How we help and serve those living with ALS.
We support people living with ALS and their families by providing care, equipment, and resources to make everyday life easier. Our services include home visits, support programs, guidance through the healthcare system, access to medical equipment, and opportunities to connect with a caring community. We also invest in research through the Alberta ALS Research Network to improve treatments and work to raise awareness about ALS in Alberta and beyond.
Facilitating care for those in need.
The Alberta health care system is complex and often difficult to navigate, even by those who work within it. Client Services Coordinators provide guidance and support to help people living with ALS, and their families, navigate the maze of services as the disease progresses. Client Services Coordinators also regularly participate in multidisciplinary ALS clinics and are considered an integral part of the care team. When families seek assistance and need someone to become an advocate for their concerns during their ALS journey, client services staff often fulfill that role as well.
Equipment to make life easier.
The ALS Society of Alberta is able to respond to the rapidly changing needs of Albertans affected by ALS. Through our provincial Equipment Loan Program, we are able to assist people affected by ALS by lending mobility aids, daily living aids, and communication aids. The Equipment Loan Program is free of charge to ensure support is available when needed. The Society covers the costs of delivery and pickup, and once the person no longer requires the equipment, it is cleaned and returned to the loan pool.
Support groups for clients.
In 2024, 66 client support groups were held. These give people living with ALS space for peer connection, emotional support, and resource sharing. Support groups are offered in a hybrid delivery model, combining in-person and virtual formats, to ensure accessibility regardless of geography or mobility.
Support for caregivers helping those with ALS.
Caring for someone with ALS can be overwhelming. We provide ALS caregivers with guidance, resources, and emotional support to help navigate the challenges of daily care. From education on equipment and therapies to connecting with support groups, we’re here to help ALS caregivers feel equipped, informed, and supported every step of the way.
Help us provide equipment.
Even the smallest donation can make a large impact on somebody affected by ALS.
AARN
Research and commitment to finding treatment and a cure.
The Alberta ALS Research Network (AARN) is committed to advancing research and improving care for amyotrophic lateral sclerosis (ALS). Through strategic investment in fundamental, translational and clinical research, AARN aims to position Alberta-based ALS research as a global leader by fostering innovation and collaboration to accelerate discoveries and enhance patient outcomes.
Creating awareness and connection in our community.
Building a stronger ALS community starts with connection. Through events, campaigns, and local initiatives, we bring together people living with ALS, their families and loved ones, ALS caregivers, and supporters. Whether it’s sharing stories, raising awareness, or celebrating milestones, our programs help create meaningful connections and ensure no one faces ALS alone.
Help us make an impact.
Even the smallest donation can make a large impact on somebody affected by ALS.