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.
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