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,

I've never had pain on my right side. However, every doctor who has

examined me (and there have been too many) has poked and prodded the liver

area and each has asked me if I had any pain. Most of these same doctors

have commented that there is little if any pain associated with liver

disease, so they must have been checking for inflammation or something

else. None have ever considered that the LUQ pain could be the left lobe

of my liver but they do say that pain there can be caused by other GI

problems like cancer - not a pleasant thought. Since my spleen is always

normal sized they never consider spleen, but the new Internist has now

raised the question about a blood clot. Not inconceivable, but I hope

that's an unlikely possibility. I still think it's muscular though

sometimes the pain is rather sharp which makes me a little anxious.

Take care,

Geri

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Micki,

I'm glad to hear your mom is feeling a little better today. I'm not a

lot of help with pain relief because I'm a grin-and-bear-it type as I

don't react well to most meds. I do think, though, that your mom would

get more relief from nsaids or ibuprofen (presuming she can " stomach "

them) than she would get from Tylenol. As for natural approaches, I use

rest, alternating heat and ice on flaring joints and I use my dumb

little magnets. I have a pretty high pain threshold so my tough it out

approach isn't for everyone but I find I can handle it as long as I just

rest and really be kind to whatever area is flaring.

a Peden

PRYAH@... wrote:

>

> From: PRYAH@...

>

> Hello everyone!

> Well my mom is doing a little bit better today...shes pretty convinced she was

having a herx...she had a few really bad days. She asked me how long they

usually last and I told her it was different for everyone. She has a very good

attitude about it though and that's in no small part because of all of you. We

feel we know what to expect. She wanted me to ask you guys what you all do for

pain relief she is basically taking a bunch of tylenol and that's it. Right now

her head is what causes her the most pain...and she was never one to get

headaches. Maybe someone knows of some natural way she can get some relief...on

another note...she sees her Dr. tomorrow..I'll write and let you know how she

does.

>

> Thanks to everyone in advance

> Micki

>

>

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Micki--

I am a big fan of ice and heat for pain relief. In the summer, I use a lot

if ice, in the winter, moist heat. Times of the year like now, when I can

use both without getting myself too hot or too cold, I use both. For

instance, I might put an ice pack on an achy shoulder for 15 minutes, then

follow it up with moist heat. Two cycles of each is the most helpful--this

takes an hour, but if I'm just watching TV or relaxing, it is a good way to

pass some time. The heat and ice in cycles are especially effective for pain

relief.

If your mom is mostly in bed, you need to be careful with the heat, to avoid

burns. I have used a Bed Buddy, available from Walgreens--it is a long

tube-sock-like tube of fabric, filled with rice. When you microwave them,

the rice gets warm and moist, and it feels great. My mom started making her

own version of the Bed Buddies, so I didn't have to pay $10 for 25 cents

worth of material. She sews up a small, long pillow-shaped piece of fabric,

just like you would make a pillow. She leaves an opening at the corner and

pours the rice in through a funnel. Then she sews the corner up by hand. She

makes up several at a time, and gives them to her sisters and me, and keeps

one for herself!

They are great for cold feet, hands, stiff necks, all sorts of things. Be

sure not to get it too hot--2 1/2 minutes works in my microwave. I think

they are much safer than heating pads, because you don't have to worry about

going to sleep and burning yourself. They just slowly cool off.

Jean

----------

>From: PRYAH@...

>rheumaticonelist

>Subject: rheumatic pain relief

>Date: Thu, Sep 23, 1999, 6:05 PM

>

> From: PRYAH@...

>

> Hello everyone!

> Well my mom is doing a little bit better today...shes pretty convinced she

> was having a herx...she had a few really bad days. She asked me how long

> they usually last and I told her it was different for everyone. She has a

> very good attitude about it though and that's in no small part because of

> all of you. We feel we know what to expect. She wanted me to ask you guys

> what you all do for pain relief she is basically taking a bunch of tylenol

> and that's it. Right now her head is what causes her the most pain...and

> she was never one to get headaches. Maybe someone knows of some natural way

> she can get some relief...on another note...she sees her Dr. tomorrow..I'll

> write and let you know how she does.

>

> Thanks to everyone in advance

> Micki

>

> >

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rheumatic pain relief

>>Date: Thu, Sep 23, 1999, 6:05 PM

>>

>

>> From: PRYAH@...

>>

>> Hello everyone!

>> Well my mom is doing a little bit better today...shes pretty convinced she

>> was having a herx...she had a few really bad days. She asked me how long

>> they usually last and I told her it was different for everyone. She has a

>> very good attitude about it though and that's in no small part because of

>> all of you. We feel we know what to expect. She wanted me to ask you guys

>> what you all do for pain relief she is basically taking a bunch of tylenol

>> and that's it. Right now her head is what causes her the most pain...and

>> she was never one to get headaches. Maybe someone knows of some natural way

>> she can get some relief...on another note...she sees her Dr. tomorrow..I'll

>> write and let you know how she does.

>>

>> Thanks to everyone in advance

>> Micki

>>

>> >

>

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

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Hi Jean.........I, too, use rice bags for moist heat. Mine are about 6 "

square, (perfect size for my hands).......... anything bigger is too heavy

for me to handle. And, when the rice (eventually) " cooks " , I just open the

bag, throw the rice out, wash the bag, and refill it. Sure does beat what

they ask for it at stores! You can also use cracked corn (like from the feed

store), but I don't care for the smell of that, personally. And, for cold

packs, have you ever tried bags of frozen peas? They contour to all body

parts, and can be refroze and reused again and again...........just thought

I'd add my two cents...........

Hi, .

I never had so much luck with the frozen peas. The brand I got refroze into

a lump. I buy small ice packs for about $3 from Sports Authority. They are

Tru-Fit brand. They also come with a neoprene wrap with velcro, which costs

$15 or so with one ice pack included, but they last a long time. They are

great for my elbows and wrists. I ice often after working all day at the

computer, so just wrapping a pack around the arm and forgetting about it for

a whole is nice.

I tried feed corn, but I have dust and mold allergies. The rice is much less

bothersome in that regard.

I know Dr. Brown recommended Ice for swollen joints for his patients in a

herx. I like heat after they calm down a bit.

Jean

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A really easy way to make rice bags is to get some 100% cotton men's tube

socks at the store and fill them with rice and tie a knot in the end. I had to

make quit a few as my whole family loves them in the chilly winter. Heat them in

a microwave for about 3 minutes (you will have to experiment with times

depending on how full you make them and how powerful your oven is). Do try them

if you have a microwave, they are so much safer than a heating pad if you are

drowsy--my mom once scorched her mattress by falling asleep with hers on and it

would have probably caught fire soon if my sister hadn't noticed it!

For me, heat in the winter and cold in the summer works best, too. These

joints just don't like extremes! Liz G

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I've read that the following relieve pain and have cancer-fighting

properties (CAPITALIZED items are particularly powerful pain

relievers):

Herbs

MAITAKE MUSHROOM (Grifola frondosa)-- alleviated pain in 83% of

patients

mistletoe (Iscador)

tumeric (particularly the curcumin in it), burdock, and ginger

reduce inflammation.

chaparral-- check with a health practitioner on hazards of this

herb before using it

angelica

noni (juice)

Goldenseal root poultices

amygdalin-- Available in the form of ground apricot pits,

found in health food stores. Do NOT exceed maximum recommended oral

dosage. Avoid eating (sweet) almonds while taking amygdalin. Do

NOT take megadoses of Vit. C while taking laetrile/amygdalin, and

do NOT use laetrile/amygdalin at times of fever. Take it with food,

in several small dosages throughout the day (NOT 1 large dosage).

Use a good brand, such as Kemdalin

(www.kemsa.com/english/kemdalindescripcion.htm) from KEM, S.A. or

Apricot Kernels from

www.americanbiologics.com/NoFrames/Products/specialtynf.htm

Miscellaneous

Vitamin B-3 (Niacin)-- 50 mg, up to 6x/day

Vit. C-- 500 mg, up to 6x/day (but I wouldn't even take that

much while taking amygdalin w/o a health practitioner's

recommendation)

CESIUM-- may take up to 3 days to be effective

coffee enemas (Check w/health practitioner before using them.)

magnets-- I would consult a health practitioner knowledgeable about

magnets before using them.

VISUALIZATION/IMAGERY, MEDITATION, & RELAXATION TECHNIQUES

Pain Control and Surgical Support Series audiotapes by Hemi-Sync

(www.hemi-sync.com/catalog)-- I've been told they can be powerfully

pain-relieving.

Alt. Medical Treatments

acupuncture

neural therapy

For healing cancer, it's best (if possible) to avoid chemical

painkillers (except perhaps aspirin).

For more info on cancer pain relief, see www.alkalizeforhealth.org

Let me know if you have any questions about any of the above.

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call the pain and stress center for a free catalog: 1 800 669 calm or see

painstresscenter.com

Also search articles on Mercola.com

[ ] pain relief

I am looking for information on pain relief for my husband. He is

suffering the most extreme pain in his esophagus from the chemo and

radiation he recieved. It has been almost two weeks and even

morphine can't relieve the burning and inflamation. He can't sleep

or eat anything even water kills him to swallow. Please give me some

advise. Thank all for any information, Sincerely, Georgia

You are digging your grave with your teeth!

Read Hundreds of Collected Cancer Testimonials and learn:

cancer-testimonials/messages/

Learn more about cancer:

http://curezone.com/diseases/cancer/

http://curezone.com/diseases/cancer/faq.asp

You are receiving this email because you elected to subscribe to the

.

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Dear Georgia,

Go to the natural food store and purchase 's Aloe Vera juice. I

had burning stomach problems, and it has helped. It is not expensive.

Maybe if he just sipped on it ever so slowly, it would promote healing

in the areas that are burning.

Hugs,

queenmama85@... wrote:

>

> I am looking for information on pain relief for my husband. He is

> suffering the most extreme pain in his esophagus from the chemo and

> radiation he recieved. It has been almost two weeks and even

> morphine can't relieve the burning and inflamation. He can't sleep

> or eat anything even water kills him to swallow. Please give me some

> advise. Thank all for any information, Sincerely, Georgia

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Hi all,

I have read and heard about dried Siitake Mushroom as having anti-Cancer

properties.

My wife who has Stage IV Cancer is taking it. She just started it so I don't

know if it will help.

Does anyone has knowledge about it.

Sincerely,

Sandip

Thanks!

Sandip Bist

201 395 2201(w)

201 395 3201(FAX)

> Re: [ ] pain relief

>

> I've read that the following relieve pain and have cancer-fighting

> properties (CAPITALIZED items are particularly powerful pain

> relievers):

>

> Herbs

> MAITAKE MUSHROOM (Grifola frondosa)-- alleviated pain in 83% of

> patients

> mistletoe (Iscador)

> tumeric (particularly the curcumin in it), burdock, and ginger

> reduce inflammation.

> chaparral-- check with a health practitioner on hazards of this

> herb before using it

> angelica

> noni (juice)

> Goldenseal root poultices

> amygdalin-- Available in the form of ground apricot pits,

> found in health food stores. Do NOT exceed maximum recommended oral

> dosage. Avoid eating (sweet) almonds while taking amygdalin. Do

> NOT take megadoses of Vit. C while taking laetrile/amygdalin, and

> do NOT use laetrile/amygdalin at times of fever. Take it with food,

> in several small dosages throughout the day (NOT 1 large dosage).

> Use a good brand, such as Kemdalin

> (www.kemsa.com/english/kemdalindescripcion.htm) from KEM, S.A. or

> Apricot Kernels from

> www.americanbiologics.com/NoFrames/Products/specialtynf.htm

>

>

> Miscellaneous

> Vitamin B-3 (Niacin)-- 50 mg, up to 6x/day

> Vit. C-- 500 mg, up to 6x/day (but I wouldn't even take that

> much while taking amygdalin w/o a health practitioner's

> recommendation)

> CESIUM-- may take up to 3 days to be effective

> coffee enemas (Check w/health practitioner before using them.)

>

> magnets-- I would consult a health practitioner knowledgeable about

> magnets before using them.

>

> VISUALIZATION/IMAGERY, MEDITATION, & RELAXATION TECHNIQUES

>

> Pain Control and Surgical Support Series audiotapes by Hemi-Sync

> (www.hemi-sync.com/catalog)-- I've been told they can be powerfully

> pain-relieving.

>

> Alt. Medical Treatments

> acupuncture

> neural therapy

>

> For healing cancer, it's best (if possible) to avoid chemical

> painkillers (except perhaps aspirin).

>

>

> For more info on cancer pain relief, see www.alkalizeforhealth.org

>

> Let me know if you have any questions about any of the above.

>

> You are digging your grave with your teeth!

> Read Hundreds of Collected Cancer Testimonials and learn:

> cancer-testimonials/messages/

>

> Learn more about cancer:

> http://curezone.com/diseases/cancer/

> http://curezone.com/diseases/cancer/faq.asp

>

> You are receiving this email because you elected to subscribe to the

> .

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I can't agree more. Abbies doctor is extremely concientious about making sure

that Abbie is in as little pain as possible. He expects us to make him aware

of issues.

Christy

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So, are most of your (meaning anyone reading this) kids on pain meds

along with meds to counteract the disease?

This makes me feel totally lame, which isn't the first time here,

because I was trying to stay away from the meds that " cover up " the

disease. know what I mean? Instead, trying to use the meds to counteract

the disease and therefore make her pain free or to the greatest extent

by controlling it all. Was that such a bad idea?

So, am I a lame mama?

The naproxen messed with her tummy. She took that for 3 weeks. She can't

even take Tylenol more then a couple of times in a row now and she used

to take that just fine. So I don't know if there is anything she

*should* be taking for pain, but the Rheumy hasn't said so (probably

cause I said no).

After hearing from you all, I am brought to the conclusion that our

Rheumy allows me to make most of the decisions, which I rather

appreciate, but not if it effects the health of my child -- to an

extent. I know that with the power of decision he has given to me, I

need to be informed.

Yet, I am afraid in all the decisions I must make in what meds my dd

takes. I am a very natural choice mother, not even giving Tylenol for a

fever under 102, (dependant on age) cause it is just a simple biological

function in my opinion. Instead I rely on herbs and such for basic

illnesses. This JRA definitely threw me for a loop. She is on mtx. and

folic acid now and is doing fairly well. Was doing really well on the

remicade also. I don't know why I even agreed (at this point anyway) to

get the Enbrel instead. But I suppose it all ends with Enbrel. Which we

finally have an appt for that on the 17th.

Anyhow, I guess I was just rambling. Sorry to do that to your list. Take

care everyone, I read your messages and feel for your children. Every

time I look into my babies eyes, I know that you are there too.

Lorie (mama to Liberty, age 4 poly JRA)

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Lorie

You are not alone by a long shot. I have one child with JRA and one with epilepsy and BOTH were on meds that required constant blood and urine monitoring to make sure that their internal organs and blood weren't being compromised. I am a person who NEVER takes or give out medication unless absolutely necessary so heavily medicating my children nearly gave me a nervous breakdown. But after much consultation with many parents (including my own sister who has a child with serious auto-immune problems), doctors and researching online, I came to the conclusion that I needed to treat the whole disease including the pain because, as bad as the meds are, experts don't really have any idea of what the stress hormones that they believe are put off when you are in pain, especially chronic pain, do to the body, especially in young bodies, in the long term. I chose to take the action of something that could actually be monitored ie. medication. There is also a theory that I have heard from several parents (corroborated by a few articles that I have read but I don't think it's mainstream) that if you treat the auto-immune disease fully there may be the chance that you can "trick" the body into believing that it has "finished" it's job (attacking itself instead of a "real" enemy) and have remission - short or long-term. So that's how I decided.

I know how agonizing the process is and I wish you the best of luck. My son (he has PA JRA) seems to be in remission now. He was on high doses of ibuprofen, along with Zantac because of stomach problems, for over a year. Should he go back into a flare we know that he will have to move up the meds chain because the Zantac no longer dents the stomach problems from Ibuprofen. I just keep my fingers crossed and pray for "permanent" remission.

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Lorie Jo.............first off, you are NOT a lame

mama!!!!!

*I* think as parents, we all do what *we* think is

right for our children at any given time.

AND........every decision we make is a difficult one,

JRA related or not.

My ds takes motrin/advil or even OTC naprosyn for his

JA symptoms and does quite well.

Ok...........my dd is not on " pain " meds regularly.

She is taking mtx,folic acid, prednisone, Enbrel, and

Zofran (to counteract the horrible sickness she gets

from the mtx). She unfortunately is allergic to most

of the NSAIDS, and Vioxx as well :(

So..........for her pain, if it is really unbearable,

I will give her tylenol. I know it's really a low end

drug, but even if it takes away the edge of pain, it's

done it's job.

Yes, my rheumy allows dd/me to take an active role in

her treatment. We come up with

suggestions/possibilities, and then we discuss them at

length.......pros and cons. Sometimes we are not in

agreement, but for the most part we are okay :)

Have a great day.

Isabel

__________________________________________________

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hi lorie..i was wondering what happened that your rheumy stopped remicade

and decided to go with enbrel..my daughter Tabitha who is sixteen and has

poly jra..was your daughters age when i found out she had this nasty

disease. She was on enbrel but her doctor thought it was doing that good

when it came to fight the poly jra. So she has been on remicade now for a

year and 1 month...and it is doing well. Her arthritis activity is low for

now..which is good..she still has pain but it isn't as bad as it was..i know

the meds work different in each child.i was just wondering why the remicade

was stopped?

Good luck to you and your child..

karen(tab16..poly)

From: Lorie Jo <loriejo@...>

Reply-

Subject: RE: Pain relief

Date: Fri, 30 Nov 2001 23:13:30 -0600

So, are most of your (meaning anyone reading this) kids on pain meds

along with meds to counteract the disease?

This makes me feel totally lame, which isn't the first time here,

because I was trying to stay away from the meds that " cover up " the

disease. know what I mean? Instead, trying to use the meds to counteract

the disease and therefore make her pain free or to the greatest extent

by controlling it all. Was that such a bad idea?

So, am I a lame mama?

The naproxen messed with her tummy. She took that for 3 weeks. She can't

even take Tylenol more then a couple of times in a row now and she used

to take that just fine. So I don't know if there is anything she

*should* be taking for pain, but the Rheumy hasn't said so (probably

cause I said no).

After hearing from you all, I am brought to the conclusion that our

Rheumy allows me to make most of the decisions, which I rather

appreciate, but not if it effects the health of my child -- to an

extent. I know that with the power of decision he has given to me, I

need to be informed.

Yet, I am afraid in all the decisions I must make in what meds my dd

takes. I am a very natural choice mother, not even giving Tylenol for a

fever under 102, (dependant on age) cause it is just a simple biological

function in my opinion. Instead I rely on herbs and such for basic

illnesses. This JRA definitely threw me for a loop. She is on mtx. and

folic acid now and is doing fairly well. Was doing really well on the

remicade also. I don't know why I even agreed (at this point anyway) to

get the Enbrel instead. But I suppose it all ends with Enbrel. Which we

finally have an appt for that on the 17th.

Anyhow, I guess I was just rambling. Sorry to do that to your list. Take

care everyone, I read your messages and feel for your children. Every

time I look into my babies eyes, I know that you are there too.

Lorie (mama to Liberty, age 4 poly JRA)

_________________________________________________________________

Get your FREE download of MSN Explorer at http://explorer.msn.com/intl.asp

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Hi ,

Very well said : ) And what you've said about remission holds true, I think, for medicated remissions, too. Some of our children with persistent JRA relapse each time we try to discontinue or lower the dose of some of their meds but if they can reach a point of having the majority of their symptoms controlled by continuing their cocktail of daily meds ... I think we've reached the same goal. Only trouble with that is the added worry about possible side effects (some very serious) from long term use of the meds or the possibility that some of the meds may lose their effectiveness over a period of time. It took me a long time to be able to accept that my son might need long term medicating rather than just a quick fix. Coming to terms with the idea that it's a chronic illness can take a lot of mental readjustment.

We all, still, have a common bond. Hoping for remissions for our children and for others like them. And continued research, leading to a better understanding and one day soon, hopefully, a cure!

All the best, to you and the children,

Georgina

You are not alone by a long shot. I have one child with JRA and one with epilepsy and BOTH were on meds that required constant blood and urine monitoring to make sure that their internal organs and blood weren't being compromised. I am a person who NEVER takes or give out medication unless absolutely necessary so heavily medicating my children nearly gave me a nervous breakdown. But after much consultation with many parents (including my own sister who has a child with serious auto-immune problems), doctors and researching online, I came to the conclusion that I needed to treat the whole disease including the pain because, as bad as the meds are, experts don't really have any idea of what the stress hormones that they believe are put off when you are in pain, especially chronic pain, do to the body, especially in young bodies, in the long term. I chose to take the action of something that could actually be monitored ie. medication. There is also a theory that I have heard from several parents (corroborated by a few articles that I have read but I don't think it's mainstream) that if you treat the auto-immune disease fully there may be the chance that you can "trick" the body into believing that it has "finished" it's job (attacking itself instead of a "real" enemy) and have remission - short or long-term. So that's how I decided. I know how agonizing the process is and I wish you the best of luck. My son (he has PA JRA) seems to be in remission now. He was on high doses of ibuprofen, along with Zantac because of stomach problems, for over a year. Should he go back into a flare we know that he will have to move up the meds chain because the Zantac no longer dents the stomach problems from Ibuprofen. I just keep my fingers crossed and pray for "permanent" remission.

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Thanks, e : )

I am catching up on the posts and notice lots of concern about pain. Keep bugging your doc if your child is in pain. It is a big buzz word these days that health care providers have to be aware of and treat. We go to Seattle Childrens and there are posters everyone about pain relief, EMLA cream , etc. Keep calling and bugging. No one should be in pain, especially for children who don't understand. Pain can cause depression, weight loss, decreased movement, increased or decreased sleep, lack of concentration etc. There are all kinds of treatments out there with medication and without. Ask and bug them. Pain is supposed to be considered the 5th vital sign (with blood pressure, temperature, heart rate and respiration rate being the other four.) Even in a flare it is amazing how much more functional a child can be when their pain is under control. Good luck to everyone and keep pushing and keep trying for the right "cocktail" as was mentioned several times. (Sorry to be on a soap box, but I have chronic pain from a work injury and I hate to see this area neglected.) --e, 14 y.o with poly

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Hi,its becki.I honestly believe the meds have to get the disease under control

before the body can get the disease under control

karens tribe wrote:

> hi lorie..i was wondering what happened that your rheumy stopped remicade

> and decided to go with enbrel..my daughter Tabitha who is sixteen and has

> poly jra..was your daughters age when i found out she had this nasty

> disease. She was on enbrel but her doctor thought it was doing that good

> when it came to fight the poly jra. So she has been on remicade now for a

> year and 1 month...and it is doing well. Her arthritis activity is low for

> now..which is good..she still has pain but it isn't as bad as it was..i know

> the meds work different in each child.i was just wondering why the remicade

> was stopped?

> Good luck to you and your child..

> karen(tab16..poly)

>

> From: Lorie Jo <loriejo@...>

> Reply-

>

> Subject: RE: Pain relief

> Date: Fri, 30 Nov 2001 23:13:30 -0600

>

> So, are most of your (meaning anyone reading this) kids on pain meds

> along with meds to counteract the disease?

> This makes me feel totally lame, which isn't the first time here,

> because I was trying to stay away from the meds that " cover up " the

> disease. know what I mean? Instead, trying to use the meds to counteract

> the disease and therefore make her pain free or to the greatest extent

> by controlling it all. Was that such a bad idea?

>

> So, am I a lame mama?

> The naproxen messed with her tummy. She took that for 3 weeks. She can't

> even take Tylenol more then a couple of times in a row now and she used

> to take that just fine. So I don't know if there is anything she

> *should* be taking for pain, but the Rheumy hasn't said so (probably

> cause I said no).

> After hearing from you all, I am brought to the conclusion that our

> Rheumy allows me to make most of the decisions, which I rather

> appreciate, but not if it effects the health of my child -- to an

> extent. I know that with the power of decision he has given to me, I

> need to be informed.

>

> Yet, I am afraid in all the decisions I must make in what meds my dd

> takes. I am a very natural choice mother, not even giving Tylenol for a

> fever under 102, (dependant on age) cause it is just a simple biological

> function in my opinion. Instead I rely on herbs and such for basic

> illnesses. This JRA definitely threw me for a loop. She is on mtx. and

> folic acid now and is doing fairly well. Was doing really well on the

> remicade also. I don't know why I even agreed (at this point anyway) to

> get the Enbrel instead. But I suppose it all ends with Enbrel. Which we

> finally have an appt for that on the 17th.

>

> Anyhow, I guess I was just rambling. Sorry to do that to your list. Take

> care everyone, I read your messages and feel for your children. Every

> time I look into my babies eyes, I know that you are there too.

>

> Lorie (mama to Liberty, age 4 poly JRA)

>

> _________________________________________________________________

> Get your FREE download of MSN Explorer at http://explorer.msn.com/intl.asp

>

>

> For links to websites about arthritis and JRA, visit:

> http://www.geocities.com/Heartland/Village/8414/Links.html

>

>

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Guest guest

e

i bugged s doctor and bugged her and then bugged the rhuemy dr

until they gave something to relieve the pain

went through a few meds till the right one worked

dont feel like your a nag this is what HAS to be done

NOW when i take to the childrens hospital they ask what her pain

scale is

then they work from that they will not release her until she is pain free

this is at the childrens hospital

i had to take her to the adult regular hospital last week because my sister

needed to go also so i figured take both to the hospital

this was a experience

the regular hospital didnt know what to do just asked had she fell i said no

but they xrayed her and asked what meds she was on and gave her a pain shot

the shot hurt worser and never did help the pain

they just told me to contact her dr because they never experienced this JRA

this is ATLANTA GA lololol home of Emory Unv the Medical college

anyway

i called her dr and she told me to medicate her with 3 meds at 1 time

with a up in dose so i did

called her and let her know it helped

this dr is great if the up in dose didnt help then it was to the childrens

hospital for

the doctors are learning about this JRA and its complications as we are

Robbin

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In a message dated 08/16/2002 12:39:44 PM Eastern Daylight Time,

meghan@... writes:

> Also, for people allergic to sulfa drugs, Celebrex is BAD BAD BAD.

> Vioxx has a similar structure to Celebrex but may cause much less of

> a reaction since it is not actually sulfa-based. It really burns my

> hide that they do not talk about that more.

>

Meghan - My doctor knew right away not to give me Celebrex as I'm allergic to

sulfa - another good reason to always use the same pharmacy for all your

rx's. Tell them your allergies, form a relationship with the pharmacist. If

your doctor misses something, many times the pharmacist will catch it - drug

allergies, interactions, etc.

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I agree with Michele totally! I'm in absolute agreement with her!

For those of you trying to manage pain with over-the-counter (OTC)

drugs, you're going to find you'll still have pain and in several

years you'll have liver and kidney damage because you haven't been

getting regular blood tests to monitor the drugs going into your body.

There are other NSAID drugs besides Vioxx. After speaking with a

pharmaceutical doctor, Vioxx and Celebrex do as much stomach damage

as other NSAIDs. But your doctor can add Nexium to the mix to protect

your stomach. Some other NSAIDs include Voltaren, Mobic, Bextra,

Relafen, Indomethicin, etc. There is an excellent list available on

the Arthritis Foundation's drug site:

http://arthritis.org/conditions/DrugGuide/nsaids.asp

In any event, with a disease like PA you really should be discussing

all your medications and pain needs with your doctor.

Best wishes,

Meghan

> I wanted to comment to the newbies who have been taking large

amounts of

> aspirin or ibuprofen/advil for their pain and are not getting the

results

> they need either.

>

> First of all, you should know that Aspirin and Ibuprofen are NSAIDS-

they are

> just sold over the counter without a prescription. However, they

will do

> just as much damage to your unsuspecting stomach as other NSAIDS

like

> Voltaren, Relafen,

> Indomethacin, etc,al.

>

> Might I suggest the following. If your pain is in the minimal to

moderate

> range, ask your doctor for a prescription for Vioxx. It is one of

the new

> COX 2 inhibitors and is not as hard on your stomach as other

NSAIDs.

> However, if you find it bothering your stomach, as it did to mine,

you may

> need a stomach protectant too. I am currently on Nexium and it

works

> extremely well- much stronger than Prilosec. Celebrex is for

> mild pain and is not rated at all to work for moderate pain, so I

would not

> bother with trying it myself) Vioxx is rated well for moderate and

acute

> pain.

>

> If the Vioxx is not enough, I would ask the doctor for his

suggestion. There

> are other drugs in the NSAID family that are quite strong, and you

could take

> a separate stomach protectant like Prilosec or Nexium with them and

be okay.

>

>

> Once you get to the point that NSAIDs don't work or there is a

medical reason

> you cannot take them (say you have a bleeding problem), then you

may have to

> discuss narcotic pain management with your doctor. Long acting (8-

12 hour)

> narcotic pain meds are considered to be the less likely to trigger

addiction

> than the every four hour types, so the drugs called Oxycontin, and

MSContin

> would be two that your doctor and you might consider trying if you

were to go

> the narcotic pain reliever route. They last 8-12 hours and will

not bother

> your stomach at all, unless you do not drink enough fluids in which

case you

> could get a case of constipation! You must also take into

consideration the

> timing of the dose of these type of meds- since it is not advisable

to drive

> on narcotic pain meds.

>

> We are all different, combinations of all the above and others I am

sure I

> missed discussing are going to be useful to all of us.

Unfortunately, we have

> to rely on ourselves and be proactive and learn what our options

are ahead of

> time in order to ask the doctor for what we want and need to get

the optimal

> quality of life we DESERVE!

>

> Keep on going friends- one day at a time- and right for what you

deserve- the

> best quality of life that is humanly possible to get! We all

deserve it.

> God wants it for us

> and our families to have as wonderful a life as is possible.

>

>

> Group founder

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I just sent a messageI didn't mean to send, yet. Finger got too

trigger happy there!!

I take Celebrex (in addition to all my other meds). I asked my RD

why he preferred Celebrex to Vioxx. He stated that Vioxx had more

side effects than Celebrex, specifically affecting high blood

pressure, and that he could increase the dosage of Celebrex with

fewer side effects than with Vioxx. And, additionally, the increase

of dosage of Celebrex would not affect your stomach as much as

Vioxx. I have been taking 200mg 2Xday of Celebrex. He also stated

that he considered 50mg of Vioxx to be considered a high dosage.

Apparently, he considered 25mg of Vioxx to be equal to 200 mg of

Celebrex.

Sandy

>

> Might I suggest the following. If your pain is in the minimal to

moderate

> range, ask your doctor for a prescription for Vioxx. It is one of

the new

> COX 2 inhibitors and is not as hard on your stomach as other

NSAIDs.

> However, if you find it bothering your stomach, as it did to mine,

you may

> need a stomach protectant too. I am currently on Nexium and it

works

> extremely well- much stronger than Prilosec. Celebrex is for

> mild pain and is not rated at all to work for moderate pain, so I

would not

> bother with trying it myself) Vioxx is rated well for moderate and

acute

> pain.

>

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Hi all,

In talking with the pharmaceutical doctor, she explained that the

difference regarding blood pressure and the risk for strokes was

negligible between Vioxx and Celebrex. They think that inhibiting COX-

2 is what may be causing the risks.

It's a catch between inhibiting COX-2 which causes inflammation and

pain, but also may help the body as well.

Also, for people allergic to sulfa drugs, Celebrex is BAD BAD BAD.

Vioxx has a similar structure to Celebrex but may cause much less of

a reaction since it is not actually sulfa-based. It really burns my

hide that they do not talk about that more.

> I just sent a messageI didn't mean to send, yet. Finger got too

> trigger happy there!!

>

> I take Celebrex (in addition to all my other meds). I asked my RD

> why he preferred Celebrex to Vioxx. He stated that Vioxx had more

> side effects than Celebrex, specifically affecting high blood

> pressure, and that he could increase the dosage of Celebrex with

> fewer side effects than with Vioxx. And, additionally, the increase

> of dosage of Celebrex would not affect your stomach as much as

> Vioxx. I have been taking 200mg 2Xday of Celebrex. He also stated

> that he considered 50mg of Vioxx to be considered a high dosage.

> Apparently, he considered 25mg of Vioxx to be equal to 200 mg of

> Celebrex.

>

> Sandy

>

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The NSAIDS are pain relievers that act at the site of the inflammation -

peripheral analgesics. The opioids act on the brain to cut out pain -

central-acting analgesics. They also act on other centers in the brain to

cause narcosis and addiction.

One synthetic analgesic is a central-acting analgesic but is not an opioid

- Tramadol, (brand names Ultram or Dromadol). Tramadol is very effective

when nothing else will stop the pain - as happens to me when a tendon is

inflamed. The standard tablets only last 4 hours but there is an extended

release type (tramadol SR) that gives 8-12 hours of relief.

Like the opioids, tramadol can cause constipation hence I only use it when

I have to.

I have found ketoprofen to be a very helpful NSAID. OTC it is called

Orudis KT. I now use a prescribed 24-hr form called Oruvail.

[Moderator's note: I guess you're lucky , because Ultram did absolutely

nothing whatsoever to relieve my joint pain when I tried it - even Asprin or

Ibuprofen worked better. I guess it just goes to show how differently we each

react to the various drugs. Ron]

On Friday, August 16, 2002, at 02:53 AM, CTNATIVE@... wrote:

> I wanted to comment to the newbies who have been taking large amounts of

> aspirin or ibuprofen/advil for their pain and are not getting the results

> they need either.

>

> First of all, you should know that Aspirin and Ibuprofen are NSAIDS- they

> are

> just sold over the counter without a prescription. However, they will do

> just as much damage to your unsuspecting stomach as other NSAIDS like

> Voltaren, Relafen,

> Indomethacin, etc,al.

>

> Might I suggest the following. If your pain is in the minimal to moderate

> range, ask your doctor for a prescription for Vioxx. It is one of the new

> COX 2 inhibitors and is not as hard on your stomach as other NSAIDs.

> However, if you find it bothering your stomach, as it did to mine, you may

> need a stomach protectant too. I am currently on Nexium and it works

> extremely well- much stronger than Prilosec. Celebrex is for

> mild pain and is not rated at all to work for moderate pain, so I would

> not

> bother with trying it myself) Vioxx is rated well for moderate and acute

> pain.

>

> If the Vioxx is not enough, I would ask the doctor for his suggestion.

> There

> are other drugs in the NSAID family that are quite strong, and you could

> take

> a separate stomach protectant like Prilosec or Nexium with them and be

> okay.

>

>

> Once you get to the point that NSAIDs don't work or there is a medical

> reason

> you cannot take them (say you have a bleeding problem), then you may have

> to

> discuss narcotic pain management with your doctor. Long acting (8-12

> hour)

> narcotic pain meds are considered to be the less likely to trigger

> addiction

> than the every four hour types, so the drugs called Oxycontin, and

> MSContin

> would be two that your doctor and you might consider trying if you were

> to go

> the narcotic pain reliever route. They last 8-12 hours and will not

> bother

> your stomach at all, unless you do not drink enough fluids in which case

> you

> could get a case of constipation! You must also take into consideration

> the

> timing of the dose of these type of meds- since it is not advisable to

> drive

> on narcotic pain meds.

>

> We are all different, combinations of all the above and others I am sure

> I

> missed discussing are going to be useful to all of us. Unfortunately, we

> have

> to rely on ourselves and be proactive and learn what our options are

> ahead of

> time in order to ask the doctor for what we want and need to get the

> optimal

> quality of life we DESERVE!

>

> Keep on going friends- one day at a time- and right for what you deserve-

> the

> best quality of life that is humanly possible to get! We all deserve it.

> God wants it for us

> and our families to have as wonderful a life as is possible.

>

>

> Group founder

>

>

>

>

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