Jump to content
RemedySpot.com
Sign in to follow this  
Guest guest

Re: Lab results...FINALLY

Rate this topic

Recommended Posts

Guest guest

judy, ra in my opinoin is based on lab results(blood),x-rays,redness, moderate

to severe pain & inflammation of the joints.... i have been on prednisone since i

was 18 yrs old. & if i had to do it all over again, I WOULD NOT TAKE IT!!! yes,

the side effects are BAD!! i also have osteo.my bones are very FRAGILE & BREAK

easily!!! yes it helps SOMETIMES but its not worth all those AWEFUL SIDE

EFFECTS! good luck in whatever you decide to do... god bless,melyndagamez

3/29/08 4:48p.m.central time

Re: [ ] Re: Lab results...FINALLY

I was advised of this too. If my SED Rate, Westgren,

anti ccp were elevated and if I responded to the

treatment then they knew inflammatory arthritis was

present.

--- J Acciarito <jacyone@...> wrote:

> Is that generally true? That if your symptoms are

> relieved with prednisone, then RA is indicated?

>

> Judy

>

> Diane wrote:

>

> Hi Sharon,

> In my opinion, I think the Doctor put you on the

> prednisone to see if

> it works...if it does, than she knows it is

> definitely RA...sometimes

> there can be other reason for a raised count or a

> false positive but

> if the prednisone works and the pain is gone, then

> she knows it is RA

> for sure...does that makes sense to you? You are

> right, prednisone

> is not the only treatment for the inflammation.

> Hope you are feeling better...be careful with the

> prednisone...it is

> a powerful and tricky medication with lots of side

> effects...

>

> I would suggest getting yourself to a good

> Rheumatologist as quickly

> as possible...I think you said she was your family

> doctor...

> .___

>

> [Non-text portions of this message have been

> removed]

>

>

________________________________________________________________________________\

____

Like movies? Here's a limited-time offer: Blockbuster Total Access for one month

at no cost.

http://tc.deals./tc/blockbuster/text4.com

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

Share this post


Link to post
Share on other sites
Guest guest

hi sharon, hope your doing well. i take pred. & i take lortabs for the pain but

it does not work, so i pretty much pop whatever i have tylenol,aleve or just

anything to relive this HORRIBLE PAIN I HAVE EVERYDAY OF MY LIFE...... god

bless, melyndagamez 3/29/08 4:54p.m.central time

[ ] Re: Lab results...FINALLY

> Hi ,

>

> That's what I was thinking too...I don't see how 5 months of Pred

> will help to control anything. I told the doctor how long I've had

> this...it's nothing new for me. It's been years!!! Every few days I

> run into another situation where I find something else I can no

> longer do. I constantly drop things...it's starting to hurt to hold

> the steering wheel on the car...my hips are getting involved and

> becoming painful now too....my hands are getting so bad that typing

> is become hard. I'm not new to this at all!! I might see if I can

> see a Rhuematologist at the clinic and see what happens with that.

> Also, I just thought about this...if you're on Pred...what can you

> take for pain? She has no pain medication for me. I heard you can

> only take a Tylenol. I have morphine pain and I can only take

> Tylenol?

> Take care,

> Sharon

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

Share this post


Link to post
Share on other sites
Guest guest

Dennis i have severe ra and ankylosing spondolysis. my dr puts me on prednisone

for flare ups. i take it about 4 times a years for about a week 3 pills or less

a day 10 mg. when i have to go on it it is the last resort. i cannot function.

on this site everyone talks so bad about the prednisone, but it has been a life

saver for me. i know the long term effects but i want to live today. i have

already been put on the fentayl pain patches and sometimes prednisone is all

that will help. good to hear someone else takes it too. how is your mobility,

do you work, can you sleep, general overall wellbeing. good to hear from

someone that sees prednisone as a must for some people. rita in georgia

[ ] Re: Lab results...FINALLY

> Hi ,

>

> That's what I was thinking too...I don't see how 5 months of Pred

> will help to control anything. I told the doctor how long I've had

> this...it's nothing new for me. It's been years!!! Every few days I

> run into another situation where I find something else I can no

> longer do. I constantly drop things...it' s starting to hurt to hold

> the steering wheel on the car...my hips are getting involved and

> becoming painful now too....my hands are getting so bad that typing

> is become hard. I'm not new to this at all!! I might see if I can

> see a Rhuematologist at the clinic and see what happens with that.

> Also, I just thought about this...if you're on Pred...what can you

> take for pain? She has no pain medication for me. I heard you can

> only take a Tylenol. I have morphine pain and I can only take

> Tylenol?

> Take care,

> Sharon

________________________________________________________________________________\

____

You rock. That's why Blockbuster's offering you one month of Blockbuster Total

Access, No Cost.

http://tc.deals./tc/blockbuster/text5.com

Share this post


Link to post
Share on other sites
Guest guest

Hi Rita in Georgia! My 15 yr old son and 8 yr old daughter both have Ankylosing

Spondylitis. Son was diagnosed 12 yrs ago and daughter 3 years ago. Any

insight into

what we can be doing as I look to their future? Neither one is doing very well

right now

with many complex problems with no answers other than they have arthritis. None

of the

drugs seem to work for very long with either one of them and they both have such

stomach pain right now that they are both off of pain meds to try to ease their

stomaches.

Prednisone hasn't been very successful for them when they have tried it.

Myndi

>

> Dennis i have severe ra and ankylosing spondolysis. my dr puts me on

prednisone for

flare ups. i take it about 4 times a years for about a week 3 pills or less a

day 10 mg.

when i have to go on it it is the last resort. i cannot function. on this site

everyone talks

so bad about the prednisone, but it has been a life saver for me. i know the

long term

effects but i want to live today. i have already been put on the fentayl pain

patches and

sometimes prednisone is all that will help. good to hear someone else takes it

too. how

is your mobility, do you work, can you sleep, general overall wellbeing. good

to hear from

someone that sees prednisone as a must for some people. rita in georgia

>

>

> [ ] Re: Lab results...FINALLY

>

> > Hi ,

> >

> > That's what I was thinking too...I don't see how 5 months of Pred

> > will help to control anything. I told the doctor how long I've had

> > this...it's nothing new for me. It's been years!!! Every few days I

> > run into another situation where I find something else I can no

> > longer do. I constantly drop things...it' s starting to hurt to hold

> > the steering wheel on the car...my hips are getting involved and

> > becoming painful now too....my hands are getting so bad that typing

> > is become hard. I'm not new to this at all!! I might see if I can

> > see a Rhuematologist at the clinic and see what happens with that.

> > Also, I just thought about this...if you're on Pred...what can you

> > take for pain? She has no pain medication for me. I heard you can

> > only take a Tylenol. I have morphine pain and I can only take

> > Tylenol?

> > Take care,

> > Sharon

>

>

>

>

>

>

________________________________________________________________________________\

____

> You rock. That's why Blockbuster's offering you one month of Blockbuster Total

Access,

No Cost.

> http://tc.deals./tc/blockbuster/text5.com

>

>

Share this post


Link to post
Share on other sites
Guest guest

Hi ,

I started my Pred yesterday and it looks like I'll be on it for a

while to come. I'm 56 years old..what is it going to do to me?

Well, I have a plan. I'm on charity care offered by out local

hospital who also runs a clinic in town. Since I had a doctor I

didn't see the need to really go to the clinic but I want to see if I

can get an appointment with a Rhuematologist at the clinic sometime

soon. I want to get a copy of my lab work from the doctor tomorrow

and then go to the hospital to talk to someone in charity care about

going to the clinic. Hopefully that will work out and I can see

someone who knows a bit more about this condition than my Internist.

I guess IF I was new to RA which I'm not maybe all this Pred would be

a good thing and she wants to see me when the treatment is over. I

don't know. I know I've had it for years but without insurance or

care I've just lived with it and suffered with it until I couldn't

stand it anymore!! I'll know more if I can see the Rhuematologist.

If not I guess I'm SOL!!

By the way, for pain relief the Pharmacist told me the only over the

counter thing I can take is Tylenol...?? It's kind of funny when you

have morphine sized pain!!

Take care,

Sharon

> > >

> > > Hi Sharon, sorry, do you see a rheumatologist?

> > You're right that

> > you need something else to control the RA. The

> > course of pred will

> > help with inflammation, but not over all disease

> > management. As for

> > the rheumatoid factor (RF) test, I think the cut off

> > for many labs is

> > <20 is normal. When I was first symptomatic my RF

> > was 20. Then

> > several years later it was much higher, I think in

> > the 50s. My rheum

> > did do baseline xrays, I think that's pretty

> > standard practice. It

> > did take me 3 visits to 3 different rheums before I

> > found one I

> > liked, it might be good to try a 2nd opinion.

> > >

> > > [ ] Lab results...FINALLY

> > >

> > > Hi everyone,

> > >

> > > I got a phone call a little while ago from my

> > doctor's office to

> > > inform me that they had my labs back and she

> > wanted to talk to me

> > > about it. My cholesterol was high...knew that it

> > would be. She

> > > suggested I get more exercise and walk 20 minutse

> > a day....if only

> > I

> > > could. SED rate is 59. Tested negative for Lyme

> > and Lupus. I

> > asked

> > > about the RA Factor and she said it was " high " ...I

> > asked if that

> > > meant positive and she said yes. I thought it was

> > like a pregnency

> > > test...either negative or positive. I didn't know

> > there were

> > numbers

> > > associated with it. Do any of you know about a

> > number associated

> > > with this?

> > >

> > > Also, they are going to put me on Pred. It's a 5

> > month

> > thing...this

> > > month 20 mil, 15 next month, 10 and then 5 and

> > after 5 months of

> > > taking that daily I am supposed to call them. I'm

> > not a rocket

> > > scientist but this isn't slowing my RA in any way.

> > It's just

> > helping

> > > with inflamation. They aren't ordering x-rays or

> > a bone

> > scan....??

> > > Don't I need a base line here? Every couple of

> > days I'm less to do

> > > what I was able to do a short time ago...how are

> > they going to

> > > regular this and measure it?? Is it me or does

> > this sound about

> > > right to any of you???

> > >

> > > Take good care,

> > > Sharon

> > >

> > >

> > >

> > >

> > > <!--

> > >

> > > #ygrp-mkp{

> > > border:1px solid

> > #d8d8d8;font-family:Arial;margin:14px

> > 0px;padding:0px 14px;}

> > > #ygrp-mkp hr{

> > > border:1px solid #d8d8d8;}

> > > #ygrp-mkp #hd{

> > > color:#628c2a;font-size:85%;font-weight:bold;line-

> > height:122%;margin:10px 0px;}

> > > #ygrp-mkp #ads{

> > > margin-bottom:10px;}

> > > #ygrp-mkp .ad{

> > > padding:0 0;}

> > > #ygrp-mkp .ad a{

> > > color:#0000ff;text-decoration:none;}

> > > -->

> > >

> > > <!--

> > >

> > > #ygrp-sponsor #ygrp-lc{

> > > font-family:Arial;}

> > > #ygrp-sponsor #ygrp-lc #hd{

> > > margin:10px

> >

> 0px;font-weight:bold;font-size:78%;line-height:122%;}

> > > #ygrp-sponsor #ygrp-lc .ad{

> > > margin-bottom:10px;padding:0 0;}

> > > -->

> > >

> > > <!--

> > >

> > > #ygrp-mlmsg {font-size:13px;font-family:arial,

> > helvetica,

> > clean, sans-serif;}

> > > #ygrp-mlmsg table {font-size:inherit;font:100%;}

> > > #ygrp-mlmsg select, input, textarea {font:99%

> > arial, helvetica,

> > clean, sans-serif;}

> > > #ygrp-mlmsg pre, code {font:115% monospace;}

> > > #ygrp-mlmsg * {line-height:1.22em;}

> > > #ygrp-text{

> > > font-family:Georgia;

> > > }

> > > #ygrp-text p{

> > > margin:0 0 1em 0;}

> > > #ygrp-tpmsgs{

> > > font-family:Arial;

> > > clear:both;}

> > > #ygrp-vitnav{

> > >

> >

> padding-top:10px;font-family:Verdana;font-size:77%;margin:0;}

> > > #ygrp-vitnav a{

> > > padding:0 1px;}

> > > #ygrp-actbar{

> > > clear:both;margin:25px

> > 0;white-space:nowrap;color:#666;text-

> > align:right;}

> > > #ygrp-actbar .left{

> > > float:left;white-space:nowrap;}

> > > .bld{font-weight:bold;}

> > > #ygrp-grft{

> > > font-family:Verdana;font-size:77%;padding:15px 0;}

> > > #ygrp-ft{

> > > font-family:verdana;font-size:77%;border-top:1px

> > solid #666;

> > > padding:5px 0;

> > > }

> > > #ygrp-mlmsg #logo{

> > > padding-bottom:10px;}

> > >

> > > #ygrp-reco {

> > > margin-bottom:20px;padding:0px;}

> > > #ygrp-reco #reco-head {

> > > font-weight:bold;color:#ff7900;}

> > >

> > > #reco-grpname{

> > > font-weight:bold;margin-top:10px;}

> > > #reco-category{

> > > font-size:77%;}

> > > #reco-desc{

> > > font-size:77%;}

> > >

> > > #ygrp-vital{

> > >

> >

> background-color:#e0ecee;margin-bottom:20px;padding:2px

> > 0 8px 8px;}

> > > #ygrp-vital #vithd{

> > >

> >

> font-size:77%;font-family:Verdana;font-weight:bold;color:#333;text-

> >

> === message truncated ===

>

>

>

>

______________________________________________________________________

______________

> You rock. That's why Blockbuster's offering you one month of

Blockbuster Total Access, No Cost.

> http://tc.deals./tc/blockbuster/text5.com

>

Share this post


Link to post
Share on other sites
Guest guest

Hi ,

I am going to find out tomorrow if I can see a Rhuematologist at the

charity care clinic. If not I guess I won't have that option. We'll

see what happens tomorrow. I'm going to go to my doctor's office and

get a copy of my labs and take it to the hospital in hopes they will

tell me who to call or maybe even make the appointment for me. I'll

know more tomorrow.

Thank you and take care,

Sharon

--- In , " " <Matsumura_Clan@...>

wrote:

>

> Sharon,

>

> The rheumatoid factor (RF) test is not like a pregnancy test.

>

> Despite its name, rheumatoid factor production is not specific to

RA. There

> are many possible reasons for a positive RF, even simply aging.

>

> In addition, there is no one standard test for RF, so the way the

results

> are determined, reported, and interpreted will vary from lab to lab.

>

> I suspect that your physician is not sure of the diagnosis and

wants to see

> how you do on prednisone; however, watching and waiting for five

months is

> not a good idea.

>

> It would be wise to find a rheumatologist for a second opinion.

>

>

>

> Not an MD

>

>

> > [ ] Lab results...FINALLY

> >

> > Hi everyone,

> >

> > I got a phone call a little while ago from my doctor's office to

> > inform me that they had my labs back and she wanted to talk to me

> > about it. My cholesterol was high...knew that it would be. She

> > suggested I get more exercise and walk 20 minutse a day....if

only I

> > could. SED rate is 59. Tested negative for Lyme and Lupus. I

asked

> > about the RA Factor and she said it was " high " ...I asked if that

> > meant positive and she said yes. I thought it was like a

pregnency

> > test...either negative or positive. I didn't know there were

numbers

> > associated with it. Do any of you know about a number associated

> > with this?

> >

> > Also, they are going to put me on Pred. It's a 5 month

thing...this

> > month 20 mil, 15 next month, 10 and then 5 and after 5 months of

> > taking that daily I am supposed to call them. I'm not a rocket

> > scientist but this isn't slowing my RA in any way. It's just

helping

> > with inflamation. They aren't ordering x-rays or a bone

scan....??

> > Don't I need a base line here? Every couple of days I'm less to

do

> > what I was able to do a short time ago...how are they going to

> > regular this and measure it?? Is it me or does this sound about

> > right to any of you???

> >

> > Take good care,

> > Sharon

>

Share this post


Link to post
Share on other sites
Guest guest

Hi Melynda,

The Pharmacist told me yesterday the only OTC pain relief I could

take with Pred was Tylenol and that everything else would tear up my

stomach. I already have GERD...I don't want an ulcer too. This is

day two for Pred...how long does it take to make you feel better??

I'm starting at 20 mil daily for the next month.

Do you have flares or are you the same all the time? I used to flare

years ago but now...it's constant.

Have a good day!!

Sharon

--- In , Melynda Gamez <melyndagamez@...>

wrote:

>

> hi sharon, hope your doing well. i take pred. & i take lortabs for

the pain but it does not work, so i pretty much pop whatever i have

tylenol,aleve or just anything to relive this HORRIBLE PAIN I HAVE

EVERYDAY OF MY LIFE...... god bless, melyndagamez 3/29/08

4:54p.m.central time

>

>

> [ ] Re: Lab results...FINALLY

>

>

> > Hi ,

> >

> > That's what I was thinking too...I don't see how 5 months of Pred

> > will help to control anything. I told the doctor how long I've

had

> > this...it's nothing new for me. It's been years!!! Every few

days I

> > run into another situation where I find something else I can no

> > longer do. I constantly drop things...it's starting to hurt to

hold

> > the steering wheel on the car...my hips are getting involved and

> > becoming painful now too....my hands are getting so bad that

typing

> > is become hard. I'm not new to this at all!! I might see if I

can

> > see a Rhuematologist at the clinic and see what happens with that.

> > Also, I just thought about this...if you're on Pred...what can you

> > take for pain? She has no pain medication for me. I heard you

can

> > only take a Tylenol. I have morphine pain and I can only take

> > Tylenol?

> > Take care,

> > Sharon

>

>

> ------------------------------------

>

>

Share this post


Link to post
Share on other sites
Guest guest

i am on humira injections. and fentayl pain patches. what are their symptoms?

i have stomach problems also because i have taken so many pain meds. i am 53.

i have an excellent rheumatologist. i have had spinal fusions by surgery. i am

so stiff. i have many bone spurs. does this sound familiar? can your children do

sports or attend school? rita

[ ] Re: Lab results...FINALLY

>

> > Hi ,

> >

> > That's what I was thinking too...I don't see how 5 months of Pred

> > will help to control anything. I told the doctor how long I've had

> > this...it's nothing new for me. It's been years!!! Every few days I

> > run into another situation where I find something else I can no

> > longer do. I constantly drop things...it' s starting to hurt to hold

> > the steering wheel on the car...my hips are getting involved and

> > becoming painful now too....my hands are getting so bad that typing

> > is become hard. I'm not new to this at all!! I might see if I can

> > see a Rhuematologist at the clinic and see what happens with that.

> > Also, I just thought about this...if you're on Pred...what can you

> > take for pain? She has no pain medication for me. I heard you can

> > only take a Tylenol. I have morphine pain and I can only take

> > Tylenol?

> > Take care,

> > Sharon

>

>

>

>

>

>

____________ _________ _________ _________ _________ _________ _

> You rock. That's why Blockbuster' s offering you one month of Blockbuster

Total Access,

No Cost.

> http://tc.deals. / tc/blockbuster/ text5.com

>

>

Share this post


Link to post
Share on other sites
Guest guest

usually for me on prednisone the 3rd day i begin to feel better. it is so

disgusting that I too feel like i am always in a flair. it scares me. rita

[ ] Re: Lab results...FINALLY

>

>

> > Hi ,

> >

> > That's what I was thinking too...I don't see how 5 months of Pred

> > will help to control anything. I told the doctor how long I've

had

> > this...it's nothing new for me. It's been years!!! Every few

days I

> > run into another situation where I find something else I can no

> > longer do. I constantly drop things...it' s starting to hurt to

hold

> > the steering wheel on the car...my hips are getting involved and

> > becoming painful now too....my hands are getting so bad that

typing

> > is become hard. I'm not new to this at all!! I might see if I

can

> > see a Rhuematologist at the clinic and see what happens with that.

> > Also, I just thought about this...if you're on Pred...what can you

> > take for pain? She has no pain medication for me. I heard you

can

> > only take a Tylenol. I have morphine pain and I can only take

> > Tylenol?

> > Take care,

> > Sharon

>

>

> ------------ --------- --------- ------

>

>

Share this post


Link to post
Share on other sites
Guest guest

My son has numbness in his foot, urinary pain/bleeding (the bleeding was a while

ago),

chest pain, constipation, swollen lymph nodes throughout GI system (called

Reactive

Lymphoid Hyperplasia), dizziness, vasculitis (at least in his legs/feet -

diagnosed by skin

biopsies), gall stones, and stomachaches. My daughter also has been having

chronic

stomachaches since last Oct. She has also been seeing spots with her vision

since Oct.

She's had a brain MRI (normal) and endoscopy (also normal). Both kids do

participate in

sports - with pain. We do have to make adjustments though when we have to be

" active "

for long periods of time - like shopping, etc. We usually end up with a

wheelchair when

available since their knees and ankles hurt them too much. They also are in

school

although they miss a lot due to Dr appointments, etc. No bone spurs or fusions!

No

reasons for all of their symptoms - we've had MANY tests and seen MANY

specialists.

Myndi

> >

> > Dennis i have severe ra and ankylosing spondolysis. my dr puts me on

prednisone for

> flare ups. i take it about 4 times a years for about a week 3 pills or less a

day 10 mg.

> when i have to go on it it is the last resort. i cannot function. on this site

everyone talks

> so bad about the prednisone, but it has been a life saver for me. i know the

long term

> effects but i want to live today. i have already been put on the fentayl pain

patches and

> sometimes prednisone is all that will help. good to hear someone else takes it

too. how

> is your mobility, do you work, can you sleep, general overall wellbeing. good

to hear

from

> someone that sees prednisone as a must for some people. rita in georgia

> >

> >

> > [ ] Re: Lab results...FINALLY

> >

> > > Hi ,

> > >

> > > That's what I was thinking too...I don't see how 5 months of Pred

> > > will help to control anything. I told the doctor how long I've had

> > > this...it's nothing new for me. It's been years!!! Every few days I

> > > run into another situation where I find something else I can no

> > > longer do. I constantly drop things...it' s starting to hurt to hold

> > > the steering wheel on the car...my hips are getting involved and

> > > becoming painful now too....my hands are getting so bad that typing

> > > is become hard. I'm not new to this at all!! I might see if I can

> > > see a Rhuematologist at the clinic and see what happens with that.

> > > Also, I just thought about this...if you're on Pred...what can you

> > > take for pain? She has no pain medication for me. I heard you can

> > > only take a Tylenol. I have morphine pain and I can only take

> > > Tylenol?

> > > Take care,

> > > Sharon

> >

> >

> >

> >

> >

> >

> ____________ _________ _________ _________ _________ _________ _

> > You rock. That's why Blockbuster' s offering you one month of Blockbuster

Total

Access,

> No Cost.

> > http://tc.deals. / tc/blockbuster/ text5.com

> >

> >

Share this post


Link to post
Share on other sites
Guest guest

Hi Rita,

I think mine is so bad beause I've had it so long and gone

untreated. It just feels out of control now. I don't remember the

last time I didn't feel it. It keeps progressing too. It's like

every couple of weeks it's in another joint.

Glad to know that maybe tomorrow I might feel a little relief from

the Pred. I'm hopeful anyway. This is day two.

>

> usually for me on prednisone the 3rd day i begin to feel better.

it is so disgusting that I too feel like i am always in a flair. it

scares me. rita

>

>

>

> [ ] Re: Lab results...FINALLY

>

> Hi Melynda,

>

> The Pharmacist told me yesterday the only OTC pain relief I could

> take with Pred was Tylenol and that everything else would tear up

my

> stomach. I already have GERD...I don't want an ulcer too. This is

> day two for Pred...how long does it take to make you feel better??

> I'm starting at 20 mil daily for the next month.

>

> Do you have flares or are you the same all the time? I used to

flare

> years ago but now...it's constant.

>

> Have a good day!!

> Sharon

>

>

> >

> > hi sharon, hope your doing well. i take pred. & i take lortabs for

> the pain but it does not work, so i pretty much pop whatever i have

> tylenol,aleve or just anything to relive this HORRIBLE PAIN I HAVE

> EVERYDAY OF MY LIFE...... god bless, melyndagamez 3/29/08

> 4:54p.m.central time

> >

> >

>

Share this post


Link to post
Share on other sites
Guest guest

The Pharmacist had suggested Vicodan toom Pris. I think my doctor

wants to see how I do on Pred on its own thinking maybe it will

reduce the inflammation and the pain will be gone. I guess it's

possible but it's just hard to imagine.

Thanks,

Sharon

>

>

>

>

> > if you're on Pred...what can you

> > take for pain?

> >

>

> Vicodan, codeine, or Percocet!

> Pris

>

>

> **************

> Create a Home Theater Like the Pros. Watch the video on AOL

> Home.

> (http://home.aol.com/diy/home-improvement-eric-stromer?

video=15 & amp;

> ncid=aolhom00030000000001)

>

>

>

Share this post


Link to post
Share on other sites
Guest guest

mine too. i usually have to get shots in my joints at least one joint every six

weeks or so.it is so freightening to know there is really NO way to stop it. If

one thing lasts a few months then it causes a reaction and then the dosage is

increased, etc. it seems like a merry go round. its like one of the nurses at

my rhemy said, she use to work at a cancer center and she said at least cancer

patients can have it taken out and be totally normal for a long time. ours

never is totally gone. i feel it every minute i breathe. love and hugs rita

[ ] Re: Lab results...FINALLY

>

> Hi Melynda,

>

> The Pharmacist told me yesterday the only OTC pain relief I could

> take with Pred was Tylenol and that everything else would tear up

my

> stomach. I already have GERD...I don't want an ulcer too. This is

> day two for Pred...how long does it take to make you feel better??

> I'm starting at 20 mil daily for the next month.

>

> Do you have flares or are you the same all the time? I used to

flare

> years ago but now...it's constant.

>

> Have a good day!!

> Sharon

>

>

> >

> > hi sharon, hope your doing well. i take pred. & i take lortabs for

> the pain but it does not work, so i pretty much pop whatever i have

> tylenol,aleve or just anything to relive this HORRIBLE PAIN I HAVE

> EVERYDAY OF MY LIFE...... god bless, melyndagamez 3/29/08

> 4:54p.m.central time

> >

> >

>

________________________________________________________________________________\

____

Never miss a thing. Make your home page.

http://www./r/hs

Share this post


Link to post
Share on other sites
Guest guest

hi sharon, i got your message.. as a matter of fact,this past weekend i had a

BAD FLARE UP!! i could not MOVE my whole right side.. so i called my rheummy &

she upped my pred. to 10mg.for a week,then 5 in half for a week then so on. YES

it does help but not to the effect that it TOTALLY takes away the pain. im

still achey & tired,no ENERGY AT ALL!! since my rheummy cut my pred. i have

NOTICE that i tend to have more BAD DAYS THAN GOOD!! when i made the comment

that i pop WHATEVER, I WAS kinda being SARCASTIC & feeling BLAH at the time..

SORRY!!!! HOPE YOU HAVE A GOOD ONE!!! god bless,melyndagamez 3/30/08

9:42p.m.central time

[ ] Re: Lab results...FINALLY

>

> Hi Melynda,

>

> The Pharmacist told me yesterday the only OTC pain relief I could

> take with Pred was Tylenol and that everything else would tear up

my

> stomach. I already have GERD...I don't want an ulcer too. This is

> day two for Pred...how long does it take to make you feel better??

> I'm starting at 20 mil daily for the next month.

>

> Do you have flares or are you the same all the time? I used to

flare

> years ago but now...it's constant.

>

> Have a good day!!

> Sharon

>

>

> >

> > hi sharon, hope your doing well. i take pred. & i take lortabs for

> the pain but it does not work, so i pretty much pop whatever i have

> tylenol,aleve or just anything to relive this HORRIBLE PAIN I HAVE

> EVERYDAY OF MY LIFE...... god bless, melyndagamez 3/29/08

> 4:54p.m.central time

> >

> >

>

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

Share this post


Link to post
Share on other sites
Guest guest

hi sharon all this talk about this and that are MAKING ME LIL CRAZY!!!! just

recently my ra levels were verey HIGH compared to OTHERS that are NORMAL!! CALL

ME CRAZY BUT WHATS NORMAL????? anyway my ra lab (blood) came back and it was at

a 9,which is TO HIGH!!the normal range is 2 or 1.. so that MEANT THAT MY RA IS

VERY ACTIVE & INFLAMMED IN ALL MY JOINTS...IT HURTS SOO BAD.. i HOPE they find

OUT what you need to know,sharon.HANG IN THERE GIRL! god bless,melyndagamez

3/30/08 11:09p.m.central time

[ ] Lab results...FINALLY

> >

> > Hi everyone,

> >

> > I got a phone call a little while ago from my doctor's office to

> > inform me that they had my labs back and she wanted to talk to me

> > about it. My cholesterol was high...knew that it would be. She

> > suggested I get more exercise and walk 20 minutse a day....if

only I

> > could. SED rate is 59. Tested negative for Lyme and Lupus. I

asked

> > about the RA Factor and she said it was " high " ...I asked if that

> > meant positive and she said yes. I thought it was like a

pregnency

> > test...either negative or positive. I didn't know there were

numbers

> > associated with it. Do any of you know about a number associated

> > with this?

> >

> > Also, they are going to put me on Pred. It's a 5 month

thing...this

> > month 20 mil, 15 next month, 10 and then 5 and after 5 months of

> > taking that daily I am supposed to call them. I'm not a rocket

> > scientist but this isn't slowing my RA in any way. It's just

helping

> > with inflamation. They aren't ordering x-rays or a bone

scan....??

> > Don't I need a base line here? Every couple of days I'm less to

do

> > what I was able to do a short time ago...how are they going to

> > regular this and measure it?? Is it me or does this sound about

> > right to any of you???

> >

> > Take good care,

> > Sharon

>

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

Share this post


Link to post
Share on other sites
Guest guest

I have been on prednisone for the last 3 years. Ranging from 5 mg per day

all the way up to 40 mg. I average 10mg unless I am flaring really bad.

My doc also prescribes Oxycontin for pain with Lortab for breakthrough pain.

Jill

On 3/29/08, Melynda Gamez <melyndagamez@...> wrote:

>

> judy, ra in my opinoin is based on lab results(blood),x-rays,redness,

> moderate to severe pain & inflammation of the joints.... i have been on

> prednisone since i was 18 yrs old. & if i had to do it all over again, I

> WOULD NOT TAKE IT!!! yes, the side effects are BAD!! i also have osteo.mybones

are very FRAGILE & BREAK easily!!! yes it helps SOMETIMES but its not

> worth all those AWEFUL SIDE EFFECTS! good luck in whatever you decide to

> do... god bless,melyndagamez 3/29/08 4:48p.m.central time

>

> Re: [ ] Re: Lab results...FINALLY

>

> I was advised of this too. If my SED Rate, Westgren,

> anti ccp were elevated and if I responded to the

> treatment then they knew inflammatory arthritis was

> present.

> --- J Acciarito <jacyone@... <jacyone%40comcast.net>> wrote:

>

> > Is that generally true? That if your symptoms are

> > relieved with prednisone, then RA is indicated?

> >

> > Judy

> >

> > Diane wrote:

> >

> > Hi Sharon,

> > In my opinion, I think the Doctor put you on the

> > prednisone to see if

> > it works...if it does, than she knows it is

> > definitely RA...sometimes

> > there can be other reason for a raised count or a

> > false positive but

> > if the prednisone works and the pain is gone, then

> > she knows it is RA

> > for sure...does that makes sense to you? You are

> > right, prednisone

> > is not the only treatment for the inflammation.

> > Hope you are feeling better...be careful with the

> > prednisone...it is

> > a powerful and tricky medication with lots of side

> > effects...

> >

> > I would suggest getting yourself to a good

> > Rheumatologist as quickly

> > as possible...I think you said she was your family

> > doctor...

> > .___

> >

> > [Non-text portions of this message have been

> > removed]

> >

> >

>

> __________________________________________________________

> Like movies? Here's a limited-time offer: Blockbuster Total Access for one

> month at no cost.

> http://tc.deals./tc/blockbuster/text4.com

>

> ------------------------------------

>

>

Share this post


Link to post
Share on other sites
Guest guest

I have AS. I was diagnosed a year and half ago. My Rhuemy says that pred

doesn't work for AS. I take MTX, Remicade, Folic Acid, and we added two

months ago Arava and Volteran(as needed). Stress is a huge factor in my

flairs. But I am much, much, much better off than I was a year ago. I can

do much more and feel like I have a life again. My recommendation is they

need to stay in communication with their doctor and talk about different

combos. What works for one isn't right for another.

Kate G

AS

Hashi's

At 08:43 AM 3/30/2008, you wrote:

>Hi Rita in Georgia! My 15 yr old son and 8 yr old daughter both have

>Ankylosing

>Spondylitis. Son was diagnosed 12 yrs ago and daughter 3 years ago. Any

>insight into

>what we can be doing as I look to their future? Neither one is doing very

>well right now

>with many complex problems with no answers other than they have

>arthritis. None of the

>drugs seem to work for very long with either one of them and they both

>have such

>stomach pain right now that they are both off of pain meds to try to ease

>their stomaches.

>Prednisone hasn't been very successful for them when they have tried it.

>Myndi

Share this post


Link to post
Share on other sites
Guest guest

Hi Melynda,

I still don't know yet what my actual numbers were. I called the

doctor's office today to get a copy of my labs and DX and they were

supposed to call back..well guess what? They didn't. Could be they

stuck it in the mail though. Maybe it will come tomorrow or at least

they'll call and I can go pick it up. Normal is 1 or 2 huh? I'll

have to see what mine is when I get the report. That's good to know.

I'm stil waiting for Pred to kick in. I had a different approach

today. I had a lot of things to do and rather than sit and complain

about how rotten I felt..I decided to get on with it and go as far as

I could. It was all stuff at my desk basically and I did accomplish

a lot. The I paid the bills and I took a little nap. I got back up

and got a few more things done...had another down time. I'm just not

going to complain about it anymore. I have really let myself get

into a complaining mode and it's making me feel even worse. I'll

save the complaining for the doctor's offices. Not to worry..I'm

hanging in there. I hope you can do the same. Thanks again for the

information.

Take good care,

Sharon

> >

> > Sharon,

> >

> > The rheumatoid factor (RF) test is not like a pregnancy test.

> >

> > Despite its name, rheumatoid factor production is not specific to

> RA. There

> > are many possible reasons for a positive RF, even simply aging.

> >

> > In addition, there is no one standard test for RF, so the way the

> results

> > are determined, reported, and interpreted will vary from lab to

lab.

> >

> > I suspect that your physician is not sure of the diagnosis and

> wants to see

> > how you do on prednisone; however, watching and waiting for five

> months is

> > not a good idea.

> >

> > It would be wise to find a rheumatologist for a second opinion.

> >

> >

> >

> > Not an MD

> >

> >

> > > [ ] Lab results...FINALLY

> > >

> > > Hi everyone,

> > >

> > > I got a phone call a little while ago from my doctor's office to

> > > inform me that they had my labs back and she wanted to talk to

me

> > > about it. My cholesterol was high...knew that it would be. She

> > > suggested I get more exercise and walk 20 minutse a day....if

> only I

> > > could. SED rate is 59. Tested negative for Lyme and Lupus. I

> asked

> > > about the RA Factor and she said it was " high " ...I asked if that

> > > meant positive and she said yes. I thought it was like a

> pregnency

> > > test...either negative or positive. I didn't know there were

> numbers

> > > associated with it. Do any of you know about a number

associated

> > > with this?

> > >

> > > Also, they are going to put me on Pred. It's a 5 month

> thing...this

> > > month 20 mil, 15 next month, 10 and then 5 and after 5 months of

> > > taking that daily I am supposed to call them. I'm not a rocket

> > > scientist but this isn't slowing my RA in any way. It's just

> helping

> > > with inflamation. They aren't ordering x-rays or a bone

> scan....??

> > > Don't I need a base line here? Every couple of days I'm less

to

> do

> > > what I was able to do a short time ago...how are they going to

> > > regular this and measure it?? Is it me or does this sound about

> > > right to any of you???

> > >

> > > Take good care,

> > > Sharon

> >

>

>

>

> ------------------------------------

>

>

Share this post


Link to post
Share on other sites
Guest guest

this is rita. what exactly is your symptoms for as??? where is your pain, etc.

thanks ritawages@...

Re: [ ] Re: Lab results...FINALLY

I have AS. I was diagnosed a year and half ago. My Rhuemy says that pred

doesn't work for AS. I take MTX, Remicade, Folic Acid, and we added two

months ago Arava and Volteran(as needed). Stress is a huge factor in my

flairs. But I am much, much, much better off than I was a year ago. I can

do much more and feel like I have a life again. My recommendation is they

need to stay in communication with their doctor and talk about different

combos. What works for one isn't right for another.

Kate G

AS

Hashi's

At 08:43 AM 3/30/2008, you wrote:

>Hi Rita in Georgia! My 15 yr old son and 8 yr old daughter both have

>Ankylosing

>Spondylitis. Son was diagnosed 12 yrs ago and daughter 3 years ago. Any

>insight into

>what we can be doing as I look to their future? Neither one is doing very

>well right now

>with many complex problems with no answers other than they have

>arthritis. None of the

>drugs seem to work for very long with either one of them and they both

>have such

>stomach pain right now that they are both off of pain meds to try to ease

>their stomaches.

>Prednisone hasn't been very successful for them when they have tried it.

>Myndi

________________________________________________________________________________\

____

No Cost - Get a month of Blockbuster Total Access now. Sweet deal for

users and friends.

http://tc.deals./tc/blockbuster/text1.com

Share this post


Link to post
Share on other sites
Guest guest

thank you jill for not stabbing perdnisone. i take it for flares only and could

not live without it. i would go weeks and not be able to move out of bed plus

due to ra i have restrictive lung disease and with a flare i get tons of

inflammation in the lungs and oxygen goes down. do you take the pred daily for

three years? besides the fragile bones and swelling what is so bad about

prednisone? i would be dead without it. my ra is severe my rhuemy has told me

it will definately shorten my lifespan it is so bad. so if i can have a few

good days every now and then with prednisone and go to church or get groceries

then thank god for prednision. this support group totally is against prednison.

is it me will i be doomed because i take it for flares????thanks rita

Re: [ ] Re: Lab results...FINALLY

>

> I was advised of this too. If my SED Rate, Westgren,

> anti ccp were elevated and if I responded to the

> treatment then they knew inflammatory arthritis was

> present.

> --- J Acciarito <jacyonecomcast (DOT) net <jacyone%40comcast. net>> wrote:

>

> > Is that generally true? That if your symptoms are

> > relieved with prednisone, then RA is indicated?

> >

> > Judy

> >

> > Diane wrote:

> >

> > Hi Sharon,

> > In my opinion, I think the Doctor put you on the

> > prednisone to see if

> > it works...if it does, than she knows it is

> > definitely RA...sometimes

> > there can be other reason for a raised count or a

> > false positive but

> > if the prednisone works and the pain is gone, then

> > she knows it is RA

> > for sure...does that makes sense to you? You are

> > right, prednisone

> > is not the only treatment for the inflammation.

> > Hope you are feeling better...be careful with the

> > prednisone.. .it is

> > a powerful and tricky medication with lots of side

> > effects...

> >

> > I would suggest getting yourself to a good

> > Rheumatologist as quickly

> > as possible...I think you said she was your family

> > doctor...

> > .___

> >

> > [Non-text portions of this message have been

> > removed]

> >

> >

>

> ____________ _________ _________ _________ _________ _________ _

> Like movies? Here's a limited-time offer: Blockbuster Total Access for one

> month at no cost.

> http://tc.deals. / tc/blockbuster/ text4.com

>

> ------------ --------- --------- ------

>

>

Share this post


Link to post
Share on other sites
Guest guest

Thanks Kate. I'm so glad to hear you say that Pred doesn't always work for AS.

It really

doesn't work for my kids. Therefore, the Dr thinks their pain isn't due to

their arthritis

when we know it is. What else would it be? My daughter's Dr is sending her to

PT which is

helping, but I still am worried about long term damage. Neither one has ever

tried

Remicade. My son tried Enbrel - no luck either. Both have done/do MTX - don't

know

how much this is helping. They both have lower leg pain mainly. Ankles hurt

the most

and then the knees. They can't stand too long or walk too long. My daughter

has been

having neck pain and has had shoulder & elbow pain as well. These haven't

lasted too

long. Sports are manageable since they are giving a lot for a short amount of

time. We're

always being told that they don't show signs of swelling so everything " looks

good " . Well,

it's my understanding that AS doesn't show obvious swelling, so then what do we

do? We

can't get MRI's every month. They have pain every day and they adjust. Great!

But, what

about long term damage? That's what is frightening me.

As for other symptoms - they have included vision problems, dizziness, GI

problems,

urinary problems, chest pain, numbness in feet, gall stones, swollen lymph nodes

in GI, GI

inflammation, vasculitis in legs (that we know of), psoriasis.... All of this

" stuff " brought on

depression in my son - who can blame him??? So, we had to add that to the list

of what

we are battling. It's never ending - and still they have pain every day!

By the way, most of the above symptoms started in my son when he had been

medication

free for almost an entire year, so they have basically ruled out the fact that

it could be due

to medication.

Still searching for answers.... Myndi

> >Hi Rita in Georgia! My 15 yr old son and 8 yr old daughter both have

> >Ankylosing

> >Spondylitis. Son was diagnosed 12 yrs ago and daughter 3 years ago. Any

> >insight into

> >what we can be doing as I look to their future? Neither one is doing very

> >well right now

> >with many complex problems with no answers other than they have

> >arthritis. None of the

> >drugs seem to work for very long with either one of them and they both

> >have such

> >stomach pain right now that they are both off of pain meds to try to ease

> >their stomaches.

> >Prednisone hasn't been very successful for them when they have tried it.

> >Myndi

>

>

>

>

>

>

________________________________________________________________________________\

____

> No Cost - Get a month of Blockbuster Total Access now. Sweet deal for

users

and friends.

> http://tc.deals./tc/blockbuster/text1.com

>

>

Share this post


Link to post
Share on other sites
Guest guest

no rita you wont be doomed! we all have our views on this HORRIBLE med but YES

it does HELP but KILLS as well!!! i know first hand what this med does for me &

what IT DOES TO MY BODY... my BONES are always fracturing or breaking, i cant

walk, i have gained soo much weight & my BONES cant TAKE IT!!! this is my reason

as for others, i dont know!!! god bless,melyndagamez 4/01/08 12:06p.m.central

Re: [ ] Re: Lab results...FINALLY

>

> I was advised of this too. If my SED Rate, Westgren,

> anti ccp were elevated and if I responded to the

> treatment then they knew inflammatory arthritis was

> present.

> --- J Acciarito <jacyonecomcast (DOT) net <jacyone%40comcast. net>> wrote:

>

> > Is that generally true? That if your symptoms are

> > relieved with prednisone, then RA is indicated?

> >

> > Judy

> >

> > Diane wrote:

> >

> > Hi Sharon,

> > In my opinion, I think the Doctor put you on the

> > prednisone to see if

> > it works...if it does, than she knows it is

> > definitely RA...sometimes

> > there can be other reason for a raised count or a

> > false positive but

> > if the prednisone works and the pain is gone, then

> > she knows it is RA

> > for sure...does that makes sense to you? You are

> > right, prednisone

> > is not the only treatment for the inflammation.

> > Hope you are feeling better...be careful with the

> > prednisone.. .it is

> > a powerful and tricky medication with lots of side

> > effects...

> >

> > I would suggest getting yourself to a good

> > Rheumatologist as quickly

> > as possible...I think you said she was your family

> > doctor...

> > .___

> >

> > [Non-text portions of this message have been

> > removed]

> >

> >

>

> ____________ _________ _________ _________ _________ _________ _

> Like movies? Here's a limited-time offer: Blockbuster Total Access for one

> month at no cost.

> http://tc.deals. / tc/blockbuster/ text4.com

>

> ------------ --------- --------- ------

>

>

Share this post


Link to post
Share on other sites
Guest guest

I

> The Pharmacist had suggested Vicodan toom Pris. I think my doctor

> wants to see how I do on Pred on its own thinking maybe it will

> reduce the inflammation and the pain will be gone. I guess it's

> possible but it's just hard to imagine.>>>>

>

For me Prednisone is the best pain pill I have ever had.

Also, he may be using it to diagnose if you have an inflammation

problem....(RA).

Pris

**************

Create a Home Theater Like the Pros. Watch the video on AOL

Home.

(http://home.aol.com/diy/home-improvement-eric-stromer?video=15 & amp;

ncid=aolhom00030000000001)

Share this post


Link to post
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
Sign in to follow this  

×
×
  • Create New...