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.

Tuesday, December 16, 2014

More Than Ever

My love for this man continues to grow and grow. As Gregory's abilities continue to disappear, I am able to find more and more to love about him.

One thing I have always done since Gregory entered Lieberman Memory Care, is to be very open about our relationship and about my love for him.

I feel no embarrassment at hugging or kissing him when I want to or when he needs me to, even if we are in a large group of people. If he cries with joy or frustration, I feel no problem in hugging him and rocking with him.

Our relationship, same sex relationship, has been accepted by Lieberman administration and staff as well as by residents and their families on Gregory's and other floors.

People will ask about our relationship and I will proudly tell them Gregory is my life partner, my significant other, my boyfriend for over forty years now. Usually they gasp in amazement and say something like, "Most marriages don't last that long."

If the person is not aware, I will not go into any detail. If the person asks what I mean, I will go into my "gay" or "married" etc description.

I am tickled when people, family of residents or residents, ask if Gregory is my son or if I am his son.

Many people, both staff and family, have commented on how lucky Gregory is to have me and I will reply, "I am lucky to have him."

People will comment on what a wonderful love we have for each other, several have mentioned never having seen such a great love, and others have said they only wish they will love someone as much in their life.

When I hear this, my first feeling is one of embarrassment due to the attention and the visibility of our love, on the other hand I work at not holding back on the love when with Gregory, so the next feeling is one of confirmation.

I guess I just love this man and am a little amazed when others are amazed. It is what we do. It is who we are. That's all. But I guess that's a lot!

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