M
Mommafirst
Guest
When my daughter was initially diagnosed (at 5 months old) she had one very very rare (like 6 people ever with it) mutation and one more typical mutation. They didn't really know what this meant so they gave her a "genetic" diagnosis, but withheld a "clinical" diagnosis for when symptoms appeared.
By the time my daughter was a year old she needed enzymes and other meds and her diagnosis was no longer referred to anything except CF.
By the time my daughter was a year old she needed enzymes and other meds and her diagnosis was no longer referred to anything except CF.