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---Hi , Welcome, I hope we can help you understand this fibro,

it is something you will have to deal with every day but I guess you

all ready know that, how somedays are better than others. I have had

this for several years and I don't have many answers. One good thing

about this place is when you can't sleep in the middle of the night

you will have some one to talk to that understand. Audie

In @y..., wrote:

>

> Hi, My name is and I am from So. Cal.

>

> Age range: 50

>

> Male/female: Male

>

> What are the symptoms? Burning, aching, tingling pain in all of

the points. And then some.

>

> Has you illness been diagnosed? Yes, last December

>

> How long did you suffer before you got help? Probably at least a

few years. I also have spinal problems with similar symptoms.

>

> Is there a time that you can remember when it started? I think

after a near divorce, just before my last neck surgery.

>

> Some of us have found lack of exercise we are overweight. Have you

> found this to be a problem also? I weigh 215 and am 5'11''. Not

to well in proportion though.

>

> Are you on disability? Disibility retirement, still working on

Social Security.

>

> If you are any pointers for others trying to get on disability?

Start as soon as possible as it takes a long time.

>

> What have you found that helps ease the pain, warm baths,

medications

> etc.? Warm bathes, showers, spas help and I am on alot of Vicodin

for the ortho stuff which helps. Often though I cant tell where the

pain originates from.

>

> Do you have sleep problems? How do you deal with it? Yes, Ambien

worked for awhile, not so well now. Elavil helps be sleep but i dont

like the effect. Have been on a number of anti-depressants but cant

tolerate them. Again dont remember which came first, the pain or the

depression.

>

> Do you have family that understands your illness? Somewhat but it

is a strain on everyone. Findind info on Fibro has helped greatly. I

thought I was going crazy before i found place like this.

>

> Some have found certain foods causes problems with CFS or Fibro,

have

> you? Nothing yet.

>

> What type of Doctor have you found that has helped you the most?

No one really.

>

> I have been in pain for so long I really cant remember when it all

started. Memory is another problem. I often feel Flu like symptoms.

I get feverish and sweaty with no temperature after little exertion.

Always tired and irratable bowel. I do occasionally feel like it

goes away for a short time and then it returns. I hope this helps

someone!!

>

>

>

>

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

>

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Guest guest

---Hi , Welcome, I hope we can help you understand this fibro,

it is something you will have to deal with every day but I guess you

all ready know that, how somedays are better than others. I have had

this for several years and I don't have many answers. One good thing

about this place is when you can't sleep in the middle of the night

you will have some one to talk to that understand. Audie

In @y..., wrote:

>

> Hi, My name is and I am from So. Cal.

>

> Age range: 50

>

> Male/female: Male

>

> What are the symptoms? Burning, aching, tingling pain in all of

the points. And then some.

>

> Has you illness been diagnosed? Yes, last December

>

> How long did you suffer before you got help? Probably at least a

few years. I also have spinal problems with similar symptoms.

>

> Is there a time that you can remember when it started? I think

after a near divorce, just before my last neck surgery.

>

> Some of us have found lack of exercise we are overweight. Have you

> found this to be a problem also? I weigh 215 and am 5'11''. Not

to well in proportion though.

>

> Are you on disability? Disibility retirement, still working on

Social Security.

>

> If you are any pointers for others trying to get on disability?

Start as soon as possible as it takes a long time.

>

> What have you found that helps ease the pain, warm baths,

medications

> etc.? Warm bathes, showers, spas help and I am on alot of Vicodin

for the ortho stuff which helps. Often though I cant tell where the

pain originates from.

>

> Do you have sleep problems? How do you deal with it? Yes, Ambien

worked for awhile, not so well now. Elavil helps be sleep but i dont

like the effect. Have been on a number of anti-depressants but cant

tolerate them. Again dont remember which came first, the pain or the

depression.

>

> Do you have family that understands your illness? Somewhat but it

is a strain on everyone. Findind info on Fibro has helped greatly. I

thought I was going crazy before i found place like this.

>

> Some have found certain foods causes problems with CFS or Fibro,

have

> you? Nothing yet.

>

> What type of Doctor have you found that has helped you the most?

No one really.

>

> I have been in pain for so long I really cant remember when it all

started. Memory is another problem. I often feel Flu like symptoms.

I get feverish and sweaty with no temperature after little exertion.

Always tired and irratable bowel. I do occasionally feel like it

goes away for a short time and then it returns. I hope this helps

someone!!

>

>

>

>

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

>

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Guest guest

Welcome, to our list. This is a very good list. We are very caring,

loving and supportive. If you have any question, let us know. Someone will

more than likely have the answer. If you have something to say, just sump

right in. We have all had our times at being angry and upset about this

fibro and we say so. Out loud. So if you want to vent, feel free.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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Hi everyone and hello to our new members. You've come to the right group. I

went to the doctors yesterday for my son I ended up having an appt to. He

squeezed me in. Well, he put me on flexeril/cyclobenzaprine for my pain and I

went back on wellbutrin SR(anti-depressant). He told me it would help my

baseline. I was on it before. My cardiologist prescribed it for my neurocronigic

sycope. When I went off of it before I noticed more pain. My family dr also gave

me a prescription for massage therapy. I need to call the insurance company

though. I hope they cover it. I still have alot of pain in my back and it

radiates up to my sternum. I hope that I start feeling better. I need to go

plant my veggies in the garden. Well, I thought I'd let you know that I went to

the doctor. He is very attentive and listens to what my symptoms are. He does

help out alot. Well, everyone have a great evening everyone!!

rox6602000 rox660@...> wrote: a lot

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

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Guest guest

Cinda, welcome to our group. It is a very good one. The people are

friendly, caring, loving and very supportive. If you have anymore questions,

ask away, someone will probably have the answer. if you feel like venting,

this is the place to do it. There is always someone to listen.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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Guest guest

Cinda, welcome to our group. It is a very good one. The people are

friendly, caring, loving and very supportive. If you have anymore questions,

ask away, someone will probably have the answer. if you feel like venting,

this is the place to do it. There is always someone to listen.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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Hi ,

when I was reading your life story, haha boy it sound like me. In

March of 2001 I was slurry my words, dropping things, tripping over

my feet for no reason at all, I had pain thru out my body. went thru

so many tests and they thought I was dx with a stoke, but that was

not it, so they couldn';t find anything wrong with me. In october

2001, I lost my memory, went thru more tests and the doc said that I

was faking and trying to get attention; and get this, she said that

my kids were out of control. What does that have to do with my test

results? Well I didn;t get the test results until about month ago

saying that I cheating, faked my tests. Tell me something WHY would

I do that... I just can't belieive some of this doctors, so I know

how you feel .

I was dx with FM in the last 3 months ago, and it is a big pain. So

let me ask a Question, my doc will not rx me any pain killers..its

because of my Bi-polar, and ADD, will along my Boardline personity

disorder, the question is , where can I get some relief for my pain?

Help!!!

In @y..., " evilwoman_21 " wrote:

> Hi everyone,

> I just wanted to give a brief hello. I was diagnosed with FM about

> a year ago and have been on ultram for pain and flexaril for

> restless leg. I however was diagnosed with FM but i do not have

the

> common pain points. As a matter of fact i only have 1 pain point

in

> my neck. I do however have mystery pain throughout my intire body

> and it is different from week to week. After seeing countless

> doctors and being told it was all in my head I finally found one

> that would believe me and is working with me to control my pain. I

> guess I am lucky though because my family doctor is great and he

> doesnt cut everything off as being " faked " . I actually had an

> orthopedist tell my family doctor that there was nothing wrong with

> me i was faking for attention. Like i really want to pay $2,000.00

> for an overnights stay in the hospital for attention. I cant

> believe some doctors these days and their bedside manner. I also

am

> pretty lucky because i dont have depression either. I do however

> have my moments just as everyone does. Well I am starting to write

> a book here and I only wanted to say hi.

> Thanks For hearing me

> stephanie

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Hi ,

when I was reading your life story, haha boy it sound like me. In

March of 2001 I was slurry my words, dropping things, tripping over

my feet for no reason at all, I had pain thru out my body. went thru

so many tests and they thought I was dx with a stoke, but that was

not it, so they couldn';t find anything wrong with me. In october

2001, I lost my memory, went thru more tests and the doc said that I

was faking and trying to get attention; and get this, she said that

my kids were out of control. What does that have to do with my test

results? Well I didn;t get the test results until about month ago

saying that I cheating, faked my tests. Tell me something WHY would

I do that... I just can't belieive some of this doctors, so I know

how you feel .

I was dx with FM in the last 3 months ago, and it is a big pain. So

let me ask a Question, my doc will not rx me any pain killers..its

because of my Bi-polar, and ADD, will along my Boardline personity

disorder, the question is , where can I get some relief for my pain?

Help!!!

In @y..., " evilwoman_21 " wrote:

> Hi everyone,

> I just wanted to give a brief hello. I was diagnosed with FM about

> a year ago and have been on ultram for pain and flexaril for

> restless leg. I however was diagnosed with FM but i do not have

the

> common pain points. As a matter of fact i only have 1 pain point

in

> my neck. I do however have mystery pain throughout my intire body

> and it is different from week to week. After seeing countless

> doctors and being told it was all in my head I finally found one

> that would believe me and is working with me to control my pain. I

> guess I am lucky though because my family doctor is great and he

> doesnt cut everything off as being " faked " . I actually had an

> orthopedist tell my family doctor that there was nothing wrong with

> me i was faking for attention. Like i really want to pay $2,000.00

> for an overnights stay in the hospital for attention. I cant

> believe some doctors these days and their bedside manner. I also

am

> pretty lucky because i dont have depression either. I do however

> have my moments just as everyone does. Well I am starting to write

> a book here and I only wanted to say hi.

> Thanks For hearing me

> stephanie

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Hi ,

when I was reading your life story, haha boy it sound like me. In

March of 2001 I was slurry my words, dropping things, tripping over

my feet for no reason at all, I had pain thru out my body. went thru

so many tests and they thought I was dx with a stoke, but that was

not it, so they couldn';t find anything wrong with me. In october

2001, I lost my memory, went thru more tests and the doc said that I

was faking and trying to get attention; and get this, she said that

my kids were out of control. What does that have to do with my test

results? Well I didn;t get the test results until about month ago

saying that I cheating, faked my tests. Tell me something WHY would

I do that... I just can't belieive some of this doctors, so I know

how you feel .

I was dx with FM in the last 3 months ago, and it is a big pain. So

let me ask a Question, my doc will not rx me any pain killers..its

because of my Bi-polar, and ADD, will along my Boardline personity

disorder, the question is , where can I get some relief for my pain?

Help!!!

In @y..., " evilwoman_21 " wrote:

> Hi everyone,

> I just wanted to give a brief hello. I was diagnosed with FM about

> a year ago and have been on ultram for pain and flexaril for

> restless leg. I however was diagnosed with FM but i do not have

the

> common pain points. As a matter of fact i only have 1 pain point

in

> my neck. I do however have mystery pain throughout my intire body

> and it is different from week to week. After seeing countless

> doctors and being told it was all in my head I finally found one

> that would believe me and is working with me to control my pain. I

> guess I am lucky though because my family doctor is great and he

> doesnt cut everything off as being " faked " . I actually had an

> orthopedist tell my family doctor that there was nothing wrong with

> me i was faking for attention. Like i really want to pay $2,000.00

> for an overnights stay in the hospital for attention. I cant

> believe some doctors these days and their bedside manner. I also

am

> pretty lucky because i dont have depression either. I do however

> have my moments just as everyone does. Well I am starting to write

> a book here and I only wanted to say hi.

> Thanks For hearing me

> stephanie

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Thanks for the welcome.

One thing I forgot to mention that helps me with pain is the

magnetic wrist band. It provides a lot of relief for a few

hours. This may have more to do with osteoarthritis than FM,

I would like to learn more if anyone has any experience or

knowledge on the subject.

Peace,

jim

> Jim~

> Welcome to the group! This group is full of understanding,

> compassion but lets not forget humor! Feel free to ask questions

> because someone useally knows the answer and also if you are

> having a bad day feel free to let it out. Welcome!!!

> ~

>

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Thanks for the welcome.

One thing I forgot to mention that helps me with pain is the

magnetic wrist band. It provides a lot of relief for a few

hours. This may have more to do with osteoarthritis than FM,

I would like to learn more if anyone has any experience or

knowledge on the subject.

Peace,

jim

> Jim~

> Welcome to the group! This group is full of understanding,

> compassion but lets not forget humor! Feel free to ask questions

> because someone useally knows the answer and also if you are

> having a bad day feel free to let it out. Welcome!!!

> ~

>

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Thanks for the welcome.

One thing I forgot to mention that helps me with pain is the

magnetic wrist band. It provides a lot of relief for a few

hours. This may have more to do with osteoarthritis than FM,

I would like to learn more if anyone has any experience or

knowledge on the subject.

Peace,

jim

> Jim~

> Welcome to the group! This group is full of understanding,

> compassion but lets not forget humor! Feel free to ask questions

> because someone useally knows the answer and also if you are

> having a bad day feel free to let it out. Welcome!!!

> ~

>

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Hello Tammi!!

Welcome to the group! Glad to have you!

, 31, CO

In a message dated Tue, 11 Jun 2002 10:07:17 PM Eastern Daylight Time,

leskadog@... writes:

> Hi all. My name is Tammie, and I am a new member to this list. I am 29 years

old, and I am from Utah. I was diagnosed in 1986, when I was 13 years old, and

if it hadn't been for a Rheumatologist believing me, and taking me seriously, I

don't know what would have happened to me. I was told by several Doctors that

this was all in my head, and I got several referrals to Psychologists. When I

was diagnosed, the term Fibrositis was used. I don't know if we'll ever know

for sure, but my parents think I had Fibromyalgia since I was little. I never

could sleep through the night, and my parents would often find me roaming the

house, even when I was 3 and 4 years old. I've always had sleep problems as far

back as I can remember.

>

> Well, I'll try to keep this message short. There's more I would like to

share, but I'll wait until next time. I look

> forward to getting to know all of you.

>

> Take care.

>

> Tammie & Leska

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Hello Tammi!!

Welcome to the group! Glad to have you!

, 31, CO

In a message dated Tue, 11 Jun 2002 10:07:17 PM Eastern Daylight Time,

leskadog@... writes:

> Hi all. My name is Tammie, and I am a new member to this list. I am 29 years

old, and I am from Utah. I was diagnosed in 1986, when I was 13 years old, and

if it hadn't been for a Rheumatologist believing me, and taking me seriously, I

don't know what would have happened to me. I was told by several Doctors that

this was all in my head, and I got several referrals to Psychologists. When I

was diagnosed, the term Fibrositis was used. I don't know if we'll ever know

for sure, but my parents think I had Fibromyalgia since I was little. I never

could sleep through the night, and my parents would often find me roaming the

house, even when I was 3 and 4 years old. I've always had sleep problems as far

back as I can remember.

>

> Well, I'll try to keep this message short. There's more I would like to

share, but I'll wait until next time. I look

> forward to getting to know all of you.

>

> Take care.

>

> Tammie & Leska

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Welcome Tammie, and everyone else who is new. I've always been a light

sleeper and found it harder than everyone else to get to sleep. My

husband always tells me " naps are wonderful things. " I tell him, " no,

they're not, they're a lot of work to go to sleep, and you feel like

crap when you wake up. " I don't nap. I'll lay down for a few minutes,

usually 10-20 minutes, but don't even come close to sleeping. On the

days where I'm really bad, I'll go into a state where I can still hear

the tv, but don't know what they're saying. That's as close to napping

as I come.

Darcy

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Welcome Tammie, and everyone else who is new. I've always been a light

sleeper and found it harder than everyone else to get to sleep. My

husband always tells me " naps are wonderful things. " I tell him, " no,

they're not, they're a lot of work to go to sleep, and you feel like

crap when you wake up. " I don't nap. I'll lay down for a few minutes,

usually 10-20 minutes, but don't even come close to sleeping. On the

days where I'm really bad, I'll go into a state where I can still hear

the tv, but don't know what they're saying. That's as close to napping

as I come.

Darcy

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-Sounds as if the massage theapist is going too deep and the rotator

cuff is already irritated. Do you have an osteopath who does

manipulations in your area? That would be your best best. You need to

rest that shoulder until it is no longer irritated and ice. Have you

had a sleep study done. Sometimes, there is an underlying sleep

problem. Star

-- In @y..., " jaxxxchic " wrote:

> Greetings Newbie here....I wanted to get some suggestions maybe

> answers of why I have so much PAIN!

> It all stems back more then a year ago. I worked at Sams club

> stocking Cigarette cases. I would complain nightly about shoulder

> pain and wake with morning stiffness. This went on for at least 6

> months...Till one day I was asked to move carts/flatbeds. Flatbeds

> are heavy metal carts. I moved approx 5 to 10 at a times. As time

> progressed I experienced more and more pain until Labor day weekend

> of last year. The pain got so bad I was choking down handfuls of

IB's

> and crying/waking away from my register.Needless to say the

spervisor

> said I need to see a DOC,not their just a doc. Which I did. This

doc

> DX me with Rotator cuff tendonitis. Time went on with him and

> aggressive therapy. The pain worstened so much I couldn't move my

> head to left.After Xrays and MRI the doc said there was nothing he

> could do for me and sent me on my way...Great doc eh?

> So Now I am seeing another doc...I have improved some in areas and

> gotten worst in others. I have trouble dressing(esp the

> bra),cleaning,driving,and doing certain things. I can lift a half

> gallon of milk without pain.The Doc has been giving me

Steroids,pain

> killers ( which don't really help),and a nerve block. I also get

> massage therapy. Now even after a year and all this I STILL am in

> great pain? After massage therapy I am so stiff and in pain I can

> barely move. I go threw weird sleep patterns...I mostly sleep 3 -5

> hours give or take a night and maybe nap during the day. I find the

> recliner more comfy and haven't slept in a bed for a year now. I

also

> have bouts of depression...just crying because I feel like a

failure

> and useless. The doc now wants me to return to work. But I feel I

> couldn't drive there plus lifting heavy items I would do more

calling

> out then being at work.Somedays are better then others but I have

> most pain at night esp while sleeping.

> So any suggestions???? I don't know if I have this...my pain is

> generalized around my left shoulder with neck pain and severe

> headaches...so bad I wanna cry.Now and then I have back pain but

> nothing a few IB's don't cure.

> so suggestions??? Ideas??? anything would be GREATFUL as I have no

> clue why I hurt so bad still???

> Thankx

> Lori

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-Sounds as if the massage theapist is going too deep and the rotator

cuff is already irritated. Do you have an osteopath who does

manipulations in your area? That would be your best best. You need to

rest that shoulder until it is no longer irritated and ice. Have you

had a sleep study done. Sometimes, there is an underlying sleep

problem. Star

-- In @y..., " jaxxxchic " wrote:

> Greetings Newbie here....I wanted to get some suggestions maybe

> answers of why I have so much PAIN!

> It all stems back more then a year ago. I worked at Sams club

> stocking Cigarette cases. I would complain nightly about shoulder

> pain and wake with morning stiffness. This went on for at least 6

> months...Till one day I was asked to move carts/flatbeds. Flatbeds

> are heavy metal carts. I moved approx 5 to 10 at a times. As time

> progressed I experienced more and more pain until Labor day weekend

> of last year. The pain got so bad I was choking down handfuls of

IB's

> and crying/waking away from my register.Needless to say the

spervisor

> said I need to see a DOC,not their just a doc. Which I did. This

doc

> DX me with Rotator cuff tendonitis. Time went on with him and

> aggressive therapy. The pain worstened so much I couldn't move my

> head to left.After Xrays and MRI the doc said there was nothing he

> could do for me and sent me on my way...Great doc eh?

> So Now I am seeing another doc...I have improved some in areas and

> gotten worst in others. I have trouble dressing(esp the

> bra),cleaning,driving,and doing certain things. I can lift a half

> gallon of milk without pain.The Doc has been giving me

Steroids,pain

> killers ( which don't really help),and a nerve block. I also get

> massage therapy. Now even after a year and all this I STILL am in

> great pain? After massage therapy I am so stiff and in pain I can

> barely move. I go threw weird sleep patterns...I mostly sleep 3 -5

> hours give or take a night and maybe nap during the day. I find the

> recliner more comfy and haven't slept in a bed for a year now. I

also

> have bouts of depression...just crying because I feel like a

failure

> and useless. The doc now wants me to return to work. But I feel I

> couldn't drive there plus lifting heavy items I would do more

calling

> out then being at work.Somedays are better then others but I have

> most pain at night esp while sleeping.

> So any suggestions???? I don't know if I have this...my pain is

> generalized around my left shoulder with neck pain and severe

> headaches...so bad I wanna cry.Now and then I have back pain but

> nothing a few IB's don't cure.

> so suggestions??? Ideas??? anything would be GREATFUL as I have no

> clue why I hurt so bad still???

> Thankx

> Lori

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-Sounds as if the massage theapist is going too deep and the rotator

cuff is already irritated. Do you have an osteopath who does

manipulations in your area? That would be your best best. You need to

rest that shoulder until it is no longer irritated and ice. Have you

had a sleep study done. Sometimes, there is an underlying sleep

problem. Star

-- In @y..., " jaxxxchic " wrote:

> Greetings Newbie here....I wanted to get some suggestions maybe

> answers of why I have so much PAIN!

> It all stems back more then a year ago. I worked at Sams club

> stocking Cigarette cases. I would complain nightly about shoulder

> pain and wake with morning stiffness. This went on for at least 6

> months...Till one day I was asked to move carts/flatbeds. Flatbeds

> are heavy metal carts. I moved approx 5 to 10 at a times. As time

> progressed I experienced more and more pain until Labor day weekend

> of last year. The pain got so bad I was choking down handfuls of

IB's

> and crying/waking away from my register.Needless to say the

spervisor

> said I need to see a DOC,not their just a doc. Which I did. This

doc

> DX me with Rotator cuff tendonitis. Time went on with him and

> aggressive therapy. The pain worstened so much I couldn't move my

> head to left.After Xrays and MRI the doc said there was nothing he

> could do for me and sent me on my way...Great doc eh?

> So Now I am seeing another doc...I have improved some in areas and

> gotten worst in others. I have trouble dressing(esp the

> bra),cleaning,driving,and doing certain things. I can lift a half

> gallon of milk without pain.The Doc has been giving me

Steroids,pain

> killers ( which don't really help),and a nerve block. I also get

> massage therapy. Now even after a year and all this I STILL am in

> great pain? After massage therapy I am so stiff and in pain I can

> barely move. I go threw weird sleep patterns...I mostly sleep 3 -5

> hours give or take a night and maybe nap during the day. I find the

> recliner more comfy and haven't slept in a bed for a year now. I

also

> have bouts of depression...just crying because I feel like a

failure

> and useless. The doc now wants me to return to work. But I feel I

> couldn't drive there plus lifting heavy items I would do more

calling

> out then being at work.Somedays are better then others but I have

> most pain at night esp while sleeping.

> So any suggestions???? I don't know if I have this...my pain is

> generalized around my left shoulder with neck pain and severe

> headaches...so bad I wanna cry.Now and then I have back pain but

> nothing a few IB's don't cure.

> so suggestions??? Ideas??? anything would be GREATFUL as I have no

> clue why I hurt so bad still???

> Thankx

> Lori

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hi stephanie~ i would first like to welcome you to the

group, although i'm sorry that you had to join it. i

can sympathize with you, i was diagnosed with CFS/FMS

right before i turned 20. i think that i've had it

since i was about 16 though. it really can change

your life. i have been researching like mad for the

past couple of years so feel free to email me. i'll

even give you my personal address because sometimes

it's easier for me to answer abbuttercup55@...

i think that it's easier sometimes to talk to poeple

your own age because they know how things affect you.

are you planning on going to college or trying? well,

i hope to get to know you in the future

take care

ali

--- rain_drop1982 rain_drop1982@...> wrote:

> hi my name is . i am 19 years old. i just

> recently found

> out that i have fibromyalgia. i am still learning

> about fibro. i

> have been having pain like this for about 3 years

> but like i said i

> just recently found out what it was. i hope to

> learn more about

> this and more things that may help the pain.

>

>

__________________________________________________

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Guest guest

hi stephanie~ i would first like to welcome you to the

group, although i'm sorry that you had to join it. i

can sympathize with you, i was diagnosed with CFS/FMS

right before i turned 20. i think that i've had it

since i was about 16 though. it really can change

your life. i have been researching like mad for the

past couple of years so feel free to email me. i'll

even give you my personal address because sometimes

it's easier for me to answer abbuttercup55@...

i think that it's easier sometimes to talk to poeple

your own age because they know how things affect you.

are you planning on going to college or trying? well,

i hope to get to know you in the future

take care

ali

--- rain_drop1982 rain_drop1982@...> wrote:

> hi my name is . i am 19 years old. i just

> recently found

> out that i have fibromyalgia. i am still learning

> about fibro. i

> have been having pain like this for about 3 years

> but like i said i

> just recently found out what it was. i hope to

> learn more about

> this and more things that may help the pain.

>

>

__________________________________________________

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Guest guest

hi stephanie~ i would first like to welcome you to the

group, although i'm sorry that you had to join it. i

can sympathize with you, i was diagnosed with CFS/FMS

right before i turned 20. i think that i've had it

since i was about 16 though. it really can change

your life. i have been researching like mad for the

past couple of years so feel free to email me. i'll

even give you my personal address because sometimes

it's easier for me to answer abbuttercup55@...

i think that it's easier sometimes to talk to poeple

your own age because they know how things affect you.

are you planning on going to college or trying? well,

i hope to get to know you in the future

take care

ali

--- rain_drop1982 rain_drop1982@...> wrote:

> hi my name is . i am 19 years old. i just

> recently found

> out that i have fibromyalgia. i am still learning

> about fibro. i

> have been having pain like this for about 3 years

> but like i said i

> just recently found out what it was. i hope to

> learn more about

> this and more things that may help the pain.

>

>

__________________________________________________

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Guest guest

Hi , My son who will be 32 the last day of August has colitis, we

though for a long time that he had crohns, he finally had the surgery to

have ever thing taken out, he works night shift and he stay tired a lot, I

am the only one in the family that has fibro I hope that he doesn't get it.

So I really know how your are suffering with both fibro and crohns.If there

is anything that I can help you with just let me know. Audie

New Member

> Hi,

> Thanks for letting me be a part of your group.

>

> Age range: 27

>

>

> Male/female: Female

>

>

> Has you illness been diagnosed? 5 years

>

>

> How long did you suffer before you got help? Not too long

>

>

> Is there a time that you can remember when it started? Yes, shortly after

I

> received a diagonsis of Crohns Disease.

>

>

> Some of us have found lack of exercise we are overweight. Have you found

> this to be a problem also? No

>

>

> Are you on disability? No

>

>

> What have you found that helps ease the pain, warm baths, medications

etc.?

> Reduce stress

>

>

> sleep problems? How do you deal with it?I don't deal with it but have

> severe sleep problems.

>

>

>

> Some have found certain foods causes problems with CFS or Fibro, have

you?

> I am on a very strict diet for the crohns and candida.

>

>

> What type of Doctor have you found that has helped you the most? None

>

>

>

>

>

> SEND POST TO: fibromyalgia-cfs

>

> HOME

PAGE:http://www.geocities.com/Heartland/Oaks/7127/fibromyalgia-cfs.html

> LIST OWNER: " Missy " Parrot004@...>

> UNSUBSCRIBE:fibromyalgia-cfs-unsubscribe

>

>

>

>

>

>

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Guest guest

Hi Audie,

Thanks for the welcome. I am sorry to hear that your sons has colitis. I

have heard of many misdiagnosed crohns cases who in actual fact have

colitis. For me, I was originally diagnosed as crohns, but it has now

developed to crohns-colitis. I am going through a bad patch now with the

crohns-colitis and fibro flaring. I'm sorry to hear that you suffer with

fibro. Thanks for being here for me. You have no idea how much it means to

me.

New Member

>

>

> > Hi,

> > Thanks for letting me be a part of your group.

> >

> > Age range: 27

> >

> >

> > Male/female: Female

> >

> >

> > Has you illness been diagnosed? 5 years

> >

> >

> > How long did you suffer before you got help? Not too long

> >

> >

> > Is there a time that you can remember when it started? Yes, shortly

after

> I

> > received a diagonsis of Crohns Disease.

> >

> >

> > Some of us have found lack of exercise we are overweight. Have you

found

> > this to be a problem also? No

> >

> >

> > Are you on disability? No

> >

> >

> > What have you found that helps ease the pain, warm baths, medications

> etc.?

> > Reduce stress

> >

> >

> > sleep problems? How do you deal with it?I don't deal with it but have

> > severe sleep problems.

> >

> >

> >

> > Some have found certain foods causes problems with CFS or Fibro, have

> you?

> > I am on a very strict diet for the crohns and candida.

> >

> >

> > What type of Doctor have you found that has helped you the most? None

> >

> >

> >

> >

> >

> > SEND POST TO: fibromyalgia-cfs

> >

> > HOME

> PAGE:http://www.geocities.com/Heartland/Oaks/7127/fibromyalgia-cfs.html

> > LIST OWNER: " Missy " Parrot004@...>

> > UNSUBSCRIBE:fibromyalgia-cfs-unsubscribe

> >

> >

> >

> >

> >

> >

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Guest guest

Welcome...

I wish the best of luck with your disability.

I have found that the Elavil I take for a good nights

sleep has really helped me as well as trying to go to

bed the same time as well as waking the same time

every day. Before, I would not pay attention to this,

but now, I do and it seems to help with the sleep.

a Faye

--- Darcy Stockstill catstamp@...> wrote:

> >

> >

> > Age range: 45

> >

> > Male/female: M

> >

> > What are the symptoms? Extreme fatique, pain from

> head to toe

> >

> > Has you illness been diagnosed? Diagnosed as

> having Fibromyalgia,

> Psoractic Arthritis and Osteoarthritis

> >

> > How long did you suffer before you got help? More

> years now that I

> look back, roughly 8-10 years

> >

> > Is there a time that you can remember when it

> started? When I moved

> from CA to CO for job promotion

> >

> > Some of us have found lack of exercise we are

> overweight.

> > Have you found this to be a problem also? YES

> >

> > Are you on disability? I am currently working

> with my insurance

> company and Social Security

> >

> > If you are any pointers for others trying to get

> on disability? Just

> be aware that Social Security will do everything in

> their power to deny

> you. Do not give up, keep fighting them and

> eventually you will win

> your benefits..

> >

> > What have you found that helps ease the pain, warm

> baths,

> > medications etc.? Warm, not hot epsom salt baths

> help a great deal,

> Advil, Ultracet (RX) positive thinking!

> >

> > Do you have sleep problems? How do you deal with

> it? I sleep less

> than 3 hours a night. The truth is that I have not

> been dealing with

> it. I am now taking Ambien and it helps.

> >

> > Do you have family that understands your illness?

> My family doesn't

> have a clue about this but my roommate is more like

> my caregiver now and

> he is with me every doctors appointments and such in

> case I forget to

> the doctor something and that I will mostly forget

> what the doctor told

> me during the visit. My roommate logs everything

> down.

> >

> > Some have found certain foods causes problems with

> CFS or

> > Fibro, have you? I have noticed this too, but I

> cannot pin point

> which ones they are!

> >

> > What type of Doctor have you found that has helped

> you the most? A

> combination of a rheumatologist and orthopedic.

> They share the same

> office and they rotate me between the two doctors.

> >

>

__________________________________________________

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