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Tawny, Shirley, , Chriss, Doreen and all the Group;

Every 2 weeks I been taking Humira injections.. So far it's been 3

injections.. It was like a miracle,, no more pain.. I got up this

morning and every joint in my body hurt.. OMG.. is this a flare??

Did my humira quit working?? Panic,, fear,, my thought have gone

wild.. Could this be a FLARE everyone talks about..

What should I do?? How long does it last?? I have sufferd so much

in the last 5 years from RA pain and fibro.. I don't think its

fibro because with fibro my muscles are tender to touch.. I saved

some prednisone but I don't want to take that.. I go to my rhuemy in

a few days and she takes blood test.. She may think I am getting it

from somewhere else... I know with the prednisome start big than

lower the dosage.. I saved about a month supply..

How long does a flare last??? Does this mean the humira don't work

anymore.. I think I am sick to my stomache this morning from

worry.. Is the humira injections not working anymore?? I don't

know what to think..

You guys have helped me so much I hate complaining.. I guess this

is a flare.. I read that we get them on occasions... I didnt think I

would get one so fast.. I just been on the Humira a little over 6

weeks.. I am looking for responses from anyone that has had this

problem with meds that worked than stopped..

gentle hugs

Clora

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Better to talk to your doc first about the prednisone. They often like to

document the flares too so that they can see the patterns of them and can tell

how you are doing with the medication. I would try to stick it ou with the

Humira you are taking since it isn't in full effect and I agree with Lori, it

could be weather and pressure changes, illness, stress, etc. that could bring

on a flare.... just when I think I am doing great ( " what do they mean I have

RA, they must have made a mistake? " ) I am humbled... I have a flare...even if

it's on a smaller scale brought on by weather, stress, etc. I sleep, or do

whatever I need to to try to get past it; call the doc if necessary or wait it

out until the next appointment- but if you've been doing well- there's a lot

to feel hopeful about!!!

Abby

In a message dated 10/6/2008 6:07:40 A.M. Pacific Daylight Time,

queenstitcher@... writes:

I wouldn't take prednisone without the doctor's approval.

**************New MapQuest Local shows what's happening at your destination.

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Hi Clora,

Has your weather changed recently? Big changes in temperature or the pressure

can make me feel pretty bad for a few days, but once my body adjusts, I'm back

to normal. You've only had 3 injections, so I really don't think that the

medication has stopped working. For me it took about 6 months to realize the

full effect of the Humira. You could also just be getting sick. The first

thing that I would do would not worry yourself sick(er). I know that's easier

said than done, but I have yet to have an experience in life where the worrying

has paid off for me. Since your seeing the Rheumotogist in a few days, I'd

either just tough it out until the appointment, or try to have the appointment

changed to an earlier date. If your note sure what to do, why don't you just

call the office and see what they say? That certainly won't hurt anything and

you won't have to worry about what's going on. I wouldn't take prednisone

without the doctor's approval. You could always take a hot bath to see if that

would help ease some of your discomfort. If you are having a flare, the doctor

will probably put you on a short course of prednisone to try to stop it.

HTH,

Lori

http://home.comcast.net/~queenstitcher/

http://stitchingqueen.multiply.com

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Aw (((((CLORA))))), I hear the fear and anxiety in your words. Hang in

there, honey. Call your Rheumatologist. You could very well be having

a flare up, but I don't think that would necessarily mean your Humira

isn't working. I don't know how long a " flare " can last. My RA/FMS is

still out of control in general. I hope you feel better soon. Keep us

posted.

Now BREATHE....Deep breath in through your nose, blow it slowly out of

your mouth....repeat...........Doreen :)

>

> Tawny, Shirley, , Chriss, Doreen and all the Group;

>

> Every 2 weeks I been taking Humira injections.. So far it's been 3

> injections.. It was like a miracle,, no more pain.. I got up this

> morning and every joint in my body hurt.. OMG.. is this a flare??

> Did my humira quit working?? Panic,, fear,, my thought have gone

> wild.. Could this be a FLARE everyone talks about..

>

> What should I do?? How long does it last?? I have sufferd so much

> in the last 5 years from RA pain and fibro.. I don't think its

> fibro because with fibro my muscles are tender to touch.. I saved

> some prednisone but I don't want to take that.. I go to my rhuemy

> in a few days and she takes blood test.. She may think I am getting

> it from somewhere else... I know with the prednisome start big

> than lower the dosage.. I saved about a month supply..

>

> How long does a flare last??? Does this mean the humira don't work

> anymore.. I think I am sick to my stomache this morning from

> worry.. Is the humira injections not working anymore?? I don't

> know what to think..

>

> You guys have helped me so much I hate complaining.. I guess this

> is a flare.. I read that we get them on occasions... I didnt think

> I would get one so fast.. I just been on the Humira a little over

> 6 weeks.. I am looking for responses from anyone that has had this

> problem with meds that worked than stopped..

>

> gentle hugs

> Clora

>

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Clora,

Honey, I am so sorry that you are in pain. The sad truth is that we

do have flares. I hope that it doesn't last long and it's good you

are seeing your rheummy in a few days.

It dosen't mean that your Humira isn't working but your rheummy may

want to look at what you are taking now and make an adjustment for

flares.

I hope you are feeling better soon.

Shirley

>

> Tawny, Shirley, , Chriss, Doreen and all the Group;

>

> Every 2 weeks I been taking Humira injections.. So far it's been

3

> injections.. It was like a miracle,, no more pain.. I got up

this

> morning and every joint in my body hurt.. OMG.. is this a flare??

> Did my humira quit working?? Panic,, fear,, my thought have gone

> wild.. Could this be a FLARE everyone talks about..

>

> What should I do?? How long does it last?? I have sufferd so much

> in the last 5 years from RA pain and fibro.. I don't think its

> fibro because with fibro my muscles are tender to touch.. I saved

> some prednisone but I don't want to take that.. I go to my rhuemy

in

> a few days and she takes blood test.. She may think I am getting

it

> from somewhere else... I know with the prednisome start big than

> lower the dosage.. I saved about a month supply..

>

> How long does a flare last??? Does this mean the humira don't work

> anymore.. I think I am sick to my stomache this morning from

> worry.. Is the humira injections not working anymore?? I don't

> know what to think..

>

> You guys have helped me so much I hate complaining.. I guess this

> is a flare.. I read that we get them on occasions... I didnt think

I

> would get one so fast.. I just been on the Humira a little over 6

> weeks.. I am looking for responses from anyone that has had this

> problem with meds that worked than stopped..

>

> gentle hugs

> Clora

>

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Doreen and group;

Awe Doreen your such a sweety pie.. Yes I was so anxious.. You,,

the group and my husband has soothed my fears.. I did everthing

everyone said.. When I read the post I felt so much better..

((breathe in)) ((breathe out)) ok thats better.. Bless your heart

what relaxing words you say..

I will see my rhuemy the 13 this month.. If I got worse I would

definately called her.. I heard that the full effects of the

injections take longer to work sometimes..

I am so so sorry your RA/FMS is still out of controll.. I feel so

helpless for you.. I can't hold you like my child or touch your

hand and say how sorry I am that you hurt.. I have prayed

intensely for you.. I remember your name a lot.. The more people

post their name the more I can put it to the Lord..

I pray for the whole group but saying the name feels so much more

when I pray.. Your suffering and yet you still reach out to comfort

everyone.. You will be blessed just keep on hanging on Gods word and

our prayers are heard.. God bless and take care.

gentle gentle hugs

Clora

> Aw (((((CLORA))))), I hear the fear and anxiety in your words.

Hang in

> there, honey. Call your Rheumatologist. You could very well be

having

> a flare up, but I don't think that would necessarily mean your

Humira

> isn't working. I don't know how long a " flare " can last. My RA/FMS

is

> still out of control in general. I hope you feel better soon. Keep

us

> posted.

>

> Now BREATHE....Deep breath in through your nose, blow it slowly

out of

> your mouth....repeat...........Doreen :)

>

>

> >

> > Tawny, Shirley, , Chriss, Doreen and all the Group;

> >

> > Every 2 weeks I been taking Humira injections.. So far it's

been 3

> > injections.. It was like a miracle,, no more pain.. I got up

this

> > morning and every joint in my body hurt.. OMG.. is this a

flare??

> > Did my humira quit working?? Panic,, fear,, my thought have

gone

> > wild.. Could this be a FLARE everyone talks about..

> >

> > What should I do?? How long does it last?? I have sufferd so

much

> > in the last 5 years from RA pain and fibro.. I don't think its

> > fibro because with fibro my muscles are tender to touch.. I

saved

> > some prednisone but I don't want to take that.. I go to my

rhuemy

> > in a few days and she takes blood test.. She may think I am

getting

> > it from somewhere else... I know with the prednisome start big

> > than lower the dosage.. I saved about a month supply..

> >

> > How long does a flare last??? Does this mean the humira don't

work

> > anymore.. I think I am sick to my stomache this morning from

> > worry.. Is the humira injections not working anymore?? I don't

> > know what to think..

> >

> > You guys have helped me so much I hate complaining.. I guess

this

> > is a flare.. I read that we get them on occasions... I didnt

think

> > I would get one so fast.. I just been on the Humira a little

over

> > 6 weeks.. I am looking for responses from anyone that has had

this

> > problem with meds that worked than stopped..

> >

> > gentle hugs

> > Clora

> >

>

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Abby and group;

I won't take the prednisone because I am going to see my rhuemy in a

few days.. I never thought about documenting the flares,, your

right.. Yes I agree with everyone.. I need to calm myself.. It's

just I was in pain for so long I didnt want it to start again.. I

love to humble myself before the Lord.. I can't think of anything

better than that.. I can deal with a flare amen to that..

I am pretty dutiful to my rhuemy she has been helpful all the way..

I can count myself forutnate to have such a good rhuemy.. Some times

she nerves me but I have to remember she has laws and medical

science to abide by.. The weather has been colder and it has been

storming.. I didnt take that into conserderation.. It was such a

shock after 4 weeks of feeling good to get a flare...

Mind you I am not painless,., I still live with osteo.CHF,, PAH,,

Sleep apnea,, Migrains for 30 years of and on.. I don't freak out

when that hurts real bad haaaaaaaaaaa. It's when something is doing

so good for so short of time and than it hit me like a ton of bricks

dropped on my head.. I know what that feels like to because a arm

to a gaurds house dropped on my head and I thought the brick

building was collasping on me for a minute.. I struggled against the

arm but it brought me down fast and hard..

Indeed I feel hopeful talking to our group and family helping me out

with their concern finally.. My family has finally come to terms

with me having RA.. It was hard enough for me too but I did.,. My

family (you guys) here has been encouraging every day.. thanks Abby

I will be ok.. I am so glad I have friends here to talk about this..

God bless and take care..

gentle hugs

Clora

> Better to talk to your doc first about the prednisone. They often

like to

> document the flares too so that they can see the patterns of them

and can tell

> how you are doing with the medication. I would try to stick it ou

with the

> Humira you are taking since it isn't in full effect and I agree

with Lori, it

> could be weather and pressure changes, illness, stress, etc. that

could bring

> on a flare.... just when I think I am doing great ( " what do they

mean I have

> RA, they must have made a mistake? " ) I am humbled... I have a

flare...even if

> it's on a smaller scale brought on by weather, stress, etc. I

sleep, or do

> whatever I need to to try to get past it; call the doc if

necessary or wait it

> out until the next appointment- but if you've been doing well-

there's a lot

> to feel hopeful about!!!

>

> Abby

>

>

> In a message dated 10/6/2008 6:07:40 A.M. Pacific Daylight Time,

> queenstitcher@... writes:

>

> I wouldn't take prednisone without the doctor's approval.

>

>

>

>

> **************New MapQuest Local shows what's happening at your

destination.

> Dining, Movies, Events, News & more. Try it out!

> (http://local.mapquest.com/?ncid=emlcntnew00000001)

>

>

>

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Shirley and group;

Awe Shirley thanks for so gently telling me... I have read about so

many flares.. I was a little shocked this morning about it but I am

ok now.. I am a little sore but everyone told me it sometimes takes

time for the full affects of humira... I was scared it wasnt going

to keep working but I know it will.. Nothing else has helped so far

but the humira injections..

My rheumy started me out on MXT but all it did was break me out into

itching hives.. I heard so much good about the MXT too.. When I

heard about the enbrel and humira I said thats for me.. I chose

humira cause its every 2 weeks for the injections.. I am grateful

there are other meds I can try also.. Thank you Shirley its always

great to read your posts you are such a darling person.. God bless

and take care..

gentle hugs

Clora

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

> Clora,

> Honey, I am so sorry that you are in pain. The sad truth is that

we

> do have flares. I hope that it doesn't last long and it's good you

> are seeing your rheummy in a few days.

> It dosen't mean that your Humira isn't working but your rheummy

may

> want to look at what you are taking now and make an adjustment for

> flares.

> I hope you are feeling better soon.

> Shirley

>

>

>

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Shirley and group;

Awe Shirley thanks for so gently telling me... I have read about so

many flares.. I was a little shocked this morning about it but I am

ok now.. I am a little sore but everyone told me it sometimes takes

time for the full affects of humira... I was scared it wasnt going

to keep working but I know it will.. Nothing else has helped so far

but the humira injections..

My rheumy started me out on MXT but all it did was break me out into

itching hives.. I heard so much good about the MXT too.. When I

heard about the enbrel and humira I said thats for me.. I chose

humira cause its every 2 weeks for the injections.. I am grateful

there are other meds I can try also.. Thank you Shirley its always

great to read your posts you are such a darling person.. God bless

and take care..

gentle hugs

Clora

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

> Clora,

> Honey, I am so sorry that you are in pain. The sad truth is that

we

> do have flares. I hope that it doesn't last long and it's good you

> are seeing your rheummy in a few days.

> It dosen't mean that your Humira isn't working but your rheummy

may

> want to look at what you are taking now and make an adjustment for

> flares.

> I hope you are feeling better soon.

> Shirley

>

>

>

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Thank you so much, Clora. I just speak (type) from my heart. You may

not be able to physically hold me like a child or touch my hand, but I

feel those things in your words as well as your prayers. Thank you so

much, sweet lady. Together and by the Grace of God, we will ALL get

through this.......Doreen :)

>

> Doreen and group;

>

> Awe Doreen your such a sweety pie.. Yes I was so anxious.. You,,

> the group and my husband has soothed my fears.. I did everthing

> everyone said.. When I read the post I felt so much better..

> ((breathe in)) ((breathe out)) ok thats better.. Bless your heart

> what relaxing words you say..

>

> I will see my rhuemy the 13 this month.. If I got worse I would

> definately called her.. I heard that the full effects of the

> injections take longer to work sometimes..

>

> I am so so sorry your RA/FMS is still out of controll.. I feel so

> helpless for you.. I can't hold you like my child or touch your

> hand and say how sorry I am that you hurt.. I have prayed

> intensely for you.. I remember your name a lot.. The more people

> post their name the more I can put it to the Lord..

>

> I pray for the whole group but saying the name feels so much more

> when I pray.. Your suffering and yet you still reach out to

> comfort everyone.. You will be blessed just keep on hanging on Gods

> word and our prayers are heard.. God bless and take care.

>

> gentle gentle hugs

> Clora

>

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Doreen and group;

Your very welcome Doreen.. I love to read where people type from their

hearts.. THe feeling comes through the post.. God bless

gentle hugs

Clora

> Thank you so much, Clora. I just speak (type) from my heart. You may

> not be able to physically hold me like a child or touch my hand, but I

> feel those things in your words as well as your prayers. Thank you so

>

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