ALS Society of Canada

Tel: 416-469-2267

Toll-free: 1-800-267-4ALS (4257)

For general enquiries: als.ca/contact-us/

als.ca 

ALS Society of Canada

ALS Society of Canada

Tel: 416-469-2267

Toll-free: 1-800-267-4ALS (4257)

For general inquiries: als.ca/contact-us/

als.ca

Since 2017 Federated Health Charities has donated more than $434,782 to the ALS Society of Canada

Being part of Federated Health Charities is very important to ALS Canada. We are 100% donor-funded, and those dollars really help us to be able to assist people within the community.

Tammy Moore, CEO, ALS Society of Canada

Click to see video transcript

Kristine L:
I was told by a neurologist that he was pretty sure I had ALS. I think I went home and cried for days.

George A:
It’s a very debilitating disease and for her to come home and say that she had ALS, it was pretty devastating.

Tammy Moore:
When somebody is given the diagnosis of ALS, they’re given two to five years to live currently. For them, it will be progressive paralysis that they will be facing. So within their community, what they’re going to be finding is needing assistance with the journey as they navigate it.

Kristine L:
I can’t do any of the day-to-day things. I can still use a spoon, but that’s leaving. My husband, he does everything for me. He does all the laundry, the cleaning, the shopping, the cooking.

George A:
We both had to retire early from our jobs. You don’t see as many people as you once did, because you don’t get I and out as much as you used to do.

Kristine L:
Caretakers don’t get enough support. They suffer from this as much as we do.

Tammy Moore:
ALS Canada is directly responsible for people living with ALS here in Ontario, as well as for advocacy, and then for the national research program, so that there will be a future without ALS.

Kristine L:
I sort of looked up ALS Canada online, and then shortly thereafter I got a phone call from Sarah, and the gist of the conversation was that I wouldn’t go through this alone.
Having Sarah come to me was the best thing ever.

George A:
She’s always there to make things enjoyable in a sort of non-enjoyable world.

Tammy Moore:
We can only imagine as we’re navigating this devastating illness, that you will want somebody that’s been there, that will be able to help you, to be able to understand what’s coming next, to be able to be in your home and to be able to see what your next supports might be that you will require.

George A:
The disease that needs support, it needs it for the funding of the day-to-day aspect of dealing with the people who are suffering.

Tammy Moore:
Being part of Federated Health Charities is very important to ALS Canada. We are 100% donor-funded, and those dollars really help us to be able to assist people within the community.

Kristine L:
We would have had to buy all the equipment or maintenance and now that I’m on disability and George had to retire, we would be in big debt. I just think it’s the greatest organisation to help us across Canada.

The ALS Society of Canada works with the ALS community to improve the lives of Canadians affected by ALS through advancing research, care, advocacy, and information. Founded in 1977, ALS Canada addresses the urgent need for better treatments, improved access to clinical care, and high-quality research to find a cure for amyotrophic lateral sclerosis (ALS).

ALS, also known as Lou Gehrig’s disease, progressively paralyzes people. In ALS, the motor neurons that transmit signals between the brain and muscles break down. As these neurons die, the brain loses the ability to communicate with the body. Over time, people living with ALS lose the ability to walk, talk, eat, swallow, and eventually breathe. Most people diagnosed with ALS die within two to five years.

While the exact cause of ALS remains unknown, researchers believe they are on the brink of breakthroughs that could significantly alter the course of the disease. More funding and better access to clinical trials are critical to make ALS a treatable, not terminal, condition.

For families, ALS is a physical, emotional, and financial challenge. In Ontario, ALS Canada provides essential support through its Equipment Program and Community Leads team, helping people navigate the healthcare system and prepare for what’s next. These services ease the burden and provide compassionate guidance from people who understand the journey.

Federated Health Charities has supported ALS Canada since 2017. Donations fund research, advocacy, and programs that empower people living with ALS and their families. “Being part of Federated Health Charities is very important to ALS Canada. We are 100% donor-funded, and those dollars really help us to be able to assist people within the community. Our work depends on the generosity of donors,” says Tammy Moore, CEO of ALS Canada.

Learn more at als.ca and donate through Federated Health Charities to make a difference today.

Click on the button below to make a donation to ALS Canada through Federated Health Charities

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Toronto, ON
M7A 0B8

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Charitable Registration No.
85413 5480 RR0001

Federated Health Charities White Logo

Contact Us

647-278-9861
federated.health.charities@ontario.ca

Address

315 Front St. West, 5th Floor
Toronto, ON
M7A 0B8

Charitable Registration No.
85413 5480 RR0001

Follow us

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