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----- Original Message -----
From: "David Moreland" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Saturday, June 29, 2002 10:55 PM
Subject: Re: David Moreland and DBS surgery


> At 08:44 PM 6/29/2002 -0400, you wrote:
> >Dear David,   My experence with DBS-STN was  okay.  the surgery took
> >away my most bothersome symptom, painful dystonia involving the entire
> >left side of my body from head to toe.              the pallidotomy I
> >had in 1998 was far superior in taking away most of my symptoms  Each
> >persons experience with PD and its medical and surgical treatments is
> >different.  I'm curious,David, how long have  you had PD? when did you
> >the pallidotomy?   Diane
> >
> >----------------------------------------------------------------------
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>
> Diane, I first noticed some of my PD symptoms in 1987 I was diagnosed in
> early 1988.the doctor was cor.myrect in his diagnosis but he was
> incompetent.I had the pallidotomy in august of 1995. THat was the best
> thing that I ever expriemnced. It took me from the hellish dyskinesia i
was
> experiencing to an almost normal life. I am now taking a ton of PD meds
and
> little by little they are starting to fail to do the job.
> I was 44 when i noticd symtoms and 45 when diagnosed. I am 59 now..
>
>
>
> Yours and His
>
> David L.Moreland
>
> ----------------------------------------------------------------------
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Just thought I would jump in here with my DBS results.    I also had a
palidotomy--mine was in 1996.  At the time I didn't think it had
accomplished very much but looking back on it I think it helped more than
I realized.  Chiefly, it did away with the terrible jerking and it also
served as a sort of plateau when I didn't get any new symptoms for a couple
of years.  That surgery which I had done in Toronto by Dr. Lozano was a
piece of cake compared to the DBS which was done at Cleveland Clinic by Dr
Razai.  I liked both my surgeons and thought both of them were very skilled.
It seems to me that the DBS is more taxing on the patient--at least I did
not react as well.  After the initial surgery I was  hospitalized for a week
and waited 3 or 4 additional weeks for the implementation of the generators.
Last Tuesday we finally got down to the process of getting them set and
finding how much improvement had been realized.  Next, I will see a Buffalo
doctor who will build on these initial settings.  I really have just two
improvements so far--my freezing when I walk has been eliminated (I don't
walk well and I still need my walker but it doesn't take me as long to get
somewhere) and  can get out of a chair easier.  I am looking forward to some
hand improvements also.

If you  have any questions please ask

Joan Holliday
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