It's that time of year again! My family and I will be participating in the #WalktoendALS. This has become a yearly tradition. We do this is honour of my father who was diagnosed approximately 10 years ago and in memory of my aunt, his sister who succumb to this terrible disease. Every year we are amazed by the amount of support we get and proud of our growing team, we can't thank you enough! Please consider supporting us once again this year and donating to this cause that is very near and dear to us.

The ALS community needs our support to provide hope and help to families affected by ALS/MND. That’s why we're joining thousands of others, a part of a passionate and motivated community to “walk” in celebration of hope and a world free of ALS, also known as Lou Gehrig’s Disease. 

Your support will help to:

• create a better day-to-day reality for people and families living with ALS by providing community-based support throughout Manitoba - like home visits and support groups – as well as necessary medical equipment like wheelchairs, liftchairs, mobility aids and other items that increase safety in the home, at no cost to those who need them.
• further scientific progress by investing in the ALS Canada Research Program, which funds promising ALS research. This program provides peer-reviewed grants to researchers whose work has the greatest potential to advance the field of ALS. There’s been more progress made in ALS research in the last five years than over the last century – we need to keep building on this momentum.

Join us in making a difference, every little bit helps! Please consider donating to this fundraising page as we work towards a world free of ALS/MND.