The Founders Walk to Cure HD honours the Huntington Society of Canada's founders, Ralph and Ariel Walker, who started the society 45 years ago, in 1973, at their kitchen table in Cambridge.
Ariel Walker often shares a story about the dragonflies that explains their significance to the community, which can be found here. It is due to the profound connection this has with HD community that you will see dragonflies incorporated throughout the walk.
Please join us in celebrating our founders at this family fun event! Stay tuned to this site for information on fun activities we have planned for the day, as well as exciting prizes!
Date: Saturday, September 19, 2020
Time: Registration 9:30 am, Walk/Run at 10:00 am
Location: Riverside Park, Cambridge, Dolph Picnic Site
1km/ 5km options available for all abilities.
**Note: We know COVID-19 makes the future of events unpredictable. We continue to monitor government directions and will keep participants advised if we choose to shift to a virtual format. The Founders Walk will happen this year regardless of format!
Register and raise $100 by August 15 to be entered into a draw for a $200 Visa Gift Card. For every $100 raised over the minimum, you will receive an additional entry in the draw.
As our thanks to you, you are eligible for ONE of the following prizes, based on the amount you raise
$150: TeamHD Tech T-Shirt
$300: TeamHD Hoodie; OR
$500: TeamHD Jacket
All proceeds raised through this event will go to support Family Services and Research to delay or stop Huntington disease.
Event Questions? Please contact: firstname.lastname@example.org
Website questions? email@example.com
Visit huntingtonsociety.ca to learn more about the organization and Huntington disease.
The Huntington Society of Canada (HSC) strives for a better future for those affected by Huntington disease (HD). There are three main areas that HSC focuses on:
1. Funding cutting edge research into slowing or stopping the progression of HD
2. Funding Family Services workers across Canada to provide support for those affected by HD
3. Raising awareness of HD, educating the public and health services professionals, as well as advocating for the rights of those affected by HD