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Hi

My name is Beth Gordon and I currently live in Northern Virginia,

USA. I knew that I had several surgeriees for ptosis as a child but

only since the birth of my daughter have I learned that I actually

have BPES. Lily is 2 months old and has had 2 surgeries to put in

slings.

My father and grandfather both have BPES, although none of our

siblings have it.

I am interested in any information about the best treatment for our

daughter. This group seems very positive and helpful.

I have not undergone genetic counseling, would be interested to find

out more about it. How could it help my family?

I am also interested in meeting anyone living nearby, particularly

with children.

I was born in 1970 in Pittsburgh, PA and my surgeries were conducted

at St. Francis Hospital by Dr. Weiser (now deceased).

thank you and best to all

Beth Gordon

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