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Medical Forum / Diseases and Disorders / Alzheimer's / July 2004

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Namenda & John

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Char - 09 Jul 2004 04:30 GMT
Dear Friends,

I think the last time I wrote I told you that John had been switched
back to 10mg of namenda as the 10 twice a day was too much---

In my opinion, the namenda probably made John worse in the long run
because he once again became really aware of what has been happening
to him.  He decided almost two weeks ago to quit all of his meds.
Been there, done that.  The old-timers will remember me writing about
sneaking meds into his food or drinks when we lived  in PR.  This time
I have decided to just do what Frederick did with June ----let it go &
let everything run its course.

I can see him getting worse but he did tell me today that this is what
he wants----he loves me &  he gave me a big hug.  This meant a lot to
me because I was beginning to think he was  really angry with me &
just taking frustaration out on me.  I know now what I really knew all
along: it is the disease when he gets "snappy"  but it still hurts.

I have found a local AD support group & will go to my first meeting
next week.  They can't possibly be better than this group but I will
be out of the house & talking to others.

Always,

Char
Evelyn Ruut - 09 Jul 2004 12:04 GMT
> Dear Friends,
>
[quoted text clipped - 22 lines]
>
> Char

Dear Char,

You will be surprised at how great a local support group can be... I know I
was.   Good Luck and I hope you get as much out of your local group as I
have!
Signature

Regards,
Evelyn

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

Darryl - 09 Jul 2004 13:57 GMT
>I have found a local AD support group & will go to my first meeting
>next week.  They can't possibly be better than this group but I will
>be out of the house & talking to others.

Hi Char,

We can't *really* see your tears in cyberspace so some one-on-one will
be good.  I'm glad that John is lucid enough to convey his wishes to
you and that you correctly understand that it's not anger.  Otherwise
I'd have to believe that *my* Dad really did think I was queer.  ;-)

Take care,
Darryl.
Adelle D. Stavis, Esq. - 10 Jul 2004 16:11 GMT
{{{{{Char}}}}}

Wishing there was a way to make things easier on both you and John.

It's hard to decide to stop medicating. Watch John's anger, though. It
becomes easier for them to lash out physically. If he starts going in that
direction, do what you need to in order to protect yourself, even if it
means hiding meds in his food again.

When my FIL's meds weren't balanced just right, he was violent enough to be
placed in the hospital mental ward.
Signature

Adelle D. Stavis, Esq.

> Dear Friends,
>
[quoted text clipped - 22 lines]
>
> Char
Mare - 15 Jul 2004 02:28 GMT
Hi Char,
We stopped my Mom @6mg daily of Exelon because she also was much
more aware of her deficits. It was heartbreaking to watch her
reactions when she knew something was wrong. But the Dr at the NH
upped her dose to 12mg daily without telling us a year after she
went into the NH. I've got to say now I'm glad since she still
smiles at us even tho she is so late stage. So maybe later
depending on the circumstances you might want to up it again.
Signature

Mare
mfcoleman@THEOLEmindspring.com
http://www.muggsmulcher.com/kstuff/a.s.a/intro.htm
alt.support.alzheimers' FAQs and Stuff Pages

> Dear Friends,
>
[quoted text clipped - 22 lines]
>
> Char
 
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