Programs & Services
Receiving an ALS diagnosis is overwhelming and leads to many questions and concerns. Whether you are living with ALS or caring for someone with ALS, there are many challenges and changes to consider. The ALS Society of BC and our provincial partners are here to help. Through fundraising and donations, the ALS Society of BC is able to provide programs and services at no cost to ALS patients and their families; however, patients must be registered to access them. There is no registration fee for ALS Patients.
Patient Registration Form – Online
Patient Registration Form – PDF
General Membership Form (for Individuals, Friends and Family Members)
The ALS Guide has been developed to provide practical information about ALS, its progression, and how people and families living with ALS can find solutions to help maintain independence. To view the ALS Guide, click here.
Statistics Overview
In 2022, the ALS Society of BC provided care for a total of 566 clients, in comparison to 498 clients in 2021 and 487 clients in 2020, through various support programs and patient services initiatives.
Support Networks
- ALS Society of BC Support Groups
- On-Line Support, Patients Like Me
- BC Caregiver Support Line: 1-877-520-3267 (Mon – Fri, 8:30am – 4:00pm)