If you have a child that suffers from EDS "Ehlers Danlos Syndrome" This is the group to join. If you fall under any of the following please join and lets share our information.
* You've adopted a child suffering from EDS
* You and your child/children suffer form EDS
* Your Spouse and child suffer from EDS
Whatever the case lets share and learn from each other. I have yet to see a list dedicated to the children. I keep reading that EDS doesn't effect children early on. I disagree Since I was 2 now 31 I have complained of unexplained pain. Yet true things have progressed with age. My daughter age 4 suffers from EDS and the pain involved. My daughter and I both have been diagnosed with Classical Type.