MS Society

Check out this video from our respected charity the MS Society.

Click to see video transcript


The MS Society of Canada, we work to support people – Canadians – who live with MS. MS is highly prevalent in Canada. We’ve got one of the highest rates in the entire world. About 77,000 Canadians live with MS and three times more likely to affect women than men. And it’s really does strike in those prime years of life – those years where we’re young, starting families, building our future.

So, the way that we support and of course we fund very important research into the cause, cure, treatments and just general understanding about the disease. But also provide very important programs and services for people living with the disease today.

Multiple Sclerosis is classified as an autoimmune disease of the central nervous system. It can manifest itself in so many different ways. And that’s one of the most challenging pieces of MS. No doctor can tell you exactly what’s going to happen.

In the relapsing remitting form of the disease, sometimes there’s recovery. You start to get better and you don’t really know when that next attack will come. And the other form of the disease, progressive MS, it just continually gets worse over time.

So, it’s really – it’s – there’s a great deal of uncertainty and unpredictability with the disease. It can be life altering for anyone that lives with it.



I was diagnosed in 2013. And it was a long hard road to that diagnosis. It was like four years of many different things that I could or could not be and many trips to the ER. So, actually when I was diagnosed, it was a little bit of a relief, because it was an answer to a question that seemed unanswerable.

But it was also crazy scary at the same time. I was 23 years old and I had just started on a career that I absolutely loved. And I was working really, really hard and was worried that this was going to change my life. And I mean, it did. It was kind of the obliteration of expectation.

I spent a good three, four years keeping my diagnosis to myself predominantly and it was not a fun place to be. I was definitely in a little bit of denial, but also just afraid of what people would think. And I didn’t see that there was any – that there could be any power to that. Or, that this was actually something that could be positive.

And the MS Society really helped me find the positive and find the community that I needed to help support me. So, I think I would just – I just certainly wouldn’t be the person I am today, without having the support of the community that the MS Society introduced me to.

I would say to the Donors that it’s incredible what your donations are doing, absolutely. You’re supporting a cause and a community with your donations. But you’re also advocating for a community of people who need advocating for.



Absolutely everything we do relies on Donor dollars, which is why we’re so grateful for campaigns like this. So, we’re so grateful for Donor dollars that allow us to do this important work. Every single piece of our work is made possible, only through donations.


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