The experience of living with dementia, or caring for someone living with dementia, can differ across Canada, depending on culture, language, racial or equity barriers, and most of all, stigma
TORONTO, April 5, 2021 /CNW/ - The experience of living with dementia, or caring for someone living with dementia, can differ across Canada, depending on culture, language, racial or equity barriers, and most of all, stigma. These barriers prevent people from all backgrounds, especially from BIPOC (Black, Indigenous and People of Colour) communities, from reaching out to a doctor or community resources for help and support. The Alzheimer Society of Canada works to support people at all stages of the disease, but BIPOC people are not well-represented in dementia research, leaving a serious gap in information about diverse communities and their needs. Based on information collected from the US & UK, dementia impacts Black people at higher rates, with some studies showing twice the occurrence than in white populations. Yet the impact of this disease has on BIPOC individuals and caregivers is unknown, because the available data is minimal at best. “The research gap means that policies, programs, and strategies don’t speak to BIPOC needs and experiences,” says Ngozi Iroanyah, Coordinator of Research, Alzheimer Society of Canada, “so people may feel even more left out and excluded, and not seek out treatment in time. People in these communities fall through the cracks — or rather, gaping holes — in the research.” Ms. Iroanyah has also experienced stigma and equity barriers as a caregiver to her father, Felix, who lives with dementia. “My personal experience navigating support for my father fuels my passion to build bridges within my own community, as well as diverse communities across Canada,” says Ms. Iroanyah. Dr. Saskia Sivananthan, Chief Science Officer at the Alzheimer Society of Canada shares that she and her team of researchers are leading several initiatives aimed at closing the equity gap in dementia treatment and support. “We are working to better understand the barriers faced by people living with dementia and their caregivers, by ensuring BIPOC voices are represented in everything we do,” says Dr. Sivananthan. The Alzheimer Society of Canada has launched the following projects: Expansion of Alzheimer Society of Canada Advisory Group The National Dementia Journey Survey The survey is open to all people living with dementia and their caregivers, though BIPOC are especially encouraged to complete the survey. Share your experience at www.alzheimer.ca/survey - the survey is available in English, French, Hindi, and Chinese (Simplified and Traditional). Developing culturally specific dementia resources and programs “We’re trying to move towards deeper community engagement whereby we have the experiences, voices, and perspectives of underrepresented communities informing the things we do,” says Ms. Iroanyah. “These efforts are crucial to enhancing the experience of people living with dementia and their caregivers, across the country.” About the Alzheimer Society SOURCE Alzheimer Society of Canada |