Love, Hope, Lyme Podcast
When Fred Diamond decided to learn more about the Lyme disease that afflicted someone he loved, his life changed. He read every book on Lyme, joined Facebook groups, attended webinars and podcasts and quickly realized that he knew hardly anything about what Lyme disease survivors go through on a daily basis. His 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 Lyme ideas and tips to support this beloved person. This podcast supports the lessons learned in the book. The book features a foreword by the top Lyme doctor on the planet, Dr. Richard Horowitz. If someone you love has been afflicted with Lyme disease epidemic, listen to this podcast now.
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RFK Jr. Lyme Roundtable Follow Up from Lyme Disease Advocates
12/22/2025
RFK Jr. Lyme Roundtable Follow Up from Lyme Disease Advocates
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.
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TiCK MiTT Founder Olivia Abrams Uses Entrepreneurship to Advance Lyme Advocacy
12/15/2025
TiCK MiTT Founder Olivia Abrams Uses Entrepreneurship to Advance Lyme Advocacy
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: 💚 The e-version of "Love, Hope, Lyme" is always free for Lyme survivors.
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Uncovering the Root Cause of Your Stalled Chronic Illness Recovery with Dr. Melanie Stein
12/02/2025
Uncovering the Root Cause of Your Stalled Chronic Illness Recovery with Dr. Melanie Stein
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.
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Breaking Down Jesse Ruben’s Monster and the Truth Lyme Survivors Know
11/17/2025
Breaking Down Jesse Ruben’s Monster and the Truth Lyme Survivors Know
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.
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What It Means to Be a Lyme Warrior with Lauren Lovejoy
11/03/2025
What It Means to Be a Lyme Warrior with Lauren Lovejoy
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
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The We Don't Have Lyme Here Myth Dr. Korine Kolivras is Disproving
10/20/2025
The We Don't Have Lyme Here Myth Dr. Korine Kolivras is Disproving
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
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How Professional Skier Athena Brownson Found Purpose Through the Challenges of Lyme Disease
10/06/2025
How Professional Skier Athena Brownson Found Purpose Through the Challenges of Lyme Disease
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
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Lyme Survivors Find Hope in the NASEM Report with Nicole Malachowski and Kent Kester
09/22/2025
Lyme Survivors Find Hope in the NASEM Report with Nicole Malachowski and Kent Kester
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
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How a Mentor Can Help Lyme Survivors!
09/07/2025
How a Mentor Can Help Lyme Survivors!
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
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Surprising Facts About Lyme, Alzheimer's and Dementia
08/24/2025
Surprising Facts About Lyme, Alzheimer's and Dementia
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: 📖 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
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Lyme, the Brain and Maintaining Important Relationships with Dr. Chris Winfrey
08/10/2025
Lyme, the Brain and Maintaining Important Relationships with Dr. Chris Winfrey
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
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How Lyme Survivors Can Get Their Energy Back with Greg Lee
07/29/2025
How Lyme Survivors Can Get Their Energy Back with Greg Lee
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": 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
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How Mary Lyn Hammer Became a Medical Detective to Heal from Chronic Lyme
07/14/2025
How Mary Lyn Hammer Became a Medical Detective to Heal from Chronic Lyme
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
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Don't Give Up Before the Lyme Disease Miracle Occurs Says Ali Moresco
06/30/2025
Don't Give Up Before the Lyme Disease Miracle Occurs Says Ali Moresco
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
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Understanding Lyme Rage and Its Impact on the Brain with Dr. Darin Ingels
06/16/2025
Understanding Lyme Rage and Its Impact on the Brain with Dr. Darin Ingels
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: 📖 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.
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Why Lyme Patients Struggle to Get Help: Dr. Monica Embers & Kevin Williams from Ravel Health Explain
06/02/2025
Why Lyme Patients Struggle to Get Help: Dr. Monica Embers & Kevin Williams from Ravel Health Explain
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
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When Love Endures Lyme and Trauma with David and Jacquie Butler
05/20/2025
When Love Endures Lyme and Trauma with David and Jacquie Butler
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
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How to Heal from Chronic Lyme: Dr. Myriah Hinchey’s 10-Step Framework
05/05/2025
How to Heal from Chronic Lyme: Dr. Myriah Hinchey’s 10-Step Framework
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
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The Strain of Lyme: A Mother-Daughter Journey to Healing
04/21/2025
The Strain of Lyme: A Mother-Daughter Journey to Healing
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
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What Makes Lyme So Complex for Women’s Physical and Mental Health with Dr. Jaquel Patterson
04/07/2025
What Makes Lyme So Complex for Women’s Physical and Mental Health with Dr. Jaquel Patterson
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
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Mold and Lyme: A Hidden Health Crisis - Insights from MoldCo's Ariana Thacker and Dr. Scott McMahon
03/24/2025
Mold and Lyme: A Hidden Health Crisis - Insights from MoldCo's Ariana Thacker and Dr. Scott McMahon
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 “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.
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Turning Pain into Purpose: How Project Lyme's Emerging Leaders Fight for Survival and Hope
03/10/2025
Turning Pain into Purpose: How Project Lyme's Emerging Leaders Fight for Survival and Hope
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!
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The Key to Healing: Amy Scher on Chronic Lyme, Trauma, and the Mind-Body Connection
02/24/2025
The Key to Healing: Amy Scher on Chronic Lyme, Trauma, and the Mind-Body Connection
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.
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Lyme Disease Care, Herbs, and Other Tick-Borne Disease Questions Answered by Dr. Bill Rawls
02/11/2025
Lyme Disease Care, Herbs, and Other Tick-Borne Disease Questions Answered by Dr. Bill Rawls
[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 . #LymeDisease #DrBillRawls #HerbalMedicine #CellularHealth #Morgellons #ChronicLyme #LoveHopeLyme #FredDiamond #HolisticHealing #NaturalHealth
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Healing Chronic Lyme at the Cellular Level: Dr. Bill Rawls on Herbs, Microbes, and Wellness
02/10/2025
Healing Chronic Lyme at the Cellular Level: Dr. Bill Rawls on Herbs, Microbes, and Wellness
[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 . 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
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From Lyme Patients to Advocates: The Journey to Driving Change for Lyme Disease Funding
01/27/2025
From Lyme Patients to Advocates: The Journey to Driving Change for Lyme Disease Funding
(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
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How Lyme Disease Affects Military Personnel and their Families with Dr. Angel Davey
01/13/2025
How Lyme Disease Affects Military Personnel and their Families with Dr. Angel Davey
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
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6 Keys to Lyme Disease Recovery: Insights from The Tick Chicks
12/30/2024
6 Keys to Lyme Disease Recovery: Insights from The Tick Chicks
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 #LymeDisease #ChronicLyme #HealingJourney #TickChicks #LoveHopeLyme
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Lyme Disease Psychiatric and Mental Health Toll Insights from Dr. Robert Bransfield
12/16/2024
Lyme Disease Psychiatric and Mental Health Toll Insights from Dr. Robert Bransfield
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 . #LymeDisease #MentalHealth #DrRobertBransfield #ChronicLyme #LoveHopeLyme
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From Trauma to Triumph: Healing Chronic Lyme Disease with Christina Kantzavelos
12/02/2024
From Trauma to Triumph: Healing Chronic Lyme Disease with Christina Kantzavelos
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. 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/.
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