All - As some of you know, I was dx'd just this past March at the age of 36 with CF. It should have been "caught" MANY years ago, but nothing I can do about it now....anyway, my mother remarried and had two other children with a different "father" (this man has always been my "dad" so it's hard for me to point out the biological difference) but my MUCH
younger (half) sister has had nearly an identical medical history as mine in the past as well as presently. Since she is only 22, I am urging her to go in and at least have a sweat test done. She is resistant to the possiblitly that she might have it since we have different "biological" fathers. Does anyone have any stats on what the probabilities could be since obviously our mother is at least a carrier??? I think my mother might have CF has well (she is 56) but she refuses to go in for the test. My mom has had many problems with "mucus" (not lung specific) and has had glands removed to slow her muchs production. My daugter (who is 16) had the sweat test, which came back at 35, doesn't really exhibit "typcial" CF symptoms, but interstingly, both my mother and "half" sister do...althought they apparently choose not to see that. I still ultimately want to have my daughter genetically tested through AMBRY, but my insurance doesn't cover the $1000+ that would cost.
Anyone have any suggestions or guidance on how I can get them (my sister and mother) in to the CF clinic to be tested?
Amy
36 w/ CF
Anyone have any suggestions or guidance on how I can get them (my sister and mother) in to the CF clinic to be tested?
Amy
36 w/ CF