About ALS

• Amyotrophic lateral sclerosis is a disease that gradually paralyzes people because the brain is no longer able to communicate with the muscles of the body that we are typically able to move at will. Over time, as the muscles of the body break down, someone living with ALS will lose the ability to walk, talk, eat, swallow, and eventually breathe.
• ALS can affect anyone regardless of gender, ethnicity or age. It most often affects people aged 40-60.
• Only about 5 to 10 per cent of ALS cases are inherited from a family member.
• An estimated 3,000 Canadians are currently living with ALS--400 of which are living in BC.
• Each year approximately 1,000 Canadians die from ALS. A similar number of Canadians are diagnosed with ALS each year.
• 80 per cent of people with ALS die within two to five years of being diagnosed.
• There are few effective treatments for ALS and no cure.
• ALS has an estimated cost to families of $150,000 to $250,000. This includes the loss of salary that often comes about when a family member leaves their job to care for their loved one full-time.

 

About ALS BC

The ALS Society of British Columbia was founded in 1981 by ALS patients, their family members and healthcare professionals to meet the physical and emotional needs of people living with ALS and their caregivers. Visit our website to learn about what we do at the ALS Society of British Columbia.
 

Mission Statement

The ALS Society of British Columbia is dedicated to providing direct support to ALS patients, along with their families and caregivers, to ensure the best quality of life possible while living with ALS. This includes access to an equipment loan program. By funding research, we are committed to find the cause of, and cure for Amyotrophic Lateral Sclerosis (ALS). Our goal is to end ALS through creating a world class ALS Centre at UBC.

 

Core Values/Beliefs

Unsurpassed Service: We are dedicated to improving the quality of life for our patients, their caregivers, and their families.

Teamwork: Our success is built on a team of dedicated staff and volunteers (Team ALS BC & Yukon) working for a common purpose.


Quality of Life: Our goal is to continually improve the services needed to improve the quality of life of those living with ALS.


Equality of Care: Everyone living with ALS has a right to equal care, no matter where they live in BC.


Dream Big: We push the envelope constantly to improve what we can do to achieve results.


Vision – Long Term Goal – Aspiration
End ALS through a world class center at UBC.