What happens when a rare condition silently disrupts a life - and no one can figure out what’s wrong? In this powerful episode of Beatwise The Podcast, I sit down with Sam Jarrett, a courageous woman navigating the complex world of amyloidosis - a rare and often misdiagnosed disease that affects the body’s organs and tissues.Together, we explore Sam’s personal and emotional path to diagnosis after months of unexplained symptoms and frustration within the healthcare system. She opens up about her life-changing experience at the National Amyloidosis Centre in London, the hope she found through participation in a clinical trial, and what she wants others living with rare diseases to know. Whether you're a medical professional, caregiver, or someone seeking answers, this episode offers deep insight into the importance of early detection, patient advocacy, and the evolving landscape of amyloidosis treatment.EPISODE HIGHLIGHTS:[00:00] Introduction to amyloidosis and why awareness matters[01:42] The beginning of Sam’s journey: symptoms and misdiagnoses[05:11] What exactly is amyloidosis? A simplified breakdown[10:56] Inside the National Amyloidosis Centre: care that changed everything[19:34] The power of clinical trials in rare disease treatment[26:32] Living well with amyloidosis: support, care, and hope[34:40] Final thoughts and what we can all learn from Sam’s storyIf you enjoyed this episode, please like, rate, and subscribe to Beatwise The Podcast. Your support helps me reach more listeners and continue providing valuable content.Don't forget to follow me on social media @sarah.theheartdoc for the latest updates, behind-the-scenes content, and more engaging discussions. Stay connected and be part of our growing community! Hosted on Acast. See acast.com/privacy for more information.

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