Transplantmommy
New member
I also think, like most, that it is not the parents. My Mom took great care of me but did not force me to take my meds and I am still here. I think that some people just have the unfortunate luck of their CF progressing a lot worse than others. I was 24 before I was told that I needed transplants (lungs and liver). I was unfortunate to get both the GI and the lungs pretty bad but was fortunate that it didn't really progress until high school.
I have met and stayed in contact with another girl for quite a while who has only the digestive part. She's older than me and has never ever had problems with her lungs but she is soooo much skinnier than I have ever been. The last time I saw her was right after I had Brady. She and her parents came to see us in the hospital. She was doing really well.
Anyway, I really don't think it's because of crappy parenting (unless they do it on purpose, which some do). I think it really has to do with what mutations the child has and how severe of a case they have.
I have met and stayed in contact with another girl for quite a while who has only the digestive part. She's older than me and has never ever had problems with her lungs but she is soooo much skinnier than I have ever been. The last time I saw her was right after I had Brady. She and her parents came to see us in the hospital. She was doing really well.
Anyway, I really don't think it's because of crappy parenting (unless they do it on purpose, which some do). I think it really has to do with what mutations the child has and how severe of a case they have.