I hope you will join us on this walk at lovely Crown Point on Sunday morning, October 6th.  

We walk to in memory of our mother, Janet. Go Team Janet!  With your help, we can help HDSA achieve their mission to improve the lives of everyone with Huntington’s disease and their loved ones.

Please register and help make a difference! (It's only $25!) If you cannot participate, please consider making a donation to my personal fundraising page by clicking the SUPPORT US above.

Every little bit helps, really.  Thank you for your support! Claire


With your help, we can help HDSA achieve their mission to improve the lives of everyone with Huntington’s disease and their loved ones.

The Huntington’s Disease Society of America is the premier not-for-profit organization dedicated to improving the lives of everyone affected by Huntington’s disease. From community services and education to advocacy and research, HDSA is the world’s leader in providing help for today, hope for tomorrow for people with Huntington’s disease and their family. 

Huntington’s disease is a fatal genetic disorder that causes the progressive breakdown of nerve cells in the brain. It deteriorates a person’s physical and mental abilities during their prime working years and has no cure.

HD is known as the quintessential family disease because every child of a parent with HD has a 50/50 chance of carrying the faulty gene. Today, there are 30,000 symptomatic Americans and more than 200,000 at-risk of inheriting the disease.

The Huntington’s Disease Society of America is the premier nonprofit organization dedicated to improving the lives of everyone affected by HD.  From community services and education to advocacy and research, HDSA is the world’s leader in providing help for today and hope for tomorrow for people with HD and their families.

Across the United States, HDSA currently supports: 
•54 volunteer led Chapters & Affiliates
•41 Centers of Excellence
•65 Social Workers 
•160 Support Groups

To learn more about Huntington’s disease and the work of the Huntington’s Disease Society of America, visit www.hdsa.org or call 1-800-345-HDSA.


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