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Tag: dementia

Enhancing safety for people with dementia

Enhancing safety for people with dementia

Imagine if someone you love goes missing. The worry can be agonizing. When the person has dementia, it takes it up a notch or two. That’s why MedicAlert Foundation Canada partnered with the Alzheimer Society of Canada in 2013 to help people living with dementia who are at risk of getting lost. MedicAlert’s service—along with its well-recognized engraved bracelet—was launched in 1961 to help emergency responders treat people quickly and effectively when they couldn’t speak for themselves. .

Can a concussion increase my risk of developing Alzheimer’s disease?

Can a concussion increase my risk of developing Alzheimer’s disease?

Did you know that head injuries, and particularly repeated concussions, may increase the risk of developing Alzheimer’s disease? A traumatic brain injury that results in the loss of consciousness has been shown to increase the risk of dementia by as much as four times [i]. According to some research, this is because head injuries may increase the levels of protein in the brain that are associated with Alzheimer’s disease, such as amyloid [ii]. Who is most affected by traumatic brain…

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Mother’s Day 2018: Why Jane Kennedy appreciates her mother

Mother’s Day 2018: Why Jane Kennedy appreciates her mother

“Your mom is so strong.” These were the words I often heard people say to describe my mom. I never really understood what they meant while I was growing up, being the youngest of six children. Why was my mom this strong person everyone kept referring to?

“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).

National Volunteer Week: Why Louise chooses to volunteer

National Volunteer Week: Why Louise chooses to volunteer

Thanks to my mother, I learned the values of being a volunteer at a young age. She set up a soup kitchen at my elementary school, ensuring that my classmates coming to school without lunch wouldn’t go hungry. When my brother and sister and I joined the Cubs, Brownies, and Girl Guides, my mother volunteered as a leader. She canvassed for various charities. She was always quick to help whenever someone asked.

Meet our Researchers: Debra Sheets, University of Victoria

Meet our Researchers: Debra Sheets, University of Victoria

For people with dementia and their caregivers, it can be difficult to find activities that strike the right balance between being supportive, being socially appropriate and, of course, being fun. As the disease progresses and abilities change, it’s common for friends to withdraw and activities to start to fall away. A person is left with few things that can offer joy, a sense of purpose and human connection. I’ve seen this firsthand—my father had dementia for 18 years. As it…

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“SMILE” – Helping dementia caregivers

“SMILE” – Helping dementia caregivers

Dr. Christopher Frank, of Kingston, Ontario, particularly appreciates the caregiver’s role—after all, he focuses on areas where caregivers provide crucial help, such as geriatric rehabilitation, acute care consultation and palliative care. In this guest blog, Dr. Frank shares five pieces of inspirational advice from one of his patient’s relatives, a caregiver herself.

Brain Awareness Week: Mario’s three keys to living well

Brain Awareness Week: Mario’s three keys to living well

Mario Gregorio resides in British Columbia. He lives with dementia. An advocate for dementia awareness, Mario was one of the faces of Alzheimer’s Awareness Month this past January. I’m celebrating my 70th birthday this year. The best decision I’ve ever made in my life was to seek an early diagnosis. I felt that I needed to take control of my medical situation. And I’m glad I did. An early diagnosis allowed me to research more about dementia. I knew that…

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

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

When we last left Phyllis Fehr, we heard about how her experiences inspired her to take on her current role as a leading advocate for human rights for people with dementia. (If you haven’t yet, check out part one of this series, Becoming a force for change—Phyllis Fehr’s story.) One of Phyllis’ current focuses is the Convention on the Rights of Persons with Disabilities, an international human rights treaty that was adopted by the United Nations almost a decade ago….

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