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!

• • • • •


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.

Saturday, June 28, 2014

Welcome to My Zoo

I do not mean this to be a comment on any of our friends or family who have come to visit Gregory at The Lieberman Center. I see it more as my problem, not theirs. But I need to write about it.

For a first visit, I will go to The Lieberman Center with a friend to visit Gregory. I can introduce the visitor to the center, help them find Gregory in his room or at his current activity, provide a buffer in case it is not a good day for Gregory or a support to the visitor if the visitor has difficulties in dealing with Gregory's "Here and Now." After that I release my need to be there to the friend's discretion.

Many people have not wanted to visit Gregory because, I understand this with my entire heart, they cannot bare seeing what he has become.

Others need to see Gregory in his present circumstances so they can come to some closure with what has taken place due to the Alzheimer's.

Others want to be there to support him and to support me.

Some have had similar experiences with their own family members due to either Alzheimer's or the need for a care facility due to illness or old age.

All of the various reasons are based on love.

BUT, sometimes I feel like a game keeper at the zoo. I am there to protect the animals but also to protect the visitors.

I put Gregory on display, hoping he will perform, will show recognition, will behave appropriately.

I will discuss the various types of training he has gone through and the various tricks he can or can no longer perform.

Step right up, step this way, see Gregory in his current condition, in his current situation. Be amazed, be amused at what Alzheimer's has wrought.

Try to explain away the situation, try to understand what is going on in that void, or not.

Ouch. All I can say. Ouch. And sorry for my rantings.

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