The Walk for Muscular Dystrophy is a fully accessible fundraising event that is fun for the whole family! Funds raised through the Walk for Muscular Dystrophy are used to assist people with neuromuscular disorders through education, information, support, advocacy and funding for research and assistive devices. There are 58 events held between April and October across Canada, and volunteers are essential to each event! From volunteers on the planning committee and coordinators of fundraisers to event day helpers who assist with set up, registration, take down and more! The Walk for Muscular Dystrophy relies on the dedication and generosity of volunteers! Read about some of the wonderful volunteers involved with the Walk for Muscular Dystrophy.
Lucy has been an active volunteer for Muscular Dystrophy Canada for many years. As a member of the Peel Region Walk for Muscular Dystrophy volunteer planning committee, an active fundraiser and participant, Lucy works hard to support a cause that is important to her.
Lucy DaSilva has come up with a way to combine her passion for raising funds and awareness for Muscular Dystrophy Canada with one of her hobbies. During the holiday season, Lucy puts her needle and thread to work and sells handmade accessories, and donates the profits to Muscular Dystrophy Canada.
“With muscular dystrophy a part of my life, I feel that giving back is rewarding. I have met a lot of friends along the way and maybe one day my work will help others to beat muscular dystrophy and find a cure,” said Lucy.
The driving force behind the Peel Region Walk for Muscular Dystrophy silent auction is Annette Sultana, a long-time Muscular Dystrophy Canada volunteer. Annette dedicates her time to the silent auction like a full time job, and it continues to be one of the reasons people look forward to the Walk every year!
Annette, who was diagnosed with SMA at the age of seven, always knew that she wanted to give back to an organization that had given to her, and has been a member of the volunteer planning committee for the past three years. “I stopped working about five years ago, and wanted to do something productive and important. So, when MDC called looking for volunteers, I agreed. Being a part of the planning committee gives me the opportunity to use my skills, discover new ones, and most importantly, to give back to an organization that has given so much to so many.”
2013 marks the launch of the Sarnia Walk for Muscular Dystrophy, and it’s all thanks to Lisa Headrick and her close-knit group of family and friends.
Having participated in the London Walk for the last few years, Lisa decided that there was a great opportunity for an event like this in her community. She had brought out at least 30 people to the London Walk and was sure more people would be interested in participating in their own community. “I got in contact with [Muscular Dystrophy Canada] and got all of the information, I discussed it with a few of the people that were interested in being on the committee and we decided to go for it,” Lisa says of her decision.
Lisa spends a lot of her free time working on the Walk and trying to spread the word. “I think the best way to raise awareness is to talk about it. I talk about the Walk to everyone I see and everyone I know, there are a generous amount of people that have never heard of muscular dystrophy and I make it my duty to explain what it is to people when they are unaware.
Thank you Lucy, Annette, Lisa and all the many wonderful volunteers who spend time on the Walk for Muscular Dystrophy planning committees and working as event volunteers!