Kitty Colbert Âû

SIGN THE PETITION + GET INVOLVED: www.eds4ire.ie - The campaign towards real healthcare for Ehlers Danlos Syndrome and Hypermobility Spectrum Disorder in Ireland.
🦓 TikTok: www.tiktok.com/@chronic_sick_kit
🦓  FB: www.facebook.com/eds4ire
🦓 IG: www.instagram.com/eds4ire & www.instagram.com/chronic_sick_kit
💕 My name is Kitty, I live in Ireland, and I have Hypermobility type Ehlers Danlos Syndrome - hEDS (+ the comormidites!). Here you'll find videos relating to EDS/ HSD, disability issues, human rights.
[Disclaimer: As always - I am not a medical professional and speak only from a patient perspective. As I note in all of my videos, only a trained rheumatologist (sometimes geneticist) can diagnose EDS and HSD, and give you advice on what tests and treatments are best suited to your unique case. My advice is simply on what treatments exist out there, and where to access care and support. For further information see www.eds4ire.ie]