2022 Team Hope Walk To Support HDSA | San Diego Events


Tidelands Park

The San Diego Chapter of the Huntington’s Disease Society of America (HDSA) will host the San Diego Team Hope Walk on Saturday, October 22nd at Coronado Tidelands Park. Registration starts at 8:00 AM and the event starts at 9:00 AM. All proceeds support HDSA’s mission to improve the lives of people affected by Huntington’s disease (HD) and their families. 

“The San Diego Team Hope Walk is always a wonderful day,” said Mindy Schroeder, HDSA’s San Diego Chapter President. “It is our most special, and my personal favorite event, because it focuses on our families and gives us all an opportunity to connect with one another. It helps us feel like we are part of a bigger community and lets everyone know that they are not in it alone! I'm so excited to see old friends, and make new ones this year!” 

Team Hope is HDSA’s largest national grassroots fundraising event, which takes place in over 100 cities across the U.S. and has raised more than $20 million for HD since its inception in 2007. Thousands of families, friends, co-workers, neighbors, and communities walk together each year to support HDSA’s mission to improve the lives of people affected by HD and their families.  

Huntington’s disease (HD) 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. Every child of a parent with HD has a 50/50 chance of inheriting the faulty gene. Today, there are approximately 41,000 symptomatic Americans and more than 200,000 at-risk of inheriting the disease. The symptoms of HD are described as having ALS, Parkinson’s and Alzheimer’s – simultaneously.

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. HDSA was founded in 1967 by Marjorie Guthrie, the wife of legendary folk singer Woody Guthrie. Woody died from HD complications when he was only 55 years old, but the Guthrie family legacy lives on at HDSA to this day.

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