THE MULTIPLE SCLEROSIS SOCIETY OF WESTERN AUSTRALIA (INC.)

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The carer role can be demanding both physically and emotionally thus it is important that carers remember to continue to take care of themselves; though this often feels easier said than done.

With disease progression, family members or friends often start to take on a support role for their loved one with MS who is no longer able to do those tasks for themselves. Whilst they maintain their relationship as husband or wife, or son or daughter, or parent or friend, the roles they undertake are then recognized by Australian legislation as being that of a ‘carer’. Hence the term ‘carer’ gives recognition to those vital unpaid roles whilst not intending to disregard the relationship.

Research shows that carers are at greater risk of injury, usually resulting from assisting with transfers and lifting. The Occupational Therapist is able to assess the environment and train carers in safer ways to provide assistance. If equipment is recommended, the Occupational Therapist will assist with trials, and sourcing funding if eligible. Ongoing assessments may be needed over time as the needs of the person with MS can change.

Support in the home and respite can help reduce the ongoing strain often experienced by the carer. Our Welfare Officer has a sound understanding of supports available in the community, financial criteria and support through Centrelink, and will discuss these with the Carer and family so that they can make informed choices. 

The emotional demands of caring, and anxiety for the future are very real for carers. Carers are able to access Counselling support at the MS Society.  There are also other sources of support and information regarding caring including Carers WA.

MSWA Programs for Carers include the following:

  • Carers support group;
  • Carers camps.

For further information or to arrange an appointment please call Occupational Therapy on 9365 4831, Welfare Officer on 9365 4835 or a Counsellor on 9365 4836 or contact us.