Raising awareness for ALS while supporting ALS families and critical ALS research.
Our Mission & Vision
Our Mission
To be a connection for people living with ALS. Through their stories, we raise awareness, connecting communities to support the search for a cure.
To raise funds to donate to Canadian charities that are researching better treatment methods and looking for a cure for ALS.
​
Our Vision
To make ALS history.
What is ALS?
Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's Disease or Motor Neurone Disease (MND), is a progressive neurodegenerative condition that affects nerve cells in the brain and spinal cord. ALS leads to muscle weakness, loss of mobility, and eventual paralysis.
​
This fatal disease currently has no cure, but with increased awareness, research, and support, we aim to change the future for those living with ALS.
​
A Voice of Resilience: Ian's ALS Story
By fall 2024, Ian has lived with ALS for about 7 years. A retired, high school teacher, Ian is still able to speak, eat and has little use of his hands. He gets around by motorized wheelchair. Ian generously shared his ALS story with us and we are sharing it with you. Not just to raise awareness about ALS, but also to share some of Ian's wisdom, having lived with ALS for some time.