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Hello,

I'm just joining the group. I've been reading many of your posts

and appreciate the information sharing, so I thought I should say

hello and not just lurk!

I was diagnosed with PA last week after 5 yrs of being told it was

OA. I don't have P. Should I add " yet? " Still in the " I'm pretty

overwhelmed by this " stage and trying to learn as much as I can. My

father's family is full of RA so for the past year I've been

thinking I had more than OA and fearing RA... now I am learning

about PA! yikes

Gwen

" You must do the thing you think you cannot do. " ... Eleanor

Roosevelt

[Editor's Note: Hi, Gwen. Welcome to the list. It can be overwhelming, but as

with anything, the key is to educate yourself as much as possible and not settle

for mediocre medical care. I am a bit concerned by the change in diagnosis

because OA usually shows up in bone density tests. It presents itself very

differently from PA or RA. Who changed the diagnosis? Are you under the care

of a rheumatologist? Did the physician who diagnosed you say why he/she

believes it is PA given you don't have P? It is very possible to have PA

without P, but usually there are signs present such as nail involvement, P on

elbows, etc. OA on the other hand, is almost always visible in bone density

tests. The same is not true for PA. Did your physician recommend a drug

regimen and if so, do you have any questions about the medication? We look

forward to hearing from you frequently. Again, welcome, Kathy F.]

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Dear Gwen, First of all Welcome to our little piece of the world. This is

a wonderful group, full of smart caring people. I'm like you as far as no

doctor can say 100% for sure if I have PA or RA, thought they are positive

I have OA. At first it really bothered me and I kept wondering which one do

I have. But I finally figured out they treat them both pretty much the

same, and it really doesn't matter too much in the long run. More people

seem to " get it " if you say you have RA, but when I look at the little clues

about each disease I sort of feel more like it's PA. My skin is involved

too, but not the same way everyone else's is. I have had 3 dermatologists

tell me it isn't P, but more likely a reactive skin rash to sunburns I had

as a small child. The problem is it got worse the same time I did. No one

can seem to get rid of it either.

A lot of literature will tell you that PA isn't as painful as RA, but I

don't believe that at all. IN fact my rheumatologist told me from the

start, PA can be more painful since so many tendons and muscles are

involved. I guess that's not always the case with RA.

Kathy is so right when she say's you need to educate yourself on the

disease. Any more you have to be your own medical advocate, because doctors

are so busy these days they don't have the time. I've learned more about PA

from this group, then from all the doctors I've seen combined. So you are

starting off in the right place.

I agree that it is very overwhelming when you first start realizing just how

bad this disease can be. Just remember there are all levels of this disease

and maybe you will be one of the lucky ones and find the right medication at

the start. Take care and let us know how everything goes and how you are

feeling. You are among friends here. Take care, Fran

[ ] Hi--I'm new to the group

Hello,

I'm just joining the group. I've been reading many of your posts

and appreciate the information sharing, so I thought I should say

hello and not just lurk!

I was diagnosed with PA last week after 5 yrs of being told it was

OA. I don't have P. Should I add " yet? " Still in the " I'm pretty

overwhelmed by this " stage and trying to learn as much as I can. My

father's family is full of RA so for the past year I've been

thinking I had more than OA and fearing RA... now I am learning

about PA! yikes

Gwen

" You must do the thing you think you cannot do. " ... Eleanor

Roosevelt

[Editor's Note: Hi, Gwen. Welcome to the list. It can be overwhelming,

but as with anything, the key is to educate yourself as much as possible and

not settle for mediocre medical care. I am a bit concerned by the change in

diagnosis because OA usually shows up in bone density tests. It presents

itself very differently from PA or RA. Who changed the diagnosis? Are you

under the care of a rheumatologist? Did the physician who diagnosed you say

why he/she believes it is PA given you don't have P? It is very possible to

have PA without P, but usually there are signs present such as nail

involvement, P on elbows, etc. OA on the other hand, is almost always

visible in bone density tests. The same is not true for PA. Did your

physician recommend a drug regimen and if so, do you have any questions

about the medication? We look forward to hearing from you frequently.

Again, welcome, Kathy F.]

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Thanks for the welcome to the group. It is a rheumatologist I'm now

seeing who is calling this PA. I'm seeing him again tomorrow with

lots of questions. Right now I'm taking Aleve and while it takes

the edge off, it hasn't produced any dramatic results.

I've been taking yoga for the last year or so. I'm interested in

knowing what exercise/workouts work for folks with PA to maintain

strength and mobility. Not sure I can afford the gym membership to

access a pool for swimming. Stationary bike, free weights??? yoga??

Gwen

>

> Dear Gwen, First of all Welcome to our little piece of the

world. This is

> a wonderful group, full of smart caring people. I'm like you as

far as no

> doctor can say 100% for sure if I have PA or RA, thought they are

positive

> I have OA. At first it really bothered me and I kept wondering

which one do

> I have. But I finally figured out they treat them both pretty

much the

> same, and it really doesn't matter too much in the long run. More

people

> seem to " get it " if you say you have RA, but when I look at the

little clues

> about each disease I sort of feel more like it's PA. My skin is

involved

> too, but not the same way everyone else's is. I have had 3

dermatologists

> tell me it isn't P, but more likely a reactive skin rash to

sunburns I had

> as a small child. The problem is it got worse the same time I

did. No one

> can seem to get rid of it either.

>

> A lot of literature will tell you that PA isn't as painful as RA,

but I

> don't believe that at all. IN fact my rheumatologist told me from

the

> start, PA can be more painful since so many tendons and muscles are

> involved. I guess that's not always the case with RA.

>

> Kathy is so right when she say's you need to educate yourself on

the

> disease. Any more you have to be your own medical advocate,

because doctors

> are so busy these days they don't have the time. I've learned

more about PA

> from this group, then from all the doctors I've seen combined. So

you are

> starting off in the right place.

>

> I agree that it is very overwhelming when you first start

realizing just how

> bad this disease can be. Just remember there are all levels of

this disease

> and maybe you will be one of the lucky ones and find the right

medication at

> the start. Take care and let us know how everything goes and how

you are

> feeling. You are among friends here. Take care, Fran

>

>

> [ ] Hi--I'm new to the group

>

>

>

> Hello,

> I'm just joining the group. I've been reading many of your posts

> and appreciate the information sharing, so I thought I should say

> hello and not just lurk!

>

> I was diagnosed with PA last week after 5 yrs of being told it

was

> OA. I don't have P. Should I add " yet? " Still in the " I'm

pretty

> overwhelmed by this " stage and trying to learn as much as I

can. My

> father's family is full of RA so for the past year I've been

> thinking I had more than OA and fearing RA... now I am learning

> about PA! yikes

>

> Gwen

> " You must do the thing you think you cannot do. " ... Eleanor

> Roosevelt

>

> [Editor's Note: Hi, Gwen. Welcome to the list. It can be

overwhelming,

> but as with anything, the key is to educate yourself as much as

possible and

> not settle for mediocre medical care. I am a bit concerned by the

change in

> diagnosis because OA usually shows up in bone density tests. It

presents

> itself very differently from PA or RA. Who changed the

diagnosis? Are you

> under the care of a rheumatologist? Did the physician who

diagnosed you say

> why he/she believes it is PA given you don't have P? It is very

possible to

> have PA without P, but usually there are signs present such as nail

> involvement, P on elbows, etc. OA on the other hand, is almost

always

> visible in bone density tests. The same is not true for PA. Did

your

> physician recommend a drug regimen and if so, do you have any

questions

> about the medication? We look forward to hearing from you

frequently.

> Again, welcome, Kathy F.]

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Hi Gwen. I haven't been diagnosed for very long, but so far I've found that

Yoga really helps me with keeping up my mobility. It's not high impact, and

still ensures that all muscles are exercised, and doesn't put a whole lot of

stress on the body. It's also an exercise that you can do in different

difficulties, depending on your degree of mobility. It's flexible :) and it

can help you become flexible too hee hee!

good luck!

Crystal

>From: " catbert1949 " <catbert1949@...>

>Reply-

>

>Subject: [ ] Re: Hi--I'm new to the group

>Date: Tue, 09 Nov 2004 04:08:53 -0000

>

>

>

>Thanks for the welcome to the group. It is a rheumatologist I'm now

>seeing who is calling this PA. I'm seeing him again tomorrow with

>lots of questions. Right now I'm taking Aleve and while it takes

>the edge off, it hasn't produced any dramatic results.

>

>I've been taking yoga for the last year or so. I'm interested in

>knowing what exercise/workouts work for folks with PA to maintain

>strength and mobility. Not sure I can afford the gym membership to

>access a pool for swimming. Stationary bike, free weights??? yoga??

>

>Gwen

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Another vote for yoga. I've been taking a weekly yoga

class for about 6 years, and practicing occaisionally

for about 10 years before that. If I had NOT done yoga

consistently for this long, I'd be much stiffer and

less mobile today.

A few months ago, I wrote a long detailed message

about how it benefits me. You can find it in the

archives.

--

=====

--------------------------

Stein

www.noblefusion.com/astein

If you're tired of fighting battles with yourself

If you want to be somebody else

Change your mind...

-- Sister Hazel

__________________________________________________

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  • 4 weeks later...

Hi Gwen, , Marie, msgenelee? (Are you new? and don't say, " No I'm 73

lol) , Alfredo, Della, quiqle, Carol(A fellow Scot?) , Laurie,

CC, Carol(AMcKenzie) Roanne, lakethundermom, Andy, Lynn, Ellen, , Beth,

Patty(pattybacon), , , deslinger and Patty(maggiemay)

Just.................. wanted.............Gasp............ to welcome you

all to the group whether your are new, coming out of lurk mode or been here for

years and I have made a mistake. lol

Hope you all get the info, advice, friendship, or/and all of the above, that

you need. I noticed that a few of you have already been pretty active in the

two/three weeks I have been away.

Good luck,

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