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Raj,

I was interested in your comments about celebrex.

How much celebrex are you taking?  And how quickly does it work for you?

  Eileen

----- Original Message -----
From: "Brightline" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Friday, February 27, 2004 10:02 PM
Subject: Re: Focus Needed... Pain & PD


> Hi Shirley:
>     We are just comparing notes. If there is a higher percentageof people
> first diagnozed with hyothyroidism (or hyperthyroidism), this may indicate
> that malfunction of thyroid and the accompanying chronic fatigueness could
> be taken as a warning as to what might follow. So also is the chronic pain
> phenomenon.  So far nobody attributes these as probable early symptoms of
> the oncoming manifestation of PD.
>     At least in my case, I am fairly confident that this is so.
>     I am just stating my personal expereince and am trying to rationalize
> what might be going on in my body. For example, as soon as I take
celebrex,
> not only my pain disappears, so do all the other symptoms of PD including
> tremer, bradykinesia, and even postural instability.
>       Celebrex is an antiinflammatory agent, and is a COX-2
(Cyclo-oxigenase
> 2) inhibitor.  It can pass through the blood brain barrier. For the
> progression of PD, COX2 function is required. If you can inhibit it, could
> we slow the progression of PD?
>     I personally think, we can.  Celebrex is relatively safer than other
> non-steroidal antiinflamation drugs (NSAIDs)  to consume.  I have started
> taking it whenever I have pain, because I do not have time to wait for the
> results of a doubleblind study, which nobody has even undertaken yet. For
me
> it is important to save my neurons from dying right now and I shall do
> anything to stop them from doing so.  Because, once we lose them, it is
very
> difficult to make fresh ones (More on this later).
>     I am just sharing my experience.  I am not giving any advise nor I am
> qualified to give one. When you see your doctor next time, you can ask
> her/him about this, if you like.
>     Raj
> **********
> ----- Original Message -----
> From: "Shirley Lund" <[log in to unmask]>
> To: <[log in to unmask]>
> Sent: Thursday, February 26, 2004 2:50 PM
> Subject: Re: Focus Needed... Pain & PD
>
>
> > i just read several entries that folks were diagnosed with
hypothyroidism
> > around the time they were diagnosed with pd.  so was i...this must be
> > common?  shirley
> > ----- Original Message -----
> > From: "Brightline" <[log in to unmask]>
> > To: <[log in to unmask]>
> > Sent: Wednesday, February 25, 2004 9:42 AM
> > Subject: Focus Needed... Pain & PD
> >
> >
> > > David:
> > >     Thanks for sharing your experience.
> > >     If we share our experiences like this, we probably should be able
to
> > get
> > > a better handle on the various symptoms that might forewarn what is
> coming
> > > next to haunt us like PD or anything for that matter.
> > >     PD as far as I know  is still diagnozed by the common symptoms
such
> as
> > > tremor, micrographia (?) or small handwriting,
> > >    dystonia, bradykinesia, postural instability etc.  These are
probably
> > the
> > > symptoms that were used to recognize this disease originally by Dr.
> > > Parkinson himself.
> > >     Unfortunately, by the time one begins to show the physical
symptoms,
> > we
> > > have lost about 70-80% of the dopaminergic neurons!  Once this has
> > happenned
> > > it is very difficult and time consuming to regain the dead neurons by
> the
> > > neuroregeneratve process that is constanly going on in our body.  As
the
> > PD
> > > progresses more and more neurons are dying not only because of PD but
> also
> > > because of aging. This makes it tough on our body to regain the lost
> > > neurons.  Therefore I think it is very important that we should be
able
> to
> > > recognize the disease early and help regeneration of the endogenous
> > neuronal
> > > stem cells, which will help retardthe progression of the disease.
> > >     More on this later.
> > >     Raj
> > > ************
> > > ----- Original Message -----
> > > From: "DAVID LEWIN" <[log in to unmask]>
> > > To: <[log in to unmask]>
> > > Sent: Tuesday, February 24, 2004 8:24 AM
> > > Subject: Re: Focus Needed... Pain & PD
> > >
> > >
> > > > To add to the list, I too was first diagnosed with hypothyroidism.
> The
> > > > synthyroid greatly reduced my fatigue for a while.  But then I was
> > > diagnosed
> > > > with PD, and that shifted my focus.   We need to know more obviously
> > about
> > > > the autoimmune response.  David
> > > >
> > > >
> > > > >From: Brightline <[log in to unmask]>
> > > > >Reply-To: Parkinson's Information Exchange Network
> > > > ><[log in to unmask]>
> > > > >To: [log in to unmask]
> > > > >Subject: Re: Focus Needed... Pain & PD
> > > > >Date: Thu, 19 Feb 2004 11:34:28 -0400
> > > > >
> > > > >My experience was slightly different.
> > > > >I was diagnozed with hypothyroidism and started taking synthroid.
> This
> > > > >eliminated my fatigue for a while.  But, my pain took over my
> > attention.
> > > > >After a few years I was diagnozed with PD. As a hindsight, I now
> > strongly
> > > > >believe that if I had controlled my pain early enough, I would have
> > > slowed
> > > > >the prgression of PD.
> > > > >Raj
> > > > >*********
> > > > >----- Original Message -----
> > > > >From: "Wendy Siegel" <[log in to unmask]>
> > > > >To: <[log in to unmask]>
> > > > >Sent: Wednesday, February 18, 2004 2:19 PM
> > > > >Subject: Re: Focus Needed... Pain & PD
> > > > >
> > > > >
> > > > > > I see some commonalities between your wife's experience and my
> > > > > > husband's, things that may or may not be coincidence.
> > > > > >
> > > > > > You wrote:
> > > > > >
> > > > > > "Does anyone else have any information that draws any
correlation
> > > > > > between
> > > > > > inflammation, autoimmune disorders and PD?  ...  The first is
> > > > > > where the Thyroid is attacked by the autoimmune system
eventually
> > > > > > causing it
> > > > > > to underperform."
> > > > > >
> > > > > > My husband has recently developed a goiter. That was what
> eventually
> > > led
> > > > > > me to diagnose his PD. After researching it and other symptoms
on
> > the
> > > > > > web, I got the diagnoses down to hyperthyroidism or PD. The
> thyroid
> > > > > > doctor said all was normal, that's when I knew it was PD. He
said
> > they
> > > > > > don't know the cause of the goiter. Rich still has it, some days
> it
> > is
> > > > > > larger than other days. So far, we can't determine what affects
> it.
> > > > > >
> > > > > >
> > > > > > You wrote:
> > > > > > "A great side effect during the course of treatment was an
almost
> > > > > > total elimination of her asthma symptoms (reduction of
> inflammation
> > in
> > > > > > lungs).  Since we have stopped the steroids it seems she is now
> > > > > > experiencing
> > > > > > more pain."
> > > > > >
> > > > > > Rich had asthma as a child, and has in the past used steroids.
He
> > > hasn't
> > > > > > had problems with asthma in years though.
> > > > > >
> > > > > > Wendy
> > > > > >
> > > > >
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