This groups is for moms of children that live with Cystic Fibrosis and the other side effects of CF. Also for moms or grandma's w/CF or that help take care of a CF child. Even if you have raised your CF child you have the experience. PLEASE join. We need you.
Hi, My son is 7 and doing pretty well. I'm wondering what others experince is on when and how much to tell your children about CF. I know he realizes his life is different...
Started by Patty on 09/29/2010 in Cystic Fibrosis Moms
Last update on 03/19/2011 by Maureen
Started by Lanor on 01/17/2011 in Cystic Fibrosis Moms
Last update on 02/17/2011 by Lanor
My daughter Adaira went from eating 4 ounces every 2 hours before clinic. After clinic her doctor up her enyzme's to 2 pills, and in the last couple of days she has been eating...
Started by Lanor on 01/04/2011 in Cystic Fibrosis Moms
Last update on 01/05/2011 by Sarah