April 30th 2016. The date doesn’t ring a bell for most that knew him. It’s not his birthday or my parent’s wedding anniversary. It’s also not the birthday of any of his siblings, kids, nieces, nephews or grandkids. Nope, it’s a seemingly ordinary day last year in April.
But for my sisters, my mom and myself April 30th 2016 holds much importance.
It was the date of last years Walk for Muscular Dystrophy (MD) in Toronto. And, the last time my dad participated in this walk with his family before he passed away in June 2016.
In early 2007, my dad was diagnosed with Inclusion Body Myositis (IB), an autoimmune disease that weakens and wastes the muscles progressively over time. And even though, his body was slowly deteriorating, his willpower and zest for life never wavered. He continued to be active in the community and one of his favourite events of the year was the Walk for Muscular Dystrophy. It was an opportunity to raise awareness and support those affected by neuromuscular disorders. It was also a way to connect with friends he had made who also lived with similar disorders and spend time walking/rolling with his family.
Muscular Dystrophy Canada provided much support to my dad (and to our family) throughout the years, generously funding devices and aides that helped him with daily activities, providing a conduit for him to reach out and share his experiences with others and also supporting our family throughout his disease.
April 29 2017. The date of this years Walk for Muscular Dystrophy. We walk in honour of my dad, keeping his legacy alive. We walk in support of everyone everywhere affected by neuromuscular disorders. We walk to help raise awareness, to fuel research and encourage advocacy.
We walk to make a difference.
I would love for you to walk with us!
Visit our team page here for more information. Hope to see you there!