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Re: Digest Number 1049

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Hi everyone,

Just wanted to invite you to the pity party I am having this evening. I am

just so frustrated right now. Last night I decided to do a little crafting

with polymer clay, making some beads. Sounds tame enough right? Well I

got up this morning in agony... my hands, arms and shoulders hurt and

burned, with sharp stabbing pains and barely any strength, as if I had

spent a day doing chin-ups or something. All because I did something I

enjoy, something completely non-strenuous. About an hour after I woke up,

when the pain meds kicked in, it was tolerable, but unfortunately I only

have 4 a day, and lately I need 2 at a time to have any effect. My doctor

has me trying neurontin before he increases the hydrocodone, but it doesn't

seem to be doing a thing. I save the other 2 pain pills for evening, after

suffering all day, but they are already wearing off. I went to bed shortly

after taking them hoping for oblivion, but no such luck. I don't know why

I am sitting here writing this now, I guess I just need somebody to

understand because I feel so alone right now. Even if the rest of the

house wasn't sleeping, I would feel alone because I can't relate it to

them. They are wonderful about it, don't get me wrong, but they don't

really know how it feels and I hate to feel like a burden. I know you will

understand I just need to vent. Has anyone else experienced exaggerated

pain like this from such seemingly minor " activity " ? The FMS literature

mentioned it, but they said the pain would only last a short time, and

after rest would go away, but it's not. If it didn't hurt so much it would

be laughable. What makes it so terribly depressing... even pleasure causes

pain. I want to slip into a nice hot tub, but to be honest, I don't even

know if I would be able to get out. Thanks for bearing with me tonight,

bless you all.

Char

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Hi everyone,

Just wanted to invite you to the pity party I am having this evening. I am

just so frustrated right now. Last night I decided to do a little crafting

with polymer clay, making some beads. Sounds tame enough right? Well I

got up this morning in agony... my hands, arms and shoulders hurt and

burned, with sharp stabbing pains and barely any strength, as if I had

spent a day doing chin-ups or something. All because I did something I

enjoy, something completely non-strenuous. About an hour after I woke up,

when the pain meds kicked in, it was tolerable, but unfortunately I only

have 4 a day, and lately I need 2 at a time to have any effect. My doctor

has me trying neurontin before he increases the hydrocodone, but it doesn't

seem to be doing a thing. I save the other 2 pain pills for evening, after

suffering all day, but they are already wearing off. I went to bed shortly

after taking them hoping for oblivion, but no such luck. I don't know why

I am sitting here writing this now, I guess I just need somebody to

understand because I feel so alone right now. Even if the rest of the

house wasn't sleeping, I would feel alone because I can't relate it to

them. They are wonderful about it, don't get me wrong, but they don't

really know how it feels and I hate to feel like a burden. I know you will

understand I just need to vent. Has anyone else experienced exaggerated

pain like this from such seemingly minor " activity " ? The FMS literature

mentioned it, but they said the pain would only last a short time, and

after rest would go away, but it's not. If it didn't hurt so much it would

be laughable. What makes it so terribly depressing... even pleasure causes

pain. I want to slip into a nice hot tub, but to be honest, I don't even

know if I would be able to get out. Thanks for bearing with me tonight,

bless you all.

Char

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Hi everyone,

Just wanted to invite you to the pity party I am having this evening. I am

just so frustrated right now. Last night I decided to do a little crafting

with polymer clay, making some beads. Sounds tame enough right? Well I

got up this morning in agony... my hands, arms and shoulders hurt and

burned, with sharp stabbing pains and barely any strength, as if I had

spent a day doing chin-ups or something. All because I did something I

enjoy, something completely non-strenuous. About an hour after I woke up,

when the pain meds kicked in, it was tolerable, but unfortunately I only

have 4 a day, and lately I need 2 at a time to have any effect. My doctor

has me trying neurontin before he increases the hydrocodone, but it doesn't

seem to be doing a thing. I save the other 2 pain pills for evening, after

suffering all day, but they are already wearing off. I went to bed shortly

after taking them hoping for oblivion, but no such luck. I don't know why

I am sitting here writing this now, I guess I just need somebody to

understand because I feel so alone right now. Even if the rest of the

house wasn't sleeping, I would feel alone because I can't relate it to

them. They are wonderful about it, don't get me wrong, but they don't

really know how it feels and I hate to feel like a burden. I know you will

understand I just need to vent. Has anyone else experienced exaggerated

pain like this from such seemingly minor " activity " ? The FMS literature

mentioned it, but they said the pain would only last a short time, and

after rest would go away, but it's not. If it didn't hurt so much it would

be laughable. What makes it so terribly depressing... even pleasure causes

pain. I want to slip into a nice hot tub, but to be honest, I don't even

know if I would be able to get out. Thanks for bearing with me tonight,

bless you all.

Char

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,

They have treid a few meds for pain, but they all make me very itchy.

The dr said it is probably an allergic reaction. The ones who will even try

the pain meds will only give them to me for a few days. They all say

narcotics are too adicting. I have tried all the anti--depressants, and even

muscle relaxants that are supposed to work for fibro and none work for

me...all they do is give me bad side effects and dont help the pain anyways.

I have been to about 15 diffrrerent Dr's and they are all the same. Tell me

to loose weight and start an aerobic exercise program. I mean really..I can

barely walk..and they want me to jog everday. I have also found out that my

estrogen level is really low...lower than that of a menopausal women, even

though I am only 27. None of the Drs can seems to explain this or even seem

to care to try. It is not common with the polycystic ovarain syndrome so now

I wonder if they even have the right diagnosis. I have also tried to take my

husband along on appts and it seems that has the opposite feect

sometimes....sometime they act like I must be some kind of baby to have to

bring him with. We have not had much luck with good Dr's. We have driven up

to 3 hours to try to find better Dr's even, with no luck tthere either. The

rheumy we went to was the worst.....he told me " You have pain, live with it

and go back to work. It wil never get any better " He was a total jerk. We

are just sooo frustarted because i have soo many thing going on in my body

right now. They cant figure out this hormone problem and no one even really

seems to care. I am just sooo frustrated, but thanks a lot for trying to

help, but most of all for understanding and responding ot my email. I

really appreciate it. =)

Vicki

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Vicki,

I feel your pain, literally. Doctors have a very annoying habit of belittling

our pain. My doctors is always telling me to diet and exercise...skinny people

have this crappy syndrome too!!! What makes them think I can run if I can

hardly walk from room to room in my house. Arrogant bastards aren't they *lol*

Keep your chin up...there are good doctors out there...it's just finding them

that's the problems.

Anne

Re: Digest Number 1049

,

They have treid a few meds for pain, but they all make me very itchy.

The dr said it is probably an allergic reaction. The ones who will even try

the pain meds will only give them to me for a few days. They all say

narcotics are too adicting. I have tried all the anti--depressants, and even

muscle relaxants that are supposed to work for fibro and none work for

me...all they do is give me bad side effects and dont help the pain anyways.

I have been to about 15 diffrrerent Dr's and they are all the same. Tell me

to loose weight and start an aerobic exercise program. I mean really..I can

barely walk..and they want me to jog everday. I have also found out that my

estrogen level is really low...lower than that of a menopausal women, even

though I am only 27. None of the Drs can seems to explain this or even seem

to care to try. It is not common with the polycystic ovarain syndrome so now

I wonder if they even have the right diagnosis. I have also tried to take my

husband along on appts and it seems that has the opposite feect

sometimes....sometime they act like I must be some kind of baby to have to

bring him with. We have not had much luck with good Dr's. We have driven up

to 3 hours to try to find better Dr's even, with no luck tthere either. The

rheumy we went to was the worst.....he told me " You have pain, live with it

and go back to work. It wil never get any better " He was a total jerk. We

are just sooo frustarted because i have soo many thing going on in my body

right now. They cant figure out this hormone problem and no one even really

seems to care. I am just sooo frustrated, but thanks a lot for trying to

help, but most of all for understanding and responding ot my email. I

really appreciate it. =)

Vicki

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Vicki,

I feel your pain, literally. Doctors have a very annoying habit of belittling

our pain. My doctors is always telling me to diet and exercise...skinny people

have this crappy syndrome too!!! What makes them think I can run if I can

hardly walk from room to room in my house. Arrogant bastards aren't they *lol*

Keep your chin up...there are good doctors out there...it's just finding them

that's the problems.

Anne

Re: Digest Number 1049

,

They have treid a few meds for pain, but they all make me very itchy.

The dr said it is probably an allergic reaction. The ones who will even try

the pain meds will only give them to me for a few days. They all say

narcotics are too adicting. I have tried all the anti--depressants, and even

muscle relaxants that are supposed to work for fibro and none work for

me...all they do is give me bad side effects and dont help the pain anyways.

I have been to about 15 diffrrerent Dr's and they are all the same. Tell me

to loose weight and start an aerobic exercise program. I mean really..I can

barely walk..and they want me to jog everday. I have also found out that my

estrogen level is really low...lower than that of a menopausal women, even

though I am only 27. None of the Drs can seems to explain this or even seem

to care to try. It is not common with the polycystic ovarain syndrome so now

I wonder if they even have the right diagnosis. I have also tried to take my

husband along on appts and it seems that has the opposite feect

sometimes....sometime they act like I must be some kind of baby to have to

bring him with. We have not had much luck with good Dr's. We have driven up

to 3 hours to try to find better Dr's even, with no luck tthere either. The

rheumy we went to was the worst.....he told me " You have pain, live with it

and go back to work. It wil never get any better " He was a total jerk. We

are just sooo frustarted because i have soo many thing going on in my body

right now. They cant figure out this hormone problem and no one even really

seems to care. I am just sooo frustrated, but thanks a lot for trying to

help, but most of all for understanding and responding ot my email. I

really appreciate it. =)

Vicki

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Vicki,

I feel your pain, literally. Doctors have a very annoying habit of belittling

our pain. My doctors is always telling me to diet and exercise...skinny people

have this crappy syndrome too!!! What makes them think I can run if I can

hardly walk from room to room in my house. Arrogant bastards aren't they *lol*

Keep your chin up...there are good doctors out there...it's just finding them

that's the problems.

Anne

Re: Digest Number 1049

,

They have treid a few meds for pain, but they all make me very itchy.

The dr said it is probably an allergic reaction. The ones who will even try

the pain meds will only give them to me for a few days. They all say

narcotics are too adicting. I have tried all the anti--depressants, and even

muscle relaxants that are supposed to work for fibro and none work for

me...all they do is give me bad side effects and dont help the pain anyways.

I have been to about 15 diffrrerent Dr's and they are all the same. Tell me

to loose weight and start an aerobic exercise program. I mean really..I can

barely walk..and they want me to jog everday. I have also found out that my

estrogen level is really low...lower than that of a menopausal women, even

though I am only 27. None of the Drs can seems to explain this or even seem

to care to try. It is not common with the polycystic ovarain syndrome so now

I wonder if they even have the right diagnosis. I have also tried to take my

husband along on appts and it seems that has the opposite feect

sometimes....sometime they act like I must be some kind of baby to have to

bring him with. We have not had much luck with good Dr's. We have driven up

to 3 hours to try to find better Dr's even, with no luck tthere either. The

rheumy we went to was the worst.....he told me " You have pain, live with it

and go back to work. It wil never get any better " He was a total jerk. We

are just sooo frustarted because i have soo many thing going on in my body

right now. They cant figure out this hormone problem and no one even really

seems to care. I am just sooo frustrated, but thanks a lot for trying to

help, but most of all for understanding and responding ot my email. I

really appreciate it. =)

Vicki

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  • 6 months later...
  • 8 months later...

Hi: I am reading about fear fear fear. I had my left hip done by treacy

8/2000 and the right hip done by treacy 5/2001. You guys should not fear

anything. You could win the lottery easier than have your resurfacing fail.

Who was the doctor who did the one that failed????? The other person

talking about having it done in March please just stop the worry. You will

laugh at yourself once you have it done and look back. If you want to call

me and talk I will be glad to make you feel much better. Margaret 321 544

7509-c -h

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Hi: I am reading about fear fear fear. I had my left hip done by treacy

8/2000 and the right hip done by treacy 5/2001. You guys should not fear

anything. You could win the lottery easier than have your resurfacing fail.

Who was the doctor who did the one that failed????? The other person

talking about having it done in March please just stop the worry. You will

laugh at yourself once you have it done and look back. If you want to call

me and talk I will be glad to make you feel much better. Margaret 321 544

7509-c -h

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