|
| |
Moving Mountains
This is my personal blog. It's simply about my life and often about my struggles and triumphs with Cystic Fibrosis and CFRD.
|
|
| |
Breathing Deeply: My Life with Cystic Fibrosis
1 review(s)
I'm an adult in my mid-twenties, married, college grade, full-time scientist and a professional freelance writer, living and thriving with CF. "Breathing Deeply" is a journal of my day to day life as an active adult enjoying every moment God gives me.
|
|
| |
CF Roundtable-a newsletter for adults with CF
1 review(s)
CF Roundtable is a newletter for adults with cystic fibrosis on-line, as well as their families, friends and caregivers. It consists of articles by and for adults living with cystic fibrosis on topics from lung transplants, dating CF related diabetes, oxygen use, and living fulfilling lives.
|
|
| |
Luke William Larson
1 review(s)
My name is Luke Larson. I was born on December 10th, 2006 and was diagnosed with CF a few weeks later. This page is a way for my parents and I to update everyone on my adventures.
|
|
| |
Chicago Cystic Fibrosis Awareness Day
1 review(s)
Web home of the annual Chicago CF family education day sponsored by the Chicagoland Adult Cystic Fibrosis Association. Site includes: programs, archives, links to CF on the internet, and contact information for CF clinics in the greater Chicago area.
|
|
| |
Sea Salt
1 review(s)
This is my daily thought process as I encounter new obstacles and run right into God's will for my life. This is my story with Cystic Fibrosis.
|
|
| |
Clayton Bates Cystic Fibrosis Support Site
1 review(s)
A site for Family and Friends to offer support to Clayton
|
|
| |
Genevieve's Cystic Fibrosis Website
1 review(s)
Gen's talks a lot about her personal journey with Cystic Fibrosis, and alternative therapies she has used to help manage her symptoms. Her choice for sharing her story is to inspire parents of CF children and CF Adults that it is not all doom and gloom. We hear a lot about the sad stuff - lets hear more of the good stuff!
|
|
| |
In Memory of Gianna Rose
1 review(s)
The site documents the life of Gianna Rose. She touched our hearts as she fought Cystic Fibrosis and Hepatoblastoma, childhood liver cancer. Gia passed away during a liver transplant surgery in July 2004. The site is filled with information about CF and Hepatoblastoma.
|
|
| |
Walk for Grace Cystic Fibrosis Page
1 review(s)
Meeting Site for Kansas City Based Grace Beshore and her Great Strides team.
|