I am new here and wanted to say hello.
I care for my mother who is 81years of age and suffers from Alzheimer's.
She lives in my home with me. I am not married so I have it all by myself.
I work during the day and she stays here alone. I come home for lunch every
day and feed her and I get off work at 3:30 and come straight home.
She is pretty coherent really but she has a memory of about 30 seconds and
an attention span of about 15 seconds. She can remember just about
anything if I remind her. Really she is not as bad, yet, as many with the
disease. But, she continues to fail more and more and it is only a matter
of time. She is getting very clumsy and falls. Last Friday I got off work
early and we went to Chick-fil-a for lunch. As we were leaving she lost her
balance and fell - it didn't really hurt her except for a skinned knee and a
big black eye. Now the bruise covers her whole face and has turned yellow
with red around her eye. Boy, she really drew a crowd at the Chick-fil-a!!
It seems now that she is getting very frustrated and stays mad all the time.
She blames me for her problem saying that I have driven her to this. Also,
she wants to be active in the house and do "housework" but makes the biggest
mess. I just let her at it and fix it when she is done.
She is taking a hand full of pills twice a day. She takes 150MG of Zoloft
each day as well as heart pills and water pills and blood pressure pills.
We are having a time.
When she gets a little worse I will have to place her somewhere. Since the
disease is not taken her out of reality except for robbing her of good
judgment, I don't know how I will get her someplace. I jokingly say I need
a tranquilizer dart and net to get her to go. She is very, very strong
willed and getting worse as it progresses. It will be an impossible task.
Please everyone, pray for me and Mom and I will you too.
Evelyn Ruut - 27 Feb 2004 23:46 GMT
> I am new here and wanted to say hello.
>
[quoted text clipped - 30 lines]
>
> Please everyone, pray for me and Mom and I will you too.
Welcome Greg.

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Evelyn
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Lee - 27 Feb 2004 23:47 GMT
I don't envy you.... being a caregiver is enough of a challenge without
having to do it all by yourself.... helps a lot to have someone to share the
load... or at least to vent to
have you looked at possibly finding someone to come in while you're at work?
Will likely be necessary, if not right away, then soon. We started by just
having someone come in 'to clean' ... my MIL was totally resistant to having
someone come in for her... but she didn't mind a cleaning lady .... we just
~happened~ to find a cleaning lady who is also a personal support worker....
it sure made things easier when we started having home care workers in for
her
> I am new here and wanted to say hello.
>
[quoted text clipped - 30 lines]
>
> Please everyone, pray for me and Mom and I will you too.
Mary Gordon - 28 Feb 2004 16:50 GMT
Presenting extra help in a facesaving way is always a good plan.
Our first foray was getting our financial planner to take over my MILs
finances. We were able to convince my MIL by putting the spin on it
that it was such a boring and time consuming job, so why should she
spend her precious time fighting with her books when she had better
things to do. Let Janet do it! We didn't let on she wasn't competent
to do it any more, or that it was in a muddle - it was more that heck,
why would you want to do it when we can get someone else to do it. We
were much helped by the fact she'd had an accountant doing the taxes
in past years, and he was much more expensive than our planner - so we
had a price selling point as well, never mind that Janet was able to
totally organize everything to make it managable..
We put a similar spin on the home care person - although she was
actually hired to make sure my MIL was bathed, fed and that the
household was in some semblance of order, we spun it that my MILs
knees and hip were bad, so we didn't want her doing tiresome housework
like oven cleaning - i.e. she was doing US a favour by accepting a
housekeeper, and besides, why should she be bothered with all those
messy and difficult tasks when we could get someone to do it! We never
let on that the real problem was that she wasn't capable of adequately
doing basic domestic tasks like her laundry or keeping the place
clean, or making sure there were basic supplies on hand. We just tried
to paint her as a lady of leisure who had better things to do with her
time, and had earned the right not to do yucky jobs. Worked pretty
well. She had a hard time at first with the idea of a strange person
in the house, but soon started to really enjoy the company.
Mary G.
spam2death - 28 Feb 2004 02:42 GMT
> I am new here and wanted to say hello.
>
[quoted text clipped - 3 lines]
> I work during the day and she stays here alone. I come home for lunch every
> day and feed her and I get off work at 3:30 and come straight home.
Your routine sounds very familiar. We are now doing live in 24 (or 36) hour
a day care.
> She is pretty coherent really but she has a memory of about 30 seconds and
> an attention span of about 15 seconds. She can remember just about
[quoted text clipped - 5 lines]
> big black eye. Now the bruise covers her whole face and has turned yellow
> with red around her eye. Boy, she really drew a crowd at the Chick-fil-a!!
If she asks questions repeatedly, just answer her and don't get angry. 15-30
secs memory is as good as it's going to get.
Loss of balance and tendency to fall comes with the territory. Watch out for
her climbing on chairs or step ladders. If you think your mom is a hand full
now, try taking care of her after she breaks a hip. Been there, done that.
> It seems now that she is getting very frustrated and stays mad all the time.
> She blames me for her problem saying that I have driven her to this. Also,
> she wants to be active in the house and do "housework" but makes the biggest
> mess. I just let her at it and fix it when she is done.
Don't set her up for failure. We tell my MIL that she is now "retired" from
any housekeeping she can't do very easily. This leaves loading (only) the
dishwasher and wiping the kitchen counter, occaisional unloading (only) the
clothes dryer and making her bed. Of course we have to check the dishwasher
before running, look for the clothes after she hides them around the house
and also help her change her sheets once a week, but at least she feels like
she has regular chores and is being helpful around the house and this seems
to make her happy. If you allow her to try things beyond her remaining
ability, you set both her and yourself up for major frustrations. Learn to
fib creatively to make her more comfortable with whatever abilities she
still has functional.
> She is taking a hand full of pills twice a day. She takes 150MG of Zoloft
> each day as well as heart pills and water pills and blood pressure pills.
> We are having a time.
Consider asking her Dr about Aricept or other drug that might slow her AD
disease progression.
> When she gets a little worse I will have to place her somewhere. Since the
> disease is not taken her out of reality except for robbing her of good
> judgment, I don't know how I will get her someplace. I jokingly say I need
> a tranquilizer dart and net to get her to go. She is very, very strong
> willed and getting worse as it progresses. It will be an impossible task.
Hopefully the strong willed tendency will decrease over time. Judgement is
already gone, so don't expect much there. We've already been through denial,
alcohol abuse, paranoia, and general meanness. Fortunately my MIL is now
rather pleasant most of the time and no longer worrying nearly as much. She
jokes about her failing memory and she is now happy just to be living with
her daughter rather than trying to live alone and being unable to function.
It is a 36 hr a day job to watch out for her and provide good care.
> Please everyone, pray for me and Mom and I will you too.
Welcome to the group. s2d
Greg F - 28 Feb 2004 14:33 GMT
Thank you. The thing you mention are good things.
Mom fell in March 2003 and broke her pelvis in three places, one of them a
nasty break. Although she had been diagnosed with Alzheimers for two years
it wasn't so bad until her fall.
> > I am new here and wanted to say hello.
> >
[quoted text clipped - 75 lines]
>
> Welcome to the group. s2d
Gwen Love - 28 Feb 2004 03:34 GMT
Welcome Greg. Sorry you need to be here. If you don't already have it, I
suggest you get a copy of "The 36 Hour Day" to read. It really will give
you much information about AD.
Gwen
===========================================================================
====
Laughing at our mistakes can lengthen our own life. Laughing at someone
else's can shorten it.
- Cullen Hightower
===========================================================================
=====
| I am new here and wanted to say hello.
|
[quoted text clipped - 30 lines]
|
| Please everyone, pray for me and Mom and I will you too.
Greg F - 28 Feb 2004 14:18 GMT
I have heard so much about that book. I will look around and try to find a
copy. Thank you. And, I am sorry that you and all the others are in this
group as well.
> Welcome Greg. Sorry you need to be here. If you don't already have it, I
> suggest you get a copy of "The 36 Hour Day" to read. It really will give
> you much information about AD.
> Gwen
===========================================================================
> ====
> Laughing at our mistakes can lengthen our own life. Laughing at someone
> else's can shorten it.
> - Cullen Hightower
===========================================================================
> =====
>
[quoted text clipped - 49 lines]
> |
> | Please everyone, pray for me and Mom and I will you too.
Tumbleweed - 28 Feb 2004 18:21 GMT
> I am new here and wanted to say hello.
>
[quoted text clipped - 3 lines]
> I work during the day and she stays here alone. I come home for lunch every
> day and feed her and I get off work at 3:30 and come straight home.
<snip>
> When she gets a little worse I will have to place her somewhere. Since the
> disease is not taken her out of reality except for robbing her of good
[quoted text clipped - 3 lines]
>
> Please everyone, pray for me and Mom and I will you too.
Greg, my dad was the same, it was a *real* struggle to get him into respite
care, and once he was there, it took about another 2 weeks before he got
used to it, and several more months before he stopped asking to go home when
we visited (after 2 weeks in respite my mother realised she couldnt cope any
more were he to come back).
Partly him accepting it is acclimatisation and partly (probably) him getting
worse.
It will probably be traumatic when she goes, and it might also be an
emergency situation, for example when you are out and she wanders off or
harms herself, in fact this seems almost inevitable to me if you leave her
alone all day, its probably just a matter of time before something
unfortunate happens. Have you looked into day care?
Good luck, one person looking after an Az person full time is pretty tough,
to say the least.

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Tumbleweed
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Laurie - 28 Feb 2004 21:35 GMT
Hi!
My name is Laurie and I've been lurking. I've learned so much here! I'm
so overwhelmed by what's happening with my dad that I haven't even been
able to write.
Below-please note I a post from Patty that looked like it got lost in
the Eddyjean shuffle. She looks like a VALUABLE resource and friend!
Guess I'm a boundary overstepper- but was so glad to find someone on
the inside of a residence!
Hi Everyone!
Laurie
Patty's post- you can nd it in the Aricept causing dementia. thread:
Hi Everyone. Excuse me...hope you do not mind me "butting" in.
My name is Patty and I live in R.I. I work in a beautiful Nursing Home.
I work on the Special Care Unit...It is a 43 Bed Closed Alzheimer's
Unit. I am the Activity Coordinator...and I am a Med Tech...(Do the Med
Passes as needed) 2 for the price of one...LOL..I have worked with
Alzheimer Residents for 10 years, and on April 1st....Been a Med Tech
since 1980.
I LOVE the Alzheimer Residents. My heart goes out to the Famiy Members
for they knew them when....
Barb...We call our "lies" Fiblets. Tell them anything that sounds
good...so they will stay calm. For example....:
Where are my children? The had to go shopping, Mom. They'll be home
soon.
Where is your Dad? He's working over-time, Mom. Let's keep his supper
warm for him. He'll be hungry when he gets home.
I want to go home....Look at your watch.....Okay let's wait until I can
get us a ride. Why don't we have some Supper now...etc. Hope this
helped...
On Aricept...I'm not an expert, but what I was taught about the Med
is....Starting on Aricept is to maintain their present level of
functioning for as long as possible.
But like someone has already stated, medication does NOT necessarily
work to the same degree on everyone. Each person is an idividual. Stay
Safe.....Patty:-)
Greg F - 28 Feb 2004 22:46 GMT
It sounds like Patty is a real nice person. I can't find her posts.
> Hi!
> My name is Laurie and I've been lurking. I've learned so much here! I'm
[quoted text clipped - 33 lines]
> work to the same degree on everyone. Each person is an idividual. Stay
> Safe.....Patty:-)
Laurie - 29 Feb 2004 03:42 GMT
It sounds like Patty is a real nice person. I can't find her posts.
Patty is #27 unber Can Aricept CAUSE dementia thread? It's the thread
down about three topics.
Laurie
Greg F - 29 Feb 2004 03:57 GMT
OK, I see her now. Thanks.
> It sounds like Patty is a real nice person. I can't find her posts.
>
> Patty is #27 unber Can Aricept CAUSE dementia thread? It's the thread
> down about three topics.
> Laurie
Patty - 29 Feb 2004 04:16 GMT
Thanks, Laurie. I just want to be of some help IF I can...
I have one thing I would like to say about your Alzheimer Parent/s....I
am PETRIFIED knowing they are home alone!! Because I fear they will
wander
off or fall down and get hurt or start a fire....???
I say that because I know the many facets of the Residents on a daily
basis.
If monitored we can do all their ADL's...activities, Medications every
day, and we know everything about them.
We are a closed unit, but they can wander all they want, have a finger
food on the run if they won't stay seated, have that 1-1 special touch,
activities, etc.
In my opinion, anyone that works on my unit, is there by THEIR choice.
Why? Because we WANT to be there. We CHOOSE to be there. We are TRAINED
to be there. And that is why we are called "The Special Care Unit" We
LOVE these SPECIAL human beings.
Although by Friday I'm ready for the bridge...after the week-end I'm
ready for another week....LOL
The above is JMHO...
And to Paul....My deepest condolences for the loss of your neice. My
heart goes out to you. Prayers are on there way.....Patty
Dennis P. Harris - 29 Feb 2004 05:27 GMT
> I have one thing I would like to say about your Alzheimer Parent/s....I
> am PETRIFIED knowing they are home alone!! Because I fear they will
[quoted text clipped - 3 lines]
> I say that because I know the many facets of the Residents on a daily
> basis.
you must realize, though, that the folks in your unit come their
*after* it's no longer safe for them to be home. i agree that
the OP needs to avoid denial and be a dispassionate observer who
can determine when they will no longer be safe alone.
Laurie - 29 Feb 2004 05:58 GMT
Dennis.
you must realize, though, that the folks in your unit come their *after*
it's no longer safe for them to be home. i agree that the OP needs to
avoid denial and be a dispassionate observer who can determine when they
will no longer be safe alone.
÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷÷
I thought I could keep my parents safe in an assisted retirement
situation. That is until my father was discovered walking on the highway
in is socks. Hopefully, most people aren't as naive as I am. but he
didn't have an AD diagnosis yet, and I had NEVER heard of wandering.
Again, I've learned so much from the posts here. Thanks!
Laurie
Dennis P. Harris - 29 Feb 2004 06:46 GMT
> Hopefully, most people aren't as naive as I am. but he
> didn't have an AD diagnosis yet, and I had NEVER heard of wandering.
> Again, I've learned so much from the posts here. Thanks!
again, the bible for caregivers is "the 36 hour day" by mace and
rabin, available at any larger bookstore. it covers about 95% of
what you need to know.
Mary Gordon - 29 Feb 2004 16:17 GMT
Here is a link to the book at Amazon
http://www.amazon.com/exec/obidos/tg/detail/-/0446610410/103-5008228-5581437?v=glance
I wore mine out. The softcover is not expensive - best 8 bucks you'll
ever spend.
I have some other books aimed at caregivers but nothing else I've seen
has as much to the point information in one volume.
Mary G.