The ALS Canada Blog is a pilot project. We will be working towards publishing content in both English and French in the coming months. Please refer to the “Français” category to access blog posts that are available in French at this time.

Le blogue de la Société canadienne de la SLA est un projet pilote. Nous poursuivrons des travaux sur la publication d’un contenu de blogue en anglais et en français dans les mois à venir. Veuillez consulter la catégorie « Français » pour accéder aux entrées de blogue qui sont disponibles en français en ce moment.

WALKing for ALS with gratitude and positivity

The Belleville-Quinte WALK for ALS


For the second year in a row, the Williams family is “trekking for ALS research – boldly going where ALS research needs to go.” These are the words of Scott Williams, who since receiving his ALS diagnosis in 2015, has...

Posted in: WALK for ALS

The impact of donor dollars on ALS research in Canada

Investing with care and consideration


The result of the 2014 Ice Bucket Challenge gave the ALS community a tremendous gift: awareness and unprecedented investment in ALS research. Thanks to the viral fundraising phenomenon that year, along with matched funds from Brain Canada (through the Canada...

Posted in: Research

A Community Connected

2017 Annual Report to the community


In 2014, the Ice Bucket Challenge gave hope to people and families living with ALS – hope that one day there would be a cure for this terminal disease. With the Ice Bucket Challenge came an immense responsibility to invest...

Posted in: Update
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Every August Until A Cure 2018


"Every August until a cure." These five words were first spoken by ALS patient and advocate, Pat Quinn, upon accepting a Webby Award for his part in creating the Ice Bucket Challenge. The social media phenomenon raised millions of dollars...

Posted in: Research

The emotional challenges of ALS

Below the surface


When someone hears about ALS, the first thought is often about the loss of physical function; for example, the progressive inability to walk, talk, eat, swallow, and eventually, breathe. Losing these functions one by one can be profoundly difficult on...

Posted in: Stories

Wrapping up ALS Awareness Month

Who do you give for?


ALS Awareness Month is all about telling stories. Over the course of the month of June, people and families affected by ALS shared their personal stories about why they gave and who they gave for. On June 27, 2018, Dr. David...

Posted in: Events