Anyone have Eds hyper mobility syndrome???

Be • Fri, Feb 22

Anyone else on here have this?

Has anyone from the UK been to bath pain centre?

164 views • 1 upvote • 7 comments

Posted at Sun, Mar 10 2019

I have Ehlers Danlos, but haven't been there.

Posted at Sun, Mar 03 2019

Yep! There's some really great Facebook groups.l, I'm pretty sure I saw one specify for EDS in the UK.

Bethany • Mar 4, 2019

Thats a shame :(

Be • Mar 4, 2019

I don’t have Facebook x

Posted at Sat, Feb 23 2019

I have this but haven’t been there sorry x

Amber • Feb 25, 2019

Not currently. I’m waiting for my referral to Stanmore which now I’ve had baby no 3 should get sorted.

Be • Feb 25, 2019

Have you done any in patient pain programs for it? X

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