biomarkers, and dapsone combination therapy. The conversation centers on a patient with a long history of Lyme disease who had an elevated phosphorylated tau 217 (p-tau217) level, an increasingly important blood biomarker associated with Alzheimer's disease. After completing a nine-week dapsone combination protocol, the patient's p-tau217 declined by approximately 63% and returned to the normal range. Her amyloid-beta 42/40 ratio also moved in a favorable direction, and she reported improved cognitive clarity. This case provides a new research question: Could infections, toxins, metabolic dysfunction, sleep disorders, microbiome disturbances, and other inflammatory drivers contribute to Alzheimer's pathology in subsets of patients—and could identifying and addressing those drivers change the course of the disease? Read the Published Study Read Dr. Horowitz's published study on SAGE Journals The case report provides the scientific foundation for much of the discussion in this episode, including the changes in p-tau217 and amyloid biomarkers following treatment. In This Episode, You'll Learn Lyme Disease and Alzheimer's Disease Dr. Horowitz reviews research that has investigated possible relationships between Borrelia burgdorferi, neuroinflammation, amyloid, phosphorylated tau, and Alzheimer's pathology. Much of the earlier work examining spirochetes and Alzheimer's disease involved brain tissue and postmortem studies. Dr. Horowitz explains why he believes studying Alzheimer's biomarkers in living Lyme disease patients may provide another way to investigate these questions. The discussion also explores an important distinction: finding an association between infection and Alzheimer's pathology does not mean every case of Alzheimer's disease is caused by Lyme disease. The Patient Who Sparked the New Case Report Dr. Horowitz describes a longtime patient with Lyme disease whose p-tau217 was substantially elevated despite her perception that her cognition was relatively good. After the patient underwent his nine-week dapsone combination protocol, repeat testing showed a substantial reduction in p-tau217, bringing the biomarker into the normal range. Dr. Horowitz also discusses changes in the patient's amyloid-beta 42/40 ratio, rheumatoid factor, and subjective cognitive function. The case led him to ask whether treatment directed at persistent infection and inflammation could influence biomarkers normally associated with Alzheimer's disease. What Is p-Tau217? A major portion of the interview focuses on the emerging use of blood-based biomarkers for evaluating Alzheimer's pathology. Dr. Horowitz discusses four primary biomarkers: p-tau217 – phosphorylated tau 217 p-tau181 – phosphorylated tau 181 Amyloid-beta 42/40 ratio Neurofilament light chain (NfL) He also discusses GFAP (glial fibrillary acidic protein) and the potential relevance of APOE genetics. Dr. Horowitz describes p-tau217 as one of the most sensitive and specific currently available blood biomarkers associated with Alzheimer's disease pathology. Amyloid May Be More Than Just “Plaque” Why does amyloid accumulate in the brain in the first place? The episode explores the concept of amyloid-beta as an antimicrobial peptide and the hypothesis that amyloid production may, in some circumstances, be part of the brain's response to biological threats. Dr. Horowitz discusses research examining potential infectious and environmental contributors to amyloid production, including: Borrelia and other bacteria Viral infections Fungal organisms Other microbes Environmental toxins The conversation then explores how a response that may initially be protective could potentially become harmful when amyloid accumulates and interferes with normal neuronal function. Amyloid, Tau and Neurodegeneration Dr. Horowitz breaks down two major features associated with Alzheimer's disease. Amyloid-beta plaques accumulate outside neurons and are associated with disrupted communication between brain cells. Tau proteins normally help stabilize structures inside neurons. Abnormally phosphorylated tau can become associated with neuronal dysfunction and neurodegeneration. The discussion also explores why some patients may have abnormal tau biomarkers without corresponding abnormalities in amyloid markers—and why much more research is needed to understand these patterns in people with chronic Lyme disease. Dapsone Combination Therapy and Cognitive Symptoms Dapsone has been a major focus of Dr. Horowitz's research into persistent Lyme disease. In this episode, he explains that his protocols involve combination therapy rather than dapsone alone and discusses his previous published work examining dapsone combination therapy in patients with persistent Lyme disease symptoms. According to Dr. Horowitz, improvements in memory, concentration, cognition, and word-finding difficulties have repeatedly been among the most notable improvements reported in his patient cohorts. He believes this observation deserves greater attention now that blood-based Alzheimer's biomarkers make it possible to investigate biological changes alongside cognitive symptoms. Dapsone, the Brain and the NLRP3 Inflammasome The discussion goes beyond dapsone's antimicrobial activity. Dr. Horowitz explains his interest in the NLRP3 inflammasome, an inflammatory pathway implicated in neuroinflammation and studied in relation to Alzheimer's disease. He proposes that dapsone could potentially have more than one relevant effect—targeting certain microorganisms as part of combination therapy while also influencing inflammatory pathways. This remains an area requiring further clinical investigation. Alzheimer's Disease May Have Multiple Drivers One of the most important themes of the interview is that Alzheimer's disease is unlikely to have a single universal cause. Dr. Horowitz applies his 16-point MSIDS (Multiple Systemic Infectious Disease Syndrome) model to cognitive decline and Alzheimer's disease. Potential contributors discussed include: Lyme disease and other infections Mold and mycotoxin exposure Heavy metals and environmental toxins Chronic inflammation Insulin resistance and blood sugar dysregulation Sleep disorders and sleep apnea Gut microbiome dysfunction Nutritional deficiencies Mitochondrial dysfunction Cardiovascular and metabolic factors Other sources of systemic inflammation Rather than focusing exclusively on amyloid or tau, Dr. Horowitz argues for investigating what may be driving those abnormalities in an individual patient. Lyme Disease Is Not the Only Possible Infectious Trigger The episode also examines the broader question of infection and neurodegeneration. Dr. Horowitz discusses scientific literature investigating organisms and infections beyond Borrelia, including Chlamydia pneumoniae, Helicobacter pylori, Coxiella burnetii, herpesviruses, and other microbial exposures. His central argument is not that every Alzheimer's patient has an infection. Instead, he believes clinicians and researchers should investigate whether infectious, toxic, metabolic, environmental, and inflammatory factors may coexist and contribute differently from patient to patient. The Challenge of Lyme Disease Testing The conversation also addresses limitations surrounding Lyme disease diagnostics. A negative standard Lyme disease test does not necessarily answer every clinical question surrounding prior exposure or persistent symptoms. The hosts and Dr. Horowitz discuss why testing methodology, timing, immune response, strain diversity, clinical history, and other factors may need to be considered when evaluating a complex patient. Dr. Horowitz also explains how he combines laboratory findings with clinical history and his MSIDS framework when evaluating patients. Why More Data Is Critical A single case can generate a hypothesis. It cannot establish a treatment standard. Dr. Horowitz repeatedly emphasizes the need for: Additional documented cases Standardized biomarker testing Long-term patient follow-up Larger patient cohorts Collaboration among Lyme-literate physicians and neurologists Shared research databases Multicenter studies Randomized controlled clinical trials The episode explores the possibility of physicians systematically collecting Alzheimer's biomarkers before and after treatment of specific MSIDS factors to determine which interventions, if any, consistently change those biomarkers. That type of data could help researchers move beyond individual clinical observations toward testable conclusions. Could Patient Data Accelerate Lyme and Alzheimer's Research? Matt and Dr. Horowitz discuss the potential for a secure research repository where physicians could contribute standardized patient data. For example, researchers could track a patient's infections, mold exposure, metabolic factors and other MSIDS variables alongside p-tau217, p-tau181, amyloid-beta 42/40 and NfL measurements. Repeating those measurements after individual interventions could help researchers identify patterns that would otherwise take years to discover through isolated clinical practices. Dr. Horowitz Is Developing an MSIDS App Dr. Horowitz also shares a major project currently in development. He says he is working with researchers from the University of California, Irvine on an application designed to translate his MSIDS framework into a digital tool. The goal is for users to enter information based on the MSIDS questionnaire and other health data, allowing the software to help guide them through the framework. Dr. Horowitz also discusses how a sufficiently large and secure database could eventually create opportunities for collecting real-world patient data and generating new research hypotheses. Lifestyle, Metabolic Health and Brain Health Not every potential driver discussed in this episode is infectious. Dr. Horowitz highlights several established areas of brain-health research, including: Mediterranean/MIND-style dietary patterns Regular physical activity Healthy blood sugar and insulin regulation Cardiovascular health Adequate sleep Addressing sleep apnea Omega-3 fatty acids Nutritional status Gut and microbiome health This reinforces one of the episode's central messages: cognitive decline may result from multiple interacting biological pressures rather than one isolated mechanism. Ending Chronic Illness The discussion also previews Dr. Horowitz's upcoming book, Ending Chronic Illness, scheduled for publication on October 13, 2026. The book expands on his 16-point MSIDS model and explores how overlapping infectious, inflammatory, environmental, metabolic, immune, neurological, and lifestyle factors may contribute to chronic disease. A separate Tick Boot Camp interview dedicated to the new book will be released this fall. Learn More About Dr. Richard Horowitz Dr. Richard Horowitz is one of the best-known physicians in the Lyme disease community and has spent decades treating patients with Lyme disease, tick-borne infections, and complex chronic illness. Tick Boot Camp has interviewed Dr. Horowitz multiple times about Lyme disease, Babesia, Bartonella, dapsone combination therapy, MSIDS, chronic inflammation, and emerging research. Visit Dr. Richard Horowitz's Tick Boot Camp page for all of our interviews, articles, and resources Additional Resources Explore all Tick Boot Camp interviews and information Key Topics Richard Horowitz, MD; Lyme disease; Alzheimer's disease; Alzheimer's biomarkers; Lyme disease and Alzheimer's; Lyme disease and dementia; cognitive decline; neuroinflammation; p-tau217; p-tau181; phosphorylated tau; amyloid beta; amyloid-beta 42/40 ratio; neurofilament light chain; NfL; GFAP; APOE4; Borrelia burgdorferi; chronic Lyme disease; persistent Lyme disease; dapsone; dapsone combination therapy; MSIDS; Multiple Systemic Infectious Disease Syndrome; biofilms; persister bacteria; brain inflammation; memory problems; brain fog; cognitive dysfunction; mold toxicity; mycotoxins; microbiome; infections and Alzheimer's disease; tick-borne disease; Lyme disease research; dementia research; Alzheimer's research.

In this episode, I have the pleasure of speaking with Dr. Neil Nathan about the intersection between brain symptoms and complex illness. Dr. Nathan has practiced medicine for over 50 years. He is one of the leading experts in complex chronic illness and mold toxicity — author of the bestselling Toxic: Heal Your Body from Mold Toxicity, Lyme Disease, Multiple Chemical Sensitivity, and Chronic Environmental Illness and The Sensitive Patient's Healing Guide. I am grateful to call Dr. Nathan a mentor and colleague. His pioneering work has been responsible for my healing from chronic illness, as well as that of many patients I've treated. Together, we co-lead a small peer group (within the larger mentoring group he provides with Marie Matheson, ND), supporting practitioners who treat those with complex chronic illness.In this episode we discuss:03:43 – Dr. Nathan's path to understanding complex illness11:20 – Why complex illness is rising and underrecognized19:30 – Why new medical ideas take decades to reach patients23:15 – Mold, Lyme, and long-COVID: the “big three” root causes25:58 – The limbic-vagal-mast cell “trifecta”30:31 – Are some people born more vulnerable?44:39 – The risk in “just do limbic retraining” advice47:35 - Biochemical contributors49:26 – Structural root: jaw and cervical instability53:58 – Differentiating Between Mold, Lyme & Long-COVID58:49 – A message of hope, and where to learn moreFull Transcript belowYou can find Dr. Nathan's books, consultations and mentoring program through his website at neilnathanmd.com. If you'd like to help get this information out into the world, please consider liking, sharing, or commenting.Until next time,CourtneyCourtney Snyder MDDr. Courtney Snyder MD is a holistic and functional child and adult psychiatrist and host of the Holistic Psychiatry Podcast and can be found at courtneysnydermd.comMedical DisclaimerThis podcast is for educational purposes only and is not intended or implied to be a substitute for professional medical advice, diagnosis, or treatment. Consult your own physician for any medical issues you may be having.Full TranscriptDr. Nathan's Path to Understanding Complex Illness03:43Courtney: I'm so glad we're doing this, and I feel like it's long overdue. As you know, in the mental health space in psychiatry, there's a lot of recognition of a dysregulated nervous system, threat response in the body, but oftentimes that's attributed to external forces or trauma, and not necessarily internal threats that we see, obviously, in complex chronic illness, which we'll be talking about. There's also not the recognition of the relationship between physical symptoms and brain-related symptoms. So I know you're going to help us connect a lot of these dots. As we sort of just lay the groundwork for what complex chronic illness is — when in your path did you start to recognize the distinction, when was the beginning of your work and appreciation of complex health issues?Neil: Okay, there are two answers to that question. First, when I went to medical school, my hope was to become a healer. And I was very disappointed that when I got there, I realized they weren't going to teach me to be a healer. And back then I used to question my professors at medical school — why do you do it this way, and how is that? And I kept feeling in all of our interactions that we were missing something. And my professors would go, “Okay, Mr. Wise Guy, smart guy, what are we missing?” And I'd go, “I don't know, I just know we're missing something.” Later I would come to recognize that we were missing the emotional and spiritual component to whatever was affecting people in their illnesses. And I have language for it now — I didn't then. The person in medical school who influenced me the most was Elisabeth Kübler-Ross, who I view as my main mentor in medical school. She, unlike anyone else, had a one-and-a-half-hour seminar once a week. Back then there weren't video cameras — you were in a small confined room with a two-way mirror, and you're sitting there watching someone do this. And she would simply interview one of her patients. She was a psychiatrist, but she was the only one in medical school who demonstrated how to really listen to people, how to really communicate with them, and not have this standard review of systems — here's my questions, here's your answers, and that's what I do, and this is what I write up. She was really listening. She was trying to really take in, okay, what happened to you, and what's going on with you? So I would want to give her credit as a role model to change how I learn to listen. Okay, that was step one.I'm going to fast forward to the early 1980s. And I am, at that point, the medical director of a regional pain clinic. And we are starting to see a whole bunch of patients who had this complicated process of fatigue, unrefreshed sleep, irritable bowel syndrome, and pain migrating all over their body. And back then we called it fibrositis. Now we call this fibromyalgia. And so whenever medicine encounters a thing that they don't know what they're looking at, it's psychological until proven otherwise. And people would get therapy, and they would take antidepressants and anti-anxiety agents. Didn't help much. And so it became clear to me that we didn't understand what this was at all. It was not psychological. Something was going on in their bodies — now I recognize it as an inflammatory process. Back then there was no concept of that at all. And then, slowly, in the early nineties, we began to find pieces of the puzzle to understand what was triggering fibromyalgia. I was working back then with Jacob Teitelbaum, who did a lot of work with chronic fatigue and fibromyalgia, and we both independently came up with an understanding that a deficiency of magnesium, DHEA, adrenal issues, thyroid issues, sex hormone deficiencies, GI dysbiosis, and food allergy — if we looked at those and treated those, the majority of people with fibromyalgia got cured. It was different for different patients. It was not like there was one thing that caused it. And as time evolved, we began to realize that there was lots of other biochemical imbalances in the body that would contribute to this kind of a process that represented chronic fatigue and fibromyalgia.We discovered that Lyme disease and coinfections was a huge piece of that. And later still we discovered that mold toxicity was a huge piece of that. And so my understanding of the complexity — and it's not really confined to chronic fatigue and fibromyalgia at this point, we're really talking about almost all chronic illness — with a huge psychological component to that. So we've begun to understand this as essentially some version of inflammation. And if we start to really dig into what are the potential causes of that inflammation, we can make a huge impact for them. So this is a multi-year evolving understanding of how a person's genetics, biochemistry, physiology impacts their whole being in every way. And that inflammation extends to the nervous system, contributing greatly, if not causing directly, a large number of what are now called psychiatric diagnoses.Courtney: Right. So even among those patients that you were seeing — you were seeing, I'm assuming, depression, anxiety, brain fog?Neil: Yeah, the vast majority of our patients with mold toxicity have brain fog and anxiety, depression, OCD behaviors, mood swings, depersonalization, derealization. I mean, all of that is super common in our patients.Complex Illness Is Rising — and Underrecognized11:20Courtney: Do you feel like this is more recognized now — or do you feel like the number of people being hit with these complex health issues is increasing — or both?Neil: Both. I would love to say that the medical profession is increasingly recognizing all of this as important, but that recognition is coming very, very slowly. The majority of folks out there, if they were to list the symptoms that they had, their doctors would basically look at them like, “I have no idea what's causing it, so this must be in your head.” And that is the message they're getting from their physicians at this point. So many patients are being gaslighted, so many patients are being told it's in your head. And the repercussions of that are the family is hearing that same message, and the families become less supportive of those people, because they're saying, “This is not real, so why would I support you? This is still in your head, go get your head fixed.” And they're wrong, and it's really a travesty. But so yes, very slowly, this awareness is growing. There are now more medical meetings that I'm aware of where psychiatrists can learn more about this than there were ten, fifteen years ago, for sure. But not enough — it's still not enough.The other part of that is some of the main triggers for this inflammatory process are increasing. So we're seeing more and more mold toxicity, we're seeing more and more Lyme and coinfections, partly because the environment that we are all exposed to has gotten extremely increasingly toxic. So it's now known, for example, that there are 350,000 new chemicals in our environment than existed 70 years ago. The vast majority of those have never been tested for safety in human beings. So human beings have a tremendous amount of chemical exposure that they never had before. Human beings have a tremendous amount of EMF, electromagnetic exposures that they never had before in the history of the human race. So these exposures are cumulative. Our major organs, like our liver and our kidney, that have to deal with toxicity, are overloaded. And so, yes, we are seeing an epidemic of a whole bunch of these conditions. In children, we are aware that autism has skyrocketed — it went from one in several thousand kids to one in thirty kids in many states now have autism. And forgive me, but the pediatric profession is not taking this seriously. It's like, “Yeah, that's sad, it's unfortunate.” It's like — really, you don't want to look at this? This means one in every three kids born are getting autism — does that not concern you? But, forgive me, the medical profession is very slow to embrace new information, and that is really to the detriment.We're seeing an epidemic of Alzheimer's, Parkinson's, ALS, all of which involve neuroinflammation. We've seen already an epidemic of chronic fatigue and fibromyalgia. And all of these things are interrelated, because — yes, I'm supposed to be an expert on mold toxicity, and I probably am — but mold toxicity doesn't exist in a vacuum. You have mold toxicity as one of multiple environmental toxins we're being exposed to. It is simply one of the most common, the easiest one to diagnose, because we have tests for it. We don't have tests for the hundreds of thousands of chemicals out there. We're just beginning to be able to have some tests that will tell us what's in someone's body that might be making them sick.Courtney: Right, right. And I would imagine that this typical medical model of looking for one cause to autism, one cause to dementia — it's a completely different way of thinking. When you get away from that and you look at complexity of the human body, that way of thinking holds back the research, it holds back any progress.Neil: What I think is helpful for people to look at is: we are all uniquely, biochemically, genetically different. And so the same inflammation in one person could trigger cardiovascular disease, and another person could trigger Alzheimer's, and another person could trigger chronic fatigue. So we need to take a step back and go, okay — and this is not a brand new idea. For the last ten years, there are many papers in the medical journals that are saying chronic illness is almost certainly an inflammatory process. Now, it hasn't really integrated into what people are being taught in medical school or in their residency program. But this is not a brand new idea, and there's tons of medical research documenting that.What behooves us as physicians is to look at every human being and go, “Okay, this is your named chronic condition — what are the triggers for you?” We have to kind of be like a medical detective and dig in and go, okay, what's triggering your inflammation, so I can treat the cause — not put a band-aid on it, which is, forgive me, in the psychiatric field, taking antidepressants and benzodiazepines. That's a band-aid. It's a helpful band-aid, it could be a very important band-aid, help someone to function. But you really need to be looking at, okay, I have this great band-aid, but wouldn't it be nice to actually cure this? And I think that would be, for me, to your audience, Courtney, my take-home message — which is always look for the root cause, because it is possible that we will find that root cause, and you won't have whatever name you've been given, depression, anxiety, OCD, for the rest of your earthly life. Maybe.And I've treated thousands of people successfully here. So this is not — I've had one or two successes here — we're talking thousands of people that have responded to this way of practicing medicine, with fabulous results. People who've been literally bedridden, incapacitated by their illness, are now out there working again and being with their family and living full lives. So that's the take-home message.Courtney: Right. Which makes it so satisfying to treat. And I mean, I can speak to that, having experienced it personally. But at the same time, you do get pushback from other areas of medicine that don't give it necessarily credibility, even though people, on the other side, are thriving and healing, and it's really amazing.New Medical Ideas & Research Take Decades to Reach Patients19:30Neil: You know, the history of all science, including medicine, is: new technology, new drugs are fast-tracked to get into our lives. Ideas, not so much. Typically it takes a generation — twenty, twenty-five years — for a new idea to come into acceptance. And the first reaction of any science, medicine included, is to get into denial, which is, “There isn't enough data to support this concept, and I can't be perceived as practicing bad medicine by embracing a concept that isn't proven yet.” But that means that all of their patients are going to have to wait twenty years — until suffering — until that person goes, “Now there's enough evidence, now I can learn how to do this, and now I'll begin to help you.” I'm not wired that way. I'm wired that if I have a suffering person, and I have something that I can offer them that might help, I'm going to try it. I'm going to do it in the safest way I know how, but I can't leave someone dangling for twenty years and say, “I'm sorry, I have to wait until my profession figures out what to do.” That's not me.I worked at the medical school at the University of Minnesota Duluth for eleven years. And I was not only on the faculty, but I was on the committee that determined what new information was put into the curriculum. For example, AIDS was just coming into vogue at that particular point, and it was obvious that we needed to have courses on AIDS for the medical students, because this was big. What a lot of people wouldn't understand is that each department in a medical school fiercely guards its time allotment. Everyone gets a certain number of hours, and they're not open to adding new things or giving up any of their time slots for anything new. And so what I would watch is, as new information came into the medical school, each department fiercely refused to add any new lectures in their department, or give up any of the time that they had to anybody else to add that information. So we're talking about university politics now — this is not even medicine, this is people guarding their turf. And I don't even think that would occur to any consumers, that that would happen like that — well, certainly, why would that happen in a medical school? Well, it's because human beings are responsible for each department, and they guard their own turf. So it's a kind of an insidious process about how new information isn't embraced by the profession, to go into the medical school curriculum.Mold, Lyme, and Long-COVID: The “Big Three”23:15Courtney: I want to come back to what you were saying about inflammation being at the core of chronic illness and complex chronic illness. And when it comes to complex chronic illness, whether it's SIRS or mast cell activation from mold or Lyme, we talk about multiple systems being affected — the central nervous system, gastrointestinal tract, endocrine, skin, just you name it. If the inflammation then is from a source of oxidative stress or a major insult — would you say that mold toxicity is the most common, or would you put Lyme or now even COVID on a par with that, as far as the deepest roots causing the inflammation? Not that the chemicals, metals, and everything else we're being exposed to aren't at play.Neil: In my experience, those three are the biggies — mold toxicity, Lyme with its co-infections, and long-haul COVID. Those are the three most common. Of those, in my experience, mold is the most common, and the one that has to be treated first if you have some or all of them. So, for example, in people who have long-haul COVID or Lyme, often their body will not respond to that treatment optimally until you first get the mold out. So there's a little hierarchy of what we do, in what order. And then within that hierarchy, there's also an order in which we do things for people to respond optimally. So, for example, mold toxicity will trigger — and Lyme and Bartonella will do the same thing — limbic dysfunction, vagal nerve dysfunction, and mast cell activation in most of our patients. Not all, but in most. And the longer they have it, the more likely those things are going to get triggered. Once somebody does not feel safe — and the systems that we have in our body to monitor that safety and to keep us safe are the limbic system, the vagal system, and mast cell activation — we have to get the body safer, or it will not be able to take what you need to take to treat mold or Lyme or long-haul COVID. People will literally shut down — their limbic system will essentially go, “Mm, I see what you're trying to do there, and I can't let you do it, because I'm not sure that's safe.” And it will literally not allow people to do it.The Limbic-Vagal-Mast Cell “Trifecta”25:58Courtney: So with one of those, or a combination of those, on board, these threat mechanisms would be kicked up — mast cell activation, limbic system dysfunction, autonomic nervous system dysfunction. If they look similar, or a timeline isn't easily helping parse out what might be primary, how able do you feel to make the distinction — versus if mold is present, starting there?Neil: If we look at our patient's symptoms, they will point us clearly to whether there's a limbic or vagal or mast cell piece, to be specific. The limbic system's job involves primarily monitoring and regulating and keeping emotion and sensitivity in check. So any symptoms that involve those two things are limbic almost by definition. So on the sensitivity side, if someone describes an increased sensitivity to light, sound, touch, smell, chemicals, EMFs, food — they're already telling me my limbic system is dysfunctional. In some ways it doesn't matter what the cause is; if someone has this increased sensitivity, regardless of the cause, I know we have to treat their limbic system first.On the vagal side, the symptoms would primarily run into symptoms that involve the autonomic nervous system, which would involve things like temperature dysregulation, palpitations, insomnia, POTS, blood pressure dysregulation, or symptoms that involve the gastrointestinal tract, because the vagus nerve controls almost the entire intestinal tract. So any GI symptoms — gas, bloating, distension, reflux, diarrhea, constipation, abdominal pain — again, that would lead me to go, the vagus is involved here. So by listening to my patient's symptoms, I can immediately know what's dysregulated here, and what my first treatment arm will be — to get the limbic and vagal systems back up and running again at a safer level, because otherwise our patients aren't going anywhere. They can do binders and antifungals and antibiotics for Lyme, and they will get worse. Their body will basically go, “I know I might need that, but why are you doing that? I can't even get to a place of safety to respond. I'm on self-preservation mode here.”And in the mast cell category — again, all of the same symptoms that could be mold or Lyme or long-haul COVID could also be mast cell. Again, it's a multi-systemic process. A tip-off, which I find very helpful, is if someone describes a symptom that comes on immediately after eating, sometimes while eating. Nothing causes that kind of reaction that fast except mast cell activation. Allergy — and most people, if they do have some symptom that comes after eating, they're going to be thinking, “It must be what I ate, what did I just eat?” But it's not food allergy, it's mast cell activation. In that context, many of our patients have already observed that they can eat a particular food one day and have a very strong reaction, and the next day, same food, nothing. And they'll go, “That doesn't make sense — if this was allergy, I ought to react the same way every time.” And so that is classical mast cell activation, which fluctuates. So — for the first part of your question — that's what I'm looking for. When I take a history, when I talk with patients, I'm going to really dig into: are they already manifesting symptoms that clearly tell me what we need to do first, to get them safer, so that now they can respond properly to the treatment that will really get at their root cause.Are Some People Born More Vulnerable?30:31Courtney: I know you take deep timelines when you meet with someone, so you're really accounting for a lot. But one of the things that I think about a lot is: who is most vulnerable? Do some of us come into the world already with a vulnerability similar to Elaine Aron's highly sensitive person model? And then maybe there's trauma, early attachment disruption — and already vulnerabilities — but then the toxic load that we're all experiencing. But then something like mold or Lyme then hits. And then, all the years and all the patients you've seen — I'm curious how many you feel already had sort of a vulnerability. Not that they ever had to really become sick necessarily, but already had a vulnerability.Neil: Honestly, I would say most. Our limbic system evolves from the time we were in our mother's uterus, so that almost no one has had a perfect childhood. And so whatever someone has had to deal with in childhood — it could be recurrent ear infections or throat infections, or it could be a surgical procedure, or it could be parents, both of whom worked and they didn't get enough time, or they could be abusive parents, sexually, physically, verbally abusive — whatever someone has been exposed to, that forces their limbic system to have to deal with it. Because that's the job of the limbic system, is to keep you safe. So your limbic system is basically going, “Okay, I'm just a little thing here, what do I need to do to cope with this?” And so their limbic system slowly, inexorably, becomes more and more hypervigilant to protect them. Let's say someone had an alcoholic parent, and they would come home, and you were never sure what their status would be — and so you'd kind of hold yourself back from that, which is, “I've got to see what this person is showing me, is it safe for me to come up and give them a hug, or do I want to hang out in my room for a bit until whatever this is settles down?” That's the beginning of this limbic hypervigilance process. And then it just goes on through life. So that if you've had difficult relationships, or surgeries, or severe infections, or anything in the physical or emotional or spiritual plane, a betrayal of some type — the limbic system becomes slowly more and more and more hypervigilant, when the straw hits the camel's back. And that straw could be COVID, or Lyme, or mold toxicity, or another infection of some type — that's the straw that breaks the camel's back. At that point the limbic system goes into shutdown, which — we know the vagal system goes into shutdown, literally, that's something the vagal system is trained to do. It's “okay, we are so unsafe that I'm shutting down my systems here.” And so that predisposes to illness. But I want to tie that back to inflammation, which — a lot of people don't understand that the vagus nerve, for example, controls inflammation in the body also. There are branches of the vagus that go to the spleen, to the gut-associated lymphoid tissue, and to the thymus, all of which are major immune organs. And if the vagus is dysfunctional, inflammation can rage out of control. So again, this comes back to understanding this complexity of inflammation, and how we need to both understand it and know where it is we want to look to get at that inflammation. So there is a profound interconnected limbic-vagal-mast cell piece. Each totally connects to the other. There's an interaction between the thousand biochemical mediators that mast cells make and the nervous system itself. So I call this interconnection the trifecta, which is: you can't just treat the limbic system in a vacuum, because if you're not also looking at the vagal and mast cell system, your treatment may be a little bit helpful, or it might not even work at all, until you combine all three — so that you really understand this is a package deal here, in terms of how we work with it.There was one more piece I wanted to add, Courtney, to understanding the inflammation piece: whether or not someone gets mold toxicity or Lyme or COVID depends on how robust their immune system is. So you could have a family living in a moldy environment — one person is really sick, several are a little bit sick, and one is not sick at all. And the one who's not sick at all can easily go, “I'm not sure what's wrong with you all, but I'm fine in this environment, it can't be my environment because I'm fine.” And what they're not understanding is: yes, they are fine, as long as their immune system stays robust. For the others, they were at risk for all of these conditions because their immune system took a hit. And for many people who were living in a moldy environment, during COVID, for example, when we isolated and people were spending twenty-four hours in their home rather than the eight hours out, they were many now being exposed to more mold at home than they were before. I don't think people began to think about that or look at that. So in that environment, whether or not they were affected depends on the hit they took. Now, the things that will hit an immune system to weaken it, and allow whatever's there to manifest, are: COVID was a biggie, any severe infection, a surgical procedure, childbirth, menopause, or any emotional upheaval will weaken that immune system, and then the immune system loses containment, and now we are off to the races. So what I try to convince people who are living in a moldy environment who are well is that they're living with a ticking time bomb. Should they take an immune hit, they will be just as sick as their family member who they're kind of lording it over, which is, “I'm not sick, what's wrong with you?” You'll be right there yourself if you take that hit — to try to help them understand, yeah, you're okay for now, but once your immune system weakens. So I'm trying to tie together the immune system, its ability to regulate inflammation, and this whole process here.Courtney: Right, right. Which I guess is why we call it complex, complex illness.Neil: It is the way human beings are. We're not making up a new word of complex illness — illness was always complex. We're just beginning to understand how complex it always has been.The Limits of Treating Symptoms Alone44:39Courtney: Right, so there's communities out there addressing mast cell activation. There's communities out there addressing POTS and dysautonomia. Communities out there addressing OCD and more obvious limbic-type issues. And then there's the whole mental health field. And the dots aren't getting connected. I mean, I've yet to see someone with OCD — I think it's like eighty to ninety-five percent have mold toxicity as part of the picture.Neil: You know, an example — and I won't name names — is there's an eminent pediatric physician who is very well known for his work in autism, who thought he was ADD his whole life until he recognized that he had mold toxicity and started taking antifungals, and all of a sudden his brain went online and he doesn't have it anymore. So that's just a very clear example of what you're talking about. And what we are talking about is: it's absolutely essential that all people who work in the medical field, all healthcare providers, embrace this complexity, because if you're only working on a piece of it, you will help some people to a certain extent, but you will not help people optimally. I mean, that is the absolute bottom line.The understanding that mast cell activation was huge came in 2016, when Larry Afrin wrote his book, Never Bet Against Occam. It was a huge game changer. When I read his book, it was like, “My goodness, I've been missing this in my patients.” And the whole world embraced this information, so that every medical center in the country now has a mast cell activation clinic. However, they're looking at it as a single thing with a label to it, and they're treating it just that way. They have not recognized that if they don't add limbic and vagal work to it, their treatment is not going to be adequate. And so, yes, they're helping people, but absolutely not optimally. And to make it worse, very few of those clinics have recognized that what's causing mast cell activation, which absolutely needs to be treated, is mold toxicity and Lyme. So people go to these clinics and get a certain amount of help, but they're not being treated comprehensively, which is a pet peeve of mine — which is, come on, if you're going to have a clinic, understand the whole interactions of whatever name it is you're working with. If you're going to be an ENT specialist, understand everything that impacts that area. If you're going to be a cardiologist, understand everything that impacts it. And we just don't see that. We see people kind of in their little box — “No, no, I've learned this, this is what I do, this is how I work” — and it's just unfortunate that they're not looking at the bigger picture.Courtney: Right, I think add to that PANS and PANDAS, because in psychiatry, people feel like they're deep diving because they're getting to PANS and PANDAS. It's like, okay, you've got to go deeper than that, because even those conferences, they talk about the need for treating relapse, and it's just going to keep reoccurring.Neil: I mean, they're using IVIG to help. That's nice, but they're not getting to cause. And we know when PANS and PANDAS first emerged on the scene, it was all about strep, and that was the focus for a long time. But as time emerged, it was very clear that this was a neurological inflammation triggered — here we go, broken record — Lyme, mold, other infectious agents had to be looked for. And if we treated those, you could cure PANS. It wasn't something that needed IVIG for the rest of your earthly life.Courtney: Even among those, would you say very often mold is underlying the mycoplasma, the candida?Neil: I think mold is one of the most missed components to illness that I can think of. If I have a goal in life, it would be to raise the consciousness of our profession as to the importance of mold toxicity, how common it is. We're talking millions and millions of people who are not diagnosed, because their doctors don't know about it, and therefore are not making the diagnosis. I'd love to see the consciousness get to the point that someone would present with these complicated stories and a doctor would say, “Why don't we think about mold toxicity?” That would be the most important thing I would have done in my career.Courtney: Yeah, well, you're certainly raising awareness.Neil: I'm working — it is slow. As we said, I'm working on a twenty-year generational issue here.Courtney: You've mentioned that the underlying source needs to be addressed, but the nervous system and immune systems need to be addressed. So one of the things that comes up with limbic system retraining is: I've had people hear the message that if they just address their limbic and autonomic nervous system, then they wouldn't need to address what I see as an ongoing threat, such as a mold toxin. So I'm hoping you can speak to that, and the importance of these programs, despite that.Neil: Sure. A couple of the better-known limbic retraining programs, the coaches get a little bit zealous about — “limbic retraining is so important, this is all you need to do alone, don't even do anything else, just do limbic retraining.” And I suspect that there are a handful, very few, but a handful of people who've gotten well just doing limbic retraining. If, for example, if you had mold toxicity, if it was relatively new, if you had not colonized, and you moved out of your mold exposure soon, it is possible that the limbic retraining would help reboot it to the point that your immune system rebooted itself and you'd be fine. I believe there are a few people like that. The vast majority of people who have limbic dysfunction — you need to do limbic retraining and vagal retraining. You may also need to do mast cell retraining, and please look for the cause of that. Those are downstream effects, those are not named diagnoses that you treat alone and it fixes it. Please look for at least mold and Lyme, which are the two most common things that are triggering this at this point. And people are getting the wrong message if they think they need to do it in a vacuum. To make it worse, they're being told, “No, no, just do limbic retraining, that's all you need.” And the truth is, no, you need to combine limbic retraining and vagal rebooting and mast cell activation most of the time. And of course you've got to get back to cause.Courtney: Right, I mean I try to liken it to — if they were in an abusive relationship or toxic relationship, they wouldn't just limbic-system their way out of that, if there was an external threat.Biochemical Contributors47:35Neil: No, you've got to fix what's primary here. I want to add to this discussion — we're focusing on inflammation from toxins and infections, but there are also other biochemical issues, some of them downstream, that need to be looked for and addressed in order for people to recover completely. So, for example, Lyme and mold will trigger kryptopyrrole issues, or imbalances in the ratio between zinc and copper, or they'll trigger methylation issues super commonly. And I just wanted to expand this discussion — I know it's complicated enough, but I don't want to oversimplify it either — that there are other biochemical things that we want to be looking for, because they're treatable, and they will help people to heal faster, if we're also addressing methylation, the need for zinc, the need for magnesium or B6 — those are common components of this whole process here. And so I just want to kind of tie that all together for a moment.Courtney: No, I'm glad you did, because those are topics that I talk about here, so it's important to connect those. The other thing I see, because I integrate the Walsh approaches with treating people that have complex health issues, is zinc seems so amazing when it comes to mast cell activation — making sure that's optimized. As well as connective tissue — and that was something else I wanted to ask you about — is structural issues that can be impacting the autonomic nervous system. I just see a lot of people — I inquire about it because I had it myself — but who have upper cervical instability as part of this whole picture.Structural Contributors49:26Neil: Again, all of these things are interrelated, and the physical structure can prevent people from moving forward in several different ways. One is the structure of the jaw and the face — the body puts a priority on teeth occluding properly. And if the teeth don't meet just quite right, and the jaw is a little bit out of structure, people often talk about TMJ — the body basically freaks out, it goes into sympathetic overdrive. And for some patients — it's not common, but I've seen several dozen — where the jaw had to be realigned by a combination of dentists specially trained in this work, working with osteopathic physicians, to realign the jaw. Often in those patients, they couldn't respond to the limbic and vagal treatment until their jaw got realigned.Same thing is true with what you're talking about, as cervical cranial instability, which is basically a weakening of the ligaments at the base of the skull, where it attaches to the first cervical vertebra. Now, these are all again intertwined — for example, it begs the question of what weakens those ligaments. And the answer is: if you have mast cell activation, some of the materials that the mast cell makes weakens the ligaments. So the ligaments get weak, and where the skull attaches to the first cervical vertebra, instead of being pulled apart, like ligaments do, it collapses. And that influences the blood flow to the brain, the nerve flow to the brain. And again, the body recognizes that as a priority, and often you can't get that better — you can't get limbic and vagal response until that gets fixed.So there are a bunch of structural issues that also need to be looked at, when people become overly sensitive and are not responding properly. And there's more in that area. So, for example, there's a chapter by Tasha Turzo, who's an expert on the jaw structure. There's a chapter in there by Andy Maxwell on cervical cranial instability. So that book would give people a really good overview of how complicated things are, and they might, chapter by chapter, get a clue of, “I haven't looked at this piece yet.” I mean, we haven't talked about oxalate or salicylate imbalances, which can add to that. So I just think that is a resource for folks that could really help them understand how they've gotten where they are, and understand the path out.Courtney: Right, right, because not everyone has all of these areas, but certainly could be held back or have a unique something that they could be getting relief from early on in the process. So I think it's both, to the degree that people are able to learn, and your book Toxic, too — it's like an encyclopedia, even if someone doesn't read straight through it, they can go to the mast cell section, or they can go to the Bartonella section.Neil: It was intended to be a readable way to understand this complexity, because it basically will talk about almost everything we've talked about today, and help people to get better understanding. I mean, we've talked about the bigger picture today. We didn't talk about, okay, how do you diagnose Lyme, how do you diagnose mold toxicity, how do you diagnose long-haul COVID, and most important, because this is very complicated, how do you decide which of those is the biggest player that you want to address first?Distinguishing Between Mold, Lyme & Long-COVID53:58Courtney: Right, I have shared resources on diagnosing mold toxicity. Would you comment on your last point — how do you recognize, are you using specific testing that you want to reference, the RealTime?Neil: I do. But I would emphasize, we're taught in medical school that if you really listen to patients, ninety-five percent of the time you will make the diagnosis by history alone. And I don't want to get too focused on testing, because listening to the patient and having them describe in detail what they're going through will really give you the little pieces you need to tease it apart to a certain degree. That's only possible to a certain degree, because there's a huge overlap between the symptoms of Lyme and Bartonella and mold and long-haul COVID and mast cell activation. Huge overlap. So there's little teeny pieces that will tend to lean more in one way than another. And honestly, that's what's required from all of us, literally years of study, to really get a handle on — someone will say something, okay, that's much more of a mold symptom than it is a Lyme symptom, something else. So I do encourage people, if they think they might have mold, to get a urine mycotoxin test. That has revolutionized our ability to make these diagnoses.Courtney: Would you still set RealTime as the preferred? That's what I've communicated to this audience.Neil: I would. Any test can help make the diagnosis, but for follow-up testing, the only one that's been really consistent is RealTime. And you want a follow-up test, so you want to know what your baseline starting is, and then you want to know, okay, am I getting these toxins out of my body? From my perspective, you know that you're done treating it when that RealTime comes back reading not present in every category. We have better tests now for Lyme than we've had in the past. Years ago, our tests were inadequate to say the least. And the CDC recognized years ago that the tests were so inadequate that it was basically a diagnosis made by a physician by examining all of the history and information that you had. That was enough — you didn't need a lab report to make the diagnosis of Lyme disease. A new test that I'm particularly fond of is Bruce Patterson's fourteen-panel cytokine test. This is a test that measures cytokines, which are the molecules of inflammation — cytokines are made by your immune system to deal with, or fight, different inflammational causes. And so what Dr. Patterson has discovered is there's a pattern of cytokines that we see with long-haul COVID, which is different than the pattern we see for Lyme. And I'm working with him now on the pattern for mold. So we can literally look at that test and look at, okay, what is inflaming this person primarily now, because I'm looking at that inflammational pattern, and I can literally read that. Some of my patients will have all of those on a particular test, or only one, but it really helps tease apart what is — I call it public enemy number one for my patient, what do I need to address as root cause right now. So our science is improving as we go here.A Message of Hope — and Where to Learn More58:49Courtney: And that's huge. Before we go — I think all of your books, but I'm thinking specifically about Toxic and The Sensitive Patient — all the information you generously share gives people a lot of hope who've been struggling out there. And I think your mentoring and teaching so many of us helps extend some of that reach. Is there anything you'd want to convey to people out there in the throes of chronic illness who are feeling hopeless and not getting the feedback from their doctors that this is something they can get beyond?Neil: Sure. My take-home message is always: everything we talked about today is treatable. Is there hope in there? You bet there is. But if you are not getting the help you need from whoever you are seeing, find someone who understands these things. For example, I do have on my website a list of physicians that I've trained over the years that I'm comfortable that they really know what they're doing — it's a growing list. There's someone like Courtney, who's been trained for years to do this, she's good at it. Find someone who knows what they're talking about, so that you can get someone who does embrace this complexity, and will look at it in its entirety, and then get you moving in the right direction, doing the right things in the right order. To me, this can be done. I mean, I have personally helped to cure four or five thousand people with mold toxicity, and an equal number of people with Lyme disease. So we can help the vast majority of people that we're seeing. So, regardless of how long you've been sick, if you haven't been properly diagnosed and you haven't gotten the right treatment, you can be helped.Courtney: Right, right, that's great. And for physicians out there who are interested in learning more about complex chronic illness — are there resources you would point to? I'll be sharing your books, because I think those are great references — but also how people can find what you're doing currently.Neil: Sure, my books — particularly with this discussion, Toxic and The Sensitive Patient's Healing Guide would be the two most appropriate. I would add that I have just finished writing a book on this whole subject of inflammation. It's currently being edited, I hope it'll be out by early next year. So if you stay tuned to my website, I'll let people know when that's going to be available. And I think, Courtney, what you're referring to is: I do have a mentorship program for healthcare providers. We now have three hundred and fifty-plus people in the mentorship program, it keeps growing. You were in one of the first groups — we started with eight, and then people kept wanting to get in on it. So we welcome people to join. If you go to my website, which is simply neilnathanmd.com, there's a whole thing which talks about the mentorship and how to sign up for it. So I certainly welcome people who want to learn more.Courtney: And then you offer consultations and professional consultations also?Neil: I do. My consultations — I am, at this point, since I'm semi-retired, not seeing people directly. But I do offer consultations with a patient and their primary treating physician — so we all get on a Zoom together, and we will go over the details of that person's history and their lab work, and I will help outline a treatment program that looks to me like it will get people well. And actually, Courtney, I actually do a lot of that — I'm not really retired, my wife will tell you. I stay pretty busy. I love helping people. I love being able to take this complicated information and tease it apart, so that I can help people to understand what they need to do, in what order, in order to get better.Courtney: And we're all grateful — grateful that you've followed your path, because so many people have benefited personally and professionally. So thank you for bringing your wisdom and expertise, really appreciate it.Neil: You're very welcome, happy to do that.You can find Dr. Nathan's information, consultations, and mentoring program through his website at neilnathanmd.com. If you'd like to help get this information out into the world, please consider liking, sharing, or commenting.Until next time,CourtneyCourtney Snyder MDDr. Courtney Snyder MD is a holistic, functional, and environmental psychiatrist for children and adults. Find her at courtneysnydermd.com and on the Holistic Psychiatry Podcast on all major platforms.Medical DisclaimerThis podcast is for educational purposes only and is not intended or implied to be a substitute for professional medical advice, diagnosis, or treatment. Consult your own physician for any medical issues you may be having. This is a public episode. If you would like to discuss this with other subscribers or get access to bonus episodes, visit courtneysnydermd.substack.com

Send us Fan MailWhat if you could have an infection, already be experiencing symptoms, and yet the diagnostic test could still tell you that you're negative? That's one of the central challenges of Lyme disease - and today we're going inside the biology and technology behind the race to detect it earlier.Dr. Joseph J. Burrascano Jr., M.D., is a physician and longtime researcher who has spent more than three decades focused on Lyme disease and other tick-borne infections.A graduate of NYU School of Medicine and trained in internal medicine, Dr. Burrascano spent approximately 25 years in primary care before leaving clinical practice and moving into biotechnology and research. He has been deeply involved in the Lyme disease field since the 1980s, is a founding member of the International Lyme and Associated Diseases Society, or ILADS ( https://www.ilads.org/ ), and has continued to educate physicians around the world about the diagnosis and management of Lyme and associated infections.Dr. Burrascano has also been involved in the development and evaluation of diagnostic technologies and currently serves as a consultant and scientific advisor to IGeneX ( https://igenex.com/ ).And that's particularly relevant to our conversation today.A recently published study in Microbiology Spectrum evaluated FDA-cleared single-step immunoblot tests developed by IGeneX and compared them with conventional standard two-tier testing.In one analysis of early-stage Lyme disease, the immunoblot approach detected antibodies in 58.3% of samples compared with 30.0% for standard two-tier testing. The researchers also reported very high specificity and performed additional discrepancy analysis on samples that produced different results between the methods.So today we're going to step back and ask a fundamental question:How good are we really at detecting Lyme disease - especially during the window when treatment may be most effective?We'll talk about what Lyme actually does inside the body, why early diagnosis can be so difficult, what today's tests are actually measuring, what an immunoblot adds to the diagnostic process, how we should interpret sensitivity versus specificity, and where Lyme diagnostics may be headed next.#LymeDisease #Lyme #LymeDiseaseAwareness #TickBorneDisease #TickBorneIllness #LymeTesting #LymeDiagnostics #Borrelia #InfectiousDisease #MedicalDiagnostics #Biotechnology #Diagnostics #Immunology #PublicHealth #PrecisionMedicine #MedicalResearch #HealthTechnology #ProgressPotentialAndPossibilitiesSupport the show

What if the test that diagnosed your Lyme disease, and the theory behind it, was never actually proven in the first place?In this episode of Integrative Lyme Solutions, Dr. K sits down with Dr. Thomas Cowan, a physician and author of The Contagion Myth, for a conversation that questions one of the most basic assumptions in the Lyme disease world: that borrelia has actually been shown to cause the illness. Dr. Cowan spent years as an ER doctor before turning his attention to what he calls the unexamined foundations of modern medicine, and in this conversation he walks through why he believes the original Lyme research, the antibody tests built on it, and even the concept of an immune system itself don't hold up to the kind of scrutiny any other medical claim would require.They get into the 1980s study that first linked spirochetes to Lyme disease, why Dr. Cowan says antibody tests can't be trusted to identify anything specific, and what he does instead when a patient walks in exhausted, in pain, and carrying a diagnosis that hasn't made them any better. If you've ever been told you have chronic Lyme disease and felt like the label explained less than it promised, this conversation offers a different way to think about what's actually happening in your body.Key Takeaways:Why Dr. Thomas Cowan argues the original Lyme disease study never proved borrelia causes the illnessThe case against Lyme antibody testing: why a positive IgG or IgM result may not mean what patients are told it meansWhy long-term antibiotic use, not lingering infection, may explain chronic Lyme disease symptoms for some patientsDr. Cowan's approach to chronic illness: treating a patient's health history instead of the Lyme disease labelWhy there is no clinical definition of Lyme disease, and what that means for anyone diagnosing themselves off a bullseye rash or brain fogSchedule a Free 15-Min Cancer/Lyme Consultation at The Karlfeldt Center: 208-338-8902Resources:The New Biology Clinic - https://newbiologyclinic.com/Medical Disclaimer: This content is for educational purposes only and is not intended to diagnose, treat, cure, or replace professional medical advice. Always consult your physician or qualified healthcare provider regarding any medical condition or treatment decisions.

Learn about lyme/bartonella/coinfection testing & diagnosis with CEO of Galaxy Diagnostics, Nicole Bell.We dive into WHY standard Lyme disease testing can miss cases, what IgM and IgG antibodies can—and cannot—tell us, and how direct-detection methods such as PCR and urine antigen testing differ from ELISA, Western blot, and FISH testing.We also discuss:Why a negative Western blot does not necessarily rule out Lyme diseaseThe difference between antibody testing and direct pathogen detectionWhy testing for Borrelia, Bartonella, and Babesia mattersHow IgM cross-reactivity can complicate test interpretationPersistent infection versus post-treatment Lyme disease syndromeWhy multiple positive antibodies do not always mean multiple active infectionsThe emerging connection between infections, neuroinflammation, dementia, and cognitive declineWhy insurance coverage for advanced testing remains so difficultHow to advocate for yourself when a diagnosis does not explain your symptomsThis conversation is a powerful reminder that receiving a diagnosis does not necessarily mean you have found the root cause. Chronic fatigue syndrome, fibromyalgia, dementia, and even PCOS describe patterns of symptoms-but the bigger question is: WHY are those symptoms happening?My Website & Work with Me: Instagram: ⁠⁠⁠⁠⁠⁠www.instagram.com/faithandfit⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.upliftfitnutrition.com⁠⁠⁠⁠⁠⁠Email for coaching & phone consults: laceydunn@upliftfitnutrition.com & fitandfaith@gmail.comFind Galazy Diagnostics at: https://www.galaxydx.com

What if some of the most powerful tools for controlling chronic bacterial infections are already living inside the human body? In this episode of the Tick Boot Camp Podcast, hosts Matt Sabatello and Rich Johannesen sit down with Dr. David A. Jernigan, DNM, DC, founder of the Biologix Center for Optimum Health, for a deep exploration of Lyme disease, bacteriophages, chronic infection, biological medicine, and his development of Induced Native Phage Therapy (INPT). Dr. Jernigan has worked with people experiencing Lyme disease and complex chronic illness since the 1990s. His journey into the Lyme world began unexpectedly when a mother and her twin sons came to his Kansas practice with Lyme disease. At a time when Lyme disease knowledge was far more limited, the experience pushed him into decades of clinical work, research, writing, and experimentation focused on understanding why some patients remain chronically ill. Today, one of the central areas of his work is bacteriophages—viruses that infect bacteria—and a therapeutic model he calls Induced Native Phage Therapy. What Are Bacteriophages? Bacteriophages, commonly called phages, are viruses that infect bacteria. They exist throughout nature and are also found in enormous numbers within the human body. Unlike broad-spectrum approaches that may affect many different microorganisms, phages can have highly specific relationships with particular bacteria. During the interview, Dr. Jernigan explains the relationship between bacteria and bacteriophages and introduces listeners to the phageome—the vast community of phages living in and around the human microbiome. He describes how certain phages can enter a lytic cycle, ultimately destroying their bacterial host, while others can exist in a more dormant or lysogenic relationship with bacteria before environmental conditions trigger a change in their behavior. This bacterial-phage relationship forms the foundation for Dr. Jernigan's work with INPT. What Is Induced Native Phage Therapy (INPT)? One of the most important distinctions in this conversation is the difference between conventional phage therapy and Induced Native Phage Therapy. Traditional phage therapy generally involves identifying phages capable of attacking a particular bacterium and introducing those phages into a patient. Dr. Jernigan's approach is fundamentally different. Rather than administering externally sourced bacteriophages, INPT is designed around the idea of influencing native phages that are already present within the body. Dr. Jernigan describes his approach as using electromagnetic or bioresonance-based information intended to influence phages associated with targeted microorganisms and encourage a shift toward bacterial destruction. He explains that development of the process took approximately five years and grew out of his earlier work with bioresonance and biological medicine. Matt and Rich push Dr. Jernigan throughout the conversation to explain exactly what he believes is happening biologically, how targeted phages are distinguished from the enormous number of phages within the body, and how this approach differs from simply attempting to kill microorganisms directly. Why Phages Could Matter in Lyme Disease The discussion then turns specifically to Borrelia burgdorferi, other Borrelia species, and Lyme disease. Dr. Jernigan argues that bacteria and their associated phages have coexisted for an extraordinarily long time and that bacteria entering the human body may already exist within complex relationships with bacteriophages. Instead of searching externally for a single phage capable of targeting Borrelia, his research asks a different question: Can the phages already present within a patient or associated with a microorganism be influenced to help control that organism? That question sits at the center of INPT. The conversation also explores monovalent versus polyvalent phages, bacterial specificity, intracellular microorganisms, and the potential ability of phages to interact with bacteria residing in difficult-to-reach environments. Lyme Disease Is More Than One Infection This episode extends far beyond phage therapy. Dr. Jernigan explains how his understanding of Lyme disease has evolved dramatically since he began treating patients in the 1990s. Early in his career, much of the Lyme community was focused primarily on finding and killing Borrelia burgdorferi. Over time, he became increasingly convinced that chronic illness could not be adequately explained by one microorganism alone. He describes what he calls Multi-Microbial Activation Syndrome, a model in which Lyme disease may occur alongside or contribute to changes involving numerous microorganisms and physiological systems. The conversation explores: Borrelia burgdorferi and other Borrelia species Bartonella and Babesia Other tick-borne infections Mold and environmental exposures Microbial interactions Toxins Metabolic dysfunction Immune dysregulation Mast cell activation Inflammation Individual biological terrain This leads to one of the central themes of the episode: two people can carry similar microorganisms yet experience dramatically different levels of illness. Dr. Jernigan therefore argues that treating a diagnosis alone can miss the larger biological picture of the person experiencing the disease. Treating the Infection vs. Repairing the Damage Dr. Jernigan uses a memorable termite analogy to explain chronic Lyme disease. If termites are discovered before they have caused significant structural damage, eliminating them may largely solve the problem. But if termites have been damaging a house for years, killing the termites does not rebuild the house. The same concept, he argues, may apply to chronic illness. Reducing microbial burden may be important, but a person may still be dealing with neurological, metabolic, inflammatory, structural, immune, or other dysfunction that developed during years of illness. That distinction becomes particularly important when evaluating whether a treatment has worked. A reduction in infection does not necessarily mean that years of physiological damage or dysregulation immediately disappear. Why Every Lyme Patient May Require a Different Approach Matt and Rich discuss Tick Boot Camp's view of Lyme disease as a polymicrobial, multisystemic, chronic infectious or post-infectious illness, and Dr. Jernigan explains why his clinical experience has led him toward a similarly individualized model. Every patient enters illness with a different history, microbiome, microbial exposures, environmental exposures, physiology, and accumulated biological stress. For that reason, Dr. Jernigan challenges what he describes as "cookbook" medicine—the idea that every patient carrying the same diagnosis should receive essentially the same protocol. Instead, his model attempts to identify what is dysfunctional in the individual patient while simultaneously reducing infectious burden and supporting the body's ability to repair itself. Phages, Biofilms, and Intracellular Bacteria Another major portion of the interview explores two difficult problems in chronic infection: biofilms and intracellular bacteria. Dr. Jernigan discusses research showing that certain bacteriophages can interact with or penetrate bacterial biofilms, potentially giving phage-based approaches characteristics that differ from conventional antimicrobial strategies. The discussion also examines whether phages can reach bacteria residing inside cells. These questions are particularly relevant to Lyme disease because persistence, bacterial morphology, biofilms, tissue environments, and intracellular localization are frequently discussed as possible contributors to treatment difficulty. Dr. Jernigan explains why he believes native phages may be capable of reaching microorganisms in environments that can present challenges for other therapeutic approaches. Herxheimer Reactions: Does Feeling Worse Mean Treatment Is Working? The episode also challenges one of the most familiar ideas in the Lyme community: Do patients have to feel worse before they feel better? Many Lyme patients are familiar with the Jarisch-Herxheimer reaction, often shortened to "Herxing," in which symptoms can temporarily intensify during antimicrobial treatment. Dr. Jernigan discusses his belief that effective treatment should not necessarily require significant suffering. He connects this idea to his model of phage-mediated bacterial destruction and explains why he believes INPT may behave differently from therapies that produce large amounts of inflammatory bacterial debris. Matt and Rich dig into this distinction and the potential relationship between microbial die-off, cytokines, inflammation, mast cells, and worsening symptoms. MCAS, Immune Activation, and Treatment Sensitivity The conversation also addresses why some people with chronic Lyme disease become extraordinarily sensitive to medications, supplements, foods, environmental exposures, and other treatments. Dr. Jernigan discusses macrophages, inflammatory cytokines, histamine, mast cell degranulation, and mast cell activation syndrome (MCAS) as part of the larger chronic illness picture. Rather than viewing these problems as completely separate diagnoses, he encourages looking for the biological processes that may be driving multiple downstream symptoms. This reflects another recurring theme throughout the episode: identifying and addressing upstream contributors rather than continually treating individual symptoms in isolation. Antibiotics, Resistance, and the Search for New Approaches Matt, Rich, and Dr. Jernigan also have an extended discussion about antibiotics and antimicrobial resistance. Dr. Jernigan is strongly critical of long-term reliance on antibiotics and argues that bacterial adaptation and antibiotic resistance make alternative antimicrobial strategies increasingly important. The conversation examines doxycycline, broad-spectrum antibiotics, environmental antibiotic exposure, bacterial adaptation, and why phage research has regained scientific interest as antimicrobial resistance becomes an increasingly important global challenge. Dr. Jernigan also makes an important distinction between his approach and conventional phage therapy, which itself is an active area of scientific research. Dr. Jernigan's Published INPT Research Dr. Jernigan discusses several publications related to his work, including his 2021 retrospective review of Induced Native Phage Therapy for Lyme disease and relapsing fever and subsequent work expanding the concept into treatment-resistant illnesses involving multiple microorganisms. He intentionally made his peer-reviewed publications open access so patients, practitioners, and researchers could review the work without encountering a paywall. During the interview, he also acknowledges the importance of additional independent research and the challenges involved in funding and validating emerging therapeutic approaches. INPT remains an emerging and unconventional approach. The mechanisms and clinical claims discussed in this episode should therefore be understood as Dr. Jernigan's research, hypotheses, clinical observations, and interpretations rather than established standards of Lyme disease treatment. From "Chasing Bugs" to Biological Medicine Perhaps the most important evolution in Dr. Jernigan's career is his movement away from simply "chasing bugs." His earliest Lyme work focused heavily on identifying and addressing microorganisms. After decades of treating complex patients, his philosophy expanded toward simultaneously considering two questions: What microorganisms are creating a burden, and what is preventing this particular person's body from returning to healthy function? That means considering infections alongside neurological function, metabolism, immune regulation, inflammation, environmental exposures, structural problems, the microbiome, and other biological systems. For patients who have spent years moving from treatment to treatment, that broader question may be one of the most valuable takeaways from this conversation. Topics Discussed Dr. David Jernigan's introduction to Lyme disease in the 1990s Congenital and persistent Lyme disease Early Lyme disease testing Natural and biological medicine Borrelia burgdorferi Bartonella, Babesia, and other tick-borne infections Polymicrobial illness Multi-Microbial Activation Syndrome Bacteriophages and the human phageome How bacteriophages infect bacteria Lytic and lysogenic phage cycles Conventional phage therapy Induced Native Phage Therapy (INPT) Native versus externally administered phages Monovalent and polyvalent phages Bioresonance and electromagnetic signaling Phages and bacterial biofilms Intracellular bacteria Antibiotic resistance Doxycycline and antimicrobial treatment Jarisch-Herxheimer reactions Cytokines and inflammation Macrophages and immune dysfunction MCAS and treatment sensitivity Mold and environmental illness Microbial terrain Personalized Lyme disease treatment Treating infection versus repairing physiological damage Biological and bioregulatory medicine Emerging research into phage-based therapies About Dr. David Jernigan Dr. David A. Jernigan, DNM, DC, is an author, researcher, clinician, and founder of the Biologix Center for Optimum Health in Franklin, Tennessee. He has worked with people experiencing Lyme disease and complex chronic illness for decades and has written extensively about Lyme disease, biological medicine, natural approaches to chronic illness, bacteriophages, and related topics. His more recent research has focused on Induced Native Phage Therapy, an approach designed to influence naturally occurring bacteriophages within the body rather than administering externally sourced phages. Learn more about Dr. David Jernigan, INPT, his Lyme disease work, publications, and the Biologix Center. Work With Dr. David Jernigan Patients interested in learning more about Dr. Jernigan, the Biologix Center for Optimum Health, and opportunities to work with him can visit: Biologix Center for Optimum Health – Dr. David Jernigan INPT Information for Doctors and Healthcare Providers Healthcare professionals interested in learning more about Induced Native Phage Therapy or becoming an INPT provider can visit PhaGenCorp: PhaGenCorp – Induced Native Phage Therapy Learn More About Lyme Disease Explore more Tick Boot Camp conversations with physicians working with Lyme disease and complex tick-borne illness: Tick Boot Camp Doctors

Anne Desjardins is a Lyme disease survivor, educator, podcaster and holistic health practitioner.She is also the creator of The Silver Lyming, a podcast and educational resource focused on Lyme disease and tick-borne illness, providing information, hope and practical guidance for people navigating their own health journeys. Her life was dramatically changed by a tick-borne illness that left her battling crippling fatigue, neurological symptoms, insomnia, cognitive problems and a loss of normal physical function. This became a seven-year search for answers, during which she was repeatedly told that nothing was wrong, eventually reaching a point where she feared she was dying. After finally receiving a Lyme diagnosis and beginning treatment, Anne began the long process of rebuilding her health and understanding the relationship between infection, the nervous system, stress, lifestyle and mental wellbeing. What emerged from that experience was a new purpose: using what she had learned to help others who find themselves facing the same uncertainty and isolation.Anne opens up about the darkest and most confronting parts of her journey, including the financial and emotional cost of years of treatment, the hypervigilance that followed repeated tick exposure, and the point where she seriously considered taking her own life. We discuss resilience, faith, intuition, personal responsibility and the importance of listening to yourself when conventional answers don't explain what you are experiencing. Anne explains how supportive communities and connecting with people who had walked similar paths helped her regain hope, and how she ultimately transformed her own struggle into an opportunity to educate and support others.Her story is ultimately about refusing to give up when the answers aren't obvious, finding the strength to keep searching, and recognising that sometimes the experience that nearly breaks you can become the foundation for your next mission.Today, Anne works with individuals through personalised programmes focused on rebuilding the nervous system, gut health and healthier relationships with themselves. I hope you enjoy this show as much as I did- Anne shares not only what she learned from surviving Lyme disease, but what she discovered about resilience, purpose and rebuilding a life after believing she might never get her health back.

What happens when a young woman who grew up surrounded by horses and the outdoors develops a mysterious red ring after spending a summer working at a horse camp in West Virginia—but no one recognizes the possibility of Lyme disease? In this episode of the Tick Boot Camp Podcast, we sit down with Hannah Green, a Lyme disease survivor, advocate, and author from England whose international Lyme journey stretches across the United Kingdom, United States, and Australia. Hannah is the author of My Lyme Success Story, a book documenting her personal experience with chronic Lyme disease, the research she conducted while searching for answers, the approaches she believes helped her recover, and the lessons she learned about listening to her body along the way. Tick Boot Camp first met Hannah after she traveled from England to Connecticut for the Lyme Warrior 10th Anniversary Gala, where patients, researchers, clinicians, authors, advocates, and Lyme community leaders gathered for an evening centered on science, advocacy, connection, and hope. Hannah's story is ultimately about much more than one treatment or protocol. It is about missed warning signs, years without answers, becoming her own researcher, learning to trust herself again, and refusing to give up on the possibility of getting better. Growing Up Around Horses—but Knowing Almost Nothing About Ticks Hannah grew up in southeast England and spent much of her childhood outdoors. Horses became one of her greatest passions, and she eventually trained professionally in riding, horse management, dressage, and eventing. She was also deeply interested in animal health. Hannah spent time working around veterinary medicine and learned about fleas, lice, worms, botflies, equine influenza, strangles, and other conditions affecting horses. Yet one subject was almost completely absent from her education: ticks and Lyme disease. Despite spending years around horses, dogs, cats, veterinary environments, fields, and the English countryside, Hannah remembers receiving virtually no meaningful education about ticks or the infections they can transmit. The West Virginia Horse Camp and Hannah's Possible Lyme Exposure At approximately 19 years old, Hannah traveled alone from England to the United States to work as a riding counselor at a horse camp in West Virginia near the Blue Ridge Mountains. It was a major adventure for someone who describes herself at that age as extremely shy. Hannah suddenly found herself responsible for a cabin of young campers while teaching multiple horseback riding lessons each day. She loved the experience. But the camp also introduced Hannah to something she had never encountered before: ticks. Hannah remembers discovering engorged ticks attached to horses grazing in long grass. After asking what they were, she and other staff members were shown how to remove them. Removing ticks from the horses soon became part of their regular routine. What Hannah does not remember receiving was comprehensive education connecting those ticks with the potential risk of Lyme disease in humans. She recalls being warned about hazards such as poison ivy and rattlesnakes, but she does not remember meaningful tick-bite prevention training for counselors or campers. There was a Lyme disease pamphlet in the staff area, but the information Hannah remembers most strongly involved severe neurological complications such as seizures and paralysis. She did not come away understanding the broad range of symptoms that could develop or recognizing how important an expanding rash could be. The Red Ring That Was Dismissed as a Spider Bite Years later, while reconstructing her medical history after finally learning about Lyme disease, Hannah remembered something important from that summer. She had developed a distinctive red ring on her lower leg. At the time, Hannah says someone told her that it was probably a spider bite and that she should simply keep the area clean and watch it. The rash did not significantly hurt or itch, and it eventually disappeared. No one, according to Hannah's recollection, asked whether she might have been bitten by a tick. She did not connect the rash with the ticks she had been routinely removing from horses, and she did not connect it with the Lyme disease pamphlet she had briefly seen. Hannah believes today that this may have been the event that began her Lyme disease journey. For practical prevention and early-action information, read the Tick Boot Camp Tick Bite Blueprint. The First Sign Something Was Wrong Hannah initially remained extremely healthy and active after leaving the United States. She returned to England and attended Aston Business School near Birmingham. But approximately six months after her time at camp, she began noticing unusual problems with her knees. She was a runner and initially assumed she had simply overtrained. Her knees would ache and sometimes lock, particularly when walking down gentle slopes or moving at certain angles. Cold weather could make the discomfort worse. Because Hannah had been a competitive runner and lifelong equestrian athlete, healthcare professionals often attributed the symptoms to physical activity and wear and tear. She was told variations of the same explanation: runner's knee, overuse, muscle imbalance, or consequences of years of athletic activity. Yet Hannah was still a young woman, and the symptoms continued. Over time, joint problems began appearing elsewhere. Her elbows became involved. Her lower back became increasingly problematic. A diagnosis of scoliosis provided another seemingly logical explanation for some of her pain. Hannah kept adapting and pushing forward. She even completed the London Marathon, although afterward her knees became so painful and locked that she struggled to walk normally for approximately a week. When Her Health Finally Collapsed After university, Hannah continued traveling internationally, including spending time in Borneo and eventually completing a round-the-world trip. Then, around 2006, everything changed. After developing what appeared to be a significant viral illness, Hannah says she never fully recovered. Her shoulder became extremely painful and effectively froze. What followed was no longer an isolated problem with her knees or back. Hannah describes developing a growing collection of debilitating symptoms that included: Severe fatigue and exhaustion Joint and musculoskeletal pain Digestive problems Insomnia Anxiety Depression Episodes of intense anger or rage Memory problems Progressively worsening neurological and systemic symptoms Difficulty maintaining normal work and daily activities She describes the illness as feeling like a combination of flu, glandular fever, and malaria. Instead of resolving, her symptoms continued getting worse for approximately six years. Trying to Keep Working While Becoming Increasingly Ill Hannah attempted to continue working despite her deteriorating health. She worked with horses and also painted portraits professionally, but even limited morning work became increasingly difficult because of overwhelming fatigue. She frequently needed time off and struggled to explain what was happening because she did not understand it herself. Later, while working in a tea shop, Hannah began noticing that her memory was also being affected. She describes 30 or 40 symptoms gradually accumulating, with insomnia, chronic fatigue, and mood changes becoming some of the most difficult to manage. Meanwhile, repeated medical testing failed to provide an explanation. Several doctors told Hannah that her results were normal and that they could not find anything wrong. She says she did not necessarily feel directly accused of imagining her illness, but over time it became easier to stop discussing what she was experiencing because she felt that people were not truly hearing her. Moving to Australia While Searching for Answers Hannah eventually moved to Australia, hoping that a different environment and lifestyle might improve her health. She would spend approximately a decade there. Initially, the excitement of the move helped her keep going. She settled in tropical Darwin and started a graphic design company. Then her health crashed again. During the first wet season, Hannah became severely ill and spent significant periods in bed. Eventually, even working a few hours per day from home became too difficult, and she had to close the company she had built. She developed severe food reactions and describes being bedridden for seven to ten days at a time. Her relationship also ended during this period. Hannah describes eventually losing her business, her apartment, her ability to ride horses, much of her independence, and a significant amount of weight. At her lowest point, she says she would sometimes visit the stables and simply hold herself against a rail while watching the horses because she no longer had the strength to ride or even interact with them normally. The Chance Conversation That Changed Everything One day at the stables, another person noticed how ill Hannah had become. Hannah explained what was happening, and the woman told her about another horse rider with similar symptoms who was seeing a doctor who periodically traveled from Perth to Darwin to work with patients experiencing chronic fatigue and unexplained illness. Hannah and the other woman both scheduled appointments. After reviewing Hannah's extensive symptoms, the physician told her he believed she had late-stage Lyme disease. Hannah says subsequent testing through Australian Biologics was positive for Borrelia. The diagnosis triggered a flood of memories—the ticks on the horses, the pamphlet in West Virginia, and the unexplained red ring on her leg years earlier. For the first time, Hannah felt that the scattered pieces of her story might belong to the same puzzle. Lyme Disease, Co-Infections, and Alternative Testing Hannah continued exploring her illness through a combination of conventional and alternative approaches. She describes undergoing PCR testing through Australian Biologics as well as bioresonance and autonomic response testing. During the interview, Hannah says these alternative assessments suggested possible Borrelia strains, co-infections, active viruses, heavy metals, parasites, yeast overgrowth, gut inflammation, and other abnormalities. Among the infections discussed during her journey were Borrelia, Bartonella, Babesia, Rickettsia, Ehrlichia, Anaplasma, and Chlamydia, as well as viral findings including Epstein-Barr virus. It is important to distinguish Hannah's personal experience from established clinical diagnostic standards. Bioresonance and autonomic response testing are not established replacements for validated medical testing for Lyme disease or tick-borne infections. Hannah is sharing what practitioners told her and how those results influenced her personal recovery decisions. Choosing a Different Lyme Treatment Path After receiving her Lyme diagnosis, Hannah says the physician treating her wanted to begin an aggressive multi-antibiotic protocol. Hannah decided not to pursue that approach. She was already extremely weak, her digestive system was severely affected, and she was concerned about medication side effects. Instead, she asked whether there were other options and ultimately chose to spend several months researching Lyme disease treatment approaches around the world. Her family and friends were frightened by the decision, but Hannah says she felt strongly that she needed to find a different path for herself. That decision became the beginning of the recovery strategy she would later document in My Lyme Success Story. Building a Staged, Whole-Person Recovery Plan Hannah describes her recovery not as one treatment, but as a staged process. Working with naturopathic practitioners and combining their guidance with her own research, she focused first on what she describes as improving her body's overall terrain before directly targeting Lyme and co-infections. Her personal strategy included: Reducing environmental stressors Simplifying her lifestyle Changing her diet Supporting gut health Addressing issues practitioners identified as heavy metals and parasites Reducing inflammation Using herbs and supplements Using binders and detoxification strategies Experimenting with bioresonance Meditation and nervous-system calming practices Emotional and trauma-focused work Creating an environment where she felt safe enough to recover Hannah emphasizes that the sequence mattered to her. She believes preparing her body first made it easier to tolerate later interventions. The Diet Change That Gave Her Hope Diet became one of the earliest major changes in Hannah's recovery. Based on the recommendations she was receiving at the time, she adopted a highly individualized, low-inflammatory Paleo-style diet. She says that after approximately four weeks of changing her diet and focusing on cleansing and lifestyle interventions, she felt better than she had in four years. That improvement became a major psychological turning point. For the first time in years, Hannah had tangible evidence that something she was doing might be helping. From there, she continued gradually working through the other areas she believed were contributing to her illness. Herbs, Bioresonance, and Individualized Treatment Hannah experimented extensively with herbs and natural products. She describes using BioPure Quintessence, a herbal tincture containing ingredients including Japanese knotweed and Andrographis, after another product did not feel appropriate for her. She also describes using binders and other detoxification strategies while gradually increasing the intensity of her treatment. Bioresonance became another major part of her personal approach. Hannah says she used a portable device at home for approximately six months and also used bioresonance testing to help guide decisions about foods, herbs, and supplements. She reports that, through the overall combination of approaches she was using, she went from being largely bedbound to symptom-free in approximately 11 months. That is Hannah's personal account and should not be interpreted as evidence that the same interventions will produce the same results for another person. The Story Behind Hannah's "Lyme-Busting Drink" One memorable moment in the interview involves something Hannah jokingly calls her "Lyme-busting drink." Hannah says she gathered several antimicrobial ingredients in her kitchen and intuitively selected ingredients to combine into a homemade preparation. She later took the mixture to her naturopath, who tested it using the bioresonance method they were working with. Hannah says the mixture tested strongly for her. The larger takeaway from this part of the story is not that listeners should reproduce Hannah's homemade mixture. Rather, Hannah uses the story to illustrate just how individualized and experimental her own recovery process became. She repeatedly emphasizes listening to her own body and adjusting what she was doing based on how she felt. Learning to Trust Her Body Again One of the strongest themes throughout Hannah's interview is intuition. Years of unexplained illness can cause people to question themselves, especially after repeated normal tests or medical appointments that fail to provide answers. Hannah says she never entirely lost the belief that her body was telling her something important. When she was told nothing could be found, she continued searching. When one explanation did not make sense to her, she kept looking. And once she finally received a diagnosis, she approached recovery with the same determination. Rich identifies this as one of the most powerful parts of Hannah's story: despite years of confusion and dismissal, she continued trusting her own observations enough to keep investigating. Mindset, Spirituality, and Asking for Help Hannah also describes a major shift in her mindset and spirituality. For much of her life, she had been fiercely independent and believed that she could solve any problem herself. At her sickest, that changed. Hannah remembers lying in a dark room, sometimes barely able to lift her head, and finally looking outside and simply asking for help. She describes this as a turning point. A housemate later gave her a book about the Law of Attraction and introduced her to meditation. Hannah says these ideas reawakened something she remembered from childhood: a strong belief that mindset, intention, and action could help shape the direction of her life. She began meditating regularly and eventually built up to approximately 45-minute sessions. Whether listeners share Hannah's spiritual framework or not, the interview makes clear that hope and belief became important psychological resources during a period when her physical circumstances gave her very little reason to feel optimistic. Trauma, NLP, and Emotional Healing Hannah's recovery eventually expanded into emotional and trauma-focused work. She describes exploring Neuro-Linguistic Programming, or NLP, after reflecting on experiences from earlier in her life. One particularly powerful realization involved her premature birth. Hannah was born approximately three months early and spent significant time in an incubator, separated from her mother. During a later meditation experience, Hannah says she suddenly connected that early experience of illness and isolation with what she was experiencing as an adult. She later participated in NLP-based work that involved revisiting and reframing those experiences. Toward the end of her recovery, Hannah also explored Faster EFT, combining tapping and other emotional-processing techniques. She says she realized that even after becoming physically healthier, she had developed significant fear about leaving her home and becoming ill again. After working through some of those fears and other emotional experiences, she felt more capable of re-entering normal life. For Hannah, physical recovery, emotional recovery, mindset, spirituality, and lifestyle became deeply interconnected parts of the same journey. From Bedbound to What Hannah Describes as Fully Recovered Hannah says she eventually went from being largely bedbound to symptom-free over approximately 11 months. She attributes that change not to one single intervention, but to the sequencing and combination of approaches she personally used. She emphasizes reducing inflammation and other stressors first, then gradually addressing the infections and other issues she believed were affecting her. Her experience shaped one of the central messages she now shares with other Lyme patients: recovery does not necessarily have to happen through the most aggressive approach available. She encourages people to work with knowledgeable practitioners, move carefully, and allow the body time to recover. As she says during the interview, she believes there is value in "slow, steady, gentle" healing, while also emphasizing the importance of appropriate medical supervision. Why Hannah Wrote My Lyme Success Story Once Hannah had recovered, she began organizing everything she had documented during her illness. Her background made that process unusually natural. Hannah had experience in graphic design, photography, writing, editing, and copywriting. She had also meticulously recorded what she tried during her illness—partly because she wanted a record in case she ever became sick again. Eventually, people began encouraging her to write a book. That became Hannah Green: My Lyme Success Story. Hannah says she wrote the book for several reasons: To document what happened to her To explain her experience to family members in England who had been thousands of miles away during the worst of her illness To process the trauma of what she had been through To organize the research and strategies she had collected To help other Lyme patients who might find value in her experience The book includes Hannah's story, the approaches she personally tried, her research, and practical resources including meal plans, shopping lists, checklists, and educational information intended to help patients and families better understand Lyme disease. Learn more about Hannah, her book, and her resources on her website: Hannah Green: My Lyme Success Story Meeting Hannah at the Lyme Warrior 10th Anniversary Gala This Tick Boot Camp interview began with an in-person connection. Hannah traveled from England to attend the Lyme Warrior 10th Anniversary Gala on May 9, 2026, at Saybrook Point Resort & Marina in Old Saybrook, Connecticut. Tick Boot Camp partnered with Lyme Warrior to help photograph, document, and amplify the event. The gala brought together Lyme patients, advocates, researchers, clinicians, authors, families, and supporters for a night focused on research, advocacy, humor, music, community, and hope. Hannah attended alongside other members of the Lyme community who traveled from England, including Kirstie Haysman, Ms Great Britain 2026. The night included appearances from leading Lyme voices including Dr. Eva Sapi, Dr. Monica Embers, Dr. Richard Horowitz, Dr. Myriah Hinchey, Nicole Bell, Jesse Ruben, and many other advocates and community leaders. Read Tick Boot Camp's full coverage of the event. A Lyme Story Across Three Continents Hannah's Lyme journey crosses three continents. She grew up in England. She believes her Lyme exposure may have occurred while working with horses in West Virginia in the United States. Her earliest symptoms emerged after returning to England. Her illness eventually became severely disabling. And in Australia, Hannah finally received the Lyme diagnosis that gave her a framework for understanding what had happened. Australia also became the place where she developed the personal recovery strategy she later documented in My Lyme Success Story. Hannah eventually returned to England in 2019 to spend more time with family. Her international experience underscores an important reality: Lyme disease does not respect borders, and gaps in tick awareness, diagnosis, and treatment can follow patients across healthcare systems. What You'll Learn in This Episode In this episode of the Tick Boot Camp Podcast, Hannah Green discusses: Growing up in England surrounded by horses and the outdoors Why she knew almost nothing about ticks despite extensive equestrian experience Traveling alone to America as a shy 19-year-old Working as a horse-riding counselor at a West Virginia summer camp Removing engorged ticks from horses without understanding the possible human health risk The Lyme disease pamphlet she remembers seeing at camp The red ring on her leg that she was told was probably a spider bite Why she now believes her Lyme exposure may have occurred in West Virginia Developing unusual knee problems after returning to England Years of migrating joint and back symptoms Running the London Marathon despite worsening knee problems The viral illness after which her health dramatically deteriorated Digestive issues, insomnia, chronic fatigue, anxiety, depression, rage, and memory problems Trying to continue working while becoming progressively sicker Repeated medical visits that failed to explain her illness Moving to Australia and eventually becoming largely bedbound How another horse rider helped connect her with the doctor who diagnosed Lyme disease Borrelia and the co-infections discussed during her journey Her experience with PCR testing, bioresonance, and autonomic response testing Why she declined the multi-antibiotic protocol initially proposed to her The three months she spent researching treatment approaches around the world Her staged approach to lifestyle, diet, gut health, and other interventions The low-inflammatory Paleo-style diet she says produced an early improvement Her use of herbs, binders, naturopathic care, and bioresonance Her homemade "Lyme-busting drink" Creating an environment dedicated to healing Learning to trust her intuition Meditation, spirituality, and asking for help Trauma work, NLP, and Faster EFT The fear of leaving home even after her physical health improved Why she believes mindset is critical to recovery Why she wrote My Lyme Success Story Her advice for people newly diagnosed with Lyme disease Why she believes patients should not give up on the possibility of healing Hannah's Advice for Someone Newly Diagnosed With Lyme Disease Near the end of the conversation, Hannah shares several lessons she wishes more people understood early in their Lyme journey. First, she encourages people not to panic. She believes a recovery mindset matters and that people benefit from knowing that others have gotten better. Second, she recommends finding a practitioner you genuinely trust and who looks at the person as a whole rather than focusing on only one symptom. Third, she emphasizes consistency and persistence rather than continually jumping from one protocol to another. And finally, Hannah advocates for a gentler approach when appropriate, saying that the body may need time and a sense of safety in order to recover. Her advice reflects her own experience rather than a universal medical prescription, but the underlying message is powerful: stay engaged, keep learning, work with qualified support, and do not surrender hope. Why Hannah Green's Lyme Success Story Matters Hannah's story is not presented as a universal Lyme disease treatment protocol. It is one person's experience of becoming severely ill, searching for answers across multiple countries, experimenting with approaches that felt appropriate for her circumstances, and eventually reaching a level of health that inspired her to describe her journey as a Lyme success story. Her experience reinforces several important messages for the Lyme community: Tick education matters before a bite ever happens. Not everyone remembers finding an attached tick. An expanding red rash deserves careful medical evaluation. Lyme symptoms can evolve and involve multiple body systems. Migrating joint symptoms can be an important part of a patient's history. People with unexplained chronic symptoms deserve to be heard. Recovery journeys can be highly individualized. Emotional and psychological support can coexist with treatment of physical illness. Community can help replace the isolation that so often accompanies chronic illness. Hope matters. Healing is possible. Final Takeaway Hannah Green's Lyme disease journey began long before she knew she was on one. A young woman from England traveled to America to teach horseback riding, encountered ticks for the first time, developed a mysterious red ring that was dismissed as a spider bite, and returned home feeling healthy. Then the clues slowly appeared. First her knees. Then other joints. Then her back. Eventually, after another illness years later, her health deteriorated dramatically. What followed was a long search for an explanation that eventually took Hannah across the world and into an intense process of research, experimentation, self-advocacy, emotional healing, and recovery. Today, she has transformed that experience into My Lyme Success Story in the hope that what she learned can help others ask better questions and feel less alone. Her exact path will not be everyone's path, and the approaches Hannah believes helped her should not be interpreted as medical advice or a universal treatment plan. But the larger message of her story belongs to the entire Lyme community: keep asking questions, keep learning, find people who take your experience seriously, and do not give up on the possibility of healing.

RHR Interviews Dr. Richard Ostfeld, a Cary Institute disease ecologist who co-directs the tick-monitoring program and is a coauthor of this paper revealing some surprising Lyme Disease findings. For more than 35 years, researchers at the Cary Institute of Ecosystem... Read More ›

This is the afternoon All Local update for September 2, 2026.

What if your symptoms weren't your enemy—but your body's way of asking for help?In this fascinating and empowering episode of Linda's Corner Podcast, we sit down with Dr. Kelly McCann to explore the deeper meaning behind chronic illness, physical symptoms, and the body's incredible wisdom. Dr. Kelly is a pioneer in Functional, Integrative, and Environmental Medicine who specializes in uncovering the root causes of complex chronic conditions like Mast Cell Activation Syndrome (MCAS), mold toxicity, Lyme disease, and persistent infections.You can learn more about Dr. Kelly and her work at Dr. Kelly McCann's WebsiteAfter navigating her own serious health challenges—including mold exposure and Lyme disease—Dr. Kelly discovered how profoundly our thoughts, emotions, beliefs, and environment influence our physical health. Through her work at The Spring Center in California, she helps patients reconnect with their bodies, restore balance, and reclaim their vitality.During this conversation, we explored the relationship many people have with their bodies. Too often, we view the body as broken, inconvenient, or even the enemy. But Dr. Kelly teaches that the body is deeply intelligent and always communicating with us. Symptoms are not random punishments—they are messages guiding us toward healing.We discussed Mast Cell Activation Syndrome, a condition where the body's defense systems become hypersensitive and overreactive. Dr. Kelly shared the powerful idea that our mindset and emotional state can influence our susceptibility to toxins and illness. Two people may experience the same toxic exposure, yet one becomes very ill while the other does not. Why? According to Dr. Kelly, our internal beliefs, stress patterns, emotional wounds, and nervous system regulation all play a significant role in how the body responds.She explained how thoughts such as “I'm not safe,” “I'm not good enough,” or “My body is failing me” can create chronic stress patterns that are reflected physically in the body. Rather than blaming ourselves, Dr. Kelly encourages us to become curious and compassionate toward our symptoms and to recognize them as invitations to heal more deeply.We also discussed her transformational masterclass, The Unforgetting Project, which teaches that we are already whole and enough—we have simply forgotten who we truly are beneath the conditioning of the world. From childhood onward, many people absorb messages that they are flawed, unsafe, or unworthy. Dr. Kelly believes healing involves “unforgetting” our true nature and reconnecting with our authentic selves.One of the most practical insights she shared was the importance of allowing emotions to fully move through the body instead of suppressing them. She explained that emotions often complete their natural cycle in about 60–90 seconds if we allow ourselves to feel them fully without resistance. By noticing sensations in the body, identifying the associated emotion, and allowing it to flow through us, we can release trapped emotional energy and create space for healing.This episode is a powerful reminder that healing is not just physical—it's emotional, mental, spiritual, and deeply personal. If you've struggled with chronic symptoms, unexplained illness, or feeling disconnected from your body, this conversation offers hope, insight, and a compassionate new perspective.In This Episode We Discuss:Listening to the wisdom of the body The mind-body connection Why symptoms may actually be messages from the bodyMast Cell Activation Syndrome and hypersensitive defense systemsMold toxicity, Lyme disease, and environmental illnessThe impact of thoughts like “I'm not safe” or “I'm not enough”Nervous system regulation and susceptibility to illnessLearning to trust the wisdom of the bodyEmotional processing and allowing feelings to complete their cycleDr. Kelly's “Unforgetting Project”Remembering that we are already enoughListen and ConnectTo learn more about Dr. Kelly McCann and her work, visit: Dr. Kelly McCann Official WebsiteListen, Share, and SupportIf this episode resonated with you, please share it with someone who may need hope today.Be sure to subscribe, leave a rating and review, and help us spread more healing and inspiration to the world.Free Resource for HealingIf you're ready to release stress, calm your mind, and begin healing from within, visit:

In this month's episode, we discuss new research looking into the relationship between tick hosts and Lyme disease prevalence, new tools to detect fire ants, and the potential link between cockroaches and mice as vectors of Salmonella. We're joined this episode by our special guest, Matthew Mehr at Hawx Pest Control!  Be sure to check out NPMA's Pestology blog for more information on the research covered in this episode!  Have questions or feedback for the BugBytes team? Email us at training@pestworld.org, we'd love to hear from you!

Intro (0:35),Acute Otitis Externa (1:52),Acute Otitis Media (3:24),Acute Sinusitis (5:41),Strep Throat (7:05),Acute Bronchitis (8:14),Community-Acquired Pneumonia (8:57),Pertussis (11:15),Impetigo (12:04),Cellulitis (13:01),Abscess (14:05),Bite Wounds (14:59),Lyme Disease (15:54),Asymptomatic Bacteriuria (17:19),Cystitis (18:18),Pyelonephritis (20:02),Prostatitis (21:22),Heliobacter pylori (22:02),Clostridioides difficile (23:22),Rapid Fire Antibiotic Prescribing Pearls (24:50),Practice Questions (26:55)

Want more exclusive content?! http://prometheuslens.supercast.com to sign up for the "All Access Pass" and get early access to episodes, private community, members only episodes, private Q & A's, and coming documentaries. We also have a $4 dollar a month package that gets you early access and an ad free listening experience!====================In this episode of The Prometheus Lens Podcast, Doc Brown sits down with author A.W. Finnegan to unpack the deep and provocative research behind The Sleeper Agent: The Rise of Lyme Disease, Chronic Illness, and the Great Imitator Antigens of Biological Warfare.What starts as a conversation about Lyme disease quickly opens into a much larger discussion about biowarfare, immune suppression, historical experiments, and the uneasy overlap between public health, defense, and hidden agendas. Adam shares the personal story that led him to spend years researching the topic, tracing connections through old papers, declassified documents, historical figures, and global programs that he believes shaped modern disease narratives.If you're interested in history, medicine, biology, or the darker corners of scientific research, this one will make you think twice about what you've been told.Topics covered:The origins of Adam Finnegan's book The Sleeper AgentLyme disease, immune tolerance, and chronic illnessHistorical biowarfare and disease experimentationEric Traub, Plum Island, and Operation PaperclipPublic health, vaccine debates, and government secrecyHow old ideas about biological warfare still echo todayGuest: A.W. FinneganWebsite: thesleeperagent.comHost: Doc Brown The Prometheus Lens PodcastIf you enjoyed this conversation, make sure to like, subscribe, and share for more thought-provoking interviews that challenge assumptions and explore the stories beneath the surface.====================

What happens when a wellness expert becomes the patient? In this episode of Let’s Talk Wellness Now, Dr. Deb sits down with Danielle to share her deeply personal and inspiring journey through thyroid cancer, Lyme disease, and the long road of recovery that followed. What emerges is a powerful story about the mind-body-spirit connection and how healing often asks more of us than medicine alone can give. Danielle opens up about how martial arts, visualization, and faith became central to her recovery, and how learning to regulate her nervous system changed the course of her healing. Her story is a reminder that even in the hardest seasons, resilience and hope can carry us further than we imagine. If you or someone you love has been navigating chronic illness and wondering whether real healing is still possible, this conversation is for you. In this episode, you will learn: Danielle’s personal journey through thyroid cancer and Lyme diseaseThe role of spiritual practices and visualization in healing How martial arts and nervous system regulation supported her recovery The powerful impact of stress and emotional health on chronic illness Why holistic, integrative approaches matter so much in health and healing Key frameworks discussed:The Mind-Body-Spirit Connection, Vagus Nerve Regulation, and Quantum Healing.Simple practices to take with you:Incorporate daily visualization and prayerPractice martial arts or Qigong to support nervous system healthMake space for holistic and spiritual well-being in your health routineIn Danielle’s words:“What we focus on is what we become.”“Healing is possible. Don’t lose hope.”“Strive to cope, not to be perfect.” Chapters:00:00 Introduction and Personal Journeys03:45 The Impact of Chronic Illness06:31 Navigating Thyroid Cancer09:37 The Spiritual Component of Healing12:22 Lyme Disease and Its Challenges15:01 The Aftermath of COVID-1917:59 Finding Healing Through Martial Arts20:41 The Role of Mindset in Recovery23:30 Current Work and Future Aspirations26:38 The Need for Accessible Healthcare29:28 Final Thoughts and Encouragement Connect with Danielle:LinkedIn: https://www.linkedin.com/in/daniellepashko/Instagram: https://www.instagram.com/thesoulhakker/Website: https://www.soulhakker.com/ Connect with us:Website: https://www.letstalkwellness.comInstagram: https://www.instagram.com/letstalk_wellnessnow/Facebook: https://www.facebook.com/LetsTalkWellnessNowPodcastLinkedIn: https://www.linkedin.com/company/lets-talk-wellness-now/ Subscribe to Let’s Talk Wellness Now so you never miss an episode, and if this one opened your eyes, share it with someone who needs to hear it.The post Episode 280: Healing Beyond Medicine: A Journey Through Thyroid Cancer and Lyme first appeared on Let's Talk Wellness Now.

What happens when Lyme disease affects the brain? Why do so many people with Lyme disease struggle with brain fog, memory problems, difficulty concentrating, and mental fatigue—even after treatment? And how can researchers better understand, measure, and treat these persistent cognitive symptoms? In this episode of the Tick Boot Camp Podcast, we sit down with Dr. Jacqueline Becker, clinical neuropsychologist, researcher, and Assistant Professor of Medicine at the Icahn School of Medicine at Mount Sinai. Dr. Becker specializes in the cognitive effects of infection-associated chronic illnesses, including Lyme disease, Post-Treatment Lyme Disease Syndrome (PTLDS), Long COVID, and ME/CFS. Drawing from both her clinical practice and groundbreaking research, Dr. Becker explains how neuropsychological testing provides objective ways to evaluate brain fog and cognitive dysfunction. She discusses why patients deserve validation for symptoms that are often invisible, how cognitive rehabilitation differs from commercial brain retraining programs, and why improving research methods is essential for developing more effective treatments. The conversation also explores the growing collaboration between researchers studying Lyme disease and Long COVID, revealing how these conditions may share biological mechanisms that could lead to future breakthroughs benefiting millions of patients. Whether you're living with Lyme disease, caring for someone experiencing cognitive symptoms, or interested in the future of neuroscience and infection-associated chronic illness research, this episode offers practical insights and hope grounded in science. What You'll Learn Why brain fog is one of the most common and disabling symptoms of Lyme disease. How neuropsychologists objectively measure memory, attention, processing speed, and executive functioning. The similarities between Lyme disease, Long COVID, and other infection-associated chronic illnesses. Why traditional clinical trials often struggle to capture the complexity of persistent Lyme symptoms. How improved research design could accelerate the development of new diagnostics and treatments. The difference between evidence-based cognitive rehabilitation and commercial brain retraining programs. Why validating patients' experiences is critical for advancing both research and clinical care. In This Episode Matt Sabatello, Tick Boot Camp Co-Founder, and Dr. Becker discuss: Dr. Becker's journey into neuropsychology and cognitive research How Lyme disease can affect the brain Understanding brain fog beyond subjective symptoms Neuropsychological testing and cognitive assessment Memory, attention, language, and executive functioning Infection-Associated Chronic Illnesses (IACI) The overlap between Lyme disease, Long COVID, and ME/CFS Cognitive rehabilitation and neuroplasticity The blood-brain barrier and emerging neuroscience Improving Lyme disease research through better study design The importance of interdisciplinary collaboration Hope for the future of cognitive recovery after infection About Dr. Jacqueline Becker Dr. Jacqueline Becker is a clinical neuropsychologist, researcher, and Assistant Professor of Medicine at the Icahn School of Medicine at Mount Sinai. She specializes in the evaluation and treatment of cognitive dysfunction associated with Lyme disease, Long COVID, ME/CFS, and other infection-associated chronic illnesses. Her research focuses on improving the scientific understanding of persistent cognitive symptoms while developing better methods for measuring outcomes and advancing patient-centered care. Resources & Links Listen to more Tick Boot Camp Podcast episodes Explore more interviews with Lyme-literate doctors Read the Tick Boot Camp Blog About Tick Boot Camp Tick Boot Camp is dedicated to helping people liberate themselves and others from Lyme disease and tick-borne illness through education, validation, and community. By bringing together leading physicians, researchers, advocates, and patients, we provide trusted information and inspiring stories that remind listeners healing is possible and no one has to face Lyme disease alone.

Shania Twain holds the record for the biggest selling country album of all time: Come On Over. Growing up poor in a Canadian mining town, who could have foreseen that the woman born Eileen Regina Twain would go on to sell over 100 million records, cross country music into pop, and become one of the most recognisable voices on the planet?Her life has been extraordinary, dotted with hit albums and huge shows, songs known by their opening line worldwide, and fans ranging from country music loyalists to Harry Styles. There've been plenty of lows too, including almost losing her voice completely to Lyme disease. Shania Twain may be a little more raspy, but she's got stories.This episode was captured at the legendary Power Station in Midtown Manhattan (the recording studio where Bruce Springsteen made his biggest albums, where David Bowie recorded Let's Dance, and Madonna crafted Like a Virgin). It was the perfect place to sit down and travel back in time with Shania, as she reflected on the little Miss Twain that became the star. Stick around after the chat for a very funny story about what happened that day at the studio. Let's just say Take 5 alumni Lin-Manuel Miranda may have been involved (and Amanda Seyfried... and Hamilton star Phillipa Soo).Shania Twain's song choices: Dolly Parton - 'Coat of Many Colors'Tanya Tucker - 'Texas (When I Die)'Olivia Newton-John - 'Hopelessly Devoted to You'Tina Turner - 'What's Love Got to Do with It'Aretha Franklin - 'Respect'00:00 Introduction and Setting the Scene at the Power Station01:50 The Legendary Power Station Studio02:35 Dolly Parton - 'Coat of Many Colors'03:15 Growing Up Poor and Dolly Parton's Influence06:45 Reflecting on Childhood and the New Album 'Little Miss Twain'07:30 Singing in Bars as a Child and Tammy Wynette09:01 Tanya Tucker - 'Texas (When I Die)'09:30 Tanya Tucker: A Voice Beyond Her Years11:00 First on Stage at Eight Years Old12:45 Singing in the Bars of Timmins, Ontario15:30 Mother's Dream: The Next Tanya Tucker16:00 Dreaming of Horses Instead of Fame17:05 Olivia Newton-John - 'Hopelessly Devoted to You'17:45 Olivia Newton-John: Crossing Genres and Breaking Boundaries20:30 Nashville, Crossing Over to Pop, and Doing It Her Way24:00 The First Video, a Target Budget, and the Belly Button Scandal27:10 Tina Turner - 'What's Love Got to Do with It'28:00 The Queen of Comebacks29:45 A 15-Year Break and Losing Her Voice30:30 Lyme Disease, Vocal Cord Surgery, and Finding a New Voice34:20 Aretha Franklin - 'Respect'35:00 Aretha's Brilliance and Owning the Song37:30 Respect, Recognition, and Not Feeling Like a Star38:30 Finding Peace in the Bush40:00 Full Circle: A Message to Little Miss Twain41:00 A Surprise Visit from Lin-Manuel Miranda, Amanda Seyfried & Phillipa Soo42:30 Next Time: Darren Hayes43:30 Double JThis episode was filmed for season 5 of Take 5 with Zan Rowe on ABC TV and ABC iview. You can stream the whole season on ABC iview now.Watch this episode of Take 5 on ABC iview:https://iview.abc.net.au/show/take-5-with-zan-rowe

EPISODE 125 |  On this episode of the Neurologic Wellness Podcast, Dr. David Traster sits down with Ali from The Tick Chicks to discuss Lyme disease, tickborne illness, chronic infections, diagnosis challenges, and the often nonlinear journey of healing. Ali shares the story behind The Tick Chicks, created following her Lyme disease diagnosis in 2009 and years of searching for answers. The conversation explores why tickborne illnesses can be difficult to identify, including situations where patients do not recall a tick bite or develop a bullseye rash. Topics include brain retraining, neurofeedback, biofeedback, nutrition, inflammatory foods, nervous system support, immune regulation, environmental factors, mold exposure, and approaches focused on improving overall resilience and function. The episode also highlights the upcoming Global Tickborne Illness Summit, taking place October 8–11, 2026. This content is for educational purposes only and is not medical advice. Locations: Boca Raton, FL | Chicago, IL | Waukesha, WI | Wood Dale, IL

Recorded 25th August 2026Follow Dave Hunter here (and watch for FAKE Accounts and being tagged into) he has over 445,000 followershttps://x.com/DaveHcontrarianMedia PicksBitten: The Secret History of Lyme Disease and Biological Weaponshttps://link.amazon/B0aMEu4py (affiliate link) Watch, learn and protect yourself: https://youtu.be/1AN37nEBebc?si=oy3_Hfj0qLExSUyvhttps://x.com/DaveHcontrarian/status/2091650837672063411State of the Markets PodcastTim Price (⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Tim's Substack⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠: https://timprice.substack.com)⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://www.pricevaluepartners.com/⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Investing Through the Looking Glass (by Tim Price)⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://amzn.to/4pXa7pw⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠and Paul Rodriguez⁠⁠https://x.com/prodr1guez⁠

Elaine tells PJ that she thought her baby boy was safe on the manicured lawns of Muckross House but days later she found tick bites on his ear because the ticks get everywhere Hosted on Acast. See acast.com/privacy for more information.

What if the experiences of thousands—or eventually millions—of Lyme disease patients could help the next patient find answers faster? In this episode of the Tick Boot Camp Podcast, we sit down with siblings Carter Bradsky and Payton Bradsky, co-founders of LymeLess Health, to explore their family's extraordinary Lyme disease journey and the technology they're building to help other patients navigate complex chronic illness. Lyme disease didn't affect just one member of the Bradsky family. Their mother became severely ill and largely bedridden while searching for answers through the conventional medical system. Carter later developed debilitating neurological and psychiatric symptoms while preparing to play college basketball. Payton experienced seizure-like episodes, was diagnosed with epilepsy, lost her driver's license, and struggled with cognitive dysfunction while beginning a promising career in technology. Their experiences ultimately inspired a much bigger question: What if Lyme patients didn't have to start from zero? That question became LymeLess, a precision care navigation platform built around an AI companion named Ella. The goal is to help patients organize complex medical histories, track symptoms and treatments, recognize patterns, prepare for medical appointments, find Lyme-literate providers, and make better use of the enormous amount of information generated throughout a chronic illness journey. A Family's Lyme Disease Journey Carter and Payton explain that their family's Lyme journey began with their mother around 2015. After relocating from South Dakota to Arizona, their mother progressively became sicker. Despite extensive medical evaluations—including care through major medical institutions—the family struggled to find an explanation for what was happening. At one point, her symptoms were attributed to psychological causes. Everything changed through a chance encounter. While attending an event surrounding Carter's high school graduation, their mother discussed her symptoms with someone familiar with Lyme disease. That conversation led her toward a Lyme-literate provider and ultimately toward the answers the family had been searching for. Her experience would later become critically important when both Carter and Payton developed their own unexplained illnesses. Carter Bradsky's Lyme Disease Story Carter was preparing for his senior year of high school and planning to play college basketball when his health began changing. During a period that also included significant emotional and physical stress, Carter began experiencing symptoms including: Brain fog and cognitive dysfunction Memory loss Dissociation Depression Anxiety Changes in his ability to function academically and athletically Because his mother had already traveled the Lyme disease diagnostic journey, she recognized similarities between Carter's symptoms and what she had experienced. That awareness allowed Carter to reach a Lyme-literate provider relatively quickly. He describes undergoing combination antibiotic therapy with herbal support and eventually reaching remission after approximately 1.5 to 2 years. His experience became an important lesson that would later influence LymeLess: Having someone Lyme-literate helping you navigate the journey can dramatically change how quickly you find the next right step. Payton Bradsky: Seizures, Epilepsy Misdiagnosis, and Lyme Disease Payton's illness presented very differently. During her senior year of college, after an intense period of stress, illness, dehydration, travel, and lack of sleep, Payton experienced what appeared to be a seizure. She was subsequently diagnosed with epilepsy. The diagnosis changed her life. Payton was placed on powerful anti-seizure medication, lost her driver's license, struggled cognitively, and found herself unable to use the brain she had relied upon throughout her life as an engineering student. This was particularly frightening because she had already accepted a job at Google and was preparing to begin her career in technology. Her family once again questioned whether there might be another explanation. That eventually led Payton toward Lyme and tick-borne disease testing and treatment. Unlike Carter's relatively shorter journey, Payton's recovery became a much longer process involving years of treatment and numerous providers. Her experience illustrates one of the central themes of this episode: There is no single Lyme disease presentation—and there is no single recovery pathway that works for every patient. From Lyme Patients to Technology Founders The siblings eventually brought very different professional backgrounds together to create LymeLess. Carter studied finance and data analytics at the University of San Diego before working in technology, media, and telecommunications investment banking in New York City. Payton studied computer engineering and entrepreneurship at Santa Clara University in Silicon Valley before spending approximately five years at Google, working as a software engineer and product manager. Her experience in technology—including exposure to privacy, security, and regulated data environments—would later become particularly relevant when designing a health platform handling sensitive patient information. Both siblings eventually left their careers to tackle a problem they understood personally: Why does navigating Lyme disease so often become a second full-time job for the patient or caregiver? What Is LymeLess? LymeLess describes itself as a precision care navigation platform designed around the patient. Instead of leaving medical information scattered across patient portals, paper binders, lab reports, physician notes, symptom journals, and a patient's memory, LymeLess is working toward creating a centralized longitudinal record of the patient's journey. The platform's AI companion is called Ella. Patients can use Ella to help: Organize their health history Track symptoms over time Track treatments and supplements Record reactions and potential triggers Upload medical documents and laboratory results Identify patterns in symptoms and treatments Prepare for doctor appointments Surface relevant resources and research Find Lyme-literate providers Remember previous treatment responses Better understand their evolving health journey Carter describes one user's characterization of Ella as a "second brain" for when Lyme brain makes remembering and organizing everything difficult. Turning the Lyme Disease Binder Into Usable Data Anyone who has navigated chronic Lyme disease knows about the binder. Years of: Bloodwork Imaging Specialist reports Medication lists Treatment protocols Symptom histories Diagnostic testing Hospital records Patients frequently carry enormous amounts of information between specialists, yet a physician working within a short appointment may have only minutes to understand it. The conversation explores whether AI could become a bridge between these two realities. Instead of expecting a physician to read hundreds or thousands of pages, AI may eventually help synthesize a patient's history into the information most relevant to that particular appointment. LymeLess currently allows patients to upload digital documents and images of physical records, while the company is working toward easier bulk uploading and potential integrations with electronic health record systems. The LymeLess "Warrior Report" One important feature discussed in the episode is the Warrior Report. Patients can export information from LymeLess into a report designed to help communicate their health journey to their provider. Carter and Payton envision this concept becoming considerably more sophisticated in the future. One possibility discussed is a provider-facing experience in which clinicians could interact with a patient's organized information, review relevant research, and ask questions in language and formats designed specifically for medical professionals. Longer term, LymeLess is exploring clinical decision-support concepts and potential integrations with electronic health record platforms. Ella Is Not a Doctor Carter and Payton emphasize an important distinction throughout the interview: Ella is not intended to replace physicians. LymeLess is not positioning Ella as an autonomous doctor that diagnoses disease or prescribes treatment. Instead, the goal is to help patients: Understand their own information Recognize patterns Surface questions Find relevant resources Organize their medical histories Communicate more effectively with their healthcare team The ultimate medical decisions remain between patients and qualified healthcare professionals. Can AI Help Patients Recognize Patterns? One of the most exciting possibilities discussed is AI's ability to analyze enormous amounts of information. Lyme and tick-borne disease patients frequently experience changing combinations of: Neurological symptoms Psychiatric symptoms Pain Fatigue Inflammation Treatment reactions Food sensitivities Environmental triggers Co-infections Medication and supplement responses Patients may recognize individual events but struggle to see patterns unfolding across weeks, months, or years. Payton explains that Ella is being designed to combine patient-specific longitudinal information with curated research and educational resources. The goal is not simply to answer a question at one moment in time, but to understand that question in the context of the patient's broader journey. Learning From Other Lyme Patients The conversation then expands beyond individual patient tracking. Could anonymized patient experiences eventually help identify broader patterns across the Lyme community? Carter describes a long-term vision for a community intelligence layer that could potentially help patients, providers, and researchers learn from real-world experiences at scale. Instead of every newly diagnosed patient beginning at zero, future patients could potentially benefit from patterns identified among people with similar symptoms, diagnoses, treatment histories, and responses. The siblings discuss the potential for properly anonymized and de-identified information to eventually contribute to research while protecting individual patient identities. Lyme Disease Research and Real-World Evidence The episode explores an even larger possibility: Could longitudinal patient data help accelerate Lyme disease research? Traditional clinical trials are essential, but they can be expensive, geographically limited, and slow. Meanwhile, Lyme patients are already trying enormous numbers of treatments in the real world. The challenge is that much of that information disappears. One patient tries a treatment. Another patient tries something different. A physician discovers something useful in clinical practice. Patients discuss experiences in Facebook groups and online forums. But those experiences rarely become structured research-quality data. LymeLess hopes eventually to help close that gap. Potential future applications discussed include: Identifying promising treatment patterns Generating real-world evidence Identifying potential clinical trial candidates Helping researchers determine which therapies deserve formal study Supporting decentralized research Connecting patients with clinical trials Helping researchers study complex combinations of Lyme disease, co-infections, and overlapping conditions Lyme Disease Is More Than Borrelia Another important research discussion centers around the complexity of the Lyme patient population. Many patients aren't navigating Borrelia alone. Their health picture may also include: Bartonella Babesia Other tick-borne infections Mold exposure Mast cell activation Dysautonomia Inflammation Neurological dysfunction Genetic differences Environmental exposures By collecting longitudinal information across complex patients, platforms such as LymeLess could potentially help researchers study the combinations and patterns that traditional Lyme research may not fully capture. Protecting Patient Privacy Health information is extraordinarily sensitive, and the episode includes an extensive discussion about privacy and security. Payton explains that protecting patient data has been considered from the beginning of LymeLess' development. According to Payton, LymeLess uses: Encryption at rest Encryption in transit Zero-data-retention policies and agreements with vendors powering the platform Patient control over their information De-identification and anonymization approaches for broader data use She emphasizes that patients should be able to benefit from AI technology while still understanding and controlling how their information is used. LymeLess and the Doctor-Patient Relationship One of the most interesting themes of the conversation is that technology could potentially improve—not replace—the relationship between doctors and patients. Patients with complex chronic illness frequently arrive at appointments carrying years of medical information. Doctors, meanwhile, may have extremely limited appointment time and may not have extensive training in Lyme and tick-borne diseases. That can create frustration on both sides. Could better-organized information help? The conversation explores how AI-generated summaries, longitudinal symptom tracking, research resources, and eventually provider-facing tools could help physicians understand complicated patients more quickly. Rather than telling patients they must become their "own doctor," the goal is to help patients become better-informed partners with their healthcare team. Can LymeLess Help Health Coaches? The siblings also discuss the growing role of health coaches in complex chronic illness. Because Lyme patients often need significant support between medical appointments, health coaches can help patients organize treatment plans, make lifestyle changes, and navigate day-to-day challenges. LymeLess could potentially serve two populations: Patients who cannot afford ongoing human health coaching may gain access to a more affordable form of between-appointment support. At the same time, professional health coaches may eventually use technology like LymeLess to organize information and support more patients efficiently. Carter's Mold Illness After Lyme Remission The episode also takes an unexpected turn when Carter shares a recent health setback. After reaching remission from Lyme and tick-borne disease, Carter moved into an older apartment in New York City's SoHo neighborhood. Over time, he began experiencing: Brain fog Severe fatigue Cognitive problems Word-recall difficulties Nervous system dysregulation Increasing sensitivity to caffeine Anxiety Eye floaters Initially, he questioned whether Bartonella or another tick-borne infection had returned. Testing eventually pointed toward mold exposure. Environmental testing of his apartment reportedly identified numerous types of water-associated mold, and subsequent testing contributed to his decision to address mold illness and leave the environment. He describes temporarily moving home, focusing on recovery, reducing caffeine and screen exposure, exercising, using sauna, and continuing to work with his healthcare team. Importantly, Carter says subsequent testing did not indicate reactivation of Lyme, Bartonella, or Babesia. His experience reinforces another reason he believes longitudinal health records are valuable: When symptoms return years later, knowing exactly what happened during previous illnesses and treatments can provide important context. Discovery, Active Treatment, and Maintenance Payton describes three broad stages LymeLess is designed to support: Discovery Someone has experienced a tick bite or unexplained symptoms and is trying to determine what should happen next. Active Treatment The patient has a diagnosis and is navigating treatments, symptoms, reactions, providers, testing, and progress. Maintenance / Remission The patient is doing better but still wants to understand their health, recognize potential triggers, remember previous treatment responses, and protect their progress. This makes LymeLess potentially relevant beyond the period when someone is acutely sick. Genetics and Precision Medicine The interview also explores another future direction: incorporating genetic information. Genetics can influence: Detoxification Methylation Medication responses Nutritional needs Inflammatory pathways Other aspects of individualized health Carter and Payton discuss a future in which genetics, laboratory testing, patient history, symptoms, environmental factors, and treatment responses could contribute to increasingly personalized health navigation. Their larger vision moves from precision care navigation toward precision care and, eventually, increasingly individualized precision medicine. How Much Does LymeLess Cost? At the time of this interview, Carter and Payton describe LymeLess as offering a one-month free trial, followed by a subscription of approximately $15 per month. They also discuss working toward making portions of the platform available more broadly and maintaining a scholarship program for people who cannot afford the subscription. Carter explains that a portion of subscription revenue is intended to help support that scholarship program. Turning Lyme Disease Into Purpose The episode ultimately becomes about much more than artificial intelligence. Both Carter and Payton discuss how illness changed their lives. They describe fear, isolation, cognitive impairment, uncertainty, faith, family support, and the challenge of trying to continue school and demanding careers while sick. They also discuss something we talk about frequently at Tick Boot Camp: finding purpose through suffering. Payton continued developing her engineering career while undergoing treatment. Carter describes spending long periods alone in church during college, trying to quiet his mind and understand what mattered most. Eventually, their experiences gave them a problem they felt compelled to solve. Their mission with LymeLess is ambitious: Learn from the unique story of every patient so future patients don't have to navigate Lyme disease through the same degree of trial, error, expense, and luck. Key Topics Discussed Carter and Payton Bradsky's family Lyme disease story Their mother's long diagnostic journey Medical dismissal and unexplained chronic symptoms Carter's neurological Lyme symptoms Brain fog, memory loss, anxiety, depression, and dissociation Payton's seizure and epilepsy misdiagnosis Neurological and psychiatric Lyme disease symptoms Lyme disease remission and recovery Lyme disease and co-infections Bartonella and Babesia Mold toxicity after Lyme disease AI and Lyme disease LymeLess Health Ella AI companion Precision care navigation Symptom and treatment tracking Longitudinal patient health data Medical record organization The Lyme disease "binder" Patient-provider communication Warrior Reports Lyme-literate provider matching Clinical decision-support technology Electronic health record integration AI pattern recognition Patient privacy and healthcare data security De-identification and anonymization Real-world evidence Lyme disease clinical trials Patient-generated health data Artificial intelligence and medical research Health coaching and Lyme disease The financial burden of chronic Lyme disease Genetics and personalized medicine Precision medicine Faith and chronic illness Post-traumatic growth Finding purpose after Lyme disease Life after Lyme disease Learn More Explore LymeLess and Ella Listen to more Tick Boot Camp Podcast episodes Explore Tick Boot Camp interviews with Lyme doctors Recently bitten by a tick? Start with the Tick Boot Camp Tick Bite Blueprint About Tick Boot Camp Tick Boot Camp is a Lyme disease awareness and advocacy platform built around a simple belief: people navigating Lyme and tick-borne illness deserve validation, community, better information, and hope. Through conversations with patients, doctors, researchers, advocates, and innovators, we share the experiences and emerging ideas helping move the Lyme community forward. You are not alone—and healing is possible.

When conventional medicine says 'there's nothing else we can do,' Dr. Marty Ross knows you're just getting started. This episode explores the overlooked co-infections, mold toxicity, and system dysfunctions behind chronic fatigue and fibromyalgia—and the terrain-based healing approach .Dr. Ross walks through a patient case: a young missionary bedridden from what appeared to be Lyme disease received eighteen months of IV antibiotics with minimal improvement. The course changed when he recognized mold toxicity as the missing link—cholestyramine alone brought 90% recovery in weeks.He reveals why treating the system—not just killing the germ—matters. He discusses testing recommendations (IgeneX for Borrelia and co-infections; Vibrant Lab or Mosaic for mold biotoxins), then three no-cost starting points: sleep hygiene (7-9 hours nightly), feeding your microbiome with polyphenols and plant-forward foods, and addressing limbic system dysfunction via tools like the Gupta Program or Primal Trust.For those suffering with Lyme diagnosis or suspect chronic illness which has terrain-based roots, this conversation offers both immediate steps and the framework to reframe your healing—plus Dr. Ross's resources for personalized guidance.about Dr. RossDr. Marty Ross is a functional medicine physician based in Seattle and one of the leading clinical voices in chronic Lyme disease, tick-borne infections, and complex chronic illness in the United States. Over 25 years, he has helped thousands of patients across the US and internationally recover from conditions that mainstream medicine often dismisses, including Lyme, mold toxicity, fibromyalgia, and long COVID.He is the founder of Treat Lyme, one of the largest chronic illness education platforms online, and is the author of Hacking Lyme Disease: An Action Guide to Wellness. He also runs a monthly live Q&A webinar and a curated supplement line in partnership with Femologist. Before opening the practice in Seattle, Marty shaped US public health legislation from the Senate. Today, he is the doctor who shows up for patients when everyone else has stopped looking.https://www.linkedin.com/in/marty-ross-md/https://www.instagram.com/martyrossmd/----In the even the podcast exceeds 300 views in the first week, The One Thing Podcast will donate at least $100 in your honor of Plus One Foundation (https://plusonefoundation.networkforgood.com/projects/194639-everyday-donation-page)

Are unexplained fatigue, brain fog, inflammation, or other chronic symptoms sometimes connected to mold exposure or Lyme disease? In this episode of Shaped by Faith Radio, Theresa Rowe welcomes Dr. Vaughn Lawrence of Spirit of Health back for Part 2 of their conversation on infectious disease. This time, they take a closer look at mold exposure, Lyme disease, chronic illness, immune health, and the body’s natural ability to heal and recover. Dr. Vaughn shares his perspective on why mold and Lyme disease can be difficult to recognize, symptoms that may be overlooked, and why it is important to look deeper when someone has been struggling with ongoing health concerns. As people of faith, we want to be informed and intentional about caring for our bodies while ultimately placing our trust and hope in God. Keep reading...

What are the real benefits of red light therapy and infrared saunas, and how could infrared therapy support detoxification, inflammation, pain, recovery, and overall cellular health? In this episode of the Health Detective Podcast, Michele Scarlet sits down with Robby Besner, Chief Science Officer and co-founder of Therasage, whose work with infrared technology began after his teenage daughter was diagnosed with Lyme disease. Robby shares his daughter's Lyme disease journey, the limitations they experienced with conventional treatment, and why he began researching infrared therapy as another way to support her quality of life. They also explore: • Red light therapy vs. infrared therapy • Near, mid, and far infrared wavelengths • Infrared sauna benefits and how often to use one • Infrared therapy for inflammation, pain, and recovery • Detoxification and supporting the body's elimination pathways • Why consistency matters more than having the “perfect” wellness routine • Full-body infrared saunas vs. targeted infrared pads • How sunlight, nature, and infrared may influence cellular health • Taking a more active role in your own health journey Robby also shares how his daughter's experience ultimately became the catalyst for his mission to make infrared technology more accessible to people looking for additional ways to support their health. If you are interested in red light therapy, infrared sauna benefits, Lyme disease, detoxification, inflammation, holistic health, or functional medicine, this conversation offers a fascinating look at the story and philosophy behind infrared therapy. GET METABOLIC REBALNCE FOR 20% OFF ⬇️ Use Code HD20  http://functionalformulas.com/buynow  Disclaimer: This podcast is for educational and informational purposes only and is not intended to diagnose, treat, cure, or prevent any disease. The information shared is not a substitute for professional medical advice, diagnosis, or treatment. Always consult your physician or another qualified healthcare professional regarding your individual health needs.

Dr. Kerri Simpson - The Well Nut Wellness and Nutrition Center 214-308-9594 - https://thewellnut.com/Sovereign Health Summit with Barbara O'Neill, October 27-31, 2026 - https://www.sovereignhealthsummit.com/?ref=permaPromo Code - TPC - 5% OffJonathan Otto's Website - https://myredlight.com/Promo Code - bb25 and bb30The Wellness Blanket -https://thewellnessblanket.com/?sca_ref=10936149.IjFZC1tt28OPromo Code - Perma - 10% OffAzure Standard - https://www.azurestandard.com/?a_aid=dd1f60ff5dPromo Code - FOODFORHEALTH1515% Off for New Customers Minimum Order $100Nesa's Hemp - https://www.nesashemp.com/#permapasturesfarmPromo Code - perma - 10% OffBon Charge Blue Light Blocking Glasses - https://boncharge.com/?rfsn=8947983.d7b6efPromo Code: Perma - 15% OffSoil Savior Products - https://www.soilsaviors.org/order?aff=654693f413fad4692e058e9eb0779d3667638550392d22d979d6d2d4daf720b3Cell Saviors - https://www.cellsaviors.org/fulvicPromo Code: detox - Get 10% OffWAVwatch - $100 Off - https://buy.wavwatch.com/?ref=billy100Promo Code: BILLY100Micronic Silver - https://www.micronicsilver.com/?ref=PERMAPASTURESFARMPromo Code - perma 10% offEMF Rocks - https://emfrocks.com/PERMAPASTURESFARMPromo Code - Perma Pastures Farm - 5% OffAir Water Healing Triad Air Filter - https://airwaterhealing.com/Promo Code: perma - Get 10% OffLiving Soil Foundation GiveSendGo - https://givesendgo.com/GE2E8?utm_source=sharelink&utm_medium=copy_link&utm_campaign=GE2E8If you would prefer to send a check:Living Soil FoundationPO Box 2098Mars Hill, NC 28754Richardson Nutritional Center https://rncstore.com/permaPromo Code: perma - Get 10% OffRedmond Products - 15% Off - https://glnk.io/oq72y/permapasturesfarmPromo Code: permaGet $50 Off EMP Shield: https://www.empshield.com Promo Code: permaAbove Phone - https://abovephone.com/perma/Promo Code - PERMA $50 OffHarvest Right Freeze Dryer: https://affiliates.harvestright.com/1247.htmlOnline Pig Processing: https://sowtheland.com/online-workshops-1Patreon: https://www.patreon.com/user

Alayna Bellquist was bitten by a tick on a trail ride in San Diego. The ER doctor gave her two pills and sent her home.What followed wasn't just a year in bed. It was a time when Alayna's life was abruptly halted, forcing her to reckon with everything that had come before it.Alayna is a marine scientist, author, and speaker who spent two decades studying how ecosystems collapse and how they bounce back. Then her own body became the ecosystem in crisis. A chronic Lyme diagnosis forced her to stop racing, stop achieving, and start looking backward at a childhood that had quietly shaped her into someone who never asked for help and never took days off. What she found on the other side wasn't just recovery. It was a completely different way of understanding what healing actually requires and how the words we use to describe our healing journey carry the most weight of all.What You Will Learn[00:14:30] Alayna's life scheduled to the minute, always racing[00:18:00] What parentification explained about her patterns[00:28:00] Three years of symptoms she called "stress"[00:34:00] Hiding Lyme disease from her family for months[00:37:30] Calling on a psychic out of pure desperation[00:45:30] Addressing Alayna's true vulnerabilities, not the tick[00:56:00] Why Alayna says "cured," not "in remission" when mentioning her experience with Lyme disease[00:59:00] A simple perspective on what healing can actually look likeResources MentionedResilient by Nature: A Memoir of Curing Chronic Lyme Disease by Alayna BellquistMia Magik - Alayna's Intuitive AdvisorLet's Connect!Alayna BellquistWebsite | Instagram | LinkedIn | Facebook | YouTubeChandler StroudWebsite | LinkedIn | InstagramHappiness Academy is now Healing Heroines, a signature space for women who are ready to feel more grounded, more peaceful, and more aligned — inside and out. Download a complimentary Healing Roadmap to discover our Past, Present, and Possible framework.Want personalized guidance for your healing journey? Book a call with Chandler!Mixing and editing provided by Next Day Podcast.Text message us questions, requests, or comments!

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There's a virus within a bacterium within a parasite, and University of Kentucky researchers are figuring out how to make them kill each other. Dr. Greg talks with a UK researcher who has been studying the Lyme issue for nearly 30 years.

From Episode #258: Lyme Disease & Alpha-Gal: The Hidden Cause & How to Heal✨ Subscribe for the Full Episode: https://beyondlabels.supportingcast.fmFind Joel Here: www.polyfacefarms.comFind Sina Here: www.drsinamccullough.comFollow on InstagramFollow on XSubscribe on RumbleSubscribe on YouTubeDISCLAIMER

Low-fat dairy shown to confer no weight, cholesterol benefits over full-fat dairy; FDA and USDA to define ultra-processed foods for first time—but what are they really? Newly discovered tick-borne Bourbon virus can be fatal—but is it more pervasive than we think? Thorne supplement maker—sold 3 years ago for $700 million—acquired by Procter & Gamble for $3.8 billion. Those dark skin blotches—are they melasma, or just age spots? Is low-mercury salmon a hype? That fishy smell—does it mean your seafood is spoiled?

Canada is in the middle of one of its worst seasons for ticks. The tick population and tick-borne diseases are climbing year-over-year, and it's not just Lyme disease that experts say we should be concerned about. Today, the Globe's health science reporter Jennifer Yang joins the show to discuss the emergent tick-borne disease causing concern in Canada, why our country's tick problem is only getting worse, and what we can do to protect ourselves. Questions? Comments? Ideas? Email us at thedecibel@globeandmail.com Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

In this special Tick Boot Camp Instagram Live, Dr. Casey Kelley returns to discuss the latest developments in Lyme disease diagnosis, treatment, clinician education, and research. Drawing on both her personal recovery journey and years of treating complex chronic illness, Dr. Kelley explains why Lyme disease requires individualized care, why more Lyme-literate clinicians are urgently needed, and how new technologies—including big data, advanced diagnostics, and innovative therapies like SOT—are shaping the future of patient care. Episode Highlights Expanding Lyme-Literate Medical Education Dr. Kelley announces an exciting partnership between the Illinois Lyme Association and Carle Health to offer the ILADS Fundamentals Course free to healthcare providers. She explains why educating more physicians is one of the fastest ways to improve Lyme disease diagnosis and treatment across the country. The conversation also explores the role of the International Lyme and Associated Diseases Society (ILADS), including its physician training programs, fellowship process, and commitment to evidence-based medicine. Dr. Casey Kelley's Personal Lyme Journey Dr. Kelley reflects on her own experience with chronic illness. After years of unexplained symptoms, multiple incorrect diagnoses, and eventually developing POTS during medical school, she discovered that Lyme disease and tick-borne infections were contributing to her illness. Her recovery ultimately inspired her to found Case Integrative Health, where she now helps patients with complex chronic illnesses using a personalized, whole-body approach. How COVID Changed the Chronic Illness Conversation The discussion examines how the COVID-19 pandemic dramatically increased awareness of infection-associated chronic illnesses. Dr. Kelley explains that greater recognition of Long COVID has also helped bring attention to Lyme disease, ME/CFS, POTS, mast cell activation syndrome, and other complex conditions that share similar biological mechanisms. AI, Big Data, and the Future of Lyme Care Matt and Rich ask whether artificial intelligence and large clinical databases will transform Lyme medicine. Dr. Kelley believes AI and big data will become valuable tools—but only when paired with experienced clinicians who understand the complexity of Lyme disease and can interpret each patient's unique presentation. Why Every Lyme Patient Is Different The conversation explores why no two Lyme patients look exactly alike. Genetics, epigenetics, immune function, microbiome diversity, environmental exposures, multiple tick bites, co-infections, and varying bacterial strains all contribute to highly individualized clinical presentations. New Advances in Lyme Diagnostics Dr. Kelley discusses promising diagnostic research aimed at distinguishing active infection from past exposure and identifying bacterial peptides unique to active Borrelia infections. These advances could help clinicians better determine whether symptoms are being driven by persistent infection or ongoing immune dysfunction. Understanding Supportive Oligonucleotide Therapy (SOT) One of the most in-depth portions of the conversation focuses on Supportive Oligonucleotide Therapy (SOT). Dr. Kelley explains how SOT is customized using a patient's own blood sample to target specific pathogens by preventing them from replicating. While not a cure, SOT has become an increasingly valuable treatment option for patients who have plateaued with conventional therapies and is often combined with treatments such as ozone therapy. There Is No Single Treatment Order Matt and Rich ask whether every patient should follow the same healing sequence. Dr. Kelley explains that there is no universal roadmap. Some patients must first stabilize mast cell activation, while others need to prioritize infections, mold exposure, parasites, or nervous system dysfunction. Successful treatment depends on understanding each person's unique biology rather than following rigid protocols. Nervous System Regulation and Neuroplasticity The discussion shifts toward brain retraining and nervous system healing. Dr. Kelley explains that many severely ill patients simply lack the energy to begin intensive neuroplasticity programs early in treatment. Instead, she often introduces passive nervous system therapies first before transitioning patients into more active brain retraining as their health improves. She also shares practical tools she frequently recommends, including: Vagus nerve stimulation Apollo Neuro Pulsetto Neurofeedback Binaural beats Breathing exercises Hypnosis Humor and intentional joy A Message of Hope Dr. Kelley closes the conversation by reminding listeners that healing is possible. While Lyme disease treatment often requires patience, persistence, and individualized care, she emphasizes that people can regain health, improve function, and achieve long-term remission—even when recovery feels impossible in the beginning. Learn More Explore the Tick Boot Camp Podcast for more Lyme disease education and recovery stories. Browse our complete collection of Doctor Interviews featuring leading Lyme-literate physicians. Learn more about Persistent Lyme Disease and the latest research into chronic tick-borne illness.

Dr. Sina McCullough unpacks some shocking origins of Lyme Disease and how Borrelia is not as modern as people think.From Episode #258: Lyme Disease & Alpha-Gal: The Hidden Cause & How to Heal✨ Subscribe for the Full Episode: https://beyondlabels.supportingcast.fmFind Joel Here: www.polyfacefarms.comFind Sina Here: www.drsinamccullough.comFollow on InstagramFollow on XSubscribe on RumbleSubscribe on YouTubeDISCLAIMER

The Journey 195. Corruption 101: Biowarfare Blues (John Loftus, A. W. Finnegan, Dan Luzadder)Websites: https://www.trineday.com https://www.trinedaily.comTrineDay socials:Facebook: https://www.facebook.com/trinedaypress Instagram: https://www.instagram.com/trinedaypress X: https://x.com/TrineDay YouTube: https://www.youtube.com/@TrineDayIn this episode, Kris Millegan and Todd Baumann speak with John Loftus, A. W. Finnegan, and Dan Luzadder regarding media, biowarfare between countries, and the stealth nature of bioweapons. Finnegan recaps the work of Dr. Erich Traub and his diabolical contributions to the biological weapons game and his concerns about our approaches in handling this problem. Finnegan also discusses how the war crosses over into the pharmaceutical and public health sectors, with some serious red flags for people from enemy countries acquiring top positions in public health in the USA A. W. Finnegan is the author of The Sleeper Agent: The Rise of Lyme Disease, and the Great Imitator Antigens of Biological Warfare (https://trineday.com/products/the-sleeper-agent-the-rise-of-lyme-disease-chronic-illness-and-the-great-imitator-antigens-of-biological-warfare), who was personally affected by Lyme disease and immune tolerance. He is a writer, graphic artist and designer, and avid researcher of history, biological warfare, esoteric philosophy, spirituality, and the Western Mystery Traditions. He has made a special study of the life and work of Erich Traub and the science of immune tolerance, collecting and translating to English all of Traub's published research. He lives in Cape Cod, Massachusetts, where he enjoys BMX biking, fitness, study, the arts, and self-development. John Loftus is a former U.S. government prosecutor, a former Army intelligence officer, and the author of numerous books, including The Belarus Secret; The Secret War Against the Jews; Unholy Trinity: How the Vatican's Nazi Networks Betrayed Western Intelligence to the Soviets; and Unholy Trinity: The Vatican, the Nazis, and the Swiss Banks. He has appeared regularly as a media commentator on ABC National Radio and Fox News. He lives in St. Petersburg, Florida. Buy America's Nazi Secret here: https://trineday.com/products/americas-nazi-secretPre-order My Client's Were Spies Here: https://trineday.com/products/myclients-were-spiesDan Luzadder is an American journalist and author whose lengthy newspaper career began as a teenaged police reporter in the last days of linotypes. He came of age amid hagiographic newsroom characters who believed shoe leather reporting, tight deadlines and well-placed sources were journalism's divinity. He has written for the New York Daily News and the New York Times, shared a Pulitzer Prize (1983) for general local reporting, won a national public service award from the American Bar Association for exposing corruption in federal courts, and is a member of the Scripps Howard Journalism Hall of Fame. He resides with his wife, Nancy, in the Pacific Northwest. He is the author of The Manchurian Journalist: Lawrence Wright, the CIA and the Corruption of American Journalism. (Trine Day). He is currently at work on a book and investigative documentary series on a cold-case crime spree in Speedway, Indiana in 1978, and is completing a book exploring the American myth of Al Capone. Buy The Manchurian Journalist: Lawrence Wright, the CIA, and the Corruption of American Journalism here: https://trineday.com/products/manchurian-journalist-lawrence-wright-the-cia-and-the-corruption-of-american-journalism

When Alysa Seeland's health began falling apart after the birth of her first baby, she was told she would likely need surgery and was left searching for answers. Instead, that journey led her to discover the power of nutrient-dense foods, healing through nourishment, and eventually building Fond Regenerative: a company dedicated to truly traditional bone broth and regenerative foods.In this conversation, Alysa shares her incredible postpartum healing story, why quality bone broth matters, the role of healthy fats during pregnancy and breastfeeding, recovering from Lyme disease, home birth experiences, homeschooling six boys, running a thriving business with her husband, and the practical systems that make large family life possible. If you've ever wondered how to nourish yourself while raising children, or how to let go of perfectionism in motherhood, this episode is packed with encouragement and practical wisdom.00:00 Trailer & Introduction03:46 Why Real Bone Broth Matters 05:24 Alysa's Postpartum Health Crisis 09:20 Healing Through Nourishment 12:20 Why Moms Need More Nutrients 19:06 Healthy Fats During Pregnancy & Postpartum 20:46 Childhood Health & Choosing Birth Centers 23:31 Fast Birth Stories & Home Births 26:18 Letting Go of Perfectionism 30:14 Babies Close Together & Pregnancy Nutrition 34:14 Lyme Disease & Pregnancy After Healing 37:27 Managing Expectations With a Large Family 43:06 Homeschooling Six Kids 49:46 Running a Business Together as Parents 52:25 The Problem With Perfectionism 56:40 Family Systems That Actually Work 60:10 Why the Company is Named FOND 61:51 Daily Routine & Work Schedule 65:05 Traveling & Building a Business With Kids 68:36 Healthy Sports Snacks for Kids 72:35 Favorite Ways to Use Bone Broth & Tallow 75:20 Are They Done Having Kids?Resources From This Episode:Use code HAAM and save 10% at Fond - https://fondregenerative.com/HAAMCheck out Fond on Instagram - https://www.instagram.com/fondregenerativeFollow Alysa on Instagram - https://www.instagram.com/alysaseeland/Dr. Morgan's Pregnancy Call Course - https://milkmedicine.com/lessonsonly/Healthy As A Mother Podcast | YouTubeHealthy As A Mother Podcast | InstagramHealthy As A Mother Podcast | TikTokHealthy As A Mother Podcast | Merch StoreFind more from Dr. Leah:Dr. Leah Gordon | InstagramDr. Leah Gordon | WebsiteWomanhood Wellness | WebsiteFind more from Dr. Morgan:Dr. Morgan MacDermott | InstagramDr. Morgan MacDermott | WebsiteUse code HEALTHYMOTHER and save 10% at EarthleyUse code HEALTHYMOTHER and save 15% at RedmondFor 20% off your first order at Needed, use code HEALTHYMOTHERSave $260 at Lumebox, use code HEALTHYASAMOTHERUse code HAAM and save 10% at Fond

Lyme disease is called "the great imitator" because it can look like growing pains, fatigue, or nothing at all and this episode shows you what to watch for. Steph sits down with naturopathic physician Dr. Jacquell Patterson, a nationally recognized expert in Lyme disease, tick-borne co-infections, and PANS/PANDAS to cover everything parents need to know about ticks and Lyme disease. You'll learn which areas to check on your kid's body, why the smallest ticks cause the most infections, and how to tell the difference between growing pains and a tick-borne illness that's being missed. Dr. Patterson also shares her own delayed Lyme disease diagnosis and what she wishes every parent knew before tick season hits. Topics Covered In This Episode: Why Tick Season Feels Scarier Than Ever Why Lyme Disease Is Called "The Great Imitator" Different Tick Species, Co-Infections, and Testing Gaps The Bullseye Rash Myth (Only Half of Cases Get One) Tick Prevention: Clothing, Sprays, and Checks That Work How Often to Check Kids and Pets for Ticks What to Do the Moment You Find a Tick Symptoms to Watch For After a Tick Bite What Every Parent Gets Wrong About Lyme Disease Show Notes: Click here to learn more about Dr. Elana Roumell's Doctor Mom Membership, a membership designed for moms who want to be their child's number one health advocate! Click here to explore Steph Greunke, RD's Mindset and Metabolism Substack, nuanced discussions on fat loss and behavior change for women. Watch this episode on our Youtube channel @medschoolformoms Listen to today's episode on our website I am a nationally and internationally recognized naturopathic physician. I am an expert in Lyme disease and other tick borne-illnesses, autoimmune conditions, PANS/PANDAS, women's health and anxiety and depression. I run a large and growing multi-disciplinary integrative medical practice composed of naturopathic physicians, nutritionist, physical therapist and acupuncture. Due to my record of clinical success, I also work as a success coach to other integrative practitioners and help them to grow and scale their businesses so that they may spread and have influence in the world of integrative medicine. I'm a sought-after speaker appearing frequently on the lecture stage, television, print, podcasts and radio. I've served in many leadership capacities, most recently as the President of the American Association of Naturopathic Physicians. This Episode's Sponsors  Discover for yourself why Needed is trusted by 15,000+ women's health practitioners, including Dr. Elana and Steph. Needed supports optimal health and nourishment throughout the Motherspan--from preconception through perimenopause. Enjoy their range of practitioner-formulated, third-party tested supplements and get 20% off with code DOCTORMOM. Visit thisisneeded.com   Active Skin Repair is a must-have for everyone to keep themselves and their families healthy and clean.  Keep a bottle in the car to spray your face after removing your mask, a bottle in your medicine cabinet to replace your toxic first aid products, and one in your outdoor pack for whatever life throws at you.  Use code DOCTORMOM to receive 20% off your order + free shipping (with $50 minimum purchase). Visit BLDGActive.com to order. INTRODUCE YOURSELF to Steph and Dr. Elana on Instagram. They can't wait to meet you! @stephgreunke @drelanaroumell Please remember that the views and ideas presented on this podcast are for informational purposes only.  All information presented on this podcast is for informational purposes and not intended to serve as a substitute for the consultation, diagnosis, and/or medical treatment of a healthcare provider. Consult with your healthcare provider before starting any diet, supplement regimen, or to determine the appropriateness of the information shared on this podcast, or if you have any questions regarding your treatment plan.

Allie Chandler went from being fit, active and adventurous to experiencing severe widespread pain and spending almost two years largely confined to bed.Her symptoms began suddenly following a backpacking trip in the Swiss Alps. After years of searching for answers, Allie was diagnosed with Lyme disease and co-infections. However, receiving a diagnosis was only the beginning of a long and often unpredictable recovery journey.In this episode of Beyond The Pain, Allie shares the physical, emotional and social impact of living with debilitating persistent pain. She discusses her experience with functional medicine, environmental triggers—including exposure to black mould—and the different approaches she explored while trying to restore her health.We also explore the turning point in Allie's recovery: recognising the role of her nervous system, mindset and identification with illness. Through limbic-system retraining, emotional work and daily practices designed to change her brain's response to perceived threats, Allie gradually began reclaiming her health and her life.Today, Allie considers herself 98% recovered. Her story offers hope, encouragement and practical insights for anyone who feels trapped by pain, illness or repeated setbacks.In this episode, we discuss:How Allie went from competitive sport and boxing to being largely bed-boundThe long search for an explanation for her widespread symptomsHer Lyme disease and co-infection diagnosesFunctional medicine, detoxification and organ supportHow black-mould exposure contributed to a significant setbackThe relationship between stress, the nervous system and persistent symptomsLimbic-system retraining and neuroplasticityMoving beyond a victim mentality and an illness-based identityThe daily habits that helped Allie rebuild her healthWhy setbacks do not necessarily mean recovery is impossibleAllie's experience is personal and should not be taken as medical advice. Anyone experiencing persistent or unexplained symptoms should seek appropriately qualified medical support.Contact AllieMeet Your Healer App: www.meetyourhealer.comBrain Retraining Programme: www.upsellhealth.com/brainContact LeighBeyond The Pain paperback: https://amzn.to/4y2HVWgBeyond The Pain ebook: https://amzn.to/4y0lH78Beyond The Pain 14-Day Programme: https://bodychek.co.uk/beyond-the-pain-programme/Pain-Free Plate Free Guide: https://www.bodychek.co.uk/freepainguide/Consult with Leigh: https://www.bodychek.co.uk/consultation

What if the missing piece in your Lyme recovery isn't another antibiotic protocol, but your brain itself?In this episode of Integrative Lyme Solutions, Dr. K sits down with Mo Pritzker, Co-Founder of re-origin, who spent two years cycling through doctors and alternative treatments for Lyme disease before finally getting better, only to relapse even harder. It wasn't until a doctor handed her a book on neuroplasticity that everything shifted. Mo shares how brain retraining calmed her dysregulated limbic system, helped her body return to homeostasis, and led to being Lyme free for ten years, including a Lyme test that eventually came back negative.This conversation goes beyond killing the pathogen and into what actually keeps people stuck: a nervous system stuck in survival mode. Mo breaks down the "pause" technique she uses to interrupt negative thought loops, why healing chronic illness is as much a crisis of the whole person as it is a physical one, and why community and coaching were just as critical to her recovery as any protocol. If you're navigating Lyme disease and feel like you've tried everything, this episode offers a piece of the puzzle you may not have considered yet.Key Takeaways:0:00 Introduction1:11 From serial entrepreneur to sudden health collapse3:07 The perfect storm that broke her body down9:20 A doctor handed her a book that changed everything11:24 Why neuroplasticity worked when other therapies didn't17:35 How her brain turned a positive Lyme test negative25:27 The pause technique for breaking negative thought loops34:01 Where to find the re-origin communitySchedule a Free 15-Min Cancer/Lyme Consultation at The Karlfeldt Center: 208-338-8902Resources:re-origin - https://www.re-origin.com/The Brain That Changes Itself by Norman Doidge - https://normandoidge.com/ Medical Disclaimer: This content is for educational purposes only and is not intended to diagnose, treat, cure, or replace professional medical advice. Always consult your physician or qualified healthcare provider regarding any medical condition or treatment decisions.

What if the biggest obstacle to healing Lyme disease isn't just the infection—but the body's inability to feel safe enough to recover? In this inspiring episode of the Tick Boot Camp Podcast, Dr. Meagan Bonnot shares her remarkable journey from being a chronically ill patient with debilitating symptoms to becoming a naturopathic doctor dedicated to helping others recover from complex chronic illnesses. Drawing from both personal experience and years of clinical practice, Dr. Bonnot explains why healing Lyme disease requires far more than simply killing bacteria. Together, Matt Sabatello and Dr. Bonnot explore the critical roles of nervous system regulation, detoxification, trauma recovery, frequency medicine, herbal therapies, and faith in creating an environment where true healing can occur. Dr. Bonnot also discusses how her clinic, Deeper Wellness, integrates biofeedback technology, individualized treatment plans, and functional medicine principles to help patients restore health. Whether you're newly diagnosed with Lyme disease or have struggled with chronic illness for years, this conversation offers practical insights and a hopeful reminder that healing is possible. In This Episode Dr. Meagan Bonnot discusses: Her personal battle with chronic Lyme disease Why Lyme testing often misses patients Childhood trauma and chronic illness connections The importance of regulating the nervous system Frequency medicine and AO Scan technology Herbal protocols for Lyme disease Detoxification before antimicrobial treatment Brain retraining and neuroplasticity Faith, resilience, and healing Practical strategies patients can begin immediately Meet Dr. Meagan Bonnot Dr. Meagan Bonnot is a naturopathic physician and the founder of Deeper Wellness, where she helps patients with Lyme disease, mold illness, Bartonella, chronic fatigue, autoimmune conditions, and other complex chronic illnesses. After spending years searching for answers to her own debilitating health challenges, Dr. Bonnot discovered that lasting recovery required addressing much more than infections alone. Today, she combines functional medicine, naturopathic therapies, herbal medicine, nervous system regulation, detoxification strategies, biofeedback technology, and personalized care plans to help patients restore health from the inside out. Her mission is to help patients understand that the body possesses an incredible capacity to heal when given the right environment and support. Dr. Bonnot's Personal Lyme Disease Story Long before becoming a physician, Dr. Bonnot experienced many of the same frustrations faced by Lyme patients today. Growing up, she struggled with chronic asthma, allergies, fatigue, digestive issues, and recurring illnesses. Despite years of medical evaluations, no one identified the underlying causes of her declining health. Eventually, she developed worsening neurological and systemic symptoms that conventional medicine struggled to explain. Even Lyme testing failed to provide clear answers. Rather than accepting that chronic illness would define her life, she pursued naturopathic medicine and began investigating the deeper drivers behind persistent disease. Her own recovery ultimately became the foundation for the clinical approach she now uses with patients worldwide. Why Killing Lyme Isn't Always the First Step One of the biggest misconceptions surrounding Lyme disease is that recovery begins with antimicrobial treatment. Dr. Bonnot explains that many patients simply are not physiologically prepared to tolerate aggressive treatment. If detoxification pathways are impaired or the nervous system remains trapped in chronic fight-or-flight mode, antimicrobial therapies may overwhelm the body rather than support healing. Instead of asking: "How do we kill Lyme?" She encourages practitioners to first ask: "Why is this person's body unable to heal?" That subtle shift changes the entire treatment strategy. The Four Foundations of Healing Throughout the interview, Dr. Bonnot outlines the sequence she frequently follows when working with patients. 1. Regulate the Nervous System Chronic infections, emotional trauma, prolonged stress, and toxic exposures can leave the nervous system stuck in survival mode. When the brain continually perceives danger, healing becomes significantly more difficult. Dr. Bonnot discusses techniques that help patients restore regulation, including: Adaptogen herbs, such as those from Supreme Nutrition & VerVita Breathwork Mindfulness Gratitude practices Restorative sleep Faith Emotional healing Lifestyle changes Brain retraining programs Consistency over perfection 2. Open Detoxification Pathways Rather than forcing detoxification, Dr. Bonnot emphasizes gently supporting the body's natural elimination systems. These include: Liver Kidneys Lymphatic system Digestive tract Skin Cellular detoxification Supportive therapies may include: Hydration Nutrition Sauna Red light therapy Movement Lymphatic drainage Herbal support Creating efficient detox pathways helps reduce inflammatory burden before antimicrobial therapies begin. 3. Address Infections Once patients are better prepared, treatment may include targeted therapies for Lyme disease and common coinfections. During the discussion, Dr. Bonnot references herbs frequently used within naturopathic protocols, including: Japanese Knotweed Cat's Claw Cryptolepis Houttuynia Chinese Skullcap Artemisia Reishi Adaptogenic herbs Rather than applying identical protocols to every patient, she individualizes treatment based on symptoms, testing, history, and response. 4. Retrain the Brain Healing often continues long after infections have been treated. Many patients continue experiencing persistent symptoms because their nervous systems remain conditioned toward chronic survival responses. Dr. Bonnot discusses the importance of neuroplasticity and brain retraining approaches that help the brain learn safety again. She explains that recovery frequently requires healing both the body and the brain simultaneously. Frequency Medicine and AO Scan Technology A unique portion of the interview explores frequency medicine and biofeedback technologies such as the AO Scan. Dr. Bonnot explains how these technologies may help identify physiological imbalances and guide personalized wellness strategies. Rather than replacing conventional diagnostics or clinical judgment, she views frequency-based tools as one component of a comprehensive functional medicine approach. She stresses the importance of integrating patient history, laboratory findings, symptoms, and clinical experience when making treatment decisions. The Connection Between Trauma and Chronic Illness Another major theme of the conversation is unresolved trauma. Dr. Bonnot discusses how childhood experiences, chronic stress, and emotional wounds can influence immune regulation and nervous system function for years. While trauma does not cause Lyme disease, it can influence how the body responds to infection and recovery. Healing often requires addressing both physical and emotional health. Faith as Part of Healing One of the most personal portions of the interview centers on Dr. Bonnot's faith. She shares how her spiritual beliefs helped sustain hope during periods when improvement seemed impossible. Faith, purpose, gratitude, and community became important parts of her own healing journey and continue influencing how she cares for patients today. Key Takeaways Throughout this conversation, Dr. Bonnot reinforces several important messages: Healing is rarely linear. Every patient is unique. Nervous system regulation matters. Detoxification should support—not overwhelm—the body. Lyme disease treatment should be individualized. Emotional healing often supports physical healing. Recovery requires patience and consistency. Hope remains essential throughout the healing journey. Listen Now If you've been searching for a more comprehensive approach to healing Lyme disease and chronic illness, this episode provides valuable perspectives from both a physician and former patient who understands the journey firsthand. More Lyme Disease Resources: Podcast Physician Interviews Lyme Disease Testing Educational Resources About Tick Boot Camp Tick Boot Camp is dedicated to educating, inspiring, and empowering the global Lyme disease community through conversations with leading physicians, researchers, advocates, and patients. Through hundreds of interviews, Tick Boot Camp shares practical information, emerging research, and real stories of hope that remind listeners they are not alone—and that healing is possible.

EVEN MORE about this episode!What if your body has been trying to tell you something all along—and you just haven't known how to listen?In this live episode of the Ask Julie Ryan Show, Julie Ryan facilitates real-time medical intuitive scans, energetic healings, spirit communication, and animal readings for callers from across the U.S., uncovering hidden clues behind chronic symptoms and offering practical guidance for healing.Julie helps callers struggling with chronic pain, Lyme disease, autoimmune symptoms, stomach cancer, elevated PSA levels, and digestive issues, while sharing intuitive insights into root causes that may not appear on traditional medical tests. Along the way, Spirit delivers comforting guidance to a grieving pet owner, and an Angelic Attendant Training™ graduate joins the live chat to share his remarkable personal cancer recovery journey and the lifestyle changes that transformed his health.Whether you're navigating unexplained symptoms, seeking spiritual guidance, or exploring the connection between energy and physical wellness, this episode offers hope, practical insights, and powerful reminders that healing often begins by understanding what your body has been trying to communicate.Episode Chapters:(0:00:00) Welcome & AAT Scholarship Announcement(0:06:43) What Your Body Is Trying to Tell You(0:21:11) Lyme Disease, Autoimmune Illness & Healing(0:34:07) Spirit Messages from a Beloved Pet(0:36:55) Cancer, Medical Intuition & Root-Cause Healing(0:47:10) A Remarkable Cancer Recovery Story(0:51:08) Prostate Health, PSA & Energy Healing(1:02:24) Closing Thoughts➡️ Subscribe to Ask Julie Ryan YouTube➡️ Julie's Intuitive Trainings✏️ Ask Julie a Question!

What if chronic illness isn't caused by the infection everyone is trying to eliminate? On this episode of The Longevity Formula, Dr. Brandon Crawford sits down with physician, bestselling author, and chronic illness expert Dr. Bill Rawls, MD, to challenge one of modern medicine's core assumptions: that killing the pathogen is the path to recovery.After his own collapse from Lyme disease, mold exposure, and burnout, Dr. Rawls abandoned symptom-chasing medicine to study cellular health, impaired autophagy, and what he calls "terrain." He explains why Lyme, long COVID, autoimmune disease, mold illness, and fibromyalgia may all trace back to the same broken mechanism.Follow Dr. Bill Rawls, MD:Facebook – facebook.com/rawlsmd/Instagram – instagram.com/rawlsmd/LinkedIn – linkedin.com/in/bill-rawls-md/YouTube – youtube.com/@rawlsmdWebsite – rawlsmd.com/resources/Products:528 Innovations LasersNeuroSolution Full Spectrum CBDNeuroSolution Broad Spectrum CBDNeuroSolution StimpodSTEMREGEN®For more information, resources, and podcast episodes, visit tinyurl.com/3ppwdfpm

JAMA Medical News Director Jennifer Abbasi and Associate Managing Editor Kate Schweitzer discuss "Will New Lyme Disease Approaches Change Patient Care?" Related Content: Will New Lyme Disease Approaches Change Patient Care?

Jody Hudson's beloved daughter began experiencing what can only be described as "mystery symptoms"; aching joints, inflammation, and random weight loss. The mystery illness progressed with no formal diagnosis when she was finally tested for Lyme Disease. Throughout her ever-changing illness, Alex forged ahead and focused on her faith, while taking time to serve others. The disease eventually caused too much damage, and Alex sadly passed at the age of 22. Jody fiercely refused to let that be the end of Alex's story. She has taken up the cause to fight against Lyme Disease by founding the Alex Hudson Lyme Foundation, dedicated to spreading awareness and educating others about Lyme disease and MCAS and supporting patients to find community and proper care. Learn more about the Alex Hudson Lyme Foundation here and purchase Jody's book, "My Promise to Alex: Through Pain Comes Purpose", here.SUPPORT His Heartbeat through Crown of Beauty Internationalhttps://www.crownofbeautyinternational.com/donateCONNECT with His Heartbeat and Crown of Beauty InternationalWebsite// Facebook//InstagramEmail: crownofbeautyinternational@gmail.comConnect with Sue Corl's Instagram//Facebook// WebsitePurchase Sue's Transformational Bible Studies and Devotionals on Amazon!Sue Corl's best-selling books: Crown of Beauty Bible Study, Broken But UndefeatedCrown of Beauty International: EMPOWERING WOMEN AROUND THE WORLD WITH GOD'S TRUTH!

You don't have to live in the woods to get bit by a tick. It can happen in your backyard, on a walk, even pulling weeds in your own garden. In this episode of The Art of Living Well Podcast®, Marnie and Stephanie sit down with Ali Moresco, a tick-borne disease survivor, healthcare publicist, and one of the most recognized Lyme disease advocates in the country. Ali spent two years searching for a diagnosis before learning she had Lyme disease along with several co-infections, and she's turned that experience into advocacy work that has helped shape federal tick-borne disease legislation as executive board chair of Project Lyme. Ali walks through what those confusing early years of unexplained symptoms actually looked like, why standard Lyme testing misses far more cases than most people realize, and the practical prevention and removal steps worth knowing before your next walk outside. She also shares what her recovery has actually required over the better part of a decade, including where the treatment protocols and research are headed next. Whether you spend your weekends on the trail, garden in your own backyard, or just want to know what to actually do if you find a tick on you, this conversation will change how you think about prevention. Key Takeaways: Lyme disease is present in all 50 states, not just the East Coast Standard two-tier Lyme tests can be 64-78% inaccurate, especially in the early weeks after a bite Fewer than half of people infected with Lyme ever develop the classic bullseye rash Never burn, smother, or otherwise irritate an attached tick — use fine-tipped tweezers and pull straight up Save a removed tick in a bag or jar; some states and universities offer free tick testing Alpha-Gal syndrome is a tick-borne meat allergy that can also cause fatigue, brain fog, and gastro symptoms Symptoms from a tick bite can surface years later, often triggered by an unrelated stressful event or illness Recovery from chronic tick-borne illness is rarely linear and often requires a combination of treatments tailored to the individual person Episode Breakdown with Timestamps:  00:00   Introduction & Meeting Ali Moresco 01:03   Does Ali Still Enjoy Being Outside After Everything She's Been Through 02:51   Life Before Lyme Disease Was Part of Her Vocabulary 07:23   The Timeline From Tick Bite to First Symptoms 08:53   The Two-Year Path to Diagnosis 10:39   Why Standard Lyme Testing Misses So Many Cases 13:40   What Her Lowest Point Actually Looked Like 17:28   The Biggest Misconceptions About Tick Bites 19:43   Beyond Lyme: Other Tick-Borne Conditions on the Rise 20:34   Understanding Alpha-Gal Syndrome 22:31   Babesiosis and Bartonella, Explained 23:24   How to Actually Prevent Tick Bites 26:36   Prophylactic Antibiotics After a Bite 27:49   The Right Way to Remove a Tick (and What Never to Do) 29:46   What to Do With a Tick After You Remove It 30:58   Can Symptoms Show Up Years After a Bite? 32:47   Reasons for Hope: New Research on the Horizon 35:55   Inside Project Lyme's Advocacy Work 37:48   What Treatment Actually Looks Like Long-Term 44:03   The Daily Habits That Help Ali Stay Well 45:34   Where to Find Ali and Her Work 46:28   "What Does the Art of Living Well Mean to You?" Guest Links: Instagram: instagram.com/alitmoresco  Moresco PR: amorescopr.com/ali-moresco Project Lyme: projectlyme.org --------------------------------------------------------------------------------------------------------- Feeling tired, inflamed, or stuck in a cycle of cravings? Join our 7-Day Fall Vitality Reboot starting September 27 and discover how much better you can feel with simple daily habits and a supportive community beside you every step of the way. Click here to save your spot: https://l.bttr.to/fNSbn --------------------------------------------------------------------------------------------------------- Subscribe to our Substack to get episode updates, wellness tips, and personal reflections from Marnie & Stephanie delivered straight to your inbox. Grab your free Midlife Travel Resilience Checklist here. If you love the show and want to support what we're building, consider a paid subscription for $30 annually. https://theartoflivingwell.substack.com/ Follow & Connect: Instagram: https://www.instagram.com/theartofliving_well/ YouTube: https://www.youtube.com/@theartoflivingwellpodcast LinkedIn: https://www.linkedin.com/company/the-art-of-living-well-podcast/ TikTok: https://www.tiktok.com/@theartoflivingwel/ Spotify: https://open.spotify.com/show/4gym3jOPdSHwrpM1BmxyJz Apple Podcasts: https://podcasts.apple.com/us/podcast/the-art-of-living-well-podcast/id1482050468  Connect with your Hosts: https://www.theartoflivingwell.us/about-us

Hello friends! Wisconsin based singer-songwriter Ruby James is my guest for episode 1589! Ruby's new album, Call It Rock & Roll on Mule Kick Records drops on August 7th and she is celebrating the release with a show at The Five Spot in Nashville on Friday, August 14th. Go to rubyjamesmusic.com for show info, music and more. Ruby and I have a great conversation about making Call It Rock & Roll with producer Kyle Crusham and a host of great Austin musicians like Rosie Flores, Harmoni Kelley, David Jimenez and more, turning a Supersuckers song into a duet with Eddie Spaghetti, adventures on the Little Steven's Garage Cruise, getting over Lyme Disease, and much more. Let's get down! Find Ruby on Spotify, Instagram, Facebook Follow us on Instagram, TikTok, X, Facebook, Spotify, Apple Podcasts, or anywhere you pod. Go to johnny-goudie.com for all things Johnny.   If you feel so inclined. Venmo: venmo.com/John-Goudie-1  Paypal: paypal.me/johnnygoudie

Hey, Heal Squad! Today we're throwing it back to one of our most eye-opening conversations with Dr. Christopher Motley, a leading expert in functional kinesiology and Chinese medicine. If you've been following our recent episodes on mold toxicity, this is the perfect next listen because mold and Lyme disease often go hand in hand, sharing many of the same frustrating symptoms. Dr. Motley explains the surprising ways Lyme can enter the body, why so many people never fully recover, and the hidden role blocked drainage pathways play in keeping you sick. From EMFs, heavy metals, and mold toxicity to trapped emotions, he reveals how these invisible stressors overwhelm your body, disrupt your lymphatic system, and prevent true healing. We also dive into how trauma can become stored in your organs, what viruses like Epstein-Barr have to do with fatigue and hormone imbalances, and why restoring your body's Qi (your electromagnetic life force) may be one of the missing pieces to lasting wellness. If you've been doing everything "right" but still don't feel like yourself, this throwback episode will help you connect the dots and finally understand what could be keeping your body stuck. Join us at our Canyon Ranch 2026 Retreat: https://www.canyonranch.com/lenox/retreats/heal-retreat-maria-menounos HEAL SQUAD SOCIALS IG: https://www.instagram.com/healsquad/ TikTok: https://www.tiktok.com/@healsquadxmaria HEAL SQUAD RESOURCES: Heal Squad Website:https://www.healsquad.com/ Heal Squad x Patreon: https://www.patreon.com/HealSquad/membership Maria Menounos Website: https://www.mariamenounos.com My Curated Macy's Page: https://stylecrew.macys.com/@mariamenounos EMR-Tek Red Light: https://emr-tek.com/discount/Maria30 for 30% off Airbnb: https://www.airbnb.com/host ABOUT MARIA MENOUNOS: Emmy Award-winning journalist, TV personality, actress, 2x NYT best-selling author, former pro-wrestler and brain tumor survivor, Maria Menounos' passion is to see others heal and to get better in all areas of life. ABOUT HEAL SQUAD x MARIA MENOUNOS: A daily digital talk-show that brings you the world's leading healers, experts, and celebrities to share groundbreaking secrets and tips to getting better in all areas of life. DISCLAIMER: This Podcast and all related content ( published or distributed by or on behalf of Maria Menounos or http://Mariamenounos.com and http://healsquad.com ) is for informational purposes only and may include information that is general in nature and that is not specific to you. Any information or opinions provided by guest experts or hosts featured within website or on Company's Podcast are their own; not those of Maria Menounos or the Company. Accordingly, Maria Menounos and the Company cannot be responsible for any results or consequences or actions you may take based on such information or opinions. This podcast is presented for exploratory purposes only. Published content is not intended to be used for preventing, diagnosing, or treating a specific illness. If you have, or suspect you may have, a health-care emergency, please contact a qualified health care professional for treatment.

Dr. Rani is one of two ophthalmologists in the country who is also certified in functional medicine. She is able to diagnose up to 200 conditions from your eyes – things like MS and diabetes, but also Lupus, and Lyme Disease. We discuss dry eyes, glaucoma, cataracts, macular degeneration, and more. This is a fascinating conversation. If you want to learn how to care for your eyes as you age and what supplements and foods to prioritize, this is the episode for you. For example, did you know you should get an eye exam every year after the age of 40? Learn more now!    KEY TOPICS Why Eye Health Matters For Midlife Women (00:00) How Functional Medicine Applies To Eye Health And Root-Cause Vision Care (02:37) Eyes As A Window To Overall Health And Systemic Disease Detection (06:30) Hormones, Perimenopause/Menopause, And Women's Higher Risk For Eye Diseases (13:30) Dry Eye In Midlife Women: Symptoms, Gland Dysfunction, And Hormone Links (14:53) Contact Lenses, Dryness, And Infection-Safety Best Practices (18:00) Cataracts: Aging Lens Changes, When To Operate, And Premium IOL Options (25:12) Macular Degeneration: Genetics, Central Vision Loss, And Prevention With Lutein/Zeaxanthin (30:13) Nutrition And Lifestyle For Lifelong Vision: Antioxidants, Omega-3s, Gut Health, And Daily Habits (32:10)    RESOURCES Join The Newsletter Subscribe on YouTube Follow on APPLE PODCASTS Follow on SPOTIFY PODCASTS Book: Design a Life You Love      GUEST RESOURCES Dr. Rani Banik's website: www.drranibanik.com Instagram: https://www.instagram.com/dr.ranibanik/ YouTube: https://www.youtube.com/channel/UC8mIi8P9tXSRXXwEdNX6aRw Book: Beyond Carrots: Best Foods For Eye Health A to Z Dr. Rani's Visionary Kitchen (Beyond Carrots) *The Her Starring Role with Michele Lamoureux podcast and content provided by Michele Lamoureux is for educational and entertainment purposes only. It does NOT constitute medical, mental health, professional, personal, or any kind of advice or serve as a substitute for such advice. The use of information on this podcast or materials linked from this podcast or website is at the user's own risk. Always consult a qualified healthcare or trusted provider for any decisions regarding your health and wellbeing. This episode may contain affiliate links.  

What if the fatigue, brain fog, joint pain, or mysterious symptoms you've been chasing for years weren't caused by stress, aging, or burnout—but by a tick bite you never even noticed? Lyme disease is one of the most misunderstood illnesses in medicine. But Lyme is rarely just one infection—it's often part of a much bigger picture involving co-infections, immune dysfunction, inflammation, gut health, and environmental triggers. In today's episode, I walk through a functional medicine approach to Lyme disease and tick-borne illness, including: Why Lyme disease is so often missed—and the hidden role of co-infections like Babesia, Bartonella, Ehrlichia, and Anaplasma The limitations of conventional testing and treatment, and how functional medicine looks beyond the infection to understand why some people recover while others remain chronically ill The role of herbs, antibiotics, gut repair, detoxification, immune support, and mitochondrial health in a comprehensive recovery plan What the latest evidence says about emerging therapies like ozone, hyperbaric oxygen therapy, and hyperthermia—as well as practical strategies to prevent tick-borne illness in the first place Lyme disease isn't always just an infection—it's often a whole-body disruption. By addressing the underlying drivers of inflammation, immune dysfunction, gut health, and cellular resilience alongside the infection itself, you give your body the best chance to heal and recover. Resources Mentioned: Track your metabolic health with Function Health: https://functionhealth.com/mark (Use code MARK2026 for $50 off your membership.) Have a question you'd love answered on Office Hours? Submit it here (0:00) Introduction to Lyme disease, overview, and Dr. Hyman's experience (4:13) Functional medicine's approach and comprehensive treatment strategies (10:51) Innovative therapies for Lyme disease (14:08) Managing die-off reactions and restoring gut health (17:18) Supporting the immune and nervous systems; prevention strategies (19:29) Future research, persistent symptoms, and conclusion (21:15) Alzheimer's disease, neuroinflammation, and call to action

For two decades, a perplexing illness has been spreading: After a lone-star tick bite, people find themselves with a severe allergic reaction to red meat. The CDC estimates up to 450,000 people in the U.S. may be affected with alpha-gal syndrome, up from just a few dozen documented cases in 2009. New research finds that in some states, more than 30% of people are positive for alpha-gal antibodies—but not all of them have the syndrome. Flora speaks with allergist Scott Commins, who has studied alpha-gal syndrome for nearly 20 years, to unpack this finding and next frontiers for treatment. Guest: Dr. Scott Commins is the William J. Yount Distinguished Professor of Medicine and associate chief for allergy and immunology at the UNC School of Medicine in Chapel Hill, North Carolina.  Other episodes you may enjoy: Instead Of A Vaccine For Lyme, How About A Vaccine For Ticks? Why Don't We Have A Vaccine For Lyme Disease? Transcripts for each episode are available within 1-3 days at sciencefriday.com. Subscribe to this podcast. Follow our show on Instagram, TikTok, Facebook, and Bluesky @scifri and sign up for our newsletters. Got a science question that's keeping you up at night? Call us: 877-472-4374 Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.