The Genetic Disease Foundation
The Genetic Disease Foundation (GDF), a 501(c) (3) corporation, was established in 1997 by patients, parents and families who have suffered from genetic diseases. The Foundation’s mission is to support research and education to prevent and cure genetic diseases and birth defects. Specifically, the GDF supports research to discover effective treatments and cures for genetic diseases and to improve and expand genetic testing to ultimately prevent these devastating diseases. Vital to the Foundation’s mission is the education of patients, physicians, and the public to increase awareness about genetic disorders as well as the availability of genetic testing and counseling.
For more information, visit www.knowyourgenes.org or www.geneticdiseasefoundation.org.


Our purpose is to raise funds for research so that we can find a cure and effective treatment for Prader-Willi Syndrome, a non-inherited and potentially life threatening genetic disorder. It is a life-long condition that affects appetite, growth, metabolism, cognitive function and behavior. By participating in our golf classic you become our partner in securing a good life for Josi, Harold and others with PWS. The more you do, the more we can do.
Thank you for helping. It's about our children, what more can we say?
Your hosts,
Ronnie and Ira Levine
Jill and Harold Wilkinson

The Prader-Willi Syndrome Association, PWSA (USA), was organized in 1975 and provides a resource for education and information about Prader-Willi Syndrome. They provide life-time advocacy for affected individuals. Visit their website.
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This event is sponsored by Josilyn Faith's Foundation a 501(c)(3) status organization.
A copy of the official registration and financial information may be obtained from the Division of Consumer Services by calling 800-435-7352 (toll-free from within Florida). Registration does not imply endorsement, approval or recommendation by the state.
© 2011 Prader-Willi Classic, all rights reserved.