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For Caregivers and Families

The Multiple Sclerosis Society of Canada is committed to assisting persons affected by multiple sclerosis and is acutely aware of the wide-ranging and growing needs of caregivers providing care to loved ones with MS. The MS Society can be a valuable source of information about the disease and provide resources and support group contacts for caregivers to help them effectively manage the ongoing stress of providing care.

The MS Society of Canada is also currently undertaking a pilot project, The Caring Balance Pilot Project: Supporting Caregivers and People with MS on Their Journey Together with the goal of increasing capacity within all levels of the MS Society to support caregivers of people with MS. The Caregiver Wellness Funding Pilot Project is the central component of this pilot and provides family members and friends who are primary caregivers of people with MS with funding for services, activities or items that help them to maintain their own health and well-being while they continue to provide assistance and support to someone with MS. All funds designated for funding caregivers’ individualized self care plans have now been allocated. Key findings from this pilot project will be posted to this site as they become available.

Taking Care: Resources for Caregivers provides caregivers with useful insights and resources to help manage their important role as a caregiver.

Caregivers interested in starting a caregiver support group in their chapter area may find The Sharing Network of assistance. This handbook is intended as a practical guide for starting and maintaining self help programs

Contact your nearest division or chapter for available information on caregiver programs in your area.

Multiple Sclerosis Society of Canada
Toll free to reach the nearest regional office: 1 800 268-7582

To locate the MS Society office near you, please select your region:

E-mail: info@mssociety.ca
(Please provide your town and province in your e-mail)

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