EDS
Ehlers-Danlos Syndrome β hypermobility, pain management, and the comorbidity maze.
- π₯ Quickanonymous
Has anyone tried specialist physiotherapy for hEDS?
Standard NHS physio made things worse β they had no understanding of hypermobility and pushed me to stretch and use resistance in ways that caused more subluxations. Finally got a β¦
β 8 - π₯ Quick
Has anyone tried specialist physiotherapy for hEDS?
EDS-specialist physio (not standard physio!) changed everything. Learning to stabilise joints properly, understanding my hypermobility patterns, and finally having exercises that dβ¦
β 19 - π₯ Quick
Has anyone tried compression garments for EDS?
Compression has helped a lot with joint stability and the POTS side of my hEDS. Knee-high compression socks basically every day. The challenge is getting ones that don't dig in or β¦
β 4 - π₯ Medium
For those with hEDS β what was the turning point in your physiotherapy? What made the difference between physio that helped and physio that made things worse?
β 12 - π₯ Quickanonymous
What other conditions were you diagnosed with alongside EDS? I'm trying to understand how common certain comorbidities actually are.
β 3 - π₯ Quick
Which joints give you the most daily trouble, and what's helped you stabilise or protect them?
β 13 - π₯ Medium
Finding a physio who actually understands hypermobility
After seeing 4 physiotherapists who made my joints worse by stretching them (stretching! the thing you should never do with hEDS!), I finally found someone who understood. The searβ¦
β 9 - π₯ Quickanonymous
Dislocations at night are ruining my sleep
My hips and shoulders sublux while I sleep and I wake up in pain constantly. A body pillow helped a little. Has anyone found a better solution? Bracing everything feels impossible.
β 0