Podcasts about lyme warrior

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.

This is episode 68 of the Love, Hope, Lyme podcast. To get your free pdf of "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know," reach out to Fred Diamond on social media. [NOTE: This podcast does not replace medical treatment. If you struggle with Lyme care, please see a Lyme Literate Medical Doctor.] What does it really mean to be a Lyme Warrior?  

Topic: Dr. Cipriano's journey from ICU nurse to Lyme disease practitioner, inspired by her son's diagnosis and the challenges of navigating the medical system. Key Takeaways: The Power of ILADS Conferences – How attending ILADS helped Dr. Cipriano learn about innovative Lyme disease treatments and naturopathic approaches. From ICU Nurse to Lyme Specialist – Dr. Cipriano shares her transition from hospital-based care to focusing on preventative medicine and helping patients get off medications. A Mother's Fight for Answers – Her son's Lyme disease journey, the difficulties of getting an accurate diagnosis, and the perseverance needed to find effective treatment. Polymicrobial Infections on the Rise – The growing complexity of Lyme disease cases, including Bartonella, Babesia, and other co-infections. Breaking Barriers in Medicine – The challenges of being an outlier in the medical field and the importance of collaboration through ILADS. The Evolution of Diagnostic Testing – Advances in Lyme disease testing, including the accuracy and comprehensiveness of iGenex panels. Chronic UTIs & Tick-Borne Infections – How Lyme disease and co-infections contribute to chronic urinary tract infections and why they require a different treatment approach. Resources & Links: Follow the latest ILADS updates at ILADS.org Learn more about Dr. Pamela Cipriano Stay connected with Tick Boot Camp: Website | Instagram | Facebook | YouTube | TikTok | Twitter (X)

Introduction Tick Boot Camp Podcast goes LIVE from the ILADS Conference with Sharon Ibanez and her daughter Mara, representatives of Lyme Warrior, a nonprofit dedicated to raising awareness and providing resources for Lyme disease patients. Sharon and Mara share their personal experiences with Lyme disease and discuss how Lyme Warrior is making a difference in the patient community. Lyme Warrior's Mission at ILADS Sharon and Mara attend the ILADS conference to build relationships with doctors and healthcare practitioners to improve patient care. Their goal is to foster better communication and collaboration between Lyme patients and providers. Mara's Lyme Disease Journey Diagnosed with Lyme disease at a young age, Mara shares how it affected her physically and emotionally. She reflects on how an earlier diagnosis could have prevented years of suffering and isolation. Sharon's Battle with Lyme Disease Sharon recounts her decades-long struggle with misdiagnoses before finally testing positive for Lyme. Symptoms such as chronic migraines, weight loss, and extreme fatigue impacted her daily life. The Challenges of Being a Lyme Parent and Patient Sharon opens up about the difficulty of managing her illness while being a mother. She emphasizes how understanding that Lyme—not her children—was causing her suffering changed her perspective. Lyme Warrior's Impact: Smile Boxes and Volunteer Work Sharon shares how receiving a Smile Box from Lyme Warrior was a turning point in her healing journey. Mara highlights the emotional impact of these care packages, which help Lyme patients feel seen and supported. How to Support Lyme Warrior Sharon discusses ways to donate, volunteer, or sponsor a Smile Box to help Lyme patients in need. The organization relies on community support to continue making a difference. Resources & Links

In this powerful episode, we sit down with Laura to explore the importance of understanding individual health journeys—especially for women navigating hormonal and immune challenges. Laura shares her own transformation story and how personalized coaching and sustainable strategies helped her achieve lasting results. With insights like “Health is a long-term game,” she emphasizes the value of consistency over quick fixes.We dive into the misconception that fat loss is impossible for women with hormonal issues, and Laura reassures listeners: “Never let hormones or any conditions be a barrier to fat loss.” Her experience with the Strong Girls methodology showcases how the right programming can be a game-changer.This episode is all about empowerment, support, and redefining what's possible for women in their health and fitness journeys. Laura Manganaro's Links:Follow Laura on IG here: https://www.instagram.com/coach_laura_manganaro/Want to work with Laura? Fill out her application here: https://www.teamstronggirls.com/laura-application-formLaura's website: https://lauramanganaro.com/about Whenever you're ready, here are two ways to help you get a stronger body, faster results, and a responsive metabolism:Join our private BODY TRANSFORMATION group and connect with women levelling up their goals: It's our Facebook community where ambitious women learn to get leaner, get faster results, and achieve more energy – CLICK HERE https://www.facebook.com/groups/teamstronggirlsWork directly with me and my team privately: If you'd like to work with me and my team to lose fat and build more lean muscle…fill out my questionnaire and tell me about your goals…I'll get right back to you CLICK HERE https://y6bawlb79dm.typeform.com/to/EIHKhwmTResources:Coach JVB Website https://coachjvb.com/Team Strong Girls Website https://www.teamstronggirls.com/Follow Jenny on social media:Instagram @coach_jvbFacebook @jennifer.vanbarneveldYouTube @JenniferVanBarneveldPe  DISCLAIMER: The opinions, beliefs, and viewpoints expressed by the hosts and guests on this podcast do not necessarily represent or reflect the official policy, opinions, beliefs, and viewpoints of Disenyo.co LLC and its employees.

https://thelymeboss.com/ In this episode 106,  Heather Gray FDN-P engages in a deep conversation with Nicole, a caregiver for a loved one with Lyme disease. Nicole discusses the challenges faced by caregivers, the importance of self-care, and her involvement in advocacy and diagnostic solutions for Lyme disease. The episode emphasizes the need for caregivers to prioritize their well-being and highlights ongoing efforts to improve Lyme disease diagnostics and research. In this podcast you will discover 01:50 - Nicole talks about her background in engineering and entrepreneurship, as well as her love for outdoor activities and coaching sports. 05:32 - Nicole discusses her connection to Lyme disease through her husband's illness, highlighting the importance of awareness and understanding in mental health professionals.. 13:51 - The conversation delves into using tragedy to fuel change and bring awareness to Lyme disease. 21:14 - Nicole reflects on the gifts of Lyme disease and discusses her efforts to power change through research and education. 24:31 - Heather mentions her participation in an event related to Lyme disease, highlighting the importance of raising awareness and supporting research efforts. 25:13 - Nicole highlights the critical role of advocacy organizations in raising awareness and funding research for Lyme disease. 26:42 - Nicole discusses the emerging link between Lyme disease pathogens and dementia, calling for increased research funding to explore alternative hypotheses. 27:24 - Reflecting on her caregiving experience, Nicole shares the challenges of balancing multiple responsibilities and stresses the importance of self-care for caregivers. 29:10 - Nicole describes her coping mechanisms, including journaling, meditation, and reaching out for support from friends, emphasizing the need for caregivers to prioritize their own well-being. 30:32 - The conversation delves into the impact of stress on health, particularly for high-performing women, and the importance of setting boundaries and prioritizing self-care. 33:42 - Nicole discusses her current endeavors, including advocacy work, collaboration with Lyme Warrior, and her involvement with Galaxy Diagnostics to improve Lyme disease diagnostics. She also shares insights from her book, "What Lurks in the Woods," and provides information on where to find her work and upcoming projects. Get Nikki click here: https://wearenikki.com/ Use code LYMEBOSS for 10% off Guest Bio :Nicole Bell is an Author, entrepreneur, and advocate for tick-borne and neurodegenerative diseases. Former engineer turned executive in medical devices. Her memoir, "What Lurks in the Woods," recounts her caregiving journey. With degrees from MIT and Duke University, she now serves as Chief Business Officer at Galaxy Diagnostics. Nicole's Website: https://www.nicoledaniellebell.com/Get healthier food into your diet with these easy, yummy, fast meals today! Get more energy, less brain fog, and LESS pain when you start eating a low-inflammatory diet Download your free video series Real Cooking For Real Life here. https://thelymeboss.com/ #thelymebosspodcast #Lymepodstcast #healinglymepodcast #FunctionalHealth #LymeDisease #MentalHealth #Caregivers #Awareness #Research #Bioenergetics #Wellness #FunctionalMedicine #HealthPodcast #thelymeboss #nicoleDaniellebell --- Send in a voice message: https://podcasters.spotify.com/pod/show/lymebossheathergray/message Support this podcast: https://podcasters.spotify.com/pod/show/lymebossheathergray/support

Imagine 15 years of pain and undiagnosed symptoms, being bedridden, and suffering through relapse after relapse, until finally reaching the diagnosis of Lyme disease. Our guest today is an influencer who has been through hell and back and ultimately became her own advocate for health. She now pours her heart and soul into fighting for better patient care and treatment for others who suffer from Lyme. This is the Story of a Lyme Warrior with Elena Krail.EPISODE VIDEO HIGHLIGHTSWatch the Entire EpisodeAn Influencer's Battle to a Lyme DiagnosisNavigating Lyme Treatments: Conventional or Functional?Lyme Treatment: How to Be Your Own AdvocateLyme Journey: How To Recover After Hitting Rock BottomBeyond Lyme: Finding Purpose in the Healing JourneyCONNECT WITH ELENA KRAILWebsite - Lena's WorldInstagramFacebookCONNECT WITH INNOVATIVE MEDICINE Website Instagram Facebook YouTube CONNECT WITH CASPAR SZULC Instagram X LinkedIn LEARN ABOUT NADOVIM - A BREAKTHROUGH IN BRAIN HEALTHDoctor-formulated, clinically-tested true NAD+ supplement for focus, concentration and cognitive support. Visit our website and save 10% on your first order by using coupon code NADOVIM10. Website Instagram Facebook 'YOUR HEALTH. YOUR STORY.' PODCAST Follow us on Spotify Follow us on iTunes Subscribe on YouTube...

This is episode 18 of the Love, Hope, Lyme podcast. Fred Diamond's popular book, "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" offers those who love someone with persistent or chronic Lyme ideas and tips to support this beloved person. It also helps Lyme survivors know how to ask for support. On today's podcast, Fred interviews TJ Nelson, author of "Walk the Lyme: From Knocking on Death's Door to Building a Multimillion-Dollar Business." As Fred conducted the research for his book “Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know,” he read dozens of books from medical practitioners and Lyme disease survivors. On this week's Love, Hope, Lyme podcast, TJ Nelson, a successful business owner, talks about his healing journey and how he was able to develop a successful business while battling Lyme disease. If someone you love has been afflicted with Lyme disease, listen to this podcast now. The e-version of Fred's book is always free for Lyme survivors. Just reach out to Fred on Facebook or LinkedIn. The print copy can be ordered at https://www.amazon.com/Love-Hope-Lyme-Partners-Survivor-ebook/dp/B0B9Q8LX7G/.

This is episode 17 of the Love, Hope, Lyme podcast. Fred Diamond's popular book, "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" offers those who love someone with persistent or chronic Lyme ideas and tips to support this beloved person. It also helps Lyme survivors know how to ask for support. On this week's Love, Hope, Lyme podcast, Fred interviews successful sales trainer Lauren Bailey. Lauren was originally interviewed on Fred's Sales Game Changers Podcast about her successful career in sales training and consulting, all while battling chronic Lyme disease.  As Fred conducted the research for his book “Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know,” he was shocked to learn how difficult it was to manage career while battling Lyme. Fatigue, anxiety, and pain often made it hard to work. Lauren talks about how she succeeded while treating her Lyme disease. If someone you love has been afflicted with Lyme disease, listen to this podcast now. The e-version of Fred's book is always free for Lyme survivors. Just reach out to Fred on Facebook or LinkedIn. The print copy can be ordered at https://www.amazon.com/Love-Hope-Lyme-Partners-Survivor-ebook/dp/B0B9Q8LX7G/.

Ever wish you had the energy to run your business like the successful entrepreneurs who seem to be everywhere at once?It's entirely possible when you learn how to tap into the power of automation.Lyme Warrior and automations queen Jess Kotzer joins me today to help you find the systems and workflows that *work* for you — so you can build a business that runs without you.BY THE TIME YOU FINISH LISTENING, YOU'LL DISCOVER: How Jess embraced her chronic illness and automated her business to six figuresWhy automations stop decision-fatigue in their tracks (saving you more time and energy)Where to start when setting up automations in your businessOne easy automation you can install today that will give you back an hour every weekThree things you can do to become a published authorCheck out Jess and Create Unforgettable Experinces Through Collaboration HERE!Support the showSupport the showLoved this episode? Leave a review: https://www.craftedtothrive.com/reviews/new/To Work With Nikita, Book A Free Discovery Call Here.Subscribe to the exclusive private-podcast series, Create Your Clarity Mondays, where I help service-based creatives and coaches living with chronic illness get unstuck and grow their businesses with ease in less than 15 minutes.Follow Nikita on Instagram

Guys this is an episode you don't want to miss! I sit down and chat with Alyssa of @holyssticbalance to talk all things confidence and how to be your best self. We dive into how to grow your business through boundaries and positivity, why investing in yourself is a life changer and how to grow your confidence through your business. Grab a coffee, cozy up  and enjoy! Listen to the complete Episode on Spotify:Listen to the complete Episode on Apple Podcasts:Find me on Instagram for daily entrepreneurial education:  https://www.instagram.com/emilywoodswellness/ APPLY FOR FOUNDATIONS OF ONLINE COACHING:  https://prodigious-innovator-3744.ck.page/500c14b1aaGET MY NICHE COURSE: https://emily-woods-wellness-llc.teachable.com/p/discovering-your-nicheMY ACE EXAM STUDY GUIDE: https://prodigious-innovator-3744.ck.page/937cd4366c 

Brain on Fire. How many of you can relate to that? Our very first episode!! How exciting. And I love the non-profit Lyme Warrior. So blessed to have them as my first guest. In this episode, we dig in deep in it's not all in your head. Listen to Sharon's Lyme story and her two daughters who also have Lyme. How she talks about being totally dismissed by Doctors calling her an attention-seeking hypochondriac. Sharon, like most of us mothers, also knew there was something up with her kiddos. And she was determined to find answers. Also find out what the nonprofit Lyme Warrior is all about, and how you can get involved! https://lymewarrior.us/ https://www.facebook.com/LymeWarriorUS And if you have Lyme and are looking for a support group, check out mine here. https://www.facebook.com/groups/509165527599122 --- Send in a voice message: https://anchor.fm/lymebossheathergray/message Support this podcast: https://anchor.fm/lymebossheathergray/support

In this episode we interview Wellness Blogger and Lyme Warrior, Carly Taylor. Carly shares her experience battling Lyme Disease from the very beginning to her final healing protocol. She shares insight on how to eat, think and heal from a chronic illness and how important your thoughts can be when healing. Carly Taylor is a wellness blogger, certified health coach, and Lyme warrior. Being diagnosed with Lyme disease in 2015, she has worked over the years to completely change her lifestyle and mindset to help heal Lyme. She also helps others to heal through social media and teaching others about a healthy toxic free lifestyle. Follow Carly at @naturallycarly Blog: Naturally Carly - Your Healthiest Self, Naturally Notes from Episode: @intentionally_mikayla @tickbootcamp Episode 125: Tick Boot Camp https://podcast.tickbootcamp.com/episode/dfea5185b6ef42fc/life-s-greatest-lesson-an-interview-with-carly-taylor

In this episode we interview Wellness Blogger and Lyme Warrior, Carly Taylor. Carly shares her experience battling Lyme Disease from the very beginning to her final healing protocol. She shares insight on how to eat, think and heal from a chronic illness and how important your thoughts can be when healing. Carly Taylor is a wellness blogger, certified health coach, and Lyme warrior. Being diagnosed with Lyme disease in 2015, she has worked over the years to completely change her lifestyle and mindset to help heal Lyme. She also helps others to heal through social media and teaching others about a healthy toxic free lifestyle. Follow Carly at @naturallycarly Blog: Naturally Carly - Your Healthiest Self, Naturally Notes from Episode: @intentionally_mikayla @tickbootcamp Episode 125: Tick Boot Camp https://podcast.tickbootcamp.com/episode/dfea5185b6ef42fc/life-s-greatest-lesson-an-interview-with-carly-taylor

There are many ways to treat Lyme Disease and debate around antibiotics vs. herbs/supplements. In today's episode, Georgia shares her journey with taking antibiotics (and herbs!) to treat her Lyme+co-infections. Georgia explains what medications she took, how she felt, and why she ultimately made the decision to start taking antibiotics as someone who works in the holistic space.  Open enrollment for the August back-to-school session of NUTRITION BUSINESS BOOTCAMP is available now!Apply today.Whole Body HealingWholeBodyHealingNutrition.comIG+TikTok: @wholebodyhealinggeorgia@wholebodyhealingnutrition.com

On this episode of When Harry Met Daphne  we interviewed Melissa Klepacki - an Acupuncturist, Serial Entrepreneur, Wellness Fanatic and TedX Speaker, Mom of 2 teen boys, Wife, Lyme Warrior, Magic Maker, 2 time Collegiate National Champion coxswain, published author, bourbon drinker and a little bit tech geek.  Founder of The Güüd Company - a voice-first wellness company. - "I stand for vibrant health for all!"Please take better care of yourself.Connect with Melissa Klepacki:   Instagram   | FacebookSupport the show

Lauren Lovejoy is the charismatic entrepreneurial founder of the Lyme service organization Lyme Warrior. She grew up and lives in rural Virginia. Ms. Lovejoy was living a life of a normal 20 something, working in a law office by day and attending graduate school studying Analytics at night. She filled her remaining time participating in social activities and training at a CrossFit gym. One weekend, when she took an 8-hour road trip, she suffered a panic attack, shaking, and an out of body experience. After returning to school, she began to suffer from disorientation and vision loss. Her symptoms continued to build to the point that she had to acknowledge she “could not continue her job or her education.” Her illness remained undiagnosed, despite visiting “piles of primary care doctors, every category of specialists (twice), and functional medicine” professionals. One renowned neurologist told her “there was nothing he or any doctor could do for [her]” and she had to accept her “life as being home bound.” Her diagnosis arrived as a gift from a nurse at a holistic clinic that rejected her as a patient. He told her “based on your symptoms, you sound like you have Lyme disease” and encouraged her to attend a specialized Lyme clinic. During her time studying Lyme disease, she discovered her story was not uncommon. She learned that the well documented disease was “still denied by [her] government, and most doctors.” This information inspired her to create the Lyme Warrior non-profit from her couch. If you would like to learn more about how Lyme Warrior Lauren Lovejoy discovered that it was her job to try to prevent her Lyme disease story “from happening to as many people as possible,” then tune in now!

In honor of Lyme Disease Awareness month, Georgia shares the best nutrition for Lyme Disease! Wherever you are in your journey, Georgia will explain what foods will and won't get your body in fighting shape against the disease. She shares simple and practical tips to get your body closer to healing. Open enrollment for the August back-to-school session of NUTRITION BUSINESS BOOTCAMP is available now!Apply today.Whole Body HealingWholeBodyHealingNutrition.comIG+TikTok: @wholebodyhealinggeorgia@wholebodyhealingnutrition.com

Today Georgia is joined by fellow Lyme warrior and host of the Lyme 360 podcast, Mimi MacLean. Mimi shares her personal journey with Lyme Disease, both past, and present. She explains some of her favorite methods for healing, how she keeps fighting despite living with long-term Lyme, and what she's learned hosting her own podcast. Mimi and Georgia also discuss the importance of Lyme testing, detox, and the Lyme/mental health connection. Mimi is full of knowledge and an amazing guest to kick off Lyme Disease awareness month! Mimi MacLeanhttps://lyme360.com/IG: @lyme.360Lyme 360 PodcastWhole Body HealingWholeBodyHealingNutrition.comIG+TikTok: @wholebodyhealing Open enrollment for the August back-to-school session of NUTRITION BUSINESS BOOTCAMP is available now! Apply today. 

VM Evolution Classic!This is a very controversial episode. The views shared at not the views of this show. 

Your brain, mindset, and nervous system play a large role in the healing process of chronic Lyme. Lindsay Mitchell, founder of Vital Side and Lyme warrior, used brain retraining to regain her health. The virtual programs provide a modern approach to finding solutions to limbic system impairment - key techniques for healing from many of the symptoms.Tune in to this episode to learn about Lindsay's journey, what brain retraining is and how you can use it to help with your chronic pains and symptoms.

Healing takes time and the timeline to get better is different for everyone - it took 10 years for her to receive a proper Lyme diagnosis and over 20 specialists to get on a healing path. As an actress in LA whose life was thrown off course due to Lyme and COVID, Christa focused on healing and building a community for other chronic illness warriors. Her biggest progress happened after discovering energy healing. She is now working on recovering, her documentary, and her book Tick Tock Lyme O'Clock launching on January 11th.Tune in to hear about Christa's journey with Lyme, how she navigated the medical system, and all about her book launch!

She used her project management training to approach her years of chronic symptoms and pain and now is on the other side of remission from Lyme. Julie Yakunich went through 5 years of undiagnosed Lyme disease and has firsthand experienced healing from a complex chronic disease. She uses her experience in her 1-1 coaching services called Get Well with Julie where she helps clients do exactly what she did...heal once and for all!Tune in to hear her tips to getting on the right track and healing as well as why mindset and calming your nerves is crucial.

Traci Weintraub is a cook, author, and Lyme warrior whose diagnosis and battle with Lyme inspired her to build an immuno-supportive lifestyle that is just as delicious as nutritious. She created Gracefully Fed to spread her recipes and healthy approach to delicious food and meals. Gracefully Fed is organic gluten and dairy-free soupery that offers local pickup in LA and nationwide shipping. Her brand mission is inspired by her healing journey and the desire to heal her chronic symptoms while maintaining a happy and not a limited lifestyle.Please tune in to hear about Traci's journey from Lyme diagnosis to Gracefully Fed, the habits she had to break and relearn to heal, and why nutrition is such a pivotal component to beating chronic pain and supporting your immune system.This week's episode is sponsored by Vital Plan, a supplement line Bill Rawls MD. He is the author of Unlocked Lyme and the founder of Vital Plans, a supplement line made of herbs that supports the immune system (made especially for Lyme warriors). Dr. Rawls offers a free online survey to help you get the right supplement protocol and be on track to a healthier life. Go to lyme360.com/DrRawls to learn more about the amazing herbal protocol I have been using.  

Stress, nutrition, and an imbalance hormone system can all lead to exacerbated chronic Lyme symptoms - it's essential to prioritize building a lifestyle that enables you to look and feel your best from the inside out. Jolene Hart is a former beauty editor and chronic late-stage Lyme warrior whose healing journey inspired her to pivot into 1-1 coaching other chronic illness warriors into feeling better. Her coaching, Beauty Is Wellness, focuses on holistic healing: everything from stress and gut health to clients' products.Tune in to hear why it's essential to have a low sugar diet and avoid cortisol spikes, the power of energy and positivity in the healing process, and her top advice for improving your lifestyle when fighting Lyme.Beautycounter sponsors this week's episode. Do you know what you are putting on your skin? What you put on your skin, which is your largest organ, is just as important as what you eat because your body immediately absorbs what is on the skin. Most of your products have not been tested for human safety, and for those struggling with your health, it is super important to use clean products. Beautycounter is the leader in cleaner, safer cosmetic and body products that work. They have done the research and taken the guesswork out of what products are safe.  Go to lyme360.com/beautycounter to learn more. 

Sometimes the path to healing is about slowing down, going back to the basics, and focusing on overall wellness. Georgia Grey is the perfect example of how sometimes even a healthy diet and wellness-based lifestyle can't fully heal you until you slow down. After years of symptoms, she was diagnosed with Lyme and celiac disease, yet her healthy lifestyle could not erase the brain fog, joint pain, and swollen limbs. Her journey with Lyme inspired her to reconsider her daily habits and focus on her overall nutritional balance. She is an INHC certified holistic coach, and her company Whole Body Healing Nutrition is focused on 1-1 coaching to help other chronic pain warriors have the right tools to heal.Please tune in to hear about her Lyme journey and the critical changes she made to overcome her chronic symptoms, why a modified paleo diet is her preferred nutritional plan, and the importance of a tight-knit support system.This week's podcast is brought to you by Air Oasis. As a Lyme warrior, I know how important it is to have clean air in the home. I've been using a room air purifier but recently purchased an all-home unit to combat mold issues throughout our house. I did some research and found a great company called Air Oasis. Their air purifiers help fight bacteria, viruses, and mold. So if you've not put an air purifier into your home, go to lyme360.com/airoasis. They carry room units as well as entire home units.

Looking to find out where Lyme originated?  Kris Newby began her investigative Lyme journey when she and her husband were both diagnosed with Lyme. While receiving treatment and recovering from the disease, Kris was left with a clear feeling that Lyme disease was misunderstood and overlooked by the medical community - no one gave her clear answers, so she started researching. Something was awry.  Through her journey of creating the film Under the Skin and writing Bitten, Kris was introduced to Willy Burgdorfer, the discoverer of Lyme microbes that admitted a stark truth of his work during the Cold War.  Tune in to hear what Willy disclosed to Kris, why she believes COVID long haulers are prioritized, and chronic Lyme warriors are overlooked, and what she has in the works as her next project.  Kris is the Tom Clansy of the Lyme world.  This is an episode you don't want to miss.To learn more about the podcast go to https://www.lyme360.comFor your free Lyme Detox Checklist please go to:  https://www.lyme360.com/detoxchecklist

This week on the Heal Podcast, Jessica Snajder talked to us about her foundation Partner in Lyme and how her family's personal battle with Lyme inspired her to find a way to help others alleviate the financial burden that comes with fighting chronic Lyme. The charity does work to provide grants to individuals who have a hard time keeping up with the living cost of Lyme disease (something not often talked about!)

Raising awareness on Lyme disease can sometimes be hard when the process of talking about one’s journey is exhausting - that is where Patricia Cosulich decided to step in and create The Great Imitator. A documentary theatre-based platform for Lyme warriors to express their stories, build community and ultimately raise awareness to a wider audience. Tune in to hear Patricia’s own battle with Lyme, how she was inspired to use theatre as a vessel for activism, and how she plans to grow her platform in order to raise funds for the community.PS: Dr. Rawls is a trusted MD whose life was upended by Lyme but was able to heal himself and use his experience to help others on their journeys battling Lyme. He is the author of Unlocked Lyme and the founder of Vital Plans, a supplement line made of herbs that supports the immune system (made especially for Lyme warriors). Dr. Rawls offers a free online survey that can help you get the right supplement protocol and on track to a healthier life. Go to lyme360.com/DrRawls to learn more about the amazing herbal protocol I have been using.  

This week Sarah is joined by Gina Valles, a fitness coach with a degree in exercise science who founded Gina's Total Fitness in Connecticut. In 2018, Gina was diagnosed with Lyme disease, which changed her life and outlook on fitness. Through her Instagram account, which has almost 180,000 followers, Gina shares her journey, workouts, and inspiration.Gina explains that she lived with undiagnosed Lyme disease for a year in 2017 before being diagnosed. She knew nothing about the disease then, but has educated herself and learned how to adjust her exercise routine and manage on a day-to-day basis. Gina was a competitive athlete throughout her life, and when she got sick she had to adjust her workout routines to focus more on lower intensity movement and listening to her body. She emphasizes that it took time, trial and error to find a fitness routine that works for her.Get the show notes and resources.

After contracting a serious case of Lyme and Bartonella in 2014, which was misdiagnosed by a dozen doctors, leading to heart failure, Dana Parish was determined to help change the status quo. She's a chart-topping Sony ATV writer and New York City-based science journalist and the co-author of Chronic, a book focused on exposing the truth of the infectious causes of chronic psychiatric and auto-immune illnesses around the world.Tune in to hear all about her experience with Lyme, how she began the journey of investigating and writing Chronic, and the advice she gives to Lyme warriors struggling right now.Dr. Rawls is a trusted MD whose life was upended by Lyme but was able to heal himself and use his experience to help others on their journeys battling Lyme. He is the author of Unlocked Lyme and the founder of Vital Plans, a supplement line made of herbs that supports the immune system (made especially for Lyme warriors). Dr. Rawls offers a free online survey that can help you get the right supplement protocol and on the track to a healthier life. Go to lyme360.com/DrRawls to learn more about the amazing herbal protocol I have been using.  

This week on the Heal Podcast we sat down with Bennett Nemser, the Senior Program Officer at the Steven & Alexandra Cohen Foundation, to talk about the initiatives he is working on, how the foundation has dispersed over $60 million dollars in grants since 2015, and his new work on the LymeX initiative. Nemser is the director of the foundation's Lyme and Tick-Borne disease initiative and looks over the grants awarded by the foundation to candidates.Tune in to learn how the Cohen Foundation is the #1 donor to the Lyme community, what the LymeX Innovation Accelerator is, and why it's imperative to get better diagnostic and treatment opportunities for Lyme patients.  Editor's Note: In the episode, we talk about the Tick-Borne Disease Working Group. The 21st Century Cures Act, enacted in December 2016, authorizes the HHS Secretary to establish a Tick-Borne Disease Working Group to serve as a Federal Advisory Committee.  The Tick-Borne Disease Working Group has 14 members - seven federal members and seven public members - with diverse disciplines and views pertaining to tick-borne diseases. The Act charges the Working Group to provide a report to Congress and the HHS Secretary on its findings and any recommendations every two years. To learn more, please visit: https://www.hhs.gov/ash/advisory-committees/tickbornedisease/index.htmlThis episode was sponsored by Air Oasis. The air quality in your home is worse than the air outside,  As a Lyme warrior, it is important to have clean air in the home. I’ve been using a room air purifier but recently invested in an all-home unit from Air Oasis to combat mold issues. Their air purifiers help fight bacteria, viruses, and mold. If you’ve not put an air purifier into your home, go to lyme360.com/airoasis for more information on Air Oasis products.

Having histamine sensitivities? Hives, rashes, over-sensitive to Amy chemicals or foods? Dr. Gail Clayton talks to us about why lyme causes our body to go into over drive and what you can do about it Her expertise is chronic illness and reducing symptoms through an in-depth look at their life patterns, diet, and amino/fatty acid testing. She is the co-founder of the Mold Detox Guide that helps educate people on how to discover, get rid of, and heal from mold toxicity. She discusses how your immune system becomes polarized and sends you into chronic inflammation and histamine sensitivity episodes. Tune in to learn why and how pH balance and other steps are key to neutralizing the polarization within your body and reaching an equilibrium that will keep histamine and mast cell reactions at bay.To learn more about the podcast go to https://www.lyme360.comFor your free Lyme Detox Checklist please go to: https://www.lyme360.com/detoxchecklist

Amanda Tiberi is a Lyme Warrior and founder of Grab A Spoon Wellness, a platform to share her story battling chronic illness as well as take on clients and help them succeed in their wellness journey. She is a licensed Holistic Coach and has a Masters of Science in Nutrition which led her to create her own line of herbal products called Olive + Grayce Apothecary. Tiberi's practice is based on clean nutrition and detoxing the body of toxins such as mold which can contribute to chronic pain - her weekly regimen includes eating for her genetic makeup, salt baths, and a strict supplement routine. Tune in to learn more about the tools Amanda used to clear clients and her own chronic symptoms.

Dr. Bill Rawls is a Lyme Warrior who healed his Chronic Lyme on a budget using herbal treatments. Tune in to learn how you can start healing now with simple protocols that treat the root cause, not just your symptoms.

In this episode Freddie invites Lauren Lovejoy, the owner of Lyme Warrior. Lyme Warrior is a nonprofit organization that supports people affected by Lyme and forming a strong and passionate community. Through her journey with Lyme, she has gone from selling shirts to creating a community that provides Lyme patients with security and a place to belong to. This episode will focus on Lauren's healing process and how Lyme Warrior has grown into what it is today. She talks about the importance of building a community, giving back, different modalities of healing with Lyme, and going back to nature. HIGHLIGHTS1:43 Lauren talks about her Lyme disease journey and how she established Lyme Warrior10:05 Freddie shares his point of view on dealing with illnesses alone and forming a community11:37 How Lyme Warrior provides a community for those suffering from Lyme16:13 Lauren talks about how Lyme Warrior gives support to caregivers of Lyme disease patients18:32 Freddie shares how he has incorporated technology in his healing process, with AmpCoil having the most impact on him. But he emphasizes that it's not all about the tech, it's also about the community.21:57 How the pandemic has affected Lyme Warrior24:00 Lauren urges everybody to give at least 1%, which can have a great impact on the cause25:53 Freddie looks back to his experience with cancer and shares his reflections in comparison to Lyme27:11 Lauren talks about how the healing process of Lyme is sometimes a lonely path29:26 Freddie and Lauren talk about Lyme disease, dating, and having proper emotional support37:50 Lauren reflects on the impact of technology on dealing with Lyme, elevating your quality of life, and going back to nature.46:15 She talks about the financial side of running a non-profit organization and learning the ropes of leadership and growth48:24 She talks about her vision for Lyme Warrior for the upcoming year51:36 Freddie talks about his friend Tyler and how people are creating platforms that bring about great change for people affected with chronic illnesses like LymeRESOURCES MENTIONEDLyme Warrior US Website - https://lymewarrior.us/lauren-lovejoy-lyme-warriorLauren Lovejoy on Linkedin - https://www.linkedin.com/in/lauren-lovejoy-1926874aUPGRADE YOUR WELLNESSActivate your Stem Cells - LifeWave.com/beautifullybrokenAmpCoil and PEMF - Discount Code - BeautifullyBrokenMagnesium Breakthrough Promo Code - BEAUTIFULLYBROKEN10Dry Farm Wines http://www.dryfarmwines.com/freddiesetgoRelax Saunas https://bit.ly/36B5z0dBiOptimizers  https://bit.ly/3lBeJA1CONNECT WITH FREDDIECheck out my website - https://freddiesetgo.com/ Instagram - https://www.instagram.com/freddiesetgo/Read my Favs - https://freddiesetgo.com/freddies-favorites/ Sing For Your Seniors - https://http://singforyourseniors.org Amp Coil - https://www.ampcoil.comABOUT FREDDIEI'm Freddie Kimmel, a Functional Health Coach, Reiki Healer, Certified Personal Trainer, Gut Health Specialist, and a proud cancer survivor. I help men and women eliminate brain fog, bloat and belly fat through gut health. I've been featured in The Wall Street Journal, the Full Plate Podcast, An Excellent Example of Being Human, State of the Arts on LA talk radio and Dance Magazine. I have a Bachelor of Fine Arts from SUNY Brockport, attended SUNY Fredonia, and graduated from the Institute of Functional Health Coaching. I can be found in NYC living each day to its fullest and focused on creating more value than what I capture. Please stand back from the awesomeness that's about to unfold.

Dr. Jaban Moore is a Lyme Warrior and Doctor of Chiropractic. Dr. Moore has now been symptom-free for over 5 years and has made it his mission to help others find the root causes of their conditions. When he first sits down with a Lyme patient, he just listens. Because if you can give a Lyme person 20 minutes to just talk, he believes that you are going to get a great amount of information is going to lead you in a direction. Tune in to listen to Dr. Moore's detoxing, fasting, and supplement tips for Lyme Warriors.

So excited to share with you a conversation I had with Sylvie Lam of Herterra. She is a somatic therapist and creator of beautiful beaded earrings at Herterra Wear. In this conversation got extra vulnerable and we discuss our journeys with Lyme disease and the things that have helped on our healing paths. Also lots of ideas  and questions about branding and developing a heart centered business. We also dive into ancestry, dance, herbalism, therapy and so much more! Let me know your favorite takeaway on instagram @thymeinthestudiopodcast Links:https://www.herterrawear.com/https://sylvielam.com/https://www.instagram.com/herterra.wear/https://www.instagram.com/inspirochete/https://www.instagram.com/sylvielamcounseling/ Links mentioned:for more information on trauma in the body and healing racialized trauma.“My Grandmother’s Hands”https://www.amazon.com/My-Grandmothers-Hands-Racialized-Pathway/dp/1942094477“The Body Keeps the Score”https://www.amazon.com/Body-Keeps-Score-Healing-Trauma/dp/0143127748/ref=sr_1_3?dchild=1&keywords=The+Body+Keeps+the+Score&qid=1599885755&sr=8-3 Thyme in the Studio links: https://www.patreon.com/thymeinthestudiohttps://www.instagram.com/thymeinthestudiopodcast/https://www.instagram.com/aida.zea.arts/https://www.facebook.com/groups/403582056803336/www.thymeinthestudio.comhttps://www.aidazea.comContact me: sara@aidazea.com Thymelights:*The somatic therapy teacher and Hakomi trainer Melissa Grace for her therapeutic insight and stance *Melissa Michels work with 5 rhythms https://goldenbridge.org/Also, the books When the Body Keeps the Score and My Grandmother's Hands for more information on trauma in the body and healing racialized trauma.Sylvie is the founder of Herterra. Where she.Making bold earrings for bold women who aren’t afraid of a little color and fringe. From her therapy site she states.Outside of the office, I feel at home in the forest, with a paintbrush in my hand, or on the dance floor. My ongoing commitment to self-growth and exploration through five-rhythms dance, yoga, and meditation continues to enhance both my personal and professional life.Credentials– Masters in Mindfulness-Based Transpersonal Clinical Counseling from Naropa University – Certified Hakomi Therapist through the Hakomi Institute – PACT Level 1 therapist – EMDR trained from the Mailberger Institute – MESA (Moving to End Sexual Assault) Hotline Volunteer – Teaching Assistant for Naropa University Human Growth and Development Courses – Teaching Assistant for Hakomi InstituteMy mission:To support individuals to work through trauma and blocks in order to return to a natural state of connection with their bodies, hearts, and spirits allowing them to live with a greater sense of agency and choice.To assist couples in working through individual and collective trauma that impacts their relationship in order to cultivate a more connected and easeful partnership. The beginning of our chat  and our super secret invocation  before we went live was especially magical and is available to patreon supporters. We're offering a pay what you can community model so you can join for as little as $1/month! Thanks for considering that option!www.patreon.com/thymeinthestudio

Kirk and Trevor are live on stage at HempFest Saskatoon for a second time!  This time Trevor talks with Sue Letwin(@LetwinSue).  Sue has Lyme Disease.  She explains how this misunderstood condition effects her life and how cannabis is helping her.  In fact she finds the THC helps her more than CBD.  And she make her own edibles.  Come learn from Sue with us! Music: The Sheepdogs https://thesheepdogs.com/ (Yes we got a SOCAN membership to use this song all legal and proper like) Additional Music: Desiree Dorion www.desireedorion.com/ Marc Clement http://marcclementmusic.com/ Links: Sue Letwin - https://www.indicapable.ca/ Twitter - https://twitter.com/LetwinSue Facebook - https://www.facebook.com/sue.letwin HempFest Canada - http://www.hempfestcanada.com

Kirk and Trevor are live on stage at HempFest Saskatoon for a second time!  This time Trevor talks with Sue Letwin(@LetwinSue).  Sue has Lyme Disease.  She explains how this misunderstood condition effects her life and how cannabis is helping her.  In fact she finds the THC helps her more than CBD.  And she make her own edibles.  Come learn from Sue with us! Music: The Sheepdogs https://thesheepdogs.com/ (Yes we got a SOCAN membership to use this song all legal and proper like) Additional Music: Desiree Dorion www.desireedorion.com/ Marc Clement http://marcclementmusic.com/ Links: Sue Letwin - https://www.indicapable.ca/ Twitter - https://twitter.com/LetwinSue Facebook - https://www.facebook.com/sue.letwin HempFest Canada - http://www.hempfestcanada.com

During our conversation, Eric and I discuss his journey in martial arts and MMA fighting, what it's like to climb 400' regularly, and his efforts with the non-profit Lyme Warrior to find a cure and better treatments for Lyme's disease.

During our conversation Eric and I discuss his journey in martial arts and MMA fighting, what it's like to climb 400' on a regular basis and his efforts with the non-profit Lyme Warrior to find a cure and better treatments for Lyme's disease.

During our conversation Eric and I discuss his journey in martial arts and MMA fighting, what it's like to climb 400' on a regular basis and his efforts with the non-profit Lyme Warrior to find a cure and better treatments for Lyme's disease.

During our conversation Eric and I discuss his journey in martial arts and MMA fighting, what it's like to climb 400' on a regular basis and his efforts with the non-profit Lyme Warrior to find a cure and better treatments for Lyme's disease.

In 'Climbing High with Eric Canfield' 's we hear about 400' towers, the Lyme Warrior charity and Eric's work to create sustainable farms.

During our conversation Eric and I discuss his journey in martial arts and MMA fighting, what it's like to climb 400' on a regular basis and his efforts with the non-profit Lyme Warrior to find a cure and better treatments for Lyme's disease.

In this episode, Amy Stark talks with Kimberly Gifford about her struggles with Lyme disease, and how she, and her three children, used energy medicine to help them heal from Lyme Disease. Kim's story is both heartbreaking and inspiring; you won't want to miss it!  You can find more information about Kimberly here: Facebook: facebook.com/kimberly.cronangifford Instagram: instagram.com/this_life_health/  Kimberly Gifford is a Holistic and Sports Nutritionist, Energy Healer, Applied Kinesiology Wellness practitioner, and badass Lyme Warrior. Everything you need to know about one of my favorite techniques, E.F.T. (tapping) can be found on my website or simply, click here!

Episode Description Kirk and Trevor are live on stage at HempFest Saskatoon for a second time! This time Trevor talks with Sue Letwin(@LetwinSue). Sue has Lyme Disease. She explains how this misunderstood condition effects her life and how cannabis is helping her. In fact she finds the THC helps her more than CBD. And she make her own edibles. Come learn from Sue with us! Music: The Sheepdogs https://thesheepdogs.com/ (Yes we got a SOCAN membership to use this song all legal and proper like) Additional Music: Desiree Dorion www.desireedorion.com/ Marc Clement http://marcclementmusic.com/ Links: Sue Letwin - https://www.indicapable.ca/ Twitter - https://twitter.com/LetwinSue Facebook - https://www.facebook.com/sue.letwin HempFest Canada - http://www.hempfestcanada.com