The Cystic Fibrosis web ring is a collection of web sites that share a common bond. CF is the number one genetic killer of children and young adults in the world today. The web sites in our Ring share valuable information about this disease and how individuals cope with daily living. Some sites offer CF related links and other include personal stories.
Well hello my loyal followers. Sorry for the delay in posts, but this place has been super busy. We left off at Halloween. November was busy with school and Thanksgiving; but also Daddy's birthday. Here I am helping him blow out the candles. December 1st, Mommy and Daddy bought us a new house!! We got to move in the very next day. Here is my new pl...
Below is a guest article from one of my readers. Jenna is a recent college graduate who shares my interest in English. I love how this blog can be a vehicle for others to share their motivational ideas, dreams, and life stories so that others can learn to better cope with chronic diseases. Thank you Jenna for your submission. Itâs a very ta...
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The Cystic Fibrosis web ring is a collection of web sites that share a common bond. CF is the number one genetic killer of children and young adults in the world today. The web sites in our Ring share valuable information about this disease and how individuals cope with daily living. Some sites offer CF related links and other include personal stories.
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.
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.
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.
Walter van Praag will be coughing on a bicycle from Paris to Istanbul between July-October 2007 to raise awareness and funds for CF Research. Read about his trip and see how you can support him in this worthy cause.
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.
