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Third Annual Golf Bowl Classic - June 7, 2010
We are proud to announce the 3rd Annual Golf Bowl Classic For a Cure to benefit the Central Ohio Chapter of the Huntington’s Disease Society of America. We will be playing golf at Heritage Golf Course followed by dinner and bowling at Ten Pin Alley. Cost for the Outing is $120 per person. For more information, please contact Wendy Vaughan at office@hdsacentralohio.org.
Central Ohio HDSA Support Group
At the June 10th support group meeting, we will be having three massage therapists, who will be talking about the benefits of massage and will offer massages to all attendees.
25th Annual National HDSA Convention
June 25 - 27, 2010 - Hilton North Raleigh - Raleigh, NC
Save the Date!
Celebration of Hope Casino Night
September 24, 2010 - Makoy Center
Huntington's Disease Parity Act of 2009
Nearly everyone affected by HD has trouble obtaining disability benefits. HDSA is leading a national campaign to address this problem, and we need your help! A bill in Congress, HR 678, The Huntington's Disease Parity Act of 2009 would revise the current Social Security Administration (SSA) guidelines for determining disability caused by HD. It would also eliminate the two-year waiting period to receive Medicare benefits after a disability determination is made by SSA. If enacted into law, HR 678 would significantly improve the lives of everyone affected by HD.
Support HDSA When You Buy Your Groceries
Help raise funds for Huntington's Disease Society of America by simply shopping at your local Kroger store.
HDSA's National Youth Alliance (NYA)
Connect with a great group of children and young adults who, with HDSA's encouragement and support, have made it their mission to ensure that theirs is the last generation with Huntington's Disease!
National Research Roster for Huntington Disease Patients and Families
The National Research Roster for Huntington Disease Patients and Families was established in 1979 at Indiana University. The goal of the Roster is to help researchers learn more about Huntington disease. To accomplish this goal, the Roster has involved nearly 3,000 families in Huntington disease research.
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