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Decentralized Democracy

House Hansard - 64

44th Parl. 1st Sess.
May 4, 2022 02:00PM
Context: House Hansard - 64 - May/4/22
Mr. Jamie Schmale (Haliburton—Kawartha Lakes—Brock, CPC)
  • 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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Context: House Hansard - 64 - May/4/22
Mr. Jeremy Patzer (Cypress Hills—Grasslands, CPC)
  • 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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