If you are someone who provides regular care to someone with MS, you play a very important role in their life. A “caregiver” can refer to anyone of any age and could be a spouse, partner, parent, child, family member or friend.
As a caregiver, it’s important that you also take care of yourself. There are many resources available to you. The MS Society of Canada has a wealth of resources for caregivers, including links to many other sources of information, which can be found at https://mssociety.ca/support-services/caregivers/information-and-resources.
Remember that the Shared Solutions nurses are also available for you to talk to, whenever you might need support.