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Dear Ray

Moneesha has a good point. If your CG goes to your place only twice a week, then she has no excuse to be inefficient in her work. Seems like she has taken you for granted.

Since you have written to her a good explanation regarding your condition (especially your speech difficulty), you have a good reason to find another CG if the present CG does not understand you.

I suggest that when you get a new CG, show her what you wrote for Kathy. Right from day 1, explain to her that you have speech difficulty and prefer to communicate through the computer.

Please keep us updated on your progress.

NK



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Subject: caregiver woes
Date: Sun, 27 Dec 2009 11:49:37 -0700








thanks so much for your commentary
 
NK - a "heart to heart" is great if you can 
talk.  I can only do  2 and 3 word answers.  Here is what I wrote 
to Kathy, my CG
 
 
"I think we need to try communication by my using 
the computer as it is becoming more and more difficult for me to speak.  I 
may get so I can't speak at all.
 
Every time I try to speak I feel like I am 
strangling.   It is impossible to modulate the tone of my 
voice.
 
People with Parkinson's are told to "speak louder" 
and doing so does not help as it gives you the impression that I am angry.  
I know that this really bothers you and I wish you wouldn't take it so 
personally.  More than that I wish I could get my life back but I will only 
get worse.  I don't know how I can make it easier for you.
 
Yes, I wish we could talk things over.  I'm 
willing to  listen."
 
I'm thinking my difficulty is something like 
Tourette's Syndrome in that unwanted sounds come out.  Imagine how you 
might sound trying to talk while being strangled.
 
Angela,  I am not suggesting Margery goes 
through the same thing I do, everybody is so different.  Also, I have 
a good friend who really tries to understand but persists in questioning 
me.  It is impossible for me to know what other Parkies 
experience  or what I will experience as the disease advances.
 
NK, I know Kathy has an unsatisfactory home 
situation, living with her daughter and her family's unscheduled life and it is 
why I have agreed to her coming whenever she can, twice a week and I store her 
stuff as she has been put in a smaller space.   Oh, she is 
also hard of hearing.
 
Moneesha, you certainly understand where I have 
gone wrong.  It should be a professional relationship from the 
beginning.  Too bad I have to learn "on the job" (but who knew she'd throw 
out Mom's ashes), but I should have known from teaching that the rules need to 
be clear from the start.  I gave her a list of chores and left her alone. 
Your observations should be heeded if someone is about to get in-home 
help.
 
My Mom once had a CG who rearranged ALL her drawers 
and cabinets, but the upside was she was a neatnik and kept things super 
clean.
 
Linda, yesterday I emailed "Alternate Homecare" in 
my area so I could start looking into getting a replacement.  You're right, 
I'm not shy about my opinions, but it is not so much about what I say as how 
I  say it.  And I have scared off some crank telephone 
callers.
 
Thanks so much, everyone.
 
Ray 
 
 
 
Rayilyn Brown
Director AZNPF
Arizona Chapter 
National Parkinson Foundation
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