People Think I'm Faking My Disability 🎤: Aiden Bloch #DisabilityHumor #ChronicIllness #standup
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Exploring the Quirks of Ehlers Danlos Syndrome
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TikTokjello_jam_kitty
“I’m Aiden Bloch, a 16-year-old stand-up comedian diagnosed with classical/hypermobile Ehlers-Danlos syndrome (EDS) when I was 2 years old. Having EDS and being an adrenaline junkie is not a good combination: I have had over 100 stitches. My whole life I couldn’t accept that I was born this way and I can’t be ‘normal’ – about six months ago I finally accepted it. My whole life I pushed through the pain but over time it got worse to the point that I had to and still do use a walker and wheelchair
0:40
“I’m Aiden Bloch, a 16-year-old stand-up comedian diagnosed with classical/hypermobile Ehlers-Danlos syndrome (EDS) when I was 2 years old. Having EDS and being an adrenaline junkie is not a good combination: I have had over 100 stitches. My whole life I couldn’t accept that I was born this way and I can’t be ‘normal’ – about six months ago I finally accepted it. My whole life I pushed through the pain but over time it got worse to the point that I had to and still do use a walker and wheelchair
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FacebookThe Ehlers-Danlos Society
Thankful every day that I’m disabled because otherwise I would be a terrible hang #disabled
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Thankful every day that I’m disabled because otherwise I would be a terrible hang #disabled
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Rare disease month. Ehlers Danlos edition. Standing and sitting are my enemies. Walking, I can work with…. But when my brain gets mad at the things I used to do with out having to overthink about it, is the hardest part. Everyday I strive to feel decent and every day is battle. I don’t go out much anymore, mostly cause I’m afraid of falling or having an attack and being by myself. So I’m re-building my foundation at home slowly and quietly. #heds #raredisease #hipdysplasiawarrior #life #stronger
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They said it’s just knee pain… EDS says it’s loose kneecaps, cartilage damage, grinding stairs, and daily battles—who else lives this reality? #ehlersdanlossyndrome #supportcommunity #zebrastrong #invisibleillness #EDS #potssyndromeawareness🦵🔥 | Ehlers Danlos Syndrome Support
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