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Screening at age 36

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Hello, I am 36 years of age and live in Melbourne, Australia. I have

a

sister and father with CMT. My sister, who is 32, is very severely

affected. I show no signs of CMT, although sometimes I think my hands

are very weak or uncoordinated. Two years ago my husband and I

visited

the genetics clinic at the major childrens teaching hospital for

counselling. We are still considering a family. My knee reflexes were

tested. Apart from that I was told they dont think I have CMT. I have

always felt this summation was unsatisfactory. I wish there was a

definitive test that could tell me if I have CMT. How rare is it that

a person of my age would show no symptoms? Have I received the right

counselling? I am afraid of pregnancy inducing CMT symptoms and

therefore already exposed the fetus to a risk I am trying to prevent.

I do not want to bring this upon someone, knowing the agony my sister

has been through. Any thoughts or comments would be helpful,

especially from those faced with the same dilemma.

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