I have only posted here about 2 times in the past 7 years. My mother was
diagnosed with AD 7 years ago. Until about a year and a half ago she was
still talking and able to do a lot of things for herself. Then she had to
be hospitalized a few times for UTI's and she really went downhill. The last
2 UTI's she had were antibiotic resistant infections and it took 2 weeks of
IV antibiotics to get them cleared up. Mom became less talkative, totally
incontinent and eventually pretty much unable to do much for herself at all.
She was in a 36 bed RCFE starting in May 2003 and last year we had to find
another place for her. She is in a 6-bed home now and the caregivers are so
wonderful with her. She almost needs total care now and my sisters and I
are worried that very soon we will have to put her in a state-run nursing
home. Mom can no longer wear her dentures because she lost too much weight
last year and since she can't co-operate with a dentist to get new ones
made, she is on a pureed diet. She has to be fed. She is totally
incontinent. She has to be bathed, dressed and groomed. She talks very
little and most of it is either gibberish or a few words strung together
that make no sense. She doesn't seem to know her children anymore. She
only responds to the caregivers. She will look at them or smile at them
when they talk to her - nothing for us though.
The mind is pretty much gone but her physical health is not that bad. We
try to make sure she gets 2 visits from us a week but it is soooooo hard to
see her now. We sit and talk to her and it's like talking to a wall. It is
getting so depressing lately. And we wonder and we wonder....... how long
can she live like this? We know there is no answer but we wish there was.
When we started on this journey with her we never imagined she would be like
this.
We think there are 2 reasons she can still stay in the Home she's in. 1 -
She still tries to feed herself at times and can get food on a spoon and to
her mouth. She can also hold a cup and drink. 2 - After she is helped out
of a sitting position, she can take small steps and with a little help can
turn herself around to get in bed. She can walk by herself. She is never
allowed to though because she would fall so the caregivers walk her several
times a day. If she needed "total" care, she could not be in a RCFE. We
are really dreading the day that she will no longer be able to stay in this
Home.
I have been reading this newsgroup on and off for the past 7 years. It has
helped so much to know that I'm not alone. Now I do feel alone though -
there is just nothing left of my mother. We have tried everything we can
think of to try to get a response from her and.... nothing. I really hate
this disease.
I guess there really is no reason for this post. I just felt like I wanted
to connect with someone tonight. Thanks for listening if you read this far.
~~~~Pat
Evelyn - 17 Jan 2007 14:14 GMT
> I have only posted here about 2 times in the past 7 years. My mother was
> diagnosed with AD 7 years ago. Until about a year and a half ago she was
[quoted text clipped - 45 lines]
>
> ~~~~Pat
Dear Pat,
I am glad you decided to share here. It is the best of all possible
reasons for this newsgroup to exist. I don't have anything to offer,
but just to say that I hear you, I sympathize, and hope your mom gets
through this illness with the least amount of suffering to all
concerned. Sadly it is the family that suffers the most with
alzheimers, and I think most of the posters here would agree.
Stay strong, and the best to you.....
Regards,
Evelyn
Bud - 17 Jan 2007 17:05 GMT
> I guess there really is no reason for this post. I just felt like I wanted
> to connect with someone tonight. Thanks for listening if you read this far.
Dear Pat. We buried my wife one week before Christmas. Hospice insured
she had no pain the last few days but it isn't any easier for me since
she is gone now. There is no easing of the hurt, just a relief from the
worry and concern of the disease process. I offer you my sympathy as I
know how you feel.
Bud
Dana Carpender - 17 Jan 2007 22:47 GMT
> I have only posted here about 2 times in the past 7 years. My mother was
> diagnosed with AD 7 years ago. Until about a year and a half ago she was
[quoted text clipped - 43 lines]
> I guess there really is no reason for this post. I just felt like I wanted
> to connect with someone tonight. Thanks for listening if you read this far.
I read the whole thing, and sympathize -- and empathize -- with all my
heart. My mom is about where yours is. I'm going to see her this
weekend (she's in care near my sister, 2000 miles away) and I'm not
looking forward to it. I know it will hurt a lot.
We, too, wish for some sort of answer to the question "How long?" We,
too, never envisioned how bad it would get.
Let us pray for a swift and painless release for our loved ones.
((((((((((((((Pat)))))))))))))
Dana
Alan Meyer - 18 Jan 2007 05:37 GMT
Sorry about your situation Pat. It is a horrible, heart-wrenching
experience to go through.
It sounds like your Mom is nearing the end. In my experience
(two parents and one mother-in-law), rapid deterioration like you
have seen was a precursor of one or another kind of fatal
illness. I wouldn't think your Mom would suffer for more than
another year or two, though we never know what will happen
until it happens.
I hope that when it does happen it will be easy and painless for
your Mom and for the family.
Best of luck.
Alan
Liz C - 24 Jan 2007 02:45 GMT
Hi Pat:
I also am a lurker here most of the time and rarely post but after
reading your post I just wanted to let you know that you are not alone.
My mom passed away just over 1 year ago now and although it has been so
hard (much harder then I thought it would be) I am happy that she is no
longer suffering here. I miss her every day and hate the disease that
took her from me and am trying to come to terms with it.
You are not alone (although at times I am sure it feels like you are)
and there are many of us out there behind you although you can't see us.
Liz C