Tuesday, October 20, 2015
Recently, I have been trying to think of things I would ask someone with CF if I didn't know anything about it. So I thought it would be fun to open this post up to everyone. Please below in the comments, ask anything that you would like to know about our life, roanans specific CF mutation, or cystic fibrosis in general. I hope everyone participates and I cannot wait to see how all the bright minds think!
at 5:13 PM