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Re: Duanes Syndrome

From: nikki norish, e-mail:
Date: 07 Aug 2000 at 21:22
Replying to: message 706.html

Hi Melinda. My daughter was diagnoised with duanes syndrome about 4 months ago, Like you, I don't really know alot about it. All i know is that there is nothing they can do for her, Some people have had surgery to correct the eye so it is more central, I like you, am so worried how duanes is going to affect her life, she will be 1 in 2 weeks time, I feel so helpless. If i find any info out i will let you know, I am from Hampshire in England and it's so hard to get any real answers, But like i say if i can find anything out i will let you know
Thanks Nikki and baby Bryony


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