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The
Reach for the Stars Foundation is dedicated to
providing individuals afflicted with Cystic Fibrosis and their
families with the resources, knowledge and support necessary
to manage their unrelenting battle with this insidious disease.
Cystic Fibrosis is not only physically debilitating, but carries
a heavy financial and psychological burden for families.
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2007
Alison Bine Spirit Award Winner, Joy Heinsohn with Jay
Fiedler, Karen Bine and Foundation President Stacey
Levy.
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Cystic
Fibrosis (CF)
compromises 30,000 children and young adults in the U.S. Tragically
only 50 percent of CF sufferers live to be 30 years of age.
CF is characterized by the body's abundant production of very
thick and sticky mucus. This mucus becomes an ideal environment
for infections and causes blockages throughout the body. Although
the disease manifests itself in many ways, it is most commonly
the constant infections and buildup of mucus plugging in the
lung tissue, that eventually lead to the destruction of the
lungs and ultimate death of these children.
…Our
efforts are designed to Bridge the Gap!
The
Reach for the Stars Foundation is
devoted to improving the quality of life for these afflicted
individuals as they await the cure, and to help ease the burden
of the families as they engage in their battle with CF: a
battle that never ends…
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