I’ve Treated People With Dementia for a Decade — Here’s What I Want Family Caregivers to Know

My first job changed my life. As a recent graduate, I landed my first role as an occupational therapist at a nursing home where I was assigned to the memory care unit. One person on my caseload was an individual living with dementia, and I naively treated it like any of my other cases. So when I asked them to come to therapy, they responded by pouring juice on me.

Obviously, having juice-stained scrubs is not a great impression for the first day of work. But the juice incident was also a wake-up call. School taught me the terminology and what happens in the brain, but I was woefully unprepared for what it takes to care for someone living with dementia. For people with cognitive impairment, the standard procedure is to ask them to come to occupational therapy, but that one-size-fits-all approach does not work for dementia. If I wanted to help my patients, I would need to rethink how to personalize my treatment sessions to fit their unique needs.

Over 55 million people worldwide have dementia and while it can happen to anyone, women are the most affected directly and indirectly. The World Health Organization reports women make up 70 percent of dementia caretakers — and just like any other job, it carries a risk of stress and burnout. 

Fortunately, you don’t need a professional degree to take care of someone with dementia. A year and a half ago, I created a company called Your Dementia Therapist. It offers digital education for taking care of people living with dementia. I create content to teach techniques and strategies to increase the quality of life for people with dementia and make caretaking easier to manage. 

Below are some important tips I’ve learned while helping others with this condition.

Learning of a loved one’s dementia diagnosis can stir up a lot of feelings. Most feel sad and heartbroken over the news, others might feel some guilt over not noticing the out-of-character behavior sooner, and some might have a sense of dread about the responsibilities that come with taking care of someone sick. These are normal reactions; it is a life-changing diagnosis. But that does not mean their life is over.

Dementia does not take away who they are — your loved one is still there. People have a tendency to believe that a dementia diagnosis is the end when it’s really learning to live with cognitive impairments.

In fact, I’ve met individuals in the early stage of dementia who continue to lead fulfilling and meaningful lives. The big factor was the supportive and inclusive environment they were in where they didn’t feel like a burden but like another person with feelings, thoughts, and interests. If we continue to focus on what dementia has robbed a person of, then all you’re going to see is everything they can’t do anymore. And the person living with dementia will also pay attention to all the things they’ve lost. Instead, if you shift the narrative and focus more on what they are still capable of doing, it’ll show that a dementia diagnosis does not define them.

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