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Hi Wanda..

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My name is Machaela, and I am a new member. I have a 2yr old daughter

who was diagnosed @ approx 10mths old. When she was born her eyes were

not open, and the doctors tried to force them open. Like , they

opened in the following days but with very small openings. We spoke to

many different peadiatricions,doctors etc. who seemed very unsure of

what the problem was. They assured us that her vision was fine but

told us they had not seen of this before. Perhaps that was because we

live in a reasonably small city. We were then referred to a specialist

in Melbourne(aus!) where they began to suspect BPES but thought she

was a little young to diagnose. By the time she was 10mths they were

confident that it was BPES. Like you, we began to search the net to

find what we could but, we too found that alot of it was very medical.

I am in the nursing field so I could understand some of it but alot

was really for surgeons etc. I was delighted to find this group and

have found it is a great place for people to share experiences,

stories etc but as I was told, the best place to get answers is a

health professional. It appears to be a very individual thing. Maybe a

geneticist would be someone of benifit for you to talk to, as we found

that very benificial. It sounds as if your has other issues

involved, but as for me, all I have to offer you is my story, and my

own individual experience...Take care! and welcome to the group!

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