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Posted

Em, I know exactly how you feel but I do want to caution you. So many things

that sound horrible to us really aren't so bad after all. We don't understand

" doctor speak " nor do we have medical degrees to totally understand what is

being written. I would try to remain calm (tough to do I know) and wait to talk

to your doctor. I do think you have a right to know EXACTLY what the tests show

and would make sure he tells you in " little people speak *lol* " . I have just

found out I have to have 4 MRI's because my neuro thinks I might have MS...now

that scares me to death and of course I've looked it up on the internet which

has only freaked me out even more. Who is your neuro? I see Dr. Harney in

.

Anne

Neuro developments

Howdy --

Been keeping my head down, working, sleeping, so I'm sorry I haven't been

keeping up with much. It's like my FM has been cutting me some slack --

haven't felt as achy as usual, although still needing lots of sleep.

I got my MRI and MRA results yesterday (head). The radiology clinic where

I had them done didn't get them to my neurologist in time for my first

appt, so I thought I'd get them myself and bring them next week just in

case. They scared me to death. I feel sure that if any of this was truly

serious somebody would have told me. But it was so hard to read them -- so

scary I wish I hadn't gotten them. Better off not wondering about

them. Evidently I have two somethings that the radiologist said might be

cysts, he wasn't sure -- one is in the sphenoid sinus (back of the head),

and the other is in the left ventricle of the brain. He did not suggest

tumors, and I'm sure that they are certainly not, or that neurosurgeon

would have said something. But the radiologist did suggest several things

that my neurosurgeon never passed along to me, and I'm bothered by

that. First off, the presence of cysts -- my sinuses are in very poor

shape, and now I can see why! I'm trying to get in to see an

otolaryngologist to see about having a sinus lavage. But there were

vascular (vein) problems that the neurosurgeon also did not tell me

about. They may be minor problems, but it makes me

angry/scared/frustratrated that he did not tell me anything. None of the

major veins have problems at all, but he thought I had something he called

" acquired microvascular disease. " I have not been able to find out even

*vaguely* what this is, except what it sounds like -- something funky with

my smaller veins.

These tests were done in June. I have been having so many neuro

weirdnesses going on in the past month, I guess I'll ask my neurologist

(not to be confused iwth the neurosurgeon I saw last summer) if I can have

another MRI of the head. And I couldn't help it -- can't help it -- I feel

so scared in the pit of my stomach. I know I should just let it lie, not

worry about it until the time comes, but it was a HUGE shock to read some

of that stuff. Most of it, to be honest, I am so far from understanding

that it doesn't mean squat to me. But some of it made sense, and what did,

scared me. And made me mad, too. Boy am I going to talk frankly with this

neurologist next week. I want to know EVERYTHING.

If anybody knows what any of this means, please let me know? I'm nto as

scared today, but man, I hate not knowing.

Best,

Em

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

It is the tale, not he who tells it.

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

Posted

Em, I know exactly how you feel but I do want to caution you. So many things

that sound horrible to us really aren't so bad after all. We don't understand

" doctor speak " nor do we have medical degrees to totally understand what is

being written. I would try to remain calm (tough to do I know) and wait to talk

to your doctor. I do think you have a right to know EXACTLY what the tests show

and would make sure he tells you in " little people speak *lol* " . I have just

found out I have to have 4 MRI's because my neuro thinks I might have MS...now

that scares me to death and of course I've looked it up on the internet which

has only freaked me out even more. Who is your neuro? I see Dr. Harney in

.

Anne

Neuro developments

Howdy --

Been keeping my head down, working, sleeping, so I'm sorry I haven't been

keeping up with much. It's like my FM has been cutting me some slack --

haven't felt as achy as usual, although still needing lots of sleep.

I got my MRI and MRA results yesterday (head). The radiology clinic where

I had them done didn't get them to my neurologist in time for my first

appt, so I thought I'd get them myself and bring them next week just in

case. They scared me to death. I feel sure that if any of this was truly

serious somebody would have told me. But it was so hard to read them -- so

scary I wish I hadn't gotten them. Better off not wondering about

them. Evidently I have two somethings that the radiologist said might be

cysts, he wasn't sure -- one is in the sphenoid sinus (back of the head),

and the other is in the left ventricle of the brain. He did not suggest

tumors, and I'm sure that they are certainly not, or that neurosurgeon

would have said something. But the radiologist did suggest several things

that my neurosurgeon never passed along to me, and I'm bothered by

that. First off, the presence of cysts -- my sinuses are in very poor

shape, and now I can see why! I'm trying to get in to see an

otolaryngologist to see about having a sinus lavage. But there were

vascular (vein) problems that the neurosurgeon also did not tell me

about. They may be minor problems, but it makes me

angry/scared/frustratrated that he did not tell me anything. None of the

major veins have problems at all, but he thought I had something he called

" acquired microvascular disease. " I have not been able to find out even

*vaguely* what this is, except what it sounds like -- something funky with

my smaller veins.

These tests were done in June. I have been having so many neuro

weirdnesses going on in the past month, I guess I'll ask my neurologist

(not to be confused iwth the neurosurgeon I saw last summer) if I can have

another MRI of the head. And I couldn't help it -- can't help it -- I feel

so scared in the pit of my stomach. I know I should just let it lie, not

worry about it until the time comes, but it was a HUGE shock to read some

of that stuff. Most of it, to be honest, I am so far from understanding

that it doesn't mean squat to me. But some of it made sense, and what did,

scared me. And made me mad, too. Boy am I going to talk frankly with this

neurologist next week. I want to know EVERYTHING.

If anybody knows what any of this means, please let me know? I'm nto as

scared today, but man, I hate not knowing.

Best,

Em

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

It is the tale, not he who tells it.

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

Posted

Em, I know exactly how you feel but I do want to caution you. So many things

that sound horrible to us really aren't so bad after all. We don't understand

" doctor speak " nor do we have medical degrees to totally understand what is

being written. I would try to remain calm (tough to do I know) and wait to talk

to your doctor. I do think you have a right to know EXACTLY what the tests show

and would make sure he tells you in " little people speak *lol* " . I have just

found out I have to have 4 MRI's because my neuro thinks I might have MS...now

that scares me to death and of course I've looked it up on the internet which

has only freaked me out even more. Who is your neuro? I see Dr. Harney in

.

Anne

Neuro developments

Howdy --

Been keeping my head down, working, sleeping, so I'm sorry I haven't been

keeping up with much. It's like my FM has been cutting me some slack --

haven't felt as achy as usual, although still needing lots of sleep.

I got my MRI and MRA results yesterday (head). The radiology clinic where

I had them done didn't get them to my neurologist in time for my first

appt, so I thought I'd get them myself and bring them next week just in

case. They scared me to death. I feel sure that if any of this was truly

serious somebody would have told me. But it was so hard to read them -- so

scary I wish I hadn't gotten them. Better off not wondering about

them. Evidently I have two somethings that the radiologist said might be

cysts, he wasn't sure -- one is in the sphenoid sinus (back of the head),

and the other is in the left ventricle of the brain. He did not suggest

tumors, and I'm sure that they are certainly not, or that neurosurgeon

would have said something. But the radiologist did suggest several things

that my neurosurgeon never passed along to me, and I'm bothered by

that. First off, the presence of cysts -- my sinuses are in very poor

shape, and now I can see why! I'm trying to get in to see an

otolaryngologist to see about having a sinus lavage. But there were

vascular (vein) problems that the neurosurgeon also did not tell me

about. They may be minor problems, but it makes me

angry/scared/frustratrated that he did not tell me anything. None of the

major veins have problems at all, but he thought I had something he called

" acquired microvascular disease. " I have not been able to find out even

*vaguely* what this is, except what it sounds like -- something funky with

my smaller veins.

These tests were done in June. I have been having so many neuro

weirdnesses going on in the past month, I guess I'll ask my neurologist

(not to be confused iwth the neurosurgeon I saw last summer) if I can have

another MRI of the head. And I couldn't help it -- can't help it -- I feel

so scared in the pit of my stomach. I know I should just let it lie, not

worry about it until the time comes, but it was a HUGE shock to read some

of that stuff. Most of it, to be honest, I am so far from understanding

that it doesn't mean squat to me. But some of it made sense, and what did,

scared me. And made me mad, too. Boy am I going to talk frankly with this

neurologist next week. I want to know EVERYTHING.

If anybody knows what any of this means, please let me know? I'm nto as

scared today, but man, I hate not knowing.

Best,

Em

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

It is the tale, not he who tells it.

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

Posted

Em, I agree with this. They have a technical name for EVERY symptom or

condition that a person has. When I was diagnosed with a sleeping disorder (no

REM) he called it " Idiopathic Hypersomnalence " sounds pretty bad huh? It means

" she is really tired and we don't know why " . The Idiopathic just means that

they don't know why. You could have a red spot on your arm from where you slept

and they would call it " hyper edema limbitis " (I just made that up :) Anyway,

with my daughter they have used scary language and it was not any thing

abnormal. They said she had some heart issue and called it a scary name (I

can't remember it now) and I was really concerned, only to find out, it was just

a description of her heart but it is common in 50% of all babies. It was a

description of her, but not a disease or abnormality, just a characteristic.

Sincerely, Pamela Rauch

Neuro developments

Howdy --

Been keeping my head down, working, sleeping, so I'm sorry I haven't been

keeping up with much. It's like my FM has been cutting me some slack --

haven't felt as achy as usual, although still needing lots of sleep.

I got my MRI and MRA results yesterday (head). The radiology clinic where

I had them done didn't get them to my neurologist in time for my first

appt, so I thought I'd get them myself and bring them next week just in

case. They scared me to death. I feel sure that if any of this was truly

serious somebody would have told me. But it was so hard to read them -- so

scary I wish I hadn't gotten them. Better off not wondering about

them. Evidently I have two somethings that the radiologist said might be

cysts, he wasn't sure -- one is in the sphenoid sinus (back of the head),

and the other is in the left ventricle of the brain. He did not suggest

tumors, and I'm sure that they are certainly not, or that neurosurgeon

would have said something. But the radiologist did suggest several things

that my neurosurgeon never passed along to me, and I'm bothered by

that. First off, the presence of cysts -- my sinuses are in very poor

shape, and now I can see why! I'm trying to get in to see an

otolaryngologist to see about having a sinus lavage. But there were

vascular (vein) problems that the neurosurgeon also did not tell me

about. They may be minor problems, but it makes me

angry/scared/frustratrated that he did not tell me anything. None of the

major veins have problems at all, but he thought I had something he called

" acquired microvascular disease. " I have not been able to find out even

*vaguely* what this is, except what it sounds like -- something funky with

my smaller veins.

These tests were done in June. I have been having so many neuro

weirdnesses going on in the past month, I guess I'll ask my neurologist

(not to be confused iwth the neurosurgeon I saw last summer) if I can have

another MRI of the head. And I couldn't help it -- can't help it -- I feel

so scared in the pit of my stomach. I know I should just let it lie, not

worry about it until the time comes, but it was a HUGE shock to read some

of that stuff. Most of it, to be honest, I am so far from understanding

that it doesn't mean squat to me. But some of it made sense, and what did,

scared me. And made me mad, too. Boy am I going to talk frankly with this

neurologist next week. I want to know EVERYTHING.

If anybody knows what any of this means, please let me know? I'm nto as

scared today, but man, I hate not knowing.

Best,

Em

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

It is the tale, not he who tells it.

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

Posted

Em, I agree with this. They have a technical name for EVERY symptom or

condition that a person has. When I was diagnosed with a sleeping disorder (no

REM) he called it " Idiopathic Hypersomnalence " sounds pretty bad huh? It means

" she is really tired and we don't know why " . The Idiopathic just means that

they don't know why. You could have a red spot on your arm from where you slept

and they would call it " hyper edema limbitis " (I just made that up :) Anyway,

with my daughter they have used scary language and it was not any thing

abnormal. They said she had some heart issue and called it a scary name (I

can't remember it now) and I was really concerned, only to find out, it was just

a description of her heart but it is common in 50% of all babies. It was a

description of her, but not a disease or abnormality, just a characteristic.

Sincerely, Pamela Rauch

Neuro developments

Howdy --

Been keeping my head down, working, sleeping, so I'm sorry I haven't been

keeping up with much. It's like my FM has been cutting me some slack --

haven't felt as achy as usual, although still needing lots of sleep.

I got my MRI and MRA results yesterday (head). The radiology clinic where

I had them done didn't get them to my neurologist in time for my first

appt, so I thought I'd get them myself and bring them next week just in

case. They scared me to death. I feel sure that if any of this was truly

serious somebody would have told me. But it was so hard to read them -- so

scary I wish I hadn't gotten them. Better off not wondering about

them. Evidently I have two somethings that the radiologist said might be

cysts, he wasn't sure -- one is in the sphenoid sinus (back of the head),

and the other is in the left ventricle of the brain. He did not suggest

tumors, and I'm sure that they are certainly not, or that neurosurgeon

would have said something. But the radiologist did suggest several things

that my neurosurgeon never passed along to me, and I'm bothered by

that. First off, the presence of cysts -- my sinuses are in very poor

shape, and now I can see why! I'm trying to get in to see an

otolaryngologist to see about having a sinus lavage. But there were

vascular (vein) problems that the neurosurgeon also did not tell me

about. They may be minor problems, but it makes me

angry/scared/frustratrated that he did not tell me anything. None of the

major veins have problems at all, but he thought I had something he called

" acquired microvascular disease. " I have not been able to find out even

*vaguely* what this is, except what it sounds like -- something funky with

my smaller veins.

These tests were done in June. I have been having so many neuro

weirdnesses going on in the past month, I guess I'll ask my neurologist

(not to be confused iwth the neurosurgeon I saw last summer) if I can have

another MRI of the head. And I couldn't help it -- can't help it -- I feel

so scared in the pit of my stomach. I know I should just let it lie, not

worry about it until the time comes, but it was a HUGE shock to read some

of that stuff. Most of it, to be honest, I am so far from understanding

that it doesn't mean squat to me. But some of it made sense, and what did,

scared me. And made me mad, too. Boy am I going to talk frankly with this

neurologist next week. I want to know EVERYTHING.

If anybody knows what any of this means, please let me know? I'm nto as

scared today, but man, I hate not knowing.

Best,

Em

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

It is the tale, not he who tells it.

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

Posted

Em, I agree with this. They have a technical name for EVERY symptom or

condition that a person has. When I was diagnosed with a sleeping disorder (no

REM) he called it " Idiopathic Hypersomnalence " sounds pretty bad huh? It means

" she is really tired and we don't know why " . The Idiopathic just means that

they don't know why. You could have a red spot on your arm from where you slept

and they would call it " hyper edema limbitis " (I just made that up :) Anyway,

with my daughter they have used scary language and it was not any thing

abnormal. They said she had some heart issue and called it a scary name (I

can't remember it now) and I was really concerned, only to find out, it was just

a description of her heart but it is common in 50% of all babies. It was a

description of her, but not a disease or abnormality, just a characteristic.

Sincerely, Pamela Rauch

Neuro developments

Howdy --

Been keeping my head down, working, sleeping, so I'm sorry I haven't been

keeping up with much. It's like my FM has been cutting me some slack --

haven't felt as achy as usual, although still needing lots of sleep.

I got my MRI and MRA results yesterday (head). The radiology clinic where

I had them done didn't get them to my neurologist in time for my first

appt, so I thought I'd get them myself and bring them next week just in

case. They scared me to death. I feel sure that if any of this was truly

serious somebody would have told me. But it was so hard to read them -- so

scary I wish I hadn't gotten them. Better off not wondering about

them. Evidently I have two somethings that the radiologist said might be

cysts, he wasn't sure -- one is in the sphenoid sinus (back of the head),

and the other is in the left ventricle of the brain. He did not suggest

tumors, and I'm sure that they are certainly not, or that neurosurgeon

would have said something. But the radiologist did suggest several things

that my neurosurgeon never passed along to me, and I'm bothered by

that. First off, the presence of cysts -- my sinuses are in very poor

shape, and now I can see why! I'm trying to get in to see an

otolaryngologist to see about having a sinus lavage. But there were

vascular (vein) problems that the neurosurgeon also did not tell me

about. They may be minor problems, but it makes me

angry/scared/frustratrated that he did not tell me anything. None of the

major veins have problems at all, but he thought I had something he called

" acquired microvascular disease. " I have not been able to find out even

*vaguely* what this is, except what it sounds like -- something funky with

my smaller veins.

These tests were done in June. I have been having so many neuro

weirdnesses going on in the past month, I guess I'll ask my neurologist

(not to be confused iwth the neurosurgeon I saw last summer) if I can have

another MRI of the head. And I couldn't help it -- can't help it -- I feel

so scared in the pit of my stomach. I know I should just let it lie, not

worry about it until the time comes, but it was a HUGE shock to read some

of that stuff. Most of it, to be honest, I am so far from understanding

that it doesn't mean squat to me. But some of it made sense, and what did,

scared me. And made me mad, too. Boy am I going to talk frankly with this

neurologist next week. I want to know EVERYTHING.

If anybody knows what any of this means, please let me know? I'm nto as

scared today, but man, I hate not knowing.

Best,

Em

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

It is the tale, not he who tells it.

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

Posted

Em, I agree with this. They have a technical name for EVERY symptom or

condition that a person has. When I was diagnosed with a sleeping disorder (no

REM) he called it " Idiopathic Hypersomnalence " sounds pretty bad huh? It means

" she is really tired and we don't know why " . The Idiopathic just means that

they don't know why. You could have a red spot on your arm from where you slept

and they would call it " hyper edema limbitis " (I just made that up :) Anyway,

with my daughter they have used scary language and it was not any thing

abnormal. They said she had some heart issue and called it a scary name (I

can't remember it now) and I was really concerned, only to find out, it was just

a description of her heart but it is common in 50% of all babies. It was a

description of her, but not a disease or abnormality, just a characteristic.

Sincerely, Pamela Rauch

Neuro developments

Howdy --

Been keeping my head down, working, sleeping, so I'm sorry I haven't been

keeping up with much. It's like my FM has been cutting me some slack --

haven't felt as achy as usual, although still needing lots of sleep.

I got my MRI and MRA results yesterday (head). The radiology clinic where

I had them done didn't get them to my neurologist in time for my first

appt, so I thought I'd get them myself and bring them next week just in

case. They scared me to death. I feel sure that if any of this was truly

serious somebody would have told me. But it was so hard to read them -- so

scary I wish I hadn't gotten them. Better off not wondering about

them. Evidently I have two somethings that the radiologist said might be

cysts, he wasn't sure -- one is in the sphenoid sinus (back of the head),

and the other is in the left ventricle of the brain. He did not suggest

tumors, and I'm sure that they are certainly not, or that neurosurgeon

would have said something. But the radiologist did suggest several things

that my neurosurgeon never passed along to me, and I'm bothered by

that. First off, the presence of cysts -- my sinuses are in very poor

shape, and now I can see why! I'm trying to get in to see an

otolaryngologist to see about having a sinus lavage. But there were

vascular (vein) problems that the neurosurgeon also did not tell me

about. They may be minor problems, but it makes me

angry/scared/frustratrated that he did not tell me anything. None of the

major veins have problems at all, but he thought I had something he called

" acquired microvascular disease. " I have not been able to find out even

*vaguely* what this is, except what it sounds like -- something funky with

my smaller veins.

These tests were done in June. I have been having so many neuro

weirdnesses going on in the past month, I guess I'll ask my neurologist

(not to be confused iwth the neurosurgeon I saw last summer) if I can have

another MRI of the head. And I couldn't help it -- can't help it -- I feel

so scared in the pit of my stomach. I know I should just let it lie, not

worry about it until the time comes, but it was a HUGE shock to read some

of that stuff. Most of it, to be honest, I am so far from understanding

that it doesn't mean squat to me. But some of it made sense, and what did,

scared me. And made me mad, too. Boy am I going to talk frankly with this

neurologist next week. I want to know EVERYTHING.

If anybody knows what any of this means, please let me know? I'm nto as

scared today, but man, I hate not knowing.

Best,

Em

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

It is the tale, not he who tells it.

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

Posted

Em, I agree with this. They have a technical name for EVERY symptom or

condition that a person has. When I was diagnosed with a sleeping disorder (no

REM) he called it " Idiopathic Hypersomnalence " sounds pretty bad huh? It means

" she is really tired and we don't know why " . The Idiopathic just means that

they don't know why. You could have a red spot on your arm from where you slept

and they would call it " hyper edema limbitis " (I just made that up :) Anyway,

with my daughter they have used scary language and it was not any thing

abnormal. They said she had some heart issue and called it a scary name (I

can't remember it now) and I was really concerned, only to find out, it was just

a description of her heart but it is common in 50% of all babies. It was a

description of her, but not a disease or abnormality, just a characteristic.

Sincerely, Pamela Rauch

Neuro developments

Howdy --

Been keeping my head down, working, sleeping, so I'm sorry I haven't been

keeping up with much. It's like my FM has been cutting me some slack --

haven't felt as achy as usual, although still needing lots of sleep.

I got my MRI and MRA results yesterday (head). The radiology clinic where

I had them done didn't get them to my neurologist in time for my first

appt, so I thought I'd get them myself and bring them next week just in

case. They scared me to death. I feel sure that if any of this was truly

serious somebody would have told me. But it was so hard to read them -- so

scary I wish I hadn't gotten them. Better off not wondering about

them. Evidently I have two somethings that the radiologist said might be

cysts, he wasn't sure -- one is in the sphenoid sinus (back of the head),

and the other is in the left ventricle of the brain. He did not suggest

tumors, and I'm sure that they are certainly not, or that neurosurgeon

would have said something. But the radiologist did suggest several things

that my neurosurgeon never passed along to me, and I'm bothered by

that. First off, the presence of cysts -- my sinuses are in very poor

shape, and now I can see why! I'm trying to get in to see an

otolaryngologist to see about having a sinus lavage. But there were

vascular (vein) problems that the neurosurgeon also did not tell me

about. They may be minor problems, but it makes me

angry/scared/frustratrated that he did not tell me anything. None of the

major veins have problems at all, but he thought I had something he called

" acquired microvascular disease. " I have not been able to find out even

*vaguely* what this is, except what it sounds like -- something funky with

my smaller veins.

These tests were done in June. I have been having so many neuro

weirdnesses going on in the past month, I guess I'll ask my neurologist

(not to be confused iwth the neurosurgeon I saw last summer) if I can have

another MRI of the head. And I couldn't help it -- can't help it -- I feel

so scared in the pit of my stomach. I know I should just let it lie, not

worry about it until the time comes, but it was a HUGE shock to read some

of that stuff. Most of it, to be honest, I am so far from understanding

that it doesn't mean squat to me. But some of it made sense, and what did,

scared me. And made me mad, too. Boy am I going to talk frankly with this

neurologist next week. I want to know EVERYTHING.

If anybody knows what any of this means, please let me know? I'm nto as

scared today, but man, I hate not knowing.

Best,

Em

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

It is the tale, not he who tells it.

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

Posted

I know you're both so right. I knew I shouldn't even READ it, because it

would be filled with this medicalese that would sound awful to me. I'm

actually pretty good with most medical terminology, but I'm speaking in

broad terms -- now when you get to the nitty-gritty of neuro-speak, you've

lost me. Like this -- " There is increased T2 and FLAIR signal seen in the

deep white matter of the left frontal lobe and left parietal lobe with

extensive atrophy of the left parietal deep white matter and intact

overlying gray matter. These findings are suggestive of periventricular

leukomalacia related to a developmental vascular insult, I cannot

definitively rule out acquired microvascular disease. "

Excuse me -- translation please??? LOLOL! T2? FLAIR? What do those

stand for? At the same time, you say " extensive atrophy " and I know what

THAT means. And what in God's good green earth is a " developmental

vascular insult? " Somebody cussed at my veins when I was a baby???

It's two pages of this kind of talk, and I do not understand 90% of it. So

I guess I'll just wait till next week, talk to my neuro dude (I see Dr.

D'Cruz in Lubbock), and maybe eventually find out what that all means.

*HUGS* THank you guys for bringing me back to earth -- when I hear about

white matter I start thinking about Alzheimer's, and oh man, can I go to

town from there. Yeesh. I need to think about something else, like where

I'm going to find a nice new menorah in Lubbock, TX.

*more hugs*

Em

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

It is the tale, not he who tells it.

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

Posted

I know you're both so right. I knew I shouldn't even READ it, because it

would be filled with this medicalese that would sound awful to me. I'm

actually pretty good with most medical terminology, but I'm speaking in

broad terms -- now when you get to the nitty-gritty of neuro-speak, you've

lost me. Like this -- " There is increased T2 and FLAIR signal seen in the

deep white matter of the left frontal lobe and left parietal lobe with

extensive atrophy of the left parietal deep white matter and intact

overlying gray matter. These findings are suggestive of periventricular

leukomalacia related to a developmental vascular insult, I cannot

definitively rule out acquired microvascular disease. "

Excuse me -- translation please??? LOLOL! T2? FLAIR? What do those

stand for? At the same time, you say " extensive atrophy " and I know what

THAT means. And what in God's good green earth is a " developmental

vascular insult? " Somebody cussed at my veins when I was a baby???

It's two pages of this kind of talk, and I do not understand 90% of it. So

I guess I'll just wait till next week, talk to my neuro dude (I see Dr.

D'Cruz in Lubbock), and maybe eventually find out what that all means.

*HUGS* THank you guys for bringing me back to earth -- when I hear about

white matter I start thinking about Alzheimer's, and oh man, can I go to

town from there. Yeesh. I need to think about something else, like where

I'm going to find a nice new menorah in Lubbock, TX.

*more hugs*

Em

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

It is the tale, not he who tells it.

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

Posted

I know you're both so right. I knew I shouldn't even READ it, because it

would be filled with this medicalese that would sound awful to me. I'm

actually pretty good with most medical terminology, but I'm speaking in

broad terms -- now when you get to the nitty-gritty of neuro-speak, you've

lost me. Like this -- " There is increased T2 and FLAIR signal seen in the

deep white matter of the left frontal lobe and left parietal lobe with

extensive atrophy of the left parietal deep white matter and intact

overlying gray matter. These findings are suggestive of periventricular

leukomalacia related to a developmental vascular insult, I cannot

definitively rule out acquired microvascular disease. "

Excuse me -- translation please??? LOLOL! T2? FLAIR? What do those

stand for? At the same time, you say " extensive atrophy " and I know what

THAT means. And what in God's good green earth is a " developmental

vascular insult? " Somebody cussed at my veins when I was a baby???

It's two pages of this kind of talk, and I do not understand 90% of it. So

I guess I'll just wait till next week, talk to my neuro dude (I see Dr.

D'Cruz in Lubbock), and maybe eventually find out what that all means.

*HUGS* THank you guys for bringing me back to earth -- when I hear about

white matter I start thinking about Alzheimer's, and oh man, can I go to

town from there. Yeesh. I need to think about something else, like where

I'm going to find a nice new menorah in Lubbock, TX.

*more hugs*

Em

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

It is the tale, not he who tells it.

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

Posted

Em,

Oh hon, I wish I could help ya out on this. I'm such a dummy

sometimes when it comes to all the jargon. I just wanted to say to

try to keep your head up and that you are in my prayers. If you need

anything, feel free to email me. Take care hon.

Love and Prayers,

Posted

Em,

Oh hon, I wish I could help ya out on this. I'm such a dummy

sometimes when it comes to all the jargon. I just wanted to say to

try to keep your head up and that you are in my prayers. If you need

anything, feel free to email me. Take care hon.

Love and Prayers,

Posted

Em, I'm reading the prescription that I'm to take to the MRI people and it reads

" MRI head and spine...double dose gd and flair...r/s MS...r/s Myelopathy.

I'm convinced that I'm going to drop dead any day now *lol* I told my mom that

he must really think I have MS because that's what he's looking for on the

MRI...do I buy a wheel chair now?? YIKES!!!!

I do tend to be a little bit of a drama queen =)

Anne

Re: Neuro developments

I know you're both so right. I knew I shouldn't even READ it, because it

would be filled with this medicalese that would sound awful to me. I'm

actually pretty good with most medical terminology, but I'm speaking in

broad terms -- now when you get to the nitty-gritty of neuro-speak, you've

lost me. Like this -- " There is increased T2 and FLAIR signal seen in the

deep white matter of the left frontal lobe and left parietal lobe with

extensive atrophy of the left parietal deep white matter and intact

overlying gray matter. These findings are suggestive of periventricular

leukomalacia related to a developmental vascular insult, I cannot

definitively rule out acquired microvascular disease. "

Excuse me -- translation please??? LOLOL! T2? FLAIR? What do those

stand for? At the same time, you say " extensive atrophy " and I know what

THAT means. And what in God's good green earth is a " developmental

vascular insult? " Somebody cussed at my veins when I was a baby???

It's two pages of this kind of talk, and I do not understand 90% of it. So

I guess I'll just wait till next week, talk to my neuro dude (I see Dr.

D'Cruz in Lubbock), and maybe eventually find out what that all means.

*HUGS* THank you guys for bringing me back to earth -- when I hear about

white matter I start thinking about Alzheimer's, and oh man, can I go to

town from there. Yeesh. I need to think about something else, like where

I'm going to find a nice new menorah in Lubbock, TX.

*more hugs*

Em

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

It is the tale, not he who tells it.

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

SEND POST TO: fibromyalgia-cfs

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

LIST OWNER: -owner

Posted

Em, I'm reading the prescription that I'm to take to the MRI people and it reads

" MRI head and spine...double dose gd and flair...r/s MS...r/s Myelopathy.

I'm convinced that I'm going to drop dead any day now *lol* I told my mom that

he must really think I have MS because that's what he's looking for on the

MRI...do I buy a wheel chair now?? YIKES!!!!

I do tend to be a little bit of a drama queen =)

Anne

Re: Neuro developments

I know you're both so right. I knew I shouldn't even READ it, because it

would be filled with this medicalese that would sound awful to me. I'm

actually pretty good with most medical terminology, but I'm speaking in

broad terms -- now when you get to the nitty-gritty of neuro-speak, you've

lost me. Like this -- " There is increased T2 and FLAIR signal seen in the

deep white matter of the left frontal lobe and left parietal lobe with

extensive atrophy of the left parietal deep white matter and intact

overlying gray matter. These findings are suggestive of periventricular

leukomalacia related to a developmental vascular insult, I cannot

definitively rule out acquired microvascular disease. "

Excuse me -- translation please??? LOLOL! T2? FLAIR? What do those

stand for? At the same time, you say " extensive atrophy " and I know what

THAT means. And what in God's good green earth is a " developmental

vascular insult? " Somebody cussed at my veins when I was a baby???

It's two pages of this kind of talk, and I do not understand 90% of it. So

I guess I'll just wait till next week, talk to my neuro dude (I see Dr.

D'Cruz in Lubbock), and maybe eventually find out what that all means.

*HUGS* THank you guys for bringing me back to earth -- when I hear about

white matter I start thinking about Alzheimer's, and oh man, can I go to

town from there. Yeesh. I need to think about something else, like where

I'm going to find a nice new menorah in Lubbock, TX.

*more hugs*

Em

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

It is the tale, not he who tells it.

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

SEND POST TO: fibromyalgia-cfs

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

LIST OWNER: -owner

Posted

At 12:36 PM 11/30/2001 -0600, Anne Scarborough wrote:

>I do tend to be a little bit of a drama queen =)

Oh I am sure that I do too! LOL! And man, I hope you do NOT have

MS. That is one of the things they are looking for for me, too. I do have

some plaque deposits, so I was upset to see that; it may be totally

unrelated, but it sorta freaked me. And look up " arachnoid cyst, " oh my

God, it sounds like my head will explode by the time I'm 40. LOLOLOL

If any of you have seen " Miss Congeniality, " you'll know why I'm now saying

" Dalai Lama, Dalai Lama " over and over again. LOLOL

And there's always " Kindergarten Cop. " " Probably a tumor. " " It's NOT A

TUMUH! "

*warm hugs to you great folks*

Em

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

It is the tale, not he who tells it.

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

Posted

<< I have just found out I have to have 4 MRI's because my neuro thinks I

might have MS...now that scares me to death and of course I've looked it up

on the Internet which has only freaked me out even more. >>

My sister and a couple of close friends have MS. My sister for at least40

years and is still hanging in there. She does what the doctor tells her and

she is taking those new shots which are working wonders on people with MS.

One of the others I see a lot of as we live in the same city. She also takes

the shots but she does not follow her doctors instructions. She drinks to

much, smokes to much and does not take the rest that she is supposed to be

getting. Stays of late partying and all ready had some complications.

The other friend lives a bit far away but does pretty well. She does smoke

and once in a while parties to late but is doing great.

What I am trying to say is that you have to do what is necessary for your

health with MS. Do as your doctor tells you to if you have MS. Some of the

things that I listed above are not necessary and I am not saying that you

drink, smoke and all the rest because I do not know. They are just examples

of the sort of thing that you need to do and not to do.

My sister has been in remisson for 30 years until just lately. They put her

on the shots and she is doing fine. You can do and live well with MS. My

sister is ample proof of that.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

Posted

<< I have just found out I have to have 4 MRI's because my neuro thinks I

might have MS...now that scares me to death and of course I've looked it up

on the Internet which has only freaked me out even more. >>

My sister and a couple of close friends have MS. My sister for at least40

years and is still hanging in there. She does what the doctor tells her and

she is taking those new shots which are working wonders on people with MS.

One of the others I see a lot of as we live in the same city. She also takes

the shots but she does not follow her doctors instructions. She drinks to

much, smokes to much and does not take the rest that she is supposed to be

getting. Stays of late partying and all ready had some complications.

The other friend lives a bit far away but does pretty well. She does smoke

and once in a while parties to late but is doing great.

What I am trying to say is that you have to do what is necessary for your

health with MS. Do as your doctor tells you to if you have MS. Some of the

things that I listed above are not necessary and I am not saying that you

drink, smoke and all the rest because I do not know. They are just examples

of the sort of thing that you need to do and not to do.

My sister has been in remisson for 30 years until just lately. They put her

on the shots and she is doing fine. You can do and live well with MS. My

sister is ample proof of that.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

Posted

<< I have just found out I have to have 4 MRI's because my neuro thinks I

might have MS...now that scares me to death and of course I've looked it up

on the Internet which has only freaked me out even more. >>

My sister and a couple of close friends have MS. My sister for at least40

years and is still hanging in there. She does what the doctor tells her and

she is taking those new shots which are working wonders on people with MS.

One of the others I see a lot of as we live in the same city. She also takes

the shots but she does not follow her doctors instructions. She drinks to

much, smokes to much and does not take the rest that she is supposed to be

getting. Stays of late partying and all ready had some complications.

The other friend lives a bit far away but does pretty well. She does smoke

and once in a while parties to late but is doing great.

What I am trying to say is that you have to do what is necessary for your

health with MS. Do as your doctor tells you to if you have MS. Some of the

things that I listed above are not necessary and I am not saying that you

drink, smoke and all the rest because I do not know. They are just examples

of the sort of thing that you need to do and not to do.

My sister has been in remisson for 30 years until just lately. They put her

on the shots and she is doing fine. You can do and live well with MS. My

sister is ample proof of that.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

Posted

Thanks Irene! I only know of one person who had MS...a friends father and he

died of it. Not exactly an encouring example =( My party days are over and

have been for a long time. I'm lucky if I can stay awake long enough to see the

news *lol* I rarely drink, never smoked, etc... I will do what the doctor

tells me. I won't know anything though until Dec. 27th.

Anne

Re: Neuro developments

<< I have just found out I have to have 4 MRI's because my neuro thinks I

might have MS...now that scares me to death and of course I've looked it up

on the Internet which has only freaked me out even more. >>

My sister and a couple of close friends have MS. My sister for at least40

years and is still hanging in there. She does what the doctor tells her and

she is taking those new shots which are working wonders on people with MS.

One of the others I see a lot of as we live in the same city. She also takes

the shots but she does not follow her doctors instructions. She drinks to

much, smokes to much and does not take the rest that she is supposed to be

getting. Stays of late partying and all ready had some complications.

The other friend lives a bit far away but does pretty well. She does smoke

and once in a while parties to late but is doing great.

What I am trying to say is that you have to do what is necessary for your

health with MS. Do as your doctor tells you to if you have MS. Some of the

things that I listed above are not necessary and I am not saying that you

drink, smoke and all the rest because I do not know. They are just examples

of the sort of thing that you need to do and not to do.

My sister has been in remisson for 30 years until just lately. They put her

on the shots and she is doing fine. You can do and live well with MS. My

sister is ample proof of that.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

Posted

Thanks Irene! I only know of one person who had MS...a friends father and he

died of it. Not exactly an encouring example =( My party days are over and

have been for a long time. I'm lucky if I can stay awake long enough to see the

news *lol* I rarely drink, never smoked, etc... I will do what the doctor

tells me. I won't know anything though until Dec. 27th.

Anne

Re: Neuro developments

<< I have just found out I have to have 4 MRI's because my neuro thinks I

might have MS...now that scares me to death and of course I've looked it up

on the Internet which has only freaked me out even more. >>

My sister and a couple of close friends have MS. My sister for at least40

years and is still hanging in there. She does what the doctor tells her and

she is taking those new shots which are working wonders on people with MS.

One of the others I see a lot of as we live in the same city. She also takes

the shots but she does not follow her doctors instructions. She drinks to

much, smokes to much and does not take the rest that she is supposed to be

getting. Stays of late partying and all ready had some complications.

The other friend lives a bit far away but does pretty well. She does smoke

and once in a while parties to late but is doing great.

What I am trying to say is that you have to do what is necessary for your

health with MS. Do as your doctor tells you to if you have MS. Some of the

things that I listed above are not necessary and I am not saying that you

drink, smoke and all the rest because I do not know. They are just examples

of the sort of thing that you need to do and not to do.

My sister has been in remisson for 30 years until just lately. They put her

on the shots and she is doing fine. You can do and live well with MS. My

sister is ample proof of that.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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