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Leading Irish neuroimmunologist Prof. Denise Fitzgerald has been awarded €6.26 million Research Professorship funding from Research Ireland to investigate ways that ageing affects how the immune system helps repair brain tissue in illnesses such as Multiple Sclerosis (MS). The funding means that over the next five years, Prof. Fitzgerald – who has, until now, been based exclusively in Queen's University Belfast – will lead a research team of ten based in Trinity College Dublin and partnering with FutureNeuro Research Ireland Centre for Translational Brain Science, St James's Hospital and Beaumont Hospital to discover why our immune cells become less able to coax brain stem cells to repair damage as we age. This research combines immunology, neuroscience and regenerative biology to tackle this complex problem. Prof. Fitzgerald said: "This ambitious programme of research will uncover new insights into fundamental changes in the older immune system that has a knock-on effect on brain repair. This new knowledge can then be used to develop pioneering regenerative treatment for MS and other neurological conditions. To speed this up, we are embedding research into new clinical trials led by consultant neurologist, Hugh Kearney. "This will increase the opportunities for people with MS in Ireland to access experimental treatments early, as well as to co-produce research with us as key public members of the research programme. Through this neuroimmunology research programme we will train the next generation of scientists, doctors and health professionals, side-by-side, in partnership with the public." Commenting on the announcement, Dr Diarmuid O'Brien, CEO of Research Ireland commented: "Research Ireland is pleased to support Prof. Fitzgerald's critically important work over the next five years, with the investment facilitating an additional 11 research positions, comprising postdocs, PhDs, research assistants and senior research fellows. Funding excellent research talent is a key part of our recently launched strategy, as is addressing Ireland's opportunities and challenges in areas such as public health. I look forward to seeing the outputs and impact of Prof. Fitzgerald's endeavours over the coming years." Through this appointment, Prof. Fitzgerald will divide her role between Trinity College Dublin and Queen's University Belfast, promoting all-island collaboration across neuroimmunology and other research areas. She will be an investigator at FutureNeuro, the RCSI-based Research Ireland Centre that aims to translate breakthroughs in understanding of brain structure and function to transform the patient journey for people with neurological diseases. She also brings extensive international collaboration with world-leading experts at Cambridge University, University College London, the University of Toronto, the Institute of Neuroscience – Alicante, the Wellcome Sanger Institute and Maynooth University. Prof. Colin Doherty, head of the School of Medicine in Trinity and a Principal Investigator with FutureNeuro said: "I have known Denise for some time and have marvelled at the quality of her research into one of the great and challenging areas of medical science. We are delighted that she will be leading a team here in Trinity while retaining her links with Queen's, strengthening all-island collaboration in neuroimmunology and creating exciting new opportunities across the wider FutureNeuro research network." See more stories here. Irish Tech News are Ireland's No. 1 Online Tech Publication and often Ireland's No.1 Tech Podcast too. You can find hundreds of fantastic previous episodes and subscribe using whatever platform you like via our Anchor.fm page here: https://anchor.fm/irish-tech-news If you'd like to be featured in an upcoming Podcast email us at Simon@IrishTechNews.ie now to discuss. Irish Tech News have a range of services available to help promote your business. Why not drop us a line at Info@IrishTechNews.ie now to find...
In this episode, Aimee sits down with Jonah Platt, actor, musician, and host of The Being Jewish Podcast. Aimee first reflects on the milestone of 200 episodes and impact of IWSTHAB on the Jewish community, before pivoting to Jonah's personal story. Jonah Platt discusses the complexities of navigating health, faith, and the public eye while trying to grow a family. This conversation is a vulnerable exploration of how chronic health challenges reshape the path to parenthood. Jonah Platt opens up about his upbringing in a musical household and his transition into fatherhood alongside his wife, Courtney, who lives with Multiple Sclerosis (MS). He describes the reality of MS—the extreme fatigue and the medical necessity for Courtney to stop life-altering medications in order to conceive and breastfeed. In discussing the lack of awareness around these specific hurdles, Jonah notes, "I think we don't talk about this story that much because her issue isn't fertility." This challenge led the couple through three distinct reproductive journeys: a natural pregnancy, IVF, and surrogacy. Jonah shares the emotional weight of supporting his partner through a taxing fertility journey and the gift of surrogacy, which allowed Courtney to be fully present for their daughter's birth. Through his story, Jonah highlights the importance of choosing a path that preserves the health of the mother while expanding options for building families. If you are navigating the difficult intersection of chronic illness and family building, this episode offers a compassionate and grounded perspective. You're not alone. More about Jonah Platt: Jonah Platt is one of America's most trusted voices on modern Jewish identity, culture, and current events. He hosts Being Jewish with Jonah Platt—the world's #1 Jewish podcast—exploring Jewish life through conversations with prominent Jews and allies like Jason Alexander, Congressman Ritchie Torres, Bernard-Henry Lèvy, Cindy Crawford, and Sheryl Sandberg. An accomplished entertainer, Jonah has starred in acclaimed projects from Broadway (Wicked) to Hollywood (Being the Ricardos), is co-writing the musical adaptation of The Giver, and producing his first feature film, The Mensch. He was honored with California's inaugural Community Excellence Award for Combating Antisemitism, Holocaust Museum LA's inaugural Roz & Abner Goldstine Advocacy Award, the 2025 American Friends of ELEM LifeSaver Award, and is currently pursuing his Master's in Antisemitism Studies at Gratz College. Connect with Jonah Platt: Website Email Instagram Facebook Threads TikTok X LinkedIn Listen to the Being Jewish with Jonah Platt: Beingjewishpodcast.com Instagram Facebook TikTok YouTube LinkedIn Aimee's Favorite Episodes: 1-Seen and Remembered: Making Space for Everyone This High Holiday Season with Rabbi Yisrael Motzen I kept nodding through this episode with Rabbi Motzen because I agreed with everything he said. As a rabbi at a large synagogue with many different kinds of family units, he has developed many unique ways to make sure everyone fits in... I loved all of its suggestions and thought they were so applicable to people in the fertility community too. 2- Finding Calm in the Chaos with Dr. Aliza Ancier Mindfulness is something anyone can use to get through stressful situations, but I had never really given it much thought until this conversation with Aliza. It's amazing how something so simple can really help. 3- Making Mikvah Meaningful with Dr. Naomi Grumet Mikvah is one of the hardest mitzvos to keep when you're struggling to have a baby. I hated every single time I went. The suggestions here were personally life-changing and helped me reframe mikvah. 4- A Decision I Never Imagined: An Anonymous TFMR Story This was the first episode we did on TFMR, and I remember being so nervous before it came out. Not because I was worried that we were doing anything wrong by sharing this incredible story, but more because I was concerned about backlash. And the amazing thing is - TFMR stories are some of the most listened to in our 200 episodes. Because people don't walk these stories openly, it's a huge gift to offer those dealing with this personally the knowledge that they are not alone. 5- Tokophobia with Yehudit Kosowsky Even as a doctor, I had never heard of tokophobia before, but I have had dozens of people/year message me that they are so grateful this episode exists. Connect with us: Website Instagram - send us a message YouTube Facebook TikTok LinkedIn
Right now, nearly 38,000 Australians are living with Multiple Sclerosis (MS), however, fewer than one in three Australians have heard of MS, and among those who have, most still don't believe people living with it can lead active, happy lives. But the modern reality can look very different.Nine in 10 Australians with the most common form of MS, relapsing-remitting MS, say they feel positive about their future. With the right support and access to modern treatments, 92% say they can live life fully. They just need the rest of us to catch up.So where did this gap come from, and why hasn't it caught up with us yet? We'll take you through the findings from the research in today's deep dive.Watch Emma's interview with Meg Maskell here.TDA team note: Today’s episode is proudly supported by Novartis, with expert input from MS Australia. As always, TDA has independently written and produced all editorial content for this podcast without commercial influence.Hosts: Emma Gillespie and Billi FitzSimonsGuests: Meg Maskell and Dr Tennille Luker, Head of Research at MS Australia.Producer: Rosa Bowden To find out more visit msaustralia.org.au.Findings from MS My Way Survey, Novartis, Australia, 2025. Data on file. AU-30416 | April 2026. Want to support The Daily Aus? That's so kind! The best way to do that is to click ‘follow’ on Spotify or Apple and to leave us a five-star review. We would be so grateful. The Daily Aus is a media company focused on delivering accessible and digestible news to young people. We are completely independent. Want more from TDA?Subscribe to The Daily Aus newsletterSubscribe to The Daily Aus’ YouTube Channel Have feedback for us?We’re always looking for new ways to improve what we do. If you’ve got feedback, we’re all ears. Tell us here.See omnystudio.com/listener for privacy information.
The image of a "gardener" isn't just a retired person in a sun hat with a perfectly manicured rose bush. Gardening is for the dreamers, the hustlers, and yes, even those of us living with chronic illness or physical limitations.We were recently moved by a story from a woman living with Multiple Sclerosis (MS) who decided that her diagnosis wasn't going to keep her from her backyard dreams. Instead of giving up, she adapted. Gardening doesn't demand perfection; it demands presence.CONNECT WITH US Show Notes | www.goldenacre.ca/podcast Instagram | thehelpfulgardenerspod Leave us a Voice Note: www.goldenacre.ca/podcast SPONSORED BY GOLDEN ACRE HOME & GARDEN Golden Acre Home & Garden is open 362 a year for all your home and garden needs. Head online or visit us in store in Calgary, AB. www.goldenacre.ca CREDITS Hosted by: Brandi Warren & Colin Hayles Voiceover by: Kaelan Shimp Music by: Forestmusic
What should a neurologist do when a routine MRI for migraine reveals incidental white matter lesions that look remarkably like Multiple Sclerosis (MS), despite the patient having no neurological symptoms? The Editors' Choice paper for the April 2026 issue of Practical Neurology is a practical guide to the clinical diagnosis and management of radiologically isolated syndrome (RIS). Author Dr. Audrey Reynolds¹ joins PN podcast editor Dr. Amy Ross Russell to discuss her work on how updated diagnostic criteria and advanced imaging markers now enable a more proactive, biological approach to the disease. Their discussion highlights the importance of risk stratification - using tools like CSF analysis and spinal imaging - to identify those most likely to benefit from early intervention with disease-modifying therapies. They also examine the delicate balance between preventing future disability and avoiding misdiagnosis in this rapidly evolving area of neurology. Read the paper: Radiologically isolated syndrome: a practical guide. (1) St Vincent's University Hospital, Dublin; University College Dublin, Ireland Please subscribe to the Practical Neurology podcast on your favourite platform to get the latest episodes. If you enjoy our podcast, you can leave us a review or a comment on Apple Podcasts (https://apple.co/3vVPClm) or Spotify (https://spoti.fi/4baxjsQ). We'd love to hear your feedback on social media - @PracticalNeurol. This episode was hosted by PN's podcast editor Dr. Amy Ross Russell. Production by Amy Ross Russell and Brian O'Toole. Editing by Brian O'Toole. Thank you for listening.
In this episode of Dishing Up Nutrition, dietitians Melanie Beasley and Brandy Buro discuss multiple sclerosis (MS) and the role of nutrition in supporting brain health and managing symptoms. Learn how inflammation, blood sugar balance, and nutrient deficiencies can impact MS, and discover how simple, practical diet strategies and real-food nutrition may help support the nervous system. If you or a loved one is navigating MS, this episode offers supportive, nutrition-focused guidance.
In this episode of Dishing Up Nutrition, dietitians Melanie Beasley and Brandy Buro discuss multiple sclerosis (MS) and the role of nutrition in supporting brain health and managing symptoms. Learn how inflammation, blood sugar balance, and nutrient deficiencies can impact MS, and discover how simple, practical diet strategies and real-food nutrition may help support the nervous system. If you or a loved one is navigating MS, this episode offers supportive, nutrition-focused guidance.
Laura bravely shares the story that has shaped her life in so many ways. Psoriasis, endometriosis, and multiple hospitalizations with a layer of MTHFR gene mutation underneath. Watch to see how Laura has mastered her own health, her own path, and her journey forward for herself and her family.00:00 - Intro00:39 - Laura's story - psoriasis, psoriatic arthritis, and more.01:44 - Stage 4 endometriosis02:46 - Fertility03:15 - First episode of Multiple Sclerosis (MS)04:35 - Crippling fatigue05:38 - Finding a functional doctor07:42 - MTHFR and folic acid08:52 - Heavy metal detox09:55 - Laura and Dr. Amy are twinning!11:09 - High-dose vitamin D12:54 - Learning to trust your body14:26 - Laura's kids17:12 - Vitamins should be healthy, but...18:19 - The impact of accidentally eating fortified foods18:51 - How MTHFR is like the Bin Man20:02 - The decision to support her immune system instead of suppressing it21:38 - Psoriasis symptoms as a gauge of health25:06 - Medicine is still not good with women's hormones25:52 - Advocating for yourself in medicine29:00 - If I'd known about MTHFR earlier33:04 - Laura's Podcast: The Understanding You PodcastThanks so much for watching! I have so many other resources for you. Here is the full-length version of this interview on YouTube: https://youtu.be/28NcHb2twF0Check out the website for lots of FREE stuff:WEBSITE: https://tohealthwiththat.com/ Order Dr. Amy's book MTHFR Easy: Get Healthy For Life: https://amzn.to/47tT31YPaperback and audiobook versions are coming soon.This story was shared graciously and generously with permission to post on the podcast, Youtube, and in print if that happens in the future.
In this episode of A Couple Takes on MS, we welcome Brian Wallace, a former University of Michigan offensive lineman who helped lead the Wolverines to four Big Ten championships and three Rose Bowl appearances. Diagnosed with Multiple Sclerosis (MS) in 1997 at age 27, Brian has spent nearly three decades navigating life with MS while continuing to move forward. Today, Brian hosts the MS Michigan Man 64 Podcast, where he shares honest conversations about life with chronic illness and the mindset it takes to keep going. Brian joins us to talk about football, life after diagnosis, the mental challenges of chronic illness, and why community and conversation matter so much in the MS world. In this episode, we talk with Brian about: His journey from Michigan football to living with MS How a competitive mindset helped shape his approach to the disease How isolation can affect people living with chronic illness and the importance of community Why he started the MS Michigan Man 64 Podcast to focus on positive, honest conversations about life with MS The emotional and mental health challenges of living with Multiple Sclerosis Why building community and sharing stories matters 👉 You can explore Brian's podcast here: MS Michigan Man 64 Podcast From our blog Reflecting on the conversation with Brian, Jennifer recently revisited an essay she wrote about the Michigan football game she missed shortly after her MS diagnosis and the lesson it taught her about living with Multiple Sclerosis without regrets. 👉 Read the essay here: The biggest Michigan game I missed and the lesson MS taught me *** Remember to rate, review, and subscribe to A Couple Takes on MS Podcast for two insightful perspectives on this one multifaceted disease.
On this episode of the Ramp. It. Up! Podcast we are observing Multiple Sclerosis (MS) Awareness Month. MS is a chronic neurological disease where the immune system attacks the central nervous system (brain, spinal cord, and optic nerves), causing symptoms like fatigue, vision loss, pain, and mobility issues.The month of March is set aside to raise awareness, promote early diagnosis, and support funding to find a cure. Our Guest for this episode of the podcast is Regina Beach, an author, an adventurer, a fellow performer of the From Where I Sit project, and a person living with MS. Regina shares about her life, her work in the arts, navigating living with MS, and how to keep things sexy with your partner, even with a disability. Ramp. It. Up!Get to Know Our GuestRegina Beach is a disabled poet and essayist. Originally from the American Midwest, she now calls the U.K. home. She is a freelance writer and editor passionate about accessibility in the arts. She is the founder of the literary magazine Lesions | Art + Words, featuring the work of creators living with chronic conditions. She hosts Writers' Hour and is the editor of the London Writers' Salon's Writing in Community anthology. She facilitates creativity workshops for the MS-UK charity and is the producer of the Living Well with MS podcast. Instagram: https://www.instagram.com/reginabeach_creativewellbeing Facebook: http://facebook.com/ReginaBeachCreativeWellbeing/ Substack: http://reginagbeach.substack.com/ Website: http://www.reginagbeach.com/ Click the links below to watch the From Where I Sit performance presented by UAB:https://www.youtube.com/watch?v=JfCYWhId-48https://www.youtube.com/watch?v=DvBSsiIQODQClick the link below to watch the From Where I Sit documentary directed by Ingrid Pfau:https://www.youtube.com/watch?v=6M3qmd4WoPgStay Connected to the PodcastInstagram: https://www.instagram.com/ramp.it.up.podcast/Facebook: https://www.facebook.com/ZoeOnWheelz/YouTube: https://www.youtube.com/channel/UCZAnH8I6sGEf7SJ9OKw8dEAEmail: rampituppodcast@gmail.comWe want to hear from you!Support the show
Multiple Sclerosis (MS) remains the leading cause of non-traumatic disability in adults aged 18–65. Because of its prevalence and the vital role of therapy in management, it is a clinical area we return to often at OT Potential.We previously explored this topic through the inspiring lens of Dr. Sarah Adam, OTD, OTR/L—a professor and Paralympic medalist living with MS. In this upcoming one-hour course, we continue the conversation by diving into the latest evidence-based research through the lens of an outpatient neurological specialist.Joining us is Makeda N. Jackson, OTD, OTR/L, MSCS, a Multiple Sclerosis Certified Specialist. Dr. Jackson will share her expert perspective on the clinical logistics of MS care, focusing on:Evidence-Based AssessmentTargeted InterventionPatient Education/ CoachingYou will walk away with practical, actionable knowledge. Plus, we are assembling a treatment guide for you to reference—synthesizing insights from this and our past conversations on MS—to help you provide the highest level of care.See full course details here:https://otpotential.com/ceu-podcast-courses/ot-and-multiple-sclerosis-treatmentSee all OT CEU courses here:https://otpotential.com/ceu-podcast-coursesCheck our our live webinar schedule here:https://otpotential.com/live-ot-ceu-webinarsSupport the show by using the OTPOTENTIAL Medbridge Code:https://otpotential.com/blog/promo-code-for-medbridgeTry 2 free OT Potential courses here:https://otpotential.com/free-ot-ceusSupport the show
When you're diagnosed with Multiple Sclerosis (MS), there's often an unspoken expectation that you'll process it, accept it, and eventually move on. But what happens when the thing you're supposed to “move on” from is a chronic, progressive disease that you carry with you every single day? In this honest and deeply personal conversation, we unpack the myth of moving on with Multiple Sclerosis, and what it really means to live with a long-term neurological condition. From dreams of walking again to small victories like standing and pivoting, we explore what it looks like to live with MS nearly three decades after diagnosis as both patient and caregiver. Is moving on even possible, or is the goal something different? In this episode, we talk about: The difference between moving on and moving forward after an MS diagnosis Living with Multiple Sclerosis for 25+ years and how perspective shifts over time Grief and chronic illness and why it resurfaces even decades later Caregiving and marriage while navigating progressive disability Society's expectations around acceptance, resilience, and “getting over it” Finding gratitude in small, everyday wins while living with MS Jennifer shares what it's like to dream about walking and wake up to the reality of mobility challenges. Dan reflects on accepting numb hands, shifting abilities, and life as a caregiver to a spouse with MS. Together, we wrestle with a question many in the chronic illness community quietly carry: Can you ever really move on from Multiple Sclerosis or is acceptance less about closure and more about courage? For those living with Multiple Sclerosis, caregiving for someone with MS, or navigating any chronic illness, this episode is a reminder that grief doesn't have an expiration date. But neither does resilience. We'd love to hear from you! Do you ever have moments where you forget you have Multiple Sclerosis? What does “moving forward” look like in your life right now? Email us at acoupletakesonms@gmail.com to help keep this conversation going. *** Remember to rate, review, and subscribe to A Couple Takes on MS Podcast for two insightful perspectives on this one multifaceted disease.
Multiple sclerosis (MS) is a chronic autoimmune condition in which the immune system mistakenly attacks the protective covering of the nerves, called myelin, in the brain and spinal cord. This damage disrupts communication between the brain and the rest of the body. Hosted on Acast. See acast.com/privacy for more information.
Host : Dawn HemingwayGuests 1 - Dr. Rheanna Robinson and Bev Tijioe, Indigionous persons with Multiple Sclerosis (MS),Guests 2 -Misia Slugocki , Women's Memorial March.
Last week, over 1,400 scientists and clinicians gathered in San Diego, California, at the 2026 Americas Committee for Treatment and Research in Multiple Sclerosis annual meeting, better known as the ACTRIMS Forum. This week, in Part One of our coverage, you'll hear from three of the experts who presented their research at the ACTRIMS Forum. Dr. Manuel Friese, a clinician-scientist at the Institute of Neuroimmunology and Multiple Sclerosis at the University Medical Center Hamburg-Eppendorf in Hamburg, Germany, where he serves as the Director of the Center for Molecular Neurobiology, and the Director of the Institute of Neuroimmunology and Multiple Sclerosis, is this year's winner of the Barancik Prize for Innovation in Multiple Sclerosis. I had an opportunity to talk with Dr. Friese about some of his truly remarkable research. Dr. Amit Bar-Or, the Director of the Centre for Neuroinflammation and Experimental Therapeutics (CNET) and Chief of the Division of Multiple Sclerosis (MS) and related disorders at the University of Pennsylvania, presented encouraging results from two important clinical trials. Dr. Bar-Or and I discussed what those results might mean for people living with relapsing-remitting and primary progressive MS. Dr. Haritha Desu, a young investigator at the ACTRIMS Forum, presented her cutting-edge research on how immune cells interact with cells already resident in the brain to drive damage or potentially promote repair. I talked with Dr. Desu about how her work could be key to stopping MS progression independent of relapse activity. We have a lot to talk about! Are you ready for RealTalk MS??! This Week: The 2026 ACTRIMS Forum :22 Barancik Prize winner Dr. Manuel Friese discusses his pioneering discoveries 1:34 Dr. Amit Bar-Or shares encouraging results from two important clinical trials 16:27 Dr. Haritha Desu discusses her research 25:27 Share this episode 32:23 Next week's episode 32:42 SHARE THIS EPISODE OF REALTALK MS Just copy this link & paste it into your text or email: https://realtalkms.com/441 ADD YOUR VOICE TO THE CONVERSATION I've always thought about the RealTalk MS podcast as a conversation. And this is your opportunity to join the conversation by sharing your feedback, questions, and suggestions for topics that we can discuss in future podcast episodes. Please shoot me an email or call the RealTalk MS Listener Hotline and share your thoughts! Email: jon@realtalkms.com Phone: (310) 526-2283 And don't forget to join us in the RealTalk MS Facebook group! LINKS If your podcast app doesn't allow you to click on these links, you'll find them in the show notes in the RealTalk MS app or at www.RealTalkMS.com Support Jon at WALK MS https://realtalkms.com/walkms Find out about ABLEnow Accounts https://ablenow.com JOIN: The RealTalk MS Facebook Group https://facebook.com/groups/realtalkms REVIEW: Give RealTalk MS a rating and review http://www.realtalkms.com/review Follow RealTalk MS on Twitter, @RealTalkMS_jon, and subscribe to our newsletter at our website, RealTalkMS.com. RealTalk MS Episode 441 Guests: Dr. Manuel Friese, Dr. Amit Bar-Or, and Dr. Haritha Desu Privacy Policy
Healing MS Naturally: Bridging Science and Soul Can you truly reclaim your health from the inside out?In this episode of Mind Body Medicine for Self Healers, I sit down with holistic transformation guide Christine Ruch to discuss her incredible 20-year journey of healing Multiple Sclerosis (MS) naturally.After moving beyond mainstream medicine, Christine utilized nervous system restoration, whole-food nutrition and spiritual practices to reconnect with her body's innate wisdom. We dive deep into the connection between autoimmune disease and the nervous system, the importance of emotional capacity and why "remodelling" your relationship with your emotions is a primary key to lasting transformation. Whether you are living with MS or seeking holistic healing for chronic illness, this conversation offers grounded practices to move from symptom management to true inner healing.Key Takeaways 01:50 Early Red Flags & Body Sensitivity Before her MS diagnosis, Christine struggled with weight issues, severe skin conditions (rosacea and eczema) & environmental allergies, signs that her body was already in a state of high sensitivity.04:31 The "Missing Piece": Nervous System Regulation After years of focusing on diet and lifestyle, Christine realized that nervous system work was the most overlooked part of her journey. She explains why this should be an integral part of healing not just "woo-woo" support.08:13 Eliminating Common Inflammatory Triggers: autoimmune conditions start by eliminating "the big four" inflammatory products; refined sugar, gluten, dairy and often egg products.08:57 The Role of Emotional Trauma: How a "disordered nervous system" and unprocessed emotional stress can feed autoimmune conditions and prevent the body from entering a healing state.10:18 Building "Emotional Capacity": We are not our emotions. Learning to hold space for uncomfortable feelings without creating a "story" or an "identity" around them is a foundational step in recovery.18:31 Developing a Body-Language Dialogue: The importance of listening to your body like a "newborn infant"—with curiosity and tenderness—to move from a place of fear to a place of internal trust.28:56 The "Type A" Stress Identity: Christine used to "thrive on stress" as a high-achieving chef, only to realize later that her high-pressure lifestyle was kept in service of a dysregulated nervous system.Christine's Bio Christine Ruch is a Holistic Transformation Guide who helps people with health conditions reconnect to their body's innate wisdom and healing potential. After spending 20 years healing her own MS naturally through whole food nutrition, nervous system restoration, spiritual practice, plant medicine, deep self-inquiry and many other Eastern and Western modalities, Christine now guides others on their own transformative healing path. Her work bridges science and soul—offering tools to move beyond symptom management and into lasting inner healing. She's here to share insight, hope, and grounded practices for listeners ready to reclaim their health from the inside out.Connect with Christine https://ChristineRuch.comInstagram: @ChristineRuch.MSSubstack: ChristineRuch.substack.comWho am I?Sarah Dawkins is a passionate Holistic Health and Healing Coach, international speaker and author of Heal Yourself. She's also a multi-award-winning entrepreneur and the award-winning host of the uplifting podcast Mind Body Medicine for Self Healers with Sarah Dawkins.With over 20 years' experience as a Registered Nurse, Sarah combines her deep understanding of conventional medicine with her own powerful self-healing journey to create a truly integrative approach. Having overcome multiple chronic health challenges herself, she now supports others in uncovering and addressing the root causes of their symptoms, helping them restore balance, reclaim their energy and create lasting, vibrant wellness.www.sarahdawkins.com#MShealing #multiplesclerosis
What happens when your body, the very thing you've spent nearly two decades teaching others to harmonize with, begins to fail you in a way you never saw coming? This week on the show, I'm sitting down with meditation teacher, and author Megan Monahan. Megan first appeared on Hurdle back in 2019, and today she returns to share a profoundly personal update. In late 2024, Megan faced a life-altering health hurdle: a diagnosis of Multiple Sclerosis (MS). Megan takes us inside the raw moments of her diagnosis—from the sudden loss of vision in her right eye to an eight-hour wait in an UCLA emergency room. We discuss the power of the "meditation muscles" she built over 16 years and how they allowed her to meet this challenge with resilience instead of a victim mindset. In this episode, we discuss: The sudden symptoms and 36-hour journey to an MS diagnosis. How a decade of spiritual practice reframed a "devastating" diagnosis into a "resurgence of purpose". The 4-7-8 breathwork framework and somatic shaking for navigating high-stress moments. Unmasking personality traits that are actually trauma responses. What it truly means to be authentic and "come home to yourself". Lessons learned from spiritual giants like Deepak Chopra and Wayne Dyer. QUOTABLE MOMENTS "You get to choose how a life-changing moment changes you. We all have the ability to author our story in whatever way we want." "There is a part of you that can't be diagnosed with MS, that can't be broken up with, that can't be broke, that can't be relocated. That is who you are." "We mistake the need to enjoy the experience or the process with finding value in it." "You are not your thoughts. You don't have to believe every thought you have." SOCIAL@megmonahan@emilyabbate@iheartwomenssports JOIN: The Daily Hurdle IG Channel SIGN UP: Weekly Hurdle Newsletter ASK ME A QUESTION: Email hello@hurdle.us to with your questions! Emily answers them every Friday on the show. Listen to Hurdle with Emily Abbate on the iHeartRadio app, Apple Podcasts, or wherever you get your podcasts.See omnystudio.com/listener for privacy information.
In this episode of A Couple Takes on MS, we're honored to welcome Sarah Locke, founder of Locke's Promise, a New Hampshire–based nonprofit born from her own lived experience with Multiple Sclerosis. Sarah shares how Locke's Promise came to life, from the six-week paperwork marathon it took to get started to the community momentum that followed. Through events like Climb the Peak, Rides & Wranglers for MS, and other grassroots efforts, the organization has raised more than $100,000 over four years and, in 2025 alone, has already donated over $42,000 to directly support six individuals living with MS. In this episode, we talk about: • Turning an MS diagnosis into a mission grounded in community • What it really takes to start a nonprofit from scratch • How grassroots fundraising creates direct, local impact • Living authentically—and honestly—after diagnosis • Why no one facing MS should ever feel invisible or alone We also talk with Sarah about her memoir, Living Out Loud, where she reflects on coming out later in life, navigating an MS diagnosis, and learning how honesty, humor, and vulnerability can coexist, even in the hardest moments. Throughout our conversation, Sarah reminds us that advocacy doesn't have to be loud to make an impact, and that real community built on connection and compassion can make all the difference. Here are the links we referenced that offer depth and insights for our conversation: Locke's Promise – Link to check out Sarah's “… compassionate nonprofit organization dedicated to raising awareness about Multiple Sclerosis (MS) while directly supporting local community members affected by this challenging condition.” Living Out Loud – Link to order Sarah's honest, personal, and inspiring memoir. *** Remember to rate, review and subscribe to A Couple Takes on MS Podcast for two insightful perspectives on this one multifaceted disease.
It started with clumsiness at high jump. Then, midway through Year 12, Deanna Renee woke up partially blind in one eye. At just 17, she was diagnosed with *Multiple Sclerosis (MS). Her classmates shunned her, convinced MS was a contagious STI. The internet told her she’d be in a wheelchair by 25. Today, she is a viral content creator, proving them all wrong. In this raw and often hilarious episode of the Well Summer Series, Claire Murphy sits down with Deanna to discuss the reality of growing up with a chronic neurological condition. They cover the isolation of high school, the darkness of her early 20s and the "bohemian doctor" who finally gave her hope. Deanna also opens up about the unique challenges of living with an invisible disability - from being "uninvited" to Schoolies to battling "Karens" in car parks who don't believe she's sick enough to park in disabled spots. Plus, we learn how she turned her MRI scans into art and became a viral advocate on TikTok. Get ready to have your perceptions challenged by a woman who refuses to let a diagnosis define her future. *MS is the most common acquired chronic neurological disease affecting young adults, often diagnosed between the ages of 20 to 40 and, in Australia, affects three times more women than men. As yet, there is no cure. There is no known single cause of MS, but many genetic and environmental factors have been shown to contribute to its development. In MS, the body’s own immune system mistakenly attacks and damages the fatty material – called myelin – around the nerves. This results in a range of symptoms, but no two people experience MS in the same way.**Content Warning: This episode discusses suicide and mental health struggles. If you’re looking for more to listen to - every Mamamia podcast is curating your summer listening right across our network from pop culture to beauty to powerful interviews there’s something for everyone, explore here. We’ll be back to regular programming Thursday15th January. THE END BITS If this episode has raised any issues for you, or if you just need someone to talk to, please reach out to: Lifeline: 13 11 14 Beyond Blue: beyondblue.org.au All your health information is in the Well Hub. Follow Deanna Renee: Instagram TikTok Learn more about MS: Visit MS Australia for resources and the wellness guide mentioned in this episode. GET IN TOUCH Sign up to the Well Newsletter to receive your weekly dose of trusted health expertise without the medical jargon. Ask a question of our experts or share your story, feedback, or dilemma - you can send it anonymously here, email here or leave us a voice note here. Ask The Doc: Ask us a question in The Waiting Room. Follow us on Instagram and Tiktok. Support independent women’s media by becoming a Mamamia subscriber. CREDITS Hosts: Claire Murphy and Dr Mariam Guest: Deanna Renee Senior Producers: Claire Murphy and Sally Best Audio Producer: Scott Stronach Video Producer: Julian Rosario Social Producer: Elly Moore Mamamia acknowledges the Traditional Owners of the Land we have recorded this podcast on, the Gadigal people of the Eora Nation. We pay our respects to their Elders past and present, and extend that respect to all Aboriginal and Torres Strait Islander cultures.Information discussed in Well. is for education purposes only and is not intended to provide professional medical advice. Listeners should seek their own medical advice, specific to their circumstances, from their treating doctor or health care professional. +++++++++++++++++++++++++++++++++++++++++++++++++++++++++++Support the show: https://www.mamamia.com.au/mplus/See omnystudio.com/listener for privacy information.
In this inspiring episode of the Eye Believe Podcast, we welcome author and advocate Rachel Sindaco, whose journey through Multiple Sclerosis (MS) and Ocular Melanoma (OM) reshaped her life in unimaginable ways—and ultimately saved it. Rachel maintains a remarkable positive outlook, openly sharing how she considers herself lucky to have MS. It was her MS diagnosis that led to increased medical monitoring, allowing her ocular melanoma to be caught early—a discovery that may have saved her life. Without MS, Rachel believes her cancer might have gone undetected until it was too late. Her book, From a Kick in the Head to a Kick in the Ass: My Involuntary Journey with Multiple Sclerosis and Ocular Melanoma, is a candid, often humorous, and deeply moving memoir about navigating serious illness, reframing adversity, and finding gratitude in the most unexpected places. This conversation is a powerful reminder that perspective matters, early detection saves lives, and even the hardest diagnoses can carry unexpected gifts.
Motivation and Inspiration Interviews with Professor of Perseverances
Amber McCollum shares her journey with MS as an Entrepreneur
Two-time Emmy and three-time NAACP Image Award-winning television Executive Producer Rushion McDonald interviewed Mori Taheripour.
Two-time Emmy and three-time NAACP Image Award-winning television Executive Producer Rushion McDonald interviewed Mori Taheripour.
Two-time Emmy and three-time NAACP Image Award-winning television Executive Producer Rushion McDonald interviewed Mori Taheripour.
In this compelling and candid episode of The Gritty Nurse Podcast, host Amie Archibald-Varley sits down with a truly inspiring guest: Emily Edwards, RN, founder of Nomad Care Consulting. Emily, a healthcare expert, shares the deeply personal and often frustrating journey of her own Multiple Sclerosis (MS) diagnosis. She details the challenges of being a patient in the very system she knows so well, often feeling unheard, dismissed, and invalidated while searching for answers. This is more than a story about chronic illness; it's a powerful masterclass in self-advocacy. Emily opens up about the immense emotional toll of MS and the sheer resilience required to keep pushing for proper care. What you'll learn in this eye-opening conversation: The shocking reality of receiving a major diagnosis as a practicing RN. Why self-advocacy is crucial—especially when dealing with complex or chronic conditions. How to push past dismissal and demand validation from your care team. The psychological and emotional landscape of living with MS. Join us for this essential conversation that will redefine how you view the patient experience and inspire you to find your own voice in the healthcare world. Where to Listen / Watch * Listen on Apple Podcasts: https://podcasts.apple.com/ca/podcast/the-gritty-nurse/id1493290782 * Watch on YouTube – https://www.youtube.com/@thegrittynursepodcast Leave a comment, Like and SUBSCRIBE! Thank you to Hospital News for being a collaborative partner with the Gritty Nurse! www.hospitalnews.com More about Emily Edwards: Emily Edwards, RN is a Registered Nurse and a highly respected expert in the dementia care space, as well as the founder of Nomad Care Consulting. With an expansive knowledge of older adult mental health and dementia, Emily's expertise is built on years of experience, including her roles as a Psychogeriatric Resource Consultant, a Long Term Care Behavioural Supports Coordinator, and an RN Team Lead for a specialized dementia care team. Emily's unique strength lies in her ability to take complex healthcare topics and translate them into actionable, manageable pieces, empowering families and caregivers to navigate the intricate healthcare system and discover effective, non-pharmacological care approaches. She is dedicated to helping people cultivate a life worth living for both their loved ones and themselves. Support Emily! https://www.gofundme.com/f/help-emily-rest-recover-return-better-than-ever Where to find Emily: Linkedin: https://www.linkedin.com/in/emilyedwardsbscn/ IG: https://www.instagram.com/thatnomadnurse/ Websites: https://www.nomadcare.ca/ https://nomadcare.kit.com/uncover?fbclid=PAZXh0bgNhZW0CMTEAc3J0YwZhcHBfaWQMMjU2MjgxMDQwNTU4AAGn4bcyAvxUxhHr4TaDy1Yu6iH5VLVO7BbOmNemtDU08WrU1KmVDxw1pvoTLvg_aem_UCvO6EjkIb0Su1nZw0HNFg
This week on the Good Humans Podcast, I sit down with Mikel Nyholt — a high-performing executive at Usher Group, where he leads sales, marketing, and culture for a $100M+ business employing over 500 people. But behind his professional success lies an incredible story of burnout, resilience, and self-healing that will leave you inspired.In his late 20s, Mikel's life came crashing down. After years of pushing himself to the edge in business, he was diagnosed with Multiple Sclerosis (MS) — told he'd need constant care, and even lost vision in one eye. But instead of accepting the bleak prognosis, Mikel chose a different path.He turned inward, exploring the power of breathwork, mindset, and holistic healing, and seven years later his doctors are still blown away by his recovery and vitality.In this powerful episode, we dive into: ✅ The personal and professional burnout that led to his MS diagnosis ✅ The moment he decided to take ownership of his healing journey ✅ How breathwork and nervous system regulation changed everything ✅ The role of purpose, balance, and mindset in sustainable success ✅ What he's learned about leadership, health, and being truly aliveMikel's story is a masterclass in self-awareness and the courage to challenge conventional thinking. From corporate burnout to deep healing, his journey shows what's possible when we stop living on autopilot and start taking responsibility for our wellbeing.Follow MikelInstagram—Send me a DM on Instagram saying "I wanna join the club" to join our FREE mindfulness and gratitude accountability community :)1% Good Club Book!!The Good Human FactoryAmazonBooktopiaCooper's SocialsInstagramTikTokThe Good Human Factory LinksInstagramWebsiteMerch – Use code PODCAST for 25% OFFWorkshop EnquiryTHE GOOD HUMAN FACTORY™️ 2020 Hosted on Acast. See acast.com/privacy for more information.
This week on the Good Humans Podcast, I sit down with Mikel Nyholt — a high-performing executive at Usher Group, where he leads sales, marketing, and culture for a $100M+ business employing over 500 people. But behind his professional success lies an incredible story of burnout, resilience, and self-healing that will leave you inspired.In his late 20s, Mikel's life came crashing down. After years of pushing himself to the edge in business, he was diagnosed with Multiple Sclerosis (MS) — told he'd need constant care, and even lost vision in one eye. But instead of accepting the bleak prognosis, Mikel chose a different path.He turned inward, exploring the power of breathwork, mindset, and holistic healing, and seven years later his doctors are still blown away by his recovery and vitality.In this powerful episode, we dive into: ✅ The personal and professional burnout that led to his MS diagnosis ✅ The moment he decided to take ownership of his healing journey ✅ How breathwork and nervous system regulation changed everything ✅ The role of purpose, balance, and mindset in sustainable success ✅ What he's learned about leadership, health, and being truly aliveMikel's story is a masterclass in self-awareness and the courage to challenge conventional thinking. From corporate burnout to deep healing, his journey shows what's possible when we stop living on autopilot and start taking responsibility for our wellbeing.Follow MikelInstagram—Send me a DM on Instagram saying "I wanna join the club" to join our FREE mindfulness and gratitude accountability community :)1% Good Club Book!!The Good Human FactoryAmazonBooktopiaCooper's SocialsInstagramTikTokThe Good Human Factory LinksInstagramWebsiteMerch – Use code PODCAST for 25% OFFWorkshop EnquiryTHE GOOD HUMAN FACTORY™️ 2020 Hosted on Acast. See acast.com/privacy for more information.
In this episode we speak with three runners from Team Abbott — a community of runners who have faced serious health challenges but didn't let those challenges define them! [powerpress] About Our Guests Elizabeth Pehota (Boston, MA): Three days out from running the 2022 Berlin Marathon, Elizabeth Pehota experienced a feeling of pins and needles in her hands, feet and thighs, and an unnatural resistance while running. Soon after, she was diagnosed with Multiple Sclerosis (MS), a chronic, unpredictable disease of the central nervous system. As someone who shares her daily life on social media, Elizabeth, @healthy_cheers on Instagram, only recently opened up about her diagnosis, but has already formed relationships with other MS patients around the world. Elizabeth is an Abbott World Marathon Major Six Star Finisher and received her seventh star in Sydney. Ed Barnes (Douglas, MA): Ed was born with a congenital heart condition and at age 15 he started to experience frequent dizziness - to the point of nearly passing out - leading him to undergo open heart surgery to receive an Abbott artificial aortic heart valve. This year, after completing the Boston Marathon, Ed became the first person with an artificial heart valve to finish all seven Abbott World Marathon Majors. Mary Tawney Suarez (Fullerton, CA): Just before the pandemic, Mary started experiencing seizures and was diagnosed with Epilepsy and a brain cyst. One year later, she started experiencing back pain and numbness in her legs, which was revealed to be the degeneration of the cerebral and lower part of her spine. Despite these obstacles, Mary has continued running, and just finished the Berlin Marathon. [box] Links Mentioned in This Episode Run Coaching. Work with an expert MTA running Coach. MetPro.co -For the first time ever, MetPro is offering MTA listeners a full 30-day experience for just $95 with absolutely no strings attached! See what it's like working with your own metabolic coach. Limited to the first 30 people. AG1 Next Gen has new flavors: new flavors: Citrus, Tropical, and Berry. Get a free Welcome Kit with your first order which includes 5 AG1 Travel Packs, a shaker bottle, metal canister, and a bottle of AG Vitamin D3+K2. The Virginia Credit Union River City Half -March 7 in Richmond, Virginia. Drury Hotels -Get 10% off your stay with our link or use the code RN2025. Team Abbott -a community of runners, many of whom have overcome health challenges, who are committed to inspiring others through their running journeys. To submit your story for a chance to join Team Abbott, visit abbott.com/marathons. [/box]
Multiple Sclerosis (MS) is a life-altering neurological condition that affects thousands of people across Ireland. It can impact mobility, speech, vision, and everyday life.Joining Andrea in the studio to talk about living with MS, and the MS Readathon is Meath Gaelic Footballer, Cillian O'Sullivan and Jamie Crawford.
Michelle was a business owner, gym junkie and busy mum when she broke a foot in December, 2017.After experiencing balance and walking issues she attributed to a second broken foot in December 2018, Michelle was eventually diagnosed with Multiple Sclerosis (MS) and Charcot-Marie-Tooth disorder (CMT) in March 2019.Both neurological conditions, MS and CMT have left Michelle unable to run or move her legs quickly.But that didn't stop her from entering - and finishing - her first (and last) triathlon at the Husky Triathlon in February 2020.Michelle tells the story in this conversation of what unfolded, her experience of crossing the finish line and what that race means to her.And trust me when I say this — you're going to need a tissue ;)
How do you keep chasing your purpose when life hits you with a diagnosis that changes everything?In this deeply inspirational and motivational episode, Reginald D sits down with rapper, producer, author, and entrepreneur Robert Cardillo, better known as B-Cide, to talk about his raw, real, and resilient journey living with Multiple Sclerosis (MS)—while still pursuing his passion for music, entrepreneurship, and impact.From growing up in upstate New York, grinding in the underground hip hop scene for over 25 years, and building his streetwear brand “55 Strong,” B-Cide opens up about what it truly means to fight for your purpose, even when your body tries to betray you. Diagnosed with MS in 2011, he shares the emotional toll, the reality of lost relationships, and how he rose again—stronger, wiser, and louder than ever.B-Cide's story is more than music—it's about faith, mental strength, and redefining success when life doesn't go according to plan.Whether you're battling chronic illness, invisible pain, or internal doubt—this episode will remind you that you are not your diagnosis, and you still have a voice.Powerful TakeawaysLearn how to transform adversity into art and advocacy—and how B-Cide channels MS into a groundbreaking album set to drop during MS Awareness Month.Discover how to redefine success beyond fame or fortune—through purpose, connection, and legacy.Get inspired by B-Cide's practical wisdom on how to push through physical and emotional pain while staying creative, resilient, and faith filled.If you've ever felt like life knocked you off course, hit play now for a motivational/inspirational speech wrapped in real-life experience, hip hop wisdom, and purpose-driven fire.B-Cide contact info:Official Website: https://www.b-cide.com Book Website: https://www.myelinmyshoes.com Instagram: https://instagram.com/bcide Facebook: https://facebook.com/bcide TikTok: https://tiktok.com/@bcide YYouTube: https://youtube.com/@btvstudio Bandcamp: https://bcide.bandcamp.cominspirational, motivational, motivational podcast, motivational speech, MS awareness, multiple sclerosis, chronic illness motivation, invisible illness inspiration, hip hop artist, , underground rap, Myelin My Shoes book, B-Cide, overcoming adversity, living with MSSend us a textSupport the showFor daily motivation and inspiration, subscribe and follow Real Talk With Reginald D on social media:Instagram: realtalkwithreginaldd TikTok: @realtalkregd Youtube: @realtalkwithreginald Facebook: realtalkwithreginaldd Twitter Real Talk With Reginald D (@realtalkRegD) / TwitterWebsite: Real Talk With Reginald D https://www.realtalkwithreginaldd.com Real Talk With Reginald D - Merchandise
We talk to Sheila all about Multiple Sclerosis (MS), her symptoms and diagnosis and what daily work and home life looks like for her. She speaks inspiringly about clinical trials, her supportive family, friends and colleagues and her unique outlook on life and humanity.
Patti Bevilacqua is in my socials a lot and her accomplishments since we last spoke 3 years ago are almost too many to count. Why is that impressive? Well, 35 years ago, Patti was diagnosed with Multiple Sclerosis – MS. Today Patti discusses: What exactly MS is Canada has highest rate of MS in the world and 3 out of 4 are women Evolution of Patti's journey Patti shares some great stories Be your own hero why people with disabilities will change the world If you have the ear of Christine Sinclair, listen in to Patti and then share this episode with Christine!! Listen now and then share this episode! Find Patti Bevilacqua at https://pattibevilacqua.com/ Learn more about Patti and find all her links at The Boomer Woman's Podcast: Patti Bevilacqua Find your nearest A&W at https://web.aw.ca/en/locations and buy a Teenburger for MS! Want to be a guest on The Boomer Woman's Podcast? Send Agnes a message on PodMatch, here: Agnes on PodMatch
Communication Queen | entrepreneurship, marketing, storytelling, public speaking, and podcasting
Learn how to share stories of medical gaslighting without getting cancelled — and turn your truth into a powerful visibility strategy. Share your story here: https://www.communicationqueens.com/podcast
What if autoimmunity wasn't the body turning against you, but a call for deeper care and understanding? In this episode of Healthily, I'm joined by Nutritional Therapist Elisa Ferguson, who specialises in supporting people with Multiple Sclerosis (MS). We explore the wider story behind autoimmune conditions – including how stress, gut health, trauma, and diet all interact in powerful ways. We take a look at the cell danger response – a protective mechanism where the body essentially "hits pause" on certain functions to deal with threat. When this response becomes chronic, it can contribute to many chronic conditions, including MS. Together, we reflect on why people often fall down rabbit holes in search of solutions, and how to find a gentler, more effective way forward. This is an episode full of insight, calm, and connection – not just for those living with MS, but for anyone curious about how to support whole-body health through the lens of autoimmunity. For more resources, support, and information on how I work, visit www.nicola-moore.com You'll find details about my clinic, courses, and services designed to support real-life health — with compassion, clarity and practicality. Are you a qualified nutritional therapist or student practitioner looking for support in clinic? My Clinical Support Groups are a warm, practical space where you can build confidence, ask questions, and learn how to simplify and personalise your client work — without overwhelm. Whether you're newly qualified or more experienced and looking for fresh perspective, you'll find honest discussion, real-world strategy, and encouragement that makes a difference. Learn more and sign up at www.nicola-moore.com One-to-One Nutritional Therapy - https://p.bttr.to/3gs8X3M Hormone Insights & Support Service - https://www.nicola-moore.com/hormone-insights-support-service Liberate Food Freedom Course - https://www.nicola-moore.com/liberate-1 Nutrition Practitioner and Student Mentoring Groups - https://www.nicola-moore.com/nmpractitionersupport Website | Facebook | Instagram https://www.nicola-moore.com/ https://www.facebook.com/NicolaMooreNutrition https://www.instagram.com/nicolamoorenutrition/
Perks and benefits are nice, but they aren't enough to retain the best talent. According to Jon Franko, co-founder of Gorilla 76, employees want transparency, growth opportunities, and a culture that supports their lives outside of work. In this episode, Vanessa Brulotte speaks with Jon about how building a culture based on core values and empathy can drive stronger employee retention. Jon shares how his Multiple Sclerosis (MS) diagnosis shaped his approach to supporting his team. Key takeaways:How to create a workplace people don't want to leaveStrategies for building high-trust environments at workWhy HR can steer the organization in the right directionKey topics:(00:00) Introducing Jon Franko(03:13) The MS diagnosis that changed Jon's leadership perspective(05:00) Hire people better than you(08:41) How Gorilla 76 encourages people to give back(13:53) Transparency that attracts top talent(17:00) Evaluating the impact of your benefits package(21:59) Retention and engagement metrics to trackKey links:Read BambooHR's blog, “5 Powerful Benefits of Transparency in Business”: https://www.bamboohr.com/blog/creating-transparency-in-workplaceRead BambooHR's blog, “Perks At Work: What Benefits Make Your Employees Happy?”: https://www.bamboohr.com/blog/creative-benefit-ideasDownload BambooHR's guide, “Learn How to Retain Top Talent in 2025”: https://www.bamboohr.com/resources/ebooks/definitive-guide-to-employee-retentionSubscribe to HR Unplugged Series: https://www.bamboohr.com/resources/podcasts/hr-unplugged/Join HR Heroes Slack Community: https://join.slack.com/t/hrheroesworkspace/shared_invite/zt-21ad3f1r8-dkWC2EdmyhxUAHw9cGLdQwBambooHR Homepage: https://www.bamboohr.com/Connect with Jon on LinkedIn: https://www.linkedin.com/in/jonfranko/Learn more about Gorilla 76: https://www.gorilla76.com/
Book your appointment with Allure Medical: https://www.alluremedical.com/schedule-an-appointment/Can conventional therapy slow down or reverse Multiple Sclerosis?In this episode, Dr. Charles Mok provides an in-depth overview of what a patient consultation for Multiple Sclerosis (MS) typically involves under his care.He discusses the two major types of multiple sclerosis, the potential role of stem cell therapy, and the reasons many patients turn to conventional treatments.Dr. Mok also explores emerging drug therapies aimed at managing MS symptoms, the significance of impaired blood-brain and bowel-blood barriers, and how low sex hormone levels may influence the progression of the disease.Tune in to Inside The Cure Podcast — The Standard Care for Multiple SclerosisSubscribe to the podcast and leave a 5-star review!You can also catch this show on our YouTube channel and on all your favorite podcast platforms.Read the latest research and advice from the doctors at Allure Medical: https://www.alluremedical.com/books/Dr. Charles Mok received his medical degree from Chicago College of Osteopathic Medicine, Chicago, Illinois in 1989. He completed his medical residency at Mount Clemens General Hospital, Mt. Clemens, Michigan. He has worked with laser manufacturing companies to improve their technologies; he has performed clinical research studies and has taught physicians from numerous other states. His professionalism and personal attention to detail have contributed to the success of one of the first medical spas in Michigan.LinkedIn: https://www.linkedin.com/in/charles-mok-4a0432114/ Instagram: https://www.instagram.com/alluremedicals/ Website: https://www.alluremedical.com/ YouTube: https://www.youtube.com/@AllureMedical TikTok: https://www.tiktok.com/@alluremedical Amazon Store: https://www.amazon.com/stores/Dr.-Charles-Mok/author/B0791M9FZQ?ref=ap_rdr&store_ref=ap_rdr&isDramIntegrated=true&shoppingPortalEnabled=true Join the Allure Medical Inner Circle Membership:https://www.alluremedical.com/inner-circle-membership/ #MultipleSclerosis #MSTreatmentOptions #AutoimmuneDisease
In today's video, we're diving deep into the transformative power of the carnivore diet and how it can help heal the gut-brain barrier, reduce inflammation, and improve symptoms of neurological conditions like Multiple Sclerosis (MS).
Join us as we discuss Logan's recent run with MS Run the US! MS Run the US is a non-profit organization who's mission is to raise awareness, raise funds, and aid those living with Multiple Sclerosis (MS).This is Logan's 3rd year being a part of this event, which is a 3,260 mile relay run across America!This year, MuuvWell PROUDLY supported this event, and we loved hearing Logan's experience running this year's event.Logan ran 155 miles from Williamsburg, Iowa to Platteville, Wisconsin. Follow MuuvWell online at linktr.ee/muuvwell
In the second part of Kate's story, we discover what shifted in her marriage that caused her once-strong sexual desire to disappear—and why sex became a low priority in her relationship.When Kate started dating her future husband, she worried the passion might fade. But to her relief, it didn't. Their sex life remained fun, exciting, and free of guilt. Everything changed, however, after they had children.Following the birth of their second child, Kate found herself constantly exhausted. While sex remained a top priority for her husband, it became the last thing on Kate's mind by the end of each day. Her husband felt hurt and began to believe she no longer loved him.For years, Kate went through the motions, having sex mainly to meet his needs—but she found little enjoyment in it. During this period, she was also diagnosed with Multiple Sclerosis (MS), which only deepened her fatigue. As her symptoms worsened, she eventually had to leave her job, and any energy for intimacy vanished.Then, Kate stumbled across Janna's Wanting It More Foundations program for women through an online ad. She took the self-paced course and recalls thinking, “I can't believe I'm not the only one!” Understanding the real reasons behind her low desire was a breakthrough. She suggested they try Doing It Together, a couples' version of the course—and her husband was fully on board.Now, Kate shares what they've learned and the steps they're taking to build a mutually satisfying sexual connection—one that truly works for both of them.Janna's Wanting It More Foundations self-paced course for women is on sale for $100 off until June 17. Learn more and join here.Join the waitlist for the Oct./Nov. 2025 round of Doing It Together here.Learn about the Doing It Together program details, schedules, testimonials, and Q&A.Leave a podcast review: We'd so appreciate your rating and review to help the podcast reach more couples.
In this eye-opening episode of the Whole Body Detox Show, David DeHaas of Living Waters Wellness Center uncovers shocking facts about everyday toxins—starting with Ziploc bags, which can leach microplastics and heavy metals into food when microwaved or frozen. Learn why switching to glass containers is critical for reducing toxic exposure.David draws from the Blaylock Wellness Report to explore the root causes of neurodegeneration, including Alzheimer's, Parkinson's, Multiple Sclerosis (MS), and ALS. He explains how brain fog, cognitive decline, and other neurological disorders are often triggered by environmental toxins, vaccinations, glutamate, and impaired mitochondrial function.You'll hear powerful stories of transformation from our 10-Day Healing Retreat, where deep detoxification, emotional healing, and muscle testing (kinesiology) have helped clients overcome symptoms like memory loss, tremors, and even regain mobility from wheelchairs.Discover the neurological power of Vitamin B6 (P5P), Riboflavin (Vitamin B2), Thiamine (Vitamin B1), and Benfotiamine, along with Green Tea Extract (EGCG)—nutrients shown to support dopamine production, reduce excitotoxicity, and enhance mitochondrial energy and brain health.David also exposes the dangers lurking in biosolids, used in city parks and farmland, which carry pesticides, heavy metals, and animal waste. Plus, learn why assisted living centers restrict access to life-saving supplements and how you can stay independent through natural detox, energy healing, and proper nutrition.Holistic tools like Trauma Plant (comfrey cream), nanocurcumin, and healing touch energy therapy are also featured—practical ways to reduce inflammation and support recovery without toxic pharmaceuticals like Tylenol.Take the first step toward holistic health and a toxin-free future.
Diagnosed with Multiple Sclerosis in 2013, Lis van Lynden has refused to let the condition define her limits. With no prior cycling experience or training, Lis set off in 2022 on a solo, unsupported ride around the entire coastline of Great Britain—covering 5,000 miles over seven months and raising over £13,000 for MS charities. Her journey didn't stop there. Lis went on to cycle the Irish coastline and most recently visited 12 of the UK's national parks by bike, with plans to complete the final 3 in 2025. Along the way, she's faced physical challenges, experienced incredible acts of kindness, and become a passionate advocate for others living with MS. Lis's story is one of courage, conviction, and living life on her own terms—no matter the obstacles. *** Catch the latest episodes of the Tough Girl Podcast, dropping every Tuesday at 7 am UK time! Don't forget to subscribe so you won't miss the inspiring journeys and incredible stories of tough women. Want to play a part in uplifting female representation in the media? Support the Tough Girl Podcast on Patreon! Your generosity helps shine a spotlight on female role models in the world of adventure and physical challenges. Join us in making a positive impact by visiting www.patreon.com/toughgirlpodcast. Thank you for your amazing support! *** Show notes Who is Lis Half Dutch, Half British Growing up abroad Moving to London and training as a teacher Losing her brother in a sailing accident Losing her father to bowl cancer Working in West Dulwich for 12 years Thinking there must be more to life Being interested in adventure travel Climbing Kilimanjaro and doing a mountaineering course Slowing the group down The first signs of having Multiple Sclerosis (MS) 2008 packing in her job and doing a history degree with the Open University Losing her mother to lung cancer Meeting someone and buying a house together Getting diagnosed in 2013 with MS Going through a divorce Heading to Svalbard in 2018 Reading “one man and his bike' by Mike Carter Book: One Man and His Bike: A Life-Changing Journey All the Way Around the Coast of Britain “Can I do this? Could this be my adventure challenge?” Having 100% conviction Being inspired by and supported by Verdangi Kulkarni Being consumed by her dream 2020 and dealing with lockdowns 2022 7th May - Ready to start the journey! No training and doing 68 miles on the first day. Ripping up the rules…. 7 months, 3 days and 1 hour 1 month into the journey and how everything had changed Going off medication and feeling free Heading to Northern Ireland Meeting Ann Whatmore on the road (her episode on the TGP goes live on 5th June 2025) MS Symptoms and dealing with it on the road Wanting to make changes in her life and live life to the fullest Trying to figure out a different way of earning income Movement, eating well and sleep The power of helping ourselves and the importance of mindset Getting through the shitty days Reframing Next challenge How to connect with Lis on social media Final words of advice for other women who want to take on a new challenge Social Media Just giving: www.justgiving.com/fundraising/lisvanlynden Instagram: @coddiwomple2wander Facebook: www.facebook.com/lis.vanlynden Twitter: @LisvlTravels
In this episode of the Brain & Life Podcast, host Dr. Daniel Correa is joined by comedian and actress Kellye Howard, who shares about her Multiple Sclerosis (MS) diagnosis process and how she manages symptoms in her daily routine. Dr. Correa is then once again joined by Dr. Lilyana Amezcua, a neurologist and MS specialist based out of Los Angeles at USC and the Keck School of Medicine. Dr. Amezcua explains MS and discusses some of the disparities in care amongst different communities. Additional Resources Expert Insights and Practical Tips for Managing Multiple Sclerosis MS-ing Around with Kellye Howard How Multiple Sclerosis Affects Black People How Exercise Helps Those with Multiple Sclerosis Other Brain & Life Podcast Episodes Voices from the Multiple Sclerosis Community We want to hear from you! Have a question or want to hear a topic featured on the Brain & Life Podcast? · Record a voicemail at 612-928-6206 · Email us at BLpodcast@brainandlife.org Social Media: Kellye Howard @kellyehoward; Dr. Lilyana Amezcua @keckschoolusc Hosts: Dr. Daniel Correa @neurodrcorrea; Dr. Katy Peters @KatyPetersMDPhD
My MS Story- Episode 183 - Transcript In this episode we join our host Stephanie Buxhoeveden and special guest Ashley Ratcliff Lundy as we dive into the personal journeys of living with Multiple Sclerosis (MS) as we share unique stories of diagnosis, the emotional rollercoaster that follows, and how perspectives on life have shifted since that moment. From the first signs of MS to the life-changing diagnosis, our guest speaks about challenges, the feelings of uncertainty, fear, and hope, while hearing the lessons they've learned along the way. With honesty and resilience, we discuss how to redefine goals, priorities, and outlook on life, offering valuable advice to those newly diagnosed. Tune in for an inspiring conversation on adapting to change, embracing strength, and finding a renewed sense of purpose in the face of MS. A special thank you to our generous sponsor Novartis. Poppy + Monarch, E-commerce business that supports the chronically ill community Jesus Year, The self-help memoir Ashley wrote about her MS diagnosis We Are ILL, The patient advocacy organization Disclaimer: This podcast provides general educational information. Can Do MS does not endorse, promote, or recommend any service, or diet associated with the content of this program.
- Join The Guild - CLICK HERE TO LEARN MORELife can change in an instant, and when it does, how do you keep going? In this deeply personal episode, I sit down with my sister, Evelyn, to talk about her journey with Multiple Sclerosis (MS)—a diagnosis that turned her world upside down.We dive into the mental and emotional battles that come with life-altering challenges, the process of grieving the life you once had, and the power of acceptance. Evelyn shares how she had to redefine success, let go of rigid goals, and find new ways to move forward when her body no longer allowed her to live the way she used to.If you've ever faced a setback—whether it's illness, weight struggles, or any unexpected life change—this episode is for you. We talk about:✔️ How to adapt when life doesn't go as planned✔️ Why comparison is the thief of joy—and how to let it go✔️ The importance of surrounding yourself with only supportive people✔️ How shifting your mindset can help you find peace, even in the hardest moments✔️ Why small wins matter more than you thinkThis episode is a powerful reminder that even when life throws a curveball, you can still take control of your mindset and keep moving forward.— Have a question for The Chris Terrell Podcast? Leave a voicemail at this link: https://podcasters.spotify.com/pod/show/christerrellcoaching/message or submit your written question for a chance to be on the show live with Chris Terrell: https://www.surveymonkey.com/r/3SC92W8 __3 ways to support the showSupport the show directly: Buy Me a CoffeeShare your favorite episode on social media. Provide a review on your favorite podcasting app.—Free DownloadsDownload my Journaling Guide today: The Free GuideHow to find your why: https://youtu.be/VkQtpSi1Tus—Additional ResourcesCoaching Website: www.christerrellcoaching.comFree Content: The Goods!My TikTok Channel: @og_chris_terrellInstagram: @OG_Chris_Terrell—
In this episode of The MSing Link Podcast, I delve into the 2024 updates to the McDonald Criteria for diagnosing Multiple Sclerosis (MS). Join me as I explain these significant changes and what they mean for patients seeking an accurate MS diagnosis. You'll gain a clearer understanding of the evolving landscape in MS diagnosis. I also discuss the addition of optic nerve involvement and changes to dissemination in time requirements, offering practical advice and questions you can take to your neurologist for a confident diagnosis. Stay informed, empowered, and ready to take action on your MS journey with this comprehensive episode filled with the latest MS diagnosis criteria insights and expert guidance. Resources mentioned in the episode: McDonald Criteria - https://mstrust.org.uk/a-z/mcdonald-criteria The MSing Link Book - https://www.drgretchenhawley.com/the-msing-link-book Additional Resources: https://www.doctorgretchenhawley.com/insider Reach out to Me: hello@doctorgretchenhawley.com Website: www.MSingLink.com Social: ★ Facebook: https://www.facebook.com/groups/mswellness ★ Instagram: https://www.instagram.com/doctor.gretchen ★ YouTube: https://www.youtube.com/c/doctorgretchenhawley?sub_confirmation=1 → Game Changers Course: https://www.doctorgretchenhawley.com/GameChangersCourse → Total Core Program: https://www.doctorgretchenhawley.com/TotalCoreProgram → The MSing Link: https://www.doctorgretchenhawley.com/TheMSingLink
In this episode of Talking Nutrition, Johan is joined by Ronja Jacobsson to talk about her journey with Multiple Sclerosis (MS). You'll learn about common misconceptions about MS and the challenges of this central nervous system autoimmune condition, how Ronja is still able to keep her mindset, health, and fitness in a great place, and how you can overcome virtually any challenge by focusing on what's within your control. Even something like MS doesn't have to define you - especially when you're stubborn about your health ;)Follow Ronja at:https://www.instagram.com/ronjaronjis/https://www.coachronja.com/If you'd like more coaching advice based on where YOU are currently at habit, routine, and goal-wise, you can fill out the free metabolism quiz here: https://bit.ly/408H4oe. After filling in the quiz, Johan will email you a personal video with the exact steps to follow for the next 30-90 days! More from Johan and Odyssey Coaching Systems:- Instagram: @johanvesters_ocs- Website: www.odysseycoachingsystems.co- E-book (FREE download): www.odysseycoachingsystems.co/e-book
Selma Blair sits down with Drew Barrymore to reveal surprising insights into her dating life and get candid about her journey with multiple sclerosis (MS). Learn more about your ad choices. Visit megaphone.fm/adchoices
The Plant Free MD with Dr Anthony Chaffee: A Carnivore Podcast
Query successful Try again without extensions In this episode of The Plant Free MD, Dr. Anthony Chaffee interviews Penny Roehr, who has had a remarkable recovery from multiple sclerosis (MS) using a carnivore diet. Penny shares her personal experience with MS, including her initial symptoms, diagnosis, and the challenges she faced with traditional treatments. She also discusses how she transitioned to a carnivore diet and the positive impact it has had on her health. Dr. Chaffee and Penny explore the potential benefits of a carnivore diet for people with MS and other autoimmune diseases. This podcast episode is for you if you are: Diagnosed with multiple sclerosis (MS) and are looking for alternative treatment options. Interested in learning more about the carnivore diet and its potential health benefits. Looking for inspiration and hope from someone who has overcome a serious health challenge. In this episode, you will learn: Penny Roehr's personal story of recovery from MS using a carnivore diet. The challenges Penny faced with traditional MS treatments. The potential benefits of a carnivore diet for people with MS. How to get started on a carnivore diet. Don't forget to like and subscribe to the Plant Free MD channel for more informative and inspiring content! ✅ Dr Chaffee's website: www.thecarnivorelife.com ✅Join my PATREON for early releases, bonus content, and weekly Zoom meetings! https://www.patreon.com/AnthonyChaffeeMD ✅Sign up for our 30-day carnivore challenge and group here! https://www.howtocarnivore.com/ ✅Stockman Steaks, Australia Discount link for home delivered frozen grass-fed and grass finished pasture raised meat locally sourced here in Australia! Use discount code "CHAFFEE" for free gift with qualifying orders! http://www.stockmansteaks.com.au/chaffee ✅ 60-minute consultation with Dr Chaffee https://calendly.com/anthonychaffeemd/60-minute-consultation Sponsors and Affiliates: ✅ Brand Ambassador for Stone and Spear tallow and soaps referral link https://www.stoneandspeartallow.com/?ref=gx0gql8b Discount Code "CHAFFEE" for 10% off ✅ Carnivore t-shirts from the Plant Free MD www.plantfreetees.com ✅THE CARNIVORE BAR: Discount Code "Anthony" for 10% off all orders! https://the-carnivore-bar.myshopify.com/?sca_ref=1743809.v3IrTuyDIi ✅Schwank Grill (Natural Gas or Propane) https://glnk.io/503n/anthonychaffeemd $150 OFF with Discount Code: ANTHONYMD ✅X3 bar system with discount code "DRCHAFFEE" https://www.kqzyfj.com/click-100676052-13511487 ✅Cerule Stem cells https://DrChaffee.cerule.com ✅CARNIVORE CRISPS: Discount Code "DRCHAFFEEMD" for 10% off all orders! www.carnivorecrisps.com ✅Shop Amazon https://www.amazon.com/shop/anthonychaffeemd?ref=ac_inf_hm_vp And please like and subscribe to my podcast here and Apple/Google podcasts, as well as my YouTube Channel to get updates on all new content, and please consider giving a 5-star rating as it really helps! This podcast is for general informational purposes only and does not constitute the practice of medicine, nursing or other professional health care services, including the giving of medical advice, and no doctor/patient relationship is formed. The use of information on this podcast or materials linked from this podcast is at the user's own risk. The content of this podcast is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Users should not disregard or delay in obtaining medical advice for any medical condition they may have and should seek the assistance of their health care professionals for any such conditions. Music Credit: Music by: bensound.com License code: MPTEUCI8DAXJOKPZ Music: bensound.com License code: FJQPPMCJLHEOYGQB Music: Bensound.com/royalty-free-music License code: KQAKMWSXIH3MJ4WX Music I use: https://www.bensound.com License code: 58NN4QOSKWJ7ASX9
What if your life was turned upside down by a diagnosis 20 years too late? Montel Williams—Emmy-winning TV icon, veteran, and health advocate—shares his decades-long struggle with undiagnosed Multiple Sclerosis (MS) and the journey that finally led to answers. After living with unexplained pain and inflammation for two decades, Montel took control of his health after receiving his MS diagnosis. Montel reveals the steps he took to manage his MS symptoms, reduce chronic inflammation, and reclaim his life—including his plant-based diet, embracing cannabis therapies, and even developing his Montel Living Well Blender. If you or someone you know has MS, this is the episode for you. Stay tuned for part 2 where we'll dive even deeper! HEALERS & HEAL-LINERS: Plant-based eating reduces inflammation: After switching to a plant-based diet, Montel saw a significant reduction in inflammation. He credits blending whole fruits, vegetables, and herbs like ashwagandha for boosting his body's natural defenses. Cannabis is medicine, not a trend: Montel has been a leading advocate for medical cannabis since 1999. Its anti-inflammatory and pain-relieving properties helped manage his chronic pain when other treatments failed Your Health Is in Your Hands. Doctors can provide guidance, but the real responsibility for managing your health rests with you. He shares how taking charge of his own wellness changed his life. -- HEAL SQUAD SOCIALS IG: https://www.instagram.com/healsquad/ TikTok: https://www.tiktok.com/@healsquadxmaria HEAL SQUAD RESOURCES: Heal Squad Website: https://www.healsquad.com/ Maria Menounos Website: https://www.mariamenounos.com My Curated Macy's Page: Shop My Macy's Storefront OUAI: https://theouai.com/ use promo code: HEALSQUAD for 15% off Nanit: https://www.nanit.com/ use promo code: DREAM20 for 20% off your first order Prenuvo: Prenuvo.com/MARIA for $300 off Montel Williams' Resources Instagram: https://www.instagram.com/montel_williams/?hl=en Books: https://www.barnesandnoble.com/s/%22Montel%20Williams%22?Ntk=P_key_Contributor_List&Ns=P_Sales_Rank&Ntx=mode+matchall ABOUT MARIA MENOUNOS: Emmy Award-winning journalist, TV personality, actress, 2x NYT best-selling author, former pro-wrestler and brain tumor survivor, Maria Menounos' passion is to see others heal and to get better in all areas of life. ABOUT HEAL SQUAD x MARIA MENOUNOS: A daily digital talk-show that brings you the world's leading healers, experts, and celebrities to share groundbreaking secrets and tips to getting better in all areas of life. DISCLAIMER: This Podcast and all related content ( published or distributed by or on behalf of Maria Menounos or Mariamenounos.com and healsquad.com ) is for informational purposes only and may include information that is general in nature and that is not specific to you. Any information or opinions provided by guest experts or hosts featured within website or on Company's Podcast are their own; not those of Maria Menounos or the Company. Accordingly, Maria Menounos and the Company cannot be responsible for any results or consequences or actions you may take based on such information or opinions. This podcast is presented for exploratory purposes only. Published content is not intended to be used for preventing, diagnosing, or treating a specific illness. If you have, or suspect you may have, a health-care emergency, please contact a qualified health care professional for treatment.
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