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Fibromyalgia

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The imprecise meaning is " muscle pain. " Fibromyalgia is a (usually)

chronic condition that appears mostly in women. It's not at all well

understood and, until recently, many physicians swore that it didn't

exist. Usually there is extreme tenderness at a minimum of 11 of 18

documented hot spots over the torso. (There's actually a chart they

can use showing where these are located.) The pain sometimes begins

after a viral infection, sometimes after trauma to the body. All

testing (X-Rays, etc) show no visible injury but the pain can be

excruciating and last for years. Some research has shown that people

with fibromyalgia have increased levels of the " P " enzyme, designated

the pain enzyme, in their spinal fluid. Therefore we feel pain when

we shouldn't. Some treatments are anti-inflammatories, muscle

relaxers, hot/cold packs, deep tissue massage (which I personally

think is sadistic.) Unlike arthritis, lifting light weights can

actually increase the muscle damage. Doctors want you to exercise but

aren't really sure what kind is best. Some people swear by particular

diets to help alleviate symptoms.

It's an extremely irritating disease.

P

>

> Re: sciatica

>

>

> > completely disabled from my fibromyalgia and arthritis pain.

Within

>

> Okay...I've seen this mentioned twice lately.

What's " fibromyalgia " ??

>

> alyssa

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I have Myofascial Pain Syndrome, which my doctor calls

a cousin of fibromyalgia. In my case, I have pain

(from mild to severe) nearly everywhere but my stomach

from my waist to the top of my head. I get

" triggerpoints " on my head, face, neck, back,

shoulders, and arms to my wrists. (As for my wrists,

I have bilateral carpal tunnel so that takes care of

that!) Oh, I forgot, I also have triggerpoints in my

butt muscles. When my triggerpoints are touched or

inflamed, pain travels to other areas of my body. I'm

on 2 different kinds of medication for it, including a

strong pain-killer. Treatment includes having my

therapist push a wooden round device into the

triggerpoint, holding it for 30 seconds and releasing.

It hurts like hell but it (temporarily) releases the

muscle. When she's done, I can actually turn my neck

and move better. I just wished it lasted!

Having said all that, if I had a choice between the

two, I would keep the MPS. I don't know that I could

handle fibromyalgia. I really feel for the people who

have it.

dee

--- wrote:

> The imprecise meaning is " muscle pain. " Fibromyalgia

> is a (usually)

> chronic condition that appears mostly in women. It's

> not at all well

> understood and, until recently, many physicians

> swore that it didn't

> exist. Usually there is extreme tenderness at a

> minimum of 11 of 18

> documented hot spots over the torso. (There's

> actually a chart they

> can use showing where these are located.) The pain

> sometimes begins

> after a viral infection, sometimes after trauma to

> the body. All

> testing (X-Rays, etc) show no visible injury but the

> pain can be

> excruciating and last for years. Some research has

> shown that people

> with fibromyalgia have increased levels of the " P "

> enzyme, designated

> the pain enzyme, in their spinal fluid. Therefore we

> feel pain when

> we shouldn't. Some treatments are

> anti-inflammatories, muscle

> relaxers, hot/cold packs, deep tissue massage (which

> I personally

> think is sadistic.) Unlike arthritis, lifting light

> weights can

> actually increase the muscle damage. Doctors want

> you to exercise but

> aren't really sure what kind is best. Some people

> swear by particular

> diets to help alleviate symptoms.

> It's an extremely irritating disease.

> P

>

> >

> > Re: sciatica

> >

> >

> > > completely disabled from my fibromyalgia and

> arthritis pain.

> Within

> >

> > Okay...I've seen this mentioned twice lately.

> What's " fibromyalgia " ??

> >

> > alyssa

>

>

>

----------------------------------------------------------------------

>

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re: fibromyalgia

> think is sadistic.) Unlike arthritis, lifting light weights can

> actually increase the muscle damage. Doctors want you to exercise but

> aren't really sure what kind is best. Some people swear by particular

> diets to help alleviate symptoms.

> It's an extremely irritating disease.

> P

My goodness...it sounds *awful*! I'm so sorry you have this!

alyssa

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re: fibromyalgia

> think is sadistic.) Unlike arthritis, lifting light weights can

> actually increase the muscle damage. Doctors want you to exercise but

> aren't really sure what kind is best. Some people swear by particular

> diets to help alleviate symptoms.

> It's an extremely irritating disease.

> P

My goodness...it sounds *awful*! I'm so sorry you have this!

alyssa

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Dear P:

I also have fibromyalgia and was wondering if you are pre or post op? I

would like to know how you are feeling. Do you notice less pain? What about

the flue like symptoms? What kind of exercise do you do? I have had the

diagnosis for about 6 years. When I first became ill, long before I knew

what it was, I started to gain weight because I stopped moving. In about 2

1/2 years I gained about 120lbs. I now exercise regularly but find that the

weight is clinging to me. I can hardly walk and for any outings, where more

than a few steps is involved, I must use a wheelchair. I try to walk as much

as possible in the house and yard. My pain is pretty chronic and some days

are much worse than others. So, I am hoping that you might be able to give

me some good news like the surgery has reduced your pain even a little. Has

the condition, in your opinion, slowed weight loss? I have spoken with a few

other people who have fibro and received mixed reviews. One person is losing

slowly but she is having a revision another has lost just fine but she still

has a significant amount of pain especially after exercise. Any thing you

feel comfortable sharing would be greatly appreciated.

Thanks

Sheryle

Dr Keshishian

10-10-01

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  • 1 year later...
Guest guest

Yes I have fibromyalgia & Dish disease of the spine & I'm beginning

to think my esophagus pain is fibromyalgia pain.....which only

Trazadone relieves. I can hardly breathe on some days with pain in

the chest & not sure what is producing it, the fibromyalgia or

Barrett's esophagus, esophageal spasms, or my Dish disease? Or Cp

shooting up bile? I have Epstein-barr virus, herpes simplex 2 on the

tailbone, and have had 2 outbreaks of shingles! Memory? I can't even

remember all the diseases I have! I have Scleraderma in my

family....does anybody with CP have Scleraderma? I wish they could

connect some of my symptoms to one disease! I also can't remember who

asked....but hopefully you will find me. Like to talk re

Fibro.....

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