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Hi. My name is Anita and I'm 36. I was really surprised and pleased

to find this group for BPES. I've had many operations, from age 2

yrs to 21 yrs. My mother also has BPES and we've been involved in

some genetic research in the UK through St 's Hospital in

Manchester. They're still unable to tell me whether I have Type I or

Type II BPES but think that it's unlikely that my fertility is

affected given that my mother has been able to have children.

I've been told that there is now a surgeon specialising in BPES at

the Manchester Eye Hospital. My surgery was very successful and I'm

sure there have been improvements since I had my operations. Most

people don't even notice that I've got anything wrong with my eyes

until I mention it. My only recollections of being in hospital are

good memories about friends I made and having time off school rather

than any of the operations themselves! I had a very normal childhood

and I hope that this offers some reassurance to parents with newly

diagnosed children facing surgery.

Anita

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