On April 28, 2025, the federal election was held in Canada, and the Liberal Party won with a minority government. The start of a fresh mandate, with many first-time Members of Parliament (MPs) and a newly appointed Minister of Health, means considerable opportunities to engage with MPs and build relationships with federal decision-makers.
Nearly 4,000 Canadians are living with ALS, and another 1,000 Canadians will be diagnosed with, and die from, ALS each year. The physical, emotional, and financial realities of an ALS diagnosis are devastating and impact the entire family. Despite its incredible toll, ALS remains an underfunded disease in Canada, even as the burden on families, the healthcare system, and the economy continues to grow. To address this, there is an urgent need for federal leadership, support, and investment in research.
This campaign is an opportunity to ensure the voices of the ALS community are heard and that the ALS community is at the forefront of the federal government’s agenda.