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Medical Forum / Diseases and Disorders / Alzheimer's / June 2005

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appts re: LTC

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Lee - 23 Jun 2005 22:22 GMT
tomorrow is the day .... finally ...

just pulled out the paperwork and so on we were given when we last talked to
our case worker re: LTC... it's dated Dec 5, 2004 .....  everything was done
except that it was left to the kids (hubby and his sisters) to make
appointments to go look at the available facilities and make a decision on
which three they preferred (and in which order)  .... has taken them long
enough to get around to it, I think!

at this point, the girls are going to the appointments with LT placement in
mind; hubby is looking at it from the p.o.v. of TRYING respite care (more to
get me off his back than because he wants it) ....  but at least they're
going.

I think hubby is a ~tad~ perturbed with me for continuing to push the
respite care issue.... after all, we ARE getting a full day and 2 nights off
in a couple of weeks .... the one sister that lives about an hour away and
is only peripherally involved (but who is on the POA with hubby)  called and
left us a message that she was coming up to stay with ma for a few days in
July so we could have a break - fortunately, she happened to hit on a time
when I'm not scheduled to teach ....   didn't know it was coming, and don't
really have a plan ... but we'll figure something out.  I'm looking forward
to a couple of days away ...don't really care what we do ....  but I also
don't think that because she's going to give us a break we should drop the
whole respite care idea.  Having someone give us a break for 2/3 days
whenever she happens to decide to do it (last time was over 2 years ago!) is
not the same as being able to look forward to regular breaks ...AND being
able to stay home and have ma gone, rather than us going to a hotel or
whatever. Plus I really want to see how my MIL handles it, even if it's only
for few days at a time.
Tumbleweed - 24 Jun 2005 08:34 GMT
> tomorrow is the day .... finally ...
>
[quoted text clipped - 9 lines]
> (more to get me off his back than because he wants it) ....  but at least
> they're going.

In my direct experience, it was respite care that lead my mother to the full
realisation that she couldnt cope any more.
And it was the social workers and care staff and doctors and so forth who
(to my surprise) also were making that case.
I beleive this may be a fairly common experience.

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Tumbleweed

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tumbleweednews at hotmail dot com

Dennis P. Harris - 24 Jun 2005 08:52 GMT
> I think hubby is a ~tad~ perturbed with me for continuing to push the
> respite care issue.... after all, we ARE getting a full day and 2 nights off
> in a couple of weeks

tell him that you want a LIFE.
Evelyn Ruut - 24 Jun 2005 12:15 GMT
> tomorrow is the day .... finally ...
>
[quoted text clipped - 26 lines]
> than us going to a hotel or whatever. Plus I really want to see how my MIL
> handles it, even if it's only for few days at a time.

Good for you for sticking to your guns, Lee.   It doesn't look to me as
though the rest of the family is to be counted on for any kind of regular
respite care.   I think you are going to really appreciate the respite.
And I think he will too, no matter what he thinks right now.

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Best Regards,
Evelyn

(to reply to me personally, remove 'sox')

Florence A - 24 Jun 2005 20:39 GMT
Lee....Is it possible to take MIL to her daughter's  home for that
respite period.  You could find out how she will respond to different
surroundings. (not that I really believe it means much) but SIL will get
the full gist of your situation.  She will need to adjust her home to
accomadate.
You might press then for longer away time {maybe?}
 

 
Lee - 24 Jun 2005 23:12 GMT
we know how she responds to being other places like that anyway - not well
....  they (2 of the 3 girls) tried taking her to a lovely resort for 2 days
more than 2 years ago - and had great difficulty managing her then  (if she
doesn't know where to go pee, she just picks a place...wherever!)

my HOPE is that she will adjust better to a nursing home  than hubby thinks
only because of the fact that she will no longer constantly feel 'all alone'
the way she does in her own home ....  plus, possibly, there would be a
reduction in tension  .... wouldn't be feeding off of my
tension/stress....AND would no longer be living with the constant fear of
doing/saying something 'wrong' and being sent to a nursing home

longer time away really isn't practical, anyway .... we do have a 7 days a
week sort of business... costs us WAY too much to be away for any extended
period of time

in an ideal world, either of the sisters in law would be able to manage her
at their homes once in a while so we could just BREATHE at home .... but if
't'were an ideal world, no one would have alzheimers and none of that would
matter anyway

> Lee....Is it possible to take MIL to her daughter's  home for that
> respite period.  You could find out how she will respond to different
> surroundings. (not that I really believe it means much) but SIL will get
> the full gist of your situation.  She will need to adjust her home to
> accomadate.
> You might press then for longer away time {maybe?}
Evelyn Ruut - 25 Jun 2005 11:42 GMT
> we know how she responds to being other places like that anyway - not well
> ....  they (2 of the 3 girls) tried taking her to a lovely resort for 2
[quoted text clipped - 16 lines]
> but if 't'were an ideal world, no one would have alzheimers and none of
> that would matter anyway

Truer words were never spoken.

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Best Regards,
Evelyn

(to reply to me personally, remove 'sox')

 
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