My Journey To hEDS Diagnosis | Ten Years Undiagnosed...

Today I'm telling you all about my ten-year process of getting diagnosed with hypermobile Ehlers-Danlos syndrome. I was told it was anemia three times, depression once, and even once told "it sounded like something" but the doctor "didn't have time to look it up". Navigating the medical system is hard, but if you're doing it right now, know that I got your back, and support you fully! :) Find me on Instagram!   / robinhahnsopran   Find me on Twitter!   / ​   Buy me a Ko-Fi! https://ko-fi.com/robinhahnsopran AMAZON AFFILIATE LINKS (thanks so much for clicking!) Headband: https://amzn.to/46BGJKM Eyeliner: https://amzn.to/3R93rVT Microphone: https://amzn.to/47pbHqp Ring light: https://amzn.to/47pbJi1 MUSIC: “Feeling Good” Music: https://audiotrimmer.com/royalty-free... Music: https://mixkit.co/​ Music: https://www.purple-planet.com/ #EhlersDanlos #ChronicIllness #MyDiagnosisStory