Hi Everyone,
This is my first post, so please bare with me.
My husband and I just adopted a 2 1/2 year old with CF. He is doing wonderfully and most of his problems are GI. He has a Bard Button and the closure on the button has worn out. We saw the GI doctor at John's Hopkins 2 weeks ago and he says the button looks great. He said we could change it if we want but that it was a procedure that our son was not going to like. My husband and I don't want to put him through that if the button itself is okay.
I'm hoping there are some other CF parents out there that have experienced this before and maybe have some creative ways of keeping the button closed. The Drs. say not to cover it. We tried tiny rubberbands, but he is so active that they were pinching his skin. Medical tape won't stick to it. Any ideas?????
We are constantly having to close it and if it comes open during the night it soaks his sheets.
If anybody has any advice we would appreciate it.
Take Care,
Mindy
This is my first post, so please bare with me.
My husband and I just adopted a 2 1/2 year old with CF. He is doing wonderfully and most of his problems are GI. He has a Bard Button and the closure on the button has worn out. We saw the GI doctor at John's Hopkins 2 weeks ago and he says the button looks great. He said we could change it if we want but that it was a procedure that our son was not going to like. My husband and I don't want to put him through that if the button itself is okay.
I'm hoping there are some other CF parents out there that have experienced this before and maybe have some creative ways of keeping the button closed. The Drs. say not to cover it. We tried tiny rubberbands, but he is so active that they were pinching his skin. Medical tape won't stick to it. Any ideas?????
We are constantly having to close it and if it comes open during the night it soaks his sheets.
If anybody has any advice we would appreciate it.
Take Care,
Mindy