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Canada

ALS Society of Quebec

December 15, 2021 by

ALS Canada Research Program

February 27, 2018 by

ALS research is at a time of unprecedented excitement and momentum: there has been more progress in the last 5 to 7 years than in the last century. Many of the top ALS researchers in the world believe the scientific community is now poised to find treatments that can significantly alter the course of the disease, and that lack of funding is the only limitation standing in the way of effective ALS treatments being developed sooner rather than later.

Pour les médecins

February 27, 2018 by

Afin de garantir aux personnes vivant avec la SLA des soins de grande qualité, il est essentiel que leur médecin de premier recours connaisse la maladie et collabore avec une équipe spécialisée en soins contre la SLA. Les ressources présentées dans cette page vous aideront à mieux comprendre la SLA afin d’appuyer vos patients qui vivent avec la maladie.

Resources for Physicians

February 27, 2018 by

To ensure people living with ALS receive the best possible quality of care, it is critical that their primary care physicians be knowledgeable about the disease and work in collaboration with an ALS specialty team. The resources on this page will help you to better understand ALS in order to support your patients who are living with the disease.

Pour les jeunes

February 27, 2018 by

Une maladie comme la SLA provoque de nombreux changements et touche tous les membres de la famille.  Les enfants et les adolescents pourraient avoir des préoccupations, des craintes et des questions auxquelles ils ne savent pas comment faire face ou comment les exprimer. Les ressources qui suivent sont spécialement conçues pour aider les enfants et les adolescents dont un membre de la famille vit avec la SLA.

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