AAIC 2017 reveals great strides in research

AAIC 2017 reveals great strides in research






By Nalini Sen, Director, Alzheimer Society Research Program I had the opportunity to attend this year’s annual Alzheimer’s Association International Conference (AAIC) in London, UK. This conference brings together some of the world’s leading researchers and clinicians in dementia treatment, detection and prevention. And with a record number of presentations—3300 in all—I have to admit, I was awestruck. Here are a few takeaways I would like to share with you: Stress can age your brain How we manage stress is even…

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People like Margaret are more than just a number.

People like Margaret are more than just a number.






Did you know that of the 564,000 Canadians with dementia, 60% will go missing or become lost at some point? These men and women are more than just a number. And so are you. You have the power to be the one who makes an impact. By making a donation today, you can help fund dementia research initiatives and support vital programs for people with dementia and their families. With your support, we can help people like Margaret and her…

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Research Video Series: Introducing Danielle Alcock

Research Video Series: Introducing Danielle Alcock






Danielle’s personal experience inspired her to pursue research in the field of continuity of care. She will assess existing services through the use of oral narratives by female, Indigenous caregivers for a loved one diagnosed with alcohol-related dementia and will make recommendations based on their experience. Coming from a First Nations family, it was difficult to navigate the healthcare system dealing with jurisdictional barriers, stigma and a lack of resources. As a caregiver, there are no existing supports for alcohol-related…

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What’s love got to do with Alzheimer’s? A lot

What’s love got to do with Alzheimer’s? A lot






By Alex Westman My wife Donna and I met when we were just teenagers—she was 18, I was 16. Despite our youth, we understood early on that we had a deep connection. It was an amazing thing, really, and still is. There was magic in her and she saw something in me. I had a reputation as a bit of a scrapper, but she soon took care of that. These days, I’m almost respectable. I’m a three-term municipal councillor in the…

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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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Racing for memories

Racing for memories






Recently, my family has joined the unfortunate ranks of those who have been impacted by Alzheimer’s disease. My mom started showing early signs of the disease a few years ago, and it has slowly and stubbornly progressed ever since. The toll that Alzheimer’s is taking on my mom is obvious and devastating. Less obvious, but just as significant, is the impact it is having on my dad. As my mom’s primary caregiver, it’s been said that my dad must ride…

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Announcing the top 10 Canadian dementia research priorities

Announcing the top 10 Canadian dementia research priorities






[Le texte en français suit l’anglais ci-bas.] By Drs. Katherine McGilton and Jennifer Bethell Over the course of the past year, we asked Canadians affected by dementia—either personally or through their work—for their unanswered questions about living with dementia, dementia prevention, treatment and diagnosis. This study, also known as the Canadian Dementia Priority Setting Partnership, set out to identify the top 10 dementia research priorities, and to share them with Canadian researchers and research funding organizations. We thank the over…

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Hope in the face of Alzheimer’s

Hope in the face of Alzheimer’s






One might think that having a disease with no cure wouldn’t leave a person with much hope to draw on. The truth is, if you’d asked me how I felt about the future after I was first diagnosed with Alzheimer’s disease, my answer would have been far from ‘hopeful.’ Then, one day, that changed.

Getting a dementia diagnosis – where do you start?

Getting a dementia diagnosis – where do you start?






It can start with something simple, like having trouble following your favourite recipe, or putting your car keys in the fridge. Maybe you’ve noticed small changes in your memory that are affecting how you do things day-to-day. If you can’t quite remember things that should be straightforward for you, or if you notice changes in your mood or ability to communicate, make an appointment to see your family doctor right away. Diagnosing dementia is a complex and difficult process. The…

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Why language matters

Why language matters






Jim Mann, a person living with Alzheimer’s, discusses the impact of language on people with dementia, and how words have the power to harm or heal.