You can download information to take to your doctors, schools, gyms, etc. to educate them about Ehlers-Danlos Syndrome whether it's EDS Awareness Month (May) or not. The only thing rare about EDS is awareness of it! Go to www.ednf.org to help. Thanks!
[Always check with your doctor - my posts should be considered my informed personal opinion which does not necessarily reflect the official position of the EDNF or any other organization or person concerned with Ehlers-Danlos Syndrome.]
I just heard about it, 5yo just diagnosed
DoddsFamilyRDI 3 years ago
I will look.
Thanks for the video.
Rekisum 3 years ago
thanks for letting me know.
i might have EDS (not sure, haven't gotten a diagnose yet)
watch my video to understand what i mean
svartebert 3 years ago
I have Ehlers-Danlos syndrome type 3 and i had no idea that there was a Ehlers-Danlos awaremess month cheers for leting me know
taurenmale 4 years ago