New member

[Guest guest]

You do belong on this list. You want to help your husband and hopefully we

can help you.

> Actually, I'm not exactly sure I belong on this list, but I'll leave that up

> to you.

>

But his FMS symptoms didn't start showing up until he was hit by a car while

walking in our neighborhood 2 years ago

FMS is often activated by an accident, stress and things of that sort. I,

myself, had a bad fall and FMS was started then.

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

My biggest concern is the depression. He has the FMS depression on top of

the head injury depression. He just recently saw a neurologist who diagnosed

him with Post Concussion Syndrome and advised him he won't get any better.

Now he has lost hope. He says he feels hollow, and is unable to feel emotion

of any kind -- positive or negative. He just shuts down. It is very

frustrating for me to see him like this.

I sometimes feel that doctors do not help any by saying that you won't get

any better. I can't speak to your husbands injury but I was diagnosed with

tinnitus about 6 years ago and the same thing was told to me. I was ready to

commit suicide. I was so depressed that I felt like I could not live any

longer with the noises in my head.

I went to see a psychologist and started counseling and taking medication and

came to my senses and realized that suicide was not the way to go. The

feeling of being hollow and unable to feel emotion goes with it. He does

need help and medication to realize that there are loved ones that wants him

and that life is going on and his family wants him to be a part of it.

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

He is in the process of being referred to a psychiatrist to evaluate his meds

(he takes Trazedone and Effexor to help him sleep), but he won't get

counseling. He says he's done that before and they didn't have a clue, and

he doesn't want to waste his time with it. I think his problem is mostly

neurochemical anyway, because of the head injury, and am hoping that the

right medication will make a big difference.

His problem is probably neurochemical but counseling would really help.

There might be other medications that he could take after consultation with a

doctor. It takes time for a medication to take effect. About 4 to 6 weeks I

believe. A good counselor would be able to help but unless your husband is

ready to listen it will not help him.

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

So for now, I joined this list for me to better understand what he is going

through, and to find different ways I can help him. I'm watching for a

treatment or a medication we haven't tried yet, as well as the kinds of

things that help all of you cope from day to day, so I can help him. Of all

the people in the world, his wife should understand, right?

This list is a very good one. Supportive and loving. There are many ways

that we have learned to cope and maybe some of those will help.

Take care,

Irene

[Guest guest]

You do belong on this list. You want to help your husband and hopefully we

can help you.

> Actually, I'm not exactly sure I belong on this list, but I'll leave that up

> to you.

>

But his FMS symptoms didn't start showing up until he was hit by a car while

walking in our neighborhood 2 years ago

FMS is often activated by an accident, stress and things of that sort. I,

myself, had a bad fall and FMS was started then.

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

My biggest concern is the depression. He has the FMS depression on top of

the head injury depression. He just recently saw a neurologist who diagnosed

him with Post Concussion Syndrome and advised him he won't get any better.

Now he has lost hope. He says he feels hollow, and is unable to feel emotion

of any kind -- positive or negative. He just shuts down. It is very

frustrating for me to see him like this.

I sometimes feel that doctors do not help any by saying that you won't get

any better. I can't speak to your husbands injury but I was diagnosed with

tinnitus about 6 years ago and the same thing was told to me. I was ready to

commit suicide. I was so depressed that I felt like I could not live any

longer with the noises in my head.

I went to see a psychologist and started counseling and taking medication and

came to my senses and realized that suicide was not the way to go. The

feeling of being hollow and unable to feel emotion goes with it. He does

need help and medication to realize that there are loved ones that wants him

and that life is going on and his family wants him to be a part of it.

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

He is in the process of being referred to a psychiatrist to evaluate his meds

(he takes Trazedone and Effexor to help him sleep), but he won't get

counseling. He says he's done that before and they didn't have a clue, and

he doesn't want to waste his time with it. I think his problem is mostly

neurochemical anyway, because of the head injury, and am hoping that the

right medication will make a big difference.

His problem is probably neurochemical but counseling would really help.

There might be other medications that he could take after consultation with a

doctor. It takes time for a medication to take effect. About 4 to 6 weeks I

believe. A good counselor would be able to help but unless your husband is

ready to listen it will not help him.

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

So for now, I joined this list for me to better understand what he is going

through, and to find different ways I can help him. I'm watching for a

treatment or a medication we haven't tried yet, as well as the kinds of

things that help all of you cope from day to day, so I can help him. Of all

the people in the world, his wife should understand, right?

This list is a very good one. Supportive and loving. There are many ways

that we have learned to cope and maybe some of those will help.

Take care,

Irene

[Guest guest]

You do belong on this list. You want to help your husband and hopefully we

can help you.

> Actually, I'm not exactly sure I belong on this list, but I'll leave that up

> to you.

>

But his FMS symptoms didn't start showing up until he was hit by a car while

walking in our neighborhood 2 years ago

FMS is often activated by an accident, stress and things of that sort. I,

myself, had a bad fall and FMS was started then.

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

My biggest concern is the depression. He has the FMS depression on top of

the head injury depression. He just recently saw a neurologist who diagnosed

him with Post Concussion Syndrome and advised him he won't get any better.

Now he has lost hope. He says he feels hollow, and is unable to feel emotion

of any kind -- positive or negative. He just shuts down. It is very

frustrating for me to see him like this.

I sometimes feel that doctors do not help any by saying that you won't get

any better. I can't speak to your husbands injury but I was diagnosed with

tinnitus about 6 years ago and the same thing was told to me. I was ready to

commit suicide. I was so depressed that I felt like I could not live any

longer with the noises in my head.

I went to see a psychologist and started counseling and taking medication and

came to my senses and realized that suicide was not the way to go. The

feeling of being hollow and unable to feel emotion goes with it. He does

need help and medication to realize that there are loved ones that wants him

and that life is going on and his family wants him to be a part of it.

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

He is in the process of being referred to a psychiatrist to evaluate his meds

(he takes Trazedone and Effexor to help him sleep), but he won't get

counseling. He says he's done that before and they didn't have a clue, and

he doesn't want to waste his time with it. I think his problem is mostly

neurochemical anyway, because of the head injury, and am hoping that the

right medication will make a big difference.

His problem is probably neurochemical but counseling would really help.

There might be other medications that he could take after consultation with a

doctor. It takes time for a medication to take effect. About 4 to 6 weeks I

believe. A good counselor would be able to help but unless your husband is

ready to listen it will not help him.

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

So for now, I joined this list for me to better understand what he is going

through, and to find different ways I can help him. I'm watching for a

treatment or a medication we haven't tried yet, as well as the kinds of

things that help all of you cope from day to day, so I can help him. Of all

the people in the world, his wife should understand, right?

This list is a very good one. Supportive and loving. There are many ways

that we have learned to cope and maybe some of those will help.

Take care,

Irene

[Guest guest]

Thanks, Irene, for your comments and your welcome. I appreciate it. You have

given me hope that the psychiatrist can help with his depression.

The last few days he actually seems a bit improved mentally. He's even going

golfing with a group this Saturday (at 5:15 in the morning -- I thought he was

pulling my leg, but he was serious!). Maybe it will work out after all.

With Father's Day this weekend and his birthday coming up shortly after that,

I'm looking for ideas for gifts. He spends about 55 hours a week on his feet at

work. He has a good pair of shoes, but his lower back, butt, thighs and knees

still get sore and stiff. He is also just starting to get the leg cramps that

everyone else is talking about. I'd like to get him something to help him feel

better. Any suggestions will be helpful.

It has been suggested that soaking in Epsom Salts would help with the cramping

and stiffness, but our bathtub isn't nearly big enough. I'm thinking about

getting a Jacuzzi room in a nearby hotel and letting him soak. Has this worked

for anyone?

Angie Madsen

" I fought the stamps, and the stamps won! "

e-mail me at madsens@...

For a complete list of standard swap rules and current swap information, please

see my new web site at http://socialstamper.tripod.com/swapcentral/

Re: New Member

You do belong on this list. You want to help your husband and hopefully we

can help you.

> Actually, I'm not exactly sure I belong on this list, but I'll leave that up

> to you.

>

But his FMS symptoms didn't start showing up until he was hit by a car while

walking in our neighborhood 2 years ago

FMS is often activated by an accident, stress and things of that sort. I,

myself, had a bad fall and FMS was started then.

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

My biggest concern is the depression. He has the FMS depression on top of

the head injury depression. He just recently saw a neurologist who diagnosed

him with Post Concussion Syndrome and advised him he won't get any better.

Now he has lost hope. He says he feels hollow, and is unable to feel emotion

of any kind -- positive or negative. He just shuts down. It is very

frustrating for me to see him like this.

I sometimes feel that doctors do not help any by saying that you won't get

any better. I can't speak to your husbands injury but I was diagnosed with

tinnitus about 6 years ago and the same thing was told to me. I was ready to

commit suicide. I was so depressed that I felt like I could not live any

longer with the noises in my head.

I went to see a psychologist and started counseling and taking medication and

came to my senses and realized that suicide was not the way to go. The

feeling of being hollow and unable to feel emotion goes with it. He does

need help and medication to realize that there are loved ones that wants him

and that life is going on and his family wants him to be a part of it.

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

He is in the process of being referred to a psychiatrist to evaluate his meds

(he takes Trazedone and Effexor to help him sleep), but he won't get

counseling. He says he's done that before and they didn't have a clue, and

he doesn't want to waste his time with it. I think his problem is mostly

neurochemical anyway, because of the head injury, and am hoping that the

right medication will make a big difference.

His problem is probably neurochemical but counseling would really help.

There might be other medications that he could take after consultation with a

doctor. It takes time for a medication to take effect. About 4 to 6 weeks I

believe. A good counselor would be able to help but unless your husband is

ready to listen it will not help him.

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

So for now, I joined this list for me to better understand what he is going

through, and to find different ways I can help him. I'm watching for a

treatment or a medication we haven't tried yet, as well as the kinds of

things that help all of you cope from day to day, so I can help him. Of all

the people in the world, his wife should understand, right?

This list is a very good one. Supportive and loving. There are many ways

that we have learned to cope and maybe some of those will help.

Take care,

Irene

[Guest guest]

Thanks, Irene, for your comments and your welcome. I appreciate it. You have

given me hope that the psychiatrist can help with his depression.

The last few days he actually seems a bit improved mentally. He's even going

golfing with a group this Saturday (at 5:15 in the morning -- I thought he was

pulling my leg, but he was serious!). Maybe it will work out after all.

With Father's Day this weekend and his birthday coming up shortly after that,

I'm looking for ideas for gifts. He spends about 55 hours a week on his feet at

work. He has a good pair of shoes, but his lower back, butt, thighs and knees

still get sore and stiff. He is also just starting to get the leg cramps that

everyone else is talking about. I'd like to get him something to help him feel

better. Any suggestions will be helpful.

It has been suggested that soaking in Epsom Salts would help with the cramping

and stiffness, but our bathtub isn't nearly big enough. I'm thinking about

getting a Jacuzzi room in a nearby hotel and letting him soak. Has this worked

for anyone?

Angie Madsen

" I fought the stamps, and the stamps won! "

e-mail me at madsens@...

For a complete list of standard swap rules and current swap information, please

see my new web site at http://socialstamper.tripod.com/swapcentral/

Re: New Member

You do belong on this list. You want to help your husband and hopefully we

can help you.

> Actually, I'm not exactly sure I belong on this list, but I'll leave that up

> to you.

>

But his FMS symptoms didn't start showing up until he was hit by a car while

walking in our neighborhood 2 years ago

FMS is often activated by an accident, stress and things of that sort. I,

myself, had a bad fall and FMS was started then.

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

My biggest concern is the depression. He has the FMS depression on top of

the head injury depression. He just recently saw a neurologist who diagnosed

him with Post Concussion Syndrome and advised him he won't get any better.

Now he has lost hope. He says he feels hollow, and is unable to feel emotion

of any kind -- positive or negative. He just shuts down. It is very

frustrating for me to see him like this.

I sometimes feel that doctors do not help any by saying that you won't get

any better. I can't speak to your husbands injury but I was diagnosed with

tinnitus about 6 years ago and the same thing was told to me. I was ready to

commit suicide. I was so depressed that I felt like I could not live any

longer with the noises in my head.

I went to see a psychologist and started counseling and taking medication and

came to my senses and realized that suicide was not the way to go. The

feeling of being hollow and unable to feel emotion goes with it. He does

need help and medication to realize that there are loved ones that wants him

and that life is going on and his family wants him to be a part of it.

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

He is in the process of being referred to a psychiatrist to evaluate his meds

(he takes Trazedone and Effexor to help him sleep), but he won't get

counseling. He says he's done that before and they didn't have a clue, and

he doesn't want to waste his time with it. I think his problem is mostly

neurochemical anyway, because of the head injury, and am hoping that the

right medication will make a big difference.

His problem is probably neurochemical but counseling would really help.

There might be other medications that he could take after consultation with a

doctor. It takes time for a medication to take effect. About 4 to 6 weeks I

believe. A good counselor would be able to help but unless your husband is

ready to listen it will not help him.

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

So for now, I joined this list for me to better understand what he is going

through, and to find different ways I can help him. I'm watching for a

treatment or a medication we haven't tried yet, as well as the kinds of

things that help all of you cope from day to day, so I can help him. Of all

the people in the world, his wife should understand, right?

This list is a very good one. Supportive and loving. There are many ways

that we have learned to cope and maybe some of those will help.

Take care,

Irene

[Guest guest]

Thanks, Irene, for your comments and your welcome. I appreciate it. You have

given me hope that the psychiatrist can help with his depression.

The last few days he actually seems a bit improved mentally. He's even going

golfing with a group this Saturday (at 5:15 in the morning -- I thought he was

pulling my leg, but he was serious!). Maybe it will work out after all.

With Father's Day this weekend and his birthday coming up shortly after that,

I'm looking for ideas for gifts. He spends about 55 hours a week on his feet at

work. He has a good pair of shoes, but his lower back, butt, thighs and knees

still get sore and stiff. He is also just starting to get the leg cramps that

everyone else is talking about. I'd like to get him something to help him feel

better. Any suggestions will be helpful.

It has been suggested that soaking in Epsom Salts would help with the cramping

and stiffness, but our bathtub isn't nearly big enough. I'm thinking about

getting a Jacuzzi room in a nearby hotel and letting him soak. Has this worked

for anyone?

Angie Madsen

" I fought the stamps, and the stamps won! "

e-mail me at madsens@...

For a complete list of standard swap rules and current swap information, please

see my new web site at http://socialstamper.tripod.com/swapcentral/

Re: New Member

You do belong on this list. You want to help your husband and hopefully we

can help you.

> Actually, I'm not exactly sure I belong on this list, but I'll leave that up

> to you.

>

But his FMS symptoms didn't start showing up until he was hit by a car while

walking in our neighborhood 2 years ago

FMS is often activated by an accident, stress and things of that sort. I,

myself, had a bad fall and FMS was started then.

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

My biggest concern is the depression. He has the FMS depression on top of

the head injury depression. He just recently saw a neurologist who diagnosed

him with Post Concussion Syndrome and advised him he won't get any better.

Now he has lost hope. He says he feels hollow, and is unable to feel emotion

of any kind -- positive or negative. He just shuts down. It is very

frustrating for me to see him like this.

I sometimes feel that doctors do not help any by saying that you won't get

any better. I can't speak to your husbands injury but I was diagnosed with

tinnitus about 6 years ago and the same thing was told to me. I was ready to

commit suicide. I was so depressed that I felt like I could not live any

longer with the noises in my head.

I went to see a psychologist and started counseling and taking medication and

came to my senses and realized that suicide was not the way to go. The

feeling of being hollow and unable to feel emotion goes with it. He does

need help and medication to realize that there are loved ones that wants him

and that life is going on and his family wants him to be a part of it.

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

He is in the process of being referred to a psychiatrist to evaluate his meds

(he takes Trazedone and Effexor to help him sleep), but he won't get

counseling. He says he's done that before and they didn't have a clue, and

he doesn't want to waste his time with it. I think his problem is mostly

neurochemical anyway, because of the head injury, and am hoping that the

right medication will make a big difference.

His problem is probably neurochemical but counseling would really help.

There might be other medications that he could take after consultation with a

doctor. It takes time for a medication to take effect. About 4 to 6 weeks I

believe. A good counselor would be able to help but unless your husband is

ready to listen it will not help him.

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

So for now, I joined this list for me to better understand what he is going

through, and to find different ways I can help him. I'm watching for a

treatment or a medication we haven't tried yet, as well as the kinds of

things that help all of you cope from day to day, so I can help him. Of all

the people in the world, his wife should understand, right?

This list is a very good one. Supportive and loving. There are many ways

that we have learned to cope and maybe some of those will help.

Take care,

Irene

[Guest guest]

We have a new member on the list.

Will you please give her a warm welcome.

isabelle@... has joined our group

Will you please introduce yourself.

Bierman

Hello, I'm Isabelle, I was diagnosed with fibromyalgia after seven

years of complaining about unexplained symptoms following a whiplash

injury in 1988 - because of the variety of symptoms, I saw about

eight different 'specialists' before getting there.

I had doubts about the diagnosis for quite a while, as the symptoms,

I felt, could be explained by the developing spondylosis in various

areas, and/or pre-existing immunological problems, having been asthmatic,

allergic, and also hypersensitive to drugs and some foods.

However, since reading a lot of information on the Web, it does seem

that I have the fairly consistent pattern of symptoms, so I have

accepted what thends to be, in the UK, a 'put up and shut up' diagnosis.

The Employment service have been very helpful for many years - I am

self-employed, making both porcelain 12th scale'people in miniature'

for dolls houses, and decorative head plaques for gardens. I have

disabled disks for parking, a support worker for eight hours a week,

and a computer with ViaVoice so I can minimise keyboard work, plus

other accessories, and have received training courses. They are all

supportive and helpful to any variation or additional help that I need.

I have no medical support, however, and on moving to my present

home, and registering with a doctor, on my first visit I got berated

at length for having 'thick notes' (i.e. hypochondriac). When I asked

to see a physio, after reading that stretching exercises are helpful

for the muscle spasm and pain, I was told that 'I was irresponsible to

work if it meant my needing medical attention, and I was a drain on the

National Health Service.' I suppose I should have responded by saying

that if I was fit I would earn enough money to continue to pay for

therapy, as I had in the past.

I am in pain all the time, and receive no treatment or specialist guidance.

My left hip started 'giving way' fourteen months ago, with right 'groin strain'

and 'swelling'of the hip and upper limb areas. Since then I have had

to give up driving beyond a radius of about 15 miles from home, I limp

painfully all the time, and have pain or discomfort sitting, standing, lying

down etc.

I can no longer attend sales fairs (even if driven) - which involve travelling

long distances, or visit friends and family as before. I have obviously

rearranged my life to accommodate this, but fibromyalgia information invariably

states that 'it is not a degenerative condition', and also '....fibromyalgia

will never cripple you.....'

As my GP has said that I have too much movement in my hip for it to be

osteoarthritis, my symptoms 'are that of fibromyalgia', and he refuses to refer

me to a rheumatologist.

I would be interested to know if any one has similar problems with

mobility, and how they have dealt with it.

regards - isabelle

.

[Guest guest]

We have a new member on the list.

Will you please give her a warm welcome.

isabelle@... has joined our group

Will you please introduce yourself.

Bierman

Hello, I'm Isabelle, I was diagnosed with fibromyalgia after seven

years of complaining about unexplained symptoms following a whiplash

injury in 1988 - because of the variety of symptoms, I saw about

eight different 'specialists' before getting there.

I had doubts about the diagnosis for quite a while, as the symptoms,

I felt, could be explained by the developing spondylosis in various

areas, and/or pre-existing immunological problems, having been asthmatic,

allergic, and also hypersensitive to drugs and some foods.

However, since reading a lot of information on the Web, it does seem

that I have the fairly consistent pattern of symptoms, so I have

accepted what thends to be, in the UK, a 'put up and shut up' diagnosis.

The Employment service have been very helpful for many years - I am

self-employed, making both porcelain 12th scale'people in miniature'

for dolls houses, and decorative head plaques for gardens. I have

disabled disks for parking, a support worker for eight hours a week,

and a computer with ViaVoice so I can minimise keyboard work, plus

other accessories, and have received training courses. They are all

supportive and helpful to any variation or additional help that I need.

I have no medical support, however, and on moving to my present

home, and registering with a doctor, on my first visit I got berated

at length for having 'thick notes' (i.e. hypochondriac). When I asked

to see a physio, after reading that stretching exercises are helpful

for the muscle spasm and pain, I was told that 'I was irresponsible to

work if it meant my needing medical attention, and I was a drain on the

National Health Service.' I suppose I should have responded by saying

that if I was fit I would earn enough money to continue to pay for

therapy, as I had in the past.

I am in pain all the time, and receive no treatment or specialist guidance.

My left hip started 'giving way' fourteen months ago, with right 'groin strain'

and 'swelling'of the hip and upper limb areas. Since then I have had

to give up driving beyond a radius of about 15 miles from home, I limp

painfully all the time, and have pain or discomfort sitting, standing, lying

down etc.

I can no longer attend sales fairs (even if driven) - which involve travelling

long distances, or visit friends and family as before. I have obviously

rearranged my life to accommodate this, but fibromyalgia information invariably

states that 'it is not a degenerative condition', and also '....fibromyalgia

will never cripple you.....'

As my GP has said that I have too much movement in my hip for it to be

osteoarthritis, my symptoms 'are that of fibromyalgia', and he refuses to refer

me to a rheumatologist.

I would be interested to know if any one has similar problems with

mobility, and how they have dealt with it.

regards - isabelle

.

[Guest guest]

We have a new member on the list.

Will you please give her a warm welcome.

isabelle@... has joined our group

Will you please introduce yourself.

Bierman

Hello, I'm Isabelle, I was diagnosed with fibromyalgia after seven

years of complaining about unexplained symptoms following a whiplash

injury in 1988 - because of the variety of symptoms, I saw about

eight different 'specialists' before getting there.

I had doubts about the diagnosis for quite a while, as the symptoms,

I felt, could be explained by the developing spondylosis in various

areas, and/or pre-existing immunological problems, having been asthmatic,

allergic, and also hypersensitive to drugs and some foods.

However, since reading a lot of information on the Web, it does seem

that I have the fairly consistent pattern of symptoms, so I have

accepted what thends to be, in the UK, a 'put up and shut up' diagnosis.

The Employment service have been very helpful for many years - I am

self-employed, making both porcelain 12th scale'people in miniature'

for dolls houses, and decorative head plaques for gardens. I have

disabled disks for parking, a support worker for eight hours a week,

and a computer with ViaVoice so I can minimise keyboard work, plus

other accessories, and have received training courses. They are all

supportive and helpful to any variation or additional help that I need.

I have no medical support, however, and on moving to my present

home, and registering with a doctor, on my first visit I got berated

at length for having 'thick notes' (i.e. hypochondriac). When I asked

to see a physio, after reading that stretching exercises are helpful

for the muscle spasm and pain, I was told that 'I was irresponsible to

work if it meant my needing medical attention, and I was a drain on the

National Health Service.' I suppose I should have responded by saying

that if I was fit I would earn enough money to continue to pay for

therapy, as I had in the past.

I am in pain all the time, and receive no treatment or specialist guidance.

My left hip started 'giving way' fourteen months ago, with right 'groin strain'

and 'swelling'of the hip and upper limb areas. Since then I have had

to give up driving beyond a radius of about 15 miles from home, I limp

painfully all the time, and have pain or discomfort sitting, standing, lying

down etc.

I can no longer attend sales fairs (even if driven) - which involve travelling

long distances, or visit friends and family as before. I have obviously

rearranged my life to accommodate this, but fibromyalgia information invariably

states that 'it is not a degenerative condition', and also '....fibromyalgia

will never cripple you.....'

As my GP has said that I have too much movement in my hip for it to be

osteoarthritis, my symptoms 'are that of fibromyalgia', and he refuses to refer

me to a rheumatologist.

I would be interested to know if any one has similar problems with

mobility, and how they have dealt with it.

regards - isabelle

.

[Guest guest]

oops....I must of missed m introduction

I am Dee in Calif.

[Guest guest]

oops....I must of missed m introduction

I am Dee in Calif.

[Guest guest]

I did not write ther is a dee in Californica. But there is a Deana in

Ca. too. So we will have to continue tous names as they are Deana

On Tue, 19 Jun 2001 17:22:01 -0700 (PDT) MY-FIBROJOURNEY@...

writes:

> oops....I must of missed m introduction

> I am Dee in Calif.

>

>

> SEND POST TO: fibromyalgia-cfs

>

[Guest guest]

I did not write ther is a dee in Californica. But there is a Deana in

Ca. too. So we will have to continue tous names as they are Deana

On Tue, 19 Jun 2001 17:22:01 -0700 (PDT) MY-FIBROJOURNEY@...

writes:

> oops....I must of missed m introduction

> I am Dee in Calif.

>

>

> SEND POST TO: fibromyalgia-cfs

>

[Guest guest]

I did not write ther is a dee in Californica. But there is a Deana in

Ca. too. So we will have to continue tous names as they are Deana

On Tue, 19 Jun 2001 17:22:01 -0700 (PDT) MY-FIBROJOURNEY@...

writes:

> oops....I must of missed m introduction

> I am Dee in Calif.

>

>

> SEND POST TO: fibromyalgia-cfs

>

[Guest guest]

I am Dee and I am in Calif.

And I wrote that. I guess If I leave I would' never be misses......Dee

Aka De Lois ......Sorry for the confusion. Good Bye

http://community.webtv.net/MY-FIBROJOURNEY/THISISMYFIBRO

[Guest guest]

I guess the first clue would of bee My-fibrojourney......is webtv and

not juno.

http://community.webtv.net/MY-FIBROJOURNEY/THISISMYFIBRO

[Guest guest]

I guess the first clue would of bee My-fibrojourney......is webtv and

not juno.

http://community.webtv.net/MY-FIBROJOURNEY/THISISMYFIBRO

[Guest guest]

I guess the first clue would of bee My-fibrojourney......is webtv and

not juno.

http://community.webtv.net/MY-FIBROJOURNEY/THISISMYFIBRO

[Guest guest]

abraxis3@...

Hi Dee,

Welcome to the group!!! There are many wonderful,

compassionate, non-judgemental people here. Wonderful

place to be! Hope you stick around!

Love,

Sue

--- MY-FIBROJOURNEY@... wrote:

> oops....I must of missed m introduction

> I am Dee in Calif.

>

>

__________________________________________________

[Guest guest]

abraxis3@...

Hi Dee,

Welcome to the group!!! There are many wonderful,

compassionate, non-judgemental people here. Wonderful

place to be! Hope you stick around!

Love,

Sue

--- MY-FIBROJOURNEY@... wrote:

> oops....I must of missed m introduction

> I am Dee in Calif.

>

>

__________________________________________________

[Guest guest]

Welcome Dee in California. We are glad to have you with us. I think that

you will enjoy the people on this list. We are all a very loving and caring

group. I am happy that you joined us, Jump in when you have something to say

and we will all be glad to hear from you.

Take care,

Irene

>

> oops....I must have missed m introduction

> I am Dee in Calif.

>

[Guest guest]

Welcome Dee in California. We are glad to have you with us. I think that

you will enjoy the people on this list. We are all a very loving and caring

group. I am happy that you joined us, Jump in when you have something to say

and we will all be glad to hear from you.

Take care,

Irene

>

> oops....I must have missed m introduction

> I am Dee in Calif.

>

[Guest guest]

Welcome Dee in California. We are glad to have you with us. I think that

you will enjoy the people on this list. We are all a very loving and caring

group. I am happy that you joined us, Jump in when you have something to say

and we will all be glad to hear from you.

Take care,

Irene

>

> oops....I must have missed m introduction

> I am Dee in Calif.

>

[Guest guest]

I am not sorry you wrote it. Is Dee your real name or is it a nickname,

cause people real close to me call me Dee. I did notmean to say

something wrong about the way you said that. I just wanted every one to

know we had to similiar. Thanks for writing. I assume you have FM too.

I do not remember getting your story. If you care to tell me about it i

would be glad to listen and you would be sadly missed if you left so

please do not and let me knw what I missed. Hope you are pain free

today. Deana in CA. Oh where are you in Ca. I live in northern part

near Sacramnto, a little town south of Sac actually, called Galt

between Elk Grove and Stockton. Hope to hear from you.

On Wed, 20 Jun 2001 00:12:39 -0700 (PDT) MY-FIBROJOURNEY@...

writes:

> I am Dee and I am in Calif.

> And I wrote that. I guess If I leave I would' never be

> misses......Dee

> Aka De Lois ......Sorry for the confusion. Good Bye

>

> http://community.webtv.net/MY-FIBROJOURNEY/THISISMYFIBRO

>

>

> SEND POST TO: fibromyalgia-cfs

>

[Guest guest]

I am not sorry you wrote it. Is Dee your real name or is it a nickname,

cause people real close to me call me Dee. I did notmean to say

something wrong about the way you said that. I just wanted every one to

know we had to similiar. Thanks for writing. I assume you have FM too.

I do not remember getting your story. If you care to tell me about it i

would be glad to listen and you would be sadly missed if you left so

please do not and let me knw what I missed. Hope you are pain free

today. Deana in CA. Oh where are you in Ca. I live in northern part

near Sacramnto, a little town south of Sac actually, called Galt

between Elk Grove and Stockton. Hope to hear from you.

On Wed, 20 Jun 2001 00:12:39 -0700 (PDT) MY-FIBROJOURNEY@...

writes:

> I am Dee and I am in Calif.

> And I wrote that. I guess If I leave I would' never be

> misses......Dee

> Aka De Lois ......Sorry for the confusion. Good Bye

>

> http://community.webtv.net/MY-FIBROJOURNEY/THISISMYFIBRO

>

>

> SEND POST TO: fibromyalgia-cfs

>