Hi! My name is Jen, I am a 30 year old who has Cystic Fibrosis. I originally started this blog to keep track of my time on the double lung transplant list. Well after 2 LONG years and a lot of bumps in the road I finally received my transplant on December 2nd, 2010. Now I write about life post-tx and all that goes along with it! :)
It's almost 2:45pm and I'm sitting with my beautiful, brave, resilient daughter Jennifer who is resting after receiving her tracheotomy. I like finding positives out of negative situations. So, I feel happy to get to see her face again! She only has a nasal tube which hopefully will come out tomorrow or Wednesday. I'll keep you posted.