Posted 2/5/2014 1:37 PM (GMT 0)
A new member came on our forum to expressly tell us about Ehlers-Danlos Syndrome. Her name is Gatheringroses. Welcome Gatheringroses! She posted on the What Else Could It Be thread and knew she wasn't supposed to so she asked me to delete it. But I copied and am pasting her post below so everyone will see it. Thanks you, Gatheringroses for caring enough to let us know.
Sherrine
I signed up solely to let you know that my DD had all of these things, and it turned out to be a genetic connective tissue disorder (Ehlers-Danlos Syndrome). It shares many of the same symptoms as fibro, lyme, and even MS.
If people have gone through all the tests, and still have migrating joint pain, it might be worth it for them to check. It's a rare disease, but I found it on a forum when googling other diseases. :) If there is anybody who is stuck/not happy with their DX, I think it could be worth checking out connective tissue disorders. There are many that share these symptoms.