缅北强奸

Diabetes disparities: 缅北强奸 researchers work with communities at risk

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Rick Bhurji was shocked to learn that, at age 47, he had type 2 diabetes.

His next thought was: What did I do wrong?

Rick鈥檚 daughter, Anjali, noticed that many of their Indo-Canadian friends and family had 鈥渕ysteriously鈥 developed diabetes. She figured her father鈥檚 diabetes was due to his love of pop and junk food.

鈥淔or many of us who are South Asians, we internalize and blame ourselves for the diabetes epidemic in our community, but that is really unfair,鈥 says Ananya Banerjee, an assistant professor at the University of Toronto鈥檚 Dalla Lana School of Public Health and a researcher with the Temerty Faculty of Medicine鈥檚 Banting & Best Diabetes Centre.

In fact, people from communities of colour across Canada are at higher risk for diabetes. is double in Black communities and triple in South Asian and First Nations communities, compared to white Canadians.

that First Nations children in Manitoba are 25 times more likely to be diagnosed with type 2 diabetes than other children. But disparities in diabetes are about more than ethnicity.

Researchers have found that location, income level, education, mental health, and experiences of racism and trauma can all profoundly impact the development and progression of diabetes.

By looking beyond basic biology, health-care providers are not only identifying which communities are at risk for diabetes, but also what interventions can make a difference.

鈥淚n health care, we tend to take a one-size-fits-all approach,鈥 says Aisha Lofters, a clinician scientist and an associate professor of family and community medicine at the Temerty Faculty of Medicine.

Lofters is also co-leader of which aims to improve the screening and prevention of cancer and chronic illnesses, including diabetes.

In practice, set guidelines and flowsheets don鈥檛 work for all individuals, explains Lofters.

Rather than 鈥渨agging the finger鈥 at a patient who, for instance, isn鈥檛 meeting the recommended amount of exercise, the BETTER WISE project works with the patient to set individualized, attainable goals 鈥 such as going for a 15-minute walk each week.

Banerjee took a similar approach with (SAADAP), providing education and prevention strategies to 80 South Asian teens with a family history of diabetes.

Through this pilot program, about eight in 10 participants reduced their intake of sweets and junk food and encouraged their family members to eat healthier.

Anjali and Rick, for instance, learned recipes for a healthy mango lassi and chickpea salad that have become staples in their home.

Outcomes of tailored diabetes programs are promising but, as obesity management expert and 缅北强奸 alumnus Sean Wharton explains, they point to larger flaws in Canada鈥檚 health-care system.

鈥淒isparity has come about because of a health-care system that isn鈥檛 serving people of colour,鈥 says Wharton.

Beyond adjusting care to fit individual patient needs, he says some of the most effective ways of treating disparities in diabetes are at the grassroots level, such as in places of worship and community centres.

鈥淭hese are spaces where the people working with the community are not biased against them, and they鈥檙e not blaming and shaming them, making them feel unrecognized or discriminated against,鈥 explains Wharton.

In an effort to dispel internalized blame or stigma related to diabetes, Banerjee, through SAADAP, highlights the social determinants of health, such as the walkability of neighbourhoods and the burden of precarious employment, and how they affect the participants鈥 health.

Those lessons made Anjali realize, 鈥淭here鈥檚 no need to feel horrible, and that you caused this, because you didn鈥檛.鈥

(FNHSSM) showed that First Nations individuals access primary care at a similar rate to others in the province. However, that care is not reducing complications from type 2 diabetes, such as amputations and kidney failure.

鈥淭he health system has made it the responsibility of the client with this simplistic idea that if you live healthy, eat healthy and exercise, you鈥檙e less likely to have type 2 diabetes. We know there鈥檚 more to it than that,鈥 says Lorraine McLeod, associate director of (DIP), a mobile program that First Nations leaders support to provide on-reserve diabetes care and treatment to more than a dozen First Nations communities in Manitoba.

Programs such as the centre鈥檚 DIP, B.C.鈥檚  and have made significant improvements in diabetes prevention and management by being created by or developed in partnership with First Nations communities.

Since the late 鈥90s in Manitoba, First Nations leaders have been calling for action and collecting the necessary data to address the growing epidemic of diabetes in Indigenous communities.

鈥淥ftentimes, research has been led by non-Indigenous researchers who have used their voice and academic lens to analyze Indigenous people, which often leads to continued stigmatization, and upholds the colonial practices and policies that were put in place to assimilate First Nations, M茅tis and Inuit people into Canadian society,鈥 says Leona Star, the centre鈥檚 director of research.

As an example of a dataset that accurately identifies First Nations according to their own indicators of well-being, Star points to (RHS), which she says was 鈥渄esigned and delivered by First Nations with our cultural framework and code of ethics.鈥

According to Star, RHS data has led to federal funding for multiple Indigenous health initiatives, including diabetes prevention. While Star emphasizes the need for First Nations people to govern their own information and data, known as 鈥渄ata sovereignty,鈥 she calls for more action.

鈥淚t is also important to look at the effectiveness and impacts of research findings,鈥 says Star. 鈥淎lthough significant investments have been made to undertake research around diabetes, the rates of diabetes continue to increase and climb especially amongst First Nations.鈥

While evidence led or co-led by First Nations is available, she says what is lacking are policies and implementation recommendations to address discrimination and disparities in health care.

Wharton says the key question is why researchers and health-care providers aren鈥檛 acting on what they already know.

To address the disparities created by bias, racism and systemic inequalities, he says it鈥檚 time that practitioners embrace the strengths of Indigenous peoples and people of colour, rather than assessing how these patients adhere to a system that wasn鈥檛 designed for or by them.

鈥淲e need to shake the foundations of how we help,鈥 he says. 

This story was originally published in .

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Temerty Faculty of Medicine