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It's about time for people with ALS to be heard.

It's about time for people with ALS to be heard.

image of It's about time for people with ALS to be heard.

When you’re living with ALS, you measure time by loss, not by months or years. Which ability will you or your loved one lose tomorrow? Will you still be able to share a hug? Say I love you? Laugh? Breathe? How long before time runs out?

Across the country, people just like Selvajothy and her family are fighting for more time together, to laugh, to love, to live. This ALS Awareness Month you can join them. Send an email to federal party leaders today, with one simple click, asking them to create a health system that improves access to ...

When you’re living with ALS, you measure time by loss, not by months or years. Which ability will you or your loved one lose tomorrow? Will you still be able to share a hug? Say I love you? Laugh? Breathe? How long before time runs out?

Across the country, people just like Selvajothy and her family are fighting for more time together, to laugh, to love, to live. This ALS Awareness Month you can join them. Send an email to federal party leaders today, with one simple click, asking them to create a health system that improves access to the proven high-quality ALS therapies of tomorrow.

For people living with ALS, the health system never moves fast enough. That’s why the health system reforms being considered by government today must take into account the needs of people living with ALS—for faster, more equitable access in the future when more proven ALS therapies are expected. There’s no time to waste. Join the fight for timely, equitable, and affordable access to tomorrow’s ALS treatments. Send your email today.

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Email Canada's party leaders

Time is running out and the lives of Canadians living with ALS are at stake. Tell your federal party leaders that it’s about time to make people living with ALS a priority.

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