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ehlersdanlossupportclub · Ehlers Danlos Support Club - A place to talk about Ehlers Danlos Syndrome
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hi I'm new....   Message List  
Reply | Forward Message #480 of 643 |
Re: [Ehlers Danlos Support Club] hi I'm new....

Hey Dawn Welcome, My name is Crystal I'm 22 years old I have Vascular EDS along
with many other things. Have you been told what type of EDS you have? Where do
you live? I'm in Southern Indiana. You have came to a good place we are all like
one big family and we are all here for you and will help you in any way
possible. With you being 19 your EDS should qualify you for Medicaid. You really
need to look into that because with EDS as time goes on you'll need to to seen
often. Mine effects my joints I've had 24 surgeries some here have more. If you
need or want to email me personally please do it's kinda nice to see someone
younger join in. My email is caw1984@....
Hugs
Crystal

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Sun Jan 7, 2007 10:09 pm

caw1984
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Message #480 of 643 |
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My name is Dawn...I'm 19 years old...I was diagnosed with Ehlers-Danlos Syndrome a little while ago...however shortly after I was diagnosed...I lost my...
wolf_lover999
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Jan 7, 2007
8:00 pm

Hey Dawn Welcome, My name is Crystal I'm 22 years old I have Vascular EDS along with many other things. Have you been told what type of EDS you have? Where do...
Crystal Williamson
caw1984
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Jan 7, 2007
10:18 pm

Hi Dawn: See what a great group this is? There isn't anything that you can't ask. We are all in this together. For a lot more info, you can go to...
foundit1999
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Jan 8, 2007
4:22 pm
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