CAREGIVER SUPPORT GENERAL INFORMATION
The consequences of brain injury impact not only the person who has the injury but also their caregivers who are parents, children, siblings, partners, husbands, wives and friends.
Caregiving can impact nearly every aspect of a caregiver’s life. As a result of the cognitive, emotional and/or physical changes and challenges resulting from a brain injury, stroke or significant chronic illness, family roles, responsibilities and routines change. The focus often becomes the ‘disability’ or the illness, and the losses the ‘client’ is facing. Caregivers may find themselves feeling overwhelmed, frustrated, anxious, sad, guilty, angry and frightened in response to the disruption to the life they had and what the future now looks like with their family member/friend
We are in the process of designing some new supports and refreshing our existing services for caregivers through surveys and focus groups. Please see link to our new Family/Caregiver Support Services brochure at the bottom of this page.
Below are some ways we are currently supporting caregivers:
In order to respond to caregiver needs, Dale Brain Injury Services (DBIS) has designed a Family & Caregiver Handbook as a resource to Caregivers and to offer reassurance and guidance as they embark on their journey.
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