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4 episodes with complex regional pain syndrome crps
11 episodes with complex regional pain syndrome crps
2 episodes with complex regional pain syndrome crps
2 episodes with complex regional pain syndrome crps
2 episodes with complex regional pain syndrome crps
2 episodes with complex regional pain syndrome crps
2 episodes with complex regional pain syndrome crps
2 episodes with complex regional pain syndrome crps
2 episodes with complex regional pain syndrome crps
Send us a textIn this episode Ryan sits down with Lexi Chambers, an adaptive athlete who has shattered expectations and set multiple world records—all while using a standard NHS wheelchair. After a below-the-knee amputation due to Complex Regional Pain Syndrome (CRPS), Lexi refused to let disability define her. Instead, she turned to endurance sports, becoming the first person to wheel from John O'Groats to Land's End (1,500km) in an everyday wheelchair. Now, she's preparing for 10 ultramarathons in 10 days (50km/day) and an even bigger challenge: wheeling coast-to-coast across the USA (5,000km) in 2027.Lexi shares her journey of resilience, how sport became her therapy, and her mission to inspire others to embrace movement—no matter their circumstances.What You'll Hear- Lexi's life-changing CRPS diagnosis, amputation, and why she refused to hang up her athletic dreams- How a kitchen “test spin” led to her first world record and eventually wheeling John O'Groats → Land's End in a standard NHS chair- The surprising role of extreme training as pain therapy and mental escape- Balancing a punishing training schedule, gruelling winds, and 4 am starts—plus the “test weeks” that make or break prep- Building and motivating a novice event-planning crew to pull off “impossible” challenges- Lessons learned fundraising hundreds of thousands, nailing keynote speeches, and embracing vulnerability on stage- Upcoming feats: 10×50 km ultramarathons in 10 days for Rugby World Cup charity, then a 5 000 km coast-to-coast across the U.S.- Lexi's simple message to anyone doubting themselves: you never know what you can do until you tryReady to rethink your limits? Tune in and get inspired to take that first (or next) rotation.
Much like me, Samantha Donbavand was born 3 months prematurely and was diagnosed with Complex Regional Pain Syndrome (CRPS) in 2004 following a near-death experience. She works to treat her incurable condition through a variety of spiritual practices.Learn more about her work via the links below: Official Website:https://samanthadonbavand.wixsite.com/liveinyourlight/homeFacebook:https://www.facebook.com/share/1J3AyHYFPS/?mibextid=wwXIfrInstagram:https://www.instagram.com/serenityshaman?igsh=MWhqaDQzYWhlMzFuZQ==If you would like to reach out feel free to send an email to: atelierfuralle@gmail.com. You can also leave a review of the podcast and follow this show on:Instagram:https://instagram.com/atelierfuralle?igshid=OGQ5ZDc2ODk2ZA%3D%3D&utm_source=qrFacebook:https://www.facebook.com/profile.php?id=61551850785306Feel free to join the "JD Dragon Disability Rights Podcast" Facebook Group:https://www.facebook.com/share/g/12Eit9sBPuR/?mibextid=wwXIfrSnapchat:https://t.snapchat.com/FVWn1jmTDiscord ServerJD DragonX (formerly known as Twitter):@JDDragonPodcast
In this episode, I chat with the inspiring Eline Duk, a chronic pain coach and disability advocate who is the founder of The Spoonies Community. After two major accidents, she was diagnosed with Complex Regional Pain Syndrome (CRPS) and Functional Neurological Disorder (FND). We explore how she has learned to live well alongside her chronic health conditions, and the incredible journey of discovering somatic work and holistic healing. Stay connected with Eline here:https://thespooniescommunity.com/https://www.instagram.com/thespooniescommunity/Want to learn how to find freedom from chronic pain and fatigue? Register for my free training: https://www.thespooniementor.com/free/ Instagram: https://instagram.com/thespooniementorWebsite: https://www.thespooniementor.com/
Rising Star in Adaptive Fashion: Nevaeh Hearn's Journey In this episode of 'Pushing Forward with Alycia,' host Alycia welcomes Nevaeh Hearn, a senior at Drexel University studying Fashion and Merchandising. Nevaeh shares her transformative journey from a promising gymnast to an advocate for adaptive fashion after a life-altering injury. They discuss her struggle with Complex Regional Pain Syndrome (CRPS), her diagnosis with Ehler-Danlos Syndrome (EDS), and her ultimate passion for making the fashion industry more inclusive. She opens up about her difficulties and triumphs in college, her experience as a top finalist for the NRF Foundation's Next Generation Scholarship, and her ambitious senior thesis focused on adaptive fashion. Nevaeh stresses the importance of perspective and passion in overcoming life's toughest challenges. Finding Purpose Through Adversity: Nevaeh Hearn's Journey into Adaptive Fashion 00:00 Introduction to Pushing Forward with Alycia 00:25 Meet Nevaeh Hearn: A Journey of Resilience 03:08 Nevaeh's Early Life and Gymnastics Dream 03:55 The Life-Changing Injury and Diagnosis 09:57 Overcoming Adversity: Walking Again 13:10 Discovering a New Passion: Fashion 14:41 College Challenges and Triumphs 19:44 Advocating for Adaptive Fashion 29:51 Future Goals and Final Thoughts Themes That Shaped the Conversation
Special Thanks to Our Sponsor: Cured Nutrition This episode of the Say Yes Anyway Podcast is brought to you by Cured Nutrition—transforming wellness with natural, holistic products that support your stress, sleep, and overall well-being. If you're seeking to feel your best and recharge, Cured Nutrition is here to help you thrive. You can receive 15% off with THIS LINK—use code: JESSDAHL to enjoy your discount! In this heartfelt and inspiring episode of the Say Yes Anyway podcast, I am thrilled to welcome the incredible Amberley Lago—a motivational speaker, best-selling author, and true warrior in the face of unimaginable challenges. Amberley's journey of resilience and transformation is nothing short of remarkable, and her story will leave you inspired to face life's challenges with renewed courage and hope. She opens up about her life-changing motorcycle accident that resulted in 34 surgeries and a diagnosis of Complex Regional Pain Syndrome (CRPS), a debilitating nerve disease often referred to as the “suicide disease.” Yet, her story doesn't stop there. Amberley candidly shares her battle with alcoholism, a struggle she turned to as a way to numb her physical and emotional pain. She vulnerably discusses the moment she realized she needed help and how choosing to say “yes” to healing became the turning point that transformed her life. Throughout our conversation, Amberley reflects on the darkest periods of her life and shares how she found strength through small, attainable goals, focusing on incremental progress to regain her independence and rebuild her life. She reveals how her powerful “why”—her daughters—kept her going, driving her resilience and reminding her of the importance of showing them that adversity can be overcome. Amberley emphasizes the necessity of community, connection, and accountability in the healing process, offering practical advice for cultivating resilience, from setting goals to surrounding yourself with supportive and optimistic individuals. Amberley also gives us a glimpse into her new book, Joy Through the Journey, where she shares how she learned to find joy even in the midst of hardship. Her story is a testament to the human spirit's ability to transform pain into purpose and emerge stronger than ever. This episode is a heartfelt reminder that no matter how challenging life may get, there is always a path to healing and empowerment through resilience, connection, and the courage to say “yes” to life.Amberley's journey will resonate with anyone facing struggles, reminding us all that we have the power to overcome adversity and create a meaningful, joy-filled life. Her authenticity, grace, and wisdom are sure to inspire you to embrace life's challenges and transform them into opportunities for growth and purpose. Don't miss this powerful episode of the Say Yes Anyway podcast. Tune in now and let Amberley's story remind you of the strength you already have within you. For more about Amberley Lago, visit:Website: https://amberlylago.com/Instagram: @amberlylagomotivation Also, stay connected with me on Instagram: @jessdahl_! Thank you for tuning in—and keep saying yes to what lights you up! Please leave a review and share this episode, it means the world to me! Thank you =)
Die Diagnose eines Complex Regional Pain Syndrome (CRPS) ist für viele Patient:innen ein einschneidendes Erlebnis. Sie sehen sich nicht nur oft mit enormen Schmerzen und anderen Symptomen konfrontiert, sondern können von einem Tag auf den anderen ihr Leben nicht mehr so führen, wie sie es sich wünschen. Je nach Therapieziel geht es dann u.a. auch darum, die Patient:innen bei der Schmerzbewältigung zu unterstützen.
This is episode 1 of the series: Chronic Illness to Remission: Navigating the New NormalEpisode 1: In this episode, Dr. Candace Pierce and her daughter Judah share their inspiring journey with Complex Regional Pain Syndrome (CRPS), highlighting Judah's recent remission. They delve into the challenges faced, emotions experienced, and the crucial support they received, emphasizing the importance of understanding and acknowledging the pain of patients with rare disorders like CRPS. The discussion also covers the need for healthcare providers to reevaluate their approach to treating patients with these complex conditions. Episode 2: In this episode, Candace and Judah share their experiences managing the challenges of an invisible illness like CRPS, discussing everything from the disbelief of others to the struggle of finding proper medical care. Candace recounts a harrowing story of a doctor blaming her for Judah's condition, emphasizing the need for understanding and support from both healthcare providers and loved ones. They highlight the emotional journey of adjusting to life in remission and the crucial importance of finding a supportive community. ---Nurses may be able to complete an accredited CE activity featuring content from this podcast and earn CE hours provided from Elite Learning by Colibri Healthcare. For more information, click hereAlready an Elite Member? Login hereLearn more about CE Podcasts from Elite Learning by Colibri HealthcareView Episode TranscriptView this podcast course on Elite LearningSeries: Chronic Illness to Remission: Navigating the New Normal
This is episode 2 of the series: Chronic Illness to Remission: Navigating the New NormalEpisode 1: In this episode, Dr. Candace Pierce and her daughter Judah share their inspiring journey with Complex Regional Pain Syndrome (CRPS), highlighting Judah's recent remission. They delve into the challenges faced, emotions experienced, and the crucial support they received, emphasizing the importance of understanding and acknowledging the pain of patients with rare disorders like CRPS. The discussion also covers the need for healthcare providers to reevaluate their approach to treating patients with these complex conditions. Episode 2: In this episode, Candace and Judah share their experiences managing the challenges of an invisible illness like CRPS, discussing everything from the disbelief of others to the struggle of finding proper medical care. Candace recounts a harrowing story of a doctor blaming her for Judah's condition, emphasizing the need for understanding and support from both healthcare providers and loved ones. They highlight the emotional journey of adjusting to life in remission and the crucial importance of finding a supportive community. ---Nurses may be able to complete an accredited CE activity featuring content from this podcast and earn CE hours provided from Elite Learning by Colibri Healthcare. For more information, click hereAlready an Elite Member? Login hereLearn more about CE Podcasts from Elite Learning by Colibri HealthcareView Episode TranscriptView this podcast course on Elite LearningSeries: Chronic Illness to Remission: Navigating the New Normal
On today's Healing Hub Podcase, we're sharing the audio from a live interview on Monday, November 4th – CRPS Awareness Day - with Cindy Perlin – CEO of the Alternative Pain Treatment Directory. This was an open forum interview and Q&A where we started off talking about my personal journey with CRPS, our treatment program at Holistic Centered Treatment, and transitioned into questions and answers.Dr. Traci Patterson traveled the world and spent in excess of $250,000 searching for help for her Complex Regional Pain Syndrome (CRPS). Many of the treatments made her worse. Now 11 years in remission, Dr. Patterson, a trained MD, is President of Holistic Centered Treatment, an intensive outpatient clinic for people with CRPS and other types of difficult-to-treat chronic pain. Dr. Patterson is telling her story and talk about her treatment program that is helping many CRPS and chronic pain patients regain their lives.This was an open forum interview and Q&A with Dr. Traci Patterson - CRPS Survivor and President, Holistic Centered Treatment and Cindy Perlin, LCSW, founder and CEO of the Alternative Pain Treatment Directory.#FacebookLive #DrTraciPattersonCRPSexpert #HolisticCenteredTreatment #crpsremission #crpstreatment #CRPSsurvivor #crps #crpswarrior #makingadifference #changinglives #premiereprogramforcrps #alternativepaintreatmentdirectory #cindyperlin #KnowYourOptions #inspiringcrpsstories #crpsawareness #CRPSAdvocate #raredisease #intractablepain #chronicpain #RSD #spoonies #fibromyalgia #amps #PediatricPain #CRPSawarnessday #chronicpain #pediatricpain #CSS #AMPS #PhantomLimbPain #HCTFoundation
TARA MOSS IS GOING TO DIETara Rae Moss is a force and a shape-shifter. She is the bestselling author of 14 books of fiction and non-fiction, an experienced keynote speaker and documentary host, an award-winning advocate, holistic healer, funeral celebrant and practicing seiðkona.Since 1999 she has written fourteen bestselling books under the name Tara Moss, published in 19 countries and 13 languages, including advocacy handbook for women and girls Speaking Out, her #1 non-fiction bestselling memoir The Fictional Woman, and the internationally bestselling postwar historical crime novels The War Widow and The Ghosts of Paris.Tara Rae is an outspoken advocate for human rights and the rights of women and children, and has been a UNICEF Australia goodwill ambassador since 2007. In 2014 she was recognised for outstanding advocacy for her blog Manus Island: An Insider's Report, which helped to break information to the public about the alleged murder of Reza Barati.Against all odds, Tara Rae is now in remission for Complex Regional Pain Syndrome (CRPS) – a rare disease she lived with for nearly eight years, marked by constant burning pain that rates on the McGill Pain Scale as more painful than childbirth or amputation of a digit. Despite being told by multiple doctors that she would never recover, she was able to get her condition into complete remission in 2023 after years of debilitating pain that impacted all aspects of her being, including her mobility, causing her to require a wheelchair.With her gothic sensibilities Tara Rae has always been fascinated by the creative aspects of mortality - so it make sense that she's planned her dream Funeral with fine and brilliant detail.Website: taramoss.comInstagram: @taramossauthor Marieke Hardy Is Going To Die is a podcast made by Marieke Hardy (IG @marieke_hardy).You can follow at IG @GoingToDiePodMusic by Lord Fascinator (IG @lordfascinator)Produced by Darren Scarce (IG @Dazz26)Video edits by Andy Nedelkovski (IG @AndyNeds)Artwork by Lauren Egan (IG @heylaurenegan)Photography by Eamon Leggett (IG @anxietyoptions)With thanks to Amelia Chappelow (IG @ameliachappelow)Camilla McKewen (IG @CamillaLucyLucy)and Rhys Graham (IG @RhysJGraham)Drop an email to mariekehardyisgoingtodie@gmail.comWhilst acknowledging the privilege that comes with having the space to discuss death and mortality, we want to also recognise that discussing these topics can raise some wounds. Should you wish to seek extra support, please consider the following resources:https://www.healthline.com/health/mental-health/online-grief-support-groupshttps://www.grief.org.au/ga/ga/Support/Support_Groups.aspxhttps://www.headspace.com/meditation/griefhttps://www.mindful.org/a-10-minute-guided-meditation-for-working-with-grief/https://griefline.org.au/get-help/ https://www.wheelercentre.com/events-tickets/season-2024/ben-shewry-is-going-to-die ★ Support this podcast on Patreon ★
Mind over matter is a powerful force. Today's guest embodies this principle, overcoming Complex Regional Pain Syndrome (CRPS), Raynaud's, allergies, and osteoarthritis through sheer mental and emotional strength. He is a health guru, CEO of a real estate development firm, and a devoted family man. His journey of self-healing and personal triumphs has inspired and helped many others to achieve the same. This is the Story of a Healing Journey with Daniel Brown.EPISODE VIDEO HIGHLIGHTS▪ Watch the Entire Episode▪ How the Mind-Body Connection Influences Healing▪ The Overlooked Power of the Mind in Modern Medicine▪ How Hidden Belief Systems Impact Health and Well-Being▪ Does Non-Religious Spirituality Offer Health Benefits?▪ Must-Read Books for Transformation and Personal Growth▪ How to Design Your Home as a Healing SanctuaryCONNECT WITH DANIEL BROWN▪ Website - BrownstoneCI▪ Instagram - Daniel Brown▪ Instagram - Brownstone Capital InvestmentsLEARN MORE ABOUT US▪ Visit our website to learn more about Innovative Medicine▪ Take our assessment and set up a free 20-minute consult to learn more about becoming a patient, or feel free to contact us▪ Follow Innovative Medicine on Instagram▪ Subscribe, watch, give us a like on YouTube▪ ‘Your Health. Your Story.' Podcast: Follow, listen, leave us a review on Spotify or Apple Podcasts▪ Follow our podcast host, Caspar Szulc on Instagram▪ Sign up for Caspar's newsletterLEARN MORE ABOUT NADOVIMDoctor-formulated, clinically-tested NAD+ supplement. Visit our website and save 10% on your first order by using code NADOVIM10.Disclaimer: The content presented on the podcast is for informational purposes only and is not intended to diagnose, treat, cure, or prevent any disease.
In this episode, we review the high-yield topic of Complex Regional Pain Syndrome (CRPS) from the Basic Science section. Follow Orthobullets on Social Media: Facebook Instagram Twitter LinkedIn YouTube --- Send in a voice message: https://podcasters.spotify.com/pod/show/orthobullets/message
Send us a Text Message.This week's episode is with Dr. Katinka van der Merwe, a Doctor of Chiropractic who focuses on nervous system rehabilitation to help those suffering from chronic pain. She grew up just outside of Johannesburg, South Africa, and immigrated to the United States to receive her Doctor of Chiropractic degree. Since then, she has received numerous awards for her work, including the prestigious Global Chiropractor of the Year award in Atlanta, Georgia, and the Award of Innovation for her ongoing work with RSD/CRPS patients in Los Angeles. In addition, she is a successful author and has recently published a new book, A Paradigm Shift in Treating EDS/POTS, which focuses on the connection between EDS/POTS and other diseases to improve treatment. Dr. Van der Merwe is also the CEO and founder of The Spero Clinic in Fayetteville, Arkansas, which treats patients from around the world. To date, she has treated patients from 47 US states and 34 countries! She has great success in treating non-retractable pain syndromes and chronic pain.In this episode, Dr. Van der Merwe and I start by exploring the Spero Clinic's Nervous System Rehabilitation program and the variety of unique therapies her clinic offers. She then shares information about Complex Regional Pain Syndrome (CRPS), what makes the condition difficult to diagnose, and the approach she takes to treat the pain. We then dive into her goals for the clinic in the upcoming years, her new book, and how she builds close relationships with all her patients. We also briefly touch on numerous interesting topics, such as medical kidnapping, Long COVID, and hypnotherapy!Additionally, she shares the mental health and psychological support her clinic offers, as mental health is often intertwined with chronic pain. So, as a warning, there is a brief mention of suicide near the end of this episode. Make sure to subscribe to The Neurological Disorder Podcast on Spotify, Apple Podcasts, or wherever you listen to your podcasts!Follow me on Instagram- @neurologicaldisorderpodcast Email me at- neurologicaldisorderpodcast@gmail.com Helpful Links:https://www.thesperoclinic.com/More about CRPS
Welcome back, dear listeners. On this episode, I had the pleasure of meeting up with Harry Macansh, a speaker and wellness coach who recovered from Complex Regional Pain Syndrome (CRPS) after initially being told that this condition was incurable. He now helps others to recover as well. Over more than half a decade, Harry has spent upwards of a quarter of a million dollars in the US & Australia acquiring an arsenal of knowledge and modalities that he now affordably delivers to others, both from stage through 1-to-1 coaching. When Harry reached out to me, I immediately jumped at the chance to connect and chat, because it just so happens that I was preparing to speak onstage about my own chronic pain recovery for the first time, and I'm fascinated by the connection between recovery and the pull to break through that nearly universal human fear of public speaking to share our stories out loud. Harry and I had a brain tingling conversation about this and I'm excited to share it with you. Here we go. You can find Harry at: https://www.instagram.com/harrymacansh/ And you can find me at: Instagram: @anna_holtzman Email: anna@annaholtzman.com Website: www.annaholtzman.com --- Support this podcast: https://podcasters.spotify.com/pod/show/from-chronic-pain-to-pass/support
In a massive 53 page treatment guideline on Complex Regional Pain Syndrome (CRPS), the authors state:“Occupational therapists are the ideal therapeutic leaders in the functional restoration process…”And, go on to devote 2 pages to what this OT care can entail. In this one hour course, we'll pull out important implications for OT practice from the entire guideline. As you'll see, when it comes to treating chronic pain, like CRPS there are a lot of best practices to draw on—but also a lot of unknowns that necessitates close attention to the individual in front of you. To help us flesh out what this means for OT practice, we'll welcome to the podcast Megan Doyle, a program manager at an outpatient pain program and a leading voice on OT's role in pain management.You can find more details on this course here:https://otpotential.com/ceu-podcast-courses/ot-complex-regional-pain-syndromeLearn more about our guest:Megan Doyle MS, OTR/L, TPS, FPS, CERT-APHPTHere's the primary research we are discussing:Complex Regional Pain Syndrome: Practical Diagnostic and Treatment Guidelines, 5th Edition.Support the Show.
In the analog corners of Utah, Libby Slem navigates the digital age with a Luddite's charm and a warrior's grit, facing Complex Regional Pain Syndrome (CRPS). This isn't your everyday pain; it's a journey through a rare nerve disease that transforms every facet of life, from motherhood's joys and trials to the heart's metallic beats, courtesy of an atrial septal defect. Libby's candid conversation unfolds the layers of CRPS, beyond the pain to the diagnosis stages, and the sheer impact on her personal and parenting life. With humor and gravity, she delves into the challenges of seeking support in a world barely scratching the surface of understanding chronic pain.Our recent chronic pain episodeFor more info on CRPSCatch the full video version of this episode on YouTubeFollow Sickboy on Instagram, TikTok and Discord!
In the analog corners of Utah, Libby Slem navigates the digital age with a Luddite's charm and a warrior's grit, facing Complex Regional Pain Syndrome (CRPS). This isn't your everyday pain; it's a journey through a rare nerve disease that transforms every facet of life, from motherhood's joys and trials to the heart's metallic beats, courtesy of an atrial septal defect. Libby's candid conversation unfolds the layers of CRPS, beyond the pain to the diagnosis stages, and the sheer impact on her personal and parenting life. With humor and gravity, she delves into the challenges of seeking support in a world barely scratching the surface of understanding chronic pain.Our recent chronic pain episodeFor more info on CRPSCatch the full video version of this episode on YouTubeFollow Sickboy on Instagram, TikTok and Discord!
In this episode of the Ketamine Startup Podcast, Sam sits down with Dr. Lara Edinger, founder of Edinger Pain Management Clinic in Los Angeles. Transitioning from a seasoned neurologist to a pioneer in pain management, Dr. Edinger shares her comprehensive journey into the niche of chronic neuropathic and musculoskeletal pain disorders. She goes in-depth at her innovative treatment approaches, including the pivotal role of ketamine therapy in treating Complex Regional Pain Syndrome (CRPS).You'll gain practical advice on starting and managing a clinic plus be reminded of the significance of creating a patient-centric environment and building a solid support team. Beyond the operational advice, this episode is packed with Dr. Edinger's personal reflections on job creation, the transition to cash-based practices, and the inception of a non-profit to support patients.Listen, enjoy, and discover essential strategies for clinicians aspiring to venture in pain management and ketamine therapy.Episode 6 show notes:00:00 Introduction00:16 Interview with Dr. Lara Edinger: A Specialist in Chronic Pain Disorders01:31 Dr. Edinger's Journey: From Neurology to Pain Medicine02:38 Establishing Edinger Pain Management Clinic03:38 Understanding Complex Regional Pain Syndrome (CRPS)06:14 Challenges of Running a Private Practice06:14 Transitioning from Traditional Healthcare to Private Practice07:46 The Complexities of Medical Billing and Insurance12:17 The Role of Ketamine in Treating CRPS19:21 The Business Side of Running a Ketamine Clinic20:19 The Impact of Personalized Care in a Ketamine Clinic26:34 The Reality of Current Healthcare System26:48 The Rise of Cash-Based Practices26:57 Starting a Non-Profit for Complex Patients27:47 Advice for Clinicians Curious About the Space28:13 The Importance of Organization and Finding the Right People29:03 The Rewarding Aspect of Creating Jobs29:57 The Importance of Preparation and Legal Assistance30:16 The Challenges of Setting Up Different Services31:13 The Expansion of Ketamine Treatment31:54 The Importance of Medical and Psychological Clearance35:30 The Challenges and Rewards of Running a Practice36:59 The Importance of Delegation and Support39:23 Desert Island Choices and Time Travel Wishes43:41 Alternative Career Choices47:18 Final Thoughts on the Ketamine IndustryThanks for listening!Connect with Dr. Edinger at:Edinger Pain ManagementInstagramWant to fast track launching your ketamine clinic? If so, download our free checklist.
Chris sat down with Brittany Kim to discuss Complex Regional Pain Syndrome (CRPS). Brittany outlines the diagnostic criteria, prognosis, communication recommendations, treatment pathways, rehabilitation management strategies, and major misconceptions involving CRPS. Watch the full episode here: https://youtu.be/Adcd9FNJZfY More about Brittany: Brittany's Website Brittany's Instagram CRPS Resources: CRPS Diagnostic Toolkit Clinical Resources Interdisciplinary Therapy Program --- Follow Us: YouTube: https://www.youtube.com/e3rehab Instagram: https://www.instagram.com/e3rehab/ Twitter: https://twitter.com/E3Rehab --- Rehab & Performance Programs: https://store.e3rehab.com/ Newsletter: https://e3rehab.ck.page/19eae53ac1 Coaching & Consultations: https://e3rehab.com/coaching/ Articles: https://e3rehab.com/articles/ Apparel: https://store.e3rehab.com/collections/frontpage --- Podcast Sponsors: Vivo Barefoot: Get 15% off all shoes! - https://www.vivobarefoot.com/e3rehab CSMi: https://humacnorm.com/e3rehab --- @dr.surdykapt @tony.comella @chrishughen --- This episode was produced by Matt Hunter
If you're dealing with overwhelming pain my guest Darci Steiner has a testimony of amazing resilience as she lives out the debilitating affects of Complex Regional Pain Syndrome or CRPS. In her book, Beauty Beyond the Thorns, Darci reveals how God cares for us in the darkest valleys in life. What she shares can benefit anyone who is dealing with pain that makes it seem like there's no way out. While we didn't discuss in detail the medical side of self-care I wanted to mention it now. If you're experiencing a crisis of mental health, emotional health of physical health, consider medical professionals and/or medication (per your doctor) in addition to your faith journey. Unrelenting pain can be a very lonely journey so Darci points us to the One who will never leave nor forsake us. God is always present, always listening and ready to tend to you. CRPS is called the suicide disease because when ranked on a pain scale, CRPS is found to be the highest pain one can feel hence the suicide disease label. People who know this level of unrelenting pain want to escape, permanently. Especially because they're told there is no cure. But God, right? Twenty years ago a fall down the steps ignited Darci's first experience with CRPS. The pain was so great that she did not have an appetite and became malnourished and was dying. Darci shares a little bit about her story of being bedridden for 2 years and the healing journey she experienced. What gripped my heart is that 5 years ago on a very special day for her family, the simple need of having to go back into the venue to grab something that she forgot and a chair topples from a stack and strikes her in the ankle. Immediately the pain seared from the injury and Darci knew she was headed back into CRPS. So at the time of this recording she is living with CRPS once again. She talked about the difference in how she engages God's heart this time. Because of her vulnerability, we get a glimpse of a maturing faith forged in deep pain that produces an intimacy with God that cannot be developed in any other context. One of the ways that Darci's faith matured is that while in God's word she received revelation on the distinction between being and doing. Darci's pain severely limited her ability to engage in some of the most simple things in life…at one point of being bedridden for 2 years, as Darci lay in bed she asked her husband to create a tent over her with the bed sheet because when it touched her skin it caused excruciating pain. As she lay in bed day in and day out she began to question the purpose of living. She couldn't do anything, she wasn't of any help, she couldn't enjoy her young daughters. Life was happening around her but without her. Even today she can only watch her grandchildren with assistance and short intervals. It's in this quiet place of simply being with God that she discovers a whole new level of intimacy with Him. The revelation that His only request for her, for any of us is to be with Him. A weight was lifted and she began to see the beauty of Christ's extravagant love for her in the humble posture of being. One last thing and we'll jump into the conversation with Darci. I especially loved how Darci shares that in the dark valleys of life God is there. I know we've heard that a thousand times but it's a great reminder that we don't have to go looking for Him. We don't have to pray for Him to find us. We don't have to check off the good Christian checklist for Him to show Himself. He's already there. We simply need to engage Him in the being. If you've been struggling with the thought that a good God would not have you suffer like this I challenge you to reframe that. God is good because despite the reality of the pain in this life, He doesn't abandon or reject us nor does He leave us to figure it out on our own. He enters into our pain with us, comforts us, leads us into healing, and untangles our fears. In short, He gives us His very presence. Darci was the absolute sweetest because despite her pain and my probing questions she has such a deep desire in her heart to share an encouraging message with others who are experiencing unrelenting pain whether it's in their mind/mental health, body/physical health, heart/emotional health. Listen in because Darci does a beautiful job of revealing the heart of God in the context of pain and suffering. Lived Loved and Thrive! @alifeofthrive.com Connect with Darci: Website: https://www.darcijsteiner.com Facebook Author: https://www.facebook.com/darcijsteiner Facebook Personal: https://www.facebook.com/darci.andersonsteiner Instagram: https://instagram.com/darcijsteiner.writer/ LinkedIn: https://www.linkedin.com/in/darcijsteiner/ X (Formerly Twitter): https://twitter.com/DarciJSteiner Goodreads: https://www.goodreads.com/darcijsteiner Pinterest: https://www.pinterest.com/darcijsteiner/ Amazon Author Page: https://www.amazon.com/author/darcijsteiner.com YouTube https://www.youtube.com/channel/UC8I8Pweui5tUt1DVvpeqEIA WomenSpeakers.com Audible Bio: Darci J. Steiner is the author of the award-winning biblically based book Beauty Beyond the Thorns: Discovering Gifts in Suffering. She is an inspirational speaker, author, writing coach, and nutritionist. Darci began writing to process her pain after a foot injury disabled her due to the nerve-pain disorder Complex Regional Pain Syndrome (CRPS). Darci writes and speaks messages that uplift and inspire audiences to always hold on to hope. She loves spending time with her husband, two adult daughters, and two grandchildren. Please visit www.darcijsteiner.com to subscribe to The Upside of Suffering Newsletter.
In this episode, we welcome back award-winning author and guide Liberty Forrest to share her A'Ha moments and deep learnings about hope, persistence, and resilience on her road to recovery after her first anniversary of a catastrophic accident. Liberty shares how her life has experienced a lot of change and how she has discovered many new things about herself, including how adaptable and creative one gets when necessary, including “I hope this one isn't TMI, but even putting on my own knickers took several weeks,” plus• How a practice of daily appreciation for having a healthy body helped.• Ways to stay positive and not fall into the ‘woe-is-me' trap.• Her experience with Complex Regional Pain Syndrome (CRPS).• The importance of creating milestones.• The world kept revolving, and so much moreMore about our Guest: Our guest, Liberty Forrest, is an award-winning author, speaker, and contributor to numerous informational publications, including Huffington Post. She is also a senior contributor at SportsEdTV. And, a lover of really dumb jokes and the creator of the “Witchy” cartoons. Check out her articles over at Medium (https://medium.com/@libertyforrestauthor). She has written numerous fiction and nonfiction books covering various topics. She loves sharing what she's learned throughout her healing journey, personal development, and spiritual study. It has been an essential part of her education and training as a Master Teacher, allowing her to fulfill her purpose of helping others achieve their highest potential. Learn more about Liberty at www.LibertyForrest.com and over at YouTube @LibertyForrest.Share this link with family and friends: www.UnderstandingAutoimmune.com/Liberty_2023* Your host is neither a doctor nor a medical professional. In the capacity of this presentation, both host and guest are speaking as everyday people trying to make sense of the world, and IS OPINION ONLY. 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. ©2023 Sharon Sayler and UnderstandingAutoimmune.com
Air Date - 01 December 2023In this episode, we welcome back award-winning author and guide Liberty Forrest to share her A'Ha moments and deep learnings about hope, persistence, and resilience on her road to recovery after her first anniversary of a catastrophic accident.Liberty shares how her life has “experienced a lot of change” and how she discovered new things about herself, including how adaptable and creative one gets when necessary, including “I hope this one isn't TMI, but even putting on my own knickers took several weeks to figure out” plus• How a practice of daily appreciation for having a healthy body helped.• Ways to stay positive and not fall into the ‘woe-is-me' trap.• Her experience with Complex Regional Pain Syndrome (CRPS).• The importance of creating milestones.• And that the world kept revolving, and so much more…More about our Guest:Our guest, Liberty Forrest, is an award-winning author, speaker, and contributor to numerous informational publications, including Huffington Post. She is also a senior contributor at SportsEdTV. And, a lover of really dumb jokes and the creator of the “Witchy” cartoons.Check out her articles over at Medium (https://medium.com/@libertyforrestauthor). She has written numerous fiction and nonfiction books covering various topics. She loves sharing what she's learned throughout her healing journey, personal development, and spiritual study.It has been an essential part of her education and training as a Master Teacher, allowing her to fulfill her purpose of helping others achieve their highest potential. Learn more about Liberty at https://www.libertyforrest.com/ and over at YouTube @LibertyForrest.* Your host is neither a doctor nor a medical professional. In the capacity of this presentation, both host and guest are speaking as everyday people trying to make sense of the world, and IS OPINION ONLY. 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.©2023 Sharon Sayler and UnderstandingAutoimmune.com#LibertyForrest #UnderstandingAutoimmune #AutoimmuneHour #Wellness #SharonSayler #Autoimmune #Health #SelfHelp #Lifestyle #InterviewsVisit the Autoimmune Hour show page https://omtimes.com/iom/shows/autoimmune-hour/Connect with Sharon Sayler at http://lifeinterruptedradio.com/Subscribe to our Newsletter https://omtimes.com/subscribe-omtimes-magazine/Connect with OMTimes on Facebook https://www.facebook.com/Omtimes.Magazine/ and OMTimes Radio https://www.facebook.com/ConsciousRadiowebtv.OMTimes/Twitter: https://twitter.com/OmTimes/Instagram: https://www.instagram.com/omtimes/Linkedin: https://www.linkedin.com/company/2798417/
Do you have questions about the Bible? Dr. Michael Rydelnik will join Dawn and Steve in the Morning to take questions from listeners and to update us on the Middle East. Dr. Michael Rydelnik is a professor of Jewish Studies at Moody Bible Institute and the Bible teacher on Moody Radio's Open Line. Author Andrea Herzer will encourage us with her book Incurable Faith: 120 Devotions of Lasting Hope for Lingering Health Issues. Having spent the last twenty years with multiple illnesses—including Complex Regional Pain Syndrome (CRPS) and non-Hodgkin’s lymphoma—Andrea Herzer is intimately acquainted with the hardships that accompany debilitating health issues. Navigating life while undergoing infusions, chemotherapy, more than 100 medical procedures, and all the complications in between has given her deep compassion for others who also suffer. Andrea’s writing has been featured in multiple devotional series on iBelieve.com and Crosswalk.com. Andrea and her remarkable husband Mark are blessed with three grown children, each of whom is their favorite child.See omnystudio.com/listener for privacy information.
In a courtroom filled with legal representatives, members of the press, and attentive members of the public, a young voice emerged, providing a harrowing account of life with a debilitating condition. Maya Kowalski, the brave teenager at the heart of a major lawsuit against Johns Hopkins All Children's Hospital, took the stand to shed light on her personal battles and the pain that has dramatically altered the trajectory of her life. "I have to live with this burning pain," Maya stated with a mix of determination and vulnerability. Her choice of words and descriptions gave those in attendance a chilling insight into the gravity of her condition known as Complex Regional Pain Syndrome (CRPS). Drawing a vivid analogy, she depicted the sensation as if she had gasoline coursing through her veins, ready to set her entire body ablaze with even the slightest trigger, whether it be a minor injury like a sprained ankle or a common ailment such as an asthma attack. CRPS, though not commonly understood by the general public, is a chronic condition characterized by severe, persistent pain. For many, describing the intensity and nature of this pain is almost impossible, but Maya's testimony provided a lucid, albeit disturbing, portrayal for the jury. By equating her pain to the volatile and explosive nature of gasoline, Maya effectively conveyed the sheer relentlessness and overwhelming nature of her symptoms. The backdrop to Maya's testimony is a multifaceted legal battle that has garnered significant attention. The Kowalski family's grievances with Johns Hopkins All Children's Hospital have unveiled a series of alleged medical missteps and subsequent institutional decisions. And while the legalities are complex, at the heart of it all is a young girl forced to navigate life with an agonizing condition. Maya's account serves as a stark reminder that behind every medical case and every lawsuit, there is a human story. Her words have shed light on the very personal struggle of living with CRPS, making it clear that her fight is not only against the hospital but also against a condition that threatens her quality of life daily. As the legal battle unfolds, Maya's powerful and evocative testimony will undeniably stand as a testament to the human side of the case, emphasizing the importance of compassion, understanding, and proper medical care in the face of life-altering challenges. Want to listen to ALL of our podcasts AD-FREE? Subscribe through APPLE PODCASTS, and try it for three days free: https://tinyurl.com/ycw626tj Follow Our Other Cases: https://www.truecrimetodaypod.com The latest on Catching the Long Island Serial Killer, Awaiting Admission: BTK's Unconfessed Crimes, Delphi Murders: Inside the Crime, Chad & Lori Daybell, The Murder of Ana Walshe, Alex Murdaugh, Bryan Kohberger, Lucy Letby, Kouri Richins, Malevolent Mormon Mommys, Justice for Harmony Montgomery, The Murder of Stephen Smith, The Murder of Madeline Kingsbury, and much more! Listen at https://www.truecrimetodaypod.com
Hidden Killers With Tony Brueski | True Crime News & Commentary
In a courtroom filled with legal representatives, members of the press, and attentive members of the public, a young voice emerged, providing a harrowing account of life with a debilitating condition. Maya Kowalski, the brave teenager at the heart of a major lawsuit against Johns Hopkins All Children's Hospital, took the stand to shed light on her personal battles and the pain that has dramatically altered the trajectory of her life. "I have to live with this burning pain," Maya stated with a mix of determination and vulnerability. Her choice of words and descriptions gave those in attendance a chilling insight into the gravity of her condition known as Complex Regional Pain Syndrome (CRPS). Drawing a vivid analogy, she depicted the sensation as if she had gasoline coursing through her veins, ready to set her entire body ablaze with even the slightest trigger, whether it be a minor injury like a sprained ankle or a common ailment such as an asthma attack. CRPS, though not commonly understood by the general public, is a chronic condition characterized by severe, persistent pain. For many, describing the intensity and nature of this pain is almost impossible, but Maya's testimony provided a lucid, albeit disturbing, portrayal for the jury. By equating her pain to the volatile and explosive nature of gasoline, Maya effectively conveyed the sheer relentlessness and overwhelming nature of her symptoms. The backdrop to Maya's testimony is a multifaceted legal battle that has garnered significant attention. The Kowalski family's grievances with Johns Hopkins All Children's Hospital have unveiled a series of alleged medical missteps and subsequent institutional decisions. And while the legalities are complex, at the heart of it all is a young girl forced to navigate life with an agonizing condition. Maya's account serves as a stark reminder that behind every medical case and every lawsuit, there is a human story. Her words have shed light on the very personal struggle of living with CRPS, making it clear that her fight is not only against the hospital but also against a condition that threatens her quality of life daily. As the legal battle unfolds, Maya's powerful and evocative testimony will undeniably stand as a testament to the human side of the case, emphasizing the importance of compassion, understanding, and proper medical care in the face of life-altering challenges. Want to listen to ALL of our podcasts AD-FREE? Subscribe through APPLE PODCASTS, and try it for three days free: https://tinyurl.com/ycw626tj Follow Our Other Cases: https://www.truecrimetodaypod.com The latest on Catching the Long Island Serial Killer, Awaiting Admission: BTK's Unconfessed Crimes, Delphi Murders: Inside the Crime, Chad & Lori Daybell, The Murder of Ana Walshe, Alex Murdaugh, Bryan Kohberger, Lucy Letby, Kouri Richins, Malevolent Mormon Mommys, Justice for Harmony Montgomery, The Murder of Stephen Smith, The Murder of Madeline Kingsbury, and much more! Listen at https://www.truecrimetodaypod.com
In this episode, Kevin takes us on a deeply personal journey as he recounts his decision to embark on a transformative experience at Eleusinia retreat. Kevin's motivation for this journey is twofold: to confront the intense pain associated with Complex Regional Pain Syndrome (CRPS) and to address the unprocessed emotions stemming from a life forever altered by a devastating car accident.
In the vibrant heart of Florida, the Kowalski family led a seemingly normal life. With strong Polish roots and deep familial bonds, the Kowalskis were pillars of their community. Yet, in 2016, they found themselves ensnared in a whirlwind of medical and legal battles that would challenge the very core of their unity and resilience. The Onset of a Mysterious Malady When Maya Kowalski, a spirited 9-year-old with a penchant for painting and playing the violin, began experiencing debilitating symptoms ranging from agonizing headaches to painful lesions on her limbs, alarm bells rang. No parent is prepared to see their child suffer, and Jack and Beata Kowalski were no exception. Desperate for answers, they navigated the complex web of the healthcare system, consulting numerous physicians and specialists. Self-advocacy and a Daunting Diagnosis It was Beata, a registered nurse with an astute sense of observation, who stumbled upon the possibility of Complex Regional Pain Syndrome (CRPS) while researching Maya's symptoms. This rare disorder, characterized by chronic pain and often triggered by an injury, was later confirmed by Dr. Anthony Kirkpatrick, a renowned specialist in the field. Seeking relief for Maya, the family even embarked on a perilous journey to Mexico to pursue an experimental treatment, the "ketamine coma," hoping it would offer their daughter some respite. Their endeavors seemed successful; Maya returned with a renewed zest for life. But this was just the calm before the storm. A Fateful Hospital Admission Less than a year after their return, a severe bout of stomach pain led Maya to be admitted to Johns Hopkins All Children's Hospital. Armed with her medical history, her parents insisted on high doses of ketamine to manage Maya's pain, an approach supported by Dr. Kirkpatrick. However, this admission set off a cascade of events that none could have foreseen. The hospital staff, rather than viewing the Kowalskis as concerned parents, eyed them with suspicion. The narrative shifted dramatically: Beata was accused of Munchausen by proxy, a condition where caregivers feign or induce illness in those they care for, seeking attention or sympathy. The Legal Nightmare With accusations flying, Maya was placed in state custody, barred from seeing her family. The trauma was immeasurable. Beata, painted as a villain by the hospital, faced public scrutiny, and emotional and psychological torment. Stripped of her maternal rights and bearing the weight of false accusations, she faced a battle on all fronts: the fight to prove her innocence, the yearning to reunite with her child, and the trauma of public defamation. Tragically, the weight became too much for Beata, leading her to take her own life, believing that her sacrifice might expedite Maya's return to her family. The Road to Vindication The aftermath of this tragedy saw the Kowalski family's fight gaining momentum. With the formidable Gregory Anderson of AndersonGlenn LLP by their side, they embarked on a mission to clear their name and bring the hospital to account. The ensuing legal battle revealed unsettling patterns, with Dr. Sally Smith, a senior child services physician, often at the center of numerous controversial child removal cases. The documentary, shedding light on the Kowalskis' ordeal, further bolstered their cause, unveiling other similar cases, indicating systemic flaws. Conclusion The Kowalski saga serves as a cautionary tale of the intricate interplay between the medical and legal systems. It underscores the importance of understanding, compassion, and due diligence in professions that wield the power to shape or shatter lives. As the Kowalskis continue their journey toward healing, their story stands as a testament to the indomitable human spirit and the enduring bonds of family. Want to listen to ALL of our podcasts AD-FREE? Subscribe through APPLE PODCASTS, and try it for three days free: https://tinyurl.com/ycw626tj Follow Our Other Cases: https://www.truecrimetodaypod.com The latest on Catching the Long Island Serial Killer, Awaiting Admission: BTK's Unconfessed Crimes, Delphi Murders: Inside the Crime, Chad & Lori Daybell, The Murder of Ana Walshe, Alex Murdaugh, Bryan Kohberger, Lucy Letby, Kouri Richins, Malevolent Mormon Mommys, Justice for Harmony Montgomery, The Murder of Stephen Smith, The Murder of Madeline Kingsbury, and much more! Listen at https://www.truecrimetodaypod.com
In the vibrant heart of Florida, the Kowalski family led a seemingly normal life. With strong Polish roots and deep familial bonds, the Kowalskis were pillars of their community. Yet, in 2016, they found themselves ensnared in a whirlwind of medical and legal battles that would challenge the very core of their unity and resilience. The Onset of a Mysterious Malady When Maya Kowalski, a spirited 9-year-old with a penchant for painting and playing the violin, began experiencing debilitating symptoms ranging from agonizing headaches to painful lesions on her limbs, alarm bells rang. No parent is prepared to see their child suffer, and Jack and Beata Kowalski were no exception. Desperate for answers, they navigated the complex web of the healthcare system, consulting numerous physicians and specialists. Self-advocacy and a Daunting Diagnosis It was Beata, a registered nurse with an astute sense of observation, who stumbled upon the possibility of Complex Regional Pain Syndrome (CRPS) while researching Maya's symptoms. This rare disorder, characterized by chronic pain and often triggered by an injury, was later confirmed by Dr. Anthony Kirkpatrick, a renowned specialist in the field. Seeking relief for Maya, the family even embarked on a perilous journey to Mexico to pursue an experimental treatment, the "ketamine coma," hoping it would offer their daughter some respite. Their endeavors seemed successful; Maya returned with a renewed zest for life. But this was just the calm before the storm. A Fateful Hospital Admission Less than a year after their return, a severe bout of stomach pain led Maya to be admitted to Johns Hopkins All Children's Hospital. Armed with her medical history, her parents insisted on high doses of ketamine to manage Maya's pain, an approach supported by Dr. Kirkpatrick. However, this admission set off a cascade of events that none could have foreseen. The hospital staff, rather than viewing the Kowalskis as concerned parents, eyed them with suspicion. The narrative shifted dramatically: Beata was accused of Munchausen by proxy, a condition where caregivers feign or induce illness in those they care for, seeking attention or sympathy. The Legal Nightmare With accusations flying, Maya was placed in state custody, barred from seeing her family. The trauma was immeasurable. Beata, painted as a villain by the hospital, faced public scrutiny, and emotional and psychological torment. Stripped of her maternal rights and bearing the weight of false accusations, she faced a battle on all fronts: the fight to prove her innocence, the yearning to reunite with her child, and the trauma of public defamation. Tragically, the weight became too much for Beata, leading her to take her own life, believing that her sacrifice might expedite Maya's return to her family. The Road to Vindication The aftermath of this tragedy saw the Kowalski family's fight gaining momentum. With the formidable Gregory Anderson of AndersonGlenn LLP by their side, they embarked on a mission to clear their name and bring the hospital to account. The ensuing legal battle revealed unsettling patterns, with Dr. Sally Smith, a senior child services physician, often at the center of numerous controversial child removal cases. The documentary, shedding light on the Kowalskis' ordeal, further bolstered their cause, unveiling other similar cases, indicating systemic flaws. Conclusion The Kowalski saga serves as a cautionary tale of the intricate interplay between the medical and legal systems. It underscores the importance of understanding, compassion, and due diligence in professions that wield the power to shape or shatter lives. As the Kowalskis continue their journey toward healing, their story stands as a testament to the indomitable human spirit and the enduring bonds of family. Want to listen to ALL of our podcasts AD-FREE? Subscribe through APPLE PODCASTS, and try it for three days free: https://tinyurl.com/ycw626tj Follow Our Other Cases: https://www.truecrimetodaypod.com The latest on Catching the Long Island Serial Killer, Awaiting Admission: BTK's Unconfessed Crimes, Delphi Murders: Inside the Crime, Chad & Lori Daybell, The Murder of Ana Walshe, Alex Murdaugh, Bryan Kohberger, Lucy Letby, Kouri Richins, Malevolent Mormon Mommys, Justice for Harmony Montgomery, The Murder of Stephen Smith, The Murder of Madeline Kingsbury, and much more! Listen at https://www.truecrimetodaypod.com
Sam Schaefer is an athlete and coach at Schaefer Adaptive Methods. After dealing with intense chronic pain from CRPS for nearly a decade, Sam had his lower left leg amputated in 2020. Since then he's worked to help other amputees build strength, advocates for those in the adaptive community, and pushes his body to the limits in a variety of fitness disciplines. In this episode, Sam shared his story of battling with Complex Regional Pain Syndrome (CRPS) for nearly 10 years before having his lower leg amputated in order to alleviate the pains of the condition. We discuss his perspective through that journey, how he trains as an adaptive athlete, advice to other amputees, upcoming fitness challenges, and more. Timecodes: (2:01) - Sam's Running Journey (3:47) - Humbling Nature of Running (5:56) - Sam's Athletic Background (7:40) - Training Fitness vs. Sport (9:28) - Complex Regional Pain Syndrome (CRPS) (12:15) - What CRPS Feels Like (13:52) - How Amputation Provided Hope (19:00) - Thoughts Going Into Amputation Surgery (21:03) - Dealing With Veteran Affairs (24:04) - Highs & Lows of Recovery (26:49) - Phantom Pains & Potential Regression (28:02) - Function of Different Prosthetics Legs (33:48) - Innovation Within Prosthesis (36:11) - Advice For Amputees Or Adaptive Athletes (39:30) - "Everything is different but everything is the same" (40:52) - Sam's Pivot Towards Running (44:17) - Signing Up For a 30K (47:25) - Challenges Running With a Prosthetic (53:29) - Training Through Intuition vs. Data (57:13) - Less Leg, More Heart Non-Profit (1:01:14) - Importance of Personalizing Healthcare For More: Follow Brock on Instagram Follow Brock on YouTube Follow Sam on Instagram Support The Podcast: switchback Electrolytes Ten Thousand | Code: COVINGTON Flux Footwear | Code: Brock --- Support this podcast: https://podcasters.spotify.com/pod/show/zero-quit-podcast/support
Complex Regional Pain Syndrome CRPS I’m David Holub, an attorney focusing on personal injury law in northwest Indiana. Welcome to Personal Injury Primer, where we break down the law into simple terms, provide legal tips, and discuss personal injury law topics. Today’s question comes from a caller who said his doctor diagnosed him with Complex […] The post Ep 225 – Complex Regional Pain Syndrome CRPS first appeared on Personal Injury Primer.
In this podcast episode, we meet Bonnie Tarbert, a self-published children's book author from Baltimore, Maryland. With over 25 years of experience in childcare and teaching, Bonnie has a special connection with children that she incorporates into her writing. She is also an illustrator and holds degrees in Art Education and Painting.Bonnie shares her journey of becoming a children's book author and discusses her passion for art and teaching. Despite starting her writing and illustrating career in 2022, she has already written multiple titles that can be found in libraries worldwide.Additionally, Bonnie opens up about her personal experience with Complex Regional Pain Syndrome (CRPS), a condition characterized by prolonged and excessive pain following an injury to an arm or leg. She describes the symptoms and challenges of living with CRPS, emphasizing the difficulty of finding effective treatments.Despite the obstacles she faces, Bonnie remains resilient and continues to inspire others through her creativity and storytelling. Her story serves as a reminder of the power of art, teaching, and personal resilience in making a positive impact on children's lives.Here are links for you to bookmark, save, follow, memorize, write down, and to share with others:Bonnie Tarbert Children's Book Author - Home (weebly.com)Bonnie Tarbert | Barnes & Noble® (barnesandnoble.com)Bonnie Beth (@bonnietarbert) • Instagram photos and videosBonnie Tarbert | LinkedInThis episode is sponsored by Freedom Federal Credit UnionHere's a podcast that I recomGet your story told and book written. Schedule a call with Mike Ulmer at Select a Date & Time - CalendlyFreedom Federal Credit Union HELPING YOU REACH YOUR FINANCIAL DREAMSDisclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.Support the showFollow the Conversations with Rich Bennett podcast on Social Media:Facebook – Conversations with Rich Bennett & Harford County LivingFacebook Group (Join the conversation) – Conversations with Rich Bennett podcast group | FacebookTwitter – Conversations with Rich Bennett & Harford County LivingInstagram – Harford County LivingTikTok – CWRB (@conversationsrichbennett) | TikTok Sponsors, Affiliates, and ways we pay the bills:Recorded at the Freedom Federal Credit Union StudiosHosted on BuzzsproutRocketbookSquadCast Contests & Giveaways Subscribe by Email ...
Welcome to That's So Chronic (or if you're a long time listener, welcome back!) a weekly podcast where Jess Brien (@jessssbrien) interviews people from around the world who are thriving - and sometimes only just surviving - with chronic illnesses, life changing injuries, and potentially disastrous diagnoses... all while having a laugh along the way. You can expect new patient stories every Tuesday, and on the final Tuesday of the month, we chat about anything and everything that's in our That's So Chronic world. Whether that be a That's So episode focusing on a book, film, or another type of content, or a Spotlight On episode where we deep dive into a person or an organisation making waves in the chronic illness and disability space. Follow on IG and Tiktok: @thatssochronic Sign up to the free monthly newsletter on Substack: thatssochronic.substack.com Application form to share your story: https://forms.gle/csebLkwfwAjiLApK9 And feel free to reach out over at www.thatssochronic.com or send me an email: hello@jessbrien.com Episodes featured in the trailer (in order of appearance): • Emily Spink & Crohn's Disease • Abbie Madden & Congenital Glaucoma • Oliva Odey & Complex Regional Pain Syndrome (CRPS) and Neural Sensitisation Syndrome • Joshua Phillips & Obsessive Compulsive Disorder (OCD) • Lee Weir & Type 2 Diabetes • Hayley Sproull & Polycystic Ovarian Syndrome (PCOS) • Sam Smith & Relapsing Remitting Multiple Sclerosis (RRMS) • Tatjana & Attention Deficit Hyperactivity Disorder (ADHD) • Carlyn Reed & Hodgkin's Lymphoma • That's So: The Uncertainty Myth by Dr Toni Lindsay • Spotlight On: Get Well Circus • Spotlight On: Exsurgo • That's So: Why Does It Still Hurt? by Dr Paul Biegler Disclaimer: Here at That's So Chronic we are sharing personal stories and are not advocating any type of treatment, therapy, procedure or intervention. Everyone is unique so please seek professional medical advice before making any decisions for yourself or for others. Hosted on Acast. See acast.com/privacy for more information.
On this week's episode of The 1 Girl Revolution Podcast, we're joined by Nancy Becher, founder of Invisible Warriors - an organization dedicated to supporting those living with chronic illness, autoimmune issues, and invisible disabilities. Nancy's own journey with invisible illness began in 2014, when her life took a drastic turn after she was hit by a car. While picking up her parents from a senior center potluck, she was struck by another attendee's car, which caused her to be thrown into a drainage ditch, resulting in twisted tendons, ligaments, and broken bones. The path to diagnosis was a long and arduous one for Nancy, involving visits to multiple doctors and enduring months of physical pain. Eventually, she was diagnosed with Complex Regional Pain Syndrome (CRPS), a debilitating condition that causes severe nerve damage. Nancy underwent numerous surgeries, received two spinal stimulators, and encountered countless medical professionals in her quest for relief from the relentless pain. Drawing on her background with a Master's in Counseling and a Ph.D. in sociology, Nancy decided to utilize her knowledge and personal experiences to create Invisible Warriors, a nonprofit organization dedicated to supporting people living with chronic illness, autoimmune issues, and invisible disabilities. The mission of Invisible Warriors is not only to provide assistance and resources to these individuals but also to initiate dialogue with medical professionals and advocate for changes in the insurance, pharmaceutical, and travel industries. Through Invisible Warriors, Nancy aims to create a community where those living with hidden chronic and autoimmune disorders can find solace, support, and a sense of belonging. By sharing her own journey and advocating for systemic changes, Nancy is determined to make a positive impact on the lives of others who are going through similar mental and physical anguish. Nancy is an advocate, who is working towards greater awareness, understanding, and resources for individuals with invisible illnesses. Nancy Becher's resilience and determination to create a supportive community for individuals with chronic illness, autoimmune issues, and invisible disabilities are truly commendable. Through her personal experiences, academic background, and unwavering passion, she has taken on the mission of empowering others and working towards a more inclusive and compassionate society. In this episode, you'll hear: Nancy's inspiring life story; The story of the accident that led to her health issues and Complex Regional Pain Syndrome (CRPS); How she decided to start Invisible Warriors and why their work is so important; About the people that Nancy and Invisible Warriors are helping; How you can get involved in their work if you're living with an invisible disability or illness; About the Silent No More Benefit Concert and how you can attend and support the event; And so much more. The 1 Girl Revolution Podcast is available on Apple Podcasts, Spotify, Stitcher, iHeartRadio, YouTube, and everywhere you listen to podcasts. For more information on Nancy Becher and Invisible Warriors, please visit: www.1girlrevolution.com/InvisibleWarriors
Katie Wrigley is a Transformational Coach, Cognomovement Practitioner, and host of the Pain Changer Podcast. She is also a former chronic pain patient who found herself disabled in her early 40s after years of severe chronic pain and losing herself in a demanding 20 year long corporate career. Traditional medicine continued to fail her as her diagnoses continued to pile up, including Fibromyalgia, Complex Regional Pain Syndrome (CRPS), slipped and bulging discs, and unrelenting chronic nerve pain and increasing weakness in her limbs. It all turned around when she was introduced to Cognomovement, a gentle but effective movement modality which interrupts the pain pathways of the brain and restores the body back to health and homeostasis. Katie shares her personal pain journey along with her experience of eliminating her pain with Cognomovement, how (and why) the method works, how to listen to yourself and your body, the many benefits of cross body learning, and much, much more. Download this positive and informative episode which has a clear message of hope, and please share it with everyone who is struggling with chronic pain to learn the magic of Cognomovement. Because our bodies have an incredible capacity to heal, and no one should suffer with chronic pain. https://katiewrigley.com/ https://www.facebook.com/katie.wrigley.maine https://www.linkedin.com/in/coachktdubs/ https://www.youtube.com/channel/UCNEkBK4IfBDU4kpntFjmjOQ https://www.instagram.com/coachktdubs/
In this episode, we review the high-yield topic of Complex Regional Pain Syndrome (CRPS) from the Basic Science section. Follow Orthobullets on Social Media: Facebook: www.facebook.com/orthobullets Instagram: www.instagram.com/orthobulletsofficial Twitter: www.twitter.com/orthobullets LinkedIn: www.linkedin.com/company/27125689 YouTube: www.youtube.com/channel/UCMZSlD9OhkFG2t25oM14FvQ --- Send in a voice message: https://podcasters.spotify.com/pod/show/orthobullets/message
Today, we take a close look at the Complex Regional Pain Syndrome (CRPS). We discuss the diagnostic criteria, pathophysiology and treatment of this condition, as well as taking a closer look at the role of opioids in the management of pain relating to CRPS. Resources for today's episode: Complex Regional Pain Syndrome: Practical Diagnostic and Treatment Guidelines, 5th Edition by Harden, R.N et al. ANZCA Blue Book 2019: The changing face of complex regional pain syndrome treatment by Russo, M., Georgius, P. & Santarelli, D. (p183) Up To Date Articles: Complex regional pain syndrome in adults: Pathogenesis, clinical manifestations and diagnosis by Abdi, S. Complex regional pain syndrome in adults: Treatment, prognosis and prevention by Abdi, S.Feel free to email us at deepbreathspod@gmail.com if you have any questions, comments or suggestions. We love hearing from you! And don't forget to claim CPD for listening if you are a consultant or fellow. Log us as a learning session which you can find within the knowledge and skills division, and as evidence upload a screenshot of the podcast episode. Thanks for listening, and happy studying!
Joanne interviews Angela Talent who lives with Complex Regional Pain Syndrome (CRPS) which robs her of the use of her hands and limits her ability to walk far distances and needs in-homecare for herself. Science is proving at the Heart Math Institute that heart focused breathing, sending coherent waves of love brings together the convergent of physical pain and relief with natural remedies. Her website www.damagedparents.com She has her own podcast Relatively Damaged, for families living with disabilities. Serraphine.com for private sessions Serra on guided journeys for fullfilling your Life Desires Video Course 3 Steps to Concise Decision Make ESA Pros.com Get a certified Psychiatric Service Dogs to go where you go and emotional support animals for house companions Anxiety Simplified Show now going Beyond Psychology On Power Me Up station on IHeart Radio Mon. at 4:30 pm Pac. M-F Anxiety Simplified Show 5pm. Pacific and 8 pm Eastern
In this episode, Lyndsay Soprano talks with Katie Wrigley a transformational coach with a specialty in pain and stress and is also a Cognomovement practitioner. She came into this niche organically through her own life experience.She was pretty lost when traditional medicine continued to fail her as diagnoses just kept piling up including Fibromyalgia, Complex Regional Pain Syndrome (CRPS), slipped and bulging discs, unrelenting chronic nerve pain, and increasing weakness in her limbs.So she decided it was time to face a few things that had happened to her when she was young and take on the trauma head-on with all the gusto in the world. In her early 40s, she finally had to face an early childhood trauma that she tried to run from her entire life, and that's when her life finally started to transform – when she faced herself!Man, that is hard to do…looking at yourself in the mirror is nothing short of brave!Let's get to the heart of how to heal. With you by my side.Visit us at thepaingamepodcast.com and follow us on all socials!You can find Katie Wrigley at:Instagram:https://www.instagram.com/coachktdubs/Facebook: https://www.facebook.com/coachktdubsYouTube: @coachktdubsLinkedIn: https://www.linkedin.com/in/coachktdubs/Website: www.katiewrigley.comPodcast: https://podcasts.apple.com/us/podcast/the-pain-changer-podcast/id1622193854
In honor of #CRPSAwarenessMonth, Dr. Lin interviews physician scientist Vivianne Tawfik, MD, PhD, who just won the ASA James Cottrell Presidential Scholar's Award for her work with Complex Regional Pain Syndrome (CRPS). Dr. Tawfik has a successful lab studying causes such as glial function, her clinical work with CRPS, as well as her work mentoring upcoming physicians and scientists. The topic is one that is intellectually challenging, with life-changing implications for people with CRPS, and one that the CSA Podcast is proud to call attention to.So many people with CRPS struggle to see the possibilities of living and thriving despite it - the podcast has pulled in an amazing advocate who managed to return to her international sports career after proper diagnosis and management - by Dr. Tawfik!This is the story of Coco Vandeweghe, an American professional tennis player. She achieved a career high world ranking of #9 in 2017, when she made the semifinals of two Grand Slam tournaments, the Australian Open and US Open. She was knocked out of her sport in early 2019 with mysterious symptoms which, after a lot of uncertain times, was diagnosed by Dr. Vivianne Tawflik at Stanford as CRPS, and she has beaten all odds to return to an elite level of professional tennis. This August, she won a professional tennis tournament in Concord, Massachusetts.
In this episode, we review the high-yield topic of Complex Regional Pain Syndrome (CRPS) from the Basic Science section. Follow Orthobullets on Social Media: Facebook: www.facebook.com/orthobullets Instagram: www.instagram.com/orthobulletsofficial Twitter: www.twitter.com/orthobullets LinkedIn: www.linkedin.com/company/27125689 YouTube: www.youtube.com/channel/UCMZSlD9OhkFG2t25oM14FvQ --- Send in a voice message: https://anchor.fm/orthobullets/message
Quite frankly, Angela is no one important. If you were to ask what she does or how she identifies, she would most likely say mom. In the last few years, she has noticed divisiveness amongst groups and wants to show the world how similar we all are in our suffering and our joy. She does that with her podcast Relatively Damaged. In addition to the podcast she hopes to effect real policy changes for those who are disabled in the United States where, when one becomes so disabled they need in-home-care, they become a hostage to their home. Angela Talent is the mother of two. At the age of 35 she was diagnosed with Complex Regional Pain Syndrome (CRPS) which would rob her of the use of her hands and limit her ability to walk. At the beginning of 2021 she realized she could use her ability to listen and have meaningful conversations to show the world how uniquely beautiful the human experience is. Facebook: @damagedparents Instagram: @damagedparents TikTok: @damagedparents Twitter: @damagedparents Website: www.damagedparents.com Key points: 1. What you look for you will find 2. And it is much more fun to live there than it is to live 3. If you think you're not valuable, then you will believe you're not valuable 4. My experience of you happens inside of me 5. Listen to and follow your heart 6. See things in 3D 7. Perspective and perception are the two deciding factors which lead to choice
PARENTS AS RARE - EPISODE 048 Parenting & Living Life With Chronic Pain - Ross McCreery Ross McCreery is a dad, husband, advocate, writer and speaker. In 2006, Ross was diagnosed with a rare disease called Complex Regional Pain Syndrome (CRPS). In 2016 he founded CRPS Awareness Day in Saskatchewan to educate the public and raise awareness for those living with the disease. Ross also serves as a board member for the SaskPain Foundation where he hopes to help improve and change the lives of those living with chronic pain. He also advocates and speaks to serve as a voice for those who suffer chronic pain, he's authored several published pieces, appeared on television programs and believes in the power of a strong community of rare disease advocates with diverse voices who can encourage change and progress for all. EPISODE HIGHLIGHTS Can you tell us a little bit about yourself and your rare disease diagnosis story? I was successful in my career, I was married and life was going in the direction I wanted it to go. I had just came back from China after adopting my first daughter and had what should have been a simple surgery. The swelling and loss of mobility in my hand that resulted was the onset of my disease symptoms and Complex Regional Pain Syndrome (CRPS) diagnosis journey. What was your experience like discussing your CRPS diagnosis with your children? We say it how it is and believe in transparency. From the earliest age that they could understand, we had conversations with them about how things needed to be done differently. Having conversations with our kids and being honest and up front with them was a daily occurrence, especially as we adapted and changed. How have your conversations evolved as they've grown older? Conversations are simpler now because they understand better and have a background living with it for awhile. We don't have to explain as much, they're more understanding of the situation and can figure out a lot themselves. We still have conversations with them at times as things continue to happen or change. What wisdom do you have to share with listeners? We don't value our stories enough. Our stories are our power and it's the power of the story that touches people. I encourage people to share their story. CONNECT WITH ROSS Contact https://painfullyoptomistic.com/contact-me Instagram https://www.instagram.com/painfullyoptomistic/ Twitter https://twitter.com/Rossco006 Facebook https://www.facebook.com/Painfully-Optomistic-192150737539022/ RESOURCES MENTIONED Painfully Optomistic Blog
ENERGY IN ACTION - EPISODE 040 Silver Linings with Sarah Kate Sarah Kate Frey is a mitochondrial disease patient who is always looking on the bright side, seeking silver linings in the darkest experiences. She is the author of Alice Eloise’s Silver Linings: The Story of a Silly Service Dog and is in the process of writing a second book about her friend and service dog, a doodle named Alice Eloise. EPISODE HIGHLIGHTS How are you connected to the mito world? Like a lot of patients, my path to a mitochondrial disease diagnosis was not a straight line. At about 12 years old, I came home from horseback riding camp really sick with a high fever and a staph infection in my throat that had me sick for months. I landed in the ER numerous times in a year for extreme dehydration and high inflammation markers. The following year in dance class, I sprained my ankle. Within the week, I received a Reflex Sympathetic Dystrophy (RSD) and Complex Regional Pain Syndrome (CRPS) diagnosis. Not long after, I had extreme GI symptoms and saw a gastric motility doctor who did gastric emptying studies and further testing. I was diagnosed with Gastroparesis and then later with Hemophagocytic lymphohistiocytosis (HLH). What led to a mitochondrial disease diagnosis was tying everything together. Can you tell us about Alice Eloise and how you came to author children's books? I love dogs and wondered how a service dog could help me. My sweet doodle, Alice Eloise, and I are a self-trained service dog team. She's my silver lining through being sick, so silver linings has become a mission for me. I decided to write a book about a girl and her dog, about silver linings and looking on the bright side. When Alice Eloise came along and stole my heart, it was time to tell our story. And that's what we're doing. The first book is written through the puppy eyes of Alice Eloise and her perspective of becoming a service dog. The biggest lessons from the story are no matter what you're going through, look for silver linings, never give up and seek the beauty in the world. What will the second book be about? It's about a trip to the zoo with Alice Eloise, which started out as a scene in the first book. We ended the first book after her service dog test, so I decided to add to the story with another book. The premise of this book is about being someone else's silver lining, and knowing that some of the best silver linings in life are the people around us and our interactions with one another. RESOURCES MENTIONED Alice Eloise’s Silver Linings: The Story of a Silly Service Dog https://sarahkatessilverlinings.com/once-upon-a-silver-lining-store/ Sarah Kate's Silver Linings Blog https://sarahkatessilverlinings.com/blog/ CONNECT WITH MITOACTION Website https://www.mitoaction.org/
Angela Talent is the mother of two. At the age of 35, she was diagnosed with Complex Regional Pain Syndrome (CRPS) which would rob her of the use of her hands and limit her ability to walk far distances. At the beginning of 2021, she realized she could use her ability to listen and have meaningful conversations to show the world how uniquely beautiful the human experience is and started her podcast Relatively Damaged. Quite frankly, Angela is no one important. If you were to ask what she does or how she identifies, she would most likely say mom. In the last few years, she has noticed divisiveness amongst groups and wants to show the world how similar we all are in our suffering and our joy. She does that with her podcast Relatively Damaged. In addition to the podcast she hopes to effect real policy changes for those who are disabled in the United States where, when one becomes so disabled you need in-home-care, they become a hostage to their home. Facebook: @damagedparents Instagram: @damagedparents TikTok: @damagedparents Twitter: @damagedparents Website: www.damagedparents.com Do you want to be featured on The Gratitude Zone? All you have to do is send me a 2 - 3 minute audio clip and include the following! Who you are What you do…(Let us know if you're a coach, podcaster, or speaker!) What you're grateful for Why are you grateful for this! Send your recorded audio clip to tamar@theroadforward.ca Be sure to add the name Gratitude Zone in the Subject of your email! Come join us for our Collaboration Zone Zoom Party! Do you want to network and collaborate with like-minded entrepreneurs in recovery? Then make sure you join our next Collaboration Zone Zoom Party. This will give you an opportunity to network with other entrepreneurs who can help you grow or complement your business! Book a FREE 30 Minute Discovery Call or Mindset Business Audit Call! Book Here: Discovery Call - Discover your purpose and get some clear direction. Book Here: Mindset Business Audit Call - Find out what beliefs might be holding you back! Social Media: Facebook: https://www.facebook.com/groups/riseinrecovery Twitter: https://twitter.com/riseinrecovery Instagram: @theroadbeyondrecovery LinkedIn: https://www.linkedin.com/in/tamarmedford/ Website: www.theroadforward.ca
Have you experience pain and suffering that was so extreme you felt as if you couldn't continue? What helped you overcome and flip the script of pain into purpose? In this segment, Darci J. Steiner talks about her journey with Complex Regional Pain Syndrome (CRPS), her Faith, writing a book, and how she sees the upside to the suffering. CRPS - Complex regional pain syndrome (CRPS) is a form of chronic pain that usually affects an arm or a leg. CRPS typically develops after an injury, a surgery, a stroke or a heart attack. The pain is out of proportion to the severity of the initial injury. See video component - https://youtu.be/7je98ZMEqrg WHO IS DARCI? Darci J. Steiner has served in the ministry as a teen and women's ministry leader, as well as assisted with church plants in Denver and Los Angeles. In 2001, Darci nearly lost her life after a debilitating fall. During her recovery, she earned her Master of Science degree in Holistic Nutrition and implemented natural remedies into her diet that helped save her life. When Darci became disabled a second time after a foot injury in 2018, she turned her focus toward ministry again by writing her debut book, Beauty Beyond the Thorns: Discovering Gifts in Suffering and its companion, Study Guide for Beauty Beyond the Thorns: Discovering Gifts in Suffering. Darci and her husband have two adult daughters and one baby granddaughter. They live in the Denver area. DARCI'S CALL TO ACTION I would like for people to visit my website and hopefully buy a copy of my book! DARCI'S CONTACT INFO https://www.darcijsteiner.com https://www.linkedin.com/in/darcijsteiner/ https://www.facebook.com/DarciJSteiner https://www.instagram.com/darcijsteiner.writer GENESIS'S INFO https://thehello.llc/GENESISAMARISKEMP CALL TO ACTION Subscribe to GEMS with Genesis Amaris Kemp Channel, Hit the notifications bell so you don't miss any content, and share with family/friends. **REMEMBER - You do not have to let limitations or barriers keep you from achieving your success. Mind over Matter...It's time to shift and unleash your greatest potential. --- Send in a voice message: https://anchor.fm/genesis-amaris-kemp/message Support this podcast: https://anchor.fm/genesis-amaris-kemp/support
For more than three years, Darci Steiner has been unable to walk after incurring a debilitating foot injury. Suffering from a nerve pain disorder called Complex Regional Pain Syndrome (CRPS), Darci reached a point where she felt she didn't want to live another day. But over time, God's "thorn in the flesh" in her life began revealing the upside of suffering. Through it all, she discovered the ability to persevere beyond her strength, courage to go where she had never been, a deeper faith in God, and an unquestionable hope. Hope Along the Journey Website: https://www.hopealongthejourney.org/ Donate: https://www.paypal.com/donate/?hosted_button_id=3ZAA66EPDVZJ4 Darci Steiner website: https://www.darcijsteiner.com/ --- Support this podcast: https://anchor.fm/mark-cravens7/support
Complex Regional Pain Syndrome (CRPS) can be a tricky beast. Luckily we have Miranda Materi on the podcast today to help us better understand this intimidating condition in order to give our patients the best possible outcome. Miranda received her professional clinical doctorate in occupational therapy from Creighton University in 2006. After practicing hand therapy for five years, she became a certified hand therapist. She has a strong interest in research and development in clinical settings and has participated in many studies. Miranda has served as an adjunct faculty member at the Mayo Clinic and currently is an adjunct faculty member at Northern Arizona University. She is also co-leader of the Hand Therapy Academy, alongside our buddy Josh MacDonald, who we talked with back in episode eight. In this episode, we dive into everything CRPS: diagnostic types, typical patient demographic, symptoms to look out for, why it's critical to diagnose and treat early, and unique treatment approaches that are backed in evidence (and require a holistic, mind-body perspective). Miranda has a way of breaking down this complex condition to help clinicians feel educated, empowered, and equipped to treat.
Third episode of Yays of our Lives this week and we have our first actual member of the yayborhood join us for a Yayborhood Watch chat. The wonderful Kate Rider shares her journey with Complex Regional Pain Syndrome (CRPS) which led to her founding The Orange Elephant to help her and others redefine productivity, success and the concept of "small" achievements. Getting more into a flow with this new yayborhood segment each week, thank you so much to everyone for your contributions - please keep them coming! I'm so used to writing and editing it all myself and it's been LOVELY having you all involved in editorial decision - I can't wait to watch this segment continue to grow. >> COMPLETE THE SURV-YAY IF YOU HAVEN'T ALREADY
After becoming disabled as a teenager with Complex Regional Pain Syndrome (CRPS), Danielle realised very quickly that even during adversity we all have a choice. You can either choose to let things outside of your control defeat you, or choose to control how you respond to it. Today on The Best Version Of You show, Danielle shares how she discovered archery at 15 years old and how three years later she was representing Team GB - jumping straight to number one in the world. Danielle managed to maintain her title as the world's best throughout her entire career whilst winning gold in Beijing and again in London in 2012 on home soil. She also became the first disabled person in history to represent England as an able-bodied competitor in the 2010 Commonwealth games. Nowadays, Danielle works as a keynote speaker, trainer and coach. She focuses on helping others unlock their true potential and break down barriers. Something she is extremely passionate about and is a reflection on the large number of people she has helped. Especially the younger generation, empowering them to develop strong foundations for success through her online program 'Your Journey To Success' which helps young people develop stronger mental health and perform better in exams. Danielle's latest achievement is publishing a book she co-authored called 'Be Your Best Self: Life skills for unstoppable kids'. A children's self-development book released in Oct 2019 with a 9 year old Nathan Kye. Today Danielle shares with us what it really means to be The Best Version Of You and how any of us can overcome adversity by not letting it defeat you! ** DON'T FORGET TO SUBSCRIBE AND SHARE TODAY'S MONDAY MOTIVATION EPISODE WITH ALL YOUR FRIENDS AND FAMILY AND MAKE SOMEONE SMILE! **
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