Hi everyone,
My husband has a nephew who has CF( he's 6 and totally amazing) so when we were pregnant his sister told us we should get genetic counselling...........well let's just say shock is a mild word for how we felt when we found out that not only was my husband a carrier (we always thought he was) but so was I. Our daughter was born healthy and CF free this June and for that we are eternally grateful.
Going through all that we did has made me not want to try for another baby "the old fashion way" so my question (and I know this is probably a very charged topic) is how do others feel about PGD. We've looked into it and I still have mixed feelings about it.
Thanks for your input.
My husband has a nephew who has CF( he's 6 and totally amazing) so when we were pregnant his sister told us we should get genetic counselling...........well let's just say shock is a mild word for how we felt when we found out that not only was my husband a carrier (we always thought he was) but so was I. Our daughter was born healthy and CF free this June and for that we are eternally grateful.
Going through all that we did has made me not want to try for another baby "the old fashion way" so my question (and I know this is probably a very charged topic) is how do others feel about PGD. We've looked into it and I still have mixed feelings about it.
Thanks for your input.