I am the mom to a 20 year with CF. My daughter who is due to deliver a baby boy in May just found out that she is definately a carrier of CF. The dad currently lives in Autralia where they will be moving to after the baby is born.
I am trying to find out the best plan of action. My state currently does not have newborn testing. Is there a particular plan that should be put into place?
I am trying to find out the best plan of action. My state currently does not have newborn testing. Is there a particular plan that should be put into place?