EDS
Ehlers-Danlos Syndrome — hypermobility, pain management, and the comorbidity maze.
- 🥄 Quickanonymous
Has anyone tried specialist physiotherapy for hEDS?
Standard NHS physio made things worse — they had no understanding of hypermobility and pushed me to stretch and use resistance in ways that caused more subluxations. Finally got a …
↑ 8 - 🥄 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 d…
↑ 19 - 🥄 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 …
↑ 4 - 🥄 Medium
For those with hEDS — what was the turning point in your physiotherapy? What made the difference between physio that helped and physio that made things worse?
↑ 12 - 🥄 Quickanonymous
What other conditions were you diagnosed with alongside EDS? I'm trying to understand how common certain comorbidities actually are.
↑ 3 - 🥄 Quick
Which joints give you the most daily trouble, and what's helped you stabilise or protect them?
↑ 13 - 🥄 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 sear…
↑ 9 - 🥄 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.
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