Home About Us Government Relations and Advocacy Media Contact Us Site Map Privacy  
Multiple Sclerosis Society of Canada Société canadienne de la sclérose en plaques
About Multiple Sclerosis Living with Multiple Sclerosis Research Treatments Donate Now Get Involved Special Events
 
Division Menu





Alberta & Northwest Territories Division
Gov Banner

Caregivers
The mission statement of the MS Society of Canada is comprehensive in scope and the phrase “enabling people affected by MS to enhance their quality of life” includes caregivers of persons with MS.  The philosophy of client services endorsed by the National Executive Committee of the MS Society of Canada in March 2004 identifies caregivers of people with MS as primary clients of its services and programs.

To fulfill its mission with respect to caregivers, the MS Society of Canada affirms that:

  • The Society recognizes and affirms caregivers for their self-declaration of that role at any point along a spectrum of care for the person with MS.
  • The Society will assist people in identifying and describing their caregiving role and, once recognized, the Society will affirm the value of that role in the context of the caregiver’s relationship to the person with MS, other family and friends, and within the broader context of their community.
  • Support for a caregiver often brings an enhanced quality of life not only to the caregiver, but also to the person with MS and others in the family or immediate support/social network.  Thus, the Society will support caregivers in a manner that acknowledges the importance of maintaining caregivers’ own health and quality of life for their own sake while also being aware of the potential, related benefits to people with MS and others. 

To read more about our mission, please click on the plus sign YAMS Spotlight: Neil Blue - full story

  • The application of resources allocated in support of caregivers must be directed to caregiver-valued supports and caregiver-identified needs.
  • The voice and choice of the caregiver must be heard, respected and addressed.
  • The Society will interact with caregivers in a manner which is flexible and sustainable, and balanced with the needs of other primary clients in terms of services and research.
  • The Society’s approach to caregiver support will incorporate services and programs with the potential for relatively equitable implementation by chapters and/or divisions across the country based on local needs and resources.
  • In all programs and services offered for caregivers, the Framework for Client Services will be applied.

The MS Society has formed a National Caregiver Advisory Group to advance the support of caregivers of people with MS within the MS Society of Canada. The advisory group will represent the varied stakeholders who are interested in and or will be affected by the implementation of the MS Society of Canada’s Strategy for Supporting Caregivers of People with MS (2005). The advisory group will conduct its work between summer 2006 and April 2009. At the end of this time the group will make recommendations regarding the necessary next steps to the National Board of Directors.

The representative for Alberta & Northwest Territories Division is Bev Babuk, Client Services Coordinator at Calgary Chapter. The National Government Relations representative is Michelle Kristinson, Director, Government & Community Relations, Calgary Chapter / Alberta & Northwest Territories Division.

Policy Related Initiatives:

The MS Society of Canada is a member of the Canadian Caregiver Coalition (CCC). As well the Director, Government & Community Relations for Calgary Chapter/Alberta & Northwest Territories Division is a member of the CCC Board of Directors.

The Canadian Caregiver Coalition is the national body representing and promoting the voice, needs and interests of family caregivers with all levels of government, and the community through:
  • Policy development and leadership
  • Research and education
  • Information, communication and resource development

The Canadian Caregiver Coalition is made up of a diverse group of individuals and organizations. Individual members include caregivers, researchers, and professional service providers. Organizational members are national, regional and local. Some exist to provide support directly to caregivers; others, like the Alzheimer Society of Canada, VON Canada and the MS Society of Canada have an interest in caregiver issues because of the work they do.

For more information about the work of the CCC please visit: www.ccc-ccan.ca


For more information, contact:
Julie Kelndorfer, Director, Government & Community Relations
780-440-8756
julie.kelndorfer@mssociety.ca




Our Mission :
To be a leader in finding a cure for multiple sclerosis and enabling people affected by MS to enhance their quality of life.
 

Alberta & Northwest Territories Division
Multiple Sclerosis Society of Canada
#150, 9405 - 50 Street
Edmonton, Alberta T6B 2T4

To locate the MS Society office near you, please select the appropriate chapter:

 

© Multiple Sclerosis Society of Canada

 

Multiple Sclerosis   Living with MS   Research   Treatments   Donate Now   Get Involved    Special Events

Home    About Us    Advocacy    Media    Contact Us    Site Map    Privacy    Français