>>> Greetings - I'm very new here and have been reading your posts for the
>>> past week. My father has mild memory impairment and was just started on
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> Don't trust them to take their own pills.... you give it to them each day.
> They really can't remember that they already took it.
Thank you all.
The idea of taking this with food and in the evening is good. Tomorrow's
dose will follow dinner.
I went over tonight and took him some pepto and also made him a grilled
cheese - very lightly grilled. He felt better. This is just his second day
on the drug. He can't remember why he's taking it and not very happy with
the upset to his system. I did decide to keep his pills with me and
administer them each day myself. I even wrote on the package the date and
time of his first dose. I'm really new to this. Although I've been helping
my Dad for a few years now it's been fairly minor. Until recently he's been
able to fix his own daily pills in a week at a time box and I just check
from time to time to see if he's taking them. I've also been keeping his
prescriptions filled for him and taking care of his finances for him. He
can't do anything with numbers.
My hope is that I can continue to convince him to take this drug. We won't
know if it will help him unless he continues to take it. He goes back to
his doctor in one month. He still does not believe there's any thing wrong
with his memory but he is thinking about it, I can tell.
I'm so glad I checked to see if this group exhisted. I know I'm going to
need you. I'm still looking for a local support group. Hoping to find
something here. I'm beginning to feel very frightened.
I'll introduce myself properly in another post.
Thanks again - Barbara H
Evelyn , by the way, I read your post in ASD - I appreciate your good sense
approach. I'm having a hard time controling my bg with the latest turn of
events. I guess it will get better.
Evelyn Ruut - 09 Jun 2007 03:02 GMT
>>>> Greetings - I'm very new here and have been reading your posts for the
>>>> past week. My father has mild memory impairment and was just started
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> sense approach. I'm having a hard time controling my bg with the latest
> turn of events. I guess it will get better.
Hi Barbara! Another great group over there. Hang in there.
The stress of this can really wreak havoc with your bg's. I know.
About the Aricept. My mother in law was put on it very early on, when we
first noticed a problem and got her diagnosed. But we never really knew if
it was working until a couple of years down the road and our doctor decided
to switch her to Excelon instead.
Well let me tell you.... it was a disaster. After the first four days we
called the doctor up and begged him to switch her back. With the very
first dose, going back on it, there was a dramatic change for the better.
So if you ever wonder if the stuff is helping, stopping will tell you if it
is.
Apparently it works by facilitating a certain brain chemical and allowing it
to have effect. But as I understand it, ultimately that particular brain
chemical ends up being in very short supply anyway, so the Aricept has
little effect anymore. On the other hand, there have been some studies
that showed it was helpful even in later stages. So only you can know by
observing how your own loved one functions with and without the drug.
--
Best Regards,
Evelyn
august - 09 Jun 2007 03:46 GMT
> Thank you all.
>
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> sense approach. I'm having a hard time controling my bg with the latest
> turn of events. I guess it will get better.
Make sure and get a full power of attorney and also a medical power of
attorney signed and notarized right now so that you have these documents
ready for further on down the road. This will save both you and your dad
many potential problems. You never know when your father might have a
drastic change of personality or medical crisis where you might need to take
full control of the situation. AW
Dennis P. Harris - 09 Jun 2007 06:53 GMT
> I'm still looking for a local support group.
check www.alz.org