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Since I'm new to this whole PA thing, I have a question. I notice that for

me, I dont have alot of consistant and constant pain, but I find that

sometimes the affected joints will almost throb, LIke my toe for

instance..PAIN NOPAIN PAIN NOPAIN PAIN NOPAIN, almost as regular as my

heartbeat. Sometimes it feels like fire in the joint, I'm suspecting that's

where you get the term " flare " ? My thumb especially suffers from the fire

joint syndrome. My pinky only seems to hurt when I extend it past it's

ability to flex, when I forget that it's affected and try to use it as

normal. The middle of my back and my neck seems to hurt only when I move.

The collarbone hurts when I lift something, or turn it wrong.

Is it normal to have different kinds of pain in different affected joints?

Is there a 'normal' anymore?

Comments?

Crystal

[Editor's Note: Crystal, many of us refer to life with PA as our " new normal "

because nothing is like it used to be. I certainly experience different types

of pain in different places. Some pain is permanent while some of it does the

" pain nopain " reggae. Great to have you here. Kathy F.]

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hay

I remember just yesturday I was walking to the car and my left foot

had a sharp pain in it that was so powerful I almost fell over. Then

like it came it left and It has not returned.

I also notice when wearing thin soled shoes, that when I step on

rocks (little pebble type rocks) that I get shockwaves of tremendous

pain. It's like the nerves are over sensitive at times. Other times

I am fine.

Luckely I only seem to get PA in my feet. One thing I have noticed

is that my quality of life improves 10 fold if I go jogging or stair

stepping in the morning before the day's swelling occures. It;s like

the excersize is loosening my joints.

>

> Since I'm new to this whole PA thing, I have a question. I notice

that for

> me, I dont have alot of consistant and constant pain, but I find

that

> sometimes the affected joints will almost throb, LIke my toe for

> instance..PAIN NOPAIN PAIN NOPAIN PAIN NOPAIN, almost as regular

as my

> heartbeat. Sometimes it feels like fire in the joint, I'm

suspecting that's

> where you get the term " flare " ? My thumb especially suffers from

the fire

> joint syndrome. My pinky only seems to hurt when I extend it past

it's

> ability to flex, when I forget that it's affected and try to use

it as

> normal. The middle of my back and my neck seems to hurt only when

I move.

> The collarbone hurts when I lift something, or turn it wrong.

>

> Is it normal to have different kinds of pain in different affected

joints?

> Is there a 'normal' anymore?

>

> Comments?

>

> Crystal

>

>

> [Editor's Note: Crystal, many of us refer to life with PA as

our " new normal " because nothing is like it used to be. I certainly

experience different types of pain in different places. Some pain

is permanent while some of it does the " pain nopain " reggae. Great

to have you here. Kathy F.]

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In a message dated 11/5/2004 5:59:23 AM Eastern Standard Time,

wodell3320@... writes:

Pain/No Pain.....absolutely. I remember walking out to get

something out of the car happy to be feeling fine...thinking it was

going to be a good day.....but 30 seconds later, I was limping back

into the house.

Oh, DO I know that oh so well. The last few days I thought I had been

improving. I guess that is because I just did things around the house and

didn't

try much walking. Today I went out to the store with my husband and no

sooner did we park and walk into the store, that enemy of mine pain started

in.

Then my knees throbbed and my ankle swelled up and I knew I was back to the

same old pain. I wonder what it is like to feel normal again.

Janet

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Hi Crystal,

This is a reply to an e-mail going back a few days, but...

I experience different types of pain in different areas as well... Some are

more consistant and always achy (like my lower and sometimes upper back), or

sharp pain " just because " , but it doesn't seem to last for long, or the pain

from moving something that is hurting or inflamed. What for me is finally

great, is to know that it is really happening and I am not just imagining it or

going crazy... For me though, the " flares " are HUGE in comparison including

major swelling, major pain and inability to move regardless of the pain (because

the inflamation is so bad)...

Hope you're doing well...

(idaho)

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, I know what you mean. For years I thought I was just imagining these

things. It is

good to have a diagnosis. Now I don't feel guilty when I am too tired to do the

house work

:) M

jerre

>

> Hi Crystal,

>

> This is a reply to an e-mail going back a few days, but...

>

> I experience different types of pain in different areas as well... Some are

more

consistant and always achy (like my lower and sometimes upper back), or sharp

pain " just

because " , but it doesn't seem to last for long, or the pain from moving

something that is

hurting or inflamed. What for me is finally great, is to know that it is really

happening and

I am not just imagining it or going crazy... For me though, the " flares " are

HUGE in

comparison including major swelling, major pain and inability to move regardless

of the

pain (because the inflamation is so bad)...

>

> Hope you're doing well...

>

> (idaho)

>

>

>

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Hi Crystal,

For me, you are in the very frustrating phase. It's like you know you are in

pain and it effects your every day life signifigantly, but nothing or no one

seems to " get it " because it isn't bad enough... This has been mostly my

expierence with PA ~ it's good and bad. The last major flare I had was so

dibilitating, but it gave me my diagnoisis and the hard core meds, so I wouldn't

trade it for the world... Sounds so sad to say, but true... I don't know if

the biologics only work when you're really flaring or what, but Remicade was my

saviour and now I'm doing acupunture and nothing else.... I have aching and

pain now and then ~ and some psorisis, but nothing major and I am glad to be off

the meds...

I wish you luck...

And I love so many of your replies ~ your sense of humor is great....

(idaho)

Turrelle LaMere <turrelle@...> wrote:

Hi , any response is more than welcome, late or otherwise :)

Sometimes I think that just regular aches and pains might be the PA showing

up in a place I didn't know about yet, is that kind of paranoia regular?

(see I didn't say normal? heh heh) I " m not sure if I have a vertebrae out

and need to go see a chiro soon, or whether the PA has migrated to the back.

It's kind of frustrating. I think when I go see the new Rhumy in Dec, I " m

going to ask if we can Xray everything and pin down what is affected and

what isn't.

I dont think I quite know what a 'flare' is, because it seems that most of

the people describing them, say that they are very dibilitating and to the

point where one is almost bed ridden. I have yet to experience that

(knocking on wood!) But then I caught mine pretty early, I'm sure, so maybe

I'm lucky.

The MTX hasn't seem to have kicked in yet, the affected joints are still

sore and swelling, but I hope something works soon.

Wish me luck, and thanks for replying.

Bright Blessings..

Crystal

>

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