welcome to oneEDSvoice
- a positively charged Ehlers Danlos Syndrome community.- join today!
- login
Syndrome Ehlers Danlos parlons en
It does not depend on any association and was simply created to exchange our fears, joys and whatever you want about Ehlers Danlos Syndrome.
For people who want to join the group and apply, we thank you in advance to check your private messages on Facebook. We send an MP to each new request to find out why you are joining us in order to avoid malicious profiles and to keep the group in a climate of confidence and benevolence.
expertly curated content related to this topic
-
Help in School: Victoria Graham is Turning Invisible Illness into Public AwarenessLooking at Victoria Graham, you would ne...
-
DEFY FoundationThe DEFY Foundation is a recognized 501(...
-
Brianna Greenspan – Ehlers-Danlos SyndromeBrianna Greenspan is a mentor for people...
-
Ehlers Danlos Syndrome (patientslikeme)We’re all in this for good. By sharing...
-
It’s not in my Head’: Hope for Sufferer of Rare Joint DisorderGendi Roberts was just eight years old w...
-
The Ehlers-Danlos Support UKEDS UK was set up in 1987 to support, ad...
-
#zebrastrong...
