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when care partners of older adults first encounter symptoms of dementia, many assume the symptoms are a normal part of aging . this lack of knowledge needs to be addressed to facilitate the first step in seeking dementia care.
south asians comprise what statistics canada reports is the country’s largest “ visible minority group ,” at 5.6 per cent of the population. that means south asians also make up a significant portion of the 747,000 canadians living with alzheimer’s or other dementia.
south asians — people who are either born in or who can trace their ancestry to south asia, including india, pakistan, bangladesh, sri lanka, bhutan, nepal and the maldives — are an ethnically diverse group with socio-cultural norms that influence their experience of living with dementia. they may also encounter specific barriers to care including language, perceived stigma regarding dementia, lack of knowledge about available services, and hesitancy to use those services.
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the process of getting care for people living with dementia can be broadly divided into three stages: recognizing the symptoms, seeking a diagnosis and using various services to access the care needed to maintain quality of life.
the first step of recognizing symptoms is in itself a significant barrier. in a study conducted in the united kingdom , most south asian people living with dementia and their care partners acknowledged their lack of awareness and knowledge of dementia. they did not know the signs and symptoms of dementia before the diagnosis.
an abundance of information about dementia is available from organizations across canada, but limited information is available in multiple languages . while almost all ( 93 per cent ) south asians in canada can carry on a conversation in english or french, 46 per cent do not use english or french at home.
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there are various steps before receiving the diagnosis of dementia . these include a visit to a family physician, referral to specialists, and physical and mental tests.
the experience of receiving a diagnosis is emotionally draining and challenging. it falls on the family member to disclose it to their loved ones as a translator , which causes emotional stress for both parties.
another issue is describing dementia in a language aside from english, as not every language may have a word for dementia.
services such as having translators present, better policies to provide financial security for care partners who have to take multiple days off from employment, physicians having an understanding of the socio-cultural norms and the perception of dementia within the community may be a helpful starting point to make the experience of seeking and receiving dementia more inclusive to the south asian community.
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however, most of these services are offered in english or french and embedded in western culture. social and recreational services often include bingo, line dancing and discussing western art and literature, which may not be inviting or appropriate to a person living with dementia from the south asian community.
support groups for care partners may be a challenge due to the cultural differences in providing care for the elderly. in western culture, a move to long-term care is often the final stage for care partners to ensure their loved ones are safe and cared for.
this is a difficult conversation in south asian communities where filial piety plays a significant role, and long-term care homes can be viewed negatively . the financial responsibility associated with long-term care may also be a factor for some families. in this way, home care becomes an integral part of dementia care in the south asian community.
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this article is republished from the conversation under a creative commons license. read the original article.
