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Hi Debbie, Welcome to the group. I hope you like it here. Margaret A. CoteTo: Group <mserslife >Sent: Fri, December 18, 2009 10:23:30 PMSubject: a NEW MEMBER -- Debbie

Comment from new member:Hi, I'm Debbie, newly diagnosed with MS. I have been living with painfor many years, but the MS diagnosis is new and quite scary. Looking forsupport.

Group: please join me in extending a warm welcome to our newest member here at MSersLife!

I know we all look forward to getting to know our new member here on the group! New Member:Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations!

Sharon (group creator/owner) This

email is a natural hand made product. The slight variations in spelling

and grammar enhance its individual character and beauty and in no way

are to be considered flaws or defects.

Link to comment
Share on other sites

Hi Debbie, I understand the constant headaches. I have had them since childhood. I am still trying to get a dxs. Margaret A. CoteTo: MSersLife Sent: Sat, December 19, 2009 12:28:54 AMSubject: RE:

a NEW MEMBER -- Debbie

Hi Sharon, Thank you for the welcome. I was actually diagnosed early this

month I just got out of the hospital the week before last. The doctor initially

thought it possible that I might have had a stroke, but when all is said and

done, the diagnosis is MS. I have had a milder form of the symptoms I am having

now (eye rolling, being able to see out of only one eye, seeing double, facial

numbness, severe headache that feels like my brain is actually being squeezed

etc) since I was 17 and they always put it off to migraines. Through the years

the symptoms have gotten progressively worse and lengthier until finally I went

to bed one Friday night, and Saturday, I woke up and thought oh darn it’s

Migraine day. But it never went away. It’s a month later now and the

symptoms are still there. There are other things that have occurred that I

think now, well yeah that makes sense, I wish someone had investigated further,

but they didn’t. I understand that. I have been living with chronic pain

and problems since 2001. I fell down a flight of stairs and injured my back.

Since then I have had seven back surgeries 6 of them spinal fusions and just

before my diagnosis of MS my surgeon said I need another surgery. He wanted me

to go to pain management for 3 months first though to see if we could get any

kind of improvement because at my last surgery, when I woke up, I couldn’t

feel my legs. Now the pain doctor won’t see me until the neurologist clears

me and until she sees some kind of progress, she doesn’t really want me to

be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of

it is the constant headache. My head just pounds and pounds. Today I felt like

my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m

not really sure what to expect. So I found this group and thought it would be a

good one to join J Debbie

From:

MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the

group Debbie. When were you diagnosed? You said you have been

living with pain for many years. What kind of pain? It wasn't too

many years ago that doctors said there was no pain with MS. Can you believe

that?!? lol What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@ yahoo.com

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

From: Sharon <wobbletowalk@ yahoo.com>

To: Group <mserslife@yahoogrou ps.com>

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment from

new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm

welcome to our newest member here at MSersLife!

I

know we all look forward to getting to know our new member here on the

group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

Hi Debbie, I understand the constant headaches. I have had them since childhood. I am still trying to get a dxs. Margaret A. CoteTo: MSersLife Sent: Sat, December 19, 2009 12:28:54 AMSubject: RE:

a NEW MEMBER -- Debbie

Hi Sharon, Thank you for the welcome. I was actually diagnosed early this

month I just got out of the hospital the week before last. The doctor initially

thought it possible that I might have had a stroke, but when all is said and

done, the diagnosis is MS. I have had a milder form of the symptoms I am having

now (eye rolling, being able to see out of only one eye, seeing double, facial

numbness, severe headache that feels like my brain is actually being squeezed

etc) since I was 17 and they always put it off to migraines. Through the years

the symptoms have gotten progressively worse and lengthier until finally I went

to bed one Friday night, and Saturday, I woke up and thought oh darn it’s

Migraine day. But it never went away. It’s a month later now and the

symptoms are still there. There are other things that have occurred that I

think now, well yeah that makes sense, I wish someone had investigated further,

but they didn’t. I understand that. I have been living with chronic pain

and problems since 2001. I fell down a flight of stairs and injured my back.

Since then I have had seven back surgeries 6 of them spinal fusions and just

before my diagnosis of MS my surgeon said I need another surgery. He wanted me

to go to pain management for 3 months first though to see if we could get any

kind of improvement because at my last surgery, when I woke up, I couldn’t

feel my legs. Now the pain doctor won’t see me until the neurologist clears

me and until she sees some kind of progress, she doesn’t really want me to

be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of

it is the constant headache. My head just pounds and pounds. Today I felt like

my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m

not really sure what to expect. So I found this group and thought it would be a

good one to join J Debbie

From:

MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the

group Debbie. When were you diagnosed? You said you have been

living with pain for many years. What kind of pain? It wasn't too

many years ago that doctors said there was no pain with MS. Can you believe

that?!? lol What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@ yahoo.com

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

From: Sharon <wobbletowalk@ yahoo.com>

To: Group <mserslife@yahoogrou ps.com>

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment from

new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm

welcome to our newest member here at MSersLife!

I

know we all look forward to getting to know our new member here on the

group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

Hi Debbie, I understand the constant headaches. I have had them since childhood. I am still trying to get a dxs. Margaret A. CoteTo: MSersLife Sent: Sat, December 19, 2009 12:28:54 AMSubject: RE:

a NEW MEMBER -- Debbie

Hi Sharon, Thank you for the welcome. I was actually diagnosed early this

month I just got out of the hospital the week before last. The doctor initially

thought it possible that I might have had a stroke, but when all is said and

done, the diagnosis is MS. I have had a milder form of the symptoms I am having

now (eye rolling, being able to see out of only one eye, seeing double, facial

numbness, severe headache that feels like my brain is actually being squeezed

etc) since I was 17 and they always put it off to migraines. Through the years

the symptoms have gotten progressively worse and lengthier until finally I went

to bed one Friday night, and Saturday, I woke up and thought oh darn it’s

Migraine day. But it never went away. It’s a month later now and the

symptoms are still there. There are other things that have occurred that I

think now, well yeah that makes sense, I wish someone had investigated further,

but they didn’t. I understand that. I have been living with chronic pain

and problems since 2001. I fell down a flight of stairs and injured my back.

Since then I have had seven back surgeries 6 of them spinal fusions and just

before my diagnosis of MS my surgeon said I need another surgery. He wanted me

to go to pain management for 3 months first though to see if we could get any

kind of improvement because at my last surgery, when I woke up, I couldn’t

feel my legs. Now the pain doctor won’t see me until the neurologist clears

me and until she sees some kind of progress, she doesn’t really want me to

be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of

it is the constant headache. My head just pounds and pounds. Today I felt like

my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m

not really sure what to expect. So I found this group and thought it would be a

good one to join J Debbie

From:

MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the

group Debbie. When were you diagnosed? You said you have been

living with pain for many years. What kind of pain? It wasn't too

many years ago that doctors said there was no pain with MS. Can you believe

that?!? lol What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@ yahoo.com

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

From: Sharon <wobbletowalk@ yahoo.com>

To: Group <mserslife@yahoogrou ps.com>

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment from

new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm

welcome to our newest member here at MSersLife!

I

know we all look forward to getting to know our new member here on the

group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

DebbieI'm glad you found us but I am so sorry you have a need. That said, at least now you know what's wrong with you so hopefully soon your docs will be able to help you feel better. The migraines must be horrible for you. I wish I had a solution for you but I don't. How did they diagnosis you? Sharonjoin me on Facebook:Sharon Mars wobbletowalk@...This email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: MSersLife Sent: Fri,

December 18, 2009 11:28:54 PMSubject: RE: a NEW MEMBER -- Debbie

Hi Sharon, Thank you for the welcome. I was actually diagnosed early this

month I just got out of the hospital the week before last. The doctor initially

thought it possible that I might have had a stroke, but when all is said and

done, the diagnosis is MS. I have had a milder form of the symptoms I am having

now (eye rolling, being able to see out of only one eye, seeing double, facial

numbness, severe headache that feels like my brain is actually being squeezed

etc) since I was 17 and they always put it off to migraines. Through the years

the symptoms have gotten progressively worse and lengthier until finally I went

to bed one Friday night, and Saturday, I woke up and thought oh darn it’s

Migraine day. But it never went away. It’s a month later now and the

symptoms are still there. There are other things that have occurred that I

think now, well yeah that makes sense, I wish someone had investigated further,

but they didn’t. I understand that. I have been living with chronic pain

and problems since 2001. I fell down a flight of stairs and injured my back.

Since then I have had seven back surgeries 6 of them spinal fusions and just

before my diagnosis of MS my surgeon said I need another surgery. He wanted me

to go to pain management for 3 months first though to see if we could get any

kind of improvement because at my last surgery, when I woke up, I couldn’t

feel my legs. Now the pain doctor won’t see me until the neurologist clears

me and until she sees some kind of progress, she doesn’t really want me to

be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of

it is the constant headache. My head just pounds and pounds. Today I felt like

my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m

not really sure what to expect. So I found this group and thought it would be a

good one to join J Debbie

From:

MSersLife [mailto:MSersLife ] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the

group Debbie. When were you diagnosed? You said you have been

living with pain for many years. What kind of pain? It wasn't too

many years ago that doctors said there was no pain with MS. Can you believe

that?!? lol What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@...

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

To: Group <mserslife >

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment from

new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm

welcome to our newest member here at MSersLife!

I

know we all look forward to getting to know our new member here on the

group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

DebbieI'm glad you found us but I am so sorry you have a need. That said, at least now you know what's wrong with you so hopefully soon your docs will be able to help you feel better. The migraines must be horrible for you. I wish I had a solution for you but I don't. How did they diagnosis you? Sharonjoin me on Facebook:Sharon Mars wobbletowalk@...This email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: MSersLife Sent: Fri,

December 18, 2009 11:28:54 PMSubject: RE: a NEW MEMBER -- Debbie

Hi Sharon, Thank you for the welcome. I was actually diagnosed early this

month I just got out of the hospital the week before last. The doctor initially

thought it possible that I might have had a stroke, but when all is said and

done, the diagnosis is MS. I have had a milder form of the symptoms I am having

now (eye rolling, being able to see out of only one eye, seeing double, facial

numbness, severe headache that feels like my brain is actually being squeezed

etc) since I was 17 and they always put it off to migraines. Through the years

the symptoms have gotten progressively worse and lengthier until finally I went

to bed one Friday night, and Saturday, I woke up and thought oh darn it’s

Migraine day. But it never went away. It’s a month later now and the

symptoms are still there. There are other things that have occurred that I

think now, well yeah that makes sense, I wish someone had investigated further,

but they didn’t. I understand that. I have been living with chronic pain

and problems since 2001. I fell down a flight of stairs and injured my back.

Since then I have had seven back surgeries 6 of them spinal fusions and just

before my diagnosis of MS my surgeon said I need another surgery. He wanted me

to go to pain management for 3 months first though to see if we could get any

kind of improvement because at my last surgery, when I woke up, I couldn’t

feel my legs. Now the pain doctor won’t see me until the neurologist clears

me and until she sees some kind of progress, she doesn’t really want me to

be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of

it is the constant headache. My head just pounds and pounds. Today I felt like

my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m

not really sure what to expect. So I found this group and thought it would be a

good one to join J Debbie

From:

MSersLife [mailto:MSersLife ] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the

group Debbie. When were you diagnosed? You said you have been

living with pain for many years. What kind of pain? It wasn't too

many years ago that doctors said there was no pain with MS. Can you believe

that?!? lol What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@...

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

To: Group <mserslife >

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment from

new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm

welcome to our newest member here at MSersLife!

I

know we all look forward to getting to know our new member here on the

group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

Hi Sharon,

It’s good to know the  dx and

yes, hopefully soon I will get to feeling better. The initial test used was the

brain scan and they followed up with the spinal tap to confirm the diagnosis. Another

brain scan will be done in 3 months and again in 6 months. The brain scan was

compared to one I had a year ago when they claim I had Meningitis but then

turned around and said I didn’t….and also a five year medical history with my neurologist

was used to make the final dx.  The migraines are horrible.  They never go

away. I’ve been on every medicine she can think of and still, every day my head

just kills me. I see the neuro Monday, so hopefully she will have some more

answers or something new for  me.

*HUGS*

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of Sharon

Sent: Saturday, December 19, 2009 11:52 AM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Debbie

I'm glad you found us but I am so sorry you have a need. That said, at

least now you know what's wrong with you so hopefully soon your docs will be

able to help you feel better. The migraines must be horrible for you.

I wish I had a solution for you but I don't. How did they diagnosis you?

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@...

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

To: MSersLife

Sent: Fri, December 18, 2009 11:28:54 PM

Subject: RE: a NEW MEMBER -- Debbie

Hi Sharon,

Thank you for the welcome. I was

actually diagnosed early this month I just got out of the hospital the week

before last. The doctor initially thought it possible that I might have had a

stroke, but when all is said and done, the diagnosis is MS. I have had a milder

form of the symptoms I am having now (eye rolling, being able to see out of

only one eye, seeing double, facial numbness, severe headache that feels like

my brain is actually being squeezed etc) since I was 17 and they always put it

off to migraines. Through the years the symptoms have gotten progressively

worse and lengthier until finally I went to bed one Friday night, and Saturday,

I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a

month later now and the symptoms are still there. There are other things that

have occurred that I think now, well yeah that makes sense, I wish someone had

investigated further, but they didn’t. I understand that. I have been living

with chronic pain and problems since 2001. I fell down a flight of stairs and

injured my back. Since then I have had seven back surgeries 6 of them spinal

fusions and just before my diagnosis of MS my surgeon said I need another

surgery. He wanted me to go to pain management for 3 months first though to see

if we could get any kind of improvement because at my last surgery, when I woke

up, I couldn’t feel my legs. Now the pain doctor won’t see me until the

neurologist clears me and until she sees some kind of progress, she doesn’t really

want me to be doing any new or innovative treatments for the back.

I am in a lot of pain and exhausted all

the time. The worst of it is the constant headache. My head just pounds and

pounds. Today I felt like my eye was shaking, and it was going to shake right

out of my head I thought.

This has all hit me really hard and

really fast, and I’m not really sure what to expect. So I found this group and

thought it would be a good one to join J

Debbie

From:

MSersLife [mailto:MSersLife ] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the group Debbie. When

were you diagnosed? You said you have been living with pain for many

years. What kind of pain? It wasn't too many years ago that doctors

said there was no pain with MS. Can you believe that?!? lol

What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@...

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

From: Sharon

To: Group <mserslife >

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment from new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in

extending a warm welcome to our newest member here at MSersLife!

I know we all look forward

to getting to know our new member here on the group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group

creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

Hi Sharon,

It’s good to know the  dx and

yes, hopefully soon I will get to feeling better. The initial test used was the

brain scan and they followed up with the spinal tap to confirm the diagnosis. Another

brain scan will be done in 3 months and again in 6 months. The brain scan was

compared to one I had a year ago when they claim I had Meningitis but then

turned around and said I didn’t….and also a five year medical history with my neurologist

was used to make the final dx.  The migraines are horrible.  They never go

away. I’ve been on every medicine she can think of and still, every day my head

just kills me. I see the neuro Monday, so hopefully she will have some more

answers or something new for  me.

*HUGS*

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of Sharon

Sent: Saturday, December 19, 2009 11:52 AM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Debbie

I'm glad you found us but I am so sorry you have a need. That said, at

least now you know what's wrong with you so hopefully soon your docs will be

able to help you feel better. The migraines must be horrible for you.

I wish I had a solution for you but I don't. How did they diagnosis you?

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@...

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

To: MSersLife

Sent: Fri, December 18, 2009 11:28:54 PM

Subject: RE: a NEW MEMBER -- Debbie

Hi Sharon,

Thank you for the welcome. I was

actually diagnosed early this month I just got out of the hospital the week

before last. The doctor initially thought it possible that I might have had a

stroke, but when all is said and done, the diagnosis is MS. I have had a milder

form of the symptoms I am having now (eye rolling, being able to see out of

only one eye, seeing double, facial numbness, severe headache that feels like

my brain is actually being squeezed etc) since I was 17 and they always put it

off to migraines. Through the years the symptoms have gotten progressively

worse and lengthier until finally I went to bed one Friday night, and Saturday,

I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a

month later now and the symptoms are still there. There are other things that

have occurred that I think now, well yeah that makes sense, I wish someone had

investigated further, but they didn’t. I understand that. I have been living

with chronic pain and problems since 2001. I fell down a flight of stairs and

injured my back. Since then I have had seven back surgeries 6 of them spinal

fusions and just before my diagnosis of MS my surgeon said I need another

surgery. He wanted me to go to pain management for 3 months first though to see

if we could get any kind of improvement because at my last surgery, when I woke

up, I couldn’t feel my legs. Now the pain doctor won’t see me until the

neurologist clears me and until she sees some kind of progress, she doesn’t really

want me to be doing any new or innovative treatments for the back.

I am in a lot of pain and exhausted all

the time. The worst of it is the constant headache. My head just pounds and

pounds. Today I felt like my eye was shaking, and it was going to shake right

out of my head I thought.

This has all hit me really hard and

really fast, and I’m not really sure what to expect. So I found this group and

thought it would be a good one to join J

Debbie

From:

MSersLife [mailto:MSersLife ] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the group Debbie. When

were you diagnosed? You said you have been living with pain for many

years. What kind of pain? It wasn't too many years ago that doctors

said there was no pain with MS. Can you believe that?!? lol

What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@...

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

From: Sharon

To: Group <mserslife >

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment from new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in

extending a warm welcome to our newest member here at MSersLife!

I know we all look forward

to getting to know our new member here on the group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group

creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

Hi Sharon,

It’s good to know the  dx and

yes, hopefully soon I will get to feeling better. The initial test used was the

brain scan and they followed up with the spinal tap to confirm the diagnosis. Another

brain scan will be done in 3 months and again in 6 months. The brain scan was

compared to one I had a year ago when they claim I had Meningitis but then

turned around and said I didn’t….and also a five year medical history with my neurologist

was used to make the final dx.  The migraines are horrible.  They never go

away. I’ve been on every medicine she can think of and still, every day my head

just kills me. I see the neuro Monday, so hopefully she will have some more

answers or something new for  me.

*HUGS*

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of Sharon

Sent: Saturday, December 19, 2009 11:52 AM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Debbie

I'm glad you found us but I am so sorry you have a need. That said, at

least now you know what's wrong with you so hopefully soon your docs will be

able to help you feel better. The migraines must be horrible for you.

I wish I had a solution for you but I don't. How did they diagnosis you?

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@...

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

To: MSersLife

Sent: Fri, December 18, 2009 11:28:54 PM

Subject: RE: a NEW MEMBER -- Debbie

Hi Sharon,

Thank you for the welcome. I was

actually diagnosed early this month I just got out of the hospital the week

before last. The doctor initially thought it possible that I might have had a

stroke, but when all is said and done, the diagnosis is MS. I have had a milder

form of the symptoms I am having now (eye rolling, being able to see out of

only one eye, seeing double, facial numbness, severe headache that feels like

my brain is actually being squeezed etc) since I was 17 and they always put it

off to migraines. Through the years the symptoms have gotten progressively

worse and lengthier until finally I went to bed one Friday night, and Saturday,

I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a

month later now and the symptoms are still there. There are other things that

have occurred that I think now, well yeah that makes sense, I wish someone had

investigated further, but they didn’t. I understand that. I have been living

with chronic pain and problems since 2001. I fell down a flight of stairs and

injured my back. Since then I have had seven back surgeries 6 of them spinal

fusions and just before my diagnosis of MS my surgeon said I need another

surgery. He wanted me to go to pain management for 3 months first though to see

if we could get any kind of improvement because at my last surgery, when I woke

up, I couldn’t feel my legs. Now the pain doctor won’t see me until the

neurologist clears me and until she sees some kind of progress, she doesn’t really

want me to be doing any new or innovative treatments for the back.

I am in a lot of pain and exhausted all

the time. The worst of it is the constant headache. My head just pounds and

pounds. Today I felt like my eye was shaking, and it was going to shake right

out of my head I thought.

This has all hit me really hard and

really fast, and I’m not really sure what to expect. So I found this group and

thought it would be a good one to join J

Debbie

From:

MSersLife [mailto:MSersLife ] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the group Debbie. When

were you diagnosed? You said you have been living with pain for many

years. What kind of pain? It wasn't too many years ago that doctors

said there was no pain with MS. Can you believe that?!? lol

What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join

me on Facebook:

Sharon Mars

wobbletowalk@...

This

email is a natural hand made product. The slight variations in spelling and

grammar enhance its individual character and beauty and in no way are to be

considered flaws or defects.

From: Sharon

To: Group <mserslife >

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment from new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in

extending a warm welcome to our newest member here at MSersLife!

I know we all look forward

to getting to know our new member here on the group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group

creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

Hi Margaret,

I’m sorry you also suffer from constant headaches. They are so

terrible  Believe me  Believe me you ever want to vent to someone who

understands, drop me a line…I’ve been living with these since I was seventeen

and it’s not easy and I am always here J

*HUGS*

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of Argaret

Cote

Sent: Saturday, December 19, 2009 10:24 AM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Hi Debbie,

I understand the constant headaches. I have had them

since childhood. I am still trying to get a dxs.

Margaret A. Cote

From: Cryselle

To: MSersLife

Sent: Sat, December 19, 2009 12:28:54 AM

Subject: RE: a NEW MEMBER -- Debbie

Hi Sharon,

Thank you for the welcome. I was

actually diagnosed early this month I just got out of the hospital the week

before last. The doctor initially thought it possible that I might have had a

stroke, but when all is said and done, the diagnosis is MS. I have had a milder

form of the symptoms I am having now (eye rolling, being able to see out of

only one eye, seeing double, facial numbness, severe headache that feels like

my brain is actually being squeezed etc) since I was 17 and they always put it

off to migraines. Through the years the symptoms have gotten progressively

worse and lengthier until finally I went to bed one Friday night, and Saturday,

I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a

month later now and the symptoms are still there. There are other things that

have occurred that I think now, well yeah that makes sense, I wish someone had

investigated further, but they didn’t. I understand that. I have been living

with chronic pain and problems since 2001. I fell down a flight of stairs and

injured my back. Since then I have had seven back surgeries 6 of them spinal

fusions and just before my diagnosis of MS my surgeon said I need another

surgery. He wanted me to go to pain management for 3 months first though to see

if we could get any kind of improvement because at my last surgery, when I woke

up, I couldn’t feel my legs. Now the pain doctor won’t see me until the

neurologist clears me and until she sees some kind of progress, she doesn’t

really want me to be doing any new or innovative treatments for the back.

I am in a lot of pain and exhausted all

the time. The worst of it is the constant headache. My head just pounds and

pounds. Today I felt like my eye was shaking, and it was going to shake right

out of my head I thought.

This has all hit me really hard and

really fast, and I’m not really sure what to expect. So I found this group and

thought it would be a good one to join J

Debbie

From:

MSersLife@yahoogrou ps.com

[mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome

to the group Debbie. When were you diagnosed? You said you have

been living with pain for many years. What kind of pain? It wasn't

too many years ago that doctors said there was no pain with MS. Can you

believe that?!? lol What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join me on Facebook:

Sharon Mars

wobbletowalk@ yahoo.com

This email is a natural hand

made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

From: Sharon

<wobbletowalk@ yahoo.com>

To: Group <mserslife@yahoogrou ps.com>

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment

from new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm welcome to

our newest member here at MSersLife!

I know we all look forward to getting to know our new

member here on the group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural hand made product. The slight variations

in spelling and grammar enhance its individual character and beauty and in no

way are to be considered flaws or defects.

Link to comment
Share on other sites

Hi Margaret,

I’m sorry you also suffer from constant headaches. They are so

terrible  Believe me  Believe me you ever want to vent to someone who

understands, drop me a line…I’ve been living with these since I was seventeen

and it’s not easy and I am always here J

*HUGS*

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of Argaret

Cote

Sent: Saturday, December 19, 2009 10:24 AM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Hi Debbie,

I understand the constant headaches. I have had them

since childhood. I am still trying to get a dxs.

Margaret A. Cote

From: Cryselle

To: MSersLife

Sent: Sat, December 19, 2009 12:28:54 AM

Subject: RE: a NEW MEMBER -- Debbie

Hi Sharon,

Thank you for the welcome. I was

actually diagnosed early this month I just got out of the hospital the week

before last. The doctor initially thought it possible that I might have had a

stroke, but when all is said and done, the diagnosis is MS. I have had a milder

form of the symptoms I am having now (eye rolling, being able to see out of

only one eye, seeing double, facial numbness, severe headache that feels like

my brain is actually being squeezed etc) since I was 17 and they always put it

off to migraines. Through the years the symptoms have gotten progressively

worse and lengthier until finally I went to bed one Friday night, and Saturday,

I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a

month later now and the symptoms are still there. There are other things that

have occurred that I think now, well yeah that makes sense, I wish someone had

investigated further, but they didn’t. I understand that. I have been living

with chronic pain and problems since 2001. I fell down a flight of stairs and

injured my back. Since then I have had seven back surgeries 6 of them spinal

fusions and just before my diagnosis of MS my surgeon said I need another

surgery. He wanted me to go to pain management for 3 months first though to see

if we could get any kind of improvement because at my last surgery, when I woke

up, I couldn’t feel my legs. Now the pain doctor won’t see me until the

neurologist clears me and until she sees some kind of progress, she doesn’t

really want me to be doing any new or innovative treatments for the back.

I am in a lot of pain and exhausted all

the time. The worst of it is the constant headache. My head just pounds and

pounds. Today I felt like my eye was shaking, and it was going to shake right

out of my head I thought.

This has all hit me really hard and

really fast, and I’m not really sure what to expect. So I found this group and

thought it would be a good one to join J

Debbie

From:

MSersLife@yahoogrou ps.com

[mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome

to the group Debbie. When were you diagnosed? You said you have

been living with pain for many years. What kind of pain? It wasn't

too many years ago that doctors said there was no pain with MS. Can you

believe that?!? lol What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join me on Facebook:

Sharon Mars

wobbletowalk@ yahoo.com

This email is a natural hand

made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

From: Sharon

<wobbletowalk@ yahoo.com>

To: Group <mserslife@yahoogrou ps.com>

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment

from new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm welcome to

our newest member here at MSersLife!

I know we all look forward to getting to know our new

member here on the group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural hand made product. The slight variations

in spelling and grammar enhance its individual character and beauty and in no

way are to be considered flaws or defects.

Link to comment
Share on other sites

Hi Margaret,

I’m sorry you also suffer from constant headaches. They are so

terrible  Believe me  Believe me you ever want to vent to someone who

understands, drop me a line…I’ve been living with these since I was seventeen

and it’s not easy and I am always here J

*HUGS*

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of Argaret

Cote

Sent: Saturday, December 19, 2009 10:24 AM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Hi Debbie,

I understand the constant headaches. I have had them

since childhood. I am still trying to get a dxs.

Margaret A. Cote

From: Cryselle

To: MSersLife

Sent: Sat, December 19, 2009 12:28:54 AM

Subject: RE: a NEW MEMBER -- Debbie

Hi Sharon,

Thank you for the welcome. I was

actually diagnosed early this month I just got out of the hospital the week

before last. The doctor initially thought it possible that I might have had a

stroke, but when all is said and done, the diagnosis is MS. I have had a milder

form of the symptoms I am having now (eye rolling, being able to see out of

only one eye, seeing double, facial numbness, severe headache that feels like

my brain is actually being squeezed etc) since I was 17 and they always put it

off to migraines. Through the years the symptoms have gotten progressively

worse and lengthier until finally I went to bed one Friday night, and Saturday,

I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a

month later now and the symptoms are still there. There are other things that

have occurred that I think now, well yeah that makes sense, I wish someone had

investigated further, but they didn’t. I understand that. I have been living

with chronic pain and problems since 2001. I fell down a flight of stairs and

injured my back. Since then I have had seven back surgeries 6 of them spinal

fusions and just before my diagnosis of MS my surgeon said I need another

surgery. He wanted me to go to pain management for 3 months first though to see

if we could get any kind of improvement because at my last surgery, when I woke

up, I couldn’t feel my legs. Now the pain doctor won’t see me until the

neurologist clears me and until she sees some kind of progress, she doesn’t

really want me to be doing any new or innovative treatments for the back.

I am in a lot of pain and exhausted all

the time. The worst of it is the constant headache. My head just pounds and

pounds. Today I felt like my eye was shaking, and it was going to shake right

out of my head I thought.

This has all hit me really hard and

really fast, and I’m not really sure what to expect. So I found this group and

thought it would be a good one to join J

Debbie

From:

MSersLife@yahoogrou ps.com

[mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon

Sent: Friday, December 18, 2009 10:29 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome

to the group Debbie. When were you diagnosed? You said you have

been living with pain for many years. What kind of pain? It wasn't

too many years ago that doctors said there was no pain with MS. Can you

believe that?!? lol What other symptoms do you have?

I look forward to getting to know you here on the group. Please send an

introduction when you feel like it.

hugs

Sharon

join me on Facebook:

Sharon Mars

wobbletowalk@ yahoo.com

This email is a natural hand

made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

From: Sharon

<wobbletowalk@ yahoo.com>

To: Group <mserslife@yahoogrou ps.com>

Sent: Fri, December 18, 2009 9:23:30 PM

Subject: a NEW MEMBER -- Debbie

Comment

from new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm welcome to

our newest member here at MSersLife!

I know we all look forward to getting to know our new

member here on the group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural hand made product. The slight variations

in spelling and grammar enhance its individual character and beauty and in no

way are to be considered flaws or defects.

Link to comment
Share on other sites

Thank you , so nice to meet you J

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of

Thallas

Sent: Saturday, December 19, 2009 2:40 PM

To: MSersLife

Subject: RE: a NEW MEMBER -- Debbie

Greetings and Welcome, Debbie!

in WY

" You get a wonderful view from the point of no

return... "

http://www.flickr.com/photos/liadains_fancies

http://practical-blackwork.blogspot.com

http://practicalblackwork.com

Link to comment
Share on other sites

Thank you , so nice to meet you J

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of

Thallas

Sent: Saturday, December 19, 2009 2:40 PM

To: MSersLife

Subject: RE: a NEW MEMBER -- Debbie

Greetings and Welcome, Debbie!

in WY

" You get a wonderful view from the point of no

return... "

http://www.flickr.com/photos/liadains_fancies

http://practical-blackwork.blogspot.com

http://practicalblackwork.com

Link to comment
Share on other sites

Cryselle, welcome to life with Multiple Sclerosis!Perhaps, if we all put our MS brains together,plaques notwithstanding, we can be of some helpto you in this long hard battle.Love to you,n Rojas, wMS and a host of other things,including disc disease (no surgeries yet), diagnosedwMS at age 19; I am now 72.5--and life looks good. . .To:

MSersLife Sent: Fri, December 18, 2009 10:29:27 PMSubject: RE: a NEW MEMBER -- Debbie

Hi , Thanks for the welcome, it’s so nice to meet you J Debbie

From:

MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com

Sent: Friday, December 18, 2009 10:28 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the. group. From NE Oklahoma. (with an ie) Sent from my U.S. Cellular BlackBerry® smartphone

From: Sharon <wobbletowalk@ yahoo.com>

Date: Fri, 18 Dec 2009 20:23:30 -0800 (PST)

To: Group<mserslife@yahoogrou ps.com>

Subject: a NEW MEMBER -- Debbie

Comment from

new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm

welcome to our newest member here at MSersLife!

I

know we all look forward to getting to know our new member here on the

group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

Cryselle, welcome to life with Multiple Sclerosis!Perhaps, if we all put our MS brains together,plaques notwithstanding, we can be of some helpto you in this long hard battle.Love to you,n Rojas, wMS and a host of other things,including disc disease (no surgeries yet), diagnosedwMS at age 19; I am now 72.5--and life looks good. . .To:

MSersLife Sent: Fri, December 18, 2009 10:29:27 PMSubject: RE: a NEW MEMBER -- Debbie

Hi , Thanks for the welcome, it’s so nice to meet you J Debbie

From:

MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com

Sent: Friday, December 18, 2009 10:28 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the. group. From NE Oklahoma. (with an ie) Sent from my U.S. Cellular BlackBerry® smartphone

From: Sharon <wobbletowalk@ yahoo.com>

Date: Fri, 18 Dec 2009 20:23:30 -0800 (PST)

To: Group<mserslife@yahoogrou ps.com>

Subject: a NEW MEMBER -- Debbie

Comment from

new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm

welcome to our newest member here at MSersLife!

I

know we all look forward to getting to know our new member here on the

group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

Cryselle, welcome to life with Multiple Sclerosis!Perhaps, if we all put our MS brains together,plaques notwithstanding, we can be of some helpto you in this long hard battle.Love to you,n Rojas, wMS and a host of other things,including disc disease (no surgeries yet), diagnosedwMS at age 19; I am now 72.5--and life looks good. . .To:

MSersLife Sent: Fri, December 18, 2009 10:29:27 PMSubject: RE: a NEW MEMBER -- Debbie

Hi , Thanks for the welcome, it’s so nice to meet you J Debbie

From:

MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com

Sent: Friday, December 18, 2009 10:28 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the. group. From NE Oklahoma. (with an ie) Sent from my U.S. Cellular BlackBerry® smartphone

From: Sharon <wobbletowalk@ yahoo.com>

Date: Fri, 18 Dec 2009 20:23:30 -0800 (PST)

To: Group<mserslife@yahoogrou ps.com>

Subject: a NEW MEMBER -- Debbie

Comment from

new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm

welcome to our newest member here at MSersLife!

I

know we all look forward to getting to know our new member here on the

group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural

hand made product. The slight variations in spelling and grammar enhance its

individual character and beauty and in no way are to be considered flaws or

defects.

Link to comment
Share on other sites

J  n, thank you for the welcome, and you all have already

been help to me just by letting me know I’m not alone, and that there are

resources and friends out there!

*HUGS*

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of marion

j rojas

Sent: Saturday, December 19, 2009 5:27 PM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Cryselle,

welcome to life with Multiple Sclerosis!

Perhaps, if we all put our MS brains together,

plaques notwithstanding, we can be of some help

to you in this long hard battle.

Love to you,

n Rojas, wMS and a host of other things,

including disc disease (no surgeries yet), diagnosed

wMS at age 19; I am now 72.5--and life looks good. . .

From: Cryselle

To: MSersLife

Sent: Fri, December 18, 2009 10:29:27 PM

Subject: RE: a NEW MEMBER -- Debbie

Hi , Thanks for the welcome, it’s

so nice to meet you

J

Debbie

From:

MSersLife@yahoogrou ps.com

[mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com

Sent: Friday, December 18, 2009 10:28 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the. group. From NE Oklahoma. (with an ie)

Sent from my U.S. Cellular BlackBerry® smartphone

From:

Sharon <wobbletowalk@ yahoo.com>

Date:

Fri, 18 Dec 2009 20:23:30 -0800 (PST)

To:

Group<mserslife@yahoogrou ps.com>

Subject:

a NEW MEMBER -- Debbie

Comment

from new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm welcome to

our newest member here at MSersLife!

I know we all look forward to getting to know our new

member here on the group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural hand made product. The slight

variations in spelling and grammar enhance its individual character and

beauty and in no way are to be considered flaws or defects.

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J  n, thank you for the welcome, and you all have already

been help to me just by letting me know I’m not alone, and that there are

resources and friends out there!

*HUGS*

Deb

From:

MSersLife [mailto:MSersLife ] On Behalf Of marion

j rojas

Sent: Saturday, December 19, 2009 5:27 PM

To: MSersLife

Subject: Re: a NEW MEMBER -- Debbie

Cryselle,

welcome to life with Multiple Sclerosis!

Perhaps, if we all put our MS brains together,

plaques notwithstanding, we can be of some help

to you in this long hard battle.

Love to you,

n Rojas, wMS and a host of other things,

including disc disease (no surgeries yet), diagnosed

wMS at age 19; I am now 72.5--and life looks good. . .

From: Cryselle

To: MSersLife

Sent: Fri, December 18, 2009 10:29:27 PM

Subject: RE: a NEW MEMBER -- Debbie

Hi , Thanks for the welcome, it’s

so nice to meet you

J

Debbie

From:

MSersLife@yahoogrou ps.com

[mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com

Sent: Friday, December 18, 2009 10:28 PM

To: MSersLife@yahoogrou ps.com

Subject: Re: a NEW MEMBER -- Debbie

Welcome to the. group. From NE Oklahoma. (with an ie)

Sent from my U.S. Cellular BlackBerry® smartphone

From:

Sharon <wobbletowalk@ yahoo.com>

Date:

Fri, 18 Dec 2009 20:23:30 -0800 (PST)

To:

Group<mserslife@yahoogrou ps.com>

Subject:

a NEW MEMBER -- Debbie

Comment

from new member:

Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain

for many years, but the MS diagnosis is new and quite scary. Looking for

support.

Group: please join me in extending a warm welcome to

our newest member here at MSersLife!

I know we all look forward to getting to know our new

member here on the group!

New Member:

Please feel free to send an introduction as soon as you wish, ask any

questions you want, share your experiences with all of us and just jump into

the conversations!

Sharon (group creator/owner)

This email is a natural hand made product. The slight

variations in spelling and grammar enhance its individual character and

beauty and in no way are to be considered flaws or defects.

Link to comment
Share on other sites

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