Call for better understanding of dementia care

Bupa and Alzheimers New Zealand call for better understanding of dementia care

Bupa and Alzheimers New Zealand are helping tackle one of New Zealand’s most significant largest heathcare challenges alongside the announcement of a global partnership.

Catherine Hall, Executive Director of Alzheimers New Zealand, said dementia already affects around 50,000 people in New Zealand and that number is set to triple by 2050 as the population ages. Therefore it is critical that NZ is well positioned to meet the needs of the growing number of people affected by dementia,” Ms Hall said.

Ms Hall’s comments came after today’s announcement of a new long-term global partnership between Alzheimers Disease International (ADI) and Bupa. The partnership’s first action is the launch of a joint 10-point global manifesto on what extraordinary dementia care looks like through the eyes of someone living with dementia.

“Although there is currently no cure, there is help available to help people affected by dementia. In 2012 we launched the Alzheimers NZ we can help campaign to encourage people to see their doctor so they can get they help that need, and to build public understanding of dementia, awareness of the services and support available to people affected by dementia” Ms Hall said.

“This new charter is another action that will help people understand the impact that dementia has, and the type of care and support people affected by dementia need so that they can still live a satisfying and enjoyable life. ,” Ms Hall adds.

Grainne Moss Director of Bupa Care Homes and Rehab, said ADI and Bupa will be seeking support for the charter from governments, individuals and organisations around the world.

“As well as containing the 10 points, the charter, ‘I can live well with dementia’, also sets out a program of ‘enablers’ – the actions needed by everyone involved to achieve a better quality of life for people with dementia,” Ms Moss said.

The 10 points of the global ADI/Bupa charter are:

1. I should have access to a doctor to check if I have dementia.

2. I should have access to information about dementia so I know how it will affect me.

3. I should be helped to live independently for as long as I can.

4. I should have a say in the care and support that I am given.

5. I should have access to high-quality care that’s right for me.

6. I should be treated as an individual, with those looking after me knowing about my life.

7. I should be respected for who I am.

8. I should have access to medicine and treatment that helps me.

9. My end of life wishes should be discussed with me while I can still make decisions.

10. I want my family and friends to have fond memories of me.

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