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I was not being disrespectful of Ray.  I went out of my way to point out I
was sure she was in full control.

No, you are not correct, dementia is not a late stage symptom.  If you start
early it can come on early.  It is not so great a concern when it is late
stage as we expect to see it in older patients to some degree or another.
Since we are talking about the subset of the population that already has PD
then my "one third" assumption is correct.  Your comparison with cancer is
flawed.  A true statement would be x% of cancer patients have x type of
cancer.  There is even a greater number of patients that are plagued with
other symptoms that fall into the "mental health category" some are a result
of the disease and others the result of the medications.  What a strange
balancing act it is to weigh the benefits of the drugs with the side
effects.

Dementia is a scary thing and it is present in a large segment of PD
patients.  Don't play it off so lightly.  Paranoid reactions are also common
to the drugs used to control PD.  Then you have the reactions to the
antipsychotic drugs used to control the psychosis caused by those drugs.
Don't forget the depression that is felt by so many people with PD.  These
are all mental problems related to PD and the drugs taken to control the
symptoms.  Unfortunately we would all feel more comfortable believing that
these conditions are in the minority.  They are not.

And yes I am certain that some responses, personal attacks, paranoid
statements etc posted on this board are in some way influenced by the
unfortunate terrible deterioration of the mental state of many people with
PD or the drugs used to control the symptoms.  If those still in control of
their full faculties would refrain from sparking attacks that may set others
off who are not in full control we would return more quickly to the main
purpose of this board.  Help each other.

Regards

Frank

----- Original Message -----
From: "Greg Wasson" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Wednesday, March 03, 2004 8:45 AM
Subject: Re: I need help. I need hope. I need guidance on dealing with this
terrible...


> Just to be clear Frank,
>
> The statement that "over a third of Parkinson's patients suffer from
dementia that robs them of the ability to communicate, make decisions, think
logically and interface with the world," is wrong, and the correction is an
important one. What is true is that "over one-third of all Parkinson's
patients will eventually suffer from some form of dementia." At any moment
in time far less than one third of PD patients suffer from dementia. It is a
late stage symptom. It would be like saying that one in four people have
cancer when the fact is that one in four will have cancer at some time in
their lives. Big difference.
>
> As for the comment  that "I could not imagine a group making these
decisions and providing all support for themselves particularly if they are
afflicted with a disease that not only robs you of your ability to care for
yourself but also frequently robs you of the ability to think clearly and
make rational and logical decisions. It seems that Ray is still in full
control of her faculties and I am glad of that," I assume that you weren't
being deliberately offensive or patronizing.
>
> Greg
>
> FrankandTeri <[log in to unmask]> wrote:
> Interesting observation Dr. Fink.
>
> It is human nature to believe that no one can possibly feel or understand
a
> condition unless they have experienced it themselves. It is unfortunate
> that someone might feel that way because they isolate themselves from a
> support organization which can help them deal with this disease. It would
> be a terrible day if only people stricken with Parkinson's were supporting
> each other. I could not imagine a group making these decisions and
> providing all support for themselves particularly if they are afflicted
with
> a disease that not only robs you of your ability to care for yourself but
> also frequently robs you of the ability to think clearly and make rational
> and logical decisions. It seems that Ray is still in full control of her
> faculties and I am glad of that. I would not wish the dementia that is so
> common in Parkinson's on anyone.
>
> Come to think of that. Most discussion on this board (at least those that
> are not attacking the president) seem to focus on movement, pain, sleep
etc.
> Somewhere over a third of Parkinson's patients suffer from dementia that
> robs them of the ability to communicate, make decisions, think logically
and
> interface with the world. Give me the shakes, stalls, falls and pain any
> day but let retain my ability to communicate and reason. Does anyone have
> any information on research and treatments focused on controlling and
> improving dementia?
>
> I believe we need each other and all that are willing to help and support.
>
> Regards
>
>
> Frank
>
> ----- Original Message -----
> From: "Robert A. Fink, M. D."
> To:
>
> Sent: Tuesday, March 02, 2004 12:03 PM
> Subject: Re: I need help. I need hope. I need guidance on dealing with
this
> terrible...
>
>
> > On 1 Mar 2004 at 17:36, Rayilyn Brown wrote:
> >
> > > Frank, do you have PD or is it Teri? Ray
> >
> > Careful, Frank, before you answer. One of Ray's usual approaches when
she
> > disagrees with what someone writes is to infer that, if the writer does
> not have
> > PD, their views are disqualified. Especially if they are a big, bad,
> nasty
> > *doctor*!
> >
> > Best,
> >
> > Bob
> >
> > **********************************************
> > Robert A. Fink, M. D., F.A.C.S., P. C.
> > 2500 Milvia Street Suite 222
> > Berkeley, California 94704-2636
> > Telephone: 510-849-2555 FAX: 510-849-2557
> > WWW: http://www.rafink.com/
> >
> > mailto:[log in to unmask]
> >
> > "Ex Tristitia Virtus"
> >
> > *********************************************
> >
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