I was diagnosed with ALS in January 2020. It's been a steep learning curve and has included many shifts in perspectives and expectations. I can no longer speak, drink or eat and have a feeding tube. However, I can still advocate and fundraise for ALS patients!
One things I've learned is that there is that the BC ALS Society provides invaluable support to people with ALS, including a medical equipment loan program
Please help me to raise funds to support the BC ALS Society. ALS is not uncurable - it is underfunded!
Thank you, Sara
The Walk to End ALS is the largest volunteer-led fundraiser for ALS Societies across Canada. Family-friendly and fun, it unites Canadians in their desire to put an end to amyotrophic lateral sclerosis. Celebrate hope for a future without ALS. Honour those we have loved and lost. Show support for the 3,000 Canadians and their families living with the disease.Your generous donations support the best ALS research in the country and enable ALS Societies to provide community-based support to people and families living with the disease.
Please help us end ALS by signing up for the Walk or making a donation.
On behalf, of the ALS Society of BC board, staff, volunteers, ALS patients and their families, we thank you for your support!