I am involved in fundraising for The Cystic Fibrosis Foundation. The CF Foundation's core mission is to assure the developement of the means to cure and control Cystic Fibrosis and to improve the quality of life for those with the disease.
I am currently in the process of planning a charity concert to benefit the CF Foundation.For those of you who are not familiar with our organization Cystic Fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that:
clogs the lungs and leads to life-threatening lung infections; and
obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food.In the 1950s, few children with Cystic Fibrosis lived to attend elementary school. Today, advances in research and medical treatments have further enhanced and extended life for children and adults with CF. Many people with the disease can now expect to live into their 30s, 40s, and beyond.I have joined this fight because I am related to two young boys that can benefit from our generosity.If you require additional information about The Cystic Fibrosis Foundation or on how to make a contribution, please contact me and I will be happy to answer any questions you may have. I thank you for your time and consideration. We look forward to whatever support you can provide.Sincerely,
Angela L. Davis
717-575-9301
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