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:
I do have MCS, just got from the Dr.
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06-10-2008, 03:04 PM
braingonebad
Magnate
Join Date: Jan 2008
Location: NW Ohio
Posts: 2,450
braingonebad
Magnate
Join Date: Jan 2008
Location: NW Ohio
Posts: 2,450
Hang around right here, Julie.
Here's a thought. Ask for a MCS forum on NT. You never know unless you ask.
Or start a topic under Rare disorders.
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momXseven
(06-10-2008)
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