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Each September, the global community recognizes World Alzheimer’s Month, a time to raise awareness, challenge stigma, and invite deeper conversations about dementia. This year, the theme is simple but powerful: #AskAboutDementia.
The rising incidence of dementia and its toll on families is one piece of a significant domino effect on public health. As a caregiver for both my parents affected by dementia, I can say firsthand that there are no words to describe the emotional and physical price of this journey. I want to explore the broader crisis we face: the cost to our communities, public health, health systems, and the stakeholders who are all invested in this space.
First, let's face the reality: the looming aging tsunami, as it has been referred to for decades, is here. It is no longer a futuristic term. With this in mind, planning is accelerating into action at the federal, state, and local levels.
The alarming statistics surrounding Alzheimer's and dementia in communities of color cannot be ignored. Black Americans are twice as likely as older Whites to have Alzheimer's or another dementia, and Latinos are 1.5 times as likely, according to the Alzheimer's Association. While higher rates of cardiovascular disease may play a role, some studies suggest that these differences disappear after accounting for overall health and socioeconomic status. Regardless of the cause, the prevalence of dementia in Black and Brown communities is a public health crisis that demands immediate attention.
Through her extensive work in supporting initiatives of DAA and her experience living with dementia, Laurie is a strong advocate for quality of life. She was diagnosed with young onset dementia in August of 2013 at the age of 55. Unable to continue a professional career she turned her focus towards helping others through their dementia journey, Laurie and her husband, Roy, work continuously to identify triggers that cause her confusion and they make adjustments to overcome obstacles. Laurie is a Dementia Mentor and is active in many support groups. On her website, dementiadaze.com, Laurie shares her feelings, challenges, symptoms, and adjustments in hopes of encouraging other individuals and families living with dementia to explore ways to live beyond dementia.
Patients with dementia form a fast-increasing proportion of those entering hospice care. Is your staff prepared to compassionately care for the unique needs of people living with dementia?
