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ehlersdanlossupportclub · Ehlers Danlos Support Club - A place to talk about Ehlers Danlos Syndrome
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Reply | Forward Message #608 of 642 |
Hi my name is Anna and I am kinda new here. I have VEDS (Or our
genetisist thinks we might possibly have a new type of EDS) and so do
all four of my children. The help I need is that we live in MN and are
looking for EDS Drs in our state. Does anyone have any suggestions or
know of any other Drs we should see? I am very ill and so is my
youngest daughter. Please could anyone help?

Anna<><
Sun Aug 24, 2008 5:05 pm

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adamsv4jesus
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Forward 		Message #608 of 642 |
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Hi my name is Anna and I am kinda new here. I have VEDS (Or our genetisist thinks we might possibly have a new type of EDS) and so do all four of my children.... 		adamsv4jesus
Offline Send Email 		Aug 24, 2008
5:06 pm

hello adamsv4jesus, here are some dr's i look't up for u in ur state it may be a bit of a drive im in the long run its well worth it! good luck and god bless! ...
Natalie White
murmaidbaby
Offline Send Email 		Aug 24, 2008
8:38 pm
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