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Boy are you lucky! My first abscess surgery was covered by BC/BS

since it was an extraction. The second one He saved the tooth so I

had to pay $1000.

Margaret B

> OK, I'll hold out until Wednesday. You are right about the

> pocketbook. I can't believe they consider dental work a luxury

> when it can come on without warning and take you out just like any

> other illness. I've got to show up Wednesday with $300 cash for

> what the insurance doesn't cover.

>

> Angie aka HarleyLady-DD

> Carson City, NV; Information Technology professional, Single, five

> children (3 at home), 2 dogs, 6 cats, snow skiing, camping, Harley

> Rider, HOG member, Blue Thong Society member, opinionated,

> outspoken, and open minded.

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> " It's always something. " ~~~Gilda Radner

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  • 2 weeks later...

Lori,

Sorry it took me so long to answer your question. I somehow

overlooked your question email and just saw the link to the Fibro

Myths. I have wondered about that myself--a lot.

I talked to my doctor about the weather affecting my pain. The way

he explains it as far as I can remember, is that your body is mostly

made of of fluid, it is like a barometer. When the weather changes,

the fluid around you joints and in the bursae around you muscles can

expand like in a barometer and cause pain.

Since I have radiological evidence of arthritis in some of my joints,

I have to discount fibromyalgia as the cause of most of my joint

pain. I will say that I sometimes have terrible hip pain, and my hip

x-rays were normal--so that pain is not in the joint although it

feels like the joint is breaking.

Since " Lyrica is an anti-epileptic drug, also called an

anticonvulsant. It works by slowing down impulses in the brain that

cause seizures. Lyrica also affects chemicals in the brain that send

pain signals across the nervous system., and it has helped some

people that have fibro " and Nuerontin (another drug given for Fibro)

works in a similar way, that makes me think that when they " slow down

or stop " the pain signals, the drug works. To me that would have

nothing to do with depression.

Its a shame that they cannot seem to make a firm connection with the

fact that depression does occur when a person is in constant pain--it

seems so obvious.

Anyway, that is my opinion. I thank you Lori for bringing this up. I

hope everybody will share their opinion and we can discuss this.

Love,

Annie

>

> Guys,

>

> I was just thinking about the fibro myths when it says it is not

the connective tissue muscles, or joint damage. Well I just started

thinking don't most of us start hurting when the weather changes? I

know I have read quite a few posts including my own stating that the

weather affects our fibro something fierce! What would that have to

do with our brain stimuli? To me that just seems more like the

muscles and the connective tissues, not the brain stimuli or

depression. If you read through those carefully it is almost

disheartening as they are saying it could be another 12 years before

they come to any more conclusions about fibro. That Dr.s still cannot

decide if it is a psychological disease caused by depression (yea

right another excuse for them) or is it something to do with our

joints and connective tissues? I feel it is still the latter. Maybe

I am not understanding it correctly and am not saying this person is

wrong. But how does your body feel? How do

> your joints feel?

> Please do not think I am putting this Myth thing down at all

because it does bring up some great points but I am just wondering

how the group really feels about what it is saying?

>

> Hope all of you are having a good day!

> Lori H

>

>

>

>

>

>

>

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

> Catch up on fall's hot new shows on Yahoo! TV. Watch previews, get

listings, and more!

>

>

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I get terrible headaches when it rains. I am a human barometer.

>

> Guys,

>

> I was just thinking about the fibro myths when it says it is not

the connective tissue muscles, or joint damage. Well I just started

thinking don't most of us start hurting when the weather changes? I

know I have read quite a few posts including my own stating that the

weather affects our fibro something fierce! What would that have to

do with our brain stimuli? To me that just seems more like the

muscles and the connective tissues, not the brain stimuli or

depression. If you read through those carefully it is almost

disheartening as they are saying it could be another 12 years before

they come to any more conclusions about fibro. That Dr.s still cannot

decide if it is a psychological disease caused by depression (yea

right another excuse for them) or is it something to do with our

joints and connective tissues? I feel it is still the latter. Maybe

I am not understanding it correctly and am not saying this person is

wrong. But how does your body feel? How do

> your joints feel?

> Please do not think I am putting this Myth thing down at all

because it does bring up some great points but I am just wondering how

the group really feels about what it is saying?

>

> Hope all of you are having a good day!

> Lori H

>

>

>

>

>

>

>

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

> Catch up on fall's hot new shows on Yahoo! TV. Watch previews, get

listings, and more!

>

>

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,

Do you think Fibro is a psychological disease caused by depression?

Or, do you think it is in our joints and connective tissue? I think

this is a basic notion that we can address in the group and come up

with some examples of our pain that do not support Fibro being caused

by depression.

I understand about your headaches. I get them if I forget to take my

sinus medicine in cold weather. I think headaches are one of the

worst pains.

I hope you have a pain free day.

Love,

Annie

> >

> > Guys,

> >

> > I was just thinking about the fibro myths when it says it is not

> the connective tissue muscles, or joint damage. Well I just started

> thinking don't most of us start hurting when the weather changes? I

> know I have read quite a few posts including my own stating that the

> weather affects our fibro something fierce! What would that have

to

> do with our brain stimuli? To me that just seems more like the

> muscles and the connective tissues, not the brain stimuli or

> depression. If you read through those carefully it is almost

> disheartening as they are saying it could be another 12 years before

> they come to any more conclusions about fibro. That Dr.s still

cannot

> decide if it is a psychological disease caused by depression (yea

> right another excuse for them) or is it something to do with our

> joints and connective tissues? I feel it is still the latter.

Maybe

> I am not understanding it correctly and am not saying this person is

> wrong. But how does your body feel? How do

> > your joints feel?

> > Please do not think I am putting this Myth thing down at all

> because it does bring up some great points but I am just wondering

how

> the group really feels about what it is saying?

> >

> > Hope all of you are having a good day!

> > Lori H

> >

> >

> >

> >

> >

> >

> >

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

> > Catch up on fall's hot new shows on Yahoo! TV. Watch previews,

get

> listings, and more!

> >

> >

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Hi Lori,

My thinking is that it is something to do with the muscles/tissues, NOT

depression/psychological. I think that since doctors can't see the fibro and

tests don't show it, then it isn't really there--and it must be " all in our

heads. "

Of course we know that the pain is really there and most of us remember a time

when we had normal (by society's standards) lives. All we want is to go back to

normal functioning so that we can live our lives with some enjoyment.

I also think that the pain and fatigue cause the depression, not the other way

around. I know that having to stay at home and deal with pain on days when I

would rather be out having fun makes me pretty darn depressed...and why wouldn't

it?

Barb

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

Be a better Heartthrob. Get better relationship answers from someone who knows.

Yahoo! Answers - Check it out.

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WHOA! Ok who said they can relate to fm with Sinusitis? I know for

a fact those are not even closely related. I may spend way too much

time at the hospital, but do not ever compare a facial migrane to

nerve pain. One is pressure in the sinus cavity and the other the

misfiring of nerves. Yes I spend alot of time up in neurology and

the pain clinc. Why? Cause my boyfriend goes there. I can safely

say that diabetic nerve pain is alot closer to fm than a sinus

headache. Want the kicker? I HAVE A SINUS INFECTION RIGHT NOW

THANKS TO THE CHANGING WEATHER! My face and chest burns, my teeth

ache, the throat sore and I have green shit coming out of my eyes.

Its freaking gross. Last time I checked fm wasn't even close. So

now that we are all a little bit more educated on Sinusitis and how

gross it can be I think it best to get off this topic before my head

explodes. Anyways night everyone and I will update everyone on our

visit to the pain specialist today.

Wolfie

> > > >

> > > > Guys,

> > > >

> > > > I was just thinking about the fibro myths when it says it

is not

> > > the connective tissue muscles, or joint damage. Well I just

started

> > > thinking don't most of us start hurting when the weather

changes? I

> > > know I have read quite a few posts including my own stating

that the

> > > weather affects our fibro something fierce! What would that

have

> > to

> > > do with our brain stimuli? To me that just seems more like the

> > > muscles and the connective tissues, not the brain stimuli or

> > > depression. If you read through those carefully it is almost

> > > disheartening as they are saying it could be another 12 years

before

> > > they come to any more conclusions about fibro. That Dr.s still

> > cannot

> > > decide if it is a psychological disease caused by depression

(yea

> > > right another excuse for them) or is it something to do with our

> > > joints and connective tissues? I feel it is still the latter.

> > Maybe

> > > I am not understanding it correctly and am not saying this

person is

> > > wrong. But how does your body feel? How do

> > > > your joints feel?

> > > > Please do not think I am putting this Myth thing down at all

> > > because it does bring up some great points but I am just

wondering

> > how

> > > the group really feels about what it is saying?

> > > >

> > > > Hope all of you are having a good day!

> > > > Lori H

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

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

> > > > Catch up on fall's hot new shows on Yahoo! TV. Watch

previews,

> > get

> > > listings, and more!

> > > >

> > > >

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In a message dated 9/30/2007 8:16:18 A.M. Pacific Daylight Time,

dodgeturbo99@... writes:

Please do not think I am putting this Myth thing down at all because it does

bring up some great points but I am just wondering how the group really

feels about what it is saying?

I have always been told that yes, fibro does involve the muscles, tendons

and connective tissue. I know that during this flare I have been in for the

past 6 days, that is where I am hurting the most.

Gentle hugs,

Debi/Ca.

CO-owner of _USMCLovedOnes4Support _

(http://USMCLovedOnes4Support /)

Proud and Blessed Mom of 3

Proud MIL of a Marine and a Swiss

Blessed Grandma to 6 and one Special Angel, he got his angel wings on

6/14/04 at only 6 days old. New baby, Gavin, born 8/05/06...hooray!!!!!!!!!

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Thanks Barb I feel that it is not enough a myth. About our jointsbeing affected

by the cold and like said the extreme heat asit can really affect me also.

Thank you.

Lori H

Hi Lori,

My thinking is that it is something to do with the muscles/tissues, NOT

depression/psychological. I think that since doctors can't see the fibro and

tests don't show it, then it isn't really there--and it must be " all in our

heads. "

Of course we know that the pain is really there and most of us remember a time

when we had normal (by society's standards) lives. All we want is to go back to

normal functioning so that we can live our lives with some enjoyment.

I also think that the pain and fatigue cause the depression, not the other way

around. I know that having to stay at home and deal with pain on days when I

would rather be out having fun makes me pretty darn depressed...and why wouldn't

it?

Barb

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

Be a better Heartthrob. Get better relationship answers from someone who knows.

Yahoo! Answers - Check it out.

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Debi,

I would say that 80% of my fibromyalgia pain is directly connected to

my muscles. I get knots in them that send shooting pains when they are

pressed on. However, I have learned to use deep tissue massage to work

the knots out of my muscles and help the muscle relax and releave the

pain. Same for the tender points, I use accupressure on them to work

through the pain and help releave it.

My joints DO hurt but not near close to the amount my muscles do.

N.

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Wolfie,

I am not saying anything about sinusitis . I have had one sinus infection in

my life and that was eough for me. I am not sure if maybe the person meant the

person just meant meant plain old sinues and allergies in general.

I lived on a farm for close to 18 years nevr had an allergy that I knew of.

then after 3 kids and living in town I started getting them. I have lived on

Decongestants and Anhistimines just about as long as I have dx'd with Fibro.

They have gotten worse just in the last 6 years. My mother after she had us and

was about my age she started having issues with sinuses and and perfumes and

certian smells just about lay her out for a day. They make her physically sick.

That use to make me so mad at her as she was always complaining.

Guess what I have that problem now. Certain smells just about make me sick.

Sometimes I feel like I am pregnant again LOL. Can't happen! I know my mom has

had fibro for years she has the sinuses, sensitivity to smells and pain for

years. But she will not admit it as she cannot bring herself to see mine and

well to see hers theres just nothing to see to tell her she has this. I also

have a brother I am pretty sure has it. I usually wake up every morning nose

all stuffed and eyes pretty gross. I do not know if it has anything to do with

fibro but like I said it has been around just as long as the fibro.

Other people can have Sinusitis without having fibro. They do not have to go

hand in hand. I am just not sure how to explain it.

Lori H

whitewolf_50112 wrote:

WHOA! Ok who said they can relate to fm with Sinusitis? I know for

a fact those are not even closely related. I may spend way too much

time at the hospital, but do not ever compare a facial migrane to

nerve pain. One is pressure in the sinus cavity and the other the

misfiring of nerves. Yes I spend alot of time up in neurology and

the pain clinc. Why? Cause my boyfriend goes there. I can safely

say that diabetic nerve pain is alot closer to fm than a sinus

headache. Want the kicker? I HAVE A SINUS INFECTION RIGHT NOW

THANKS TO THE CHANGING WEATHER! My face and chest burns, my teeth

ache, the throat sore and I have green shit coming out of my eyes.

Its freaking gross. Last time I checked fm wasn't even close. So

now that we are all a little bit more educated on Sinusitis and how

gross it can be I think it best to get off this topic before my head

explodes. Anyways night everyone and I will update everyone on our

visit to the pain specialist today.

Wolfie

> > > >

> > > > Guys,

> > > >

> > > > I was just thinking about the fibro myths when it says it

is not

> > > the connective tissue muscles, or joint damage. Well I just

started

> > > thinking don't most of us start hurting when the weather

changes? I

> > > know I have read quite a few posts including my own stating

that the

> > > weather affects our fibro something fierce! What would that

have

> > to

> > > do with our brain stimuli? To me that just seems more like the

> > > muscles and the connective tissues, not the brain stimuli or

> > > depression. If you read through those carefully it is almost

> > > disheartening as they are saying it could be another 12 years

before

> > > they come to any more conclusions about fibro. That Dr.s still

> > cannot

> > > decide if it is a psychological disease caused by depression

(yea

> > > right another excuse for them) or is it something to do with our

> > > joints and connective tissues? I feel it is still the latter.

> > Maybe

> > > I am not understanding it correctly and am not saying this

person is

> > > wrong. But how does your body feel? How do

> > > > your joints feel?

> > > > Please do not think I am putting this Myth thing down at all

> > > because it does bring up some great points but I am just

wondering

> > how

> > > the group really feels about what it is saying?

> > > >

> > > > Hope all of you are having a good day!

> > > > Lori H

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

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

> > > > Catch up on fall's hot new shows on Yahoo! TV. Watch

previews,

> > get

> > > listings, and more!

> > > >

> > > >

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Try reading about Trigger Points (different from Tender Points of FM)

Trigger points can be relieved by massaging the knots in the muscles

and reduce pain

-- In Fibromyalgia_Support_Group , " Mystic "

wrote:

>

> Debi,

>

> I would say that 80% of my fibromyalgia pain is directly connected to

> my muscles. I get knots in them that send shooting pains when they

are

> pressed on. However, I have learned to use deep tissue massage to

work

> the knots out of my muscles and help the muscle relax and releave the

> pain. Same for the tender points, I use accupressure on them to work

> through the pain and help releave it.

>

> My joints DO hurt but not near close to the amount my muscles do.

>

> N.

>

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High sed Rate?

To: Fibromyalgia_Support_Group@...: jathorn@...:

Tue, 2 Oct 2007 17:55:20 +0000Subject: Re: Question/Angie

For me the lack of a high sed rate was one of the things that led them to the

FMS dx. Every single blood test they ran was normal so effectively they ruled

out everything else and said " Fibromyalgia. " So I'm not sure if the high sed

rate is universal among us.

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