About ALS Society of Canada
ALS Society of Canada: Improving Lives through Support, Advocacy, and Research
The ALS Society of Canada is a non-profit organization that is dedicated to improving the lives of people affected by Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. The organization was founded in 1977 and has since been working tirelessly to provide support, advocacy, and investment in research for a future without ALS.
Support for People Living with ALS
One of the primary goals of the ALS Society of Canada is to provide support for people living with ALS. This includes providing information about the disease, connecting people with resources in their community, and offering emotional support through peer groups and counseling services.
The organization also provides financial assistance to help cover the costs associated with living with ALS. This can include things like home modifications, assistive devices such as wheelchairs or communication aids, and respite care for caregivers.
Advocacy for People Living with ALS
In addition to providing direct support to people living with ALS, the society also advocates on their behalf. This includes advocating for better access to healthcare services and treatments that can improve quality of life.
The society also works closely with government agencies at all levels to ensure that policies are in place that protect the rights of people living with disabilities. They advocate for changes in legislation related to disability benefits programs such as CPP Disability Benefits or Employment Insurance Sickness Benefits so that they are more accessible and fairer.
Investment in Research
Finally, one key area where the society invests its resources is research into finding a cure or effective treatment options for those affected by this devastating disease. The society funds research projects across Canada aimed at understanding more about how this disease progresses over time so we can develop new therapies or drugs which could slow down its progression rate significantly.
Through these efforts towards supporting those affected by this debilitating condition - whether it be through direct assistance or advocacy work - we hope one day soon there will be no need left anymore because we will have found a cure!
als.ca
