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new member & a parent of daughter with Blepharophimosis

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Hi, Everyone!

I've just discovered this site and I am thrilled. My daughter is 20 and we have never had any support. She is the first in our family on all sides. When I read the e-mail from Loka, I want more info and want to give more about my daughter. has morphea and linear scleroderma. She got the morphea about 6 months after her second surgery. Because I have to get back to work I will write alot more later. Any body who wants to e-mail me please do. We live in Edgerton, Wisconsin. Thanks! Terry

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Hi Terry, You and your daughter have my support. My ptosis was acquired. I am now 35. Ask me anything...gotta run aTerry Helgestad <terryahelge@...> wrote: Hi, Everyone! I've just discovered this site and I am thrilled. My daughter is 20 and we have never had any support. She is the first in our family on all sides. When I read the e-mail from Loka, I want more info and want to give more about my daughter. has morphea and linear scleroderma. She got the morphea about 6 months after her second surgery. Because I have to get back to work I will write alot more later. Any body who wants to e-mail me please do. We live in Edgerton, Wisconsin. Thanks!

Terry FareChase - Search multiple travel sites in one click.

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