Hi everyone,
I was wondering how you were all diagnosed I just want a bit more information before I go back to my rheumatologist and we discuss all of this.
Such as;
what age
What made you go in the first place
Did you diagnosed with hyper mobility before
How do you deal with it day to day
Do you have extreme pain
Anything other information would be hugely appreciated, if you don’t want to share on here please could you message me
Advice for a Hypermobility sufferer 
More than just benign hypermobility syndrome?? 
Not wanting to feel socially isolated 
Hypermobile EDS & Endometrosis
Do you ever wonder whether you have been misdiagnosed or have another illness running alongside EDS?
