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Listening to People Affected by MS

Listening to People Affected by MS

Thanks to everyone who participated in the Listening to People Affected by MS on-line survey. We heard from over 5,000 Canadians about their quality of life needs, priorities and barriers. We are now reviewing the survey results and continuing with the other aspects of the initiative. Stay tuned for more information.

What is the Listening to People Affected by MS Initiative?

This initiative is a multi-pronged evaluation which has the single purpose of hearing from Canadians affected by MS about their quality of life priorities, needs, and barriers so that the MS Society of Canada can better inform decisions that relate to our programs, services and advocacy. We have sought your input in a number of ways including the recent on-line survey and a poll that was conducted in November 2012. There will also be several small focus groups as well as an environmental scan which will help us further explore aspects of quality of life and MS.

The responses we receive from the survey, poll, and focus groups will provide critical information about quality of life and MS. Your feedback will allow the MS Society of Canada to make informed decisions related to programs and services, and advocacy.

If you have questions, please direct them to: info@mssociety.ca.

Read about the Multiple Sclerosis International Federation (MSIF)’s quality of life principles. These principles were endorsed by the MS Society of Canada in 2009 and were used to structure the survey to be launched this fall, 2012.


Multiple Sclerosis Society of Canada
Toll free to reach the nearest regional office: 1 800 268-7582

To locate the MS Society office near you, please select your region:

E-mail: info@mssociety.ca
(Please provide your town and province in your e-mail)

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