Senior African American couple reading

Valentine’s Day: A Couple’s Devotion While Facing Alzheimer’s During COVID-19

Valentine’s Day can be a particularly sentimental time for couples affected by Alzheimer’s or dementia, as they adjust to dual roles as both romantic partners and care partners. This day is also a reminder that love is not only what brings couples together, but it is often what keeps couples going through this difficult journey. Continue reading Valentine’s Day: A Couple’s Devotion While Facing Alzheimer’s During COVID-19

The messy nobility of being a caretaker

When their bodies or minds (or both) leave them unable to keep up with the tasks of living, and it becomes our duty to take up the tasks for them. We put our plans, ideas, hopes and futures on hold and our worlds begin to spin on the axis of someone else’s needs. Continue reading The messy nobility of being a caretaker

Advance Directives: Make Your Wishes Known

Every adult should have “advance directives.” There are several basic types of these legal documents that describe how you want medical decisions to be made for you if you are unable to make them yourself. Continue reading Advance Directives: Make Your Wishes Known

Exercise for your brain and body

Physical activity is a valuable part of any overall wellness plan and is associated with a lower risk of cognitive decline. The new year is a great time to start integrating exercise into your daily life to help improve the health of your brain and body. Continue reading Exercise for your brain and body

Marie Raschko: My Advocacy Story

Marie devoted her career as a social worker to the fields of aging and mental health and has been a long time advocate for various organizations with the goal of working towards a better future for aging community members. Continue reading Marie Raschko: My Advocacy Story

My Advocacy Story: Kevin Kvarda

Hello Friends! My name is Kevin Kvarda or you can call me “K-Squared.” Since June of 2019, I’ve had new friends in my life — a diagnosis of Alzheimer’s and Primary Progressive Aphasia (PPA). I’ve not necessarily been one to stand up on the public stage, but my diseases have pulled me out and given me a voice…a positive voice and hope. Continue reading My Advocacy Story: Kevin Kvarda