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  • Home
  • SMA
    • About SMA
    • Newly diagnosed
  • Community
    • About Us
    • Membership
    • Fundraising
    • Resources
  • Events
    • Upcoming events
    • SMA Camp
  • Care
    • Treatments
  • Contact Us
  • Donate A Car
  • Donate
  • Français

Yearly Archives: 2018

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  2. 2018

A picture is worth 1000 words

Member Update, Research NewsBy ebessoApril 3, 2018

These photos were recently sent to Cure SMA Canada from James Radke, President at Zeal Access Inc. with the caption, “A picture is worth 1000 words”. Susi Vander Wyk speaks…

Cure SMA Awards $50,000 Grant to Rashmi Kothary, PhD, University of Ottawa

Grants, Research NewsBy ebessoApril 3, 2018

Cure SMA has awarded a $50,000 research grant to Rashmi Kothary, PhD, at the University of Ottawa, for his project, ” The shifting landscape of SMA research: towards a better…

Cure SMA Awards $150,000 Grant to Robin Parks, PhD, University of Ottawa

Grants, Research NewsBy ebessoApril 3, 2018

Cure SMA has awarded a $150,000 research grant to Robin Parks, PhD, at the University of Ottawa, for his project, “Serum-derived exosomes as a biomarker for Spinal Muscular Atrophy.” Dr.…

Community update Action needed!

camps, Member UpdateBy ebessoMarch 16, 2018

Dear Cure SMA Canada Community and supporters, Thank you for your continued vigilance in our many efforts for fighting for access to treatment.  Cure SMA Canada has been working hard…

Please help the Canadian SMA Community!!!

Member UpdateBy ebessoFebruary 20, 2018

Please help the Canadian SMA Community!!! Sign and share this petition for access to the only treatment for SMA. We need the Canadian government to hear us!! Please sign and…

Cure SMA Canada has been working feverishly in our fight for broad access to treatment. 

Member Update, Research NewsBy ebessoFebruary 16, 2018

Dear Cure SMA Canada Community,    Cure SMA Canada has been working feverishly in our fight for broad access to treatment.   A short but important update in these meetings and…

As seen on Global Drug researcher disputes rare disease medication pricing

Member Update, Research NewsBy ebessoJanuary 31, 2018

Drug researcher disputes rare disease medication pricing.

HOW MUCH LONGER WILL SMA PATIENTS HAVE TO WAIT TO GET THE APPROVED TREATMENT?

Member Update, Research NewsBy ebessoJanuary 25, 2018

    If it were not for bad news, the spinal muscular atrophy (SMA) community in Canada would have no news at all. At least in the past couple of…

Progress Needed to Help Canadians affected with SMA

Member Update, Research NewsBy ebessoJanuary 23, 2018

Cure SMA Canada urges timely, committed negotiations to provide coverage of first-ever and life-saving treatment for debilitating childhood disease. Cure SMA Canada, on behalf of Canadians diagnosed with Spinal Muscular…

Progress Needed to Help Canadians affected with SMA

Member UpdateBy ebessoJanuary 20, 2018Leave a comment

Cure SMA Canada urges timely, committed negotiations to provide coverage of first-ever and life-saving treatment for debilitating childhood disease     Cure SMA Canada, on behalf of Canadians diagnosed with…

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