What is Ehlers-Danlos Syndrome?
 
Thank you to our EDS Network CARES families & our EDS families in Canada which are also part of EDS Network CARES foundation. We are finally able to get some positive and hopeful EDS research started. The last time EDS research was done, was back in 2004-2005. That's not good enough. Research needs to be continuous, if we want to see progress for Ehlers-Danlos Syndrome. Raising Money and doing Fundraisers will help us keep this important EDS research going.

Without your donations we wouldn't have this first time EDS hope. This has been a long time coming for all our EDS Families. I'm proud to say, we all are making it happen. We couldn't have done this without all the fundraisers, all our awareness videos, donations and all the people who put their time & talent into helping us too. We are so grateful for all our volunteers who worked so hard to get us to where we are today.

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Our EDS Family & Friends Holiday Letter Template. Feel free to make this letter your own by adding your personal EDS story to the letter...

A big thank you goes to Dr. Hal Dietz for caring so much about our EDS families and for working extremely hard to help us find a cure.


We can't thank you enough!!
Thank you so much for giving EDS Families
"HOPE"!


Lynn Sanders Founder/President
Please Keep Our "Hope" Alive Donate To EDS Research

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