mbrandazzo
New member
Hi Everyone,
The impact of my son's CF hits me at different times, and unfortunately today was one of those days.
He is almost two now, and I remember right after he was first diagnosed we went to a CF Education Night at his hospital. It was a wonderful presentation that gave us a lot of hope for Logan's future... However one thing that was said rang in my head today. It was that by the time a Cf'er is two, their pancreas pretty much shot (at least with those who are PI, which my son happens to be).
So my question is, for those of you who are older now, or for anyone who has heard anything that could be of help, what implications does having "bad" pancreas have? I know he will take enzymes for the rest of his life, but are there any other "side effects" that happen later in life from not having your pancreas function, and can they be treated.
Just wondering and concerned...
The impact of my son's CF hits me at different times, and unfortunately today was one of those days.
He is almost two now, and I remember right after he was first diagnosed we went to a CF Education Night at his hospital. It was a wonderful presentation that gave us a lot of hope for Logan's future... However one thing that was said rang in my head today. It was that by the time a Cf'er is two, their pancreas pretty much shot (at least with those who are PI, which my son happens to be).
So my question is, for those of you who are older now, or for anyone who has heard anything that could be of help, what implications does having "bad" pancreas have? I know he will take enzymes for the rest of his life, but are there any other "side effects" that happen later in life from not having your pancreas function, and can they be treated.
Just wondering and concerned...