Improving the quality of life of Quebec families touched by ALS
Learning you have ALS is devastating. The diagnosis stirs up all kinds of emotions — fear, worry, sadness and anger. From diagnosis to end-of-life care and bereavement support, our dedicated team of psychosocial counsellors and coordinators provide compassionate and knowledgeable
“Today, we want to give you a little respite and acknowledge your dedication towards your loved ones” says Leigh Stephens, psychosocial counsellor at the Society, setting the tone for the third edition of Caregiver Recognition Day as part of Caregivers Week. On Sunday, November 6th, approximately 30 caregivers
“Wow, wow, wow!!!! FREEDOM!!! What a terrific day. I’ve been imprisoned inside my body for years, and I never thought it possible to experience such a feeling of freedom…” says Ginette Beaudreault, who took part in a sailing excursion organized last summer at the Pointe Claire Yacht Club.
In 2001, Martin and Anick were planning their lives together, looking forward to great adventures, determined to climb their respective career ladders and to start a family. But fate had decided otherwise.
The Society expands its regional outreach
In 2015, one of the Society’s priorities was to extend its outreach to members across the province and to diversify its activities held outside the metropolitan area. As a result during this year, the Society traveled to thirteen administrative regions, organized more support groups
When we share our ideas, energy and philanthropic contributions we create a community that is truly stronger. Together, we’ve accomplished a great deal in 2015. We have made sustainable investments in our services and contributed to major research grants in Canada.
A CROP survey of our members, caregivers and healthcare
Supporting families as they navigate the progression of ALS
Last fall, The ALS Society of Quebec was pleased to announce that over 79,000 generous Quebecers raised $2,660 000 through the Ice Bucket Challenge. The funds are being allocated to two important areas: the national research program with ALS Canada, in which
Message from the President of the Board and the Executive Director
As we look back on the past year, we can’t help but feel overwhelmed with how much we’ve accomplished. We remain astonished by the incredible success of the ALS Ice Bucket Challenge. This phenomenal fundraising campaign inspired by
Caring for someone with amyotrophic lateral sclerosis (ALS) isn’t easy. It is a 24-hour a day, seven-day a week job that takes a tremendous physical and emotional toll on caregivers. To help caregivers cope, the ALS Society of Quebec is expanding the services available to those looking after a