There is Hope!

Paula has EDS and describes, in her own words, what it is like to deal with this disorder.

 

Paula describes the practical aspects of how Ehlers-Danlos Syndrome impacts her daily activities.

Leave a Reply

Your email address will not be published. Required fields are marked *

Get Webinar Announcements And Our FREE Guide

Support EDS Awareness

See all upcoming events

Popular Article Topics

Current Poll

How long until you received a proper diagnosis for EDS?

View Results

Loading ... Loading ...
More Polls

Support Group Activities

OUR VISION

EDUCATIONAL

OUR PROGRAM

Copyright © 2023 EDS Awareness. All rights reserved. Website designed by BM Web Creation

%d bloggers like this: