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Hi Everyone,

That greeting seems a little awkward, but I copied it from the

listmaster , so I guess it's ok.

First the basics:male, age 54,married,two kids,eighteen and

thirteen.Psoriasis symptoms started

about age thirty or so, mostly confined to the scalp which is the most

annoying.I also have a small

amount on the knees and elbows.I have been using Dovonex ointment and

Nizoral shampoo for

the scalp with so-so success.My usual routine is to apply the Dovonex to

the scalp for 2 or 3 days

then do nothing for a few days untill the itching and flaking start the

process all over again.

I realize that my symptoms are extremely mild compared to most people

afflicted with this disease

or condition.

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The first time I really started to notice PA symptoms was about a year

ago,but I think it probably

began in my forties.I used to do a bit of running, no ironman stuff,

just keeping in shape. I began

to get persistant pain in my achilles tendons,knees,back,etc.I fooled

around with different

treatments for awhile but finally had to give up running.Since then,I've

confined my physical activities

to pedalling a stationary bike,lifting weights,moderately, a bit of

tennis and the usual yard work,

walking the dog, etc.I've always had a bit of joint stiffness and

moderate levels of discomfort in

one place or the other,usually, one or two Aleve tablets would take care

of the symptoms.About

a year ago I started to get an allergic reaction to the Aleve,my face

and chest would break out in

a severe rash,I tried other over the counter meds with no luck.That's

when the real PA symptoms

kicked into high gear,from reading other web sites I belive I have

symmetrical polyarthritis.The

pain and stiffness usually occur in both shoulders,knees,feet,etc.,I

knew I was in trouble when the

back of my knees started to hurt,that's something I never felt

before!The symptoms quickly

increased in severity and I was having trouble buttoning my shirts

because of the stiffness and

weakness in my fingers and thumbs.

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I finally got an appointment with a rheumy and he diagnosed the

PA,x-rays showed no joint damage

or inflammation.He prescribed 2000 mgs of Disalcid per day,after a week

or so I began to feel fine,

however the rash started to come back and I was forced to stop taking

the drug after two weeks.

My PA symptoms stayed at a very mild level for a few months,but started

creeping back about six

weeks ago,at that time I tried taking 500mgs of the Disalcid per day to

see if there would be any

reactions.There weren't any, so I upped the dose to 1000mgs..At the

present time this seems to be the

right balance between meds and PA symptoms.

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As I've stated before,I realize my symptoms are almost non-existent

compared to other members on

the list,but from checking other websites,newsgroups,etc I've come to

the conclusion that PA is not

static, chances are that the intensity of my symptoms will increase at

some point.I feel that I need

PA mailing lists and newsgroups,not just for support but to be on the

cutting edge for info about

new meds, treatments, etc.I hope that by providing a sympathetic ear or

eye? to other members

I'll be of some value.

Dennis Newman

newman@...

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Dennis--

While it's true that PA is not static, it doesn't necessisarily go from bad to

worse. PA can go into a remissive state. I was lucky enough to have a seven

month remission a few years ago. It may not sound like much, but it gave me a

new perspective on life. I was Feeling great and doing " normal " things again.

The PA came back, but the time without constant pain gave me great hope for

the future. I wish I knew what triggered the remission, my doctors said it

was common to see it happen in PA. Maybe research will find what causes PA

and find out how we can all go into a permanent remission.

Emma

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On Mon, 30 Nov 1998 13:10:35 EST, Emaline2@... wrote:

>From: Emaline2@...

>

>Dennis--

>

>While it's true that PA is not static, it doesn't necessisarily go from bad to

>worse. PA can go into a remissive state. I was lucky enough to have a seven

>month remission a few years ago. It may not sound like much, but it gave me a

>new perspective on life. I was Feeling great and doing " normal " things again.

>The PA came back, but the time without constant pain gave me great hope for

>the future. I wish I knew what triggered the remission, my doctors said it

>was common to see it happen in PA. Maybe research will find what causes PA

>and find out how we can all go into a permanent remission.

>

>Emma

I used to go *years* between flare ups. Unfortunately this time it

just keeps going and going....

Steve

http://www.zoomnet.net/~steve

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