WOW---WHAT A SCARE!!

The doctor is not always the best solution. Education is. Many of those so
called docs just dont get it. Keeping them in the loop is not always in ones
best interest since trial and error seems to be the choice of so many .
Keeping a journal of reactions and meds can be your best friend when things
just dont seem right.  Many doctors fortunately do understand the Parkinson
"life"  but they seem to be in the minority.

Drugs and their dosages like any other treatment for just about anything
need to be scheduled that only requires common sense and discipline. I'm
still enjoying life everyday.    Rob

----- Original Message -----
From: "Maureen Potts" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Sunday, January 11, 2009 3:37 AM
Subject: Re: question re dosage


> Do not ever, and I mean ever, go off your medications without telling your
> doctor.  You can develop what they call Neuroleptic Malignant Syndrome,
> where your blood pressure goes sky high, you pass out, and worse.  Some
die.
> Drugs for Parkinsons are pretty strong stuff.  You are taking your life in
> your  hands by not being more disciplied about your medications.  You are
> tempted to phase out the drugs because you feel better.  But it is the
drugs
> that are making you feel better.  Trust me, the day will come when you
will
> be infinitely grateful for those drugs.
>
>  My brother bought me one of those big plastic pill boxes with
compartments
> for every day of the week and for a daily schedule.  It helped me remember
> and to take my drugs on time.  You have  to commit to counting and sorting
> for an hour or so a week.  It is well worth it.
>
> Please dont stop your meds without medical advice.  Just remember,
> Neuroleptic Malignant Syndrome.  Sounds awful, and it is.
>
> Maureen Thompson (I have been around, just quiet)
>
>
>
> ----- Original Message -----
> From: "Murray Kastner" <[log in to unmask]>
> To: <[log in to unmask]>
> Sent: Saturday, January 10, 2009 10:24 AM
> Subject: Re: question re dosage
>
>
> >I am afraid I am the laggard of the group and the spacing of my  dosages
> >has been all over the clock. I have been prescribed 25/100  Sinemet three
> >times a day along with 75 mg Mirapex and 5 mg  Selegilene. I also take
> >Flomax CR (1x Day)and Novo oxybutnin (1x day).  1 mg  Folic Acid, calcium
> >2x daily. i am very erratic in taking the  meds, and try to keep to three
> >times a day but no fixed times. And I  usually forget them altogether one
> >to three times a week.
> >
> > I am sorely tempted to give up the meds completely, or to phase them
out.
> > I think I have read that there are cases where the meds  contribute to
the
> > symptoms rather than alleviate them. I also have  osteoporosis for which
I
> > have just completed an 18-month program with  Eli Lilly's new drug,
Forteo
> > wherein I injected myself every morning.  This past week I took a
> > bone-density scan and Wednesday I am hoping to  get the results,
expecting
> > 20-25% increase in density. This may allow  for spinal surgery. which I
am
> > not too crazy about.
> >
> > My worst symptoms are camptocormia which means I cannot straighten
myself
> > when standing or walking. I can lay down perfectly straight and
> > semis-straight when sitting. But the camptocormia has brought on
> > shortness of breath, especially if I walk without a walker. It has  been
> > suggested that my bent-over posture has been crushing my lungs  and so I
> > also now have a 'puffer' 3x a day.
> >
> > I am growing weary and am tempted to give up all the meds and see what
> > happens. Before I do that I will enquire as to the consequences.
> > Fr'instance: can the PD and accompanying symptoms get worse with no
> > returning to the meds to regain the balance I have now?
> >
> > I will discuss this with my neuro at my next visit -- scheduled every
4-5
> > months. since 1998 the only deterioration I have experienced is  the
> > damned camptocormia, apparently a rare condition which my neuro  (one of
> > two movement disorder specialists in Montreal) has seen only  in 3-4
> > others. He feels it may have been triggered by a fall I took a  couple
of
> > years ago which crushed 1-2 vertebrae when I landed on my  coccyx.
> >
> > Phew! Thank you for bearing with this. I have probably left out even
more
> > meds, like the anti-depression pills (150 mg) bupropion SR.
> >
> > Every once in a while I wonder whether I really have PD or whether it
is
> > something with similar symptoms.
> >
> > Anyway I think I have rambled on enough and will appreciate input from
> > anyone in a similar situation.
> >
> > Murray
> >
> > Ray,  I received the pins and they are already being displayed all  over
> > Montreal. Thanks!
> >
> >
> >
> > On 6-Jan-09, at 6:33 PM, rayilynlee wrote:
> >
> >> I recently got some carbo/levo from my neuro to try once more.  When  I
> >> first tried it it helped but never again even tho I took it for a
year.
> >> He gave me 25/100 3 times a day and I've forgotten how you  space the
> >> dosages.  Do you take it at night or just daytime?  I've  forgotten.
in
> >> 2003 I had DBS and tried  Comtan and Stalevo  afterwards but it didn't
> >> help.
> >>
> >>
> >> Ray
> >
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