hi im 17 and have Ehlers danlos syndrome
since ive started this blog ive gotten to talk to lots of you with eds and for me its been a great support
so if you ever need to talk about eds or want to know about it my ask is always open :)
Follow me on twitter :D : @Ehlersdanloss
just saw this on google images
i think this is such a good pic to use about raising awarness for eds
ive once had a doctor sit in front of me and google it because she didnt know what it was, so i think it needs a lot more awarness
because a lot of people/Doctors dont have a clue about it….
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