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Name: Shay

Married/single: Happily Married

Does family understand your illness: They try, but no, they do not.

Male/female { some names one can't tell}: Female

Age area: 29

Area of the world do you live in: Mid-West; USA

Country/City/Farm life: Wichita, Kansas

How bad is it: The disease is horrible and ravaging me daily.

How long have you had Fibromyalgia or CFS: I was dx 81/2 years ago, but have

probably had it for much longer.

Did a trauma in your life start it: Yes.

What have you found works for you: Tanning in a tanning bed actually helps my

muscles a great deal!

What kind of Dr do you find works best in helping you with this disease? GP

Do you have sleep problems: YES!!!

Does diet effect you: No.

Feel better with cold/hot weather: Any extreme condition hurts it.

Most people with Fibro are overweight I think for lack of activity, do

you find this to be true with you: Yes. I was very slender before the

disease....

What time of the day is the best time for you: Early afternoon

Do you have good days then bad ones or all of them bad: I have periods of

about 6 months bad, 2 good.....

On disability:Yes, but it was a long hard road.

If so hints on how you were able to get it since it is hard to get:The best

doctor in the world fought hard for me.

> Have to have helpers: Yes, my whole family helps when possible.

> Work out or stay at home:Stay at home. No other choice, or you better

> believe I'd be out working when the kids are at school.

>

> Do you have " Now what am I here for times " :Yes.

Join my new Diabetic Recipes group @

http://groups.yahoo.com/group/Recipes4Diabetes

God Bless You All, Shay/Shalynn and the rescue gang;

Max, Samson

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Name: Shay

Married/single: Happily Married

Does family understand your illness: They try, but no, they do not.

Male/female { some names one can't tell}: Female

Age area: 29

Area of the world do you live in: Mid-West; USA

Country/City/Farm life: Wichita, Kansas

How bad is it: The disease is horrible and ravaging me daily.

How long have you had Fibromyalgia or CFS: I was dx 81/2 years ago, but have

probably had it for much longer.

Did a trauma in your life start it: Yes.

What have you found works for you: Tanning in a tanning bed actually helps my

muscles a great deal!

What kind of Dr do you find works best in helping you with this disease? GP

Do you have sleep problems: YES!!!

Does diet effect you: No.

Feel better with cold/hot weather: Any extreme condition hurts it.

Most people with Fibro are overweight I think for lack of activity, do

you find this to be true with you: Yes. I was very slender before the

disease....

What time of the day is the best time for you: Early afternoon

Do you have good days then bad ones or all of them bad: I have periods of

about 6 months bad, 2 good.....

On disability:Yes, but it was a long hard road.

If so hints on how you were able to get it since it is hard to get:The best

doctor in the world fought hard for me.

> Have to have helpers: Yes, my whole family helps when possible.

> Work out or stay at home:Stay at home. No other choice, or you better

> believe I'd be out working when the kids are at school.

>

> Do you have " Now what am I here for times " :Yes.

Join my new Diabetic Recipes group @

http://groups.yahoo.com/group/Recipes4Diabetes

God Bless You All, Shay/Shalynn and the rescue gang;

Max, Samson

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>

> Name: Irene Duffield

>

> Married/single: Married

> Does family understand your illness: Yes, I am very lucky in that.

Male/female { some names one can't tell}: Female

> Age area: 65

Area of the world do you live in: Texas

> Country/City/Farm life: City

> How bad is it: Very bad and getting worse every day

> How long have you had Fibromyalgia or CFS: About 6 years that I know of.

> Did a trauma in your life start it: Yes. I had a very bad fall. Could

> barely get out of bed for three days after the fall.

> What have you found works for you: Hot tub for a short time. Pain

> medication.

> What kind of DR do you find works best in helping you with this disease?

> Rheumatologist

> Do you have sleep problems: Yes

> Does diet effect you: Yes. There are things that I eat that cause me

> problems.

> Feel better with cold/hot weather: Feel better in cold weather.

> Warm baths are heaven sent dealing with pain: I don't think so. At least

> not in my case. I also have a hard time getting out of bathtub.

> Most people with Fibro are overweight I think for lack of activity, do

> you find this to be true with you: I am overweight but because I was given

> a steroid drug that causes you pain. I have lost some of it. No longer

> take any steroids.

> What time of the day is the best time for you: Late morning. By evening I

> am in so much pain that all I can do is rest. I try to get all of my

> chores done in the late morning so I will be able to rest. I have a

> cleaning lady that comes in once a week to help. She is also very

> understanding about the fibro and she cleans thing above and beyond the

> call of duty.

> Do you have good days then bad ones or all of them bad: I have more bad days

> than good but still the good days are really not good. It just means that

> I am going to be able to cope a little better on that day and not fall

> apart.

> On disability: No

f so hints on how you were able to get it since it is hard to get: NA

>

> Have to have helpers: Yes. My husband and my daughter who lives next door.

> I don't know what I would do without either of them. I love my husband

> dearly and I hope that he will be with more for my lifetime.

Work out or stay at home: I am blessed in being able to stay home.

> Do you have " Now what am I here for times " : Yes, because I have tinnitus,

> fibromyalgia, polyarthritis, glaucoma suspect and a lump in my breast that

> so far seems to be nothing and mini strokes.

> Share your funny memory problem story: I am sorry to say that I can't

> remember any funny stories. I do have a Charlie Brown picture of him

> laying in bed and saying , " Why me " and the Lord answers " No reason, your

> name just happened to come up. " That is how I feel every time I am

> diagnosed with something new.

>

>

>

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>

> Name: Irene Duffield

>

> Married/single: Married

> Does family understand your illness: Yes, I am very lucky in that.

Male/female { some names one can't tell}: Female

> Age area: 65

Area of the world do you live in: Texas

> Country/City/Farm life: City

> How bad is it: Very bad and getting worse every day

> How long have you had Fibromyalgia or CFS: About 6 years that I know of.

> Did a trauma in your life start it: Yes. I had a very bad fall. Could

> barely get out of bed for three days after the fall.

> What have you found works for you: Hot tub for a short time. Pain

> medication.

> What kind of DR do you find works best in helping you with this disease?

> Rheumatologist

> Do you have sleep problems: Yes

> Does diet effect you: Yes. There are things that I eat that cause me

> problems.

> Feel better with cold/hot weather: Feel better in cold weather.

> Warm baths are heaven sent dealing with pain: I don't think so. At least

> not in my case. I also have a hard time getting out of bathtub.

> Most people with Fibro are overweight I think for lack of activity, do

> you find this to be true with you: I am overweight but because I was given

> a steroid drug that causes you pain. I have lost some of it. No longer

> take any steroids.

> What time of the day is the best time for you: Late morning. By evening I

> am in so much pain that all I can do is rest. I try to get all of my

> chores done in the late morning so I will be able to rest. I have a

> cleaning lady that comes in once a week to help. She is also very

> understanding about the fibro and she cleans thing above and beyond the

> call of duty.

> Do you have good days then bad ones or all of them bad: I have more bad days

> than good but still the good days are really not good. It just means that

> I am going to be able to cope a little better on that day and not fall

> apart.

> On disability: No

f so hints on how you were able to get it since it is hard to get: NA

>

> Have to have helpers: Yes. My husband and my daughter who lives next door.

> I don't know what I would do without either of them. I love my husband

> dearly and I hope that he will be with more for my lifetime.

Work out or stay at home: I am blessed in being able to stay home.

> Do you have " Now what am I here for times " : Yes, because I have tinnitus,

> fibromyalgia, polyarthritis, glaucoma suspect and a lump in my breast that

> so far seems to be nothing and mini strokes.

> Share your funny memory problem story: I am sorry to say that I can't

> remember any funny stories. I do have a Charlie Brown picture of him

> laying in bed and saying , " Why me " and the Lord answers " No reason, your

> name just happened to come up. " That is how I feel every time I am

> diagnosed with something new.

>

>

>

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In a message dated 9/10/2001 1:47:20 PM Pacific Daylight Time,

mary_bierman@... writes:

> Name: Connell

> Married/single: Married for one year on Sept. 12

> Does family understand your illness: My husband has always understood. It

>

> Male/female { some names one can't tell}: Female

> Age area: 23

> Area of the world do you live in: Magalia CA (Northern CA)

> Country/City/Farm life: I live in a foresty area.

> How bad is it: Very Severe. I think there is also something else wrong with

> me. Autoimmune diseases run in my family.

> How long have you had Fibromyalgia or CFS: Since I was 15, so 8 years

> Did a trauma in your life start it: No, it came on very gradually.

> What have you found works for you: Bengay and Neurontin

> What kind of Dr do you find works best in helping you with this disease?

> Well, I go to a pain specialist but he's been blowing me off latley.

> Do you have sleep problems: I take benadryl for allergies so that lets me

> sleep.

> Does diet effect you: I'm not sure.

> Feel better with cold/hot weather: Any extreme weather or a big drop in

> temperature always gets me.

> Warm baths are heaven sent dealing with pain: Yes!!

> Most people with Fibro are overweight I think for lack of activity, do

> you find this to be true with you: No, I weigh 114. I actually had a doctor

> tell me that this was overweight. He was very very thin himself.

> What time of the day is the best time for you: Evening

> Do you have good days then bad ones or all of them bad: I'm in pain

> everyday but I do have some days when I can't stand up.

> On disability:I'm in the middle of applying.

> If so hints on how you were able to get it since it is hard to get:

>

> Have to have helpers: My husband loves to clean!

> Work out or stay at home: I stay at home

>

> Do you have " Now what am I here for times " : Yes.

> Share your funny memory problem story: I don't have anything too funny but

> my husband is constantly finding things in the fridge that shouldn't be

> there (things that aren't even food).

>

>

>

>

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In a message dated 9/10/2001 1:47:20 PM Pacific Daylight Time,

mary_bierman@... writes:

> Name: Connell

> Married/single: Married for one year on Sept. 12

> Does family understand your illness: My husband has always understood. It

>

> Male/female { some names one can't tell}: Female

> Age area: 23

> Area of the world do you live in: Magalia CA (Northern CA)

> Country/City/Farm life: I live in a foresty area.

> How bad is it: Very Severe. I think there is also something else wrong with

> me. Autoimmune diseases run in my family.

> How long have you had Fibromyalgia or CFS: Since I was 15, so 8 years

> Did a trauma in your life start it: No, it came on very gradually.

> What have you found works for you: Bengay and Neurontin

> What kind of Dr do you find works best in helping you with this disease?

> Well, I go to a pain specialist but he's been blowing me off latley.

> Do you have sleep problems: I take benadryl for allergies so that lets me

> sleep.

> Does diet effect you: I'm not sure.

> Feel better with cold/hot weather: Any extreme weather or a big drop in

> temperature always gets me.

> Warm baths are heaven sent dealing with pain: Yes!!

> Most people with Fibro are overweight I think for lack of activity, do

> you find this to be true with you: No, I weigh 114. I actually had a doctor

> tell me that this was overweight. He was very very thin himself.

> What time of the day is the best time for you: Evening

> Do you have good days then bad ones or all of them bad: I'm in pain

> everyday but I do have some days when I can't stand up.

> On disability:I'm in the middle of applying.

> If so hints on how you were able to get it since it is hard to get:

>

> Have to have helpers: My husband loves to clean!

> Work out or stay at home: I stay at home

>

> Do you have " Now what am I here for times " : Yes.

> Share your funny memory problem story: I don't have anything too funny but

> my husband is constantly finding things in the fridge that shouldn't be

> there (things that aren't even food).

>

>

>

>

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Below you will find my answers :)

>I have made this up for new subscribers so maybe they will share with

>us.

>

>Name: Jeane Rae Watkins

>Married/single: married, May 1, 2001

>Does family understand your illness: he tries and gets better at it every day!

>Male/female { some names one can't tell}: female ;-)

>Age area: I will be 55 on Oct. 25

>Area of the world do you live in: Hemet, Riverside Co, California (about 1

>1/2 SE of Los Angeles . . . hot and dry farmland/valley surrounded by

>beautiful mountains)

>Country/City/Farm life: a wonderful combination of them all!

>How bad is it: right now, better than it's been in years! VERY bad flair

>from Aug, 2000 thru April, 2001 (after my mother's death). I didn't think

>I'd make it though that one.

>How long have you had Fibromyalgia or CFS: diagnosed Winter, 96, but I

>have probably had it for well over 20 years

>Did a trauma in your life start it: Hmmm...difficult to answer. The pain

>increased noticeably when I began travelling over 3000/month when I was

>teaching at 4 different colleges in the LA/Riverside/San Bernardino

>area. However, I can look back and see years of increasing/decreasing

>pain patterns.

>What have you found works for you: Effexor! yeah! Don't know if the

>Ritalin has an effect since it was prescribed at the same time. Water is

>wonderful . . . swimming, loafing in the jacuzzi, relaxing baths with

>scented candles. Getting out with friends has also been a help . . . hard

>at first, but then I relax and enjoy the company and I stop

> " concentrating " on my pain.

>What kind of Dr do you find works best in helping you with this

>disease? I've only been to my internal medicine doc, as he alwo treats me

>for my diabetes, which is his main/only? concern...sigh!

>Do you have sleep problems: yes. I have to carefully watch caffine

>intake. Also, since it's hard to get out of bed, I tend to stay in bed

>and doze for hours, thus making it difficult to sleep that night. I am

>very fortunate in that ibuprophen (1600 mg) at night usually reduces my

>pain enough to allow me to sleep. Still, there are times when no matter

>what, I can't fall alseep. Those are hard.

>Does diet effect you: Probably, although at something slightly over 100

>pounds overweight, diet is obviously not something I pay a great deal of

>attention to. A good friend who has just been diagnosed with rheumatoid

>arthritis says she has gotten much relief from eliminating certain foods,

>such as cheese. I probably should give my diet more attention...sigh again!

>Feel better with cold/hot weather: rofl...I live in Southern Ca...how can

>I tell? It never really gets cold here. The heat (90/100/110) doesn't

>seem to bother the FM at all...gives me more opportunity to swim!

>Warm baths are heaven sent dealing with pain: YES! . . . but try

>surrounding the tub with scented candles.

>Most people with Fibro are overweight I think for lack of activity, do

>you find this to be true with you: Most definitely! I was an athelete,

>dancer, and actress/singer for years. As the pain got worse, my

>activities lessened, I gained weight, the pain got worse, etc.

>What time of the day is the best time for you: Definitely NOT

>mornings. I hate mornings! Probably midday, as by evening I tend to get

>physically tired, even if the pain doesn't worsen.

>Do you have good days then bad ones or all of them bad: Like a flippin'

>rollercoaster! Also, I can feel great and 15 minutes later be close to

>tears with pain. Makes it difficult to plan anything!

>On disability: Yes, for about 2 years.

>If so hints on how you were able to get it since it is hard to

>get: Patience and persistence and a good lawyer who showed a circular

>relationship between my FM and depression, explaining that one made the

>other worse which in turn worsened the other, etc. Confused the judge, I

>think. He also really emphasized the fact that even though I had good

>days, I was unemployable because I could not be reliable.

>

>Have to have helpers: yes...husband helps a lot. Occasionally, friends

>have come over to help with " deep " cleaning.

>Work out or stay at home: Home, but " work " on the puter a lot. Also, I

>volunteer as a speaker for HIV/AIDS education and hope to become involved

>with the Ramona Pageant here in Hemet.

>

>Do you have " Now what am I here for times " : Actually, no. Even when I'm

>not too sure of the answer, I always know that I'm here for a very

>definite reason and that reason WILL become clear.

>Share your funny memory problem story: ROFL . . . I can't remember

>it! Actually, there's been so many. Actually, once I saw this really

>cute dress and bought it. When I showed it to my husband, he went into my

>closet and brought out the very same dress, which I had bought about a

>month before!

Scorpi's World at http://www.geocities.com/scorpijeane/ is my web page. My

poetry tells even more about me.

Jeane

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>Name: Brunson

>Married/single: Single

>Does family understand your illness: They try awfully hard.

>Male/female { some names one can't tell}: f

>Age area: 38

>Area of the world do you live in: Texas

>Country/City/Farm life: Small city

>How bad is it: The city or the FM? ;) The city's not bad, and the FM

>goes in cycles; pred shots help, but only with the pain, not the

>tiredness. I work a 40-hour week but it's very hard to keep it up.

>How long have you had Fibromyalgia or CFS: Not really sure. It started

>with mononucleosis in May 2000, I think.

>Did a trauma in your life start it: I had a great number of major life

>events in the 3 years preceding the diagnosis -- two moves of over 2,000

>miles; fired from a great job; dxed with generalized anxiety disorder and

>obsessive compulsive disorder. I dont' know if any of these things started

>my FM or not, but I think stress is a big factor for me.

>What have you found works for you: I try to eat right. I've lost

>weight. I try not to bring my disease to work with me, put on a game

>face. But nothing I've tried has really made any significant difference

>except simple sleep, and lots of it.

>What kind of Dr do you find works best in helping you with this disease? I

>haven't found a good one yet. My rheumatologist is good but too sexist;

>I'm going to try to arrange to see another one.

>Do you have sleep problems: All my life -- slow-sleeper insomniac. Once I

>get to sleep I stay that way, but almost always require sleep aids to get

>to sleep.

>Does diet affect you: I can't really tell. Fatty/rich foods set off my

>IBS, so I avoid those for the most part. I am a strict vegetarian, and

>feel best that way, for many reasons. As far as its impact on FM, I don't

>know. I don't know if it helps, but it almost certainly isn't hurting me

>to avoid meat.

>Feel better with cold/hot weather: Cold.

>Warm baths are heaven sent dealing with pain: I guess. I have not had a

>tub in my apartment until now, only shower stalls, so am rediscovering how

>nice baths are.

>Most people with Fibro are overweight I think for lack of activity, do you

>find this to be true with you: I am no longer as active as I once was, but

>I am not sedentary. I am carrying about 40 extra pounds, down 45 so far,

>but my weight seems to be tied in with hormones in some way.

>What time of the day is the best time for you: Late afternoon/early evening.

>Do you have good days then bad ones or all of them bad: Alternates; some

>are okay, some are pure misery.

>On disability: I don't have this.

>Have to have helpers: not yet

>Work out or stay at home: work at a hospital

~~~~~~~~~~~~~

It is the tale, not he who tells it.

~~~~~~~~~~~~~

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>Name: Brunson

>Married/single: Single

>Does family understand your illness: They try awfully hard.

>Male/female { some names one can't tell}: f

>Age area: 38

>Area of the world do you live in: Texas

>Country/City/Farm life: Small city

>How bad is it: The city or the FM? ;) The city's not bad, and the FM

>goes in cycles; pred shots help, but only with the pain, not the

>tiredness. I work a 40-hour week but it's very hard to keep it up.

>How long have you had Fibromyalgia or CFS: Not really sure. It started

>with mononucleosis in May 2000, I think.

>Did a trauma in your life start it: I had a great number of major life

>events in the 3 years preceding the diagnosis -- two moves of over 2,000

>miles; fired from a great job; dxed with generalized anxiety disorder and

>obsessive compulsive disorder. I dont' know if any of these things started

>my FM or not, but I think stress is a big factor for me.

>What have you found works for you: I try to eat right. I've lost

>weight. I try not to bring my disease to work with me, put on a game

>face. But nothing I've tried has really made any significant difference

>except simple sleep, and lots of it.

>What kind of Dr do you find works best in helping you with this disease? I

>haven't found a good one yet. My rheumatologist is good but too sexist;

>I'm going to try to arrange to see another one.

>Do you have sleep problems: All my life -- slow-sleeper insomniac. Once I

>get to sleep I stay that way, but almost always require sleep aids to get

>to sleep.

>Does diet affect you: I can't really tell. Fatty/rich foods set off my

>IBS, so I avoid those for the most part. I am a strict vegetarian, and

>feel best that way, for many reasons. As far as its impact on FM, I don't

>know. I don't know if it helps, but it almost certainly isn't hurting me

>to avoid meat.

>Feel better with cold/hot weather: Cold.

>Warm baths are heaven sent dealing with pain: I guess. I have not had a

>tub in my apartment until now, only shower stalls, so am rediscovering how

>nice baths are.

>Most people with Fibro are overweight I think for lack of activity, do you

>find this to be true with you: I am no longer as active as I once was, but

>I am not sedentary. I am carrying about 40 extra pounds, down 45 so far,

>but my weight seems to be tied in with hormones in some way.

>What time of the day is the best time for you: Late afternoon/early evening.

>Do you have good days then bad ones or all of them bad: Alternates; some

>are okay, some are pure misery.

>On disability: I don't have this.

>Have to have helpers: not yet

>Work out or stay at home: work at a hospital

~~~~~~~~~~~~~

It is the tale, not he who tells it.

~~~~~~~~~~~~~

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>Name: Brunson

>Married/single: Single

>Does family understand your illness: They try awfully hard.

>Male/female { some names one can't tell}: f

>Age area: 38

>Area of the world do you live in: Texas

>Country/City/Farm life: Small city

>How bad is it: The city or the FM? ;) The city's not bad, and the FM

>goes in cycles; pred shots help, but only with the pain, not the

>tiredness. I work a 40-hour week but it's very hard to keep it up.

>How long have you had Fibromyalgia or CFS: Not really sure. It started

>with mononucleosis in May 2000, I think.

>Did a trauma in your life start it: I had a great number of major life

>events in the 3 years preceding the diagnosis -- two moves of over 2,000

>miles; fired from a great job; dxed with generalized anxiety disorder and

>obsessive compulsive disorder. I dont' know if any of these things started

>my FM or not, but I think stress is a big factor for me.

>What have you found works for you: I try to eat right. I've lost

>weight. I try not to bring my disease to work with me, put on a game

>face. But nothing I've tried has really made any significant difference

>except simple sleep, and lots of it.

>What kind of Dr do you find works best in helping you with this disease? I

>haven't found a good one yet. My rheumatologist is good but too sexist;

>I'm going to try to arrange to see another one.

>Do you have sleep problems: All my life -- slow-sleeper insomniac. Once I

>get to sleep I stay that way, but almost always require sleep aids to get

>to sleep.

>Does diet affect you: I can't really tell. Fatty/rich foods set off my

>IBS, so I avoid those for the most part. I am a strict vegetarian, and

>feel best that way, for many reasons. As far as its impact on FM, I don't

>know. I don't know if it helps, but it almost certainly isn't hurting me

>to avoid meat.

>Feel better with cold/hot weather: Cold.

>Warm baths are heaven sent dealing with pain: I guess. I have not had a

>tub in my apartment until now, only shower stalls, so am rediscovering how

>nice baths are.

>Most people with Fibro are overweight I think for lack of activity, do you

>find this to be true with you: I am no longer as active as I once was, but

>I am not sedentary. I am carrying about 40 extra pounds, down 45 so far,

>but my weight seems to be tied in with hormones in some way.

>What time of the day is the best time for you: Late afternoon/early evening.

>Do you have good days then bad ones or all of them bad: Alternates; some

>are okay, some are pure misery.

>On disability: I don't have this.

>Have to have helpers: not yet

>Work out or stay at home: work at a hospital

~~~~~~~~~~~~~

It is the tale, not he who tells it.

~~~~~~~~~~~~~

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Country/City/Farm life:LOL LOL LOL Duh, I didn't even realize what I had

put here, until I saw that everyone else had answered it in the context in

which it was meant...I put Wichita, Kansas......for one, it is very much a

city, for two, I no longer even live in Wichita...I moved about a month

ago...oh well, one good thing about this disease...I can always use the

phrase brain fog....lol

Join my new Diabetic Recipes group @

http://groups.yahoo.com/group/Recipes4Diabetes

God Bless You All, Shay/Shalynn and the rescue gang;

Max, Samson

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Country/City/Farm life:LOL LOL LOL Duh, I didn't even realize what I had

put here, until I saw that everyone else had answered it in the context in

which it was meant...I put Wichita, Kansas......for one, it is very much a

city, for two, I no longer even live in Wichita...I moved about a month

ago...oh well, one good thing about this disease...I can always use the

phrase brain fog....lol

Join my new Diabetic Recipes group @

http://groups.yahoo.com/group/Recipes4Diabetes

God Bless You All, Shay/Shalynn and the rescue gang;

Max, Samson

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Name: Kay

Married/single: Happily and safely single now

Does family understand your illness: Academically, but I think they're

puzzled a bit. They understand enough that they don't get excited if I

can't do something, and celebrate with me the times when I can exceed my

own expectations.

Male/female { some names one can't tell}: Female

Age area: 48

Area of the world do you live in: Pennsylvania

Country/City/Farm life: City, I guess (15,000 pop.) in a rural area.

How bad is it: Depends on the day. Haven't had a good one in ages. I

can still work as a secretary but my sewing business is suffering, as is

the presentability of my house. Will be selling the house to re-enter

apartment living in hopes of making life more simple, less demanding on

my physical abilities.

How long have you had Fibromyalgia or CFS: Dx two years ago or so,

probably had it six or more.

Did a trauma in your life start it: Probably -certainly seems at least

coincidental with having had a multitude of intense emotional upheavals

within a short span of time following a rear-end accident that at the

time seemed of minor consequence.

What have you found works for you: Nothing conclusively. Management

mostly consists of making the mental adjustment to seriously reduced

activity, and getting to recognize when I'm setting myself up for

disaster.

What kind of DR do you find works best in helping you with this disease?

So far my GP and chiropractor have done the work of suggesting non-drug

management.

Do you have sleep problems: You betcha!!

Does diet affect you: Not that I've noticed.

Feel better with cold/hot weather: Cold. Days leading up to storms are

hellish, damp weather is terrible.

Warm baths are heaven sent dealing with pain: Not really.

Most people with Fibro are overweight I think for lack of activity, do

you find this to be true with you: Yes. Coupled with thyroid problems,

which I understand can be a component of FMS.

What time of the day is the best time for you: From around 10 a.m. to

3-ish.

Do you have good days then bad ones or all of them bad: Bad ones are

becoming much more frequent. I try not to quantify my days by pain,

though. Otherwise I get mean.

On disability: No

Have to have helpers: If I could afford it, I'd have someone do the

cooking, cleaning and carrying/moving of things. In the absence of that,

I've seriously revised my definition of a clean house and do a lot of

ignoring of dirt and mess. Instead of doing difficult jobs all at once

(since I can't) I do them in steps and make myself be patient.

Work out or stay at home: Been staying in. But my brother just made me

a set of weights since I've been told that it can help to exercise those

muscles. Unless you mean " work outside the home " in which case I still

work in an office.

Do you have " Now what am I here for times " : Yes. I've been able to drag

myself up from those depths by being matter of fact about it -- so you

can't do this any more, let's do something you _can_ do.

Share your funny memory problem story: Ain't been too funny, actually.

Messes up my job, plays havoc with my sewing business even if I do make

lists. Downright pisses me off because I used to have a great memory.

The one thing I've had the hardest time reconciling myself to.

Kay

________________________________________________________________

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Name: Kay

Married/single: Happily and safely single now

Does family understand your illness: Academically, but I think they're

puzzled a bit. They understand enough that they don't get excited if I

can't do something, and celebrate with me the times when I can exceed my

own expectations.

Male/female { some names one can't tell}: Female

Age area: 48

Area of the world do you live in: Pennsylvania

Country/City/Farm life: City, I guess (15,000 pop.) in a rural area.

How bad is it: Depends on the day. Haven't had a good one in ages. I

can still work as a secretary but my sewing business is suffering, as is

the presentability of my house. Will be selling the house to re-enter

apartment living in hopes of making life more simple, less demanding on

my physical abilities.

How long have you had Fibromyalgia or CFS: Dx two years ago or so,

probably had it six or more.

Did a trauma in your life start it: Probably -certainly seems at least

coincidental with having had a multitude of intense emotional upheavals

within a short span of time following a rear-end accident that at the

time seemed of minor consequence.

What have you found works for you: Nothing conclusively. Management

mostly consists of making the mental adjustment to seriously reduced

activity, and getting to recognize when I'm setting myself up for

disaster.

What kind of DR do you find works best in helping you with this disease?

So far my GP and chiropractor have done the work of suggesting non-drug

management.

Do you have sleep problems: You betcha!!

Does diet affect you: Not that I've noticed.

Feel better with cold/hot weather: Cold. Days leading up to storms are

hellish, damp weather is terrible.

Warm baths are heaven sent dealing with pain: Not really.

Most people with Fibro are overweight I think for lack of activity, do

you find this to be true with you: Yes. Coupled with thyroid problems,

which I understand can be a component of FMS.

What time of the day is the best time for you: From around 10 a.m. to

3-ish.

Do you have good days then bad ones or all of them bad: Bad ones are

becoming much more frequent. I try not to quantify my days by pain,

though. Otherwise I get mean.

On disability: No

Have to have helpers: If I could afford it, I'd have someone do the

cooking, cleaning and carrying/moving of things. In the absence of that,

I've seriously revised my definition of a clean house and do a lot of

ignoring of dirt and mess. Instead of doing difficult jobs all at once

(since I can't) I do them in steps and make myself be patient.

Work out or stay at home: Been staying in. But my brother just made me

a set of weights since I've been told that it can help to exercise those

muscles. Unless you mean " work outside the home " in which case I still

work in an office.

Do you have " Now what am I here for times " : Yes. I've been able to drag

myself up from those depths by being matter of fact about it -- so you

can't do this any more, let's do something you _can_ do.

Share your funny memory problem story: Ain't been too funny, actually.

Messes up my job, plays havoc with my sewing business even if I do make

lists. Downright pisses me off because I used to have a great memory.

The one thing I've had the hardest time reconciling myself to.

Kay

________________________________________________________________

GET INTERNET ACCESS FROM JUNO!

Juno offers FREE or PREMIUM Internet access for less!

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Name: Kay

Married/single: Happily and safely single now

Does family understand your illness: Academically, but I think they're

puzzled a bit. They understand enough that they don't get excited if I

can't do something, and celebrate with me the times when I can exceed my

own expectations.

Male/female { some names one can't tell}: Female

Age area: 48

Area of the world do you live in: Pennsylvania

Country/City/Farm life: City, I guess (15,000 pop.) in a rural area.

How bad is it: Depends on the day. Haven't had a good one in ages. I

can still work as a secretary but my sewing business is suffering, as is

the presentability of my house. Will be selling the house to re-enter

apartment living in hopes of making life more simple, less demanding on

my physical abilities.

How long have you had Fibromyalgia or CFS: Dx two years ago or so,

probably had it six or more.

Did a trauma in your life start it: Probably -certainly seems at least

coincidental with having had a multitude of intense emotional upheavals

within a short span of time following a rear-end accident that at the

time seemed of minor consequence.

What have you found works for you: Nothing conclusively. Management

mostly consists of making the mental adjustment to seriously reduced

activity, and getting to recognize when I'm setting myself up for

disaster.

What kind of DR do you find works best in helping you with this disease?

So far my GP and chiropractor have done the work of suggesting non-drug

management.

Do you have sleep problems: You betcha!!

Does diet affect you: Not that I've noticed.

Feel better with cold/hot weather: Cold. Days leading up to storms are

hellish, damp weather is terrible.

Warm baths are heaven sent dealing with pain: Not really.

Most people with Fibro are overweight I think for lack of activity, do

you find this to be true with you: Yes. Coupled with thyroid problems,

which I understand can be a component of FMS.

What time of the day is the best time for you: From around 10 a.m. to

3-ish.

Do you have good days then bad ones or all of them bad: Bad ones are

becoming much more frequent. I try not to quantify my days by pain,

though. Otherwise I get mean.

On disability: No

Have to have helpers: If I could afford it, I'd have someone do the

cooking, cleaning and carrying/moving of things. In the absence of that,

I've seriously revised my definition of a clean house and do a lot of

ignoring of dirt and mess. Instead of doing difficult jobs all at once

(since I can't) I do them in steps and make myself be patient.

Work out or stay at home: Been staying in. But my brother just made me

a set of weights since I've been told that it can help to exercise those

muscles. Unless you mean " work outside the home " in which case I still

work in an office.

Do you have " Now what am I here for times " : Yes. I've been able to drag

myself up from those depths by being matter of fact about it -- so you

can't do this any more, let's do something you _can_ do.

Share your funny memory problem story: Ain't been too funny, actually.

Messes up my job, plays havoc with my sewing business even if I do make

lists. Downright pisses me off because I used to have a great memory.

The one thing I've had the hardest time reconciling myself to.

Kay

________________________________________________________________

GET INTERNET ACCESS FROM JUNO!

Juno offers FREE or PREMIUM Internet access for less!

Join Juno today! For your FREE software, visit:

http://dl.www.juno.com/get/tagj.

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Share on other sites

Name: Marie

Married/single: Divorced twice and now living with my boyfriend of two years

Does family understand your illness: They try, but not really. Thet either

overreact or just don't get how it's a constant big struggle. My boyfriend is

pretty good. He gets a little frustrated, though, sometimes. My friends think

I'm a drama queen.

Male/female { some names one can't tell}: Female

Age area: 29

Area of the world do you live in: Hollywood, CA

Country/City/Farm life: That would be a city :)

How bad is it: How bad is what? The city?LOL! No, I asumme you mean the

disease. It's in the mid-range, I'd say, maybe a little worse. It keeps

getting worse.

How long have you had Fibromyalgia or CFS: I don't know how long. I got

diagnosed last year in the November, but probably several years before that.

Did a trauma in your life start it: I don't know. I never thought about it.

Yes, I was in a really horrible marriage and very stressed out, so probably.

And the symptoms started after I had breast enhancement surgery, so that may

have had something to do with it, too.

What have you found works for you: St. 's Wort, Kava-Kava, Valerian Root,

Vicodin, eating better, and I'm starting to work out more. Also a lot of

water, I quit coffee, I'm trying to quick tobacco and alcohol and I use alot

of lotions and muscle gels.

What kind of Dr do you find works best in helping you with this disease?:

Haven't found one yet. I'm starting therapy and I'm looking for an

herbalist/nutritionalist.

Do you have sleep problems: YES!!!!!!!!!!!!!!!!!!!!!!!

Does diet affect you: I've put on so much weight and I can't take it off. I

used to be supermodel skinny and now I'm buxom. I'm cutting out carbs and

meat and sugar.

Feel better with cold/hot weather: Hot, I guess.

Warm baths are heaven sent dealing with pain: I'm not a bath person, I'm

can't stay still that long. I'm sure they would be, though.

Most people with Fibro are overweight I think for lack of activity, do

you find this to be true with you: See above, although I'm a dancer, so my

daily life is pretty active. I think your metabolism slows down because your

body tries to protect itself.

What time of the day is the best time for you: Early afternoon

Do you have good days then bad ones or all of them bad: good and bad but i

always have some pain.

On disability: No

If so hints on how you were able to get it since it is hard to get:

Have to have helpers: No, unless you count my boyfriend who has to do almost

everything physical for me.

Work out or stay at home: Work out

Do you have " Now what am I here for times " :

Share your funny memory problem story: I don't know............I put the

remote control in the freezer once and took the portable phone to work. I

forget stuff so much it's just part of the daily routine. I forgot my phone

number the other day.

>>

The world is it's own magic!

< lll

> :*)~

< lll

*mmmeeeooowww*

*ppppuuuurrrr*

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Share on other sites

Name: Marie

Married/single: Divorced twice and now living with my boyfriend of two years

Does family understand your illness: They try, but not really. Thet either

overreact or just don't get how it's a constant big struggle. My boyfriend is

pretty good. He gets a little frustrated, though, sometimes. My friends think

I'm a drama queen.

Male/female { some names one can't tell}: Female

Age area: 29

Area of the world do you live in: Hollywood, CA

Country/City/Farm life: That would be a city :)

How bad is it: How bad is what? The city?LOL! No, I asumme you mean the

disease. It's in the mid-range, I'd say, maybe a little worse. It keeps

getting worse.

How long have you had Fibromyalgia or CFS: I don't know how long. I got

diagnosed last year in the November, but probably several years before that.

Did a trauma in your life start it: I don't know. I never thought about it.

Yes, I was in a really horrible marriage and very stressed out, so probably.

And the symptoms started after I had breast enhancement surgery, so that may

have had something to do with it, too.

What have you found works for you: St. 's Wort, Kava-Kava, Valerian Root,

Vicodin, eating better, and I'm starting to work out more. Also a lot of

water, I quit coffee, I'm trying to quick tobacco and alcohol and I use alot

of lotions and muscle gels.

What kind of Dr do you find works best in helping you with this disease?:

Haven't found one yet. I'm starting therapy and I'm looking for an

herbalist/nutritionalist.

Do you have sleep problems: YES!!!!!!!!!!!!!!!!!!!!!!!

Does diet affect you: I've put on so much weight and I can't take it off. I

used to be supermodel skinny and now I'm buxom. I'm cutting out carbs and

meat and sugar.

Feel better with cold/hot weather: Hot, I guess.

Warm baths are heaven sent dealing with pain: I'm not a bath person, I'm

can't stay still that long. I'm sure they would be, though.

Most people with Fibro are overweight I think for lack of activity, do

you find this to be true with you: See above, although I'm a dancer, so my

daily life is pretty active. I think your metabolism slows down because your

body tries to protect itself.

What time of the day is the best time for you: Early afternoon

Do you have good days then bad ones or all of them bad: good and bad but i

always have some pain.

On disability: No

If so hints on how you were able to get it since it is hard to get:

Have to have helpers: No, unless you count my boyfriend who has to do almost

everything physical for me.

Work out or stay at home: Work out

Do you have " Now what am I here for times " :

Share your funny memory problem story: I don't know............I put the

remote control in the freezer once and took the portable phone to work. I

forget stuff so much it's just part of the daily routine. I forgot my phone

number the other day.

>>

The world is it's own magic!

< lll

> :*)~

< lll

*mmmeeeooowww*

*ppppuuuurrrr*

Link to comment
Share on other sites

Name: Marie

Married/single: Divorced twice and now living with my boyfriend of two years

Does family understand your illness: They try, but not really. Thet either

overreact or just don't get how it's a constant big struggle. My boyfriend is

pretty good. He gets a little frustrated, though, sometimes. My friends think

I'm a drama queen.

Male/female { some names one can't tell}: Female

Age area: 29

Area of the world do you live in: Hollywood, CA

Country/City/Farm life: That would be a city :)

How bad is it: How bad is what? The city?LOL! No, I asumme you mean the

disease. It's in the mid-range, I'd say, maybe a little worse. It keeps

getting worse.

How long have you had Fibromyalgia or CFS: I don't know how long. I got

diagnosed last year in the November, but probably several years before that.

Did a trauma in your life start it: I don't know. I never thought about it.

Yes, I was in a really horrible marriage and very stressed out, so probably.

And the symptoms started after I had breast enhancement surgery, so that may

have had something to do with it, too.

What have you found works for you: St. 's Wort, Kava-Kava, Valerian Root,

Vicodin, eating better, and I'm starting to work out more. Also a lot of

water, I quit coffee, I'm trying to quick tobacco and alcohol and I use alot

of lotions and muscle gels.

What kind of Dr do you find works best in helping you with this disease?:

Haven't found one yet. I'm starting therapy and I'm looking for an

herbalist/nutritionalist.

Do you have sleep problems: YES!!!!!!!!!!!!!!!!!!!!!!!

Does diet affect you: I've put on so much weight and I can't take it off. I

used to be supermodel skinny and now I'm buxom. I'm cutting out carbs and

meat and sugar.

Feel better with cold/hot weather: Hot, I guess.

Warm baths are heaven sent dealing with pain: I'm not a bath person, I'm

can't stay still that long. I'm sure they would be, though.

Most people with Fibro are overweight I think for lack of activity, do

you find this to be true with you: See above, although I'm a dancer, so my

daily life is pretty active. I think your metabolism slows down because your

body tries to protect itself.

What time of the day is the best time for you: Early afternoon

Do you have good days then bad ones or all of them bad: good and bad but i

always have some pain.

On disability: No

If so hints on how you were able to get it since it is hard to get:

Have to have helpers: No, unless you count my boyfriend who has to do almost

everything physical for me.

Work out or stay at home: Work out

Do you have " Now what am I here for times " :

Share your funny memory problem story: I don't know............I put the

remote control in the freezer once and took the portable phone to work. I

forget stuff so much it's just part of the daily routine. I forgot my phone

number the other day.

>>

The world is it's own magic!

< lll

> :*)~

< lll

*mmmeeeooowww*

*ppppuuuurrrr*

Link to comment
Share on other sites

> Name:

'girl' - sorry, i only use my ID

> Married/single:

Divorced but in in long term relationship. 3 children

ages 11-1/2, 9-1/2 & 6-1/2

> Does family understand your illness:

not as much as i would like but they are only kids

after all. my sweetheart understands tho and is very

supportive of me.

> Male/female { some names one can't tell}:

all female :)

> Age area:

30

> Area of the world do you live in:

chicago suburbs

> Country/City/Farm life:

somewhat country but just enough city for me

> How bad is it:

it does not seem to be as bad as it was while i was a

kid but then i think that is because i have adjusted

to the pain over the last 20+ years. there are more

things tho that bother me no than there were as a kids

> How long have you had Fibromyalgia or CFS:

the Dr. just Dx it this year but said he feels that i

have had it all my life

> Did a trauma in your life start it:

i do not think so. i was about 3 when i started

having trouble.

> What have you found works for you:

slowing down. taking more rests during the day.

meditation

> What kind of Dr do you find works best in helping

> you with this disease?

my primary care has been great and the rheumy that he

sent me to has been awesome. my previous primary care

did not know how to handle this and would never

address my questions.

> Do you have sleep problems:

i have had sleep problems since i was about 10. i

always feel as if i could use another few hours of

sleep. i have not had a restful night in ages

> Does diet effect you:

i have not found that diet effects me in any way. i

try to eat healthy any way due to family history.

> Feel better with cold/hot weather:

warm weather works best for me. the midwest winters

so far have been hellish for me but i like it here too

much to want to make a change right now. really, it

does not seem to be the whole time of the cold

weather, it is more the first couple of weeks of a

weather transition from hot to cold

> Warm baths are heaven sent dealing with pain:

the warm baths with bath salts do not help my leg

pains but they do help my back pains. they also help

in relaxing me and allowing me to take my mind to

other areas.

> Most people with Fibro are overweight I think for

> lack of activity, do

> you find this to be true with you:

as a child i was over weight. as a teen and in my

20's, i was underweight. now that i am 30 and working

a desk job for the first time in my life, i am a

slight bit over weight again. for me, it is not lack

of activity tho due to pain. it is lack of activity

due to time. i was very active in my dance activates

for many years. now i am not able to participate in

those activities and have not found ones that interest

me. i refuse to allow the pain to take away from me

things that i enjoy. i just have to modify what i do

around the pain

> What time of the day is the best time for you:

mid-morning and early after noon are the best time of

day for me

> Do you have good days then bad ones or all of them

> bad:

my good and bad days are all spread out. i have had a

few times where i had nothing but bad days for several

months, even landed in the hospital having a spinal

tap done during one of those times. most of my days

tho are just mediocre.

> On disability:

no

> Have to have helpers:

no

> Work out or stay at home:

i work 40 hours a week outside of the home and then

have all the house work, kids homework etc to do when

i get home. My sweetheart and i do not live together

and he is out of time much of the time so everything

falls back onto me

>

> Do you have " Now what am I here for times " :

my 'brain farts' are just starting. i have always

been a great cook but all of a sudden i am forgetting

stuff on the stove or in the oven. i have burnt more

meals in the last couple of months than i think i did

in 20 years previous. i think that this is the most

agrivating for me, even over the pain. it also scares

me

Additional info:

the rheumy that i saw also feels that my 6yo is

suffering from FM as well. he has the leg pains just

like i have always had. the rheumy does not believe

in 'growing pains' and has asked that my 6yo's primary

care keep an eye on him

__________________________________________________

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Share on other sites

> Name:

'girl' - sorry, i only use my ID

> Married/single:

Divorced but in in long term relationship. 3 children

ages 11-1/2, 9-1/2 & 6-1/2

> Does family understand your illness:

not as much as i would like but they are only kids

after all. my sweetheart understands tho and is very

supportive of me.

> Male/female { some names one can't tell}:

all female :)

> Age area:

30

> Area of the world do you live in:

chicago suburbs

> Country/City/Farm life:

somewhat country but just enough city for me

> How bad is it:

it does not seem to be as bad as it was while i was a

kid but then i think that is because i have adjusted

to the pain over the last 20+ years. there are more

things tho that bother me no than there were as a kids

> How long have you had Fibromyalgia or CFS:

the Dr. just Dx it this year but said he feels that i

have had it all my life

> Did a trauma in your life start it:

i do not think so. i was about 3 when i started

having trouble.

> What have you found works for you:

slowing down. taking more rests during the day.

meditation

> What kind of Dr do you find works best in helping

> you with this disease?

my primary care has been great and the rheumy that he

sent me to has been awesome. my previous primary care

did not know how to handle this and would never

address my questions.

> Do you have sleep problems:

i have had sleep problems since i was about 10. i

always feel as if i could use another few hours of

sleep. i have not had a restful night in ages

> Does diet effect you:

i have not found that diet effects me in any way. i

try to eat healthy any way due to family history.

> Feel better with cold/hot weather:

warm weather works best for me. the midwest winters

so far have been hellish for me but i like it here too

much to want to make a change right now. really, it

does not seem to be the whole time of the cold

weather, it is more the first couple of weeks of a

weather transition from hot to cold

> Warm baths are heaven sent dealing with pain:

the warm baths with bath salts do not help my leg

pains but they do help my back pains. they also help

in relaxing me and allowing me to take my mind to

other areas.

> Most people with Fibro are overweight I think for

> lack of activity, do

> you find this to be true with you:

as a child i was over weight. as a teen and in my

20's, i was underweight. now that i am 30 and working

a desk job for the first time in my life, i am a

slight bit over weight again. for me, it is not lack

of activity tho due to pain. it is lack of activity

due to time. i was very active in my dance activates

for many years. now i am not able to participate in

those activities and have not found ones that interest

me. i refuse to allow the pain to take away from me

things that i enjoy. i just have to modify what i do

around the pain

> What time of the day is the best time for you:

mid-morning and early after noon are the best time of

day for me

> Do you have good days then bad ones or all of them

> bad:

my good and bad days are all spread out. i have had a

few times where i had nothing but bad days for several

months, even landed in the hospital having a spinal

tap done during one of those times. most of my days

tho are just mediocre.

> On disability:

no

> Have to have helpers:

no

> Work out or stay at home:

i work 40 hours a week outside of the home and then

have all the house work, kids homework etc to do when

i get home. My sweetheart and i do not live together

and he is out of time much of the time so everything

falls back onto me

>

> Do you have " Now what am I here for times " :

my 'brain farts' are just starting. i have always

been a great cook but all of a sudden i am forgetting

stuff on the stove or in the oven. i have burnt more

meals in the last couple of months than i think i did

in 20 years previous. i think that this is the most

agrivating for me, even over the pain. it also scares

me

Additional info:

the rheumy that i saw also feels that my 6yo is

suffering from FM as well. he has the leg pains just

like i have always had. the rheumy does not believe

in 'growing pains' and has asked that my 6yo's primary

care keep an eye on him

__________________________________________________

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Share on other sites

> Name:

'girl' - sorry, i only use my ID

> Married/single:

Divorced but in in long term relationship. 3 children

ages 11-1/2, 9-1/2 & 6-1/2

> Does family understand your illness:

not as much as i would like but they are only kids

after all. my sweetheart understands tho and is very

supportive of me.

> Male/female { some names one can't tell}:

all female :)

> Age area:

30

> Area of the world do you live in:

chicago suburbs

> Country/City/Farm life:

somewhat country but just enough city for me

> How bad is it:

it does not seem to be as bad as it was while i was a

kid but then i think that is because i have adjusted

to the pain over the last 20+ years. there are more

things tho that bother me no than there were as a kids

> How long have you had Fibromyalgia or CFS:

the Dr. just Dx it this year but said he feels that i

have had it all my life

> Did a trauma in your life start it:

i do not think so. i was about 3 when i started

having trouble.

> What have you found works for you:

slowing down. taking more rests during the day.

meditation

> What kind of Dr do you find works best in helping

> you with this disease?

my primary care has been great and the rheumy that he

sent me to has been awesome. my previous primary care

did not know how to handle this and would never

address my questions.

> Do you have sleep problems:

i have had sleep problems since i was about 10. i

always feel as if i could use another few hours of

sleep. i have not had a restful night in ages

> Does diet effect you:

i have not found that diet effects me in any way. i

try to eat healthy any way due to family history.

> Feel better with cold/hot weather:

warm weather works best for me. the midwest winters

so far have been hellish for me but i like it here too

much to want to make a change right now. really, it

does not seem to be the whole time of the cold

weather, it is more the first couple of weeks of a

weather transition from hot to cold

> Warm baths are heaven sent dealing with pain:

the warm baths with bath salts do not help my leg

pains but they do help my back pains. they also help

in relaxing me and allowing me to take my mind to

other areas.

> Most people with Fibro are overweight I think for

> lack of activity, do

> you find this to be true with you:

as a child i was over weight. as a teen and in my

20's, i was underweight. now that i am 30 and working

a desk job for the first time in my life, i am a

slight bit over weight again. for me, it is not lack

of activity tho due to pain. it is lack of activity

due to time. i was very active in my dance activates

for many years. now i am not able to participate in

those activities and have not found ones that interest

me. i refuse to allow the pain to take away from me

things that i enjoy. i just have to modify what i do

around the pain

> What time of the day is the best time for you:

mid-morning and early after noon are the best time of

day for me

> Do you have good days then bad ones or all of them

> bad:

my good and bad days are all spread out. i have had a

few times where i had nothing but bad days for several

months, even landed in the hospital having a spinal

tap done during one of those times. most of my days

tho are just mediocre.

> On disability:

no

> Have to have helpers:

no

> Work out or stay at home:

i work 40 hours a week outside of the home and then

have all the house work, kids homework etc to do when

i get home. My sweetheart and i do not live together

and he is out of time much of the time so everything

falls back onto me

>

> Do you have " Now what am I here for times " :

my 'brain farts' are just starting. i have always

been a great cook but all of a sudden i am forgetting

stuff on the stove or in the oven. i have burnt more

meals in the last couple of months than i think i did

in 20 years previous. i think that this is the most

agrivating for me, even over the pain. it also scares

me

Additional info:

the rheumy that i saw also feels that my 6yo is

suffering from FM as well. he has the leg pains just

like i have always had. the rheumy does not believe

in 'growing pains' and has asked that my 6yo's primary

care keep an eye on him

__________________________________________________

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Hello, My name is Jo. I have answered the question you sent below.

Name:Jo

Married/single: Single

Does family understand your illness:They try! But not really. I look normal,

so I should be able to ignore, get it out of my head, buck up...the usual lines.

Problem is, that just doesn't work with FMS.

Male/female { some names one can't tell}: Female

Age area: 40

Area of the world do you live in: Washington State, USA

Country/City/Farm life: Country

How bad is it:Don't understand question...how bad is what?

County life? Not bad at all. Rather be in the country anytime! Fibro: It's

bad. Hurt all the time!

How long have you had Fibromyalgia or CFS: Diagnosed in January of 2000. But

have had some symptoms all my life. I just thought everyone felt like this!

Did a trauma in your life start it: I think so. I was sexually abused as a

child, but the tiggering event that I can think back to when it started getting

worse was the death of my mom from cancer. She had an extremely hard time. The

last three days of her life were spent in my livingroom, and she was in extreme

pain, and having convulsions etc. For those three days, I neither ate or slept

and I think this was the triggering factor.

What have you found works for you: Not much. I am still in the " discovery "

stage. Going through test,etc to rule out anything else. I am on several meds.

They work only about half the time.

What kind of Dr do you find works best in helping you with this disease? I

don't know yet! My GP was the one who diagnosed the FMS/CFS. But I haven't

gotten to the appointment with a rheumentologist yet. That happens next week.

My GP is a kind and up to date physician who listens well and has been good to

believe me and try to help. I saw a neurologist, who promptly put me in the

overweight, depressed, female category with a sleeping problem. I won't see him

again!

Do you have sleep problems: YES! I rarely sleep more than four hours at a

time, and that's with meds prescibed for sleep! I am exhuasted all the time.

Does diet effect you: Sometimes. I have become a " near " vegatarian. I eat a

small amount of chicken, tuna, fish, eggs and dairy. I try and eat very little

fat. I have discovered an allergy to peanuts.

Feel better with cold/hot weather: Either one to the extreme causes me great

stress! I'd rather have it about 70 degrees. That seems to fit me best!

Warm baths are heaven sent dealing with pain: Yes!

Most people with Fibro are overweight I think for lack of activity, do you

find this to be true with you:I am overweight, but I have been for a long while.

Before FMS/CFS I was still very active. Now I can hardly get out of bed

sometimes. The exercise prescribed by some docs only makes things worse for me.

Because of the exhuastion I face everyday.

What time of the day is the best time for you: Usually early afternoon when

all the meds have kicked in.

Do you have good days then bad ones or all of them bad: Sometimes I have a day

where everything is tolerable to the point that I can do things. Most of the

time I am in considerable pain and in total exhaustion.

On disability: Not yet. My employer has been extremely tolerant of my

illness. Right now as I am going through all of the tests, they have put me on a

kind of permenant sick leave. This won't last forever thought.

If so hints on how you were able to get it since it is hard to get: I would

like some hints myself!

Have to have helpers: Not yet. I still can move around enough to help myself

most of the time. My sister does live with me right now and she is a huge help

and relief! She is doing most of the housework right now.

Work out or stay at home: I work only a few hours a week right now. See

answer to disability above for more.

Do you have " Now what am I here for times " : ALL THE TIME! I was a pretty

active person, now I can't do hardly anything I have done before. I know that

my work will have to change (if I can continue to work at all) And that leaves

me in a panicky state. I have no financial support without a job, so I don't

know what I will do.

Share your funny memory problem story: Well, don't know if it's too funny, but

I have overdrawn myself several times at the bank because I have forgotten to

write down checks. NEVER have done that in my life!

Hope this helps. I look forward to reading other people's responses.

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Hello, read your post regarding info. I saw that you live in the chicago

suburbs. So do I was hoping you could email me and maybe we could find out if

we are close to each other or not. I think it would be great to find someone

in this group who actually lives near you. If you don't feel you want to

share that info with me than I understand .

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Hello, read your post regarding info. I saw that you live in the chicago

suburbs. So do I was hoping you could email me and maybe we could find out if

we are close to each other or not. I think it would be great to find someone

in this group who actually lives near you. If you don't feel you want to

share that info with me than I understand .

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Hello, read your post regarding info. I saw that you live in the chicago

suburbs. So do I was hoping you could email me and maybe we could find out if

we are close to each other or not. I think it would be great to find someone

in this group who actually lives near you. If you don't feel you want to

share that info with me than I understand .

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