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Cystic fibrosis (CF) is the number-one genetic killer
of children and young adults in this country.
Approximately 30,000 people in the United States have
CF. A defective gene causes the body to produce an
abnormally thick, sticky mucus. This abnormal mucus
leads to chronic and fatal lung infections and impairs
digestion. Currently there is no cure.
Scientist supported by the Cystic Fibrosis Foundation
are writing a remarkable medical success story. CF
researchers are quickly translating what they learn
about the CF gene and CF cells in the laboratory into
promising new treatments. Based on their success,
landmark gene therapy studies and clinical trials on
new drug treatments are now underway.
Thanks to all who have bought us this far, another
thanks to those who will bring us that much closer in
the future. |
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