The nephew of our founder, James, was recently diagnosed with cystic fibrosis, an all to common disease that affects over 30,000 children and young adults in the United States alone. While most healthy children are entertained with the thought of what they may be when they are adults, CF sufferers are faced with the all-too-real possibility of never seeing adulthood...a thought nobody should ever have to bear, especially not a child.
There's Hope
When the Cystic Fibrosis Foundation began in 1955, few children with CF lived to attend elementary school. Today, the median age of survival for a person with CF extends into the early 30's. Research is making a real difference; yet, precious lives continue to be lost. More must be done. The CF Foundation believes that an investment in CF medical research is an investment in the present and the future of all people with the disease.
How can I help?
Please raise awareness in your community about CF and of the strides being made toward a cure. Volunteer at your a local chapter, click here to learn more. You can also donate to the Cystic Fibrosis Fountation here.
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