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In this video, my mum and me will be answering some of the questions you’ve asked about my experience with POTS syndrome. I’ll delve into topics like: Does my mum feel guilty about her genetics? How did we both feel when I received my diagnosis? Do you still meet the diagnostic criteria for POTS? How can you deal with chronic illness when you don't have a supportive family? What's it like going from playing sports to nothing as a teen girl with dysautonomia? Whether you're a parent worried about your child or someone struggling to get answers, this video will give you insights into living with POTS and multiple chronic illnesses and navigating the healthcare system for a proper diagnosis. Growing Up with POTS Syndrome: My Story of Living with Chronic Illness, A Conversation with My Mum • Growing Up with POTS Syndrome: My Story of... Check out my previous videos: Exercise with POTS Syndrome + EDS | A Look at My Training Routine w/ Leah Hollingsworth • Exercise with POTS Syndrome + EDS | A Look... POTS Alex's Story: Diagnosis to Thriving | How to live with POTS syndrome + Dealing with Negativity • POTS Alex's Story: Diagnosis to Thriving |... SUBSCRIBE and click the BELL to get notified when new videos are uploaded! SOCIALS Instagram: @thepotscoach Instagram 2: @thepotscoachapproach TikTok: @thepotscoach POTS, Chronic Illness, Dysautonomia, Postural Orthostatic Tachycardia Syndrome Thanks for watching! Xx HI! My name is Rosie. I have suffered with multiple chronic illnesses for a majority of my life, including POTS, EDS, MCAS and chronic fatigue. Now, I specialise in helping people with similar chronic illness to get their life back. I am a competitive bodybuilder and will be sharing tip and tricks, as well as showcasing what IS possible when you have multiple chronic illnesses. #POTS #POTSSyndrome #ChronicIllness