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House Hansard - 64

44th Parl. 1st Sess.
May 4, 2022 02:00PM
  • May/4/22 2:04:26 p.m.
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Mr. Speaker, Canada has one of the highest rates of multiple sclerosis in the world, with over 90,000 Canadians diagnosed with the disease. MS is three times higher among women, and COVID-19 amplified the income insecurity faced by women with disabilities. Diagnosed with MS in 2008, Michelle Hewitt shares how difficult it is to make ends meet. She says, “I regularly speak to women who are no longer able to work and have no avenues for income once their medical EI is finished. They are not seen as 'disabled enough'.... The system is failing them.” Our government recognizes the urgent need to address this issue and plans to introduce a new Canada disability benefit to support Canadians with disabilities and lift them out of poverty. Today, in honour of MS Awareness Month, I join the MS Society's virtual carnation pinning campaign to support a world free of MS. I encourage all of my colleagues to wear their carnations today and join in this effort.
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  • May/4/22 2:05:42 p.m.
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Mr. Speaker, multiple sclerosis is the most common neurological disease affecting young adults. Research has shown that more than 60% of people with MS become unemployed at some point. This disease is episodic, meaning that people alternate between relapses into disability and periods of stability. At the moment, employment insurance offers them a mere 15 weeks of sickness benefits without any flexibility. It is obvious that the EI system needs a complete overhaul. Today, in honour of MS Awareness Month, we are taking part in the MS Society of Canada's virtual carnation pinning campaign, part of the #TakeActionForMS movement, in the hopes of improving quality of life for people living with multiple sclerosis.
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  • May/4/22 2:13:59 p.m.
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Mr. Speaker, I can personally attest to the devastating impact multiple sclerosis has on families. As some may know, my mother succumbed to a progressive form of MS a few years ago. I can still remember the impact that diagnosis had on her, from coming to terms with the news, to planning home renovations that included a wheelchair ramp and accessible bathroom. As it worsened, it left a loved one with a perfectly healthy mind trying to operate in a body that just would not respond. That was only one small snapshot of a story too many Canadians are forced to experience. In fact, 12 Canadians are diagnosed with MS every day. It can happen to anyone, without warning, and sadly it is often known as Canada’s disease. Fortunately, this country is home to some of the best MS researchers. There have been many life-altering advancements in treatments over the past two decades, including the exciting recent discovery that the Epstein-Barr virus might be a trigger for MS. Today, in honour of MS awareness month, I am participating in the MS Society’s virtual carnation-pinning to show my commitment to creating a better quality of life for Canadians affected by this disease and, hopefully very soon, creating a world free of MS.
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  • May/4/22 2:20:15 p.m.
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Mr. Speaker, the month of May is MS Awareness Month, and today is carnation day. Every day in Canada, another 12 people are diagnosed with multiple sclerosis, so I want to speak to those 12 people today. A diagnosis is not the end of life as we know it. There are many people and families all across Canada who are going through, and have gone through, what those diagnosed are dealing with here today. They are not alone on this journey. It was only a short year ago that my wife received her official MS diagnosis. I know the emotions of the day run high, but thanks to improvements in detection and treatment, my wife is working every day and continues to be the amazing wife and mother she has always been. She is not letting MS define who she is or limit her in what she can or cannot do. In conclusion, we do not know how strong we are until being strong is all we have left.
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