Greater Los Angeles Chapter |
HDSA LOS ANGELES 5K WALK/RUN September 19, 2009 The HDSA LA 5K walk/run is an annual fund raising effort by the Los Angeles Chapter of the Huntington’s Disease Society of America (HDSA). It is run by a number of up and coming young television and motion picture actors, writers and behind the scenes people all dedicated to helping find the cure for Huntington’s Disease (HD). Proceeds from the walk go toward funding the HDSA Center of Excellence at UCLA and also toward funding HDSA research grants to places such as the University of California at Irvine (UCI). A portion of the proceeds fund the Marion Dougherty Fund that provides an annual travel experience for an HD family as a way for them to get some family time away from the rigors of the disease. The run is held on September 19, 2009 at the CBS Radford lots in Studio City, California. Walk chair is actor Billy Aaron Brown.
What is Huntington’s Disease? Huntington's Disease (HD) is an inherited, progressively degenerative brain disorder that results in a loss of both mental faculties and physical control. Symptoms usually appear in an individual between 30 to 50 years of age and progress over a 10 to 25 year period.
Every person who inherits the HD gene will eventually develop the disease.
Who is At-Risk? Approximately 30,000 Americans have HD and over 200,000 more are at-risk of inheriting it from a parent. This is roughly the same as ALS or Lou Gehrig’s Disease. Once thought of as a rare disease, HD is now considered to be one of the more common hereditary diseases. HD does not skip generations; if one does not inherit the gene, one cannot pass it on.
An End to HD? The outlook for solving the puzzle of Huntington’s Disease is promising. In 1993, researchers were finally able to identify the gene that causes HD. Momentum in HD research continues to increase our understanding about the Huntington's gene and how it functions. Current research projects or those in development could provide the next major discovery at any time. The Huntington’s Disease Society of America (HDSA) funds both clinical and basic research at leading hospitals and research facilities through the HDSA Coalition for the Cure, the HDSA Grants and Fellowships program and through our HDSA Centers of Excellence for Family Services. With your help, our continued commitment to research funding will solve the puzzle of HD. What is the Huntington’s Disease Society of America? The Huntington’s Disease Society of America (HDSA) is a national voluntary non-profit organization dedicated to finding a cure for Huntington’s Disease while providing support and services for those patients and families, caregivers and medical professionals who are living with HD. Founded in 1967, HDSA promotes and supports both basic and clinical HD research, aids families throughout the continuum of HD and educates families, the public and healthcare professionals about this devastating disease. HDSA’s Programs How You Can Help...
Benefits:
Gold Sponsor: $1,000 Benefits:
Silver Sponsor: $500 Benefits:
Bronze Sponsor: $300
Greater Los Angeles Chapter HDSA/LA 9903 Santa Monica Blvd #106 Beverly Hills, CA 90212 (800) 686-9868 Helpline: (888)4-HDSALA |