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Hi Everyone!

........Ann-Marie, you and I must be on the same wave-length! The nurse at

my doctor's office called me just two minutes ago with my latest CPK

results.......I, too, am normal! Mine was 174 where the normal range is

from 35 to 232. Whhoooo hooooo! It has been bouncing in and out of the

normal range since December and it looks like things are on a positive

swing!

It's always good to have the lab results back up one's improvements,

especially since I have taken an 'alternative' route to my recovery by using

the antibiotics. The antibiotic, Minocin, is no longer considered

alternative in treating rheumatoid arthritis, and these diseases are closely

related, though.

I hope everyone is able to enjoy these summer days. Let's take a

'vacation' from all of these illnesses and try not to think about them any

more than necessary, OK?

hugs to you all,

Connie (dermatomyositis since Aug '96, started Minocin in Feb of '98)

Checking in

> Dear Everybody,

> YEEEHAAAA! I went to the rheumatologist yesterday and my CPK is down to

> 118!!! I am " normal... " and passed my strength tests with flying colors.

I

> get to continue decreasing the Prednisone. My goal?

> to see cheek bones!!! Looks like my flare has " un-flared " and I hope it

> lasts a good long time.

>

> Vicki, I empathize with you. I always want to shoot people (even when I'm

> feeling somewhat better) who tell me I look so good. And all those folks

> who insinuate that it could be worse. I'm like " let's see YOU live with

PM

> for a month! " Tiwanda!!!!!

>

> Take care all.

>

> Ann-Marie

> ________________________________________________________________________

> Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com

>

>

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Ann-Marie....Hey, sounds like a hot fudge sundae event tonight. (Works

for me) I'm so happy for you. Decreasing your Prednisone is the best

ever.... Pretty soon those check bones will pop right out. I didn't

start to see mine until I got down to 20mg.... It's the little pouches

on the jar line that haven't gone yet.....

My stomach, in that last few days, has also come down a little. It does

seem to take a while but it's so much fun watching the changes take

place....

Ann-Marie...if anyone said to me " it could be worse " , I don't know how

the heck I would handle that.... My own doctor describes this disease as

being one of the nastiest disease that has no rhyme or reason.....

I'm with you.... I would like just one person thats healthy to have this

disease for one day and see what they feel like.

Not that I wish this on anyone...

Take care,

Vicki-PM

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  • 1 month later...

Dear Everyone,

Just checking in..., welcome to the group. I will keep Mattie in

my thoughts and in my prayers. Ralph and Cari will be great resources for

you.

I had the vampire moment last Wednesday (labs!!!) and I will call in on

Monday to see if my CPK is still good. If so, I can taper to 12.5 mg. of

Prednisone---woooo-wooo! Last time, though, my labs were in cyberspace (or

so I thought!) Actually they got sent to the wrong doctor and I made about

5 calls to track them down. Isn't it fun to have a chronic illness--the

things we get to do for kicks that others never dream of!!! I just want to

SHOOT the nuns who whine because they have to go to the doctor for

something. Sometimes I've just smiled and said, " Well, my doctors are on my

Christmas card list because I get to see them so often. We've really gotten

to know one another... " Sorry, I'm a little crabby tonight--what was your

first clue?!? I have been working to set up my classroom and I think I

overdid it energy wise.

Frustrating--I thought I had this figured out! Guess I'm not gifted--LOL!

Sleep tight all!

Love,

Ann-Marie--MCTD/PM

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