Love, Hope, Lyme Podcast

This is episode 81 of the Love, Hope, Lyme podcast. This podcast does not replace medical care. If you're struggling with Lyme symptoms, please seek proper medical care. The pdf of Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivors Need to Know is always free for chronic Lyme survivors. Reach out to Fred Diamond on social media for your copy. Healing Starts When You Trust Your Body with Wendi Lindenmuth In this episode of the Love, Hope, Lyme Podcast, Fred Diamond sits down with Wendi Lindenmuth, author of Listen to Your Body, to explore what it really takes to heal from chronic Lyme disease and chronic pain. Wendi shares her powerful journey from a competitive athlete suddenly unable to walk, to becoming a guide for others navigating the complexities of Lyme. Her message is clear: healing begins when you believe it's possible and learn to listen to your body with compassion and intention. We go deep into the mindset shifts and practical strategies that can help Lyme survivors move forward, including: 💚 Why believing you can heal is the first critical step 💚 How to navigate the overwhelm of Lyme communities and information 💚 The role of nutrition in reducing inflammation and supporting recovery 💚 Why sleep may be the most underrated healing tool 💚 How reconnecting with nature can restore your energy and mindset 💚 The importance of finding the right kind of support 💚 What it means to "communicate with your pain" and why it matters Wendi also shares simple, accessible ways to begin regulating your nervous system including the use of healing frequencies even on your hardest days. If you're living with Lyme disease, supporting someone who is, or searching for hope in the middle of chronic illness, this conversation will meet you where you are and help you take the next step forward. 👉 Learn more about Wendi's book Listen to Your Body 👉 Subscribe for more conversations that bring hope, healing, and understanding to the Lyme community About the Podcast The Love, Hope, Lyme Podcast is dedicated to helping Lyme survivors and their loved ones find support, understanding, and practical strategies for healing. #LymeDisease #ChronicIllness #HealingJourney #LymeRecovery #MindsetMatters #ChronicPainSupport

This is episode 080 of the Love, Hope, Lyme podcast. This podcast does not replace medical treatment. If you are suffering from Lyme and other tick-borne disease, please seek proper medical treatment. "Love, Hope, Lyme" is available on Amazon. To get the PDF for free, reach out to Fred Diamond on Facebook or LinkedIn. What does it really take to keep going when Lyme disease changes everything? In this powerful episode of the Love, Hope, Lyme Podcast, Fred Diamond sits down with Nicole O'Donnell, author of "Resilient Hope," along with Christa Nannos and Jasmin Perdomo, to share real, raw lessons from their Lyme journeys. This conversation goes beyond treatments. It's about what actually helps people move forward. 👉 Here's what you'll hear: 💚 Why community can become your lifeline 💚 The truth that healing is not linear—and that's okay 💚 How to stop chasing the "magic cure" and start listening to your body 💚 Why nervous system regulation is essential for healing 💚 How to navigate grief, identity loss, and still choose hope One of the most powerful takeaways: "Even on the hardest days, hope is a choice." If you're a Lyme survivor or love someone who is this episode will meet you where you are.

This is episode 079 of the Love, Hope, Lyme podcast. This podcast does not replace medical treatment. If you are suffering from Lyme and other tick-borne disease, please seek proper medical treatment. Purchase "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" on Amazon. What if the pain you've been told to "live with"… is actually treatable? In this powerful episode of the Love, Hope, Lyme Podcast, Fred Diamond speaks with integrative nurse practitioner and Lyme survivor Dr. Penni Vachon about one of the most misunderstood aspects of Lyme disease: chronic pain and how to overcome it. Dr. Vachon shares her deeply personal journey, including how Lyme disease impacted multiple generations of her family and how a life-changing moment in the NICU pushed her to fully dedicate her work to helping Lyme survivors heal. Together, they dive into: ✔️ Why Lyme pain is so often misdiagnosed (arthritis, lupus, fibromyalgia) ✔️ The real root causes of pain—beyond what traditional medicine addresses ✔️ Differences between neurological, joint, and muscle pain in Lyme ✔️ Effective treatment approaches—from botanicals to advanced therapies ✔️ The critical role of inflammation and the nervous system ✔️ Why "suffering is optional" and what Lyme patients must demand from their care Dr. Vachon delivers a powerful message: You do NOT have to live in constant pain. If you or someone you love is struggling with Lyme disease, this episode offers both validation and real hope—along with actionable insights to pursue more effective healing. 🎧 Love, Hope, Lyme Podcast is dedicated to helping Lyme survivors and their loved ones find answers, support, and a path forward. 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.

This is episode 078 of the Love, Hope, Lyme podcast. This podcast does not replace medical treatment. If you are suffering from Lyme and other tick-borne disease, please seek proper medical treatment. Pennsylvania has been called a ground zero of the Lyme disease epidemic in the United States. On this episode of the Love, Hope, Lyme Podcast, Fred Diamond speaks with two powerful advocates who are working to change that reality. Eric Huck and Amy Tiehel from the Pennsylvania Lyme Resource Network share their deeply personal Lyme journeys and explain why advocacy, education, and community support are critical for Lyme survivors and their families. Eric's story began in 2009 after a tick bite while hiking the Appalachian Trail. Despite early treatment, his health rapidly deteriorated and he was eventually diagnosed with Lyme disease along with multiple co-infections including Babesia, Bartonella, Ehrlichiosis, and Anaplasmosis. His experience navigating the healthcare system ultimately led him to help build one of the largest Lyme advocacy organizations in the state. Amy's journey began while she was living in Los Angeles. After years of debilitating symptoms, Bell's palsy, and visits to more than 25 doctors, she was finally diagnosed with Lyme disease and Babesia. Her experience with misdiagnosis and medical dismissal pushed her into advocacy so that other patients would not have to navigate the system alone. In this powerful conversation, we discuss: • Why Pennsylvania has become a Lyme disease hotspot • The mission of the Pennsylvania Lyme Resource Network  • The challenges patients face with diagnosis and treatment  • The mental and emotional toll Lyme takes on families • Prevention through the Dare 2B Tick Aware education program • What must change to improve care for Lyme survivors Eric and Amy also share details about the Pennsylvania Lyme Patient Conference taking place April 18 in King of Prussia, where patients, doctors, and advocates will gather to learn, connect, and support one another. Learn more about the Pennsylvania Lyme Patient Conference: https://palyme.org

What happens when Lyme disease steals a child's health and a family's sense of normal? In this powerful episode of the Love, Hope, Lyme Podcast, Fred Diamond speaks with Dr. Somer Delsignore, CEO and Founder of Hudson Valley Integrative Health and a member of International Lyme and Associated Diseases Society (ILADS), about the hidden realities of pediatric Lyme disease. Dr. Somer specializes in neuro-immune conditions in children and adolescents, uncovering root causes behind complex autoimmune and psychiatric symptoms related to tick-borne illness. Together, Fred and Dr. Somer explore what no one tells parents at diagnosis — including: Why the Lyme journey is rarely linear The guilt many parents carry — and why it's misplaced Gaslighting, medical trauma, and rebuilding trust The emotional toll of identity loss and grief in chronic illness How schools can better support children with fluctuating symptoms Navigating family dynamics when others "don't see" the illness Realistic hope vs. toxic positivity Dr. Somer also shares insights on congenital Lyme, teenage independence during chronic illness, caregiver burnout, and how small wins become powerful milestones in long-term healing. This episode is especially important for parents of children and teens with Lyme disease — but it will resonate with any caregiver navigating chronic illness. As Dr. Somer reminds us, "Hope isn't toxic positivity. Stability is success." If you or someone you love is walking this road, this conversation offers clarity, compassion, and grounded hope. 👉 Subscribe for more conversations that support Lyme survivors and the people who love them. #LoveHopeLyme #PediatricLyme #ChronicIllness #LymeDisease #CaregiverSupport Order "Love, Hope, Lyme: What Family Members, Partners and Friends Who Love a Chronic Lyme Survivor Need to Know" on Amazon. The PDF is always free. Contact Fred Diamond on Facebook or LinkedIn.

This is episode 76 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.] In this episode of the Love, Hope, Lyme Podcast, Fred Diamond, author of "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor" sits down with Dr. Jennifer Miller, who oversees clinical and scientific operations at Galaxy Diagnostics, for one of the most important conversations we've ever had about Lyme disease. We discuss the basics. Not just what Lyme does, but why it happens in the first place. Dr. Miller brings decades of deep scientific experience studying Borrelia burgdorferi and explains: ✅ How ticks actually become infected ✅ Why nymph ("seed") ticks are the biggest threat to humans ✅ What happens biologically inside the tick and inside your body ✅ Why Borrelia is so hard for the immune system (and antibiotics) to find ✅ How co-infections like Bartonella and Babesia complicate diagnosis and recovery ✅ Why some people develop neurological symptoms while others don't ✅ Why today's antibody tests often miss active infections and how Galaxy is working on direct detection methods to change the standard of care We also talk about: 🧬 Immune dysregulation 🧠 Blood–brain barrier crossing 🧪 False negatives and outdated testing 🦠 Why Borrelia behaves unlike almost any other bacteria Dr. Miller shares insights from her presentation at International Lyme and Associated Diseases Society (ILADS) and her personal journey into Lyme research inspired by growing up in tick-heavy Southern Maryland and watching her father care for Lyme patients as a primary care physician. If you've ever asked yourself: 👉 Why me? 👉 How did this actually start? 👉 Why is Lyme so hard to diagnose? 👉 What's really happening inside my body? …this episode is for you. 🎧 Listen now and please share this episode with anyone who needs a deeper understanding of Lyme disease. #LoveHopeLyme #LymeDisease #TickBorneIllness #LymeEducation #ChronicLyme #GalaxyDiagnostics #VectorBorne #LymeTesting #InvisibleIllness

This is episode 75 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.] In this powerful episode of the Love, Hope, Lyme podcast, host Fred Diamond is joined by Lyme advocate Marjorie Veiga for an honest, practical conversation about managing the overwhelm of Lyme disease and tickborne illnesses. Marjorie shares her personal journey with tickborne illness, which began in 1999, and her experience caring for her daughter through years of Lyme coinfections. Drawing on her background as a senior manager at Verizon and her deep involvement in the Lyme community, Marjorie explains why organization, documentation, and support systems are critical to healing. At the center of the conversation is "My Lyme Guide," the comprehensive resource Marjorie created to help Lyme patients and caregivers track medications, appointments, symptoms, insurance, school accommodations, and more especially when brain fog and fatigue make daily management overwhelming. Together, Fred and Marjorie discuss: 💚 Why Lyme disease creates unique and ongoing overwhelm 💚 How organization can accelerate healing and reduce stress 💚 Managing medications, pulsing and rotating treatments, and symptom tracking 💚 Supporting children with Lyme and navigating schools, 504 plans, and IEPs 💚 Using technology, apps, and patient portals to stay organized 💚 Frequency-based and bioresonance therapies as complementary healing tools 💚 Practical advice for caregivers and families walking this journey together 💚 How hope, teamwork, and adaptability matter at every stage of healing Marjorie also shares encouragement for those early or deep into their Lyme journey, reminding listeners that healing is not one-size-fits-all and that there are always new paths forward. This episode is especially valuable for: ✔️ Lyme survivors ✔️ Parents and caregivers ✔️ Those overwhelmed by complex treatment plans ✔️ Anyone seeking practical tools, structure, and hope 💚 You are not alone. There is help. There is hope.

This is episode 74 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.] In this powerful and deeply human episode of the Love, Hope, Lyme podcast, host Fred Diamond is joined by two respected Lyme disease advocates and fellow podcasters. Anne Desjardins and Tanya Hoebel join Fred for an honest conversation about healing, advocacy, and hope. Anne, host of The Silver Lyming podcast, shares her journey through years of misdiagnosed Lyme disease, how discovering the truth changed her life, and why practices like hot yoga, holistic medicine, and self-advocacy became critical to her healing. She also discusses her work educating communities through the PA Lyme Resource Network and her mission to help others believe recovery is possible. Tanya, host of Lyme and Beyond with Tanya, opens up about her 13-year journey to wellness, including years without a diagnosis, profound financial loss, and the mental-health toll of chronic Lyme disease. She explains why nervous system regulation, sleep, sound therapy, and mindset are foundational components of healing, and why no one should feel ashamed for struggling. Together, Anne and Tanya discuss: 💚 Why Lyme disease is often misunderstood and misdiagnosed 💚 The emotional and psychological impact of chronic illness 💚 Practical, low-cost tools to support healing 💚 The importance of becoming your own best advocate 💚 Why hope and community can be life-saving Fred also reflects on why he wrote Love, Hope, Lyme, the heartbreaking realities of suicide risk in the Lyme community, and why sharing stories of resilience and recovery matters so deeply.  This episode is for: 💚 People living with Lyme or other tick-borne illnesses 💚 Family members, partners, and caregivers seeking understanding 💚 Anyone looking for real stories, practical ideas, and genuine hope 🎧 Listen, share, and remind someone today: you are not alone—and healing is possible.

This is episode 73 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.] In this powerful and deeply moving episode of the Love, Hope, Lyme Podcast, host Fred Diamond welcomes back Rabbi Melinda Bernstein and Gregg Kirk, two extraordinary guests for an honest, soulful conversation about the spiritual dimensions of chronic illness, healing, and personal transformation. Gregg Kirk, author of The Gratitude Curve and his newest book Your Love Will Make the Difference, shares how Lyme disease became a catalyst for profound awakening, gratitude, and purpose. He opens up about his journey through illness, remission, grief, and healing and why chronic Lyme can be information pointing us toward necessary life change. Rabbi Melinda Bernstein brings a grounded yet expansive spiritual perspective, exploring how faith, surrender, nervous system regulation, and embodiment practices can support healing when medicine alone falls short. Drawing from her own decade-long Lyme journey, Melinda explains how constriction, loss, and suffering can become doorways to growth, balance, and renewed vitality. Together, Fred, Melinda, and Gregg discuss: 💚 The spiritual initiation that chronic illness often becomes 💚 Why Lyme is not just physical—but emotional, energetic, and existential 💚 The role of faith, frequency, and nervous system regulation in healing 💚 Practical spiritual practices for Lyme survivors  💚 What Lyme remission looks like and how to stay there 💚 Why there is more to you than Lyme disease This episode is especially meaningful for anyone navigating chronic Lyme, tick-borne illness, grief, or long-term healing and for loved ones seeking to better understand the journey. 👉 If you're searching for hope, meaning, and a deeper understanding of healing beyond symptoms, this conversation is for you. Listen. Reflect. Heal.

This is episode 72 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.] Historic Moment for Lyme Advocacy. RFK Jr. Roundtable Reactions & What Comes Next In this special episode of the Love, Hope, Lyme Podcast, host Fred Diamond, author of Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know, convenes a powerful panel of Lyme advocates, researchers, and survivors to reflect on a pivotal week for the Lyme community. Just days after the RFK Jr. Lyme Disease Roundtables in Washington, D.C., this episode captures real-time reactions to what many are calling a historic turning point when federal leadership publicly acknowledged chronic Lyme disease, condemned medical gaslighting, and outlined tangible steps toward research, funding, and accountability. 🎙️ Featured Panelists Ali Moresco – Founder of Moresco PR, Board Chair of Project Lyme, longtime advocate and communications leader in the tick-borne illness space  Nikki Schultek – Research leader, founder of multiple pathobiome initiatives, Lyme survivor, and board member of ILADEF Meghan Bradshaw – Executive Director of the Center for Lyme Action, leading federal policy and funding advocacy efforts Together, they discuss: 💚 What made this week's HHS and White House engagement different from past hearings 💚 Why statements like "Lyme patients will no longer be gaslit" matter—and what must follow 💚 Federal funding, diagnostics, Medicare coverage, and clinical trials 💚 The urgent need for collaboration between government, clinicians, researchers, and advocates 💚 How patients, caregivers, and supporters can turn momentum into lasting change This conversation is both hopeful and grounded celebrating progress while emphasizing that advocacy, accountability, and action must continue.

This is episode 71 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.] In this episode of the Love, Hope, Lyme Podcast, host Fred Diamond sits down with Olivia Abrams, founder of TiKK MiTT and a Lyme disease survivor who turned prevention into purpose. Olivia shares her personal Lyme story beginning with arthritis symptoms at age seven and how growing up in a tick-endemic area inspired her to create TiKK MiTT, a chemical-free, reusable glove designed to help people and pets detect ticks before they embed. The conversation explores prevention, entrepreneurship, advocacy, and what it was like pitching TiKK MiTT on Shark Tank, where Olivia famously received and declined two offers. Beyond the product, this episode dives deep into: 💚 Why tick checks and prevention are still overlooked 💚 The growing need for Lyme disease awareness and advocacy 💚 Olivia's work with organizations like Project Lyme and the Center for Lyme Action 💚 How passion projects can bring hope and purpose during and after chronic illness This conversation is especially meaningful for Lyme survivors, caregivers, and anyone looking for practical prevention tools and real hope. 🎧 Listen if you care about Lyme prevention, patient advocacy, mission-driven entrepreneurship, and turning personal experience into impact. 🔗 Learn more about TiKK MiTT: https://tikkmitt.com 💚 The e-version of "Love, Hope, Lyme" is always free for Lyme survivors.

This is episode 70 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.] Why do so many people with chronic Lyme and other persistent infections do everything right… yet still not get better? In this episode of Love, Hope, Lyme, host Fred Diamond sits down with Dr. Melanie Stein a naturopathic physician, author, and expert in identifying the underlying drivers of chronic illness. Dr. Stein explains why some patients stall, how trauma and nervous system dysregulation contribute to persistent symptoms, and the holistic steps that can restart healing.  If you've felt stuck despite antibiotics, herbs, treatments, and lifestyle changes this conversation offers hope, clarity, and a roadmap to rebuild resilience and progress again. ✨ What You'll Learn 💚 The most overlooked root causes behind stalled recovery 💚 Why nervous system healing must come first 💚 The role of environmental toxins, chronic stress, and stealth infections 💚 How to re-establish communication between the brain and body  💚 Steps patients can take today to support deeper healing 📘 About Dr. Melanie Stein Dr. Stein helps patients with chronic Lyme, mold illness, and long-haul infections uncover the blockages preventing recovery. She's based in Portland, Oregon and is the author of "Breaking Through Chronic Illness: The Science of Cellular Repair and the Path to Lasting Recovery" (2025). 🎧 Listen to More Love, Hope, Lyme Episodes Stories, solutions, and support for Lyme warriors and their loved ones.

In this powerful episode of Love, Hope, Lyme, Fred Diamond sits down with singer-songwriter and Lyme advocate Jesse Ruben for a deep, honest, and emotional breakdown of his song "Monster." Jesse opens up about the terrifying return of his Lyme and Babesiosis, the years of misdiagnosis, the isolation, the brain fog, the burning pain, and the desperate search for answers that so many Lyme survivors know all too well. For the first time, Jesse walks through Monster line by line — how the lyrics came to him during the darkest hours of his illness, why he nearly kept the song off the album, and why he ultimately decided the Lyme community needed to hear it. We talk about: How Lyme changed Jesse's life, relationships, identity, and career The emotional toll of not being believed by doctors, family, and friends The fear of losing the "young and healthy" version of yourself Why Monster resonates so deeply with people living with chronic illness Jesse's new album, his return to performing, and what comes next If you've ever felt dismissed, misunderstood, or alone in your Lyme journey, this conversation will speak directly to you. 🎵 Get Jesse's album (vinyl or CD): jesseruben.com 🎧 Follow Jesse Ruben: @jesseruben 💚 Learn more about Generation Lyme: generationlyme.org If this episode moves you, please like, subscribe, and share. It helps more Lyme survivors find the support they deserve.

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?  💚 In this powerful episode of Love, Hope, Lyme, host Fred Diamond talks with Lauren Lovejoy, founder of Lyme Warrior, about her 12-year journey from losing her health and career to leading one of the most passionate advocacy communities in the Lyme world. Lauren shares how she went from seeing over 60 doctors with most dismissing her symptoms as "stress" to finally receiving a clinical Lyme diagnosis and re uilding her life through alternative healing methods. Her honesty about the emotional toll, financial burden, and daily fight for recognition will move and inspire you.  🌿 You'll hear Lauren discuss:  💚 Why antibiotics aren't always the answer and what helped her heal 💚 How Lyme Warrior empowers survivors through awareness, 5Ks, and "Kid's Smile Boxes" 💚 The unseen emotional struggle of advocates and caregivers 💚Why believing Lyme patients is the first and most powerful act of care 💚The hope for accurate testing and meaningful medical progress ahead 💪 "Being a Lyme Warrior doesn't mean running a 5K. It means not giving up today." – Lauren Lovejoy 🎧 Listen. Learn. Believe. Share. Because together, we are all Lyme Warriors. 🔗 Connect with Lyme Warrior: [lymewarrior.us] 📘 Learn more about Fred's book: Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know"  #LymeWarrior #LoveHopeLyme #ChronicLyme #LymeAwareness #LymeDisease #LymeCommunity #HealingJourney #LymeSupport

In this episode of Love, Hope, Lyme, Fred Diamond speaks with Dr. Korine Kolivras, professor of geography at Virginia Tech, whose groundbreaking research challenges the long-held belief that "we don't have Lyme here." Dr. Kolivras, author of a chapter in Appalachian Epidemics: From Smallpox to COVID, shares how geography, land use, and even bird migration contribute to the spread of Lyme disease across Virginia, Appalachia, and beyond. She explains why the maps we rely on underestimate the true reach of Lyme, how land development and resource extraction may accelerate tick expansion, and what needs to change in medical education and public awareness. 🎧 Topics include: How geography and land use shape Lyme's spread Why "reported cases" don't reflect reality The role of birds, deer, and mice in tick migration How Appalachia's land changes may drive new Lyme hotspots What healthcare providers need to ask every patient 💬 Dr. Kolivras's message is clear — Lyme disease exists far beyond the maps, and awareness must rise everywhere. 📘 Learn more about her work in Appalachian Epidemics: From Smallpox to COVID (University of Kentucky Press). 🎙️ Love, Hope, Lyme is the podcast that brings together Lyme survivors, doctors, and advocates to share truth, research, and hope. #LymeDisease #VirginiaTech #Appalachia #TickBorneDiseases #LymeAwareness #LoveHopeLyme

This is episode 66 of the Love, Hope, Lyme Podcast. In this special Love, Hope, Lyme podcast with Fred Diamond, Athena Brownson shares how she went from the heights of professional skiing to the depths of chronic illness. After years of competing around the world, a Lyme diagnosis forced her to rebuild her life from the ground up. In this heartfelt conversation, Athena shares how she faced unimaginable physical and emotional challenges from misdiagnoses and loss of identity to rebuilding her health, career, and sense of purpose. Her story is one of courage, reinvention, and hope. Through Lyme, she discovered a new calling: helping others find meaning, resilience, and light in their own healing journeys. 🎧 Listen as she explores: ⛷️ The mindset of a professional athlete facing chronic illness 🤞🏻 How she found purpose and healing through adversity 💚 Why self-compassion, community, and small daily wins matter most If you're searching for strength or inspiration in your Lyme journey, Athena's story will remind you that healing begins with hope. Fred Diamond offers the e-version of his popular book "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" for free to Lyme survivors. Reach out the him on social media for your copy. The print copy of the book is on Amazon. #LoveHopeLyme #LymeDisease #LymeAwareness #HealingJourney #ChronicIllness #Resilience #Inspiration #AthenaBrownson

This is episode 65 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.] In this powerful conversation, Fred Diamond welcomes back Col. (Ret.) Nicole Malachowski, the first female Thunderbird pilot and a leading Lyme advocate, alongside Dr. Kent Kester, infectious disease physician and executive director at CEPI. Together, they unpack the groundbreaking NASEM Report (Charting a Path Toward New Treatments for Lyme Infection-Associated Chronic Illnesses) and what it means for patients. 🔹 Nicole shares how her life was changed by a tick bite, why she's dedicated herself to patient advocacy, and what serving on the NASEM committee taught her. 🔹 Dr. Kester explains why this report is a historic moment: the U.S. government is officially recognizing Lyme Infection-Associated Chronic Illnesses as real—and why patient-centered research and treatments can't wait. 🔹 Together, they discuss the six key recommendations of the report, the role of patient voices, and the urgent need for science, funding, and compassion to align.  ✨ "For the first time ever, the United States of America is saying Lyme IACI is real." Nicole Malachowski If you or someone you love has battled Lyme disease, this episode offers validation, hope, and a roadmap for change. 📖 Fred Diamond's book: Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" is available on Amazon. The pdf is always free for Lyme survivors. #LymeDisease #LoveHopeLyme #ChronicIllness #LymeAwareness #PatientAdvocacy #Hope

This is episode 64 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.] 🎙️ In this powerful episode of Love, Hope, Lyme, Fred Diamond sits down with Kristen Harris, Education and Grants Manager at the Global Lyme Alliance (GLA), to explore the vital role of mentoring in the Lyme disease community. Kristen shares her deeply personal Lyme journey beginning with a tick bite at just 8 years old in New York and how decades of struggle with fatigue, neurological issues, chronic pain, and misdiagnosis ultimately led her to remission, relapse, and finally to a place of giving back. At GLA, Kristen now helps lead the Peer-to-Peer Mentor Program, connecting Lyme survivors, caregivers, and family members with mentors who have walked this difficult path before them. These mentors don't provide medical treatment but they do offer something just as powerful: understanding, compassion, and emotional support. In this episode, you'll hear about: 💚 Why Lyme survivors seek mentors while other illnesses rarely do 💚 How the GLA mentorship program supports both patients and caregivers 💚 The rigorous process mentors go through to prepare for this role 💚 The unique challenges of the Lyme journey, from misdiagnosis to isolation 💚 Kristen's insights on why community support is more needed than ever ✨ Whether you're a patient, caregiver, or advocate, this conversation is a reminder that no one should walk the Lyme journey alone. 🔗 Learn more about GLA's resources and mentorship program: https://www.gla.org

This is episode 63 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.} In this powerful episode of the Love, Hope, Lyme Podcast, host Fred Diamond talks with Nikki Schultek, founder of Intracell Research Group and co-founder of the Alzheimer's Pathobiome Initiative (AlzPI). Nikki shares her personal journey with chronic infections and how it led her to uncover critical connections between Lyme disease, other infections, and neurodegenerative conditions such as dementia and Alzheimer's. You'll learn: How chronic infections like Lyme, co-infections, viruses, and even fungi may impact brain health Why physicians often miss infections as a root cause of cognitive decline The concept of the "pathobiome" and why it matters for understanding Alzheimer's disease Hopeful research showing some cases of dementia may improve with targeted infection treatment How Nikki and her global research team are bridging silos to uncover answers If you or a loved one are living with Lyme disease—or worried about its long-term effects—this episode offers both hope and cutting-edge insight. 🔗 Learn more about Nikki's work: alzpi.org 📖 Learn more about Fred's book: Love, Hope, Lyme 👉 Don't forget to like, share, and subscribe for more conversations bringing hope and answers to the Lyme community. #LymeDisease #Alzheimers #Dementia #ChronicIllness #Hope #LoveHopeLyme

This is episode 62 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.} How does Lyme disease affect your brain, your energy, and even your closest relationships? In this episode of Love, Hope, Lyme, psychiatrist Dr. Chris Winfrey shares powerful insights from his work with chronic Lyme survivors covering everything from mitochondrial health and strength training to the emotional hijacking of the limbic system. You'll learn: ☑️ Why true recovery is about more than symptom scores ✅ How to boost energy and brain clarity by supporting your mitochondria ✅ The critical role strength training plays in Lyme healing ☑️ How Lyme damages brain function and impacts relationships ✅ The connection between faith, motivation, and long-term recovery "You can fight the infection all day long, but if you don't have energy, it's not going to work." Dr. Chris Winfrey Whether you're a survivor, caregiver, or health professional, this conversation will change the way you think about Lyme disease and mental health. #LymeDisease #ChronicLyme #BrainHealth #Mitochondria #MentalHealth #LymeTreatment #LoveHopeLyme #Healing

This is episode 61 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.} When brain fog and gut pain derailed Greg Lee's career as a NASA engineer, he turned to acupuncture and herbal medicine—and ultimately transformed his own life. Now, after three decades and more than a thousand patients, he's helping Lyme survivors overcome the pain, brain inflammation, coinfections, and fatigue that mainstream medicine often overlooks. 🎤 In this powerful Love, Hope, Lyme episode, Greg shares the advanced protocols he uses at the Lyme Research & Healing Center in Frederick, MD—from frequency-based scans and photoactivated antimicrobials like methylene blue and curcumin, to intranasal bee venom and essential oil liposomes. These treatments are delivered with precision to reach deep into the brain, past biofilms, and inside damaged cells. 🕷️ Whether you're new to Lyme or deep into a complex healing journey, Greg's holistic approach—paired with spiritual insight and scientific rigor—offers a roadmap for restoring vitality, clearing infection, and reclaiming your life. 👉 Download his free "Innovative Anti-Lyme Co-infection Treatments": https://www.lymeresearchcenter.com/LOVE Topics we cover include: ✅ Why frequency-specific microcurrent can regenerate tissue ☑️ How advanced scanning detects over 1,000 pathogens in real time ✅ Methylene blue + red light therapy for neurological Lyme ☑️ Essential oils as potent antimicrobial tools ✅ Bee venom therapy for Babesia in the brain ☑️ The role of diet, sleep, and spiritual connection in long-term healing 🎧 Hosted by Fred Diamond, author of Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know. Learn more about the Lyme Research Center at https://www.lymeresearchcenter.com/ #LymeDisease #LoveHopeLyme #GregLee #LymeHealing #ChronicLyme #AlternativeMedicine #MethyleneBlue #BeeVenomTherapy #FrequencyHealing #LymeRecovery #LymeResearch #HealingChronicIllness #BiofilmBusting #EssentialOils #HerbalMedicine

This is episode 60 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 if your doctor missed something critical—and you had to save yourself and your child? That's exactly what happened to Mary Lyn Hammer. After six and a half years of misdiagnosis, Mary Lyn finally learned she had Lyme disease—a revelation that turned her into a relentless medical detective. She's the author of, "Over My Dead Body: What I Learned During My Decade‑long Journey to Heal from Lyme Disease and Coinfections." In this deeply personal episode of Love, Hope, Lyme, she shares how she battled chronic Lyme, a life-threatening blood infection, and a maze of co-infections—all while raising her daughter as a single mom. 💡 Learn how she cracked the biofilm puzzle. 🧬 Hear how she uncovered hidden infections, including bovine tuberculosis, before science confirmed it. 👧 And experience the emotional moment when her daughter finally felt well enough to say, "Mom, today was the best Monday of my life." If you're struggling to get answers or feel like no one understands the complexity of chronic Lyme, this conversation is for you. Mary Lyn's story is not just about surviving—it's about healing, advocacy, and hope. 👇 Listen now and share with someone who needs to hear this.  #LymeDisease #ChronicLyme #Biofilm #MedicalDetective #LymeAwareness #LoveHopeLyme #HealingJourney #CoInfections #LymeAdvocate #MaryLynHammer

This is episode 59 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.} In this powerful Love, Hope, Lyme episode, Fred Diamond sits down with Lyme warrior and healthcare PR expert Ali Moresco for an unforgettable conversation about resilience, advocacy, and purpose. After a fast-paced early career in celebrity PR, Ali's life came to a halt when she was hit with a wave of debilitating symptoms. It took two years to be diagnosed with Lyme disease and multiple tickborne infections—including Babesia, Bartonella, ehrlichiosis, and relapsing fever. She became, as she puts it, a "professional patient." But Ali didn't stop there. Today, she's the Board Chair of Project Lyme, a leader in advocacy with the Center for Lyme Action and Two Alpha Gals Foundation, and the founder of a fast-growing healthcare PR firm that centers the patient voice. 🔹 In this episode, Ali shares: 💚 Why "Don't give up before the miracle occurs" became her guiding mantra 💚 How chronic illness taught her to value resilience—and build a thriving business around it 💚 The importance of accurate testing, individualized treatment, and public awareness 💚 How every Lyme survivor can find a way to contribute, no matter their capacity Whether you're a chronic Lyme survivor, caregiver, or ally, Ali's story will inspire you to stay hopeful and take action—on your own terms. 💚 ""Lyme may have changed my life, but it didn't take away my power. I used it to build something that helps others find hope, answers, and their voice." – Ali Moresco 📲 Connect with Ali on Instagram: @alimoresco 📘 Fred's book: Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know." 👉 Subscribe to the podcast for more powerful stories of healing, hope, and advocacy in the Lyme community. #LymeDisease #ChronicIllness #LymeAwareness #AlphaGalSyndrome #ProjectLyme #LoveHopeLyme #TickborneIllness #PatientAdvocacy

This is episode 58 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 is Lyme rage—and why does it change who you are? In this powerful episode of Love, Hope, Lyme, host Fred Diamond talks with Dr. Darin Ingels, a Lyme-literate naturopathic doctor and Lyme survivor, about one of the most misunderstood aspects of chronic Lyme disease: the emotional and neurological impact of Lyme rage. Dr. Ingels shares his personal journey—from bullseye rash to relapse, from failed antibiotics to healing through Chinese herbal medicine—and breaks down why Lyme disease and co-infections like Bartonella can lead to brain inflammation, emotional dysregulation, personality shifts, and even explosive rage. 💬 "It's not just 'mood swings.' It's inflammation in the brain." You'll learn: 💚 What Lyme rage feels like—and why it's not just anger 💚 How co-infections, autoimmunity, and mast cell activation drive brain symptoms 💚 Natural and clinical strategies to reduce inflammation and restore emotional balance 💚 Ways to rebuild relationships damaged by Lyme-induced emotional shifts. A message of hope for survivors and families affected by neuropsychiatric Lyme. Whether you're living with chronic Lyme or love someone who is, this episode offers validation, clinical insights, and practical steps toward healing. 🔗 Learn more about Dr. Ingels and his work: https://dariningelsnd.com 📖 Get Fred's book "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know." The pdf is always free for Lyme survivors.

This is episode 57 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.] For decades, Lyme disease survivors have faced an uphill battle—dismissed by doctors, forced to wait years for appointments, and left without clear paths to healing. In this powerful episode of the Love, Hope, Lyme Podcast, Fred Diamond speaks with Dr. Monica Embers, a leading Lyme disease researcher at Tulane University and contributor to The Quiet Epidemic, and Kevin Williams, co-founder of Ravel Health and a chronic Lyme patient of 18 years. Dr. Embers shares the hard truth: "There is no central place for patients to turn." She explains why outdated diagnostic tools, lack of federal investment in treatment research, and misinformation have left millions without answers—and how new tests and targeted therapies are finally changing the game. Kevin Williams opens up about the deeply personal reasons he and co-founder, Jaime Intile, created Ravel Health: to spare others the years of pain and medical gaslighting they endured. Ravel now offers accessible, virtual, Lyme-literate care across 46 states with no waitlists and personalized treatment plans. 🎧 If you or someone you love is navigating Lyme or a related chronic illness, this episode will inform, validate, and give hope. 📌 Learn how Ravel is partnering with science leaders like Dr. Embers to change the future of Lyme care. #LoveHopeLyme #LymeDisease #ChronicIllness #RavelHealth #LymeTreatment #MonicaEmbers #TheQuietEpidemic

This is episode 56 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 happens to a relationship when both partners are battling invisible illnesses, trauma, and years of misdiagnosis? In this deeply emotional episode of the Love, Hope, Lyme Podcast, David and Jacquie Butler share their raw, unfiltered story of love, resilience, and healing. From David's decades-long battle with undiagnosed Lyme disease, neuropsychiatric symptoms, and Lyme rage — to Jacquie's own experience with Hashimoto's, PCOS, and years of medical gaslighting — this is a candid conversation about surviving illness as a couple. You'll hear: 🧠 How trauma, both childhood and medical, shapes chronic illness 💔 Why many relationships don't survive Lyme — and how theirs did 🗣 The truth about "Lyme rage," misdiagnosis, and psychiatric medication  💪 How orgone-based psychotherapy helped them reclaim their lives 👶 Their unexpected pregnancy after years of infertility and healing 💚 A message of hope for couples on the edge Whether you're a Lyme warrior, caretaker, or someone who has loved through suffering, David and Jacquie's vulnerability will move you — and may even help you begin your own healing.  #LymeDisease #ChronicIllness #MarriageAndIllness #LymeRage #MedicalGaslighting #LymeSupport #LoveHopeLyme #ChronicLyme #MentalHealthAwareness #HealingTogether

This is episode 55 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.] In this powerful episode of the Love, Hope, Lyme Podcast, naturopathic physician Dr. Myriah Hinchey shares the 10 essential steps she uses to help Lyme survivors reclaim their health—starting with rebuilding the immune system from the ground up. Whether you're newly diagnosed or have been living with chronic Lyme for years, Dr. Hinchey offers a clear, actionable roadmap rooted in clinical experience, integrative medicine, and deep compassion. 🎧 Topics we cover: ✔️ What the "10 Bs" are—and why they matter ✔️ The importance of detoxification and drainage  ✔️ How to balance hormones and rebuild the gut ✔️ What most treatment plans are missing 📣 "There's no one-size-fits-all solution. But there is a system—and it starts with fixing the immune system first." 🔔 Subscribe for more expert conversations and hope-filled healing stories. #LymeDisease #ChronicLyme #LymeHealing #LymeHope #DrMyriahHinchey #NaturopathicMedicine #TickBorneIllness #LoveHopeLymePodcast #LymeAwarenessMonth #ImmuneSupport

This is episode 54 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 happens when Lyme disease rips apart everything you thought you knew about yourself, your health, and your family? In this deeply emotional episode of Love, Hope, Lyme, Ilana shares her harrowing journey through chronic Lyme, Bartonella, and Babesia — and the devastating psychiatric symptoms that followed. Alongside her is her mother, Terry, whose role transformed from mom to full-time caregiver and anchor. 🔊 "Sometimes love isn't enough. You have to believe in healing." – Ilana 🛑 "You can't keep apologizing for being sick. You didn't cause this." – Terry Together, they lay bare: 💚 The unspoken emotional toll Lyme takes on families 💚 The guilt and grief of losing independence 💚 The strain – and strength – in a mother-daughter bond 💚 How boundaries, belief, and brutal honesty became their survival tools 💚 Why love is essential — but not always the cure 🎧 Whether you're a chronic Lyme survivor, a caregiver, or someone trying to understand what your loved one is going through, this episode will change the way you think about healing, support, and what it means to show up — even when you feel powerless. 💬 Join the OPLAC group on Facebook (Overcoming Psychiatric Lyme and Co-Infections) for connection and support. "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" https://www.amazon.com/Love-Hope-Lyme... #LoveHopeLyme #LymeDiseaseAwareness #CaregiverSupport #MentalHealthMatters #ChronicLyme #InvisibleIllness #MotherDaughter #LymeHealing #LymeAndMentalHealth #OPLAC #StrippedDownBook #LymeSurvivor

This is episode 53 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.] Why does Lyme disease often hit women harder — physically, emotionally, and hormonally? In this powerful episode of Love, Hope, Lyme, I speak with Dr. Jaquel Patterson, a nationally-recognized naturopathic physician and author of Women and Lyme: An Integrative Guide to Better Health. Dr. Patterson shares her personal experience with Lyme, Bartonella, and Babesia, and breaks down how tick-borne illness uniquely impacts women at every life stage — from menstruation to menopause. We explore the often-dismissed symptoms, the role of hormones, psychiatric implications, and the systemic gaps in care that many women face. Whether you're a woman navigating chronic Lyme, a loved one trying to understand, or a practitioner seeking deeper insight, this episode offers knowledge, validation, and hope. 🔹 Topics covered: – The connection between hormones and Lyme symptoms – Why women are often misdiagnosed or dismissed – Psychiatric challenges like anxiety, depression, and "Lyme rage" – How to advocate for yourself or a loved one – Herbs and lifestyle strategies that can support healing – The importance of compassionate, informed care 📘 Learn more about Dr. Patterson's work and her book. 🎧 Subscribe to Love, Hope, Lyme for more episodes supporting the chronic Lyme community. #LymeDisease #WomensHealth #ChronicLyme #HormonesAndLyme #DrJaquelPatterson #LoveHopeLymePodcast #TickBorneIllness #LymeHealing

This is episode 52 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 happens when mold exposure and chronic Lyme collide? In this powerful episode of Love, Hope, Lyme, Fred Diamond sits down with Ariana Thacker, founder of MoldCo, and Dr. Scott McMahon, an expert in mold-related illness. Together, they shed light on the misunderstood connection between mold and chronic Lyme—and why so many patients are misdiagnosed, dismissed, and left to figure things out on their own. 🎙️ Key topics: 💚 The shocking overlap between mold illness and Lyme symptoms 💚 How mold triggers the innate immune system—just like Lyme 💚 Ariana's personal story of losing her health (and nearly her future) to mold 🩺 Why Dr. McMahon believes CIRS (Chronic Inflammatory Response Syndrome) and chronic Lyme are two sides of the same coin. If you've been gaslit, misdiagnosed, or told it's all in your head, this episode is for you. 👉 Learn more at https://www.moldco.com "Without the will to live or to regain your health, you just stay stuck—and it gets worse from there. MoldCo was born because I couldn't get answers from mainstream medicine. I had to figure it out on my own—just like so many others."" Ariana Thacker  🔔 Subscribe for more interviews that support Lyme survivors and the people who love them. 💬 Have you dealt with mold on top of Lyme? We see you.  #LymeDisease #MoldIllness #MoldCo #ChronicLyme #LoveHopeLyme #CIRS #ShoemakerProtocol #InvisibleIllness #MoldToxicity #LymeWarrior #MoldAwareness

This is episode 51 of the Love, Hope, Lyme podcast. To get your free e-version 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.] In this powerful episode, Fred Diamond sits down with Ashley Baker and Maria Johnson, passionate advocates from Project Lyme's Emerging Leaders Board. They share their personal journeys with chronic Lyme disease, the fight for proper recognition and treatment, and the relentless push to educate others about the realities of this misunderstood illness. Key Highlights: 🌱 Ashley Baker's Journey: From losing two jobs at 23 due to undiagnosed Lyme to being featured in the documentary I'm Not Crazy, I'm Sick, Ashley's story is a testament to resilience and the power of advocacy. 🎨 Maria Johnson's Path: Diagnosed after years of chronic symptoms, Maria discusses her battle with disbelief—from her workplace to her own doubts—and her mission to spread awareness through her design skills. 🚨 The Fight for Belief: Both advocates reveal the heartbreaking challenge of convincing others that their symptoms are real, highlighting the urgent need for education and support within the Lyme community. ✨ Hope for the Future: Discover the impact of community, the role of Project Lyme, and why Ashley's TEDx talk could be a game-changer in bringing chronic Lyme to the forefront. If you've ever felt alone in your Lyme battle or want to support someone who is, this episode is a must-listen. 👉 Don't forget to like, subscribe, and share to help spread the word!  #LymeDisease #ChronicLyme #ProjectLyme #LymeAdvocate #InvisibleIllness #LoveHopeLyme #LymeWarrior #TEDxTalk #PodcastEpisode

This is episode 50 of the Love, Hope, Lyme podcast. To get your free e-version 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.] Join host Fred Diamond as he sits down with healing expert and chronic Lyme survivor Amy Scher. In this episode, Amy opens up about her 10-year battle with chronic Lyme disease—including neurological challenges and crippling anxiety—and how she transformed her journey into a powerful healing practice using energy psychology. What You'll Discover: • The Mind-Body Connection: Learn why treating chronic illness isn't just about addressing physical symptoms but also healing deep-seated emotional trauma. • Breaking Through Trauma: Amy shares how unresolved childhood traumas and ingrained beliefs impact your health—and how releasing these burdens can unlock true healing. • Practical Energy Psychology Techniques: From the Sweep Technique to Thymus Test & Tap and Alternate Temple Tapping, get an inside look at the tools Amy created to reprogram the subconscious and calm the nervous system. • Everyday Healing Tips: Discover simple practices like slowing down your pace of life and mindful movement to signal safety to your body. • Community & Support: Find out why connecting with a positive, uplifting community can be a game changer for chronic Lyme survivors and anyone on a healing journey. About Amy Scher: Amy is not only a chronic Lyme survivor—she's an author of the bestselling "How to Heal Yourself When No One Else Can" series and the memoir "This Is How I Save My Life." Her candid storytelling and innovative healing methods have empowered hundreds of thousands to find hope, resilience, and a path to recovery. Take Action: 👉 Subscribe to the Love, Hope, Lyme Podcast for more heartfelt conversations and healing insights. 👉 Like & Share if you or someone you know can benefit from these powerful messages. 👉 Connect with Amy: Visit amybscher.com to access a free guided energy clearing and explore more resources. Remember, even when healing seems slow, it's always on its way. Open your heart, embrace hope, and join us on the journey toward wellness. #ChronicLyme #LymeDisease #EnergyPsychology #HealingJourney #TraumaRecovery #MindBodyHealing #AmyScher #LoveHopeLymePodcast

[NOTE: This podcast does not replace medical treatment. If you struggle with Lyme care, please see a Lyme Literate Medical Doctor.] 🌿 Exclusive Bonus Episode: Dr. Bill Rawls Answers Your Lyme Disease Questions! 🎙️ In this special bonus episode of Love, Hope, Lyme, host Fred Diamond sits down again with Dr. Bill Rawls to tackle pressing questions about herbs, Lyme disease treatments, and cellular health—questions that we didn't have time for in our first conversation. If you're navigating the complexities of chronic Lyme disease, this episode is packed with expert knowledge and actionable advice. Dr. Rawls tackles these questions: ❓ What are Dr. Rawls' thoughts on iv-er*n in the treatment of chronic Lyme? ❓ What we could be doing to treat Morgellons?  ❓ Mold comes up all the time. Treat mold or the Lyme/Bartonella first? What are your thoughts on treating for mold and what do you recommend? ❓ What about neuro Lyme. As you mentioned, the spirochetes are searching for somewhere to sit. I've spoken to a lot of people with neuro Lyme where the bacteria gets into the brain, or the parasites. Do herbs cross the blood-brain barrier? ❓ What herbs can safely be used while trying to conceive, during pregnancy, breastfeeding to prevent congenital transmission of Lyme and co-infections? ❓ Does he have any opinions on Methylene blue? ❓ Can he explain SOT treatment, and does he have any thoughts on it?  If you're navigating the complexities of chronic Lyme disease, this episode is packed with expert knowledge and actionable advice. 🔹 Watch now and share your thoughts in the comments! 📚 Get Dr. Rawls' book: The Cellular Wellness Solution 🎧 Listen to the full herb-focused episode at https://youtu.be/lPSEkv2n4JQ. #LymeDisease #DrBillRawls #HerbalMedicine #CellularHealth #Morgellons #ChronicLyme #LoveHopeLyme #FredDiamond #HolisticHealing #NaturalHealth

[NOTE: This podcast does not replace medical treatment. If you struggle with Lyme care, please see a Lyme Literate Medical Doctor.] What if healing from chronic Lyme disease isn't just about killing bacteria but restoring your cellular health? In this episode of Love, Hope, Lyme, host Fred Diamond sits down with Dr. Bill Rawls, author of "The Cellular Wellness Solution," to dive deep into the science behind Lyme disease, the role of stealth infections, and why understanding symptoms at the cellular level is the key to recovery. 🔬 Topics Covered: ✔️ How Lyme microbes invade and persist in the body ✔️ The link between cellular stress and chronic illness ✔️ Why conventional antibiotics may not be the best long-term solution ✔️ The power of herbal medicine for Lyme recovery ✔️ A foundational approach to healing: sleep, nutrition, stress management, and detoxification Dr. Rawls shares insights from his own Lyme journey and explains why restoring cellular function—not just targeting microbes—is essential for healing. If you or a loved one are struggling with Lyme, this episode is packed with valuable information to help you take control of your health. 🔔 Subscribe for more expert insights on Lyme disease. "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" is available on Amazon at https://www.amazon.com/Love-Hope-Lyme-Partners-Survivor-ebook/dp/B0B9Q8LX7G/. The pdf of "Love, Hope, Lyme" is always free for Lyme survivors.  Please contact Fred Diamond via Facebook Messager for your copy. 💬 Join the conversation: Share your experiences in the comments! #LymeDisease #ChronicLyme #CellularHealth #HerbalMedicine #DrBillRawls #LoveHopeLyme #HealingLyme #FredDiamond

(Note: This video does not replace proper medical treatment. If you need medical advice, please seek a Lyme literate medical professional.) In this powerful episode of Love, Hope, Lyme, we dive into the world of Lyme disease advocacy with Meghan Bradshaw and Johanne Schwartz from the Center for Lyme Action. 🦠 Meghan shares her journey from being a Lyme patient to becoming the Center's Government Relations Manager, leading grassroots advocacy efforts like the upcoming Virtual Fly-In on February 18-19, 2025. Johanne opens up about her first experience advocating on Zoom and how sharing her story has been both impactful and healing. 💪💚 It's important right now. I asked my friend Chat (on January 27, 2025), "Is Trump for or against Lyme disease federal funding?" He replied: "While these funding decisions are made by Congress, the administration's stance on broader health funding could influence future allocations. Notably, the Trump administration has proposed significant budget cuts to federal health agencies, including the NIH and CDC, which may impact research and prevention efforts related to Lyme disease."  📅 Why You Should Watch: ✅ Learn how Lyme disease patients and allies can make a difference in Congress. ☑️Hear inspiring personal stories of resilience and advocacy. ✅ Discover how the Center for Lyme Action is fighting to increase federal funding for Lyme research. 📣 Want to get involved? Whether you're a seasoned advocate or just starting, sign up for the Virtual Fly-In and join the fight against Lyme disease: centerforlymeaction.org. 🔗 Listen now and be part of the change!  #LoveHopeLyme #LymeDisease #LymeAdvocacy #VirtualFlyIn2025 #CenterForLymeAction #Podcast #TickBorneDiseases

Lyme disease can devastate military personnel and their families. In this eye-opening episode of Love, Hope, Lyme: A Lyme Disease Podcast, Fred Diamond sits down with Dr. Angel Davey to discuss the Congressionally Directed Medical Research Programs (CDMRP) and specifically the Tick-Borne Disease Research Program, its impact on the military community, and why Lyme disease is a critical issue for service members and their families. 🪖 Highlights Include: 💚 Shocking statistics: Over 7,000 service members and 63,000 family members diagnosed with tick-borne diseases from 2006 to 2022. 💚 Why military personnel are at higher risk for Lyme and other tick-borne illnesses. 💚 The vital role of advocacy in securing federal funding for research and treatment. 💚 Stories of resilience from heroes like retired Colonel Nicole Malachowski and other military personnel affected by Lyme disease. 💚 Cutting-edge research initiatives, including the MilTICK program aimed at advancing diagnostics and prevention. 🎙️ Discover how the CDMRP incorporates the voices of Lyme disease survivors and families into its research priorities and why this collaboration is essential to transforming healthcare for service members and civilians alike. 🔗 Resources Mentioned: 💚 Learn more about CDMRP's Tick-Borne Disease Research Program: https://cdmrp.health.mil. 💚 Explore MilTICK and SURE Path for tick-borne disease surveillance. 💚 Hear the inspiring story of Colonel Nicole Malachowski: [Link to previous episode]. Don't forget to like, subscribe, and hit the notification bell for more inspiring episodes of Love, Hope, Lyme. #LymeDisease #TickBorneDiseases #MilitaryHealth #LymeAwareness #ChronicLyme #LoveHopeLyme

In the most listened to Love, Hope, Lyme podcast of 2024, Fred Diamond welcomes Ali from The Tick Chicks and host of the Lyme Time Podcast. Ali shares her inspiring journey from struggling with Lyme disease to achieving healing and dedicating her life to helping others navigate their own paths. This episode focuses on six key strategies Ali used during her recovery that offer hope and practical advice for Lyme survivors and their families: 💫 Your Recovery Journey: Ali explains the role of antibiotics, the potential for Herxheimer reactions, and why it's worth trying even if you're far along in your journey. 🌟 Surrendering the Fight: Discover how letting go of the obsession with "curing" Lyme and focusing on symptom control transformed her healing process. ⭐ Alternative Healing: From herbal protocols to nerve health treatments, Ali reveals how opening her mind to non-traditional therapies made a difference. 💫 Symptom Relief: Learn how eliminating environmental triggers like humidity and focusing on clean eating helped alleviate her symptoms. 🌟 Supplementation & Detox: Ali discusses the importance of targeted supplements, vitamin IVs, and detox strategies, including infrared sauna use. ⭐ Brain Retraining: Hear about the transformative power of brain retraining to calm the nervous system, tap into the vagus nerve, and foster long-term healing. Ali also touches on her advocacy efforts, including her website, private support group, and retreats, all of which provide valuable resources to Lyme survivors and their loved ones. 👉 For more from Ali, visit The Tick Chicks or follow her on Instagram @thetickchicks. 💚 Love, Hope, Lyme is your source for authentic conversations about the challenges and triumphs of living with chronic Lyme disease. Subscribe for more inspiring stories and actionable advice. The e-book version of "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" is always free for Lyme survivors—just reach out to Fred on Facebook or LinkedIn. To purchase the print version, visit Amazon at https://www.amazon.com/Love-Hope-Lyme-Partners-Survivor-ebook/dp/B0B9Q8LX7G/  #LymeDisease #ChronicLyme #HealingJourney #TickChicks #LoveHopeLyme

This is episode 44 of the Love, Hope, Lyme podcast. [NOTE: This podcast does not promote any specific medical treatment and should not be seen as a replacement for medical advice.] 🎙️ In this powerful episode of Love, Hope, Lyme, "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" author Fred Diamond sits down with Dr. Robert Bransfield, a renowned psychiatrist and expert in Lyme-related mental health, to explore the profound psychiatric and mental health toll Lyme disease takes on its survivors. Dr. Bransfield shares decades of experience treating Lyme patients with psychiatric symptoms, shedding light on: ✅ How Lyme and co-infections impact the brain, causing depression, anxiety, and even suicidal ideation. ✅ The physiological and psychological mechanisms behind personality changes, sleep disorders, and neuroinflammation. ✅ Why understanding immune system responses is critical to managing chronic Lyme's psychiatric effects. ✅ The systemic challenges Lyme patients face, from misdiagnosis to lack of support, and how these contribute to mental health struggles. 💡 With over 500 peer-reviewed studies linking Lyme disease to psychiatric symptoms, Dr. Bransfield offers actionable insights, hope, and strategies for healing—emphasizing the need for collaborative, open-minded medical approaches. The e-book version of "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know" by Fred Diamond is always free for Lyme survivors—just reach out to Fred on Facebook or LinkedIn. To purchase the print version, visit Amazon at https://www.amazon.com/Love-Hope-Lyme-Partners-Survivor-ebook/dp/B0B9Q8LX7G/. #LymeDisease #MentalHealth #DrRobertBransfield #ChronicLyme #LoveHopeLyme

In this deeply insightful episode of Love, Hope, Lyme, host Fred Diamond dives into the transformative journey of chronic illness with Christina Kantzavelos, a therapist, chronic Lyme warrior, and advocate for holistic healing. Christina shares her personal battle with Lyme disease, her professional expertise in trauma-informed therapy, and her mission to empower others through practical, evidence-based tools. She explains the importance of nervous system regulation, trauma healing, and the mind-body connection in overcoming chronic illness. Topics include: The role of medical trauma and how to rebuild trust in the healing journey. Groundbreaking therapies like EMDR and Constructed Awareness. Practical mindfulness techniques, from breathwork to tapping, that calm the nervous system. The impact of chronic illness on relationships and how to navigate challenges with compassion and understanding. Whether you're a chronic Lyme survivor, a caregiver, or someone looking for hope and actionable insights, this episode will leave you inspired and equipped to take the next step in your healing journey. Resources Mentioned: 👉 Visit Christina Kantzavelos' website for free resources and tools. Begin Within Today: Mental Wellness and Chronic Illness Therapy The e-book version of Love, Hope, Lyme is always free for Lyme survivors—just reach out to Fred on Facebook or LinkedIn. To purchase the print version, visit Amazon at https://www.amazon.com/Love-Hope-Lyme-Partners-Survivor-ebook/dp/B0B9Q8LX7G/.

This is episode 42 of the Love, Hope, Lyme Podcast. Note: This podcast does not promote specific medical treatments and is not a substitute for medical advice. In this deeply moving episode of Love, Hope, Lyme, host Fred Diamond welcomes Dr. Jennifer Gardella, author of Listen for the Whispers of Abuse. Together, they explore the powerful intersection of trauma, chronic Lyme disease, and surviving domestic violence. Dr. Gardella shares her courageous journey of escaping abuse, rebuilding her life, and helping others recognize and address the patterns of trauma that impact survivors of both domestic violence and chronic illnesses like Lyme disease. Key Topics Covered: ✅ The link between unresolved trauma and the challenges of chronic illness recovery ✅ Dr. Gardella's healing journey, including crisis counseling, trauma therapy, and EMDR ✅ Similarities between survivors of Lyme disease and domestic violence, from disbelief to retraumatization ✅ Practical advice for finding healing, support, and hope for survivors and their loved ones ✅ The essential role of community in overcoming trauma, and why "It's not your fault" ✨ "We don't out-trauma each other, but we can support each other." — Dr. Jennifer Gardella Whether you're managing a chronic illness, supporting a loved one, or navigating personal trauma, this episode offers hope, understanding, and actionable insights. 💚 📖 Learn more about Dr. Gardella's work in Listen for the Whispers of Abuse. 🎧 Explore more episodes of Love, Hope, Lyme for conversations with leading experts and advocates. 🔔 Don't forget to like, comment, and subscribe for updates on new episodes. Share this episode with someone who needs it! 💚 The e-book version of Love, Hope, Lyme is always free for Lyme survivors—reach out to Fred on Facebook or LinkedIn. To purchase the print version, visit Amazon. #ChronicLyme #TraumaHealing #DomesticViolenceSurvivor #Podcast #LymeDiseaseWarrior

This is episode 41 of the Love, Hope, Lyme podcast. [NOTE: This podcast does not promote any specific medical treatment and should not be seen as a replacement for medical advice.] In today's episode, Fred Diamond sits down with Rabbi Melinda Bernstein, a resilient Lyme survivor and practicing rabbi. Together, they explore the profound challenges and spiritual questions that arise when battling chronic Lyme disease and its relentless coinfections. Rabbi Melinda offers unique insights on connecting with a higher power during this struggle, sharing how maintaining faith can open doors to healing and offer a sense of purpose amid the journey. Through her own experiences, Rabbi Melinda reveals how faith can be both tested and strengthened by Lyme disease, providing hope to those on a tumultuous path to recovery. When researching his widely acclaimed book, "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know," Fred encountered many Lyme survivors and caregivers grappling with their faith. Some found comfort and commitment in their beliefs, while others experienced doubt. Even Fred faced a crisis of faith after a deeply personal loss, making this discussion particularly close to his heart. In Love, Hope, Lyme, Fred provides family members and friends with practical advice to support their loved ones battling chronic Lyme. For Lyme survivors, the book offers guidance on how to ask for support and cultivate resilience in relationships. If you or someone you love is affected by Lyme disease, this conversation is for you. Gain insights on finding strength, holding onto hope, and reconnecting with spirituality in the face of illness. You can schedule a meeting with Rabbi Melinda at https://calendly.com/melinda-bernstein/15min?month=2024-11 or visit her website at https://melindabernstein.com/about/. The e-book version of Love, Hope, Lyme is always free for Lyme survivors—just reach out to Fred on Facebook or LinkedIn. To purchase the print version, visit Amazon at https://www.amazon.com/Love-Hope-Lyme-Partners-Survivor-ebook/dp/B0B9Q8LX7G/.

This is episode 40 of the Love, Hope, Lyme podcast. [NOTE: This podcast does not promote any specific medical treatment and should not be seen as a replacement for medical advice.] On today's episode, Fred brings on Sami Kirschbaum of the Lyme Resilience Collective to discuss brain spotting and other ways to deal with the trauma that often comes with chronic disease. They discuss how to handle shame and grief that often come with the loss. Sami took Fred through a brain spotting session and they discuss how it might work for you.  When Fred was doing the research for his popular book "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know," he was ignorant of the sometimes perpetual traumas that chronic Lyme survivors might face throughout their healing journey. Many survivors have lost relationships, livelihoods, and joy. But, healing from the trauma is possible. 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 disease ideas and tips to support this beloved person. It also helps Lyme survivors know how to ask for support. If someone you love has been afflicted with Lyme disease, watch this podcast now. If you have Lyme disease, listen for ways to get the support you need. 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 39 of the Love, Hope, Lyme podcast. [NOTE: This podcast does not promote any specific medical treatment and should not be seen as a replacement for medical advice.] 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 disease ideas and tips to support this beloved person. It also helps Lyme survivors know how to ask for support. On today's episode, he discusses how to ensure you find the best doctor if you have chronic Lyme disease with ILADS president Dr. Amy Offutt. Lyme disease can be a complex and often misunderstood illness. For those dealing with it, finding a knowledgeable and compassionate doctor can be crucial to healing optimally. On today's Love, Hope, Lyme podcast, Dr. Amy Offutt, current president of the International Lyme and Associated Diseases Society (ILADS), has spent her career educating doctors and treating patients with chronic Lyme disease. In this podcast, we explore her ideas for Lyme disease survivors on finding the right medical doctor. When Fred was doing the research for his popular book "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know," he did not know there were challenges educating medical professionals to treat and care for Lyme disease survivors. If someone you love has been afflicted with Lyme disease, watch this podcast now. If you have Lyme disease, listen for ways to get the support you need. 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 38 of the Love, Hope, Lyme podcast. [NOTE: This podcast does not promote any specific medical treatment and should not be seen as a replacement for medical advice.] 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 disease ideas and tips to support this beloved person. It also helps Lyme survivors know how to ask for support. On today's episode, he catches up with Lyme survivor and advocate Olivia Goodreau from the LivLyme Foundation. They discuss how she created the foundation when SHE WAS 12 years old. They also discuss her advocacy and recovery journey that she shared in her book "But She Looks Fine." Olivia discussed her journey of meeting with dozens of doctors until she received the proper treatment to recover from Lyme disease and its coinfections. Now a college student at UCLA, she also talked about her new Tick Tracker app and how it can help people stay clear of ticks. When Fred was doing the research for his popular book "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know," he didn't know how Lyme disease affected children and teenagers and the struggle they face in recovery. Olivia's story is unique and an example of how Lyme disease survivors need to be their own advocates and can also help thousands of other find peace. If someone you love has been afflicted with Lyme disease, watch this podcast now. If you have Lyme disease, listen for ways to get the support you need. 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 37 of the Love, Hope, Lyme podcast. [NOTE: This podcast does not promote any specific medical treatment and should not be seen as a replacement for medical advice.] 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 disease ideas and tips to support this beloved person. It also helps Lyme survivors know how to ask for support. On today's episode, we discuss Alpha Gal Syndrome, a tick-borne disease that caused red meat allergies, Lyme testing updates, and new treatments in the works. His guests are Global Lyme Alliance CEO Laura MacNeill and then GLA Chief Scientific Officer Tim Sellati. They discuss the work GLA is doing to develop better diagnostics, tests and treatment for tick-borne diseases including Lyme and the coinfections Bartonella and Babesiosis. They discussed work they are funding with Dr. Brandon Jutras at Northwestern University and other research projects in the Lyme and chronic illness world. When Fred was doing the research for his popular book "Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know," he was ignorant about the work happening at universities to find better diagnostics, treatment, and mental health solutions for the millions of chronic Lyme disease survivors around the globe. If someone you love has been afflicted with Lyme disease, watch this podcast now. If you have Lyme disease, listen for ways to get the support you need. 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 36 of the Love, Hope, Lyme podcast. [NOTE: This podcast does not promote any specific medical treatment and should not be seen as a replacement for professional medical advice.] Fred Diamond's internationally acclaimed 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 episode, Fred interviews Michelle McKinzie, a licensed integrative therapist with specialized training in integrative medicine for mental health professionals. She supports professional women grappling with chronic Lyme disease to help them manage the overwhelming stress, isolation, and challenges that come with the disease so they can confidently advocate for themselves, boost their energy, and effectively navigate their medical treatments. Fred said that after speaking or messaging thousands of chronic Lyme survivors, he learned that maintaining life balance could be very difficult. He addresses this in his book and delves deep on this topic with his guest. If someone you love has been afflicted with Lyme disease, watch this podcast now. If you have Lyme disease, listen for ways to get the support you need. 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 35 of the Love, Hope, Lyme podcast. Fred Diamond's internationally-acclaimed 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 episode, Fred interviews Dr. Mo Elamir from the Aviv Clinic to discuss hyperbaric oxygen therapy for chronic Lyme disease. According to the Aviv Clinic, Hyperbaric oxygen therapy (HBOT) is a medical treatment that involves breathing 100% pure oxygen in a pressurized HBOT suite (often called a hyperbaric oxygen chamber). This process increases oxygen levels in the body 10–15 times higher than normal, and has been long-proven to speed up the body's healing and rejuvenation abilities. After speaking or messaging with thousands of chronic Lyme survivors, Fred realized how many were desperate to seek medical or alternative treatments that would ease the horrific symptoms that they would experience. HBOT is one that has come up ofter and on this show, he goes deep with Dr. Mo to understand how it may help. If someone you love has been afflicted with Lyme disease, watch this podcast now. If you have Lyme disease, listen for ways to get the support you need. 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 34 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 episode, Fred interviews Dr. Neil Nathan to discuss his new book "The Sensitive Patient's Healing Guide: Top Experts Offer New Insights and Treatments for Environmental Toxins, Lyme Disease, and Emfs." When Fred was first discovering the trauma related to tick-borne diseases, one of the first books he read was Dr. Nathan's classic "Toxic: Heal Your Body from Mold Toxicity, Lyme Disease, Multiple Chemical Sensitivities, and Chronic Environmental Illness." It helped him understand how difficult mold allergies can be to treat and how much interplay there is with Lyme disease. Dr. Nathan discussed many of the complications sensitive patients go through in finding treatments to get healthy. Fred digs deep so that Lyme survivors can find some peace and suggestions on how to get treatment, and, as he always does, how those who love and want to support someone they love with Lyme disease can support them. If someone you love has been afflicted with Lyme disease, watch this podcast now. If you have Lyme disease, listen for ways to get the support you need. 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 33 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 episode, Fred interviews patient-centered healthcare advocate Bruce Alan Fries. It's incredible that Lyme and other tick-borne diseases have political implications. For scores, entities such as the CDC and the Infectious Diseases Society of America (IDSA) refused to acknowledge that chronic Lyme disease even existed and recommended minimal treatment protocols that, in many cases, did not even come close to treating the diseases. Bruce discussed some of the political initiatives he created or participated in to bring more government awareness of these troubling diseases. If someone you love has been afflicted with Lyme disease, watch this podcast now. If you have Lyme disease, listen for ways to get the support you need. 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://a.co/d/ifi9Wne.

This is episode 32 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 episode, Fred interviews Dr. Krzysztof (Chris) Majdyło of the St. Luke's Center in Gdańsk, Poland on the challenges of treating tick-borne illness patients across Europe. He discusses what Lyme looks like in Europe and offers some strategies on treatment he provides at his medical facility. Lyme disease and its co-infections are challenging to treat anywhere around the globe. He gives his perspective on what Lyme survivors might want to consider. He also discusses why he has committed his practice to tick-borne diseases. If someone you love has been afflicted with Lyme disease, watch this podcast now. If you have Lyme disease, listen for ways to get the support you need. 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/.