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Reply | Forward Message #4023 of 4129 |
Re: Also new

lost the continuation too !! ,,,, nothing great I am doing ok and have faith in
the theorpy.

Harry

--- In dysosmia@yahoogroups.com, "harryony1" <harryony1@...> wrote:
>
> Well, here it is and I did just get back from a 23 state tour of the USA with
8750 miles of driving and 2075 nautical miles (Caribbean Cruise) on the great
Atlantic.
> We left the great Northeast USA on Feb 17 and visited Dr. Harkin on the 19th,
a scheduled appointment. I took my daily report sheets which indicated how I
was smell/tasting for the previous several months from my first meeting,
percentage wise to what I thought. Update: apparentyly I was not at 0 when
first diagnosed, as I called it a sensation. These sensations are taste/smell
but unable to identify what I was eating. The sensations were still there,
however, now I have these distortions that made bad smelly things the object of
a dinner craving???? WOW I think I blew the ole doc away when I suggested that
a flavor that was "something really bad" would have been a favorable meal. :)
Well it certainly answered a few questions for me.
>
> to be continued!! ( I have posted prior to this and lost lenghty post)
>
> --- In dysosmia@yahoogroups.com, "O'Hare, Mick (RBI-UK)" <Mick.O'Hare@>
wrote:
> >
> > Back last week Harry. Hopefully you've missed the worst of the winter.
> >
> > M
> >
> > > ----------
> > > From: dysosmia@yahoogroups.com on behalf of Harry O
> > > Reply To: dysosmia@yahoogroups.com
> > > Sent: Monday, February 16, 2009 2:43 PM
> > > To: dysosmia@yahoogroups.com
> > > Subject: RE: [dysosmia] Re: Also new
> > >
> > > Sure thing Mick. Arn't you there now for business, if I recall
correctly.
> > >
> > > H
> > >
> > > --- On Mon, 2/16/09, O'Hare, Mick (RBI-UK) <Mick.O'Hare@> wrote:
> > >
> > >
> > > From: O'Hare, Mick (RBI-UK) <Mick.O'Hare@>
> > > Subject: RE: [dysosmia] Re: Also new
> > > To: dysosmia@yahoogroups.com
> > > Date: Monday, February 16, 2009, 4:46 AM
> > >
> > >
> > > Harry, let me know how your DC visit goes
> > >
> > > Mick
> > >
> > > > ----------
> > > > From: dysosmia@yahoogroup s.com on behalf of harryony1
> > > > Reply To: dysosmia@yahoogroup s.com
> > > > Sent: Sunday, February 15, 2009 11:06 PM
> > > > To: dysosmia@yahoogroup s.com
> > > > Subject: [dysosmia] Re: Also new
> > > >
> > > > I just knew one of the smells I get was something I used in my
> > > > lifetime and you made that happen. Thank You. Playdough, duh!!
> > > > Right now I am continuing the fried onion smell that I cooked 3 days
> > > > ago, which is very strong. They did agree it was strong while I was
> > > > cooking them but presnetly they can not smell onion anymore. Oh
> > > > Well !
> > > > The first ENT you went to, was just as insensitive as mine, however
> > > > he did 87 more discoveries then mine. Mine just said "you should
> > > > have it back in 12 months or less" and that was 2 years ago!! Of
> > > > course that was after the ct, mri, and poking a rod up my nasel
> > > > passage.
> > > > Use the saline rinse and it should help with the odors.
> > > > I believe that I am at the stage you are in but I came from ZERO, so
> > > > anything I can smell/taste now is a holiday ;). Few and far inbetween
> > > > but never-the-less still a happening even if it is at 25 percent.
> > > > I am visiting Washington D.C. for my second appointment with Dr.
> > > > Henkin this thursday and will update from there.
> > > >
> > > > Good Luck
> > > > Harry
> > > >
> > > > --- In dysosmia@yahoogroup s.com, "Jeannie" <jeanjeannie@ ...> wrote:
> > > > >
> > > > > Hello to all. I've been reading posts on this for quite some time -
> > > >
> > > > > but only became a member today. I wanted to thank those who have
> > > > > taken the time to share their story...as it provides insight to me
> > > > > (and how to apply to my personal case). While everyone's story and
> > > > > perspective is unique, it's good to know that there are others who
> > > > > provide support.
> > > > >
> > > > > As for me, my symptoms began in 5/2008. I'd been diagnosed in
> > > > > February with RSV and told to wait it out. In early May I
> > > > > experienced such terrible congestion - I could barely function. I
> > > > > had used Flonase (combined with Allegra-D) in the past for
> > > > allergies,
> > > > > so my physician suggested to try Flonase again.
> > > > >
> > > > > Admittedly, it's difficult to determine the exact cause of the
> > > > > onset...whether it was due to the URI, or the Flonase. There was
> > > > one
> > > > > time where I used it and experienced a radiating pain on the left
> > > > > side of my head and face. Within days, I noticed that I could
> > > > barely
> > > > > smell anything.
> > > > >
> > > > > As of now, there are still odors/vapors that I cannot smell - while
> > > > I
> > > > > can distinguish that the odor of the air changes...I cannot
> > > > > distiguish a specific scent associated with it. For quite some
> > > > time,
> > > > > this was the same with all odors, but some have improved over time.
> > > > >
> > > > > In the summer of 08, the absence of smell changed for many odors
> > > > for
> > > > > me. Detergents and shampoos smelled of asphalt (if the detergent
> > > > or
> > > > > shampoo was non-floral, berry scented). Coffee, urine, body odor,
> > > > > diesel fuel, extreme skunk were also categorized as my "bad smell",
> > > > > which smells of chemicals, rotting flesh, playdough and burnt >
> > > > > coffee. In truth, this was (and continues to be) the most
> > > > > disconcerting for me.
> > > > >
> > > > > In September, I visited my Neurologist who referred me to an
> > > > > ENT...which was a miserable experience. He had me sniff upwards of
> > > > > 85 scratch and sniff cards and put salt and sugar on my tongue. He
> > > > > said that since I only missed 5 - that I should get over it.
> > > > >
> > > > > Initially, I felt deflated, as I consider myself to be the opposite
> > > > > of a hypochondriac - and I felt rather insulted. More recently,
> > > > I've
> > > > > seen a different ENT who seems open to entertaining my symptoms and
> > > > > has scheduled a sinus CT scan this week.
> > > > >
> > > > > Admittedly, there are times when it feels like I'm living life with
> > > > > the lights half on - however I have experienced some relief. The
> > > > > asphalt smell has diminished quite a bit. I can smell things now >
> > > > > that I couldn't six months ago. Sometimes it depends on the day.
> > > > > There are things that I still cannot smell at all (garbage), and
> > > > > there are times when the bad smell becomes overwhelming.
> > > > >
> > > > > Nonetheless, I feel happy to have stumbled upon this group - as
> > > > it's
> > > > > provided ideas and clinics to visit - and most of all a glimmer of
> > > > > hope.
> > > > >
> > > > > Thanks,
> > > > > Jeannie
> > > > >
> > > >
> > > >
> > > >
> > > >
> > > >
> > >
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Wed Apr 15, 2009 12:13 am

harryony1
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Message #4023 of 4129 |
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so here is this rich text editor that I just noticed??? will it let me post??? two continuations lost .... site has a problem I think!!!! ... USA with 8750...
harryony1
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Apr 15, 2009
12:15 am

lost the continuation too !! ,,,, nothing great I am doing ok and have faith in the theorpy. Harry...
harryony1
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Apr 15, 2009
12:14 am

Well I didn't use the beta for the second post but it took and now that is how I am getting it done. continuation: Nothing special , I am doing ok mentally...
harryony1
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Apr 15, 2009
12:17 am

Hi Harry Nice to have you back. Stick with the treatment! Mick...
Mick O'Hare
Mick.O'Hare@...
Send Email
Apr 20, 2009
8:48 am

I was disappointed in the lack of postings.. Please don't give up people!!! If any of you have regained any part of your sense, please share it with us so we...
harryony1
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Apr 20, 2009
1:33 pm

Hello everyone... It has been awhile since I posted anything. This site gave me so much information and hope, after I lost my sense of smell. It let me know...
DANNA FRANKS
df8484
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Apr 20, 2009
2:35 pm

Dana, The only treatments you have had are steroids and using the netti pot?? Harry...
harryony1
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Apr 25, 2009
8:52 pm

Hi all , here is my two pennies worth : I am currently one sodium valproate tablets , and had been for now a month , and it seem to be working great with only...
Luke Sampson
lukesampson78
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Apr 20, 2009
4:46 pm

Luke - what are your symptoms? Are you just experiencing anosmia or do you suffer from parosmia or phantosmia? anne christie...
Anne
christie5519
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Apr 21, 2009
10:14 pm

Hi Anne , I have been diagnosed with Cyclical Parosmia by the ENT Hospital in London! Here are my symptoms , i have cheated slightly and copied this from an ...
Luke Sampson
lukesampson78
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Apr 21, 2009
10:25 pm

Hi Luke, I know you are on vacation. I just don't think sodium valproate will help you. I was put on that for a year for phantosmia and it did nothing. I...
Anne
christie5519
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May 4, 2009
10:52 pm

Hi Anne Thanks for the message, if I am honest I am confused ! , I know Mick will agree it doesn't take much!! When I emailed Dr Henkin , he replied back and...
Luke Sampson
lukesampson78
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May 12, 2009
7:02 pm

* Parosmia -- distorted sense of smell * Phantosmia -- olfactory hallucinations With parosmia there is a chemical substance that normally produces a certain...
Wuensch, Karl L
klwuensch
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May 12, 2009
9:26 pm

See reading that (Call me thick) , i am not entirely sure what i have got ! One doctor is saying one , and the other doctor is saying the other ! Argghhh...
Luke Sampson
lukesampson78
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May 12, 2009
9:34 pm

Hi Luke I reckon treatment will be very similar, yes. Mick ... I ... month ... my ... mg ... of ... the ... r===================== DISCLAIMER...
Mick O'Hare
Mick.O'Hare@...
Send Email
May 13, 2009
8:50 am

Mick, I have to disagree with you on this. Marjorie and I discussed your posts about parosmia vs phantosmia. They are very different disorders and they are...
Anne
christie5519
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May 17, 2009
6:20 am

Hi Anne I am still confused whether i have parosmia or phantosmia , and am not big on technical/medical words. Emailing Dr Henkin he says i have phatosmia ,...
Luke Sampson
lukesampson78
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May 17, 2009
8:12 am

Luke, as a former patient of Dr Henkin's (though not a fan of his) I'm guessing he would recognize a case of phantosmia if he heard it described to him. I had...
Anne
christie5519
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May 17, 2009
4:09 pm

Yes I did explain my symptoms to Dr Henkin and he went with phantosmia , after I said I was from the UK and needed to find out cost, but he couldn’t give...
Luke Sampson
lukesampson78
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May 17, 2009
4:43 pm

Hi Anne Sorry for the delay in replying...... i had a letter back from the hospital in London today which was sent to my doctor , I was CC’ed/ Saying ,...
Luke Sampson
lukesampson78
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Jul 13, 2009
7:27 pm

Luke. You definitely have parosmia, that¹s the term that covers ALL distortions, so Dr Lund is correct. What type is the question. If you smell weird stuff...
Mick O'Hare
Mick.O'Hare@...
Send Email
May 18, 2009
8:25 am

Happy to bow to your greater knowledge Anne. Thanks Mick ... in ... and ... am ... an ... me! ... normal ... it can ... me to ... and ... to ... always ... do...
Mick O'Hare
Mick.O'Hare@...
Send Email
May 18, 2009
8:18 am

Hi Luke/Anne Officially parosmia is a wide-ranging term to describe any type of distortion in olfaction. Phantosmia (while still being a parosmia) is more ...
Mick O'Hare
Mick.O'Hare@...
Send Email
May 13, 2009
8:48 am

Luke You are being treated in England I guess and with one theropy? Sodium valproate ?? What is that? Would you expand on that for me please?? tks Harry...
harryony1
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Apr 25, 2009
8:53 pm

Hi Harry sorry i am on holiday at present but will reply in more depth later J Luke From: dysosmia@yahoogroups.com [mailto:dysosmia@yahoogroups.com] On Behalf...
Luke Sampson
lukesampson78
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May 4, 2009
5:06 pm

Man, I am suffering from this disease. Today it has been very rough. Terrible in fact. Mark Nichols From: dysosmia@yahoogroups.com...
Nichols, Mark
tiodiego2004
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May 4, 2009
7:55 pm

Hi Sorry Harry what is it you wanted to know ..... e.g what sodium valproate is ? I am being treated through the Royal Ear Nose and Throat Hospital in...
Luke Sampson
lukesampson78
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May 12, 2009
6:43 pm
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