Multiple Sclerosis Society of Canada

Information

Website:
Company Overview:
Founded in 1948, the Multiple Sclerosis Society of Canada is the only national voluntary organization in Canada that supports both MS research and services for people with MS and their families.
For information, call 1-800-268-7582.
Mission:
To be a leader in finding a cure for multiple sclerosis and enabling people affected by MS to enhance their quality of life.

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Société canadienne de la sclérose en plaques
http://www.facebook.com/pages/Societe-canadienne-de-la-sclerose-en-plaques/12713282418

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Disclaimer: The views expressed, comments made and material posted by users of this Page (excluding content posted by the Multiple Sclerosis Society of Canada) do not represent the views of the Multiple Sclerosis Society of Canada and remain the beliefs/opinions and the responsibility of the party posting the information.

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Displaying 3 of 14 posted items

JET SET FOR MS! Fundraiser - Wednesday July 9th - C Lounge, Toronto

1 post by 1 person. Updated on Jul 7, 2008 at 7:42 AM.

Moving Through MS-July 10th-Toronto

1 post by 1 person. Updated on Jun 30, 2008 at 9:31 PM.

CHARITY TOURNEY FOR MS

1 post by 1 person. Updated on Jun 10, 2008 at 12:49 PM.
Displaying 5 of 48 wall posts.
Stewart wrote at 8:25pm on August 21st, 2008
I'm running a marathon for multiple sclerosis! Please support me:
https://msofs.mssociety.ca/2008bike/Sponsor.aspx?L=2&PID=1060823
Kelly wrote at 2:25pm on August 13th, 2008
I would like to say that the drug Lyrica has been by far the most effective drug I have been on for my neuropathic pain , it take a a few months for the levels to maintain but it is well worth it, balance is still off but the pain is gone and i can get things done I need to... A big fan so far
Claude wrote at 6:46am on August 13th, 2008
Hello all,
Here are a couple of great sites some of you might be interested in. I have made some great friends on these sites and lots of great info to help in answering questions or just to not feel so alone sometimes.

http://www.msif.org/en/
http://www.multiplesclerosissucks.com/
Debbie wrote at 10:08am on August 12th, 2008
Hello Ruwaydah,There are alot of sites to go to to read about m.s.I find the main site for the multiple sclerosis society of canada the best for info.The are other sites to that deal with around the world.You can go to the main site of the multiple sclerosis society of canada and read info on it.That is where i go for all my info
Ruwaydah wrote at 1:01pm on August 11th, 2008
hi my name is ruwaydah i am 27yrs old and my mum has had MS for about ten years now. she was diagnosed in the u'k as the docotors in kenya had no clue as t what she had. she was on copaxone from israel for awhile but hat adversely accellerated the ms and also muked around with the pigmentation of her skin. we tried apitherapy(bee therapy) seemed to work for awhile but then became too painful for her. she was regulating on diet and physio as i come from a country where not many people know or care to know about ms and its just basically me and my younger siblings and my dad. she is now completely bed ridden, in diapers and using a tube through her nose to feed and cannot really talk. she is on meds for her nerves Nurontin and baclofen for circulation.....is there any more literature i can perhaps read because it is abit disheartening to see her like that although she always tries to smile and look cheerful i know she is depressed. but most of all i just miss talking to my mum!!

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MS is too big to face alone. Because of donor support, the MS Society of Canada is here to ensure that no one has to. Ways to give