Love.  This.  So. Much.

Thanks to a fellow EDS’er for posting it on one of the support groups, and for allowing it to be shared.  Please help spread Ehlers Danlos Awareness!

The following is a link to various myths and facts about Ehlers-Danlos Syndrome.

http://www.ehlersdanlosnetwork.org/myths-facts.html

For the record, if anyone happened to catch the House episode recently about Ehlers Danlos, it was NOT an accurate depiction of the disease.  One woman’s blog I follow, wrote about the episode, and I found that her feelings about it happened to echo my thoughts as well. 

Great informational article about EDS and it’s manifestations.  Gotta love the humor sprinkled throughout…

I came across a couple of interesting blog posts by eye doctor, Diana Driscoll about EDS and POTS, and the possible MS connection.  You can read them here.  (It makes more sense to read the second one first and then scroll up to read the first one.)