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Tag: national dementia strategy

Make your voice heard: Tell your candidates to support a national dementia strategy

Make your voice heard: Tell your candidates to support a national dementia strategy

By Pauline Tardif, CEO, Alzheimer Society of Canada Voting day is arriving soon. No matter which party forms government, it’s vital that dementia remains a top priority. Each year, dementia costs the Canadian economy and health-care system more than $10.4 billion. And our population is aging – the number of Canadians living with dementia today will nearly double in less than 12 years. We simply can’t afford to ignore the cost of dementia. But here’s the good news: we can…

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What Canadians are saying: Why does a fully-funded national dementia strategy matter?

What Canadians are saying: Why does a fully-funded national dementia strategy matter?

Though the national dementia strategy has been announced, more work needs to be done. Not only does the strategy need to be fully funded, we also must ensure that it remains a top issue in Ottawa throughout and beyond the federal election in October. We asked people living with dementia, caregivers and researchers for their thoughts on why a fully-funded national dementia strategy matters. Here’s what they have to say: It will foster a network of support for people with…

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Four reasons to celebrate

Four reasons to celebrate

By Pauline Tardif, CEO, Alzheimer Society of Canada Every day, I hear the stories of Canadians who are living with the realities of dementia in all its forms, whether they are experiencing the disease first-hand or as caregivers. I learn about successes—and failures—in research. I digest statistics and information to help me understand the ever-growing scope and magnitude of what we are facing as a country when it comes to Alzheimer’s disease and other dementias. It can be overwhelming at…

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Let’s talk about help for today

Let’s talk about help for today

When I last spoke with you, I asked what you thought about dementia research in Canada and the challenges we face together. Supporters like you, speaking from your own personal experience, agreed that this isn’t a tomorrow problem for Canada—it’s our problem today! Today, I’m reaching out again to give you an update and ask for more of your insights. An update on the national dementia strategy As CEO of the Alzheimer Society of Canada, I am pleased to have…

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Let’s talk about research

Let’s talk about research

Today, I’m reaching out because I want to know what you think about dementia research in Canada. Your own experience and the wisdom of your insights can help the Alzheimer Society amplify the voices of people like you – ensuring that these voices are heard and action is taken. I hope you will join the conversation. Since coming on board as CEO, the goodwill, expressions of support and advice from individuals across the country have been heartwarming and deeply appreciated….

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“I am a person with dementia and a person with rights.” (part three)

“I am a person with dementia and a person with rights.” (part three)

Previously in our series on human rights and dementia, we looked at how past experiences inspired Phyllis Fehr to advocate for dementia rights (Part one: Becoming a force for change—Phyllis Fehr’s story). Then, Phyllis showed us how seven articles in the United Nations’ Convention of Human Rights can improve the quality of life for Canadians living with dementia right now (Part two: Understanding dementia from a human rights’ perspective).

“I am a person with dementia and a person with rights.” (Part one)

“I am a person with dementia and a person with rights.” (Part one)

Part one: Becoming a force for change—Phyllis Fehr’s story This blog series is based on the webinar, “I am a person with dementia and a person with rights,” hosted by brainXchange and presented by Phyllis Fehr on December 13, 2017 (part one) and January 17, 2018 (part two). One day, Phyllis Fehr walked through the doors of a grocery store, and found confusion. Phyllis, who had been given a working diagnosis of early-onset Alzheimer’s along with Lewy Body dementia at…

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The importance of palliative care for people living with dementia

The importance of palliative care for people living with dementia

In her opening remarks to the Senate Committee on Social Affairs, Science and Technology, Alzheimer Society of Canada CEO Pauline Tardif led with an alarming fact. “Right now, well over half a million Canadians are living with dementia—and the numbers keep growing,” she said. “Access to palliative care has become even more important today.” Pauline had taken to Parliament Hill to support Bill C-277, An Act providing for the development of a framework on palliative care in Canada. If passed,…

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Canada to become 30th country with national dementia strategy

Canada to become 30th country with national dementia strategy

The Alzheimer Society of Canada celebrates the passage of Bill C-233, An Act respecting a national strategy for Alzheimer’s disease and other dementias. Canada will now become the latest country to develop a national dementia strategy to address the overwhelming scale, impact and cost of dementia. “For the more than half a million Canadians living with dementia and their families, this is an important milestone,” says Pauline Tardif, CEO of the Alzheimer Society of Canada. “A national strategy enables a…

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This election, support a National Dementia Strategy

This election, support a National Dementia Strategy

On October 19, 2015 the Canadian federal election will be held. And we want to reaffirm that every vote matters. On May 6 of this year, our chance for a national dementia strategy becoming enshrined into Canadian law through MP Claude Gravelle’s private member’s bill C-356 was sadly defeated 140-139. Yes, by one vote. When we hear about people who think votes don’t matter it’s disheartening, because regardless of context, every vote matters. Right now, each one of us gets…

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