Sounds like diagnosing MS torturous and expensive

[Guest guest]

I go for my 2nd MRI today, and have heard about lumbar puncture,

to diagnose, then the drugs they'll want to put me on....is it worth it?

What do I say to my grown children. they both are living out of town,

i eat a gluten free diet, but the symptoms seem to be coming like a freight

train, however a friend prayed for complete healing for me, and so for 2 days,

each tingle, and cramp, I " ve rebuked it, and it seems to be working.

I started taking colostrum in July - not very consistent- but the MS plaque they

found in the first MRI didn't " light up " whatever that means, so maybe the

colostrum worked.

any comments would be appreciated!!!

I use diatematious earth for pest control and understand it, I also have lately

been taking some pro biotics.

My hubby has had an overactive immune system for decades and with God's help and

my research I put him on colostrum 8 years ago when vasculitis kicked him into

a downward spiral, and even though only 10 % go 5 years, he's 10 years out and

feeling great!

We are both in our early 50s.

Thanks for your comments to come. I really need some input!

SW

[Guest guest]

I HAVE NEVER WRITTEN MY STORY OF MS AND HOW IT CHANGED MY LIFE, BUT I THOUGHT

IT WAS ABOUT TIME. I AM NOT SURE WHERE TO BEGIN BUT AT THE BEGINNING.

My husband had just retired after twenty years in the navy.We were in

california, my children and I had been born there, but we were moving to Kansas

and it was a stressful time. I only add this as I know stress has a lot to do

with this. It was a long trip, and I did not want to go

but I was determined to try, and kept up a good front. My husband had been

overseas in Vietnam and had come home a different man that I had married.

After we arrived, I managed to get a god job working for the State of Kansas,

I had put the children in school, we had bought land and a home and started life

over. My husband, Chuck, and his brother started a business. For awhile it

seemed all would go well. Until the symptons began.

I awoke one morning, totally numb on ones ide of my body. I almost fell when I

got up, and so I called my Dr.' You are too young for a stroke' he said'I think

it is nerves and depression', and he wrote a prescription for valium and an

antideppresant and I just looked at hime and did't know what to think. I began

to take the pills, and years later regretted it. But after a few days rest the

numbness went away and I returned to work, just thinking it was nerves. Shortly

later my feet would begin to b urn, my legs would go heavy, and i would have

tingling in my hands. I ignored it and kept working.

Things at home were not good, and just to save time I will say, I took my

children back to California and sought a divorce. Ignoring the symptoms. I found

a job at a communication company and began to work on a switchboard.

My right hand had become numb, and it was hard to operate a switchboard. I had a

job as a switchboard operator and had worked my way up to supervisor. And so I

went to a neurologist who diagnosed it as carpul tunnel syndrome, and did

surgerey. It was painful, and I lost the use of my hand. Looking back now, I

realize it was not necessary. While I was in the hospital another Dr. saw me,

and did a spinal tap. MRI " S were not available then. The results were abnormal.

I kept working, until one day I had a sharp pain in my eye, and lost some

vision. I could no longer ignore this, and I knew it. I had to be driven home

that day as I could not see to drive.

By that time, I had relocated to San Diego, calif. and had remarried and until

that day did the best I could to live a normal life. My new husband, Norman,

took me the best neuoroligist in the city. He did a lot of painful tests, and

one day called me into his office, and I will never forget the words he used at

the diagnosis that would change my life. Dr Raffer said to me, 'I have good

news and I have bad news, the good news is that you do not need any more tests,

he looked directly at me and said you have multiple sclerosis.''

He gave me a book to read, and when I did I knew, It had taken ten years to

diagnose this, the MRIS were available and there was no doubt.

As the years went on I had paralysis as well. But then went oon to voc rehab

and went on to college determined to go one. Ms would go completly away and I

would go into remissiion after the use of IV steriods. It kept me going, until

due to bone loss and fractured they could no longer use them.

To make a long story short, I am now out of the wheelcahair and In a nursing

home in Iowa. My vision returned, and I walk wiith a walker, I am a free lance

writer who wanted to share my story,

Thank you,

Becky worth

________________________________

To: mscured

Sent: Wed, September 1, 2010 7:54:27 AM

Subject: Sounds like diagnosing MS torturous and expensive

I go for my 2nd MRI today, and have heard about lumbar puncture,

to diagnose, then the drugs they'll want to put me on....is it worth it?

What do I say to my grown children. they both are living out of town,

i eat a gluten free diet, but the symptoms seem to be coming like a freight

train, however a friend prayed for complete healing for me, and so for 2 days,

each tingle, and cramp, I " ve rebuked it, and it seems to be working.

I started taking colostrum in July - not very consistent- but the MS plaque they

found in the first MRI didn't " light up " whatever that means, so maybe the

colostrum worked.

any comments would be appreciated!!!

I use diatematious earth for pest control and understand it, I also have lately

been taking some pro biotics.

My hubby has had an overactive immune system for decades and with God's help and

my research I put him on colostrum 8 years ago when vasculitis kicked him into

a downward spiral, and even though only 10 % go 5 years, he's 10 years out and

feeling great!

We are both in our early 50s.

Thanks for your comments to come. I really need some input!

SW

[Guest guest]

Hi SW

I'm from Australia and was dxd without the need of a lumbar puncture.

MRIs of brain and spine were all that was needed.

From what I've heard and from what I know, Australian Neurologists don't tend to

do the Lumbar Puncture thing to dx people.

The drugs are also generally covered by our Government's Healthcare System, so

the drugs aren't expensive there.

YOUR situation will, of course, depend on your country's healthcare system AND

your feelings about medication.

I am on the Best Bet Diet and the recommended Supplements and it's a lot better

than when I was on Avonex for a year and a half.

I've been tested for CCSVI and have stenosis in both jugulars - I am now waiting

on the time and date for the procedure (both will be paid for by my hubby as the

UK Healthcare system doesn't cover it).

The MSDiet Yahoo group is a good group to help with following the Dietary

approach.

There are ways around the drugs if you wish to take the 'alternative' route -

'MS' is, and should always be, about following the path that YOU are more

comfortable with.

I wish you a world of luck with conquering the 'MonSter'!

'What we do in life, echoes through eternity.'

MARCUS AURELIUS (121 - 180 A.D.)

To: mscured

From: skywatcher4him@...

Date: Wed, 1 Sep 2010 12:54:27 +0000

Subject: Sounds like diagnosing MS torturous and expensive

I go for my 2nd MRI today, and have heard about lumbar puncture,

to diagnose, then the drugs they'll want to put me on....is it worth it?

[Guest guest]

Hi SW

I'm from Australia and was dxd without the need of a lumbar puncture.

MRIs of brain and spine were all that was needed.

From what I've heard and from what I know, Australian Neurologists don't tend to

do the Lumbar Puncture thing to dx people.

The drugs are also generally covered by our Government's Healthcare System, so

the drugs aren't expensive there.

YOUR situation will, of course, depend on your country's healthcare system AND

your feelings about medication.

I am on the Best Bet Diet and the recommended Supplements and it's a lot better

than when I was on Avonex for a year and a half.

I've been tested for CCSVI and have stenosis in both jugulars - I am now waiting

on the time and date for the procedure (both will be paid for by my hubby as the

UK Healthcare system doesn't cover it).

The MSDiet Yahoo group is a good group to help with following the Dietary

approach.

There are ways around the drugs if you wish to take the 'alternative' route -

'MS' is, and should always be, about following the path that YOU are more

comfortable with.

I wish you a world of luck with conquering the 'MonSter'!

'What we do in life, echoes through eternity.'

MARCUS AURELIUS (121 - 180 A.D.)

To: mscured

From: skywatcher4him@...

Date: Wed, 1 Sep 2010 12:54:27 +0000

Subject: Sounds like diagnosing MS torturous and expensive

I go for my 2nd MRI today, and have heard about lumbar puncture,

to diagnose, then the drugs they'll want to put me on....is it worth it?

[Guest guest]

I HAVE NEVER WRITTEN MY STORY OF MS AND HOW IT CHANGED MY LIFE, BUT I THOUGHT

IT WAS ABOUT TIME. I AM NOT SURE WHERE TO BEGIN BUT AT THE BEGINNING.

My husband had just retired after twenty years in the navy.We were in

california, my children and I had been born there, but we were moving to Kansas

and it was a stressful time. I only add this as I know stress has a lot to do

with this. It was a long trip, and I did not want to go

but I was determined to try, and kept up a good front. My husband had been

overseas in Vietnam and had come home a different man that I had married.

After we arrived, I managed to get a god job working for the State of Kansas,

I had put the children in school, we had bought land and a home and started life

over. My husband, Chuck, and his brother started a business. For awhile it

seemed all would go well. Until the symptons began.

I awoke one morning, totally numb on ones ide of my body. I almost fell when I

got up, and so I called my Dr.' You are too young for a stroke' he said'I think

it is nerves and depression', and he wrote a prescription for valium and an

antideppresant and I just looked at hime and did't know what to think. I began

to take the pills, and years later regretted it. But after a few days rest the

numbness went away and I returned to work, just thinking it was nerves. Shortly

later my feet would begin to b urn, my legs would go heavy, and i would have

tingling in my hands. I ignored it and kept working.

Things at home were not good, and just to save time I will say, I took my

children back to California and sought a divorce. Ignoring the symptoms. I found

a job at a communication company and began to work on a switchboard.

My right hand had become numb, and it was hard to operate a switchboard. I had a

job as a switchboard operator and had worked my way up to supervisor. And so I

went to a neurologist who diagnosed it as carpul tunnel syndrome, and did

surgerey. It was painful, and I lost the use of my hand. Looking back now, I

realize it was not necessary. While I was in the hospital another Dr. saw me,

and did a spinal tap. MRI " S were not available then. The results were abnormal.

I kept working, until one day I had a sharp pain in my eye, and lost some

vision. I could no longer ignore this, and I knew it. I had to be driven home

that day as I could not see to drive.

By that time, I had relocated to San Diego, calif. and had remarried and until

that day did the best I could to live a normal life. My new husband, Norman,

took me the best neuoroligist in the city. He did a lot of painful tests, and

one day called me into his office, and I will never forget the words he used at

the diagnosis that would change my life. Dr Raffer said to me, 'I have good

news and I have bad news, the good news is that you do not need any more tests,

he looked directly at me and said you have multiple sclerosis.''

He gave me a book to read, and when I did I knew, It had taken ten years to

diagnose this, the MRIS were available and there was no doubt.

As the years went on I had paralysis as well. But then went oon to voc rehab

and went on to college determined to go one. Ms would go completly away and I

would go into remissiion after the use of IV steriods. It kept me going, until

due to bone loss and fractured they could no longer use them.

To make a long story short, I am now out of the wheelcahair and In a nursing

home in Iowa. My vision returned, and I walk wiith a walker, I am a free lance

writer who wanted to share my story,

Thank you,

Becky worth

[Guest guest]

I HAVE NEVER WRITTEN MY STORY OF MS AND HOW IT CHANGED MY LIFE, BUT I THOUGHT

IT WAS ABOUT TIME. I AM NOT SURE WHERE TO BEGIN BUT AT THE BEGINNING.

My husband had just retired after twenty years in the navy.We were in

california, my children and I had been born there, but we were moving to Kansas

and it was a stressful time. I only add this as I know stress has a lot to do

with this. It was a long trip, and I did not want to go

but I was determined to try, and kept up a good front. My husband had been

overseas in Vietnam and had come home a different man that I had married.

After we arrived, I managed to get a god job working for the State of Kansas,

I had put the children in school, we had bought land and a home and started life

over. My husband, Chuck, and his brother started a business. For awhile it

seemed all would go well. Until the symptons began.

I awoke one morning, totally numb on ones ide of my body. I almost fell when I

got up, and so I called my Dr.' You are too young for a stroke' he said'I think

it is nerves and depression', and he wrote a prescription for valium and an

antideppresant and I just looked at hime and did't know what to think. I began

to take the pills, and years later regretted it. But after a few days rest the

numbness went away and I returned to work, just thinking it was nerves. Shortly

later my feet would begin to b urn, my legs would go heavy, and i would have

tingling in my hands. I ignored it and kept working.

Things at home were not good, and just to save time I will say, I took my

children back to California and sought a divorce. Ignoring the symptoms. I found

a job at a communication company and began to work on a switchboard.

My right hand had become numb, and it was hard to operate a switchboard. I had a

job as a switchboard operator and had worked my way up to supervisor. And so I

went to a neurologist who diagnosed it as carpul tunnel syndrome, and did

surgerey. It was painful, and I lost the use of my hand. Looking back now, I

realize it was not necessary. While I was in the hospital another Dr. saw me,

and did a spinal tap. MRI " S were not available then. The results were abnormal.

I kept working, until one day I had a sharp pain in my eye, and lost some

vision. I could no longer ignore this, and I knew it. I had to be driven home

that day as I could not see to drive.

By that time, I had relocated to San Diego, calif. and had remarried and until

that day did the best I could to live a normal life. My new husband, Norman,

took me the best neuoroligist in the city. He did a lot of painful tests, and

one day called me into his office, and I will never forget the words he used at

the diagnosis that would change my life. Dr Raffer said to me, 'I have good

news and I have bad news, the good news is that you do not need any more tests,

he looked directly at me and said you have multiple sclerosis.''

He gave me a book to read, and when I did I knew, It had taken ten years to

diagnose this, the MRIS were available and there was no doubt.

As the years went on I had paralysis as well. But then went oon to voc rehab

and went on to college determined to go one. Ms would go completly away and I

would go into remissiion after the use of IV steriods. It kept me going, until

due to bone loss and fractured they could no longer use them.

To make a long story short, I am now out of the wheelcahair and In a nursing

home in Iowa. My vision returned, and I walk wiith a walker, I am a free lance

writer who wanted to share my story,

Thank you,

Becky worth

[Guest guest]

No, the lumbar puncture hurts, causes side effects in some people and it is not

a definitive test. I did it and the only thing that was found out is that

protein was in my spinal fluid. The kind of protein was not determined.

I did a VEP (Visual Evoked Potential) test and the only information that I got

was that I was abnormal! That test is not definitive either.

Clinical problems are the best way to determine if you MS, MRIs are the way that

it is diagnosed. People with MS tend to have a reflex on the bottom of their

feet that makes the toes curl up when the bottoms of the feet are touched.

Babies have this reflex but most adults tend to turn their toes under. It's

called the Babinski Reflex.

If your MRI shows an area called Dawson's Finger, that is a clear sign of having

MS.

I used DE at one time but I didn't notice a difference. That doesn't mean that

it wasn't working. I did a lot of things at the same time at that juncture and

I couldn't always tell what did what.

Probitics are a good thing but start slow because if you take a bunch you may

have a die-off reaction. Colostrum has helped many people but some people

think that anything dairy is bad. I drink raw milk, eat raw butter and cheese

and I am stronger today than I was a few months ago. It depends on your

metabolic type what you should eat (IMO). Everything has two sides. What may be

good for me may not be good for you.

Tell your children that you have a health issue that you will be able to

correct!

>

> I go for my 2nd MRI today, and have heard about lumbar puncture,

> to diagnose, then the drugs they'll want to put me on....is it worth it?

[Guest guest]

No, the lumbar puncture hurts, causes side effects in some people and it is not

a definitive test. I did it and the only thing that was found out is that

protein was in my spinal fluid. The kind of protein was not determined.

I did a VEP (Visual Evoked Potential) test and the only information that I got

was that I was abnormal! That test is not definitive either.

Clinical problems are the best way to determine if you MS, MRIs are the way that

it is diagnosed. People with MS tend to have a reflex on the bottom of their

feet that makes the toes curl up when the bottoms of the feet are touched.

Babies have this reflex but most adults tend to turn their toes under. It's

called the Babinski Reflex.

If your MRI shows an area called Dawson's Finger, that is a clear sign of having

MS.

I used DE at one time but I didn't notice a difference. That doesn't mean that

it wasn't working. I did a lot of things at the same time at that juncture and

I couldn't always tell what did what.

Probitics are a good thing but start slow because if you take a bunch you may

have a die-off reaction. Colostrum has helped many people but some people

think that anything dairy is bad. I drink raw milk, eat raw butter and cheese

and I am stronger today than I was a few months ago. It depends on your

metabolic type what you should eat (IMO). Everything has two sides. What may be

good for me may not be good for you.

Tell your children that you have a health issue that you will be able to

correct!

>

> I go for my 2nd MRI today, and have heard about lumbar puncture,

> to diagnose, then the drugs they'll want to put me on....is it worth it?

[Guest guest]

  Hi , tell me about the Best Bet Diet....what is involved?

              Jen

Subject: RE: Sounds like diagnosing MS torturous and expensive

To: " MSCured " <mscured >

Date: Wednesday, September 1, 2010, 10:53 AM

Â

Hi SW

I'm from Australia and was dxd without the need of a lumbar puncture.

MRIs of brain and spine were all that was needed.

From what I've heard and from what I know, Australian Neurologists don't tend to

do the Lumbar Puncture thing to dx people.

The drugs are also generally covered by our Government's Healthcare System, so

the drugs aren't expensive there.

YOUR situation will, of course, depend on your country's healthcare system AND

your feelings about medication.

I am on the Best Bet Diet and the recommended Supplements and it's a lot better

than when I was on Avonex for a year and a half.

I've been tested for CCSVI and have stenosis in both jugulars - I am now waiting

on the time and date for the procedure (both will be paid for by my hubby as the

UK Healthcare system doesn't cover it).

The MSDiet Yahoo group is a good group to help with following the Dietary

approach.

There are ways around the drugs if you wish to take the 'alternative' route -

'MS' is, and should always be, about following the path that YOU are more

comfortable with.

I wish you a world of luck with conquering the 'MonSter'!

'What we do in life, echoes through eternity.'

MARCUS AURELIUS (121 - 180 A.D.)

To: mscured

From: skywatcher4him@...

Date: Wed, 1 Sep 2010 12:54:27 +0000

Subject: Sounds like diagnosing MS torturous and expensive

I go for my 2nd MRI today, and have heard about lumbar puncture,

to diagnose, then the drugs they'll want to put me on....is it worth it?

[Guest guest]

  Hi , tell me about the Best Bet Diet....what is involved?

              Jen

Subject: RE: Sounds like diagnosing MS torturous and expensive

To: " MSCured " <mscured >

Date: Wednesday, September 1, 2010, 10:53 AM

Â

Hi SW

I'm from Australia and was dxd without the need of a lumbar puncture.

MRIs of brain and spine were all that was needed.

From what I've heard and from what I know, Australian Neurologists don't tend to

do the Lumbar Puncture thing to dx people.

The drugs are also generally covered by our Government's Healthcare System, so

the drugs aren't expensive there.

YOUR situation will, of course, depend on your country's healthcare system AND

your feelings about medication.

I am on the Best Bet Diet and the recommended Supplements and it's a lot better

than when I was on Avonex for a year and a half.

I've been tested for CCSVI and have stenosis in both jugulars - I am now waiting

on the time and date for the procedure (both will be paid for by my hubby as the

UK Healthcare system doesn't cover it).

The MSDiet Yahoo group is a good group to help with following the Dietary

approach.

There are ways around the drugs if you wish to take the 'alternative' route -

'MS' is, and should always be, about following the path that YOU are more

comfortable with.

I wish you a world of luck with conquering the 'MonSter'!

'What we do in life, echoes through eternity.'

MARCUS AURELIUS (121 - 180 A.D.)

To: mscured

From: skywatcher4him@...

Date: Wed, 1 Sep 2010 12:54:27 +0000

Subject: Sounds like diagnosing MS torturous and expensive

I go for my 2nd MRI today, and have heard about lumbar puncture,

to diagnose, then the drugs they'll want to put me on....is it worth it?

[Guest guest]

Hi,

(Apologies for stepping in but I saw this and thought, as I have a

couple of minutes, I might be able to save you some time.)

The Best Bet Diet (BBD) is a diet very similar to the Paleolithic Diet.

http://www.msrc.co.uk/index.cfm/fuseaction/show/pageid/8

It eliminates gluten grains, lactose, legumes, tomatoes and egg which are

implicated in molecular mimicry (see articles in their site above) wherein, in

simplistic terms, these foods are seen as its own myelin and the body attacks

itself.

I myself have been on it 3 1/2 years and take all their suggested supplements

too plus a load more for CCSVI. (PPMS 15 years, wheelchair dependent.) I also

removed all my amalgam fillings and had food allergy tests, heavy metal tests,

Lyme Disease test, syndrome test... I have changed my lifestyle to one

that incorporates swimming and/or yoga daily, is stress-free, and is in a

temperate climate, and have CST (cranio-sacral therapy) fortnightly. Whether

any of these can be proved to help MS is not of any concern to me, I am not

taking any pharmaceutical drugs and I FEEL loads better.

I am still in a wheelchair but have beaten all my other little symptoms (brain

fog, fatigue, tinnitus, neuralgia, odd sensations, bear hug, blurred vision,

slurred speech, etc. I still have absolutely no balance and my legs won't work

but other than that, hey MS isn't so bad! (Note to any newcomers here, normally

MS doesn't get you in a wheelchair.)

The diet sounds horrendous when you start it but you soon get used to it and

know what you can/can't eat. I used to be tempted to take a bit out of

someone's bread roll as I passed their table in a restaurant, now I actually

feel sorry for them having to eat it!

Keep smiling!

Janet

To: mscured

From: volleyjen0416@...

Date: Wed, 1 Sep 2010 13:28:56 -0700

Subject: RE: Sounds like diagnosing MS torturous and expensive

Hi , tell me about the Best Bet Diet....what is involved?

Jen

[Guest guest]

Hi,

(Apologies for stepping in but I saw this and thought, as I have a

couple of minutes, I might be able to save you some time.)

The Best Bet Diet (BBD) is a diet very similar to the Paleolithic Diet.

http://www.msrc.co.uk/index.cfm/fuseaction/show/pageid/8

It eliminates gluten grains, lactose, legumes, tomatoes and egg which are

implicated in molecular mimicry (see articles in their site above) wherein, in

simplistic terms, these foods are seen as its own myelin and the body attacks

itself.

I myself have been on it 3 1/2 years and take all their suggested supplements

too plus a load more for CCSVI. (PPMS 15 years, wheelchair dependent.) I also

removed all my amalgam fillings and had food allergy tests, heavy metal tests,

Lyme Disease test, syndrome test... I have changed my lifestyle to one

that incorporates swimming and/or yoga daily, is stress-free, and is in a

temperate climate, and have CST (cranio-sacral therapy) fortnightly. Whether

any of these can be proved to help MS is not of any concern to me, I am not

taking any pharmaceutical drugs and I FEEL loads better.

I am still in a wheelchair but have beaten all my other little symptoms (brain

fog, fatigue, tinnitus, neuralgia, odd sensations, bear hug, blurred vision,

slurred speech, etc. I still have absolutely no balance and my legs won't work

but other than that, hey MS isn't so bad! (Note to any newcomers here, normally

MS doesn't get you in a wheelchair.)

The diet sounds horrendous when you start it but you soon get used to it and

know what you can/can't eat. I used to be tempted to take a bit out of

someone's bread roll as I passed their table in a restaurant, now I actually

feel sorry for them having to eat it!

Keep smiling!

Janet

To: mscured

From: volleyjen0416@...

Date: Wed, 1 Sep 2010 13:28:56 -0700

Subject: RE: Sounds like diagnosing MS torturous and expensive

Hi , tell me about the Best Bet Diet....what is involved?

Jen

[Guest guest]

Hi,

(Apologies for stepping in but I saw this and thought, as I have a

couple of minutes, I might be able to save you some time.)

The Best Bet Diet (BBD) is a diet very similar to the Paleolithic Diet.

http://www.msrc.co.uk/index.cfm/fuseaction/show/pageid/8

It eliminates gluten grains, lactose, legumes, tomatoes and egg which are

implicated in molecular mimicry (see articles in their site above) wherein, in

simplistic terms, these foods are seen as its own myelin and the body attacks

itself.

I myself have been on it 3 1/2 years and take all their suggested supplements

too plus a load more for CCSVI. (PPMS 15 years, wheelchair dependent.) I also

removed all my amalgam fillings and had food allergy tests, heavy metal tests,

Lyme Disease test, syndrome test... I have changed my lifestyle to one

that incorporates swimming and/or yoga daily, is stress-free, and is in a

temperate climate, and have CST (cranio-sacral therapy) fortnightly. Whether

any of these can be proved to help MS is not of any concern to me, I am not

taking any pharmaceutical drugs and I FEEL loads better.

I am still in a wheelchair but have beaten all my other little symptoms (brain

fog, fatigue, tinnitus, neuralgia, odd sensations, bear hug, blurred vision,

slurred speech, etc. I still have absolutely no balance and my legs won't work

but other than that, hey MS isn't so bad! (Note to any newcomers here, normally

MS doesn't get you in a wheelchair.)

The diet sounds horrendous when you start it but you soon get used to it and

know what you can/can't eat. I used to be tempted to take a bit out of

someone's bread roll as I passed their table in a restaurant, now I actually

feel sorry for them having to eat it!

Keep smiling!

Janet

To: mscured

From: volleyjen0416@...

Date: Wed, 1 Sep 2010 13:28:56 -0700

Subject: RE: Sounds like diagnosing MS torturous and expensive

Hi , tell me about the Best Bet Diet....what is involved?

Jen