Living With Cystic Fibrosis by Jeremey Moore
Photo of Jeremey Moore
My Story
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Cystic Fibrosis Foundation

My name is Jeremey Moore and I am from Greeneville, Tennessee. I have a genetic disorder/disease called Cystic Fibrosis.  I was diagnosed at  3 days old.  Now I am 20 years old and I am still striving on the best I can! I have always had to take some form of medicine but never had too many complications with my Cystic Fibrosis.

Throughout my family history it has not been discovered that anyone has had cystic fibrosis. This would mean that the defective gene has skipped every generation in the history of my mother and fathers' family's until I was unfortunately the one to be diagnosed. There is no cure for this disorder as of yet.

I have also been diagnosed with Diabetes. Now there is a history in my family of this but I more and likely have it because of my cystic fibrosis. Patients of CF usually find themselves being diagnosed with diabetes, most cases do.

I am creating this site to raise awareness of Cystic Fibrosis because I'm not the only one sickened with this disease, as a matter a fact there are around 65,000 with CF around the world
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Remember those lost to and those fighting cancer.
For those who wish, donations to the
Jeremey Moore Lung Transplant Fund
May be mailed to :
Consumer Credit Union
CCU Blvd. Greenville, TN. 37745
Remember those lost on September 11th, 2001
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