Dementia: The Path Beyond the Tears

Alzheimer’s: We weather an anxiety attack

August 8, 2008 · 1 Comment

My friend had what I interpret as an anxiety attack – big time. Keep reading →

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Alzheimer’s: “I don’t know what’s wrong with me”

July 12, 2008 · No Comments

My friend Carl is saying, “I don’t know what’s wrong with me.”  And I don’t know what to say back to him – that’ll be any help.

It’s not a good situation – not encouraging at all – for either of us. Keep reading →

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Alzheimer’s Disease and Sundowning

July 1, 2008 · No Comments

Sundowning syndrome – also referred to as sundowning and sunsetting – is a pattern of more severe behavioral symptoms in the late afternoon and evening.  This pattern is common in people with Alzheimer’s disease and dementia.
Keep reading →

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Alzheimer’s: I Wish I Could Help More

June 20, 2008 · 2 Comments

I wish I could do more to help Carl.  I wish, to the most wonderful stars in Mr. Sagan’s Cosmos, that I had some way to do more to help my friend.  To help my best friend in the world – at this time, when he needs help more than he has ever, in his life, needed help.  At this time, when there’s no other person or place or power he can look to for help.

But that’s exactly what every other Alzheimer’s caregiver feels, isn’t it?  Millions and millions and millions of people.  Even if their situation isn’t exactly the same as mine, they fervently hurl an identical plea into the implacable ether. Keep reading →

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Alzheimer’s: The Path Beyond the Tears

June 15, 2008 · No Comments

“As we walked, every two minutes, I would seize up, surging close to convulsing into tears.”

Those were my words. I wrote them in my initial post to this blog, a little over six months ago. Keep reading →

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Alzheimer’s Disease and the Full Moon

June 7, 2008 · No Comments

The banging rang along the halls of the nursing home. A moment before, it was quiet. Now, the regular, rhythmic pounding echoed through the vaulted open area.

I was seated at a conference table. I was attending my second evening meeting with this Alzheimer’s Association caregiver support group.

I knew that the building was built only a few years ago. So the utility systems shouldn’t be making that kind of racket. At least, not quite this soon. Keep reading →

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Alzhimer’s Association – Northern Delaware Support Group – Men only

May 17, 2008 · No Comments

This past Monday morning, I attended my first meeting of a men only Alzheimer’s support group – sponsored and supported by the local Alzheimer’s Association. Keep reading →

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New Beginning – Writing – Again

May 5, 2008 · No Comments

Hi there! I’m back.

There’s a row of Poplar trees behind our house. In winter, the branches are bare, and I can see through the trees to the scrub beyond.

Today it’s spring, and the Poplars’ foliage is filling in – once again.

As leafy life returns to the trees outside my window, I am returning to my blogging. Keep reading →

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Small pleasures

February 25, 2008 · 3 Comments

The neurologist characterized Carl’s “progress,” along his rocky Alzheimer’s road, as “medium”.

Thinking about it later, I wondered what “medium” means – really. I must ask when I can.

I’m wondering whether Carl could be on the not-so-good side of “medium”. Or maybe even a bit beyond that. Keep reading →

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Mocha Flavored Irony

February 14, 2008 · 1 Comment

As I was getting Carl settled this morning, on the couch in the livingroom, with his breakfast Cheereos, coffee, and newspaper, I thought about the several times, in our 33 years together, when he would playfully suggest that I make his coffee – or that I get him some fresh coffee – or whatever other amusing idea popped into his head.

I always declined. Completely apart from the fact that the suggestion was playful, I was wary of getting into that sort of pattern – with coffee – or with any other routine need.

The bitter sweet, ironic agony is that’s exactly what I’m doing today.

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