When Alzheimer’s disease becomes part of a marriage, or a family, caregivers can usually find resources to support the member facing memory loss or to support the family caregiver seeking peer connections and information. Yet, until the last few years, there wasn’t much designed to support the evolving spousal or parent/child relationship itself.
Matthew Hollingshead recently joined Hebrew SeniorLife as the executive director of Assisted Living and Memory Care at NewBridge on the Charles. His energetic, resident-centric approach and skill in leading large teams is already making a difference in the lives of our residents. I recently spoke to Matt about the rewards and challenges of his work.
Taking care of a family member with Alzheimer’s disease and/or a related dementia can be as exhausting as it is meaningful. Both physically and emotionally, caregiving takes a toll that we can all appreciate. Occasional breaks – whether for a few hours, a day, or a week or more – are important in order to recharge. Family caregivers need rest and support in order to continue to provide the best possible care to loved ones.
There are many supports available for family caregivers: