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Ehlers Danlos Syndrome – Friendship & Advice Group


This is a group for people with Ehlers Danlos Syndrome, regardless of the type EDS that you have …..We welcome family and friends of EDSERS to chat here as well…This group is for people seeking advice / info and friendship…We will do our best to ALWAYS ensure that ALL posts are replied to…Our goal is to ensure that fellow EDSERS are not left feeling alone , frustrated and scared! Zebras need to stick together and that’s what we are here for..to offer any info , support and friendship that we can…Please note replies in this group are from fellow EDSers (Of all Types). We are not medical professionals..so please take note of this when reading the replies and it would be in your best interest to take whatever information you are given here and consult it with your doctor..

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