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What if one of the most powerful wellness tools was literally at your fingertips?In this episode, we welcome Susan Shane, founder of Vitality Fusion, licensed acupuncturist, educator, and longtime advocate for holistic health. Susan shares how an unexpected journey into Traditional Chinese Medicine led her to discover Korean Hand Therapy—a unique approach that uses the hand as a map of the entire body.Susan explains why this technique has gained attention around the world, how it can complement other wellness practices, and why it has become one of her favorite tools for helping people support their health and wellbeing.She also gives a preview of the Korean Hand Therapy workshop she'll be leading at the 45th Annual ANMA Convention in Las Vegas.In This Episode:- How Susan's career in natural health began- What Korean Hand Therapy is and how it works- The connection between the hands and the body's meridian system- Why stress may be affecting more of your health than you realize- How Eastern and Western healing philosophies can work together- What attendees will learn during Susan's ANMA convention workshop- Simple ways to support physical, emotional, mental, and spiritual wellbeingAbout This Podcast:Promoting and Protecting Naturopathy is powered by ANMA, the nation's oldest and largest naturopathic association. Each month, we share insights for naturopathic professionals, students, and anyone passionate about natural health.Not a member? Join ANMA today for legislative alerts, educational opportunities, member discounts, and professional community support. Visit anma.orgConnect with us:Stay tuned for updates on the 45th Annual ANMA Convention at anma.orgAmerican Naturopathic Medical Association: ⁠https://www.anma.org⁠American Naturopathic Medical Certification Board: ⁠https://www.anmcb.org⁠American Naturopathic Medical Accreditation Board: ⁠https://www.anmab.org⁠Society of Complementary Alternative and Holistic Practitioners: https://www.scahp.orgEmail: admin@anma.orgThis podcast is produced by Espresso Podcast Production: https://www.espressopodcastproduction.com/Disclaimer: This podcast is for educational purposes only and should not be taken as medical advice. Consult your doctor before implementing any information shared. Views expressed are those of the speakers and do not necessarily reflect ANMA or ANMCB positions.

A mother tells her child that one “impure” thought could mean eternal fire and she claims she can read minds. That fear becomes the fuel for a family-run, high-control religious group where confession lasts until 3 a.m., “demons” explain every human impulse, and doubt is treated like a moral failure. Peggy, author of *Surviving the Family Kingdom* and a psychotherapist, unpacks what it's like when the cult leader is also your parent. Peggy walks us through the early chaos that made her mother vulnerable to extreme beliefs, the Pentecostal influence that normalized spiritual spectacle, and the slow shift from searching for faith to building a closed system of control. We talk about coercive control tactics like sleep deprivation, isolation, punishments, the “hot seat,” and how love bombing can flip into fear the moment someone stops complying. Then we follow the moment everything breaks open: motherhood. Peggy describes how parenting clarified what she could no longer accept, how she stopped policing her own mind, and why leaving required a strategy that protected her from manipulation. We also explore the harder, less-discussed part of cult recovery and religious trauma: rebuilding identity, living with triggers, and navigating a complicated relationship with an aging parent who never offers acknowledgement. Peggy shares how EMDR helped neutralize the images and body memories that kept her feeling haunted. If this conversation helps you, subscribe, share it with someone who needs it, and leave a rating and review so more listeners can find stories of survival and recovery.Send us Fan MailSupport the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...

On this episode, Raphael Gaspard joins Liane to talk about his amazing project for 2026, riding across Canada seeking an answer to one simple question from riders…what's your definition of happiness?Guest: Raphael Gaspard, Photographer & DirectorEmail: raphael.degaspard@gmail.comAMSS: Liane LangloisWebsite: ab-amss.orgEmail: info@ab-amss.orgPodcast ProducerBryn Griffiths / Mighty Mouth CommunicationsWebsite: bryngriffiths.com Email: bryng@bryngriffiths.com

In this week's passage, Peter is exhorting believers in times of great trial. Listen to hear the progression of trials that God took Peter through to bring him to this level of confident faith.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Chrisy and Dr. Kingzett, two women I met when we were all trying to raise our rare voices a little louder. Christine “Chrisy” Klavitter and Dr. Kristen Kingzett are both rare disease advocates, but more importantly, they are people living this reality every single day. Chrisy lives with Stiff Person Syndrome and Myositis. Kristen is an Internal Medicine physician and an ultra-rare cancer survivor. Together, we talk about what life with rare disease actually looks like—beyond the statistics. From delayed diagnoses (which can take years, even decades) to the emotional and physical toll of navigating a fragmented healthcare system, this conversation is honest, eye-opening, and necessary. More than 30 million people in the U.S. are living with a rare disease—defined as affecting fewer than 200,000 people. Yet despite those numbers, patients are still too often misunderstood, misdiagnosed, or left to navigate care on their own. Chrisy and Kristen share what an average day can look like, the full-time job of managing health (or caring for someone who is), and what happens when patients have to push back—even redirect—the so-called experts. We also dig into the bigger questions: Why does diagnosis still take so long—and how do we fix it? What do providers, institutions, and policymakers still not understand? What do you say to someone who believes “there's nothing I can do”? And where are we actually seeing progress in healthcare? What stands out most is this: patients are not passive participants in their care—they are often the ones holding it all together. About my guests: Dr. Kristen Kingzett is an Internal Medicine physician, educator, and advocate who brings both professional expertise and lived experience, including Juvenile Idiopathic Arthritis, Common Variable Immune Deficiency, and an ultra-rare cancer. She serves on Michigan's Rare Disease Advisory Council and Legislative Disability Caucus. Chrisy Klavitter is a healthcare policy and patient advocate, biologist, and recreation therapist. Living with Stiff Person Syndrome and Myositis, she works to bridge communication gaps between patients, providers, researchers, and policymakers to improve care for complex conditions. The takeaway? Rare disease may be defined by numbers, but its impact is anything but small. And if we build a healthcare system that works for rare disease patients, we build one that works better for everyone. Like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

The podcast content may contain sensitive topics. Listener discretion is advised. CAPACITY.  It's the single most important and often most overlooked factor in protecting children from online exploitation. Parents often ask, “What age is safe for a child to be online?”  But age isn't the real question.Capacity is.Does your child have the maturity, reasoning skills, and emotional grounding to navigate a digital world sharedwith 5.5 billion people, including individuals who intentionally target minors?Do they understand enough about adult behavior and boundaries to recognize grooming when it begins and not after it's too late? And perhaps most importantly, is your relationship strong enough that they will come to you themoment something feels wrong?On this episode of the Protect & Prevent Podcast (P3 Kids), Opal Singleton Hendershot of MillionKids.org, one of the leading voices in keeping kids safe from predators, breaks down what “capacity” really means and why it matters more than ever. You'll learn how to build a positive, instructive relationship to help young people recognize both the value and dangers of being online. We will explore helpful conversations andeven written agreements that can assist parents and minors before they find themselves in danger.  The online world is evolving daily. Your child's ability to navigate it safely depends on more than filters, apps, or rules. It depends on their capacity to recognize danger, setboundaries, and to know when to reach out for help. This episode gives parents the tools to build that capacity before a crisis ever begins. For more info and to donate tothis 501(c)3 charity, you can reach Million Kids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook:https://www.facebook.com/IEMillionKidsInstagram:https://instagram.com/MillionKidsTeen

On this episode host Jonathan Chance talks with guest, respected clinical researcher and consultant Bill Cavanaugh about an intriguing phenomenon when treating cancer that is known as the Abscopal Effect. On this episode Jonathan and Bill discuss: ·       What exactly is the Abscopal Effect?·       Why is there so much excitement about this? ·       Are researchers trying to reproduce it and see how the body's own immune system helps to fight cancer?·       When men are currently battling advanced or recurrent prostate cancer, what should they understand about the research taking place today? ·       As somebody involved in clinical research especially when it comes to prostate cancer is there one area that Bill is mot most excited about?For more information about Bill Cavanaugh and his research, visit his website at: https://www.abscopalevents.com/blogProstate Cancer Aware is grateful to the Jevan and Ruzanna Chimayan Foundation for their generous donation, which helps fuel our podcast and website to raise critical awareness about prostate cancer and the PSA test around the world.Prostate Cancer Aware is a copyrighted production.  No content maybe rebroadcast or reproduced without the expressed written consent of the Friedman Sidrow Foundation.  For more information about prostate cancer, the PSA test, men's health and Jonathan's inspiring new book Unaware, which is about his battle with prostate cancer.Visit our website at:  https://www.iknowmypsa.orgEmail us at:  https://www.iknowmypsa.org/contactus/Follow Prostate Cancer Aware on social media at:Facebook -  https://www.facebook.com/iknowmypsa Twitter -  https://twitter.com/iknowmypsa or @iknowmypsaThank you for listening!  Remember, Stay Aware and Stay Healthy.™

On this episode, Nelson Santos of the Princess Auto Ride for Dad Edmonton joins Liane to talk about the ride, its importance and what's new for 2026!Guest: Nelson Santos, Ride for Dad EdmontonWebsite: https://ridefordad.ca/Email: info@ridefordad.caAMSS: Liane LangloisWebsite: ab-amss.orgEmail: info@ab-amss.orgPodcast ProducerBryn Griffiths / Mighty Mouth CommunicationsWebsite: bryngriffiths.com Email: bryng@bryngriffiths.com

Jesus promised His believers that they would escape the wrath that is to come upon the world in judgment. Listen to this week's message to be assured of this hope.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

“Behind every breakthrough are countless failures no one ever sees—but that's exactly what makes progress possible.” Dr. Thomas Kaiser. When I have scientists on the podcast: they're some of the coolest, smartest, funniest people, and they're always willing (and excited) to explain what they do in ways you can actually understand. Dr. Tom Kaiser is no exception. He lives and works in Durham, North Carolina, and brings together an impressive mix of scientist, physician, and entrepreneur. His work focuses on designing better medicines using cutting-edge technology. He began his career at Emory University in Dennis Liotta's lab, working on antiviral drug discovery, and later helped pioneer early machine learning approaches in drug design. His research spans RSV, cancer, and neurodegenerative diseases, and he went on to earn his medical degree from the University of Oxford. Tom is now the co-founder and Chief Scientific Officer of Avicenna Biosciences, where he's leading the development of innovative therapies aimed at improving and saving lives. And my favorite detail from his bio? He ends it by mentioning the love of his life, his wife. I'll be honest, when I first met him, I told Dr. Kaiser he seemed like someone who must have been in a movie. He's just that cool. His Company: Dr. Thomas Kaiser shares the story behind his company's name, Ibn Sina, also known as Avicenna a true Renaissance figure of the Islamic Golden Age. A physician, philosopher, and scientist, Ibn Sina embodied the kind of multidisciplinary thinking that still drives innovation today. It's a powerful reminder that the roots of modern medicine, and the spirit of discovery stretch back centuries. The Part We Don't Talk About Enough Science is not a straight line. Not even close. Experiments fail. Clinical trials don't work. Hypotheses fall apart after years of effort. Funding can disappear. Progress can stall in ways that are frustrating and sometimes heartbreaking especially when patients are waiting. Dr. Kaiser speaks about this with a clarity and calm that really stayed with me. Because the truth is: scientists have to keep going anyway. They carry the weight of those disappointments and start again. They adjust, rethink, rebuild, and try again. Over and over. And that persistence? That's where breakthroughs come from. From the outside, it's easy to celebrate the wins ... the new drug, the successful trial, the headlines. But behind every one of those moments are countless failures no one ever sees. For families like ours, waiting, hoping, advocating it matters to understand that this difficult process is also what makes progress possible. Living the Dream What if you actually got to live the dream you had as a kid? In this conversation, Dr. Thomas Kaiser shares something surprisingly personal: he feels lucky to be doing exactly what he dreamed of as a child. That early curiosity grew into a career designing new medicines and pushing the boundaries of science. From imagination to impact, his journey is a reminder that sometimes those childhood passions really can shape the future. Go to Dr. Kaisers website:  https://www.avicenna-bio.com Like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

Financial Sextortion: Words Every Parent Should Know (and Never Have to Deal With)The podcast content may contain sensitive topics. Listener discretion is advised.Financial sextortion is not a “rare online scam.” It is a heart‑breaking, fast‑growing crime that has already stolen the lives of more than 40 bright, successful young people across the United States. These were athletes, scholars, and leaders with futures. Many had parents who had never even heard of financial sextortion until it was too late.Million Kids is determined to change that.Because NEVER AGAIN should a family lose a child simply because no one warned them how this crime works.On this episode of the Protect & Prevent Podcast (P3 Kids), Opal Singleton Hendershot of MillionKids.org, one of the leading voices in keeping kids safe from predators, provides not just information but also prevention, protection and a lifeline.What Parents Need to Know Right Now…Financial sextortion almost always begins with organized overseas criminal networks. These are not “kids being kids online.” These are highly coordinated groups operating out of places like Nigeria, Ivory Coast, Myanmar, Pakistan, and the Philippines. They especially target high‑achieving young males who look confident, successful, and connected.Here's the pattern:A criminal pretends to be a cute girl who “knows” them or their friends.She sends a photo. She asks for one back.The boy sends something — sometimes fully clothed, sometimes a partially nude image. It doesn't matter as thecriminals can use AI and deepfake tools to alter the image into something explicit.And then the blackmail begins. The threats are instant, relentless, and terrifying.The victim believes his entire world, his family, his friends, his reputation are about to collapse.He has no idea he has been targeted by international criminals, not a peer. He panics and feels trapped.Far too many young men have made a tragic, irreversible decision in that moment of fear. This is why parents mustunderstand this crime. This is why teens must hear the truth before a predator reaches them. This is why this podcast matters.When teens learn about sextortion before it happens, they respond differently. They recognize the signs and they know it is a scam. They reach out for help instead of hiding in shame. But they can only do that if we, the adults, understand the threat first.This episode gives parents the knowledge, language, and confidence to protect their kids. It breaks down the tactics, the psychology, the technology, and the red flags. It gives families a plan.Start by educating yourself and your community today. Share this podcast with friends, schools, churches, teams, and youth groups. Then have a calm, honest conversation with your teens.Explain what financial sextortion is, how it works, and why they will never be in trouble asking for help.Do a full digital profile check as a family. See what strangers can see about your family online. Set every app to private and remove photos of your children from public spaces.Create a family code word. Something simple that means: “I need help right now.”Together as adults we must work together to educate our family and communities. For more info and to donate to this 501(c)3 charity, you can reach Million Kids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like ourposts on:Facebook: https://www.facebook.com/IEMillionKidsInstagram: https://instagram.com/MillionKidsTeen

Send us Fan MailThe Podcast for today is one Vicki and I recorded August 14, 2023. The topic is our “Identity.” It is our most listened to podcast of the 178 we're recorded. I think it is still one of the most critical issues of life and of our advancing years. Who are we? What does our identity of being “in Christ” mean in terms growing older? What is life “in Christ” all about? Here it is again, just as we recorded it then. I hope you'll enjoy it again.Pressing on for all that God has for us “in Christ.”HalWe exist to call a generation of retiring boomers and aging believers to leverage their lives for the fame of Jesus and the glory of God. -------Hal's wife, Vicki, shares her heart about the importance of “Identity” in all of life, and particularly, in the aging years. Perhaps nothing is as important in life than knowing who God created us to be and to see ourselves as He sees us through the life and death of His Son, Jesus. Satan attempts to pull us away from that incredible truth by tempting us to see our value through what we do. Vicki speaks out of her own heart to women, but the truth of her heart speaks to men as well. Let's press deeper into our identity in Christ and stay focused on His purposes as we grow older.Support the show"Finishing Well Ministries aims to encourage and inspire aging Christians to understand and embrace God's calling in their later years, equipping them to actively pursue and fulfill His calling. FWM provides materials, events, and other on-line resources that provide shared insights focused on finishing our lives well. We also recruit and train volunteers who lead and encourage small groups around the world to fulfill God's mission for them in these critically important years." - Hal HabeckerWebsite: www.finishingwellministries.orgEmail us: Hal@finishingwellministries.orgFollow us on Facebook: https://www.facebook.com/finishingwellministriesSupport Our Ministry: https://www.finishingwellministries.org/donateAre there biblical principles to help us understand how to finish well?Explore the Seven Essentials for Finishing Well. Learn more.Thanks for listening as we all strive to live and finish life well!

On this episode, Liza Miller of Women Riders World Relay (WRWR) joins Liane to talk about the first relay in 2019 and the updated version running in 2026. This relay's sole purpose is to connect women riders around the world, creating a larger sense of community and celebrating women who ride!Guest: Liza Miller, CEOWebsite: https://womenridersworldrelay.com/Email: info@wrwrapp.comAMSS: Liane LangloisWebsite: ab-amss.orgEmail: info@ab-amss.orgPodcast ProducerBryn Griffiths / Mighty Mouth CommunicationsWebsite: bryngriffiths.com Email: bryng@bryngriffiths.com

“Everybody has a little bit of ADHD” is one of those phrases that sounds harmless until you measure impact. ADHD isn't just distractibility or being late sometimes. It's a neurodevelopmental disorder that can shape attention regulation, executive dysfunction, working memory, impulse control, and emotional dysregulation in ways that strain jobs, relationships, sleep, and self-trust.We sit down with Leah, an ADHD life and mindset coach, to unpack what adult ADHD looks like in real life and why the label can be both clarifying and confusing. We get into ADHD types (inattentive, hyperactive-impulsive, combined), why so many women were missed as kids, and how ADHD can be misread as anxiety, depression, bipolar disorder, OCD, autism (AuDHD), or “just stress.” Leah also breaks down how the ADHD diagnosis process can differ across countries and clinics, and why support shouldn't stop at a prescription.From there, we move into what actually helps: shifting self-talk from shame to neutral reflection, understanding how executive functions create a domino effect, and building low-friction systems that make follow-through easier. Think night-before setups, habit stacking (yes, meds on the coffee machine), and a regulation toolbox that can include journaling, breathwork, sensory supports, and yoga nidra (non-sleep deep rest). The takeaway is simple but powerful: pick one or two changes, give them two weeks, and let consistency compound.If you found this helpful, subscribe, share the episode with a friend who needs it, and leave a rating and review so more listeners can find the show. What's one small step you're willing to try this week?Send us Fan MailSupport the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...

Living Fully with CF: Christopher Cornejo's Journey from Diagnosis to Avatar This fast-moving and deeply engaging conversation features Christopher Cornejo, who brings a fresh and powerful voice to the cystic fibrosis community. Diagnosed with CF as an adult just three years ago, Christopher has quickly become an advocate, sharing his story on stage at a UCLA CF symposium and being honored by the Cystic Fibrosis Foundation as one of Southern California's Finest. What makes Christopher's story especially compelling is his perspective, shaped not only by his diagnosis, but by his career in film, including his work as a technical director on Avatar 2 and 3. In this heartfelt interview, Christopher opens up about his late diagnosis, navigating medical challenges, and how openness, community, and resilience have shaped his journey. We talk about his later diagnosis, balancing his health and his demanding film career, the importance of community and support along with his mental health and resilience.    Like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

In this passage, we see how Christ wants to encourage us.  Listen to hear His plan for our hope and security in eternal life.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

The podcast content may contain sensitive topics. Listener discretion is advised.About 40% of relationships now begin online. Many turn into beautiful, healthy, lifelong partnerships.On this episode of the Protect & Prevent Podcast (P3 Kids), Opal Singleton Hendershot of MillionKids.org, one of the leading voices in keeping kids safe from predators, talks about the other side of online relationships that no one wants to believe could happen to them.Teens. Adults. Seniors. People looking for connection… and instead finding manipulation, grooming, blackmail, or heartbreak engineered by someone who never existed in the first place.And here's the part most people don't realize: We're not just meeting a few strangers online anymore. We're sharing digital space with 5.5 BILLION people, many who havethe same tools we do, such as:• Geo‑location tools• Global money transfer for extortion • AI-generated deepfakes• Massive amounts of personal data about us like where we live, work, and who we loveDigital relationships feel real because the brain releases the same dopamine as in-person connection. And when people feel safe behind a screen, they share more including more emotion, more vulnerability, more intimate content… and sometimes, even more than they ever intended.We discuss risk factors to consider, indicators that you might be being groomed or seduced, and suggested discussions in talking with your teen about healthy vetting processesin online relationships.  If you or someone you love is considering or navigating online dating, online friendships, or online “connections,” this episode is not optional. It's essential.Protect yourself. Protect your family. Listen now to the Protect & Prevent podcast.For more info and to donate to this 501(c)3 charity, you can reach Million Kids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook: https://www.facebook.com/IEMillionKidsInstagram: https://instagram.com/MillionKidsTeen

On this episode, Kirk Pelletier of Moto Instincts joins Liane to talk about the life of an instructor, what it takes and why do it! Kirk also shares his personal journey into motorcycle riding, the process of actually becoming a licensed instructor in Alberta, and the innovative approach of Moto Instincts in motorcycle education. Discover tips for new riders, insights into licensing, and how continuous learning shapes expert riders.Guest: Kirk Pelletier, Senior Instructor, Moto InstinctsWebsite: https://motoinstincts.com/Email: leeroy@motoinstincts.comAMSS: Liane LangoisWebsite: ab-amss.orgEmail: info@ab-amss.orgPodcast PoducerBryn Griffiths / Mighty Mouth CommunicationsWebsite: bryngriffiths.com Email: bryng@bryngriffiths.comChapters00:00Introduction to Kirk Pelletier and His Journey04:49Becoming a Motorcycle Instructor09:07The Process of Becoming a Licensed Instructor14:35The Importance of Licensed Instruction20:26Moto Instincts: A New Era in Motorcycle Training

Jesus calls believers to trust God and not to worry. Listen to hear the steps we can take that result in God's peace, not tumultuous worry. Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

A mother, advocate and one woman's global fight for access. Beth Vanstone is working to ensure rare disease patients don't have to wait for the treatments they need to survive. Sometimes the most powerful friendships begin in the most unexpected places.  Beth Vanstone and I first connected on social media. At the time, we were simply two moms navigating the complicated, emotional, and relentless world of cystic fibrosis. But eventually the online messages turned into something more meaningful. Then, Beth attended one of The Bonnell Foundation's Gala events. That's when we finally met in person.  And from that moment on, we became dear friends.  It's proof that social media, when used for connection and purpose, can build incredible relationships. But what inspires me most about Beth isn't just our friendship. It's her relentless determination. Beth is the mother of Madi, who was diagnosed with cystic fibrosis at just eight months old. Suddenly Beth was navigating a healthcare system, researching treatments, learning medical language, and fighting for her daughter's future. Beth didn't stop there. Instead of focusing only on her own family, she chose to fight for every family. Today, Beth is a powerful advocate in Canada and a member of the Ontario Rare Action Group, where she works to improve access to life-saving therapies for people living with rare diseases like Cystic Fibrosis. And the reality she's fighting against is one many people don't understand. Most healthcare systems, not just in Canada but around the world were built to treat common diseases. They weren't designed for rare conditions that affect smaller populations. Because of that, patients with rare diseases often face enormous barriers: long approval timelines, delayed access to medications, and exhausting advocacy battles just to receive treatments that already exist. In some cases, patients wait months — even years — for medications that could dramatically improve or extend their lives. Beth is working to change that. Through her advocacy, she's pushing for reforms that could make a real difference for patients across Canada and beyond: • Faster access to innovative therapies • Improved newborn screening programs • Better diagnostic pathways • Centers of excellence for rare diseases • Removing financial barriers like deductibles that prevent families from accessing public programs And she's also raising an important global conversation. Here in the United States, lawmakers have debated policies like the Most Favored Nation Model, which look to international drug pricing systems like those in Canada and Europe as a model. But Beth reminds us that every system has challenges, and for rare disease patients, those challenges can be life-changing. Because when access to medication is delayed… Access is denied. And that's why advocacy across borders matters. She's not just advocating for her daughter. She's advocating for every patient still waiting for their breakthrough. And today, we're talking about what needs to change and how all of us can help make it happen. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

The podcast content may contain sensitive topics.Listener discretion is advised.A story broke recently that should shake every parent totheir core. In Southern California, the Riverside County Child Exploitation Team identified 500 suspects and arrested 42 individuals in a massive child‑exploitation sting called Operation Volcano. The alleged offenders weren't the “monsters in the shadows” we imagine. They allegedly included a child psychologist, an ex–law enforcement employee, a hospital CTO, and two corporate vice presidents.The very people families are taught to trust.On this episode of the Protect & Prevent Podcast (P3Kids), Opal Singleton Hendershot of MillionKids.org, one of the leading voices in keeping kids safe from predators, talks about CSAM (previously called “child pornography,”) and how technology has supercharged it into a global, industrial‑scale criminal economy. Today, predators can access, trade, and sell images ofminors through dark‑net markets, bulletproof hosting sites, and peer‑to‑peer networks with terrifying ease. One global CSAM ring had over 1.6 million paid subscribers.Most parents have no idea how quickly a predator can groom a young person, obtain illicit images, and funnel them into these networks or how those images are used, multiplied, and monetized forever. This episode pulls back the curtain.We look at how CSAM has evolved from isolated crimes toglobal, tech‑driven criminal enterprises, the technologies predators now rely on, who these offenders really are and why they collect thousands of images from minors and what actually happens to a photo once a predator gets it.We'll also discuss how to talk to your child so theyunderstand the real‑world consequences and what to do immediately if you suspect your child is a victim of CSAM, sextortion, or a deepfake.Parents can't protect their kids from a threat they don'tunderstand. This episode gives families the clarity, language, and action steps they need to navigate one of the most urgent dangers facing young people today. For more info and to donate to this 501(c)3 charity, you canreach Million Kids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook: https://www.facebook.com/IEMillionKidsInstagram: https://instagram.com/MillionKidsTeen

Raelynn Torzone joins the ANMA podcast to share her journey from conventional medicine into the world of bioenergetic healing and practitioner training. As the founder of the BEST Institute and creator of BioEnergetic Rebalancing Therapy (BRT), Raylene has built a system designed to help practitioners better understand energetic imbalances and apply practical techniques within their own practices.In this conversation, Raylynn shares how her personal health challenges led her to explore muscle testing, frequency-based approaches, and whole-body wellness. The episode also dives into practitioner communication, legal considerations around titles and language, and the importance of helping clients better understand the healing process.Raylynn also gives a preview of her upcoming hybrid training experience at the 2026 ANMA Convention and what attendees can expect from the hands-on program.In this episode, we discuss:Raylynn's transition from conventional medicine to energy healingCommon misconceptions about muscle testingWhy practitioner language and state laws matterThe role of emotional and energetic balance in wellnessWhat attendees can expect from her ANMA convention trainingAbout Raelynn Torzone:Raelynn Torzone is the founder of the BeST Institute and creator of BioEnergetic Rebalancing Therapy (BRT). Her background includes decades in conventional medicine, beginning in cytotechnology and later practicing as a Physician Assistant across multiple specialties including hospital medicine, urgent care, OB/GYN, and family practice.After facing her own severe health challenges, Raelynn began exploring energy healing, frequency-based therapies, and holistic approaches to wellness. That journey led her to develop a unique system that blends clinical knowledge with bioenergetic techniques designed to support whole-body healing. Today, through the BeST Institute, Raelynn trains practitioners around the country in practical, hands-on methods focused on energetic balance, client communication, and integrative wellness.Connect with Raelynn: https://bioenergetixtraining.com/Cell Phone: 667-391-1444Email: info@bioenergetixtraining.comRaelynn's Personal Email: bestntp@icloud.comANMA 45th Annual ConventionAugust 28-30, 2026 | Westgate Las Vegas ResortRegister and learn more here: https://www.anma.org/conventionAbout This Podcast:Promoting and Protecting Naturopathy is powered by ANMA, the nation's oldest and largest naturopathic association. Each month, we share insights for naturopathic professionals, students, and anyone passionate about natural health.Not a member? Join ANMA today for legislative alerts, educational opportunities, member discounts, and professional community support. Visit anma.orgConnect with us:Stay tuned for updates on the 45th Annual ANMA Convention at anma.orgAmerican Naturopathic Medical Association: ⁠https://www.anma.org⁠American Naturopathic Medical Certification Board: ⁠https://www.anmcb.org⁠American Naturopathic Medical Accreditation Board: ⁠https://www.anmab.org⁠Society of Complementary Alternative and Holistic Practitioners: https://www.scahp.orgEmail: admin@anma.orgThis podcast is produced by Espresso Podcast Production: https://www.espressopodcastproduction.com/Disclaimer: This podcast is for educational purposes only and should not be taken as medical advice. Consult your doctor before implementing any information shared. Views expressed are those of the speakers and do not necessarily reflect ANMA or ANMCB positions.

On this episode, Lee Fryberger, Vice President of the Canadian Motorcycle Association joins Liane to share insights into the organization's history, its current initiatives, and the importance of a unified national voice for motorcycling in Canada. Discover how CMA is working to promote safety, recognition, and growth across all riding disciplines.Guest: Lee Fryberger, Vice-President, Canadian Motorcycle AssociationWebsite: https://www.motorcyclingcanada.ca/Email: info@motorcyclingcanada.caAMSS: Liane LangloisWebsite: ab-amss.orgEmail: info@ab-amss.orgPodcast ProducerBryn Griffiths / Mighty Mouth CommunicationsWebsite: bryngriffiths.com Email: bryng@bryngriffiths.comChapters00:00Introduction to Lee Fryberger and CMA06:10Understanding the Canadian Motorcycle Association10:06CMA's Committees and Their Importance16:43Reviving the CMA: Community Involvement20:41The Role of CMA in Motorcycle Safety23:39On-Road Safety Tips for Riders27:33Supporting the CMA and Its InitiativesResourcesCanadian Motorcycle Association (CMA)Federation of International Motorcyclists (FIM)Tuco Motorcycle School

Because God loves us, He has given us His Holy Spirit to protect us from evil. This week, we hear how we receive His help, by prayerfully obeying His Word. Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Unhealthy relationships can feel like a whirlwind, and that speed can be the point. We sit down with Laurilyn to trace how early conditioning around silence, safety, and approval can echo into adulthood as people pleasing, self-abandonment, and repeating the same relationship dynamics. Her story moves from a childhood shaped by fear and consequences to the reality of emotional abuse, violence, and the complicated question of when it's safe to speak your truth.From there, we get practical about healing. Laurilyn explains why personal safety is her top core value, how she exits conversations that aren't safe, and what it looks like to rebuild self-trust one choice at a time. We also dig into concrete self-love practices that aren't fluffy, including daily journaling, “dating yourself,” and learning to stop outsourcing your worth to partners. The big shift is moving from need and negotiation to alignment and boundaries.Then the lens widens to communication skills. Laurilyn shares what solo travel taught her about nonverbal communication, tension, and the power of the unspoken. She breaks down her CHAT Communication System, a communication styles framework designed to help you meet people where they are, whether you're navigating dating, family dynamics, leadership, or workplace conflict. You'll also hear actionable tips for writing emails and CVs that land with different communication styles.Subscribe to Multispective, share this conversation with someone who needs it, and leave a review so more listeners can find these stories.Send us Fan MailSupport the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...

Bridging Two Countries, One Mission: Cesar and Nora Hernandez Fight for Spanish-Speaking CF Families “When Alex was diagnosed, we felt fear and responsibility. If we had access to information in Spanish, other families should too. No one should feel lost because of language.” Nora Hernandez From Mexico to Mission: How Cesar and Nora Hernandez Are Closing the CF Information Gap for Hispanic Families. “I came to this country to build a better future for my family. I never imagined that future would include fighting for awareness about cystic fibrosis, but now it's part of our mission.” Cesar Hernandez Cesar and Nora Hernandez were both born in Mexico, where accurate and accessible information about cystic fibrosis has not always been readily available. While progress is being made, with more experienced physicians and improving CF care, there is still significant work to do. In the United States, members of the Hispanic community are often underdiagnosed or diagnosed later than others. That gap in awareness and access is one of the reasons The Bonnell Foundation launched its CF Familia page, offering reliable information in both English and Spanish to help families navigate the complexities of cystic fibrosis. Cesar and Nora serve as ambassadors for this effort, creating videos that provide education, updates, and reassurance to Spanish-speaking families. Cesar also serves as a board member of The Bonnell Foundation, and we are deeply grateful for his leadership and heart for this community. Cesar originally came to the United States to build a better life and financially support his family in Mexico. After meeting Nora, he made the decision to stay and make the U.S. his permanent home. Together, they are raising two children, Scarlett and Alex, who was diagnosed with cystic fibrosis. Their story is one of resilience, faith, cultural pride, and advocacy. Transcript is also available on this podcast.     Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

The podcast content may contain sensitive topics. Listener discretion is advised. We're suggesting a different kind of conversation about social media — one that goes beyond rules, restrictions, and arguments about screen time. For years, families have wrestled with what to allow, what to block, and how to keep kidssafe online. I wanted to share something I heard recently because it changes everything.Your teen has been using social media and online technology for a long time now. You've taught them well. You trust their judgment. And you know they would never intentionally do something that could harm themselves or embarrass your family.But here's the truth that is hard to admit: Sextortion isn't new but the technology behind it is.  And the way predators operate today is nothing like what we as adults are familiar with and taught our kids to watch out for.Most teens genuinely believe they'll “know” if they're being catfished. They believe they'll recognize a predator. They believe they'll see danger coming.On this episode of the Protect & Prevent Podcast (P3 Kids), Opal Singleton Hendershot of MillionKids.org, one of the leading voices in keeping kids safe from predators, shares how the world changed around 2022.  The entire globe became connected by 5G high‑speed internet. At the same time, we all began usingtechnologies that didn't exist a decade ago:• geo‑location tracking• globalmoney transfer• mass‑audience live streaming• artificial intelligence capable of altering images and identitiesThis combination created a perfect storm.For the first time in history, your child can reach the entire world and the entire world can reach your child, instantly, invisibly, and with tools that make a criminal in Nigeria or Myanmar look like a cute 14‑year‑old from your child's school.This isn't fear‑mongering.It's reality.And it means the old conversations about “don't talk to strangers online” are no longer enough.This podcast dives into what has changed, why it matters, and how parents and teens can navigate this new digital landscape together. It's not about blame. It's not about shame. It's about understanding the technology that now shapes our children's lives and the criminals who know exactly how to exploit it.This may be one of the most important conversations you ever have with your family.  And it starts with understanding what's really happening out there.Listen to the podcast. Share it. Talk about it.Your child's safety depends on it.  For moreinfo and to donate to this 501(c)3 charity, you can reach Million Kids at:Website:https://MillionKids.orgEmail:info@MillionKids.orgBe sure tofollow and like our posts on:Facebook:https://www.facebook.com/IEMillionKidsInstagram:https://instagram.com/MillionKidsTeen

Because He loves us, God wants to define the boundaries of relationship intimacy. Join in as we hear how to apply His word to our lives.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Finding Strength After Loss: A Conversation with Margarete Cassalina I first met Margarete Cassalina when we were hosted for dinner by Bob Emmelkamp at the North American Cystic Fibrosis Conference (NACFC). We connected immediately. There was an ease to our conversation, a shared understanding that doesn't require much explanation in the cystic fibrosis community. And I have to say, her husband Marc is just as wonderful. They are the kind of people you feel grateful to know. I'm so glad we are in this CF life together. Margarete is an author, speaker, and longtime advocate and fundraiser for the Cystic Fibrosis Foundation. But long before the stages, the fundraising events, and the national advocacy, she was a mom navigating the daily realities of cystic fibrosis. In 2006, her 13-year-old daughter, Jena, died from CF. In the depths of unimaginable grief, Margarete made a powerful decision: she would honor Jena's life not only with love, but with action. Since then, she has dedicated herself to storytelling, advocacy, fundraising, and speaking across the country about resilience, motherhood, loss, and the urgent need for continued research. Margarete's son, Eric, also lives with CF, and in this episode you'll hear more about how he's doing and what life looks like for their family today. This dynamic, incredible woman will inspire you. Her story is not only about loss it's about purpose. It's about choosing to move forward when standing still might feel easier. And it's about doing great things in the name of someone you love. To find her books go to Amazon.     Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

The podcast content may contain sensitive topics. Listener discretion is advised.For more than a decade, Million Kids has carried a mission that no family ever wants to need. It is the Million Kids Missing Kids program. It began with heartbreaking conversations:parents sitting across from us, voices shaking, describing the moment their teenager vanished. The fear. The confusion. The unbearable silence that follows when a child you love disappears seemingly without a trace.Thanks to the generosity of our supporters, we've been able to send out thousands of flyers, each one carrying the face of a child who deserves to be found. Those flyers matter. They save lives. And they give families hope in the darkest moments of their lives.Recently, our community watched the case of Celeste Hernandez, a beautiful young girl whose story ended in a tragedy too painful for words. Our hearts ache for her family. While this loss is devastating, it's important to rememberthat most cases do not end this way. Many young people are found. Many families are reunited. And every successful recovery fuels our determination to keep going.On this episode of the Protect & Prevent Podcast (P3 Kids), Opal Singleton Hendershot of MillionKids.org, one of the leading voices in keeping kids safe from predators, takes a look at why young people run. In our experience, a runaway is almost always doing one of two things: They're either running FROM something or someone or running TO something or someone.We'll explore the pressures, conflicts, and vulnerabilities that push teens to leave and the strategies that can prevent a moment of crisis from turning into a lifelong tragedy. Because with the right conversations, the right awareness, and the right support, many of these young people can avoid becoming victims of exploitation once they're outon their own.And to every supporter who stands with us: you make this work possible. You help us bring kids home. You help us protect families. And you help us shine a light into places where too many young people feel alone.This is a conversation every parent, guardian, and community member needs to hear.For more info and to donate to this 501(c)3 charity, you can reach MillionKids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook: https://www.facebook.com/IEMillionKidsInstagram: https://instagram.com/MillionKidsTeenX: https://x.com/IEMillionKids

How does God want to help us rest in hope and not be overcome with worry? In this week's message, we hear how Paul's faith was strengthened even though he was going through difficult trials. Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Natasha Pierre spent years carrying a secret that shaped every room she walked into: the fear of being found out. Under the ambition and the “I've got this” energy lived survivor's guilt, PTSD, panic, depression, disordered eating, and a bipolar diagnosis she didn't feel safe naming out loud. The most powerful part of her story isn't just what she survived, it's how she learned to stop letting shame run the show.We start with her childhood where she learned ownership early by helping run a tourist shop and chasing big dreams. She shares about school life, feeling unlikeable, getting teased, being sick often, and later discovering old journal entries that revealed how early depression had really begun. We also talk about why adults should treat kids' behavior as information, not attitude, and how curiosity and support can change a life.She shares about mental health treatment and self-advocacy. Natasha breaks down what hypomania can feel like, why sleep is a non-negotiable, how “medication roulette” works in real life, and why symptoms can overlap with ADHD and autism. She also shares what shifted when she finally told the truth publicly, and how her books connect to reclaiming happiness and using imposter syndrome as a signal for growth.Subscribe for more honest conversations about mental health, trauma recovery, and living well with a diagnosis, and if this resonated, share it with someone who needs it and leave a review. What's one “clue” about your mental health you understand differently now?Send us Fan Mail Support the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...

Education, connection, and community are at the heart  of our CF community. On Saturday, April 18th from 11:00 a.m. to 1:30 p.m. we gathered at the Next Step Gallery in Ferndale. Set in a bright gallery space surrounded by art, the event offered a welcoming environment for meaningful conversation, learning, and connection. It was pure joy with the smell of great food in the air. Food from my sister in laws restaurant, Bangkok Cuisine (in Royal Oak) filled the air, it smelled amazing and filled the air. Education Day is more than a traditional event. It's an opportunity for people living with cystic fibrosis, parents, caregivers, healthcare professionals, and advocates to gather in one space to share experiences and support one another. A highlight of the afternoon was our “live” podcast recording, offering attendees a chance to hear authentic conversations about life with cystic fibrosis, advocacy, and the challenges and hopes shaping the community today. We all talked about education, advocacy, and what lies ahead for the CF community. The relaxed setting allowed people to connect not just through information, but through shared experiences. Events like Education Day help strengthen the bonds within the CF community by reminding everyone that they are not alone in their journey. Whether you are living with CF, raising a child with the disease, working in healthcare, or supporting someone you love, this gathering is meant to inform, inspire, and bring people together. Every story matters. Every voice matters. And every person who attends becomes part of the conversation. To watch the the premiere of our Embracing Egypt podcast enjoy it here:  https://youtu.be/SlMscQ6Spjg   Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

THE WORLD HAS SHIFTED… Have you noticed?And whether we've noticed or not, our kids are alreadyliving in a new reality.Today, 5.5 billion people are online. Nearly all of themhave access to the same powerful tools your family does including 5G speed, global money transfer, geolocation tracking, AI-driven data mining, anddeepfake technology that can make anyone look like someone you trust.That means this anyone, anywhere in the world, can appearto be your teenager's “friend.”On this episode of the Protect & Prevent Podcast (P3Kids), Opal Singleton Hendershot of MillionKids.org, one of the leading voices in keeping kids safe from predators, talks about the conversations that are needed with teens about healthy versus unhealthy and dangerous onlinerelationships.When you ask a teen about online exploitation, most willconfidently say: “I'll know if someone is trying to blackmail me or sextort me.”But parents this is the moment to lean in and ask: “How?What exactly are you looking for? What's your criteria?”Because here's the truth most families don't realize: Theold safety rule of “I only talk to people I know or people my friends know” no longer works.Organized criminal networks overseas can now run a fullprofile on your child in minutes. They can see their followers. They can see who they interact with. They can mimic their humor, their interests, their friend group. And suddenly, they're not a stranger but the “new best friend” who seems to know everything.This episode breaks down:-         How to talk with your teen about what a healthy online relationship looks like and not just “someone I know,” but real, measurable signs of safety.-          How to help them recognize the red flags of adangerous online relationship even when the person seems familiar, friendly, or connected.-           How overseas criminal groups run financialsextortion operations targeting teens and why even smart, confident, high-achieving kids are getting trapped.If you're a parent, grandparent, educator, or youthleader, this conversation is no longer optional.It's essential.Your teen is navigating a digital battlefield.This podcast gives you the tools to help guide themthrough it. For more info and to donate to this 501(c)3 charity, you canreach Million Kids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook: https://www.facebook.com/IEMillionKidsInstagram: https://instagram.com/MillionKidsTeenX: https://x.com/IEMillionKids

SHOW NOTES:On this episode host Jonathan Chance talks with guest, Dr. Perter Rossi about Whole Gland vs. Targeted Therapy for prostate cancer. Jonathan and Dr. Rossi discuss: ·       The difference between treating the whole prostate and just targeting the tumor.·       What men should they know about, when choosing a prostate cancer treatment option.·       Active surveillance as opposed to immediate treatment for prostate cancer.·       How we're moving toward a future - where more men can avoid aggressive treatments·       What is focal therapy and brachytherapy for treating prostate cancer  Prostate Cancer Aware is grateful to the Jevan and Ruzanna Chimayan Foundation for their generous donation, which helps fuel our podcast and website to raise critical awareness about prostate cancer and the PSA test around the world.Prostate Cancer Aware is a copyrighted production.  No content maybe rebroadcast or reproduced without the expressed written consent of the Friedman Sidrow Foundation.  For more information about prostate cancer, the PSA test, men's health and Jonathan's inspiring new book Unaware, which is about his battle with prostate cancer.Visit our website at:  https://www.iknowmypsa.orgEmail us at:  https://www.iknowmypsa.org/contactus/Follow Prostate Cancer Aware on social media at:Facebook -  https://www.facebook.com/iknowmypsa Twitter -  https://twitter.com/iknowmypsa or @iknowmypsaThank you for listening!  Remember, Stay Aware and Stay Healthy.™

Jamie MoCrazy is a former professional freestyle skier, X Games record-setter, and critical traumatic brain injury survivor. Once known for pushing the limits in big air and slopestyle, her life changed dramatically during a competition in Whistler, Canada. Now, she uses her platform to raise awareness about the long-term effects of TBI and the importance of proper diagnosis, treatment, and recovery.Grace “Fruit” Mauzy (MA in Psychology, PhD candidate in Mind-Body Medicine) is Jamie's mother, who played a critical role as both a caregiver and researcher throughout Jamie's recovery. She brings a unique dual perspective, combining academic expertise with lived experience navigating the complexities of brain injury care.In this powerful episode of the Concussion Coach Podcast, host Bethany Lewis sits down with Jamie and Grace MoCrazy to discuss their remarkable journey through severe traumatic brain injury and recovery. Jamie shares the story of her 2015 skiing accident—which left her in a coma with a death report written before she left the mountain—and how she has no memory of the event or the two months following. Grace describes the harrowing moment she received the call, the breaking of protocol in stimulating Jamie's system in ways that contradicted hospital protocol (touching, singing, massaging, playing music), and the science that supported those instincts.Together, they explore the similarities and differences between severe TBI and concussion, and why healing cannot happen when the nervous system is stuck in sympathetic (fight/flight) mode. Grace explains the gut-brain axis, how the microbiome shrinks under stress and craves processed foods, and why nausea is the gut telling the brain it isn't healing. Jamie introduces her powerful reframing tool: “Let's stop and look at the view”—a strategy that transforms guilt into grace. The episode closes with details on the MoCrazy Method (a 6-week virtual mind-body therapy program) and the iFly Alive to Thrive in-person event, both designed to help brain injury survivors and their caregivers rebuild connection, joy, and a thriving “2.0” life.Resources MentionedMoCrazy Strong Foundation (Jamie & Grace):Website: www.MoCrazyStrong.orgEmail: jamie@mocrazystrong.org | info@mocrazystrong.orgInstagram: @MoCrazyStrongFoundationFacebook: @MoCrazy Strong Brain Injury FoundationUpcoming Events (as of recording):The MoCrazy Method (6-week virtual mind-body therapy program with psychoeducation)Starts: April 29, 2026 | Wednesdays, 6:00–7:00 PM MTRegistration: https://www.zeffy.com/en-US/ticketing/mocrazy-method-spring--2026iFly Alive to Thrive (indoor skydiving + lunch + social connection)Date: May 14, 2026 | 9:30 AM – 5:00 PM MT (skydiving 9:30–11:00 AM)Location: Ogden, UT (iFly + Ogden Library)Cost: $45 (lunch included; scholarships available)Registration: https://www.zeffy.com/en-US/ticketing/alive-to-thriveConnect with Bethany:Website: https://theconcussioncoach.com/Free Guide: "5 Best Ways to Support Your Loved One Dealing with a Concussion" on the websiteFree Coaching Consultation: https://theconcussioncoach.com/free-consultation

Persecution was a daily reality to this church in Thessalonica. Listen in to hear how God uses a community of believers to strengthen and grow their faith in troubled times. Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

We talk a lot about physical health, but what about the emotional side of it?In this episode, Nancy Buono joins the conversation to share her decades of experience working with Bach Flower Remedies and the role emotions play in overall wellbeing. After more than 40 years, her perspective is simple: we can't ignore how we feel and expect it not to show up somewhere else.Nancy is a long-time supporter of ANMA and an international educator and consultant specializing in Bach Flower Remedies. She is the founder of Bach Flower Education, where she trains and supports practitioners and teachers across North America. She is also a Certified Bach Flower Remedy Counselor and serves as Director of the Bach International Education Program, where she developed curriculum used by educators worldwide. With a background in psychology and education, along with extensive experience in meditation and business, Nancy brings both practical and emotional insight into her work.Nancy's program Bach Flower Institute is an ANMCB approved Continuing Education Program where you can earn your CEUs for your Board Certification. Nancy explains how Bach Flower Remedies are used, what makes them different from other approaches, and why the focus isn't on treating symptoms, but understanding the person behind them.We also talk about something that doesn't get discussed enough—how practitioners absorb emotional energy from others, and what it looks like to actually take care of yourself while caring for other people.This episode is less about quick fixes and more about awareness—paying attention to what's going on internally, and what might be asking to be addressed.In This Episode:How Nancy's personal experience led her to Bach Flower RemediesThe connection between emotional stress and physical symptomsWhy suppressing emotions doesn't make them go awayA simple way to start paying attention to your internal stateHow practitioners can stay grounded while supporting othersLearn more about Bach Flower Education: www.bachflowereducation.comANMA 45th Annual ConventionAugust 28-30, 2026 | Westgate Las Vegas ResortRegister and learn more here: https://www.anma.org/conventionAbout This Podcast:Promoting and Protecting Naturopathy is powered by ANMA, the nation's oldest and largest naturopathic association. Each month, we share insights for naturopathic professionals, students, and anyone passionate about natural health.Not a member? Join ANMA today for legislative alerts, educational opportunities, member discounts, and professional community support. Visit anma.orgConnect with us:Stay tuned for updates on the 45th Annual ANMA Convention at anma.orgAmerican Naturopathic Medical Association: ⁠https://www.anma.org⁠American Naturopathic Medical Certification Board: ⁠https://www.anmcb.org⁠American Naturopathic Medical Accreditation Board: ⁠https://www.anmab.org⁠Society of Complementary Alternative and Holistic Practitioners: https://www.scahp.orgEmail: admin@anma.orgThis podcast is produced by Espresso Podcast Production: https://www.espressopodcastproduction.com/Disclaimer: This podcast is for educational purposes only and should not be taken as medical advice. Consult your doctor before implementing any information shared. Views expressed are those of the speakers and do not necessarily reflect ANMA or ANMCB positions.

Part of being imitators of Christ is being faithful to Him and being available for opportunities He provides. Listen to this week's podcast to be encouraged as a Christian.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

PTSD doesn't always look like movie flashbacks. Sometimes it looks like a body that can't downshift, a mind stuck on alert, and a craving for intensity that turns “normal life” into something flat and unbearable. Mark knows that terrain firsthand. He walks us through the path from working class Philly to the Marines, then back into civilian life carrying hypervigilance, depression, heavy drinking, and the quiet isolation many veterans feel when the structure disappears and the adrenaline is gone. We also get honest about what comes after survival: risky behavior, identity built around being “high strung,” and the kind of suicidal thinking people hide because they're still functioning on paper. Parenthood becomes the turning point, the moment he decides he needs real mental health support if he's going to be a father. From there, the conversation opens into spirituality and mindfulness without the fog machine, where “spiritual” means how you treat your family, how you drive in traffic, and whether you can meet your own inner chaos without running from it. Mark's Zen meditation approach is radically simple and surprisingly hard: sit down, expect nothing, and pay attention. We talk Zen Mind, Beginner's Mind, why guided practices can accidentally plant outcomes, how to relate to a wandering mind, and why breath awareness becomes powerful over years instead of minutes. He also shares a memorable blue light story that connects meditation, grief, and community in a way that feels both mystical and practical. If you want a realistic way to start a daily meditation practice for stress, trauma recovery, and nervous system regulation, this one gives you a method you can actually do today. Subscribe, share this with a friend, and leave a rating and review so more listeners can find the show.Send us Fan Mail Support the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...

“Being a CF aunt has shaped so much of my life. Now I get the opportunity to turn that love and connection into helping even more people at Breathe Strong CF."  Julie Dunn Eichenberg didn't just find the cystic fibrosis community, she's been part of it for more than 30 years as a proud CF aunt. That personal connection is what makes this next chapter so meaningful. Julie recently stepped into the role of Executive Director at BreatheStrong CF, where the focus is on helping people with cystic fibrosis live stronger, healthier lives through exercise, education, and empowerment. And while she brings decades of experience in leadership, fundraising, and relationship-building, she's honest about getting used to the role. She's learning. Listening. Figuring out the day-to-day. And really taking the time to understand how she can best serve the community in this new position. Before this, Julie spent 20 years at Turner Broadcasting System (now part of Warner Bros. Discovery), and later held leadership roles at Florida State University and Fan Data Insights. But no matter where her career took her, the CF community was always part of her life. She's also been deeply involved with the Cystic Fibrosis Foundation, serving as Chair of the Georgia Chapter and contributing at the national level. We talk about what it feels like to step into a leadership role that's so personal. The excitement, the pressure, and the responsibility that comes with it. Julie shares what she's learning, what's surprised her, and why her connection as a CF aunt continues to guide every decision she makes. Because for Julie, this isn't just a job,  it's personal. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

Send us Fan Mail"Hope is not destroyed by suffering - it is developed by it." With the certainty of hope that only God instills, Dr. Randy Marshall shares his journey with metastatic prostate cancer.  His story will encourage every listener.Randy emphasizes the importance of faith, hope, and community, noting how his illness has become a mission field, providing spiritual support to other patients. He discusses the significance of maintaining a positive attitude, focusing on eternal hope, and the role of humor and prayer in coping. Randy also highlights the importance of family support and the discipline of saying no to maintain peace and focus.Support the show"Finishing Well Ministries aims to encourage and inspire aging Christians to understand and embrace God's calling in their later years, equipping them to actively pursue and fulfill His calling. FWM provides materials, events, and other on-line resources that provide shared insights focused on finishing our lives well. We also recruit and train volunteers who lead and encourage small groups around the world to fulfill God's mission for them in these critically important years." - Hal HabeckerWebsite: www.finishingwellministries.orgEmail us: Hal@finishingwellministries.orgFollow us on Facebook: https://www.facebook.com/finishingwellministriesSupport Our Ministry: https://www.finishingwellministries.org/donateAre there biblical principles to help us understand how to finish well?Explore the Seven Essentials for Finishing Well. Learn more.Thanks for listening as we all strive to live and finish life well!

In today's message, we learn Jesus' resurrection is a proven hope that is still available today for us and our future. This hope comes from believing and receiving what Christ has already done for us. Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Men with CF and Infertility: The Science, The Options, The Hope. Pete Proimos is an entrepreneur, a chronic illness advocate, and the founder of the Filotimo Foundation, a nonprofit dedicated to supporting individuals and families affected by cystic fibrosis. Diagnosed with CF as an infant, Pete kept his diagnosis private for decades. It wasn't until his forties that he chose to speak publicly about living with the disease, and that brave decision has changed lives. Pete is married to Annie, and together they are raising three children. His journey into fatherhood is part of what fuels his passion to make sure others with CF understand their options when it comes to building a family. Joining him in this important conversation is Colin Thomas, who leads the Family-Building Program at the Filotimo Foundation. Colin also lives with CF and became a father of five through IVF. In addition to his advocacy work, he serves as Vice President of Operations at IVY Fertility. He brings both professional expertise and deeply personal experience to this discussion, sharing honestly about the challenges and triumphs of becoming a parent with CF. One critical truth we discuss: Men with cystic fibrosis are not infertile because they don't produce sperm. Most are born without a connected vas deferens — the tube that carries sperm — which makes natural conception difficult. But with medical support, including sperm retrieval and IVF, biological fatherhood is often absolutely possible. This episode dives into the mission behind the Filotimo Foundation and the powerful work being done through its infertility and family-building program, work that is giving hope, clarity, and real options to families navigating CF. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

(The podcast content may contain sensitive topics. Listenerdiscretion is advised.)This week, our team dug into two recent cases of sextrafficking involving young girls and women. These cases were so brutal and heartbreaking they make you stop in your tracks. As we read and analyzed them, one conviction rose to the surface: never again should another young person beviolated, manipulated, or sexually exploited.On this episode of the Protect & Prevent Podcast (P3Kids), Opal Singleton Hendershot of MillionKids.org, one of the leading voices in keeping kids safe from predators, speaks directly to all moms about the conversations that can protect their daughters long before a predator ever enters the picture. Today's pimps and exploiters use every doorway availableincluding social media, dating apps, gaming chats, school hallways, malls, even friendships to access, seduce, groom, and ultimately trap their victims. One trafficker openly admitted he targeted girls with “low self‑esteem.” To the girl, it feels like a relationship. To the exploiter, it's a strategy. Too often it turns into a nightmare she thinks she can't escape.We break down how to build the kind of confidence andclarity that makes a young person hard to recruit. Because self‑esteem isn't something you're born with, it's a decision you make every day.We encourage young people to write down their values, define who they are, and decide what they stand for. We talk about what a healthy relationship looks like, what red flags to run from, and how sex (in the right context) is a bond, not a weapon. But in the wrong hands, it becomes a tool ofcontrol, shame, and pain.And above all, we dismantle one of the most destructive lieskids so often believe. We want them to know there is no such thing as “damaged goods.” No matter what has happened, it is never too late to step out of a harmful situation. You are valuable. You are loved. You can choose differently starting today.Because sometimes the four most powerful words a youngperson can hear are: “I believe in you.”TWO RECENT CASES:  Stockton man found guilty of sextrafficking, abusing foster youth David Hall case. Foster youth.  12, 13, 17Western District of Washington | California man convicted of sex trafficking victimsacross the United States | United States Department of Justice For more info and to donate tothis 501(c)3 charity, you can reach Million Kids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook: https://www.facebook.com/IEMillionKidsInstagram: https://app.parler.com/millionkidsX: https://x.com/notificationsLinkedIn: https://www.linkedin.com/in/opal-singleton-48641/

On this episode host Jonathan Chance talks with guest, former AZ State Rep. Lorenzo Sierra, about staying strong through prostate cancer. Jonathan and Lorenzo talk about.·       When active surveillance turns into a prostate cancer diagnosis.·       Keeping a positive outlook after a cancer diagnosis.·       The importance of early detection for prostate and other cancers.·       Being proactive for prostate cancer by getting a PSA test. ·       Lorenzo's new book, Fight Like Hell: Love, Politics and the Will to Live.For more information about Lorenzo Sierra and his new book visit his website at: Lorenzosierra.com Prostate Cancer Aware is grateful to the Jevan and Ruzanna Chimayan Foundation for their generous donation, which helps fuel our podcast and website to raise critical awareness about prostate cancer and the PSA test around the world.Prostate Cancer Aware is a copyrighted production.  No content maybe rebroadcast or reproduced without the expressed written consent of the Friedman Sidrow Foundation.  For more information about prostate cancer, the PSA test, men's health and Jonathan's inspiring new book Unaware, which is about his battle with prostate cancer.Visit our website at:  https://www.iknowmypsa.orgEmail us at:  https://www.iknowmypsa.org/contactus/Follow Prostate Cancer Aware on social media at:Facebook -  https://www.facebook.com/iknowmypsa Twitter -  https://twitter.com/iknowmypsa or @iknowmypsaThank you for listening!  Remember, Stay Aware and Stay Healthy.™

In this episode of the Hungarian Heritage Podcast, I speak with my talented guest  Suzanne Ócsai, who shares all about her Hungarian heritage and her continued quest to feel connected to her Hungarian community. We talk about her family's Hungarian heritage and her search for a feeling of belonging, and what that means when you are searching for your community. We discuss Suzanne's life-long love for art, how it has inspired her professional career, as well as, the art she creates. We specifically discuss her current wired art collection that is on display at the American Hungarian Foundation in New Brunswick, NJ.If you are interested in seeing Suzanne's Hungarian wired art collection that is currently on display at the American Hungarian Foundation in New Brunswick, NJ, her collection will be there until June. You can view the collection during one the upcoming events being held at the American Hungarian foundation, or by calling AHF to schedule a visit. If you're interested in seeing the collection AND meeting Suzanne, then make sure you attend the Hungarian Festival on June 6, 2026.. All of this information will be listed below, along with Suzanne's website and social media information so you can contact her and give a follow!If you have feedback or questions about this episode or you would like to connect with me at the podcast, you will also find that information below. If you've enjoyed this episode and you're interested in learning more about this Hungarian Heritage community, please do not hesitate to reach out. I would love to hear from you. Our theme music is Hungarian Dance by Pony Music, used with special license from Envato Market. Don't forget to subscribe, rate and review wherever you listen to your podcasts. Thanks again for listening, and until next time, make sure you Stay Hungarian Heritage Strong!  SziastokCONNECT with Suzanne ÓcsaiWebsite: www.suzanneocsai.comEmail: info on websiteInstagram: @suzanneocsaiFacebook: Suzanne Ócsai CONNECT with the PodcastWebsite: www.myhungarianheritage.comEmail: Christine@myhungarianheritage.comInstagram: @hungarianheritagepodcastFacebook: Hungarian Heritage Podcast  Contact the American Hungarian Foundation to view Suzanne's CollectionWebsite: www.ahfoundation.orgEmail: info@ahfoundation.orgInstagram: @americanhungarianfoundationFacebook: American Hungarian Foundation  Phone: 732-846-5777Address: 300 Somerset Street, New Brunswick, NJ 08903

In this episode, Alisha shares her journey through depression, anxiety, and suicidal thoughts, and how years of searching for answers left her feeling hopeless and exhausted.At her lowest point, when she finally stopped searching for external solutions, something unexpected happened — everything began to shift.After attending a talk that deeply resonated with her, Alisha was introduced to the world of mind-body healing and subconscious work. What followed was a powerful transformation that changed not only her mental health, but her relationships, purpose, and life direction.Today, she is a mind-body mentor, helping others uncover and release subconscious blocks, emotional pain, and limiting beliefs.✨ In this episode, you'll learn: The connection between mental health and the subconscious mind Why traditional approaches didn't work for her  How mind-body healing can help with depression and anxiety Practical steps to start your own healing journey  How to release emotional blocks and find inner peace If you've ever felt stuck, overwhelmed, or like nothing is working — this conversation may give you a new perspective on healing.

Three decades caring for patients with CF, that's Dr. Alan H. Cohen. His experience continues to shape everything he does today. As a pediatric pulmonologist (board-certified) , he has walked alongside patients through some of their hardest moments, including advanced lung disease and transplantation. Dr. Cohen was previously co-director of the largest pediatric lung transplant program in North America.Those years at the bedside are what ultimately led Dr. Cohen into drug development, where he has spent more than 25 years working to turn scientific innovation into real-world therapies for people who are still waiting for better options. As the Chief Medical Officer of Arcturus Therapeutics, he brings both clinical perspective and urgency to the company's work in mRNA-based therapies for cystic fibrosis and other rare diseases.“Clinical trials aren't just about science, they're about people who are willing to help move the field forward.”In this thoughtful and engaging conversation, Dr. Cohen reflects on how cystic fibrosis care has evolved over the past 35 years, from symptom management to breakthroughs in gene therapy and mRNA technology. Dr. Cohen discusses why clinical trials are essential to progress, especially for rare diseases, and why patient participation plays such a critical role in moving new therapies forward. Dr. Cohen also shares how the strength of the CF community continues to inspire his work, offering both realism and hope for the future of CF research.You'll also hear more about the personal side of this wonderful scientist! The Arcturus team packed Bonnell Foundation Hospital Bags with comfort products for caregivers, and CF adults for California CF Clinics. #teamworkClinical trials are an important step to understand whether a medicine works for its intended purpose.  Please see our active clinical trials below. For any questions email:  Community@ArcturusRx.com. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

I've known Julie McCaffrey for years. She lives about 40 minutes from me, in Romeo, Michigan. Julie and her husband, Curtis, are raising four daughters, and their oldest, Jenna—now 20—lives with cystic fibrosis.What still makes me smile is how Julie and I were connected long before we ever met through the CF community… and we had no idea. We worked in the same building, in the same industry, at the same time. Both of us were in radio. I was a news reporter at WWJ, while Julie was a producer at WYCD. Even our podcast editor worked at another station in that very same building. Proof that sometimes the universe plants people in your orbit long before it tells you why.Julie's career path reflects both her curiosity and her compassion. She's worked in radiology, orthopedics, and labor and delivery. She's supported students as a paraprofessional in an elementary school and worked in a group home for adults with intellectual disabilities. Today, she works at Target—and genuinely loves it. Wherever she goes, she brings the same energy: presence, kindness, and care.At the heart of everything Julie does is a simple but powerful mission—to spread joy. She is deeply passionate about mental health advocacy, especially within the cystic fibrosis community. And despite the very real financial strain that comes with healthcare and insurance challenges, Julie continues to show up with an unwaveringly positive spirit. Not a performative positivity—but a grounded, generous kind that makes people feel seen.If you take just one thing from Julie today, let it be this:You are brilliant.You are beautiful.And you can do anything.(Suicide was discussed in this episode. Anyone needing help can call or text #988).  Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y