Published in Research on October 30, 2019
Tags: ALS Canada Research Program, ALS research, finding a cure for als, funding als research, genetic research, motor neuron disease, research, research community, Research update
ALS Research Update, October 2019 Welcome to the October 2019 ALS Research update. This month, you’ll learn about the progress researchers have made in: transforming the way clinical trials are conducted; understanding the roles that the microbiome and protein clumping may play in ALS; and identifying the mechanisms by which different genes may contribute to […]
Published in Fund Development on August 12, 2019
Tags: community engagement, Donate to ALS, donating to ALS, finding a cure for als, funding als research, fundraising, Get Involved, How to donate to ALS research, research funding
In late 2018, Facebook began offering the option for Canadians to create fundraisers for nonprofit organizations or for personal causes. Since then many of you have reached out to us with questions about how these giving options can be used to support ALS Canada. We know Facebook can be a quick and easy way to […]
Published in Advocacy, Fund Development, Stories on July 26, 2019
Tags: ALS, ALS awareness, community, community engagement, Donate to ALS, donating to ALS, finding a cure for als, funding als research, fundraising, giving
Last spring, Mike Leech, 59, approached his plant manager to request a 2-month leave from work to complete a bike ride across Canada for charity. An avid cyclist, he dreamed of cycling coast to coast but he wanted to make it more than just a physical challenge. He wanted to raise awareness and money for […]
Published in Advocacy on June 25, 2019
Tags: 2019-personal-stories, ALS awareness, ALS Awareness Month, als stories, finding a cure for als, funding als research, fundraising
Miles4Matty is part of Adam Foley’s search for meaning after losing his brother, Matthew (aka Matty), who passed of ALS in 2014 at the age of 38. Adam and Matthew were roommates at the time of the diagnosis. When Matthew’s mobility became a significant challenge, they moved into a more accessible apartment together where Adam […]
Published in Events, Walk To End ALS on June 21, 2019
Tags: 2019-personal-stories, ALS awareness, ALS Awareness Month, als stories, community, families with ALS, finding a cure for als, living with ALS, walk to end als
On June 15, Don Doan participated in the Walk to End ALS in Brampton for the fourth time. It’s been three years since he was able to walk the course, but his positive outlook hasn’t changed. There are always people around, including his wife, Pam, to help with his wheelchair. “Generally, it’s a fight over […]
Published in Events, Walk To End ALS on June 18, 2019
Tags: ALS researching, find a cure for ALS, finding a cure for als, funding als research, how to live with als, living with ALS, motor neuron disease
Lise Michaud’s brother, Eddy Lefrançois, made every day count. He lived nearly three decades with ALS, proudly defying the odds and outliving his “expiry date” (EXP: 04.97) which he tattooed on the inside of his forearm as a reminder to live with passion and purpose. Eddy’s personal motto – “Let’s Roll” – always kept him […]
Published in Walk To End ALS on June 13, 2019
Tags: als canada, als diagnosis, ALS research, als society of canada, Donate to ALS, donate to als research, donating to ALS, finding a cure for als, finding out you have ALS, having als, how to handle als, supporting people with als, walk to end als
At the rink where he has coached boys’ ice hockey for more than 10 years, Adam Welburn-Ross, 43, is fondly known as “Coach Sunshine.” He wears his positivity as a badge of honour and now that he is living with ALS, his disposition is helping everyone around him appreciate every precious moment of the day. […]
Published in Events, Walk To End ALS on June 6, 2019
Tags: 2019-personal-stories, ALS research, Donate to ALS, donating to ALS, finding a cure for als, fundraise for ALS, fundraising for als, how to donate to ALS, How to donate to ALS research, how to help ALS, how to help people with als, walk to end als
An active mother of three young children, Stephanie Christiansen Hall wants people to know she has ALS – but she wants everyone to know that her disease is only part of her story. Apart from living with ALS, Stephanie is – and has always been – a selfless person with a positive nature, a desire […]
Published in Events, Walk To End ALS on June 3, 2019
Tags: 2019-personal-stories, ALS funding, ALS research, ALS research and funding, canadian ALS research, find a cure for ALS, finding a cure for als, funding als research
Brian Bower has always been passionate about sports. Above all, he is an ardent fisherman, known on occasion to snatch 15 minutes from his day for the joy of casting a line in one of the abundant waterways in and around Welland, where he lives. Brian also loves soccer, tennis, lacrosse, hockey and baseball. An […]
Published in Events, Walk To End ALS on May 29, 2019
Tags: 2019-personal-stories, als canada, als ontario, ALS research, als support, clinical trials als, end als, finding a cure for als, funding als, funding als research, funding als trials, funding research for als, researching als, the walk to end als, walk to end als
Talking about his dad’s ALS diagnosis, Connor Stratton, 17, says, “It’s a hard thing to understand at times, but it’s good to try to look at the bright side because my dad still has his spirits up. He’s still happy around us, and that’s something that reflects on all of us.” Kerry Stratton, a well-known […]
Published in Events, Walk To End ALS on May 29, 2019
Tags: 2019-personal-stories, als canada, als clinical trials, als ontario support, ALS research, als support, clinical trials als, end als, finding a cure for als, funding als, funding als research, funding als trials, support als ontario, the walk to end als, walk to end als
Since receiving his ALS diagnosis in February 2018, Mark Ianniello’s life has changed in profound ways. He is a 49-year-old father to three teenagers and can no longer work to help support his family. ALS has affected his speech and his mobility. Mark admits to having ups and downs. Despite the challenges, he says ALS […]
Published in Events, Walk To End ALS on May 15, 2019
Tags: 2019-personal-stories, ALS, als cure, als research is important, als research matters, Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis cure, finding a cure for als, finding a cure for motor neurone disease, motor neuron disease, motor neurone disease cure, treating als, walk to end als
According to Kevin, there’s one word that sums up ALS: a thief. “ALS is a thief – and a remorseless one at that,” he explains in writing. Now that he can no longer speak, he uses eye gaze technology to type messages with his eyes – his only method of communicating. “The sooner we can arrest […]
Published in Advocacy on April 26, 2019
Tags: 15 day fitness challenge, als canada research, ALS research, als research for a cure, als research in canada, canadian research, canadian scientific research, finding a cure for als, finding an ALS cure, fitness, fitness challenge, orangetheory fitness, science research, scientific research
For the second year in a row, Orangetheory Fitness is giving its members (and the community) a way for you to make an impact while getting in a good workout. It’s a win-win! On May 1, 2019, Orangetheory Fitness is launching a campaign throughout Canadian studios to benefit the ALS Canada Research Program. Their inaugural […]
