Late last year, our Noni’s battle with ALS came to an end. She was an active lady who loved being outdoors walking the trails with family and friends. We slowly watched her lose her strength and stamina to walk the trails and eventually the ability to live a dignified life. Losing a loved one to ALS is an incredibly painful experience which has left us with unseen scars in our hearts.

This summer we will be participating in the Walk to End ALS. Now more than ever, 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. Please consider supporting us and donating towards this important cause.

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. Please consider donating to this fundraising page as we work towards a world free of ALS/MND.

Your support is needed now more than ever - we are stronger together!