Not quite. There is a one in four chance that the child of two CF carriers would be born with the disease. Both parents must be carriers for any of their offspring to get CF. However, unaffected children would be carriers and potentially pass the disease on to their children, if they had kids with another carrier. The vast majority of people have no idea if they are carriers of CF or most other genetic diseases. (My sister was misdiagnosed with CF many years ago)Originally Posted by carole
My brother suffers from Hemachromatosis, the most common genetic disease among caucasions. He is the only affected person on any side of his family(we have different mothers so he has some different relatives than I do). His specialist says the disease has been in our family somewhere for generations, but it requires specific triggers to activate it. Big bro' just happened to do the things that set it off. He had three kids by the time he was diagnosed.
If everyone decided not to have kids because of some genetic possiblity, no one would have them! Every family has a diabetic, an alcoholic, a cancer patient, ect, ect, ect......
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