Understanding Cystic Fibrosis (CF)

Cystic Fibrosis is a genetic disease affecting approximately 30,000 children and adults in the United States.

CF causes the body to produce an abnormally thick, sticky mucus, due to the faulty transport of sodium and chloride (salt) within cells lining organs such as the lungs and pancreas, to their outer surfaces. The thick CF mucus also obstructs the pancreas, preventing enzymes from reaching the intestines to help break down and digest food. Specialized treatments are available to address these problems at CF Foundation-Supported Care Centers across the country.

SYMPTOMS

CF has a variety of symptoms. The most common are: very salty-tasting skin; persistent coughing, wheezing or pneumonia; excessive appetite, but poor weight gain; and bulky stools. The sweat test is the standard diagnostic test for Cystic Fibrosis. This simple and painless test measures the amount of salt in the sweat. A high salt level indicates that a person has CF.

TREATMENTS

The treatment of CF depends upon the stage of the disease and which organs are involved. One means of treatment, Chest Physical Therapy, requires vigorous percussion (by using cupped hands) on the back and chest to dislodge the thick mucus from the lungs. Antibiotics are also used to treat lung infections and are administered intraenously, via pills, and/or medicated vapors which are inhaled to open up clogged airways. When CF affects the digestive system, the body does not absorb enough nutrients. Therefore, people with CF may need to eat an enriched diet and take both replacement vitamins and enzymes.

FACTS

One in 31 Americans (one in 28 caucasians)~more than 10 million people~is an unknowing, symptom less carrier of the defective gene.

An individual must inherit a defective copy of the CF gene~one from each parent~to have cystic fibrosis. Each time two carriers conceive a child, there is a 25 percent chance that the child will have CF, a 50 percent chance that the child will be a carrier, and a 25 percent chance that the child will be a non-carrier.

PROGRESS TOWARD A CURE

Since the defective CF gene was discovered in 1989, the pace of CF research has greatly accelerated. In 1990, scientists successfully made copies of the normal gene, and added them to CF cells in laboratory dishes, which corrected the defective cells. The next major step was achieved in early 1993 when the first experimental gene therapy treatment was given to a patient with CF. Researchers modified a common cold virus to act as a delivery vehicle-carrying the genes to the CF cells in the airways. Several Foundation-Supported studies are underway to test new gene delivery methods, such as fat capsules (liposomes) and synthetic vectors.


HOME

PICS OF AZREA

MORE PICS OF AZREA

AND MORE PICS OF AZREA

NEW PICS OF AZREA

AZREA'S LIFE

LINKS TO CF WEBSITES
1
Hosting by WebRing.
Navigation by WebRing.