The Manitoba election is underway and we want to ensure that all candidates across the province know how important it is to #TakeActionForMS. Can you spare a minute to send a letter to the candidates in your riding, telling them about the priorities of the MS community?

Canada has one of the highest rates of MS in the world, with more than 90,000 Canadians living with the disease. In Manitoba, there are concrete actions elected officials can take to support the MS community, but we must take a proactive approach. 

Join us and tell candidates to:


Make Access a Reality

Provide better access to care, treatment, and rehabilitation for Manitoba’s MS community. Access to treatment and care has been especially challenging in recent years, and it is critical the next provincial government takes action to address these challenges.


Improve Diagnosis

A report commissioned by MS Canada found the COVID-19 pandemic led to delayed MS diagnoses for many Canadians. Delays in receiving an MS diagnosis delays starting on disease-modifying therapies (DMTs), which reduce relapses and slow disability progression in MS. 


Make Ends Meet

Ensure the forthcoming federal Canada Disability Benefit, designed to lift Canadians living with disabilities out of poverty, aligns with provincial benefit programs so Manitobans living with disabilities are better supported. Ensure no provincial support programs for people living with disabilities are decreased because of this new federal benefit.

Let your candidates know you’re voting for someone who will #TakeActionForMS and address these challenges to provide better care to Manitoba’s MS community.

» Expand to Read the Letter

Dear [Mr., Ms.] [Candidate last name]:

As a voter in [your riding], I am writing to my candidates in this provincial election and asking them to #TakeActionForMS.

[Personal comments inserted here]

Canada has one of the highest rates of multiple sclerosis (MS) in the world. This disease usually strikes a person in the prime of their lives, between the ages of 20 and 49, and impacts women at three times the rate as men.

MS is the most common neurological disease among young adults in Canada and is a costly disease for both the health system and Canadian society more broadly. To better understand the effects of the pandemic on the well-being of our community, and inform potential solutions, MS Canada commissioned a report on the impact and economic cost of COVID-19 on MS in Canada. The findings raise significant concerns. The reduction in health service access, coupled with the social and physical isolation from lockdowns, resulted in the accumulation of unmet health needs including:

  • Delayed MS diagnosis.
  • Delayed, altered, or halted treatments.
  • Suspended or altered rehabilitation.
The ongoing effects of unmet health needs, combined with the overall strain on the health system in Canada, continues to compound the challenges faced by the MS community. Challenges like the financial difficulties as families try to make ends meet, the struggles faced in the workplace, the frustrating barriers to accessing treatments, and MS care and housing.

There are clear ways to address the burden:

Make Access a Reality
Provide better access to care, treatment, and rehabilitation for Manitoba’s MS community. Access to treatment and care has been especially challenging in recent years, and it is critical the next provincial government takes action to address these challenges.

Improve Diagnosis
A report commissioned by MS Canada found the COVID-19 pandemic led to delayed MS diagnoses for many Canadians. Delays in receiving an MS diagnosis delays starting on disease-modifying therapies (DMTs), which reduce relapses and slow disability progression in MS.

Make Ends Meet
Ensure the forthcoming federal Canada Disability Benefit, designed to lift Canadians living with disabilities out of poverty, aligns with provincial benefit programs so Manitobans living with disabilities are better supported. Ensure no provincial support programs for people living with disabilities are decreased because of this new federal benefit.

Please let me know if I can count on you to #TakeActionForMS this election by replying to my email and by posting on your social media channels tagging MS Canada and using the hashtag #TakeActionForMS.

Sincerely,

[First and Last Name]
[Postal Code]

Personalize your letter:

We know that MS affects each person differently, and while our priorities might be common, every story is unique. If you'd like, please share your MS story, or add your comments here, to encourage canddiates to #TakeActionForMS. Your comments will be inserted automatically in your letter once it's sent.

The information you provide will be protected according to our privacy policy.