Beyond My Diagnosis with Michele Weston

Michele Weston

Welcome to Beyond My Diagnosis, the podcast that brings real conversations, real stories, and real breakthroughs in health, healing, and hope. I’m your host, Michele Weston—Holistic Health and Wellbeing Coach—and I'm here to help you look past the symptoms and into the deeper story of living with your chronic condition.Each week, we go beyond the chart and challenge the status quo of conventional care. From powerful patient journeys to expert insights in functional medicine and integrative practitioners, using mindset and lifestyle medicine, you’ll get the tools and inspiration to become the most informed, empowered version of yourself.This is not just about managing illness—it’s about reclaiming your health, your voice, and your life.Let’s get curious. Let’s get courageous. And let’s go Beyond My Diagnosis.

  1. 3d ago

    When Chronic Illness Interrupts Life: Michele’s Unexpected Hospital Stay

    Send us Fan Mail This episode of Beyond the Diagnosis was not the episode Michele planned to record. After spending several days in the hospital, Michele is finally home, and her friend Julie DeLucca-Collins has stepped behind the microphone for an unexpected podcast takeover. This time, instead of Michele asking the questions, Julie turns the conversation around and asks Michele what happened and what this experience has reminded her about living with a chronic condition. Michele shares how a long, hot day in New York was followed by a persistent headache that felt different from what she normally experiences. As the discomfort moved toward the eye where she had previously experienced optic neuritis, Michele knew she needed to pay closer attention. Her neurologist ordered blood work and a urine test, and concerns about dehydration and her kidney function eventually became part of a much larger medical evaluation. 50-Wellness Wednesday Julie DeLucca.txtTXT The conversation also explores the realities of managing more than one piece of your medical history at the same time. Michele has lived with MS for years and also has a history of bariatric surgery, which can make something as seemingly simple as drinking enough water more complicated. Julie and Michele talk about why general health recommendations still have to be considered in the context of the individual person and why patients need to be able to tell their healthcare professionals what is realistic for their bodies. Michele also shares what it felt like to become the patient again, including dealing with hospital safety protocols because of her drop foot and balance issues. She talks about the frustration that can come with losing some independence while also recognizing that the nurses caring for her have protocols they need to follow. One of the most personal parts of the conversation is Michele’s reminder that self-advocacy does not have to mean becoming adversarial. Even when she was tired, uncomfortable, and ready to go home, she tried to remember that the people caring for her were doing their jobs under difficult circumstances too. Now that she is home, wellness looks much simpler. It means seeing her dog, getting outside for a short walk, enjoying some fresh air, resting, and giving her body time to recover. Julie closes this special Wellness Wednesday conversation with a reminder that wellness practices do not always have to be complicated. A few minutes of intentional breathing, turning off notifications, listening to something calming, getting outside when you can, prioritizing sleep, or simply allowing yourself to rest can all be meaningful ways of caring for yourself. Going beyond a diagnosis does not mean pretending your diagnosis never affects your life. Sometimes it means knowing your body well enough to recognize when something has changed, communicating that clearly to your healthcare team, and accepting that there are moments when pushing through is no longer the right answer. What You’ll Hear Why Julie took over Michele’s microphone for this unusual episodeWhat happened before Michele ended up spending several days in the hospitalHow heat affects Michele personally when she is managing MSWhy the location and persistence of Michele’s headache concerned herHow her previous experience with optic neuritis affected the way she interpreted her symptomsWhy Michele’s neurologist ordered blood work and additional testingHow Michele’s history of bariatric surgery affects the way she approaches hydrationWhy knowing your own body is an important part of communicating with your healthcare teamWhat Michele experienced when hospital staff took additional precautions because of her drop foot and balance issuesWhy Michele believes kindness and self-advocacy can exist together in healthcareWhat Michele needed most when she finally came homeHow small wellness practices can support us when our bodies are asking for rest

  2. Sep 9

    Mindfulness, Mini-Meditations, and Chronic Illness: From The Archives

    Send us Fan Mail Mindfulness, Mini-Meditations, and Chronic Illness: A Healing Conversation with Simone Giangiordano In this episode of Beyond My Diagnosis, I talk with Simone Giangiordano, Compassion-Based Business and Lifestyle Coach and creator of the BalanceUP® Community. Simone joins me to explore the real, daily experience of living with chronic illness, and why mindfulness, mini-meditations, and self-compassion can change not only how we cope, but how we live. We talk about fatigue, fear, stigma, neuroplasticity, and the emotional layers of managing chronic illness in a world that doesn't slow down. Simone shares how contemplative practice helped her heal, how compassion reduces second-level suffering, and why mindfulness is not about perfection, but presence. In this episode, you will learn: • How mindfulness and mini-meditations help calm the nervous system • Why self-compassion is essential for anyone living with chronic illness • How neuroplasticity allows the brain to rewire emotional patterns • Why mindfulness reduces stress, stigma, and emotional overwhelm • Small, simple ways to bring awareness into daily tasks like walking, dishes, or brushing your teeth • How to use breath, intention, and presence to navigate pain and fatigue About Simone: Simone Giangiordano is a CCT Certified Instructor, chronic illness advocate, and the founder of the BalanceUP® Community. She teaches individuals how to build meaningful, sustainable lives and businesses that honor their health. Her signature program, The Power of I Can’t®, empowers people to find creative pathways around health limitations so they can flourish. Simone’s Links: 🌐 Website: https://www.simoneg.net 📄 Full Bio: https://drive.google.com/file/d/1Ck56wNRTAbFgjzVWdaLzzaVXDJ4OMMwj/view

  3. Sep 2

    Understanding Neurodivergence: How Different Brains Learn and Thrive with Lisa Richer

    Send us Fan Mail What if the problem is not that someone is unwilling to learn, communicate, or participate, but that the way we are asking them to do it does not work for their brain? In this episode of Beyond My Diagnosis, Michele Weston welcomes neurodivergent success partner and advocate Lisa Richer for a wide-ranging conversation about ADHD, autism, learning differences, late diagnosis, executive functioning, dysregulation, and what it really means to meet people where they are. Lisa was diagnosed with ADHD in her late 40s after spending decades wondering why certain expectations in school and the workplace felt so much harder for her than they seemed to be for everyone else. Her understanding of neurodivergence began even earlier as a parent. Both of her sons entered early-intervention services as toddlers, and their different learning and developmental needs eventually helped Lisa understand her own brain more clearly. Together, Michele and Lisa explore why taking notes, using captions, needing visual examples, avoiding eye contact, fidgeting, asking “why,” or requiring practical application are not signs that someone is lazy, disrespectful, or less intelligent. They may simply reflect a different way of processing information. Lisa also explains dysregulation and why behaviors such as shutting down, fidgeting, pacing, hand movements, or becoming overwhelmed can be signals that a nervous system needs support, not judgment. She shares a powerful story about realizing that requiring her autistic son to make eye contact actually made it harder for him to listen. The conversation moves from classrooms to workplaces, relationships, parenting, coaching, and leadership. Lisa challenges parents, educators, managers, and colleagues to replace assumptions with better questions: What do you need to be successful? What did you hear me say? What would help this make sense? This episode is ultimately about patience, with ourselves and with one another. Different brains learn differently. Different people communicate differently. And inclusion is not a once-a-year training or a checklist. It is the ongoing practice of creating environments where people can understand, contribute, and belong. If you have ever wondered why something that seems “easy” for one person feels impossible for another, this conversation may change the way you think about learning, communication, and success. Key TakeawaysDifferent does not mean less capable. A person can be highly intelligent and still need information presented in a different way. Memorizing something is not the same as understanding it, and understanding often improves when information is connected to practical application. Late diagnosis can reframe decades of experience. Lisa describes receiving an ADHD diagnosis in her late 40s and recognizing that many past workplace and learning struggles were not character flaws or a lack of intelligence. Learning preferences matter. Notes, captions, visual examples, hands-on practice, repetition, or extra processing time can help information become usable rather than simply heard. Eye contact is not a universal measure of listening or respect. Lisa shares that her autistic son found it harder to listen when he was required to make eye contact. The larger lesson is to avoid assuming one communication behavior works for everyone. Dysregulation can look many different ways. It may show up as fidgeting, shutting down, repetitive movements, visible anxiety, pacing, or escalating behavior. What helps one person regulate may not help another. Better questions reduce judgment. Instead of “Why don’t you get it?” Lisa encourages language such as “Tell me more,” “What did you hear me say?” or “What would help this make sense?” True inclusion is an ongoing practice. Lisa argues that inclusion cannot be reduced to a yearly training or checklist. It requires reflection, implementation, practice, evaluation, and a willingness to change systems and communication. Sometimes the best support is knowing when to hand off. Michele and Lisa discuss recognizing when a student, client, or employee needs a different kind of expertise rather than forcing one method to keep working. About Lisa RicherLisa Richer is a Neurodivergent Success Partner and Advocate who helps students, athletes, parents, professionals, schools, and organizations move from stuck to success. She is the creator of the Clarity | Confidence | Courage Journey Map™, which helps people identify internal, relational, and systemic roadblocks and build practical paths forward. Lisa combines professional experience in business, HR, career development, training, and neurodiversity consulting with more than two decades of lived experience parenting neurodivergent children and navigating her own late ADHD diagnosis. Her work centers on helping people better understand how they learn, process, communicate, and thrive. Connect with Lisa RicherJourney2Bloom Resources: https://journey2bloom.com/resources/ Instagram: https://www.instagram.com/journey2bloom/ LinkedIn: http://linkedin.com/in/lisa-richer-6040b74/ YouTube: https://www.youtube.com/@Journey2bloom Listener ResourcesCDC: ADHD in Adults Current information about how ADHD can present in adulthood, including organization, attention, restlessness, relationships, and workplace accommodations. https://www.cdc.gov/adhd/about/adhd-in-adults.html CDC: Autism Spectrum Disorder An overview of autism as a developmental disability involving differences in the brain, with wide variation in communication, learning, and support needs. https://www.cdc.gov/autism/about/index.html CDC: Autism Signs and Symptoms Includes information about differences in social communication, eye contact, movement, learning, and attention. https://www.cdc.gov/autism/signs-symptoms/index.html Job Accommodation Network (JAN) A practical U.S. resource for workplace accommodations and disability inclusion. https://askjan.org/ CHADD Education, advocacy, and support for people affected by ADHD. https://chadd.org/ Journey2Bloom Helpful Resources Lisa’s resource collection for parents, learners, educators, and professionals navigating neurodiversity and learning differences. https://journey2bloom.com/resources/ Know a parent, teacher, manager, coach, or colleague who keeps saying, “Why don’t they just get it?” Share this episode with them. Then visit Journey2Bloom to learn more about Lisa Richer’s work supporting neurodivergent students, families, professionals, and organizations.

  4. Aug 26

    When a Cough Isn’t Just a Cough: Living With Sjögren’s Disease with Julie DeLucca-Collins

    Send us Fan Mail What happens when a cough simply will not go away? In this episode of Beyond My Diagnosis, Michele Weston welcomes her friend, and fellow chronic-illness patient Julie DeLucca-Collins for a candid conversation about Julie’s journey to being diagnosed with Sjögren’s disease, a systemic autoimmune disease that can affect far more than the eyes and mouth. Julie’s story began around 2008 with a persistent cough. Antibiotics did not solve it. Allergy testing provided few answers. Visits to an ENT and pulmonologist still left questions. Then one physician looked beyond the cough. He asked about dry eyes, dry mouth, fatigue, and joint and muscle pain. Those questions eventually led Julie to a rheumatologist, additional testing, and a diagnosis that finally began connecting symptoms that had seemed unrelated. Today, Julie’s Sjögren’s journey includes managing chronic dryness, fatigue, respiratory symptoms and cough-variant asthma while learning to recognize the warning signs that tell her when her body needs her to slow down. Julie and Michele also talk about what it means to become an active participant in your healthcare rather than assuming one doctor has every answer. Julie shares why she researches, asks questions, seeks specialists when necessary, and pays attention to what her own body is telling her. The conversation becomes especially personal as Julie reflects on contracting COVID while already managing an autoimmune condition affecting her respiratory system—and the long road back after losing much of the strength and stamina she had worked years to build. But Julie’s approach to chronic illness is not centered on perfection. It is centered on progress. Her goal is not simply to grow older. It is to grow “wellderly”—stronger, healthier, more informed, and more intentional about the choices she can control. Your diagnosis may explain part of your story. It does not get to write the whole thing. In this episode: The symptoms that led to Julie’s Sjögren’s diagnosisWhy dry eyes and dry mouth were important cluesChronic cough and respiratory involvementLearning to advocate for yourself in medical appointmentsFinding doctors who listen and investigateRecognizing personal warning signs before a flareJulie’s experience recovering from COVIDExercise, yoga, strength and rebuilding after illnessCreating intentional margin in your scheduleProgress instead of perfectionWhy living beyond a diagnosis means asking, “What can I do today to help myself?”Key Takeaways Sjögren’s is more than dry eyes and dry mouth Sjögren’s disease is a systemic autoimmune condition. While dryness is common, patients may also experience fatigue, joint and muscle pain, neurological symptoms and respiratory involvement. A chronic dry cough can matter Sjögren’s can affect the throat, airways and lungs. Chronic dry cough and airway irritation are recognized respiratory manifestations, although every patient’s experience is different. Symptoms that seem unrelated may belong to the same story Julie initially viewed her cough, fatigue, dry eyes, dry mouth and body discomfort as separate concerns. A physician willing to look at the whole picture helped move her toward the eventual diagnosis. Self-advocacy does not mean rejecting medical care Julie works with physicians while asking questions, researching, seeking appropriate specialists and bringing information into appointments. Your body gives you information Learning personal warning signs can help someone decide when to slow down, seek care or adjust expectations before symptoms become more disruptive. Progress beats perfection Health does not require perfection. Julie focuses on what she can do today to support herself. Resources for Listeners Sjögren’s Foundation Patient education, symptoms, research, clinical guidelines and support. https://sjogrens.org/ NIDCR: Sjögren’s Disease Overview of symptoms, causes, diagnosis and treatment. https://www.nidcr.nih.gov/health-info/sjogrens-disease Sjögren’s Disease Signs and Symptoms A useful overview showing how systemic the disease can be beyond dry eyes and dry mouth. https://sjogrens.org/understanding-sjogrens/sjogrens-disease-signs-and-symptoms About Julie DeLucca-Collins Julie DeLucca-Collins is a business strategist, TEDx speaker, award-winning #1 bestselling author, podcaster, coach, and entrepreneur who helps women build profitable, sustainable businesses with greater clarity, confidence and visibility. After more than two decades in the corporate world, Julie founded Go Confidently Services and later co-founded Casa De Confidence Productions with her husband, Dan Collins. She is the author of Confident You: Simple Habits to Live the Life You Have Imagined and the host of the Casa De Confidence podcast. Julie is certified in the Tiny Habits® methodology and as a Thrive Global coach. In this episode, she steps away from her usual role as strategist and coach to share her personal experience living with Sjögren’s disease, advocating for her health, and learning to pursue progress rather than perfection. Connect With Julie Go Confidently Coaching: https://www.goconfidentlycoaching.com/ Julie’s Speaker & Author Website: https://juliegoconfidently.com/ Casa De Confidence Podcast: https://casadeconfidence.buzzsprout.com/ Apple Podcasts: https://podcasts.apple.com/us/podcast/casa-de-confidence-podcast-grow-your-business-life/id1510255268 LinkedIn: https://www.linkedin.com/in/goconfidentlyjulie/ Instagram: https://www.instagram.com/julie_deluccacollins/ Facebook: https://www.facebook.com/jdelucca TikTok: https://www.tiktok.com/@juliedeluccacollins YouTube: https://www.youtube.com/@JulieDeLuccaCollins/streams Pinterest: https://www.pinterest.com/juliedelco/ Confident You on Amazon: https://www.amazon.com/gp/product/B08PZHVJTC TEDx Talk: How Habits Give Us the Confidence to Dance in Life: https://www.youtube.com/watch?v=WrcJisG_wmc

  5. Aug 19

    You Can Do Hard Things: A Sister-to-Sister Conversation About Living With Chronic Illness

    Send us Fan Mail Living with chronic illness can make ordinary accomplishments invisible. Getting out of bed. Making it to an appointment. Going for a walk when your body would rather stay still. Asking a doctor one more question. Starting a new job. Finding the right job your body can tolerate. Choosing to try, again, after a difficult day. In this personal episode of Beyond My Diagnosis, Michele Weston welcomes her sister, Amy, for an honest conversation about chronic illness, family, mental health, work, medication management, stress, and learning to keep moving forward. Amy shares her experiences with gastroparesis, PCOS, insulin resistance, diabetes, chronic kidney disease, Graves’ disease, depression, and weight management. Michele reflects on living with multiple sclerosis, bariatric surgery, osteopenia, anxiety, mobility challenges, and the emotional impact of chronic illness. Together, they discuss why there is no competition in illness, why the right doctor-patient relationship matters, how work can provide purpose, and why asking for help is part of self-advocacy. They also explore the small choices that create momentum: going for a walk, keeping an updated medication list, tracking your mood, asking better questions, changing doctors when necessary, and recognizing that one difficult day does not define your future. As Amy says: “Living with chronic illnesses reminds me of making a layer cake, you may need to keep making room for more layers.” You can let chronic illness sit on top of you—or place it beside you and learn how to work it into your life. Your diagnosis may be part of your story, but it does not get to be the whole story. In this episode:  Living with multiple chronic conditions  Family support and honest communication  Mental health and depression  Work, purpose, and changing jobs  Medication management and multiple specialists  Finding doctors who listen  Personal experiences with GLP-1 medications  Building sustainable habits one step at a timeSubscribe to Michele’s free Substack at: https://micheleweston.substack.com/ Learn more about Michele’s coaching and patient advocacy work at: https://michelewestoncoach.com/ If this episode resonates with you, leave a review or share it with someone who needs to hear that they are not alone. This episode is intended for education and personal empowerment. It is not a substitute for medical diagnosis, treatment, or individualized advice. Always speak with a qualified healthcare professional before making changes to medications, treatment, nutrition, or physical activity.

  6. Aug 12

    Inflammation Myths, Part 2: What Should We Really Be Eating?

    Send us Fan Mail Inflammation is one of those words that can make eating feel complicated very quickly. Search social media for “anti-inflammatory diet” and you may find a growing list of foods you are told to avoid. Seed oils. Dairy. Nightshades. Sugar. Processed foods. Red meat. Fried foods. Before long, eating can feel like one more thing you are afraid to get wrong. But is that really what the science tells us? In Part 2 of her two-part inflammation series, Michele Weston continues the conversation from “Inflammation: The Good, the Bad and the Chronic” by asking a more useful question: What should we really be eating? Michele begins by returning to an important point from Part 1. Inflammation itself is not automatically the enemy. Acute inflammation is part of the body’s normal protective response to injury or infection. The concern is chronic inflammation, when inflammatory activity persists over time and may be associated with chronic health conditions. So the goal is not to eliminate every trace of inflammation from the body. The better question is how we can support our health and our body’s ability to regulate inflammatory processes. That brings us to food. Michele challenges the idea that a single food can magically cause chronic inflammation in everyone who eats it, or that a single “superfood” can switch inflammation off. Instead, she focuses on the overall pattern of what we eat and how that pattern fits our individual bodies, medical conditions, lifestyles, budgets, cultures, medications, activity levels, and health goals. For anyone living with chronic illness who has spent years trying to find the “perfect” diet, that distinction matters. The science is more nuanced than the headlines. Michele walks through foods and ingredients often labeled inflammatory and asks listeners to look beyond the blacklist. Red and processed meats are frequently included in discussions about inflammation and chronic disease. Refined carbohydrates and foods high in added sugars can be part of dietary patterns associated with poorer metabolic health. Fried foods and diets high in ultra-processed foods also raise important questions about nutrition. But context matters. One hamburger, French fry, dessert, or packaged food does not define an entire eating pattern. She also makes an important distinction between processed and ultra-processed foods. Processing alone does not automatically make a food unhealthy. Frozen vegetables, canned beans, plain yogurt, tofu, whole-grain crackers, and canned fish are examples of foods that undergo processing and can still fit into a nutritious eating pattern. Fresh, frozen, and canned fruits and vegetables can all be nutritious choices, with sodium and added sugars to watch for in packaged versions. The same individualized thinking applies to dairy and gluten. Lactose intolerance, milk allergy, celiac disease, and non-celiac gluten sensitivity are not the same thing. Some people may need to limit or avoid certain foods because of a diagnosed condition or individual symptoms. That does not mean the same restriction is appropriate for everyone. Then Michele tackles some of the biggest inflammation myths circulating online. Myth number one: Seed oils are inflammatory. Michele encourages listeners to look more closely at the evidence, the quantities consumed, and the foods in which these oils appear, rather than assuming the oil itself is responsible for every health concern. Current American Heart Association guidance does not support a broad avoidance of seed oils because they contain omega-6 fats. Myth number two: All processed food causes inflammation. Michele points to foods such as frozen fruits and vegetables, canned beans, canned fish, pre-washed lettuce, and tofu as practical examples. The word “processed” is not enough information to determine whether a food supports your goals. Myth number three: Everyone should avoid nightshades. Tomatoes, peppers, eggplant, and potatoes are frequently accused of causing inflammation. Michele reminds listeners that individual allergies or intolerances matter, but universal elimination rules are very different from personalized nutrition. Current evidence does not support routinely eliminating nightshade vegetables for everyone because of inflammation. Myth number four: Dairy is bad for everyone. For someone with a milk allergy or lactose intolerance, dairy may need to be modified or avoided. Other people tolerate dairy without difficulty. Personalization matters. Research reviews do not support the idea that dairy is inherently inflammatory for everyone. Myth number five: Sugar in any form is inflammatory. Michele distinguishes between added sugars and the naturally occurring sugars found in whole foods. A banana, an orange, or a handful of berries is nutritionally different from a doughnut or a sugar-sweetened drink. Rather than creating another rigid rule, she asks listeners to focus on the pattern over time. FDA nutrition labeling also distinguishes naturally occurring sugars from added sugars. So what does a supportive eating pattern look like? Michele explores Mediterranean-style eating, as well as the DASH and MIND approaches. What these patterns have in common is not one miracle ingredient. They emphasize combinations of nutrient-dense foods such as fruits, vegetables, whole grains, beans and legumes, nuts and seeds when appropriate, fish, adequate protein, and unsaturated fats such as olive oil and avocado. DASH is designed as a flexible, heart-healthy eating pattern, while research continues to examine the Mediterranean and MIND-style eating patterns in relation to brain health. They also leave room for real life. You do not have to swear off dessert forever, promise never to eat another hamburger, or throw away everything in your pantry. Instead, Michele asks practical questions: What are you eating most of the time? What foods make up the foundation of your meals? Are you getting enough fiber and protein? Are you eating a variety of plants? Are you choosing nutrient-dense foods regularly? Are you staying hydrated in a way that meets your individual needs? And most importantly, is the way you are eating sustainable for you? Because the best eating pattern is not necessarily the most restrictive one. It is one that nourishes you, supports your health goals, fits your life, and is realistic enough to continue. Food is also only one piece of the conversation about inflammation. Michele brings movement, sleep, and stress back into the picture. Walking, strength training, yoga, tai chi, resistance bands, and other sustainable forms of movement can all be part of self-care. Sleep and stress matter too, especially for people already navigating chronic illness. Even Michele’s beloved ginger tea gets put in perspective. A warm cup may be comforting, help with hydration, or create a quiet moment in the day. It is not a miracle cure for chronic inflammation, and it does not need to be. The goal is not perfection or fear, nor another list of 25 things you have to change by Friday. The goal is to become more informed about your body and make choices that are sustainable for you. If living with a chronic condition has made eating feel like another test you are constantly failing, Michele wants you to hear this: your body is not a textbook. Personalization matters. Your diagnosis may be part of your story, but it does not get to be the whole story. Listen to Part 2 of this Beyond My Diagnosis inflammation series and share it with someone who is tired of nutrition fear and conflicting food rules. Michele Weston’s Substack micheleweston.substack.com Michele Weston Coach michelewestoncoach.com

  7. Aug 5

    Root Cause Healing, Ayurveda, Functional Medicine, and Your Responsibility as the Patient

    Send us Fan Mail What if chronic illness is not just something to manage, but something to better understand? In this episode of Beyond My Diagnosis, Michele welcomes back Cindi Acree, RN, a lifelong nurse, educator, and integrative health advocate. With decades of experience in neonatal medicine and advanced nursing practice, Cindi has seen firsthand how Western medicine excels at acute care. But she also recognized its limitations when it comes to prevention, root cause healing, and long term vitality. After retiring from clinical practice, Cindi expanded her education into Applied Positive Psychology, Integrative and Functional Medicine, Yoga, and Ayurveda, the 5,000 year old sister science to yoga. She now blends biomedical knowledge with complementary and functional approaches to support sustainable health. This episode is a powerful reminder that doctors do medicine, but patients take care of patients. In this conversation, you will hear about: • The difference between biomedicine and integrative medicine  • Ayurveda and the three doshas, vata, pitta, and kapha  • Agni, the digestive fire, and why food combinations matter  • Ama, toxins in food, water, air, and daily products  • Ojas, vitality and resilience  • Functional medicine pillars, sleep, hydration, stress, and movement  • Why elimination diets can uncover hidden triggers  • The dangers of unregulated supplements  • Vitamin B12 excess and unintended consequences  • The microbiome and antibiotic recovery  • Forest bathing, grounding, and restorative movement  • Appreciative inquiry and positive reframing  • The power of coaching and asking better questions Cindi shares practical examples of root cause investigation, including cases where symptoms that looked like autoimmune disease were actually nutritional deficiencies or supplement overload. This episode is not about rejecting medicine. It is about expanding the lens. It is about asking better questions. It is about understanding your role in your own healing journey. Because it is your body.

  8. Jul 29

    Inflammation: The Good, the Bad and the Chronic | Part 1

    Send us Fan Mail Inflammation is one of the most misunderstood words in conversations about chronic illness. We hear it connected to autoimmune disease, arthritis, neurological conditions, gut health, nutrition, weight, sleep, mood, aging, heart health, and more. With so many warnings about “inflammatory” foods and habits, it can begin to sound as though all inflammation is dangerous. But inflammation is not automatically bad. In Part 1 of this two-part Beyond My Diagnosis conversation, Michele Weston begins with the question we need to answer before discussing how to manage inflammation: What is inflammation actually doing in the body? Acute inflammation is part of the body’s protective response. When you experience a paper cut, bee sting, sprained ankle, broken bone, cold, infection, or another injury, the immune system responds. Blood flow increases, immune cells move toward the affected area, and you may notice redness, warmth, swelling, or pain. These changes can be uncomfortable, but they are often part of the healing process. Acute inflammation shows up, does its job, and ideally settles down once the immediate threat has passed. Chronic inflammation is different. Instead of resolving, the inflammatory response remains active over time. The body continues sending signals and inflammatory cells, sometimes affecting healthy tissues and organs. Chronic inflammation can be associated with or play a role in many conditions, including cardiovascular disease, diabetes, obesity, certain cancers, arthritis, inflammatory bowel disease, and autoimmune disorders. For people living with autoimmune or neurological conditions, the conversation becomes even more complicated. Michele draws from her own experience living with multiple sclerosis and explains why inflammation cannot be reduced to one symptom, one food, or one lifestyle habit. In MS, the immune system mistakenly attacks myelin, the protective covering around nerve fibers in the central nervous system. That makes inflammation part of a much larger story involving the immune system, nervous system, symptoms, medical care, nutrition, sleep, movement, stress, and daily life. Michele’s central message is simple: the body is interconnected. Chronic inflammation is not always easy to recognize. Its possible signs can be vague and may overlap with chronic illness itself. A person may experience persistent fatigue, neurofatigue, low energy, pain, stiffness, disrupted sleep, digestive concerns, anxiety, depression, or changes in mood. These symptoms do not automatically prove that someone has chronic inflammation, but they can be part of a pattern worth discussing with a qualified healthcare professional. The episode explores how symptoms can begin feeding one another. Pain may interfere with sleep. Poor sleep may increase fatigue. Fatigue can make movement and exercise more difficult. Reduced activity and the stress of managing symptoms can affect mood, energy, and daily routines. Inflammation may disrupt sleep, while sleep disruption can affect circadian rhythms, the gut microbiome, stress, and immune function. It can feel like playing whack-a-mole with your health. You work on one issue, only to have another appear. This does not mean every symptom is caused by inflammation. It means the body’s systems do not exist in isolation. Michele also examines the relationship between the gut microbiome, diet, and immune function. Diet quality, fiber intake, ultra-processed foods, added sugars, refined grains, excess sodium, and some dietary patterns may influence the gut environment and overall health. At the same time, nutrition is only one part of a much larger picture that can include genetics, environmental exposures, microbiome imbalances, psychological stress, poor sleep, physical activity, smoking, medical history, and existing chronic conditions. That is why there is no single magic food that can erase a chronic inflammatory condition. People living with chronic illness are often handed oversimplified lists of foods to eliminate. One day it is seed oils. The next day it is nightshades, dairy, sugar, or processed foods. The rules change constantly, and social media often turns complicated health questions into fear-based headlines. Michele does not want listeners to fear food or believe that managing chronic inflammation rests entirely on personal willpower. She encourages people to become informed, notice patterns, ask better questions, and work with their physicians, registered dietitian nutritionists, and other qualified professionals when making decisions about treatment, nutrition, movement, sleep, smoking cessation, or symptom management. Helping yourself does not mean curing a chronic condition alone. It means taking a proactive role in your care while recognizing that medical conditions, bodies, and life circumstances are different. In this episode, Michele also discusses the emotional impact of chronic inflammation and chronic illness. Persistent pain, fatigue, and poor sleep can affect concentration, productivity, relationships, and quality of life. Depression and anxiety may become part of the experience, especially when symptoms are ongoing or unpredictable. These concerns deserve the same attention and compassion as physical symptoms. This first episode is not a list of foods to avoid. It is the foundation listeners need before trying to manage inflammation. In This Episode, You Will Learn Why acute inflammation is a necessary part of healingHow chronic inflammation differs from a short-term responseWhy chronic inflammation may be difficult to recognizeHow pain, fatigue, sleep, stress, mood, movement, and gut health can interactWhy autoimmune and neurological conditions make the conversation more complexWhy nutrition matters without being the entire answerWhy one “bad” food is unlikely to explain every symptomHow to approach inflammation with curiosity instead of fearDo I understand what inflammation is actually doing in my body? Could the symptoms I have been treating separately be more connected than I realize? Michele closes Part 1 with the message at the heart of this conversation: We do not need to fear inflammation. We need to understand it. That understanding prepares us for Part 2, when Michele will take on the endless list of foods people are told to fear and begin separating nutrition science from social media noise. Subscribe to Michele’s free Substack at MicheleWeston.Substack.com for personal insights, expert takeaways, and additional resources to help you stay informed, empowered, and one step closer to the clarity you deserve. If this episode helps you better understand your body, leave a review and share it with someone who may be overwhelmed by conflicting inflammation advice. Keep asking questions. Keep trusting yourself. And keep going Beyond My Diagnosis.

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About

Welcome to Beyond My Diagnosis, the podcast that brings real conversations, real stories, and real breakthroughs in health, healing, and hope. I’m your host, Michele Weston—Holistic Health and Wellbeing Coach—and I'm here to help you look past the symptoms and into the deeper story of living with your chronic condition.Each week, we go beyond the chart and challenge the status quo of conventional care. From powerful patient journeys to expert insights in functional medicine and integrative practitioners, using mindset and lifestyle medicine, you’ll get the tools and inspiration to become the most informed, empowered version of yourself.This is not just about managing illness—it’s about reclaiming your health, your voice, and your life.Let’s get curious. Let’s get courageous. And let’s go Beyond My Diagnosis.