June Highlights ALS Awareness Month

June marks ALS Awareness Month, bringing attention to Amyotrophic Lateral Sateralosis (ALS), a progressive motor neuron disease impacting thousands of Canadians. This nervous system disorder affects muscle movements, making activities like walking and talking increasingly difficult.

Contrary to common misconceptions, ALS is not exclusively a hereditary disease and can affect individuals regardless of their family history. While symptoms vary, living with ALS presents significant challenges. Although the disease is not curable, various treatments are available in Canada, primarily aimed at managing symptoms rather than halting its progression.

Support for those living with ALS is crucial, and awareness is the first step. Organizations such as the ALS Society of Saskatchewan are actively involved in fundraising and public education. Events like the 2026 Walk to Cure Regina aim to generate funds for research and support services.

Paula Trefiak, who was diagnosed with ALS at 34 after symptoms began in her mid-20s, described the experience as "exhausting and it's an emotional rollercoaster." She emphasizes the need to clear up misconceptions about the disease and increase public understanding. Global News correspondent Sania Ali provided further details in an accompanying video report.

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It’s exhausting and it’s an emotional rollercoaster; the amount of care that has to happen increases quite quickly.