Podcasts about invisible illness

Text Dr. Lenz any feedback or questions This episode deviates from the norm to feature excerpts from a heartfelt interview with Chuck Carroll, host of the Exam Room podcast, as shared on the Fit Vegan podcast. Chuck, known as the weight loss champion, opens up about his life beyond losing over 200 pounds and adopting a plant-based diet. He discusses his battles with fibromyalgia, chronic fatigue syndrome, and gut-brain interaction disorders, exploring how these conditions are often misunderstood and overlooked, particularly in men. The conversation delves into Chuck's personal struggles with addiction, severe binge eating, and the emotional rollercoaster that accompanied his journey towards better health. He provides insights into how stress and emotional turmoil exacerbated his condition, despite his diligent adherence to a healthy diet. This episode is particularly timely during fibromyalgia awareness month and aims to shed light on the intricate relationship between diet, mental health, and chronic illness.00:00 Introduction: Challenging Beliefs About Chronic Pain and Weight00:06 Meet Chuck Carroll: The Weight Loss Champion's Hidden Struggles02:39 Chuck's Early Life and Struggles with Food Addiction04:41 The Turning Point: Considering Gastric Surgery08:53 Life After Surgery: The Battle with Food Cravings09:29 Exploring a Plant-Based Diet for Recovery14:13 The Onset of Chronic Illnesses16:19 Navigating the Medical Maze: Searching for Answers17:27 The Role of Stress and Emotional Turmoil21:22 Living with Chronic Pain: Daily Struggles and Coping Mechanisms23:23 The Importance of Holistic and Compassionate Care32:24 Facing Public Scrutiny and Misunderstanding38:01 Finding Hope and Moving Forward38:46 Conclusion: A Message of Resilience and Support Click here for the Fibromyalgia 101 link.Click here to connect with Joy Lenz. Support the showWhen I started this podcast—and the book that came before it—I had my patients in mind. Office visits are short, but understanding complex, often misunderstood conditions like fibromyalgia takes time. That's why I created this space: to offer education, validation, and hope. If you've been told fibromyalgia “isn't real” or that it's “all in your head,” know this—I see you. I believe you. You're not alone. This podcast aims to affirm your experience and explain the science behind it. Whether you live with fibromyalgia, care for someone who does, or are a healthcare professional looking to better support patients, you'll find trusted, evidence-based insights here, drawn from my 28+ years as an MD. Please remember to talk with your doctor about your symptoms and care. This content doesn't replace personal medical advice.* ...

Margo is joined by business coach and podcast host Nikita Williams in a conversation on building a business—and a life—that honors your whole self. Living with multiple chronic illnesses, Nikita has learned how to redefine success, make peace with limitations, and turn her lived experience into a source of power and purpose. She and Margo explore what it looks like to craft a creative path that makes space for rest, joy, and authenticity—without burning out or hiding who you are. They discuss the real and raw journey of navigating health challenges as a creative woman of color, how podcasting became a lifeline and legacy, and the importance of building businesses based on actual capacity. Nikita invites listeners to rethink hustle culture and embrace the art of doing what you can, when you can—with intention, honesty, and hope.   Margo and Nikita discuss: How living with chronic illness shapes identity, business, and self-advocacy Turning your limits into superpowers—what resilience really looks like The unique layers of being a woman of color with invisible illnesses The three phases of chronic illness: “newbie,” awareness, and OG Designing a business around your capacity (not your ideal self) Why storytelling and being witnessed are critical for healing Moving from hustle to harmony: redefining productivity and rest Structuring your work and life to honor flare days and energy rhythms Managing comparison, creative permission, and celebrating your own pace Connect with Nikita: www.thrivewithnikita.com www.instagram.com/thrivewithnikita https://www.craftedtothrive.com/   Connect with Margo: www.windowsillchats.com www.instagram.com/windowsillchats www.patreon.com/inthewindowsill  

This week we're joined by Lili Higgins.On the outside Lil looks like she has everything - successful career, an incredible family, a beautiful smile and a strong social media following... but no one sees Lili's daily struggle. This isn't a story of tragedy, rather a story of maintaining hope and positivity through adversity.In this episode we break down what life looks like for someone struggling with a chronic illness, how to find healing through the pain and how we (as a society) can do better do support those struggling.Lili Higgins: @lilihigginss (insta) and @lilihiggins (TikTok)

When Grayson Murphy swapped from soccer to running in college, she never anticipated that she'd find such great success. Now a two-time world champion, the Montana-based runner has hard a whirlwind rise to success in sport — but that hasn't come without many hurdles. The most recent: A diagnosis with Crohn's Disease. In this week's episode, she shares how she's coping with the news and how the illness impacts her regularly.IN THIS EPISODE(5:07) The importance of grace to Grayson when it comes to her day-to-day(7:15) The symptoms that Grayson experienced that were indicative of Crohn's disease(9:36) How Grayson felt when she first learned about Crohn's(13:38) Grayson shares why she stopped playing soccer(20:40) What joy looks like for Grayson today(25:30) Grayson talks about starting her own stationary company, Wild Strides Paper Co.(28:55) How Grayson has navigated her grief and anger over the past year(35:53) Grayson talks about how finding early success in running was actually very difficult for her mentally(41:41) Grayson talks about severe pre-race anxiety, and how she had some pretty difficult intrusive thoughts before competing(48:10) Grayson talks about what she could see herself doing work-wise in the futureSOCIAL⁠@racin__grayson⁠⁠⁠⁠⁠⁠⁠@emilyabbate⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠@hurdlepodcast⁠⁠⁠⁠⁠⁠⁠OFFERSAG1 | Head to DrinkAG1.com/Hurdle to get a free vitamin D3K2 and five travel packs in your welcome kitBOSTON EVENTS: Live show with Des Linden at Brooks Hyperion House on 4/19, plus I'll be talking recovery at 10 a.m. with Kristina Centenari at the Birkenstock store on Boylston 4/20! For RSVP links, check out @emilyabbate stories on Instagram this week!JOIN: ⁠⁠⁠⁠⁠⁠⁠⁠THE *Secret* FACEBOOK GROUP⁠⁠⁠⁠⁠⁠⁠⁠SIGN UP: ⁠⁠⁠⁠⁠⁠⁠⁠Weekly Hurdle Newsletter⁠⁠⁠⁠⁠⁠⁠⁠JOIN: ⁠⁠⁠⁠The Daily Hurdle IG Channel⁠⁠⁠ASK ME A QUESTION: ⁠⁠⁠⁠⁠⁠⁠⁠Leave me a voice message⁠⁠⁠⁠, ask me a question, and it could be featured in an upcoming episode!⁠

He looked fine—until he wasn't. Just eleven weeks after sharing his struggles, Charlie was gone. In this powerful episode, Betsy Thibaut Stephenson reveals how depression lied to her son and why telling the hard truth is key to healing.In today's episode, I'm joined by Betsy Thibaut Stephenson, a writer, communications professional, and mother based in Alexandria, Virginia. After the unexpected death of her 21-year-old son, Charlie, by suicide, Betsy began writing as a way to process her grief, eventually shaping her reflections into the poignant and powerful book Blackbird. With decades of experience helping others find their voice, she now uses her own to break the silence around suicide, mental health, and the complexities of loss. Her work is grounded in compassion, clarity, and the belief that honesty is essential to healing—offering hope to anyone navigating the aftermath of profound sorrow.Throughout this episode, Betsy brought those same qualities—honesty, courage, and clarity—to the forefront as she reflected on her family's decision to be fully transparent about Charlie's death. She shared how that openness not only helped their loved ones support them more effectively, but also created space for deeper community understanding. We explored the deceptive nature of depression, the emotional and physical toll of grief, and how writing became a lifeline in her healing journey. Betsy also discussed the structure and purpose behind Blackbird—a collection of short, digestible entries designed to meet grieving readers where they are. Her reflections serve as a powerful reminder that telling our stories, even when painful, can become a vital source of strength and connection.Tune in to episode 326 as Betsy Thibaut Stephenson shares how embracing openness, writing through sorrow, and honoring her son Charlie's life helped her navigate the depths of grief and find a path toward healing and connection.In This Episode, You Will Learn:Choosing radical openness after suicide (01:33)Making sense of an incomprehensible loss (06:31)“The brain lies to you” - Understanding depression (9:11)Letting go of guilt while living with it (12:51)Why and how she wrote Blackbird (15:20)Coping with loss and moving forward (17:48)Grief and the fog of memory (21:01)The book she needed but couldn't find (23:00)The hard things need to be said (31:30)Connect with Betsy Thibaut Stephenson:WebsiteInstagramLinkedInFacebookGet Betsy's book!Let's Connect:WebsiteLinkedInFacebookInstagramTwitterPinterestThe Grief and Happiness AllianceBook: Emily Thiroux Threatt - Loving and Living Your Way Through Grief Hosted on Acast. See acast.com/privacy for more information.

SummaryIn this conversation, Jess shares their journey of writing the book 'Being Sick Enough', which explores themes of invisible illness, childhood trauma, and the complexities of living with chronic conditions. The discussion delves into the challenges faced as a sick child, the misunderstandings surrounding invisible illnesses, and the process of writing personal stories while navigating relationships and self-acceptance. In this conversation, the speakers delve into the complexities of navigating trauma, the importance of meditation, and the intersection of medication and wellness. They discuss the significance of honest conversations about medication, the balance between solitude and community, and the role of spirituality in personal healing. The dialogue also touches on societal challenges and the need for empathy, as well as practical travel tips for those with chronic illness.Keywordsinvisible illness, chronic illness, trauma, writing, personal stories, mental health, self-acceptance, authenticity, healing, Jess, trauma, meditation, wellness, medication, spirituality, empathy, chronic illness, travel tips, community, solitude Hosted on Acast. See acast.com/privacy for more information.

Joe is joined by Michele Roys, ahead of the launch of her book: But You Look Just Fine: My Journey to Rediscover Joy Amidst Chronic Pain and Invisible Illness, where she discusses the struggles she faces daily as someone suffering from an invisible illness Hosted on Acast. See acast.com/privacy for more information.

Here's what to expect on the podcast:Marisela's journey from young immigrant to successful entrepreneur and community advocate.SCDS symptoms, available treatment options, and its impact on Marisela's daily life and work.How Marisela inspires others to become entrepreneurs.What readers can expect from Hispanics and Latinos in Vallejo.And much more! About Marisela:Marisela Barbosa is a serial social entrepreneur and community catalyst renowned for her unwavering dedication to driving positive change. With a career marked by innovative ventures, she has demonstrated a passion for leveraging entrepreneurship to address critical societal issues.As a community catalyst, she has spearheaded initiatives that tackle challenges head-on, delivering sustainable solutions that empower individuals and communities. Her commitment to education, community engagement, civic participation, and sustainable business development is a testament to her determination to create a better world.Marisela is also a published author of "Hispanics and Latinos in Vallejo" and has been featured by numerous news organizations. She is the recipient of several awards and enjoys bird watching, as well as cherishing time with her husband, two daughters, and two beloved dogs. Connect with Marisela Barbosa!Websites: https://www.mariselabarbosa.com/ | https://www.thetimeisya.com/Email: marisela@thetimeisya.comInstagram: https://www.instagram.com/thetimeisya/LinkedIn: https://www.linkedin.com/in/mariselabarbosa/ Book Available on Amazon:Hispanics and Latinos in Vallejo (Images of America) https://tinyurl.com/44pahfn5-----If you're struggling, consider therapy with our sponsor, BetterHelp.Visit https://betterhelp.com/candicesnyder for a 10% discount on your first month of therapy.*This is a paid promotionIf you are in the United States and in crisis or any other person may be in danger -Suicide & Crisis Lifeline Dial 988----- Connect with Candice Snyder!Website: https://www.podpage.com/passion-purpose-and-possibilities-1/Facebook: https://www.facebook.com/candicebsnyder?_rdrPassion, Purpose, and Possibilities Community Group: https://www.facebook.com/groups/passionpurposeandpossibilitiescommunity/Instagram: https://www.instagram.com/passionpurposepossibilities/LinkedIn: https://www.linkedin.com/in/candicesnyder/Shop For A Cause With Gifts That Give Back to Nonprofits: https://thekindnesscause.com/Fall In Love With Artists And Experience Joy And Calm: https://www.youtube.com/@movenartrelaxation

The newest episode of The Chemical Sensitivity Podcast is available now! It's called “Illnesses You Have to Fight to Get.” It features a conversation with Melina Sherman, Ph.D. Melina is a critical science and health communication scholar and Visiting Assistant Professor at Fairfield University in Connecticut in the U.S. You'll hear Melina explore how:·      People with chronic illness are often “invisibilized” by Western medicine.·      The medical system is not able to address illnesses caused by environmental toxicants.·      People with MCS and other illnesses often create community online to support one another and lobby for change.·      And more!Thank you for listening!   Please subscribe where you get your podcasts and leave a review. It helps others find the podcast.Melina Sherman:https://melinasherman.com/  #MCSAwareness #MCS #MultipleChemicalSensitivity #TILT #MultipleChemicalSensitivityPodcast DISCLAIMER: THIS PROJECT DOES NOT PROVIDE MEDICAL ADVICE  The information, including but not limited to, text, graphics, images, and other material from this project are for informational purposes only. None of the material is intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health care provider with any questions you may have regarding a medical condition or treatment and before undertaking a new health care regimen, and never disregard professional medical advice or delay in seeking it because of something you have heard or read from this project. Support the showThank you very much to the Marilyn Brachman Hoffman Foundation for its generous support of the podcast.If you like the podcast, please consider becoming a supporter! Support the podcast. Find the podcast on Patreon. If you like, please buy me a coffee. Follow the podcast on YouTube! Read captions in any language. Please follow the podcast on social media:FacebookInstagramXBlueSkyTikTokSponsorship Opportunites Are you an organization or company interested in helping to create greater awareness about Multiple Chemical Sensitivity and Chemical Intolerance and/or looking for sponsorship opportunities? Please email us at info@chemicalsensitivitypodcast.org

Amanda joins me on the show this month to deep dive into the life of the zebra - AKA invisible illness. I have an official diagnosis for a connective tissue disorder called Ehlers Danlos Syndrome (EDS). Amanda shares the same disorder just minus the official diagnosis, so this show really dives deep into the similarities and uniqueness people with chronic illness share. We touch on all kinds of topics from being super bendy (but somehow also super stiff??), pushing through the pain and usually overdoing it, mental health and its connection to physical health, and the importance of clutter piles in our lives.1 in 20 people have a rare disease - EDS is one of them, affecting an estimated 1 in 5000. It is also one of the most misunderstood and under-diagnosed disorders and having real conversations about the reality of living with it is a great way to help change that. I also touch on my Everesting for EDS Fundraiser - I am raising $29,029 for EDS research this year while I prepare for the 29029 Everesting Event in Stratton Vermont this October (DONATE AND FOLLOW HERE!!).I hope you enjoy this episode - it is one of my personal favorites! Send us a text

I'm thrilled to welcome back Jessica Graham, an incredible author, trauma expert, and meditation teacher, to talk about their brand-new book, Being (Sick) Enough: Thoughts on Invisible Illness, Childhood Trauma, and Living Well When Surviving is Hard. If you've ever felt the weight of trauma, chronic illness, or just navigating life in a challenging world, Jessica's wisdom will resonate deeply. In this conversation, we explore the complexities of healing, mindfulness, and finding balance in a world that often feels overwhelming. After listening, my hope is that you'll walk away with not only a better understanding of the connection between trauma and physical health but also actionable insights for living well—even when surviving feels hard. What you'll hear: What sparked Jessica's new book and how it supports those navigating trauma and chronic illness (17:52) Why we often need science to trust ourselves and what that reveals about healing (21:29) The science of “limbic resonance” and how rewiring our attachment systems can transform relationships and choices (26:48) How mindfulness isn't a one-size-fits-all practice (31:59) Jessica's journey of coming out as nonbinary and finding healing through alignment (37:27) Strategies for living well in a world full of political, environmental, and societal challenges (48:55) Plus, a coaching episode update on Christina about getting out of her comfort zone! (58:11) Resources: Join me for free group coaching calls on January 21st and January 23rd! Private Coaching with Andrea Jessica's website Episode 643: Sexuality and Spiritual Awakening Jessica Graham Episode 623: Gene Keys, Personal Discovery, and Purpose with Tracie Cornell Andrea's psychedelic therapy private podcast feed Episode 648: Coaching session w/ Christina on getting out of her comfort zone Book recommendations: I love a good personal development book, and you do too, right? I've compiled a list of book recommendations, as mentioned in past episodes. Check out these amazing book recommendations here. Happy reading!   MSN is supported by: We love the sponsors that make our show possible! You can always find all the special deals and codes for all our current sponsors on our website: andreaowen.com/sponsors/ Episode link: http://andreaowen.com/652 Learn more about your ad choices. Visit megaphone.fm/adchoices

TLDR: Kee had words with a pharmacist, one step forward...three steps back, and something nice for your girls. How do you balance being positive while grieving the body you once had? How can you move forward when an invisible illness leaves you feeling stuck? And how common is chronic illness, really? This week, Kee and Lucy support Anon through a mental and physical rough patch. SUBMIT YOUR MELTDOWN THINGS WE MENTIONED: ABS: Key findings on long-term health conditions and chronic conditions, and prevalence in Australia Bras N Things HOSTS & PRODUCERS Lucy Neville / @lucymneville⁠ Kee Reece Searles / @keereece AUDIO PRODUCTION: Emmeline Peterson ARTWORK: Hollie Dempsey THEME SONG:  Extra Fries By The Fly Guy Five (Epidemic Sound) The content of this podcast is general and anecdotal, not professional, and intended for entertainment purposes only. We acknowledge the Gadigal people of the Eora Nation, the Traditional Custodians of the land we record on, and pay our respects to their Elders past and present.

Send us a textIn this episode, Crystal and Samantha explore the concept of "hidden agreements"—the unspoken stories we believe about what needs to happen for us to be happy, okay, or fulfilled. While they often go unnoticed, these stories weigh us down and create a lot of unnecessary suffering.We discuss... What "hidden agreements" are and how they show up in our livesWhy tying our happiness to specific outcomes leads to unnecessary sufferingHow to get curious about the agreements we've made with ourselvesPractical examples of living with more lightness, even in the face of chronic illness or life's challengesThis episode reminds us that life doesn't needs to go a particular way for us to experience joy, peace, and contentment.Links Mentioned:Caffeine for the Soul Episode: "Would You Sign That Contract?"Connect with Us:Follow us on Instagram and Facebook for more insights and updates.Join our free Patreon community to leave a comment about this week's episode. Support the Show:If you enjoyed this episode, please share it with a friend or leave us a rating and review wherever you're listening—it's the easiest way to help others discover the podcast.We'd also love for you to join our Patreon. Free subscribers gain access to bonus content, personal updates, polls, and more. Support the show

https://renegadehealthboss.comIn episode 138 Heather Gray FDN-P  welcomes Lynne McTaggart . Lynne McTaggart renowned author and researcher whose groundbreaking work has transformed the way we understand healing and consciousness. Lynn takes us through her journey from investigative journalism to pioneering the science of intention and healing. She shares the story behind her book The Field and how it uncovered a new understanding of human energy and the power of thoughts.In this podcast you will discover00:00 Heather Gray FDN-P welcomes Lynne McTaggart  renowned author and researcher03:42 Lynne's transition from investigative journalism to exploring alternative health practices 06:53 Discovering the science of human energy fields and the breakthrough that led to The Field.08:11 The creation of the Intention Experiment and large groups of people can heal through collective intention.13:04 The evolution of The Power of Eight and small groups can create miraculous healing effects.15:13 Lynne shares transformative healing stories, including individuals overcoming paralysis16:27 Lynne's personal experience with hip dysplasia and her recovery journey through alternative treatments.21:19 The power of group dynamics collective intentions can lead to remarkable healing outcomes25:42 The conversation turns to the emotional power of group healing, including a touching story of a man named Jerry28:12 Lynne explains the groundbreaking brainwave studies on group healing30:52 The profound idea that we are all part of the healing field is explored, emphasizing the sense of oneness 31:57  Lynne shares inspiring stories of life-changing results from their courseThank you to our amazing sponsors, without them our podcast would not be possible.  n1o1 Nitric Oxide by Dr.Nathan BryanMHP VitaminsPlease learn more about our sponsors here.https://renegadehealthboss.com/sponsors/Guest Bio: Lynne McTaggart is a leading authority on science and consciousness, the award-winning author of seven books, including The Intention Experiment and The Field. She is the architect of the Intention Experiments and was featured in Dan Brown's The Lost Symbol. Lynne is a highly sought-after speaker and documentary participant, with appearances in What the Bleep?! and The Living Matrix. She is also the co-owner and editorial director of What Doctors Don't Tell You, a respected health magazine in 14 languages.To learn more, visit https://lynnemctaggart.com/courses/your-intentional-future/From nutrition and stress management to restorative practices, this ebook is your essential companion for a balanced and vibrant life. Perfect for anyone looking to make lasting changes to their health and well-being, this guide empowers you with the knowledge and tools needed to take control of your health naturally. Start your healing journey today FREE mini eBook [Foundations of Health]https://rhbcourses.com/products/free-mini-ebookGet the Foundation of Health Course here. Lose the brain fog, have more energy, and get your gut working right. https://rhbcourses.com/discount/ACTION this link saves you $100 on the course.#PowerOfIntention #TransformationThroughIntention #EnergyHSend us a textGet Transcripts here https://drive.google.com/drive/folders/1rIazw0fXYfj5_bkR_W8EuywI5sVJ3VYg?usp=drive_link

Amy Kurtz is the author of the trailblazing book Kicking Sick: Your GO TO GUIDE for Thriving with Chronic Health Conditions, a health and wellness coach, patient advocate, and speaker. Facing debilitating pain and health issues since her teenage years, patient advocate and author Amy Kurtz well knows the frustration, fear and isolation that comes with chronic illness. Life long Chronic Health Conditions – from Celiac Disease to major parasite infections to a thyroid condition– led Amy on an intense journey through doctors' offices, medical clinics, IV labs, specialist offices and assorted spiritual communities. Through these experiences – the trials and the errors, Amy learned the importance of identifying her individual needs and putting a team together to support the whole of her body/mind/spirit. She became an active participant in her own health and got more involved, educated and invested in the healing process. She supports her clients in finding the right system so they can focus on healing instead of being mired in managing their care. Prior to starting her private practice, Amy built the health coaching program at The Morrison Center, a top integrative practice in NYC as a means of better supporting the patient by providing individualized guidance regarding their health condition and treatment plan. Key Topics: - Amy's story about healing from chronic disease - How to advocate for yourself when you know something isn't right - How to give yourself permission to empower yourself - The importance of making the mind-body connection - The process of moving from victim to empowered advocate - How to go slowly and trust your gut instinct - How to calm the inner critic and stay in the driver's seat You can learn more about Amy and get her book at amykurtz.com and on Instagram at @amykurtz. Sign up for Erin's monthly tips and recipes here: https://mailchi.mp/adde1b3a4af3/monthlysparksignup

Join Dr. Danielle and Aria as they dive into the complexities of invisible illness—conditions that aren't apparent to others but deeply impact those who live with them. From personal stories of navigating Hashimoto's, Lyme disease, and hypermobility to offering practical advice on advocating for yourself and building a support system, this episode is a compassionate guide for anyone feeling unseen or misunderstood. Whether you're battling an invisible illness or supporting someone who is, you'll find validation, encouragement, and actionable steps toward healing.SERVICES & MEMBERSHIPS:

A Connecticut lab is embarking on a groundbreaking initiative to study endometriosis, a painful condition that impacts people with a uterus. Endometriosis is just one of the many invisible illnesses that impact an estimated 10% of the American population, according to Disabled World, an independent Health and Disability news source. This hour, we talk about why invisible illnesses are difficult to diagnose and how scientists are trying to change that. GUESTS: Michayla Savitt, State Government Reporter, Connecticut Public Jennifer Crystal, Author of “One Tick Stopped the Clock” Kelsi Carolan, Assistant Professor and licensed clinical social worker, University of Connecticut Support the show: http://wnpr.org/donateSee omnystudio.com/listener for privacy information.

Author Kate Weinberg has adapted her personal ordeal of living with long Covid into a funny and philosophical novel There's Nothing Wrong With Her. 

On this episode of the Another Way To See It podcast, we talk about living with a chronic invisible illness. This vulnerable episode is a reach toward others who may be experiencing life with these challenges, and toward others who may live with or know someone experiencing symptoms of chronic illness. How do we see our suffering? How do we use our pain? Do you want to recover from or learn through? All this and more on today's episode. We always love to hear from you, reach out:https://www.instagram.com/anotherwaytoseeitpodcast/Support our show:   https://www.buzzsprout.com/1694878/supporters/new Coaches: Kim Moranhttps://www.kimmorancoaching.com/https://www.instagram.com/kimcalifornia/ Tracy Holemeyerhttps://www.uncontrollablyme.com/https://www.instagram.com/uncontrollably_me/ Produced by: Kim MoranMusic: A Rush of Inspiration by Evan Mac Donald  Support the show

Today on Where We Live, a Connecticut lab is embarking on a groundbreaking initiative to study endometriosis, a painful condition that impacts people with a uterus. Endometriosis is just one of the many invisible illnesses that impact an estimated 10% of the American population, according to Disabled World, an independent Health and Disability news source. This hour, we talk about why invisible illnesses are difficult to diagnose and how scientists are trying to change that. GUESTS: Michayla Savitt, State Government Reporter, CT Public Jennifer Crystal, Author of “One Tick Stopped the Clock” Kelsi Carolan, Assistant Professor and licensed clinical social worker, University of Connecticut Support the show: http://wnpr.org/donateSee omnystudio.com/listener for privacy information.

In today's episode, Elizabeth sits down with Hannah Kleinfeld, COO of Omni-Biotic U.S., to discuss all things gut health: from Hannah's healing journey from tick born diseases, to leaky gut, the role of the microbiome and antibiotic repair. Hannah has become a gut health authority and an inspiration to many health seekers; she has a BA from Yale, an MBA from Harvard, and worked in healthcare consulting for McKinsey before spearheading the launch of Omni-Biotic in the U.S. After being diagnosed with Lyme Disease after months of struggling with mysterious and debilitating symptoms, Hannah's healing journey, following extensive antibiotic treatment, required a complete overhaul of her gut health. This commitment not only gave her a new lease on life, working wonders in the management of her lingering symptoms, but also led her to dedicate her career to helping others access the transformative power of healing via the gut.The two discuss the gut brain axis & connection between gut health and mental health, as well as all your frequently asked probiotic questions, like when to take it, if refrigeration matters and how to navigate them simultaneously with antibiotics. Omni-Biotic, Europe's leading probiotic and a brand rooted in 30 years of gut microbiome research & clinical testing, changed the game for Hannah (and Elizabeth). Enjoy!Hannah's IG: https://www.instagram.com/hannahxkleinfeld/Omni-Biotic IG: https://www.instagram.com/omnibioticlife/?hl=enShop Omni-Biotic (code: PROCESS for 15% off!): https://omnibioticlife.com/For additional, weekly tea-filled episodes, join the TWP PatreonFollow us on Instagram: www.instagram.com/wellnessprocesspodFollow us on TikTok: https://www.tiktok.com/@thewellnessprocessProduced by Peoples Media Hosted on Acast. See acast.com/privacy for more information.

Spotlighting up and coming comics creators is one of my favorite things to do. And this one comes highly recommended by a friend of the show! Today, artist Ryan Oakley joins the podcast to talk about her art career, inspirations, and why she REALLY wants to break into mainstream comics. About Ryan:Born in Los Angeles, California and raised in Greensboro, North Carolina, Ryan Oakley is a 2016 graduate of Wake Forest University with a B.A. in Studio and Spanish. She is a multimedia artist creating anything from digital works of art and logos to traditional drawings and oil paintings. She is inspired by comic book art and diverse and strong women, which is often reflected in her work.In 2018, Ryan was 1 of 50 artists selected out of 3,000 submissions for Power to the Polls, a national voter registration drive and traveling art exhibitions. This led to a commission to create women's rights posters for NARAL: Pro-choice America and Unite for Justice for their national day of action August, 26, 2018.Currently, Ryan has been immersing herself and learning about the comics industry. She recently had a piece featured in the back of the comic book Bitter Root (Issue #3) and has a short comic in the anthology Invisible Illness.Follow Ryan on Instagram: @ryanoakleyart For More from Comics Are Dope:Get This Week in Comics, our weekly e-mail newsletter: http://thisweekincomics.comSubscribe on YouTube: http://youtube.com/@comicsaredopeJoin our online Discussion Communities:Facebook - http://bjkicks.link/communityDiscord - http://bjkicks.link/discord

This week's “How She Finds Purpose” insight comes from Diana Daniele. She says - We are helping others and that our words are like pearls to them. “There's a danger with everyone turning to you where you feel like you're giving, giving, giving, and you're kind of giving yourself away and that you don't have any time just for you because people are kind of knocking down your door, and you have to figure out your own path. But I think if we women see that when someone's turning to us, that that is empowering and that we are helping others and that our words are like pearls to them and they are holding them and they are beholding them and treasuring them, that there's a lot of bang for that buck.” Diana is a tireless advocate for invisible illness and mental health, and she is a writer and publicist living in Los Angeles. And in addition to writing about mental health and invisible illness, she writes about female friendship and family dynamics for publications like Newsweek and Business Insider. Diana is also currently writing a book entitled Damn Girl. It's a miraculous memoir of motherhood, migraine, and madness, which was recently long listed in the Tall Poppy Writers Contest. In this episode we discussed: her miraculous healing of chronic migraines and hearing of her resilience and the power of never giving up on yourself how Diana's insights about living with invisible illness led to her advocating for mental health, especially among adolescents the importance of women supporting women and nurturing those female friendships that help us through any life challenges ‌ Connect with Diana at: Instagram: https://www.instagram.com/DianaDanielePR Would you prefer to watch or listen to the podcast on YouTube?Head on over to https://www.youtube.com/@leadershippurposepodcast   Want to connect? Connect with Dr. Robin on  LinkedIn: https://www.linkedin.com/in/robinlowensphd/ Facebook: https://www.facebook.com/robinlowensphd Instagram:  https://www.instagram.com/robinlowensphd/ Email: Robin@LeadershipPurposePodcast.com   Thank you for listening! Rate, review, & follow on Apple Podcasts or your favorite podcast player. Talk to you soon!   This episode was produced by Lynda, Podcast Manager for GenX Creative Entrepreneurs at https://www.ljscreativeservices.co.nz

We have officially been a podcast for 3 years and 125 episodes! On this episode, we are talking with Diana Daniele.  Diana is a tireless advocate for invisible illness and mental health.  She endured years of chronic migraine and depression before finding healing.  Diana writes about invisible illness, mental health, female friendship, and family dynamics, contributing to various publications.  She is also a sought-after publicist for luxury brands.  Diana is a pirate at heart with a make-it-happen attitude. Where to find Diana: Website: dianadanielepr.comIG: @dianandanielepr * * * If you are enjoying Pirate Living Podcast and all the content we bring to you each week, you can support us and buy us a coffee at ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://www.buymeacoffee.com/pirateliving⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠. Other ways you can show your support:  Subscribe/Follow Pirate Living Podcast, Rate and Review our show, Share the podcast with your friends Grab your Pirate Living Guidebook to Start Your Pirate Life here: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://www.blurb.com/bookstore/invited/9817705/e9d00fd5eafd109a68b9eb4381f9d981c86f164f⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ You can find us on Instagram ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠@piratelivingpodcast⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ to keep up with the latest episodes, awesome guests, and bonus clips. Pop in and say hi, we love chatting with fellow pirates.    Ask Caron about her online nutrition program and the in person programs she's creating for teens.  For the little pirates in your life, check out Kristin's Books ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Abracadabra I Know What to Do⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠, ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠My Words Are My Wand⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠, and ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠My Wins Journal⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ on Amazon or her ⁠⁠⁠⁠⁠⁠Emotions Toolkit at ⁠⁠⁠⁠⁠⁠⁠⁠⁠www.kristinjoycoaching.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠.  And keep creating good trouble. To show your pirate spirit and create good trouble, visit our merch shops: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Pirate Living Podcast Shop⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ and ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠TeePublic⁠⁠⁠⁠⁠⁠⁠.

Have you ever met someone whose resilience in the face of adversity not only defines them but also uplifts those around them? Meet Candi—a beacon of strength, grace, and determination, balancing being a mom, and active community-volunteer, with the reality of battling five autoimmune disorders. Our latest episode introduces you to this remarkable individual, whose story will grip your heart and inspire your spirit. Candi reveals how pageantry became her refuge, a place where camaraderie triumphs and women empower one another amidst life's relentless demands. Her candid reflection on living with conditions like Crohn's Disease and Fibromyalgia is a vivid illustration of the grit required to face invisible battles while maintaining a semblance of normalcy.Please be sure to checkout our website for previous episodes, our psych-approved resource page, and connect with us on social media! All this and more at www.thelylaspodcast.com

Lyme disease is a serious illness that can have debilitating symptoms, but it is often misdiagnosed or ignored. In this video, Dr. Brad Montagne, PSc.D., a leading expert on Lyme disease, exposes the truth behind this invisible illness. Dr. Montagne will discuss the following: What is Lyme disease and how is it transmitted? What are the symptoms of Lyme disease? Why is Lyme disease so often misdiagnosed? What are the latest treatment options for Lyme disease? What can be done to raise awareness of Lyme disease and improve the lives of those affected? If you or someone you know has been struggling with Lyme disease, this video is a must-watch. Dr. Montagne's insights and advice will give you hope and help you on your journey to recovery. #lymediseasetreatment #invisibleillness Dr. Brad Montagne, PSc.D., #symptoms #diagnosis #treatment #awareness #recovery Share this video with your friends and family to help raise awareness of Lyme disease. If you have any questions or comments, please leave them below. Get your first FREE individual session at https://calendly.com/ejwcoaching/timewithedna. --- Send in a voice message: https://podcasters.spotify.com/pod/show/keepingitrealonpurpose/message

Nelly Thomas is a multi-talented comedian, author and broadcaster. She has her own podcast called 'Dear Nelly', she's won the national RAW comedy award and she happens to be a great mate of Yvie's.  But she's also raising two daughters who have invisible illnesses. She speaks to Yvie about her journey to diagnosis with her kids, the similarities her daughter and Yvie have with their illnesses and what she's learnt from them.  Nelly also shares how she went through a divorce during Covid and what differences she's found between dating men and women.  LINKS Yvie Jones @yvie_jones Nelly Thomas @nellythomascomedian Nova Podcasts Instagram @novapodcastsofficial Don't forget you can ask us a question anytime by emailing twogirls@novaentertainment.com.au Listen to Nelly's chat with Reuben Kaye here; https://shows.acast.com/638d32ebc48dee0011541fd3/646ca2b02c81c5001139723a  CREDITSHost: Yvie Jones Guest: Nelly Thomas Executive Producer: Rachael Hart Supervising Producer: Ricardo Bardon Show Artwork By: @ellymalone Find more great podcasts like this at novapodcasts.com.au Nova Entertainment acknowledges the traditional custodians of the land on which we recorded this podcast, Wurundjeri people of the Kulin Nation, and the Gadigal people of the Eora Nation. We pay our respect to Elders past and present. See omnystudio.com/listener for privacy information.

Episode 355 - Sara Bohling - When Grit and Grace Collide - Persevering Through Life's Challenges With Grit and God's GracePrematurity. Perseverance. Invisible Illness. Faith.See how these elements collide in an inspiring true life story. Nurse turned patient; fighting rare and invisible illness. It is filled with determination, love, community and hope.Come along on the journey, to witness the power of God and finding joy amidst challenging circumstances.The author is a wife, mom and nurse with 20 years experience. She bravely shares some of her life's challenging moments- providing vulnerability, honesty and encouragement to her readers about what life is like when the road isn't always easy. From weighing 2 pounds at birth, to later being shunned by medical providers who were unwilling to take a deeper look into her invisible illness. Her raw relationship with God during this time and finding hope & joy in unexpected places. This is a journey you surely don't want to miss!Sara BohlingAuthor/Nurse/Wife/MomI'm a wife, Mom to 2 daughters and a sunset enthusiast. I'm Nurse with 20 years experience- Neonatal bedside nurse, APRN-CNS, and am now providing holistic wellness coaching.I've endured a significant health challenge the past several years, with a rare, invisible illness that left me completely bedbound for nearly a year. I've spent the next 5 years relearning to walk, drive and more. It has transformed my view and approach to helping and healing others.I have shared my journey of faith, health and grace in my book: When Grit and Grace Collide: Persevering Through Life's Challenges with Grit and God's Grace.https://cedarwellnesscoaching.cohere.live/Support the showhttps://livingthenextchapter.com/Want to support the show and get bonus content?https://www.buzzsprout.com/1927756/subscribe

Ep. 141 In this episode of Fearless Fridays with Maryann, we meet Nadia Monsano, the visionary behind the anthology "The Beautiful Face of the Invisible Illness: Masking the Pain We Endure."  Nadia's story is marked by a life-threatening heart condition that required medical intervention to reset her heart's rhythm. This episode delves deep into the emotional and psychological impact of her diagnosis while also revealing how she built an empire of support for others through her company and her work in publishing.  Key Takeaways: Chronic Illness and the Power of Advocacy: Understanding one's condition and advocating for oneself in the healthcare system are crucial for receiving proper care and treatment. The Impact of Confidence and Representation: Building confidence and embracing one's identity can be transformational on both personal and professional levels. The Importance of Service and Purpose: Finding and fulfilling one's purpose by serving others can lead to a meaningful and satisfying professional life. Notable Quotes: "The most beautiful thing we can walk into a room with is our confidence." "I am living boldly and fearlessly by doing what I love. And I know my purpose. I know my purpose is to serve, is to serve others." Resources: My Sister Keeper - Nadia Monsano's Branding, Marketing, and Graphic Design Agency - mysisterkeeper.biz Victoria's View Press - Catholic-based Publishing Company Out of the Box Press - Fictional Publishing Company Pre-Order the Anthology: The Beautiful Face of the Invisible Illness  Connect with Maryann Website: https://www.maryannriveradannert.com IG: https://www.instagram.com/maryannriveradannert/ FB: https://www.facebook.com/MRDEmpowermentSolutions Linkedin: https://www.bit.ly/maryannriveradannert About the Guest: Nadia Monsano is a driven and visionary entrepreneur, acknowledged as the creative force behind the anthology "The Beautiful Face of the Invisible Illness: Masking the Pain We Endure." Founder of My Sister Keeper, a branding, marketing, and graphic design agency, Nadia also leverages her talent to foster community and empowerment. Her expertise extends to working with Victoria's View Press, a Catholic-based publishing company, while also serving as a graphic designer for Out of the Box Press. With her roots in Trinidad and Tobago and her bold advocacy for self-acceptance, Nadia's story is not only motivational but a testament to overcoming adversity and fostering confidence. Chapters: 0:00:00 Introduction to Season Six 0:01:12 Nadia shares the inspiration behind the anthology project 0:02:50 Nadia reveals her invisible illness 0:04:12 They Stopped by Heart to Restart My Life 0:05:11 Working as a Publisher 0:06:08 Finding confidence 0:08:15 The desired takeaways for readers of the anthology 0:09:43 Advice for aspiring writers on starting the writing process 0:10:50 The meaning behind the name "My Sister Keeper" for Nadia's business 0:11:56 Importance of hiring a graphic designer for your business 0:13:17 My Sister Keeper is more than a branding and marketing agency 0:13:29 Living a fearless life by serving others 0:15:10 Upcoming projects and events in 2024 0:17:29 Connect with Nadia

In this episode of The Autoimmune Hour, host Sharon Sayler engages in a powerful conversation with return guest compassion lifestyle and business coach Simone Giangiordano, lovingly known as Simone G. Sharon and Simone  explore the transformative impact of self-compassion, especially for individuals struggling with autoimmune challenges and other health and well-being issues.Share this link with your family and friends: www.UnderstandingAutoimmune.com/Simone_2024Simone highlights how compassion can help manage chronic health conditions, including societal and personal stigma. She shares skills for advocating for a life fueled by understanding and kindness towards oneself and others. Plus, she offers insights from her journey of becoming a compassion trainer, and together, Sharon and Simone explore diverse aspects of compassion, including • How compassion differs from empathy, • The importance of setting boundaries for self-care, • Techniques for developing a compassionate relationship with oneself and others. Their conversation also touches on a Compassion Training Program, highlighting its evidence-based approach and benefits for emotional and physical well-being. And much more...More About Our Guest: Simone Giangiordano, also known as Simone G, is a compassion trainer, and lifestyle and business coach who believes in the power of admitting "I CAN'T." Based on her own experiences, she knows that acknowledging our limitations can actually set us free. Simone's mission is to bring hope to those who face invisible health challenges that affect the quality of their lives and their business success. She believes that societal and cultural norms often limit us more than our own limitations and that compassion can help us overcome misconceptions and stigmas around chronic health conditions. Learn more at SimoneG.net * Your host is not a doctor nor a medical professional. Medical professionals appearing on the show are sharing opinions only during our presentation. The information presented in this interview cannot substitute for the advice of your physician or other trained medical, healthcare, legal, or other professionals. Host(s) and guest(s) are not diagnosing specific conditions during the show. This show is not intended to diagnose, prevent, or treat autoimmune diseases or other conditions or illnesses. The information provided on UnderstandingAutoimmune.com, Life Interrupted Radio.com, and The Autoimmune Hour is for educational purposes only and opinion only. It is not a substitute for your own medical, legal, or other professional advice and care.©2024 Sharon Sayler and UnderstandingAutoimmune.comIf you've listened to the show, you know it's what my friends call my irrational passion... Please help us continue to offer help and hope for those with autoimmune and long-term health challenges by supporting The Autoimmune Hour podcast: https://www.spreaker.com/podcast/the-autoimmune-hour--2935987/support.

Keisha Hickson's life changed when a diagnosis threatened her life expectancy. Faced with a renewed appreciation for time, Keisha is determined not to waste it and now urges all of us to combat complacency in all areas of our lives. This woman's story is not just moving – it's a masterclass in living life to the fullest despite the toughest of blows. Join us as we celebrate Keisha's journey, explore the lessons she's gathered along the way, and perhaps, find the encouragement we need to chase our own "Next Best Thing." Subscribe to the NEXT Nuggets Newsletter for a transcript and the lessons from this  interview: https://thenextbestthingact.com/Join The NEXT Best Thing community on IG/TikTok @nextbestthingpod Stay in touch with Keisha:Website: https://keishahickson.com/LinkedIn: https://www.linkedin.com/in/keisha-hickson/IG: https://www.instagram.com/thereal_keishahickson/

Episode 138: Meet Davetta as she talks about navigating an HR career of over 30 years with an invisible illness, what that illness is, and how she found the strength to push forward, become an author, and start her own business. Hello & Welcome to season five of the Fearless Fridays with Maryann podcast! I'm excited that you are here and have decided to spend some time with us. I look forward to connecting with you, and I can be found... Website: https://www.maryannriveradannert.com IG: https://www.instagram.com/maryannriveradannert/ FB: https://www.facebook.com/MRDEmpowermentSolutions LinkedIn: https://www.linkedin.com/in/maryannriveradannert/ Bio and Contact for our guest: Davetta Henderson is a native of Washington, DC, still residing in the DMV area. She has a B.S. Degree in Organizational Management and has a successful professional career in Human Resources in the areas of Compensation, Benefits and HR Systems. Beyond God, Family, and Corporate America, Davetta is a multipreneur. She is committed to being her authentic self with a focus on her diverse passions and God-given gifts.  ​Davetta inherited a love for writing from her mother—a published poet. Davetta is a published author. Her first book—The Seed-The Soil-The Sower—is the introduction of a soon-to-be released, five-book series which explores our ability to reap God's spiritual harvest. She is also co-author in two Bestselling anthologies, Step Into Leadership Greatness and We All Grieve Differently. ​Davetta transformed her love for writing into a vehicle to help others share their story. She is the CEO of Full Faith Publishing, LLC—providing full-service book publishing and editing services. Full Faith is committed to helping their clients make human connections by transforming their life stories into written communication. Website:  https://www.davettahenderson.com/ Other Website:  https://www.davettajewels.com/

I was feeling lonely today and hopped on the mic after receiving an incredibly kind message from a listener.  Join me in this nonsensical, yet much needed time of rambling and fun!Wild Theory CBDCheck out wildtheory.com for all your CBD needs and use code: victory4uThe Healthy PlaceCheck out my friends at findyourhealthyplace.com and use code: victory4uDisclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.Support the show

Hello & Welcome to season five of the Fearless Fridays with Maryann podcast! I'm excited that you are here and have decided to spend some time with us. In today's episode, we meet – April Hogan and you will find her contact information at the end! I look forward to connecting with you, and I can be found... Website: https://www.maryannriveradannert.com IG: https://www.instagram.com/maryannriveradannert/ FB: https://www.facebook.com/MRDEmpowermentSolutions Linkedin: https://www.bit.ly/maryannriveradannert Libsyn website: http://fearlessfridayswithmaryann.libsyn.com/website Bio and Contact for our guest: April Hogan, founder of A Rich Innovations, LLC & A Rich Financial Management Inc 501(c)3. The vision behind A Rich Innovation is to help build up, empower, connect, and educate current and future business owners as well as individuals and families through our journey to financial wellness and business success.  "Stay Ready, so you don't have to get ready"  (O): 321-364-5644 (W): arichinnovations.com (E): april@arichinnovations.com WOSB | VOSB | Certified Scrum Master

Have you been experiencing unusual symptoms that Western medicine has been unable to help you with? I know this feeling wholeheartedly, as I've been sharing my experiences in decoding this mystery throughout the podcast since my initial episode back in August 2022. So many conditions are undiagnosed in Western medicine, often being put into a label called "autoimmune conditions", or "chronic illness" - but is this truly chronic, or are there stones left unturned that can help you heal in a more natural and holistic way of living? These are some of the secrets uncovered on this episode with one of the founders of the FIG (Food is Good) app, Andrew Hollar. I have no idea how I was guided to this app, but it was Divine intervention as I truly do believe having this powerful resource at my fingertips has helped me cut through the noise online about what foods can help heal versus trigger the symptoms I was experiencing. If medicine is prescribed that is taken through the mouth, why isn't the Food you eat also considered as medicine? This episode will reveal all, including how to heal the "invisible illness" through any dietary restrictions you have without feeling restricted by a list of 5-10 foods! From a Vegan or Pescatarian diet, to Gluten, Soy, and Dairy free needs, to the Low Histamine diet (which inspired Andrew's journey and my own), the FIG app will help you release the food anxiety, and learn how feel the FIG (food is good) again! About Andrew:Andrew Hollar is the co-founder of Fig, an app that helps people with dietary restrictions find food they can eat. Andrew started Fig after discovering that a modified diet was the answer to years of mysterious health issues in his own life. He and the Fig team are committed to helping everyone feel their best through food.Connect with Andrew + Learn more about FIG:FIG app - https://foodisgood.comInstagram -  https://www.instagram.com/foodisgoodco/Support the showConnect with me: Join my Live Vibrant Sisterhood -it's not too late to join! - DM me for deets or click here to preview! I'm on the Gram! Find me on Instagram @mozen_wellness, click here to DM! Would love to hear how you're experiencing this episode + the pod. Are you on the new Threads? Follow me for a daily dose of ALIVENESS! Come ALIVE with me - click here to see what's new: https://bio.site/mozenwellness Support the show + help us continue healing mental health through this podcast!

In this episode, I discuss true Stoicism, our emotions, two different mind exercises I learned to fight against PTSD flashbacks, and how life isn't a pursuit of happiness, but a pursuit of peace.STAY IN THE FIGHT.Wild Theory CBD Check out wildtheory.com for all your CBD needs and use code: victory4uThe Healthy Place Check out my friends at findyourhealthyplace.com and use code: victory4u Disclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.Support the show

In this heartfelt episode, join me on a deeply personal exploration of 11 ways to cope with invisible illness, delving into the hidden struggles that shape the spiritual path to wellness. From addiction and mental health battles to chronic pain, autoimmune disorders, and perimenopause, I'm shining a light on the unseen challenges of dealing with chronic or relapsing health issues often overlooked by society. We'll navigate the complexities of the medical system, seeking recognition and understanding, and bridge the worlds of Western medicine and alternative healing.  Learn essential coping strategies for navigating the invisible illness terrain, including the importance of managing expectations, celebrating small victories, and finding support in your tribe. Together, we delve into the transformative power of self-care, stress management, and the significance of being your own advocate. Listen to the end to hear the most important and powerful action you can take to start healing NOW. WORK WITH ME --- Send in a voice message: https://podcasters.spotify.com/pod/show/mysticalheartoracle/message

When Selena from MyLoopyLife found herself facing the realities of lupus, she didn't just learn to live with it—she learned to thrive. This episode is a heartfelt exploration of her journey from the shock of diagnosis to a life of empowerment and purpose, offering a personal glimpse into the power of transformation that awaits anyone experiencing chronic illness. Selena and I peel back the layers of emotional resilience and discuss how reclaiming control of one's life is not just possible; it's a path to discovering extraordinary inner strength.Connect with Selena: Selena • Lupus Warrior, Advocate + Coach (@myloopylife) • Instagram photos and videosCLICK THE LINK BELOW TO JOIN the JOURNEY TO LIMITLESS COMMUNITY:Community — Journey to Limitless (jtl-lifecoaching.com)Community member perks: Be apart of an interactive WhatsApp Community with other cyclebreakers where you will have access to back pocket community support & inspirationReceive FREE/DISCOUNTED admission into our monthly eventsBe the FIRST to know about coaching offers & events- there will also be INCREDIBLE bonuses available to community members ONLY!Connect with your host, Court:Court | Podcast Host (@journeytolimitless_) • Instagram photos and videosLove the Journey to Limitless Podcast?Leave us a 5-star rating and review on your favorite listening app! Take a screenshot of the Journey to Limitless podcast on your phone and share it to your Instagram stories! Make sure you tag @journeytolimitless_ so that I can personally say “Hey thanks!” Showing your support for the podcast is SO appreciated and I definitely don't want it to go unnoticed!

I first learned about “Default aggressive" from former US Navy SEAL's  Leif Babin & Jocko Willink ( check out Jocko Podcast or read their book "Extreme Ownership" for more intel).  This concept is an awesome way to approach life and we should remember it! "Default Aggressive" means that you're being proactive instead of reactive. It means that you're taking action in life, rather than being a passive bystander watching your life go by."Miguel Johnson - Unexplored Moon" is under a Creative Commons (CC BY-NC 3.0) license   / migueljohnson  https://migueljohnson.bandcamp.com/Music promoted by BreakingCopyright: https://bit.ly/unexplored-moon-songSupport the show

 "Well-being is realized by small steps, but is truly no small thing" -ZenoIn this episode, we discuss "thinking small", how that benefits our lives, and what may  come in succession of it.  LIFE is going to happen regardless of how you feel about it. What we should focus on is what we are going to DO about it.  STAY IN THE FIGHT.Support the show

Michelle Bauman joins the SOLO 2.0 Podcast to discuss her experience living with Lyme Disease and what YOU should know about the #1 fastest growing infectious disease in the country! Michelle is a busy mom of two boys who has spent the last 12 years working in healthcare operations and management. She has always been passionate about health, wellness, nutrition and fitness, but that was taken to a new level after she came down with a case of pneumonia towards the end of 2019. In early 2020 her world was turned upside down when she became incredibly sick with a wide variety of bizarre symptoms that seemed to appear out of nowhere... During this conversation we cover: How Michelle got sick with Lyme and other co-infections including Pots syndrome and black mold. Facts to know about Lyme disease, top symptoms, medication / treatment options & testing Problems with the traditional medical model for those with Lyme & other chronic health conditions The difficulty of living with “invisible” illness that is misunderstood, not recognized universally (w/ little to no insurance coverage)   The financial strain / impact on career for those struggling with chronic health conditions   Navigating relationships with friends & family when you're chronically sick The need for better HR practices for those with chronic illness How people can support individuals in their lives struggling with chronic health conditions TICK PREVENTION: Prevention Spray: Ranger ready (can also use essential oil based products) FILMS: The Quiet Epidemic (Apple TV) YouTube: Under Our Skin (Exposing the Hidden Epidemic of Lyme Disease) CONNECT WITH MICHELLE: Instagram: @michelle_bauman/ CONNECT W/ RYE & JESS: Instagram ⁠⁠⁠⁠⁠⁠⁠@solo2.0podcast⁠⁠⁠⁠⁠⁠⁠ Follow Jess ⁠⁠⁠⁠⁠⁠⁠@bodyblissbyjess⁠⁠⁠⁠⁠⁠⁠ Follow Rye ⁠⁠⁠⁠⁠⁠⁠@ryeburch⁠⁠⁠⁠⁠⁠ Follow Your Hormone Balance ⁠⁠⁠⁠⁠⁠@yourhormonebalance

Beatrice King is an experienced actress who has appeared in an array of critically acclaimed and fan favourite projects (X-Men Origins: Wolverine, Mortal Kombat Legacy, The 100, and Loudermilk) and a well-respected acting coach, working primarily with young people on projects for Universal, Disney, and Netflix. Beatrice recently added a new title to her already impressive filmography: director. Beatrice makes her directorial debut with You Are The Blue, an atmospheric and beautifully composed coming-of-age film she wrote about invisible illnesses and the mental health toll of keeping them secret.You Are The Blue follows teenage dancer Kay, played with nuance and steely vulnerability by Eden Summer Gilmore (Family Law). Kay, like 313 million people on the planet, lives with an autoimmune disease – and she's struggling: not just with the diagnosis, but also with grief and losing a sense of control over her life during a time that's already hard for young people.You Are The Blue premiered at the Edmonton International Film Festival, screened last month at the Vancouver Asian Film Festival, and screens this weekend at the 2023 Whistler Film Festival (where Eden was named one of the festival's Stars to Watch). In this fascinating and emotional interview with Sabrina Rani Furminger, Beatrice talks about the real-life inspiration for her directorial debut, and the toll that keeping invisible illnesses a secret can have on a person's mental health and sense of self.Episode sponsor: UBCP/ACTRA

Thank YOU for being with us today. I hope you gained benefit from this podcast in some way. Please know that YOU are appreciated.  STAY IN THE FIGHT.Did you know?CVP has been crowd funded since it began in 2019! Please consider donating to support the podcasts hosting fees. You can donate @chronicvictorypodcast on Venmo or click the "Support the show" link at the bottom of this page for Patreon.  Thank you!Support the show AND get something for yourself too! Use coupon code VICTORY at the following affiliate links!- The Healthy Place -Contact Info:Instagram:  @chronicvictorypodcastEmail:  chronicvictorypodcast@gmail.com(Music by 'The Anix'. Licenses Acquired by FiXT music LLC.)The Healthy Place Support the podcast & an awesome small business! Go to findyourhealthyplace.com - use code: victoryDisclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.Support the show

Have you ever wondered how podcasts could be a lifeline for those with invisible illnesses? Come and be part of an enriching dialogue with our esteemed guests, Professor Melanie Finney and the brains behind a startling study, Kate Peterson. Kate was inspired to do the study because her sister is living with POTS, one of the invisible illnesses that falls under the umbrella of fibromyalgia. We'll unravel the layers of isolation experienced by the invisible illness community and the surprising solace they find in podcasts. According to Kate's study, a staggering 97% felt less isolated, and an alarming number expressed a lack of empathy from their healthcare providers. As we move forward, we discuss fibromyalgia, an invisible illness with its unique set of challenges, and the pivotal role podcasts play here. The majority, 94%, found the information shared by podcast hosts invaluable, and three-quarters could trust the host they tuned into. We also tackle the conundrum of making podcasts more interactive, considering it's often a one-way communication. But, we also celebrate the power of storytelling and the platform podcasts offer for these unsung heroes to share their narratives. Join us as we shed light on these invisible battles being fought every day. Thank youSupport the showDr. Michael Lenz practices general pediatrics and internal medicine primary care, seeing patients from infants through adults. In addition, he also will see patients with fibromyalgia and related problems and patients interested in lifestyle medicine and clinical lipidology.

Ever wish your loved ones knew how to show up for you and support you? Well, this is the one for you to send to your loved ones! Today I offer 5 ways that our healthy loved ones can work to show up for us with actionable tips - as well as a few ways that they probably think they're being supportive when it really comes across as telling you you're not doing enough or downplaying what you're going through! So click that share button and send this to anyone who needs to hear it! Please don't forget to click that subscibe button whereever you listen to the podcast and do me a HUGE favor and leave a review! These two things help others find the podcast, find our community, and feel a little less alone in their journey through life with chronic illness!   Join us on Instagram: https://www.instagram.com/teamvasculitis Join the Email List: https://teamvasculitis.com/team-vasculitis-email

Daniel is a remarkable individual who has faced the challenges of living with epilepsy for 27 years. His journey is a testament to courage, tenacity, and that good ol' human spirit that just won't quit. Little Danny, just a wee tot of four, was on a family adventure in Montreal. And then, bam! Out of nowhere, he's hit with a grand mal seizure that sends him zooming to the nearest hospital. Thus began his epic odyssey through the land of pills, scans, and a gazillion doctors' appointments. Some treatments worked like magic, while others... well, let's just say, as they say on the island, they were about as useful as a fart in a mitt. Fast forward to the working world, and Daniel faced the cold, hard truth of living with an invisible illness. Pesky nighttime seizures would pop up, causing him to miss work leading to job loss and accusations of misconduct. His mental health suffered, and the stigma surrounding epilepsy only compounded his struggles. Join the fellas in this episode as Daniel shares his remarkable journey, from the darkest moments of despair to newfound hope. His story sheds light on the challenges faced by those living with epilepsy and the importance of raising awareness about invisible illnesses.

This EP features Heather Hausenblas.  Heather is a health psychology expert, international award-winning scientist, public speaker, and best-selling author. Her research focuses on how our health habits affect our well-being. She is ranked in the top 1% of the most influential scientists in the world.  Heather has published 7 books and over 110 peer-reviewed scientific articles. She frequently appears on podcasts and her work has been featured in magazines such as SELF, Real Simple, Women's World, O The Oprah Magazine, and dozens more as well as in news publications such as The Times London and The Chicago Tribune.Even with her vast education on wellness, Heather's outlook shifted when her eldest son was diagnosed with Crohn's disease in 2018. She was forced to rediscover what it means to live a healthy, happy life for her family. Her journey is captured in her No. 1 new release book, Invisible Illness, a guide to reducing overwhelm and achieving optimal health while living with an autoimmune disease. Through eye-opening research and personal stories, Heather provides science-backed solutions, simple health tips, and nutritious recipes that everyone can use on their wellness journey.Beyond all her accomplishments she is a wife and mother of three growing boys. Please enjoy!If you liked this EP, please take the time to rate and comment, share with a friend, and connect with us on social channels IG @Kingopain, TW @BuiltbyScott, LI+FB Scott Livingston. You can find all things LYM at www.LYMLab.com, download your free Life Lab Starter Kit today and get busy living https://lymlab.com/free-lym-lab-starter/Please take the time to visit and connect with our sponsors, they are an essential part of our success:www.MatrixFitness.comwww.VALD.com https://bstrong.training/ - Take advantage of 10% savings and use the coupon code LYMBstrong

Have you ever experienced a hardship that is seemingly invisible to others? On today's episode of "Happiness Through Hardship" - The Podcast, author Francesca Grossman shares her experience with chronic pain and navigating the many layers of a disease that most don't understand. As discussed on this episode and in her book, "Not Weakness: Navigating the Culture of Chronic Pain," Francesca has dealt with chronic pain ever since she was young. She talks about navigating the pain, aggravation and turmoil as well as includes valuable tips that apply universally. Francesca's journey is inspirational and teaches us all about having hope and finding connection even when life feels tough. SHOW NOTES 3:27 – Francesca shares her experience with chronic pain 8:58 – Common themes across chronic pain stories 13:34 – Tips for dealing with chronic pain 17:18 – How books can help through pain 19:53 – Where to begin when dealing with chronic pain 20:47 – Acceptance and redefining success 30:13 – Francesca's tips for dealing with hardships CONNECT with Francesca Her book - "Not Weakness:" https://amzn.to/45dB4KP Writing Workshops: https://francescagrossmanbooks.com/writing-workshop/ Instagram: https://www.instagram.com/francescagrossman/ CONNECT with us www.CarynSullivan.com/podcast www.Instagram.com/prettywellness www.Facebook.com/PrettyWellness www.Twitter.com/PrettyWellness To Buy the Book: “Happiness through Hardship” - The Book: amzn.to/39PAjuT To Donate a Book to a Cancer Center: www.CarynSullivan.com/book To Donate to Metastatic Breast Cancer (MBC) Research: The Cancer Couch Foundation is a privately funded, non-profit (501c3) organization that has funded $5 million dollars in metastatic breast cancer (MBC) research since our founding in 2016! 100% of donations and event proceeds are ​​​matched and go to fund MBC research at Dana-Farber Cancer Institute and Memorial Sloan Kettering Cancer Center! www.thecancercouch.com/donations.html

From chronic fatigue to Lyme's disease to COVID to autoimmune conditions, "invisible" illnesses and those who suffer from them are often disbelieved. It's often a struggle to receive a diagnosis, and more often than not, sufferers do not receive the adequate care they need. Lack of knowledge and understanding from medical providers may lead women to remain silent and hide their suffering, live with persistent symptoms, as well as facing isolation, depression, and anxiety. So where does one even start if suffering from an invisible illness and how does one begin the journey towards reclaiming your own life? Tune into today's episode of On Health to find out My guest today, Meghan O'Rourke, is the author of the New York Times bestseller and absolute must-read, The Invisible Kingdom: Re-Imagining Chronic Illness. In her twenties, Meghan began suffering from mysterious symptoms ranging from crushing fatigue to rashes to strange neurologic symptoms. The decade long search for a diagnosis led her down a long path of discoveries about conventional, integrative alternative medicine - and herself! Her book and wisdom is a healing balm for anyone struggling with or who loves someone with chronic disease. In this episode, we discuss: What an invisible illness is, and some of the most common known conditions for which women are most commonly dismissed Meghan's journey of seeking a diagnosis and treatment for a constellation of symptoms while redefining her sense of self as someone with an invisible illness. Medical gaslighting, self-gaslighting, and gender as obstacles to women receiving proper medical care The role online groups and alternative medicine played in finally getting a diagnosis Why it's so important to deeply trust her your body and learn to discern is -- and isn'tt -- working for you from medical interactions to conventional and alternative therapies Non-negotiables for living well, and navigating work and motherhood, with a chronic condition The impact of long-COVID on raising awareness and changing the cultural and medical narrative about chronic, invisible illnesses How to advocate for yourself in conventional medicine and integrative wellness Many of you listening will find yourself in Meghan story. I hope this interview and her book give you a feeling of being less alone and remind you of the need for compassion for yourself or those in your life. Thank you so much for taking the time to tune in to your body, yourself, and this podcast! Please share the love by sending this to someone in your life who could benefit from the kinds of things we talk about in this space. Make sure to follow your host on Instagram @dr.avivaromm and go to avivaromm.com to join the conversation. Follow Megan @meghanor and grab a copy of her book at meghanorourke.com.