Periodically I will add posts here if the sources provide additioanl informaiton on how to think about and deal with Dementia/ Alzheimer's Disease.


SCROLL DOWN FOR TEXT and BIBLIOGRAPHY from DAI WEBINAR 2/22-23/2017. You can also find this information on my website:

Even though this blog is now dormant (see info below) there are many useful, insightful posts. Scroll back from the end or forward from the beginning. My guess is that you could spend a lot of time here and maybe learn or experience a thing or two about living with and loving someone with Dementia/Alzheimer's or maybe come away with the feeling that "you are not alone" in YOUR work with the same!

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Happy New Year 2016. With a new year comes new beginnings and sometimes endings. If I am personally progressing and if I am doing a good job in my grieving Gregory's death; if I have been able to learn my lessons in living and loving someone diagnosed with Dementia/ Alzheimer's; if I am to get on with my life ... I need to bring this Alzheimer's blog to an end since my writing has been dealing less with Dementia/ Alzheimer's and more with life after Dementia/ Alzheimer's.

Of course, I will always continue to work for and support fair treatment on behalf of people with Dementia/ Alzheimer's and may post here from time to time. Also, there are many wonderful posts here through which you may browse.

With this change, I will continue and reinvigorate my "michael a. horvich writes" blog which deals with grieving Gregory's death, life lessons, personal experiences, observations, memoirs, dreams, and humor in essay and poetry, as well as an attempt now and then at sharing a piece of fiction.

Please follow me there by clicking or click the link located on the right side of this page.

Finally, COMMENTS are always important to me and you can still comment on the posts on this blog! CLICK "Comments" and sign in or use "Anonymous." Leave your name or initials if you wish so I'll know it's you? Check the "Notify Me" box to see my reply to you.

Wednesday, March 25, 2015

Documentary Day 3

Today the Documentary Crew and I went to visit Michael's Museum, shot some footage there, then returned to Skokie to visit Gregory. We spent approximately 30 minutes with him then it was time for dinner. We were able to set up in a way that the cameras did not invade the privacy of the other residents but their ambient noise did create a wonderful background of what life on the fifth floor of Lieberman is like.

Gregory has developed a cold so his engagement was slightly reduced but he did end up being able to feed himself more often then I have ever seen him do so! Dinner tonight was lamb stew with mushrooms, mixed vegetables, and orzo.

It was somewhat difficult to get food into his mouth when I was doing the work because he was so badly bent over to the right. When he does not feel well or is tired, his neck seems to give out and rests uncomfortable to the right. I have had OT/PT working on this but haven't seen any improvement yet.

Dessert was canned plums and I was very tempted to have one for myself. But I resisted temptation.

Gregory did feed himself, as I mentioned, but he was less engaged then he usually is if only because of his cold/cough. I told him that I felt bad he wasn't feeling well and I really did mean it! I am just getting over a cold myself so I know how bad one can feel.

After dinner we went back to his room, camera crew in tow, said our goodbyes and left. This time Gregory did not seem too upset that I was leaving. I told him, "I'll  see you tomorrow, OK?" and he replied to the affirmative.

This is the second time of shooting at Lieberman and we will be back tomorrow for whatever shots might come up but mainly for Gregory's "Painting" session. He has not been too successful with his finger painting but we decided to try once more for the benefit of the camera and the documentary. We think that his struggling with the painting backed with stills of some of his wonderful art work will help show some of the changes that have occurred over time.

Will keep you in touch as we continue. Actually this post was staged so that the camera could capture my doing a post. Earlier I had talked about how I turned to the computer, as Gregory continued to fail in his abilities, as a way of processing what I was experiencing, as a way to deal with my emotions, and as a way to keep family and friends up to date without my having to tell the same story over and over again.

When you watch the documentary then, you might see my fingers flying across the keyboard!

1 comment:

  1. I'm really excited about the documentary, and about following it as you go. I had also hope to do a documentary about my journey with mom, but I'm not sure if that will ever happened. If it does, it will have to be using my own amateur footage so… Perhaps not to be :-)

    I will just have to live vicariously through you and Gregory and your documentary team.


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