The survey was a joint initiative between Summerset, Dementia New Zealand and The New Zealand Dementia Cooperative who partnered together in the hope of gaining a better understanding of Kiwi awareness and perceptions of dementia.

According to the results, more than 60% of New Zealanders have a current personal experience with dementia, and nearly 50% of respondents say they would like to learn more about how to better look after people with dementia and those caring for them.

Yet despite dementia being the disease Kiwis most fear getting, second only to cancer, it is also one of the least understood, with more than 20% believing dementia is a natural part of ageing.

Summerset, Dementia New Zealand and The New Zealand Dementia Cooperative say the research shows there is a clear need for a national conversation and strategy to reduce stigma, diagnose and combat the disease, and better care for Kiwis and their families living with dementia.

They are calling on the government to recognise dementia as a major health priority for New Zealand, to create and implement a national plan for supporting and providing care for the increasing numbers of people living with dementia, and to support community organisations working with those with the disease.

As a starting point, they say one of the biggest risks for New Zealand currently is we don’t record the number of people with dementia in our health system, meaning there is no accurate data on the number of Kiwis diagnosed with, living with or dying from dementia.

But according to overseas statistics extrapolated to New Zealand, around 170,000 people will be diagnosed with dementia by 2050, triple the current figures, with a cost to the economy of nearly $NZ3 billion.

Paul Sullivan is the CEO of Dementia New Zealand, an agency that aims to support the delivery of high quality services by dementia organisations working in local communities.  Its organisations cover 70% of New Zealand’s population, with Affiliates in Auckland, Waikato, Lakes, Hawke’s Bay, Wellington and Canterbury.

He says the survey results demonstrate a clear need for more information and knowledge on dementia as an illness.

“All community dementia providers could serve their communities more effectively if they knew how many cases were in their area, and what level of support was needed across these,” says Sullivan.

“Our ideal situation would be a universally accepted primary diagnostic code for all dementia diagnoses, and the ability for District Health Boards to accurately gauge the overall prevalence and the incidence of dementia through this coding,” he says, adding that consistency of diagnosis is also lacking.

“Some doctors diagnose a person as having a Mild Cognitive Impairment at the onset of dementia, and this diagnosis is not updated as a person’s symptoms worsen. Until this coding and diagnostic consistency is achieved we are unlikely to be able to answer the simple question of ‘How many people in New Zealand are living with a diagnosis of dementia?’” questions Sullivan.

Summerset CEO Julian Cook says his organisation is pioneering a new type of dementia care in New Zealand.

In 2016, Levin’s Summerset by the Ranges opened a 20-bed pilot dementia facility, the first of its kind in New Zealand. The centre is modelled on international design standards for dementia care and allows residents to live in their own apartment with personal items, pets and to have family members to stay, all in a secure environment.

Cook says it’s about thinking about what people need, not what the disease needs.

“We are in the process of becoming a dementia friendly organisation and have developed our new memory care concept for those who need secure care. But there is so much that we can all do in society to help those with all stages of dementia.”


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