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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.
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