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In a message dated 12/15/00 9:05:03 PM Pacific Standard Time, nneW5@... writes:

When I had my 2nd acute attack this past Oct, had severe joint pain which the doc advised was part of the hep. Within 24 hrs of starting prednisone, the pain was gone. I am currently on 20 mg prednisone, have been since before Thanksgiving. Over the past few days, joint pain has returned, severe enough that it is starting to limit my activity...I am also having more sleep disturbances (more than I had with the prednisone) and more fatigue. Can anybody share their experiences along these lines?

I can't give you much help, as I'm not very knowledgeable and because throughout my life, I've tended to not call doctors until problems progressed to big, big trouble. I don't recommend this mind-set for others.

When I've complained of joint pain, I'm told it's "Just the Prednisone." I sleep very, very heavily, but I'm told that's not typical of Prednisone users. Fatigue -- oh, well.

Here's one stray bit of information, although I'm not sure it's applicable. My LiverDoc isn't very talkative, to say the least. However, when I last saw him (in May), he said I might feel WORSE rather than better as the Prednisone is reduced, as it acts as an upper for some people.

I don't understand this remark: "I am also having more sleep disturbances (more than I had with the prednisone) and more fatigue." You're taking prednisone now, right?

Good luck, and BE CAREFUL. This is YOUR life, and you have to take good care of it. Do you have an advice nurse you can call on weekends?

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marianne..... We are given prednisone because of its ability to do more

than one thing....two of which are: (1) as an immunosupressant....to

suppress the proliferation of the antibodies that are mistakenly

attacking our liver cells and (2) as an anti-inflammatory..... AIH

causes inflammation of the liver by the action of the anti-bodies

attacking it... the auto immune disease also inhibits the bodys release

of certain corticosteoids that usually fight inflammations of other

types...hence our joints become inflammed and pain results... the

predisone augments the body`s productionn of these corticosteroids which

are hormones produced by the adrenal glands and diminishes the pain...

in othe words te prednisone doesn`t cause the pain but rather lessens

it... too much use of prednisone can atrophy the adrenals and natural

production is slowed or stopped..if you aren`t getting enough of these

hormones the pain returns therefore the dosage of prednisone you are

taking may not be enough to augment your natural abiiity to lessen the

inflammation in your joints ....... it is the hepatitis...the liver

disase itself that causes the fatigue NOT the prednisone. Fatgue itself

can cause inflammation. But the SIDE efffects of prednisone may

contribute. prednisone can cause insomnia which enhances fatigue...as

you aren`t getting enough sleep and it can cause depression which also

can contribute to inflammation

remember that prdnisone is prescribed as an antiinflammatory and then as

an imunosupressant....the goal of most doctors is to get as low a dose

of prednisone as possible to augment your own production of anti

inflammatories - to fight your hepatitis induced inflammed liver and

still supress the overactive antibodies which is why they add imuran to

the mix . imuran is chiefly an immunosuppressant . You want as low of

dose as possible of prednisone because of its many well documented side

effects and still fight inflammation (which will eventually kill

-cirrhos - the liver cells if left untreated) with imunos. to inhibit

the production of those maverick antibodies. I know this is wordy but I

don`t know how else to explain it. I suffered joint and back pain-

sometimes severe - for 2-3 years before I was Dxd AIH.when I was given

prednione 40mgs. the pain went away-- as the dosage was lowered--now

10mgs.-- the pain came back . I use Advil and a heating pad as well as

wet heat to treat it when it becomes too bad that plus a little pain

management by meditation (which I`m not too informed about.) Maybe your

doctor can prescribe some pain meds. (others here use it) but I don`t

think you want to be on high doages of prednisone for long periods of

time as you know the side effects it carries. Hope this was of some

help...

love and serenity

jerry

Want to see if I have anything to be concerned about, that is, if my

present regimen of prednisone is not doing the trick..I would call the

doc..but am having blood work on Tuesday as it is...just wondering if

I might be in for some new fun and games....

When I had my 2nd acute attack this past Oct, had severe joint pain

which the doc advised was part of the hep. Within 24 hrs of starting

prednisone, the pain was gone. I am currently on 20 mg prednisone,

have been since before Thanksgiving. Over the past few days, joint

pain has returned, severe enough that it is starting to limit my

activity...I am also having more sleep disturbances (more than I had

with the prednisone) and more fatigue. Can anybody share their

experiences along these lines?

I've been waiting for the pain to go away...and I haven't called the

doc before now cause if I do I cant deny it's there anymore....might

lose my title as Queen!

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Jerry, thanks for your very helpful summary of prednisone's uses and characteristics.

Re: . . ."too much use of prednisone can atrophy the adrenals and natural

production is slowed or stopped. . ."

I've been concerned with the possibility that the adrenals won't go back to normal production after high dosages of prednisone, resulting in something resembling 's disease, I think. (I'm currently too lazy to go back to the references I read this summer.) I've read that this is sometimes a problem. Have any of you run into that problem?

Harper

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I believe you are correct..... I read that same thing somewhere in my

readings but like you, am too lazy to look it up.( Is laziness the

problem to which you are refering?)

Jerry, thanks for your very helpful summary of prednisone's uses and characteristics.

Re: . . ."too much use of prednisone can atrophy the adrenals and natural

production is slowed or stopped. . ."

I've been concerned with the possibility that the adrenals won't go back to normal production after high dosages of prednisone, resulting in something resembling 's disease, I think. (I'm currently too lazy to go back to the references I read this summer.) I've read that this is sometimes a problem. Have any of you run into that problem?

Harper

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Thanks for the input, Harper. I will be talking to the nurse re the

joint pain. Guess I am just hoping that I am not going backwards.

I was surprised by your remark that your doc said the prednisone

caused the joint pain. As Jerry described, it suppresses

inflamation, and in doing so should not be causing joint pain.

Much as prednisone can cause problems, the relief I experienced the

first day I was on it was ...oh lord... To go from not wanting to

move at all because of pain, to being able to walk, write and most

importantly hug my kids was incredible.

> In a message dated 12/15/00 9:05:03 PM Pacific Standard Time,

> nneW5@e... writes:

>

>

> > When I had my 2nd acute attack this past Oct, had severe joint

pain

> > which the doc advised was part of the hep. Within 24 hrs of

starting

> > prednisone, the pain was gone. I am currently on 20 mg prednisone,

> > have been since before Thanksgiving. Over the past few days, joint

> > pain has returned, severe enough that it is starting to limit my

> > activity...I am also having more sleep disturbances (more than I

had

> > with the prednisone) and more fatigue. Can anybody share their

> > experiences along these lines?

> >

>

> I can't give you much help, as I'm not very knowledgeable and

because

> throughout my life, I've tended to not call doctors until problems

progressed

> to big, big trouble. I don't recommend this mind-set for others.

>

> When I've complained of joint pain, I'm told it's " Just the

Prednisone. " I

> sleep very, very heavily, but I'm told that's not typical of

Prednisone

> users. Fatigue -- oh, well.

>

> Here's one stray bit of information, although I'm not sure it's

applicable.

> My LiverDoc isn't very talkative, to say the least. However, when I

last saw

> him (in May), he said I might feel WORSE rather than better as the

Prednisone

> is reduced, as it acts as an upper for some people.

>

> I don't understand this remark: " I am also having more sleep

disturbances

> (more than I had with the prednisone) and more fatigue. " You're

taking

> prednisone now, right?

>

> Good luck, and BE CAREFUL. This is YOUR life, and you have to take

good care

> of it. Do you have an advice nurse you can call on weekends?

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Thank you Jerry...I appreciate the information, very much. I know

that the lack of sleep is contributing to the fatigue feeling...but

the fatigue I have had lately is different than what I had 2 weeks

ago.more overwhelming, I guess...I had not considered depression as

contributing to fatigue..altho I have some concern along those

lines... seems that instead of prednisone making me...

ummmm...belligerent, as my husband had feared..lol...it has instead

made me rather weepy at times...takes a little more effort some days

to get out of bed and not do the pity party thing. But the weepy

stuff has been there the whole time...not just lately.

> marianne..... We are given prednisone because of its ability to do

more

> than one thing....two of which are: (1) as an

immunosupressant....to

> suppress the proliferation of the antibodies that are mistakenly

> attacking our liver cells and (2) as an anti-inflammatory..... AIH

> causes inflammation of the liver by the action of the anti-bodies

> attacking it... the auto immune disease also inhibits the bodys

release

> of certain corticosteoids that usually fight inflammations of other

> types...hence our joints become inflammed and pain results... the

> predisone augments the body`s productionn of these corticosteroids

which

> are hormones produced by the adrenal glands and diminishes the

pain...

> in othe words te prednisone doesn`t cause the pain but rather

lessens

> it... too much use of prednisone can atrophy the adrenals and

natural

> production is slowed or stopped..if you aren`t getting enough of

these

> hormones the pain returns therefore the dosage of prednisone you are

> taking may not be enough to augment your natural abiiity to lessen

the

> inflammation in your joints ....... it is the hepatitis...the liver

> disase itself that causes the fatigue NOT the prednisone. Fatgue

itself

> can cause inflammation. But the SIDE efffects of prednisone may

> contribute. prednisone can cause insomnia which enhances

fatigue...as

> you aren`t getting enough sleep and it can cause depression which

also

> can contribute to inflammation

> remember that prdnisone is prescribed as an antiinflammatory and

then as

> an imunosupressant....the goal of most doctors is to get as low a

dose

> of prednisone as possible to augment your own production of anti

> inflammatories - to fight your hepatitis induced inflammed liver and

> still supress the overactive antibodies which is why they add imuran

to

> the mix . imuran is chiefly an immunosuppressant . You want as low

of

> dose as possible of prednisone because of its many well documented

side

> effects and still fight inflammation (which will eventually kill

> -cirrhos - the liver cells if left untreated) with imunos. to

inhibit

> the production of those maverick antibodies. I know this is wordy

but I

> don`t know how else to explain it. I suffered joint and back pain-

> sometimes severe - for 2-3 years before I was Dxd AIH.when I was

given

> prednione 40mgs. the pain went away-- as the dosage was lowered--now

> 10mgs.-- the pain came back . I use Advil and a heating pad as well

as

> wet heat to treat it when it becomes too bad that plus a little pain

> management by meditation (which I`m not too informed about.) Maybe

your

> doctor can prescribe some pain meds. (others here use it) but I

don`t

> think you want to be on high doages of prednisone for long periods

of

> time as you know the side effects it carries. Hope this was of some

> help...

> love and serenity

> jerry

>

>

> Want to see if I have anything to be concerned about, that is, if my

> present regimen of prednisone is not doing the trick..I would call

the

> doc..but am having blood work on Tuesday as it is...just wondering

if

> I might be in for some new fun and games....

>

> When I had my 2nd acute attack this past Oct, had severe joint pain

> which the doc advised was part of the hep. Within 24 hrs of starting

> prednisone, the pain was gone. I am currently on 20 mg prednisone,

> have been since before Thanksgiving. Over the past few days, joint

> pain has returned, severe enough that it is starting to limit my

> activity...I am also having more sleep disturbances (more than I had

> with the prednisone) and more fatigue. Can anybody share their

> experiences along these lines?

>

> I've been waiting for the pain to go away...and I haven't called the

> doc before now cause if I do I cant deny it's there anymore....might

> lose my title as Queen!

>

>

>

>

>

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Thanks Don..yes..the relief that first day was wonderful!..My doc does

have plans to taper..trying to get me down to 5 mg...He started me @

60, and within 2 weeks was down to 20, which is where I am now. He

had wanted to drop me to 15 2 weeks ago , but altho my enzymes were

down,it wasn't as much as he had wanted, so he kept me @ the same

level for a couple more weeks.

He has already told me that if he cannot get me down to @ least 10mg,

then will look at adding MP6 so he can get the prednisone low and

maybe reduce the possible prednisone problems.

I do miss that rush of the high dosage tho! At 20 mg I get by...but

seems to take about 4 to 5 hours after waking before I become even

marginally functional...not like it was @ 60...talk about

zooming!..LOL

> > In a message dated 12/15/00 9:05:03 PM Pacific Standard Time,

> > nneW5@e... writes:

> >

> >

> > > When I had my 2nd acute attack this past Oct, had severe joint

> pain

> > > which the doc advised was part of the hep. Within 24 hrs of

> starting

> > > prednisone, the pain was gone. I am currently on 20 mg

prednisone,

> > > have been since before Thanksgiving. Over the past few days,

joint

> > > pain has returned, severe enough that it is starting to limit

my

> > > activity...I am also having more sleep disturbances (more than

I

> had

> > > with the prednisone) and more fatigue. Can anybody share

their

> > > experiences along these lines?

> > >

> >

> > I can't give you much help, as I'm not very knowledgeable and

> because

> > throughout my life, I've tended to not call doctors until

problems

> progressed

> > to big, big trouble. I don't recommend this mind-set for

others.

> >

> > When I've complained of joint pain, I'm told it's " Just the

> Prednisone. " I

> > sleep very, very heavily, but I'm told that's not typical of

> Prednisone

> > users. Fatigue -- oh, well.

> >

> > Here's one stray bit of information, although I'm not sure it's

> applicable.

> > My LiverDoc isn't very talkative, to say the least. However,

when I

> last saw

> > him (in May), he said I might feel WORSE rather than better as

the

> Prednisone

> > is reduced, as it acts as an upper for some people.

> >

> > I don't understand this remark: " I am also having more sleep

> disturbances

> > (more than I had with the prednisone) and more fatigue. " You're

> taking

> > prednisone now, right?

> >

> > Good luck, and BE CAREFUL. This is YOUR life, and you have to

take

> good care

> > of it. Do you have an advice nurse you can call on weekends?

>

>

> eGroups Sponsor

>

> Paid Net2phone Advertisement - Click Here!

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>

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