Act Now

Thank you for taking action! Here’s some ways that you can Act Now. Become a volunteer, host a Walk and Roll or a fundraising event or take part in Awareness Month initiatives.

Creating awareness of our rare neuromuscular conditions GBS, CIDP, MMN, and variants will improve patient outcomes. Supporting our program initiatives through donation improves the patient journey and every dollar donated stays in Canada.

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Volunteer

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Walk and Roll

GBS mobile

May is GBS/CIDP Awareness Month

MMN mobile

February is MMN Awareness Month

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Host Your Own Fundraising Event

Walter Keast Award

The Walter Keast award is given to an individual for exemplary service to the GBS, CIDP, and MMN community.

Past winners

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Jenny Rybie
2024
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Miranda & Ameliya Pellett
2023
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Nancy Galaski
2022
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Cheryl Dean
2021
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Jason Kent
2019
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Dean Lower
2018
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Holly Gerlach
2017

Know someone who deserves this award?

We accept nominations for the Walter Keast award from September 1 - November 15 each year, for a community member who has made an outstanding contribution.

Check back on September 1st to nominate someone!


    Help Us Help Others

    Now more than ever, we continue to need your support to help those afflicted with GBS, CIDP, MMN, and variants. Donate to help us improve the quality of life for individuals and families affected.

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