Message from Leona Aglukkaq, Minister of Health

ALS Awareness Month (Lou Gehrig's Disease)

June 2010

As Minister of Health, I am proud to recognize June as Amyotrophic Lateral Sclerosis (ALS) Awareness Month in Canada.

ALS, also known as Lou Gehrig's Disease, is a neurodegenerative disease affecting approximately 2,500 to 3,000 of Canadians.

ALS can strike anyone, regardless of gender, age or lifestyle. Those living with the disease experience progressive paralysis and, in its late stages, their muscles become so weak that they lose the ability to swallow or breathe. There is currently no cure for this disease.

The Government of Canada recognizes the devastating impact of ALS in Canada.  Working with Canada's major neurological charities, including the ALS Society of Canada, the Government is investing in a four-year national population study of Canadians affected by neurological diseases. This study will inform decisions on how we can better meet the needs of Canadians affected by neurological diseases such as ALS.

During this month, blue cornflowers are sold as a fundraiser to support individuals living with ALS. This flower, hearty despite its fragile appearance, is symbolic of those inflicted with this disease.

Please join me in recognizing those Canadians living with ALS, the family and friends who serve as their caregivers, the ALS Society for its commitment to research and public awareness efforts, and those involved in the fight for a cure. I encourage Canadians to become better informed about this disease and offer support to those who are affected.

For more information on ALS, please visit the website of the  ALS Society of Canada.

Leona Aglukkaq
Minister of Health
Government of Canada