Peter Fragiskatos, London Centre
Linked statement
“June is ALS Awareness Month. Over 4,000 Canadians live with ALS, a disease that slowly takes away a person's ability to walk, talk, and breathe. I want to recognize the people living with ALS, their families, and the researchers and groups working to help them.”
“Mr. Speaker, more than 4,000 Canadians live with ALS, and June is ALS Awareness Month. ALS has been called a rare disease, but that does not take away from the very real impacts it has on people who are living with it. ALS attacks the nerve cells that are responsible for movement; therefore, basic human functions such as walking, speaking, breathing and much more are impacted. While the effects are gradual, they are absolutely devastating. For the month of June, when we reflect on ALS and what it means for those living with it, we also celebrate the resilience of those who have this terrible disease. We also think of their family, their friends, their health care workers and of course the researchers. The researchers are doing so much, not only to bring awareness to ALS but also to provide hope. “Research”, of course, is another word for hope. I thank them. I thank the ALS Society of Canada and ALS Action Canada, two incredible advocacy organizations doing so much as well. We will continue this fight together.”
Mr. Speaker, more than 4,000 Canadians live with ALS, and June is ALS Awareness Month. ALS has been called a rare disease, but that does not take away from the very real impacts it has on people who are living with it. ALS attacks the nerve cells that are responsible for movement; therefore, basic human functions such as walking, speaking, breathing and much more are impacted. While the effects are gradual, they are absolutely devastating. For the month of June, when we reflect on ALS and what it means for those living with it, we also celebrate the resilience of those who have this terrible disease. We also think of their family, their friends, their health care workers and of course the researchers. The researchers are doing so much, not only to bring awareness to ALS but also to provide hope. “Research”, of course, is another word for hope. I thank them. I thank the ALS Society of Canada and ALS Action Canada, two incredible advocacy organizations doing so much as well. We will continue this fight together.