Jays From the Couch has launched an online merchandise store where 100% of profits will be donated to the ALS Society of Canada
If you are a regular follower of Jays From the Couch and JFtC Radio, you would be aware that I have begun a campaign to fight ALS – Amyotrophic Lateral Sclerosis. This campaign has already made a great start toward raising awareness and funds for the ALS Society of Canada. But, I’m kicking it up a notch!
I am proud to introduce the Jays From the Couch vs ALS Store! We have created an online store at Teespring where you can find some great Jays From the Couch swag like shirts and hoodies, for both men and women, and a lot more! By shopping at the JFtC vs ALS Store, you will be helping our efforts to beat this terrible disease. 100% of the profits raised will be donated directly to the ALS Society of Canada.
So, head on over to the Jays From the Couch vs ALS Store and get some great swag that you will look great in and you can feel great about.
You can also head to our Jays From the Couch vs ALS Fundraising page to make a tax deductible donation directly to ALS Canada.
Support from the Jays From the Couch fundraising site and our online store will help to create a better reality for people and families living with ALS by enabling access to expensive support services and equipment. Funds raised will also support research so that one day soon ALS will be a treatable, not terminal disease. Many leading ALS researchers believe that effective treatment options are now a matter of when, not if and that research discovery is limited only by the amount of funding available to pursue it. This makes the Jays From the Couch ALS fundraising site an important vehicle for progress, so please support our efforts.
ABOUT ALS CANADA
ALS Canada is a national organization responsible for the ALS Canada Research Program – funding peer-reviewed research grants and fostering collaboration amongst Canadian researchers, helping to nurture new ideas and build capacity. ALS Canada has a role in Ontario, similar to that of the Provincial Societies, providing services and support for people living within our provinces – they help fill the gaps between the healthcare system and needs of people living with ALS. They advocate federally, provincially and locally on behalf of people and their families for better government support and access within the healthcare system.
The ALS Canada Research Program brings together top Canadian researchers in collaboration through our annual research conference, helping to nurture new ideas and build capacity. With the help of an International Peer-Review Panel, grants are awarded to the best ALS research projects possible that will move us closer towards finding a treatment for ALS.
The ALS Canada Research Program aims to accelerate research impact through a comprehensive national program focused on translating scientific discoveries into treatments for ALS, and fostering Canada’s strong and networked ALS research community to build capacity and collaboration. Support for the ALS Canada Research Program is made possible by the generosity of donors, the ALS Societies across Canada, Brain Canada and the federal government’s Canada Brain Research Fund
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