The MS Society of Canada is undertaking a survey of MS patients and their caregivers as part of the Listening to People With MS initiative. The intent is to gather information which will help to improve the Society's programs and service and therefore help to improve the live of Canadians with MS.
"Who can take the survey?
Those living with a diagnosis of Multiple Sclerosis (MS) or Clinically Isolated Syndrome (CIS);
Those waiting for a diagnosis with respect to MS;
Those with a close relationship with someone with MS or CIS (family member, spouse or partner, friend);
Those who are unpaid caregivers of someone with MS or CIS (family member, spouse, partner or friend who provides care some of the time or all of the time)."
So all you Canadians out there: mummy, Candy, Wobbly, Mike Shuswap, Rena, DiannaKw, littlelawbear, and anyone else who may see this, please take a few minutes to complete the survey. I did so and that's all the time it took.
Here's the link:
http://mssociety.ca/listening/index.htm