Advocacy, Resources, Toward better care

what if everything we’ve been taught about dementia care is a lie?

That’s what Dr. David Sheard asked himself in 1995, along with “What if people with dementia don’t have any behaviours?” and “What if we’re actually killing them?”

Based on the answers to those questions, he founded Dementia Care Matters and developed the Butterfly Household Model of Care, a framework that transforms the care home cultures and environments into ones in which people living with dementia can thrive instead of just die.

This Toronto Star video shows what that transformation looks like, and fills me with hope for the future:

More on the in-depth story entitled “The Fix,” by the Toronto Star’s Moira Walsh here.

https://myalzheimersstory.com/2018/05/24/5-ways-to-make-toast-in-long-term-dementia-care/

https://myalzheimersstory.com/2016/04/23/5-ways-we-rob-people-with-dementia-of-their-dignity/

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Care Partnering, Hope, Inspiration, Joy, Love

courageous vangaros united by love in life and death

Pops and Vince Vangaro

Albert Anthony “Pops” Zangaro

April 1st, 1942 – April 10th, 2018

For fourteen years, Vince Zangaro cared for his “Pops” who lived with Alzheimer’s disease. During that time, Vince developed a deep and abiding love, compassion and a gentleness of spirit that endeared him to care partners around the world. He shared some of his feelings on Facebook the day he and his family said farewell to Pops.

Besides being the primary care partner to his father, Zangaro is a musician and the main driver behind the Alzheimer’s Music Fest. His posts and videos documenting the loving care he and his wife Amy give Pops inspired and will no doubt continue to inspire thousands.

As Zangaro and his family approached their final days together, Vince took the time to recognize Chappie Bird, his father’s feathered friend. Here’s that Facebook post as well:

See a video of the Zangaro family caring together here.

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Care Partnering, Hope, Inspiration, Joy, Love

son thanks pops’ caregiver bird at alzheimer’s end

Vince Zangaro is an extraordinary person. He’s cared for his “Pops” who lives with Alzheimer’s disease for fourteen years. During that time, he has developed deep and abiding love, compassion and a gentleness of spirit that have endeared him to care partners around the world.

Besides being the primary care partner to his father, Zangaro is a musician and the main driver behind the Alzheimer’s Music Fest. His posts and videos documenting the loving care he and his wife Amy give Pops inspire thousands.

Now, Zangaro and his family are approaching their final days together, and true to form, Vince takes time to recognize Chappie Bird, his father’s feathered friend. Here’s the Facebook post:

See a video of the Zangaro family caring together here.

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Care Partnering, Hope, Inspiration, Joy, Love

don’t waste your time hating alzheimer’s disease

dont-waste-your-time-hating-alzheimers-disease-2

“Someone asked me the other day if I hated Alzheimer’s disease,” wrote Vince Zangaro on his Facebook page.

Besides being the primary care partner to his father, whom he calls Pops, Zangaro is a musician who is the main driver behind the Alzheimer’s Music Fest. His posts and videos documenting the loving care he and his wife Amy give Pops inspire thousands.

“I told them that for the first several years it was a battle,” Vangaro wrote on. “I realized that if I continued to hate Alzheimer’s that I would reflect that anger onto my father. I decided to build a relationship with the disease so I could continue to have one with my dad.

“It’s not like we do not get angry but anger only gets you so far. Pops and I have had a relationship with this disease going on thirteen years. To accept and not hate has made our family much more at peace. This is just where we are at in life.

“Each of us has to do what we have to to find a sense of clarity through this journey. So do I hate Alzheimer’s? No. It is a part of my father and I love him with all my heart. We accept this and don’t spend our time hating, we rather spend our time loving the moments we have.”

I went through the same kind of transformation that Vince Zangaro describes here. Although he was in his early thirties and I was in my late fifties when it happened, I discovered the same truths that Vince, Amy and Pops did. There’s no point hating Alzheimer’s disease or other dementias. It’s so much more sensible, productive and enriching to spend your time and energy loving the people who live with it, and helping them engage life for as long as they possibly can. The rewards for everyone are priceless and immeasurable.

Here’s the Zangaro family in action:

 

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Care Partnering, Death & Dying, Life & Living

life is a death sentence

shequotes-life-is-a-death-sentence-cropped

I read and hear a lot about what a terrible disease Alzheimer is.

I think we need to work hard at changing this perception for the benefit of the people who have dementia as well as the sanity of those who are their care partners. My personal experience is that while the disease is certainly horrible and tragic, there are moments of great joy and healing to be found in the journey.

I have learned as much as I have lost in the process of navigating the choppy waters of the last decade or so as I have become more acquainted with dementia and people who live with it.

I wrote in another blog post:

“Being doesn’t require remembering, thinking or doing; and recognizing love and compassion doesn’t require recognizing individuals.

It helps that I see people with dementia as engaging, vibrant and fully human beings rather than as lesser versions of themselves or worse, as empty shells.”

Life itself is a death sentence. But we don’t grieve the birth of a new life, we celebrate it. We would all be well served if we started looking at all types of dementia in a different way. I’m not saying dementia is not heart wrenching and soul destroying. It is. But the people who have it are still people, and they’re not dead while they’re still alive.

Advocates such as Kate Swaffer, Rick Phelps, Harry Urban and others who have been diagnosed with dementia are adamant they should not be dismissed because of their diagnosis. On the contrary, they actively contribute to the ongoing conversation about the disease and how they are the ones best positioned to educate the rest of us.

Let’s help people with dementia live the best lives they can until the end instead of whingeing and whining and moaning about how sad we feel about what we perceive, perhaps mistakenly, our collective losses to be. Let’s focus on how we can make life with dementia full, engaging and rewarding no matter which side of the care coin you find yourself on.

End of rant. Or beginning of a bigger rant, depending on what happens…

P.S. Some interesting quotes and thoughts on life and death here.

https://myalzheimersstory.com/2016/08/20/dying-with-my-mom/

https://myalzheimersstory.com/2018/02/25/3-wise-thoughts-on-being-with-someone-you-love-as-they-die-which-also-apply-to-being-with-someone-with-dementia-as-they-live/

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Books, Challenges & Solutions, Death & Dying, Hope, Life & Living, Quotes

what matters most

 

Atul Gawande fears or hopes

 

If you or anyone in your family plans on growing older, you must read bestselling author Dr. Atul Gawande’s book Being Mortal: Medicine and What Matters in the End.

It’s full of amazing wisdom, thought-provoking ideas, shocking statistics, heartwrenching stories and down-to-earth information about aging and dying with grace and dignity.

I absolutely love it!

I also love the idea of life being a stairway to heaven…

 

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Books, Challenges & Solutions, Death & Dying, Life & Living, Quotes

imagine aging differently

 

MAS AG MD meaning in old age is new

 

If you plan on growing older or anyone in your family does, you must read bestselling author Dr. Atul Gawande’s new book Being Mortal: Medicine and What Matters in the End.

A real eye-opener!

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