Boydette,
Mine doesn't have the laugh but she has this nasty taunting voice that
just makes me feel like screaming. Why do they continue to be able to
press our buttons?
I'm totally convinced dealing with a spouse with AD is far easier then a
parent because there''s so much more baggage to contend with.
raven
> I have called and talked to people agencies and senior services til my
> face is turning blue...NO ONE will help NO ONE has any solutions....my
> mom is out of her mind and shouldnt be living alone...but she angers me
> so with her evil little comments and she has this laugh that makes your
> skin crawl....(ANYBODY remember Bette Davis???)...LOL..
Just pray that you go into a mental coma.It's either that
suicide, being permanentyly high on drugs or continuosly bombved out of
your bra9n ob booze. There's no chance of peace otherwise. You are SO
RIGHT ABOUT THE HELP AGERNCIES THEY DON'T GIVE A F**K .
My wife's not like your mum she's a good person but i am so f**ked inmy
head with all the hurt and the rejection and ebeing scared with this
permanetn war zone in my head and yet they all think i can cope with the
very minimum of help.

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Tumbleweed - 06 Feb 2005 11:50 GMT
>> I have called and talked to people agencies and senior services til my
>> face is turning blue...NO ONE will help NO ONE has any solutions....my
[quoted text clipped - 11 lines]
> permanetn war zone in my head and yet they all think i can cope with the
> very minimum of help.
No one, repeat no one, repeat absolutely no one, can look after someone with
severe Az 24 x 365. It isnt possible, eventually you'll crack. I suspect
that if you say she needs to go into a home, and you are giving up, you'll
suddenly get a lot more help. There was family in the UK a few months back
who just left their father at a hospital because they said they couldnt get
the help they needed. All ofa suden it seems the social services could give
the help. I'm sure this wasnta one-off.

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Tumbleweed
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tumbleweednews at hotmail dot com
Evelyn Ruut - 06 Feb 2005 11:56 GMT
>> I have called and talked to people agencies and senior services til my
>> face is turning blue...NO ONE will help NO ONE has any solutions....my
[quoted text clipped - 11 lines]
> permanetn war zone in my head and yet they all think i can cope with the
> very minimum of help.
TJ, nobody can cope with this illness with "a very minimum of help"..... It
is a devastating awful disease and it wears the caregiver down in ways that
cannot be described. You need ALL the help you can get and then some.
My husband and I worked together at caring for my mother in law, but both of
us were still depressed and exhausted all the time. We barely managed to
get anything else done because it is so exhausting. He took the "night
shift" getting up with her every time she needed to use the toilet, guiding
her back to her bed, cause she didn't remember which was her room sometimes.
He had to make sure she didn't have a wet "depend" when she went back to bed
each and every time. She'd remove it sometimes and then wet the bed, so
you had to watch her to be sure she got back in bed OK.
Having that continually broken sleep, left him cranky and sleep deprived.
I took care of most of the day duties, and that meant meals, dressing and
undressing, etc.
But in reality both of us were on duty all the time and we were BOTH
zombiefied. Those three and a half years were like a blur. No social
life to speak of, and too tired to enjoy it when there was.
Please get all the help you can. Don't give up, keep on looking and asking
for help. Going through the caregiving experience alone has to be one of
the hardest things anyone can do.

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Regards,
Evelyn
(to reply to me personally, remove 'sox")
We sought help also, and felt like we were beating our heads against a
wall. Nobody would help
Has your mother been diagnosed with alzheimers? Would her doctor write a
letter stating her condition? A lawyer might be able to help you get
guardianship.