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Dear Laura,
I am 55 will be 56 in August. I have had PD for 5 and a half years, I am
doing well and so you will too, read as much as you can and learn as much as
you can on this. Welcome to the list there are a lot of good people here.
You will have good days and bad ones just roll with them and have a bright
out look on it and you will feel better. Janice
----- Original Message -----
From: Laura Kreisler <[log in to unmask]>
To: <[log in to unmask]>
Sent: Friday, February 21, 2003 8:31 PM
Subject: New List Member


> Hello,
>
> I am Laura, I am a 47 year old accountant with two grown children and a
> beautiful grandson, and I was diagnosed with PD four months ago.  I have
> however, had symptoms for five years and I suppose I wanted to be able to
> deny that there was a real problem.
>
> For the last three years my family physician was treating me for essential
> tremor (common among PWP I now read.)  This last year I have begun to have
> many symptoms that I did not realize were related.  I spent most of the
year
> thinking "I'm not that old, I can't be having this many problems."  My
> husband has been quite distraught about the tremor and then the dragging
> foot and I finally asked the Dr. "I know the two are not related to each
> other, but my husband wanted me to ask?"  He then asked if I wanted to go
to
> a Neuro and I said I guess it would make my husband happy.  I was sure
there
> wasn't anything really wrong, just many little things.
>
> When the Neuro told me she suspected I had PD, I remained very calm.  And
> even after her many tests and the confirmation that I have PD I did not
> think much of it.  I also didn't tell anyone except by immediate family.
> Finally at New Years we decided to tell our extended family, some friends
> and my co workers.  Once I told people it really hit me hard  and I guess
I
> have finally accepted it.  The worst part is that in accepting the reality
> of PD I have become much more stressed and the symptoms are much more
> pronounced.
>
> I am happy to join the list so that I can "hear" what other PWPs have to
say
> and how you are all dealing with PD.  This is probably the most I have
> "spoken" about it.
>
> Thank you for allowing me to be included in the list.
>
> Laura
>
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