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HI Norma,

I agree with others that persistent abnormal smells are common in PD.  I had them
in fact prior to actually being diagnosed!  At the same time loss of sense of
smell is also common. I have had both, but I didn't find out how common a symptom
it was(or that it was related at all to PD) until I joined the list

I disagree with Janet that you ought to consider dumping your MD if he didn't know
about that as a symptom of PD however.  If he is otherwise competent. it is a
common although largely unwritten about symptom that can and does occur.  While it
may indicate some inexperience with PD- unless he/she is giving other indications
that he is not knowledgeable about more major aspects of PD I would let it go
by.    I know a number of neurologists that do(did) not know about that symptom
and are otherwise competent. Also In all my experience with PD specialists I never
have been asked that as a diagnostic question in spite of the symptoms prevalence.

Charlie

"J. R. Bruman" wrote:

> Paul Myhre wrote:
> > My name is Norma Myhre and new to the PARKINSN list.  I started having
> > tremors 3 1/2 - 4 years ago and was diagnosed with PD this past March.  I am
> > a participant in a 2 year study and I am taking either Sinemet or
> > Ropinirole.  The tremors seem to be mostly under control but am having
> > trouble with cramping in my arms, hands and slightly in the legs, sleepless
> > nights and achiness.  Thank you all for sharing information on these
> > problems and others.
> >
> > I have an odd problem in that I have experienced a persistent abnormal smell
> > for the last 2 1/2 years.  No one  in the family, friends, and especially
> > those who claim to have a very keen sense of smell can detect the odor.
> > After CAT scans, x-rays and other tests of the sinuses and nostrils, I was
> > told it was something I probably will have to live with.  I even went to a
> > hypnotist without any help.  Very frustrating!  In reading the "The PDF
> > NEWS" Fall/Winter 1998-1999 issue under "Mary's Mailbag" on page 14 there is
> > an article "What's That Smell?".   It says "We've heard from some PWPs
> > who've lost their sense of smell, from others who complain of persistent
> > abnormal smells, .........".  Last Monday I sent an e-mail to the PDF
> > Organization asking for help but have not heard from them.  I have also
> > asked for help from the neurologist but to no avail.
> >
> > Any information or referrals you might have will be greatly appreciated.
>
> It sounds a bit odd but I too have had olfactory hallucinations (not
> recently or often). The sensation was a kind of "chemical" odor related
> to, but unlike, turpentine, toluene, benzole, etc. that I knew weren't
> really present. I thought hallucinations came with the various dopamine
> agonists for PD, but I don't take any. Cheers,
> Joe
> --
> J. R. Bruman   (818) 789-3694
> 3527 Cody Road
> Sherman Oaks, CA 91403-5013

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Charles T. Meyer,  M.D.
Middleton (Madison), Wisconsin
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