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Posted

My 25 month old son had an MRI & EEG the other day after being

referred to a pediatric neurologist due to his delayed speech. He

babbles, but has no actual vocabulary. Sometimes he'll repeat what we

say, but it's rare. His hearing is fine, and he's working with a

speech therapist and special education teacher provided through Early

Intervention. I would appreciate any feedback from others who have had

these tests performed on their children. How long does it take to

interpret the tests and what sort of informtion do these tests provide.

Thank you........

T64

Posted

hi! my son is currently ungoing the same tests. we had the EEG last week and

this week we did the MRI. the EEG lady told us that his brain waves were

beautiful but we could see a minor gap in them when he would attempt speech. my

son will be 4 next month and my 2 year old talks better than he does. his

neurologist told us that she wanted the tests done to more or less see if there

is any explanation as to WHY he has a speech disorder, ie.. brain damage,

epelepsy, or some type of nuerological problem that has been inflicted....i knew

that he had not had a head injury so i knew that the problem started at birth if

not before, but it is all in the name of research i guess so maybe they can find

a cause and a " fix " for our little ones. i honestly believe that my sons tests

were ordered and done for precautionary purposes...but i do not know. we just

did the MRI yesterday, so i will know something on that the first of next week

when we go back to the doctor. Did they have to

sedate your little one for the MRI? they did mine so that he would lay

still...i hate that...i hope that this has been of some kind of help...although

i think i have just as many questions as you do....lol. well good luck, and keep

us posted on what you find out as i will do the same about my little jacob.

With love for all of us parents,

's mom

Leah

With Love Always,

Tommie Leah

[ ] MRI & EEG

My 25 month old son had an MRI & EEG the other day after being

referred to a pediatric neurologist due to his delayed speech. He

babbles, but has no actual vocabulary. Sometimes he'll repeat what we

say, but it's rare. His hearing is fine, and he's working with a

speech therapist and special education teacher provided through Early

Intervention. I would appreciate any feedback from others who have had

these tests performed on their children. How long does it take to

interpret the tests and what sort of informtion do these tests provide.

Thank you........

T64

________________________________________________________________________________\

____

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Posted

Hi-

We have had 3 MRI's and they take only a couple days to get a

preliminary report on usually. I would just call the neuro's office

and a couple days after the test to see if they have any results yet.

The dr. should be able to tell you the basics over the phone. Waiting

for a follow-up appt. for results is torture! No experience with the

EEG.

Katrina

>

> My 25 month old son had an MRI & EEG the other day after being

> referred to a pediatric neurologist due to his delayed speech. He

> babbles, but has no actual vocabulary. Sometimes he'll repeat what we

> say, but it's rare. His hearing is fine, and he's working with a

> speech therapist and special education teacher provided through Early

> Intervention. I would appreciate any feedback from others who have

had

> these tests performed on their children. How long does it take to

> interpret the tests and what sort of informtion do these tests

provide.

> Thank you........

> T64

>

Posted

Hi-

We have had 3 MRI's and they take only a couple days to get a

preliminary report on usually. I would just call the neuro's office

and a couple days after the test to see if they have any results yet.

The dr. should be able to tell you the basics over the phone. Waiting

for a follow-up appt. for results is torture! No experience with the

EEG.

Katrina

>

> My 25 month old son had an MRI & EEG the other day after being

> referred to a pediatric neurologist due to his delayed speech. He

> babbles, but has no actual vocabulary. Sometimes he'll repeat what we

> say, but it's rare. His hearing is fine, and he's working with a

> speech therapist and special education teacher provided through Early

> Intervention. I would appreciate any feedback from others who have

had

> these tests performed on their children. How long does it take to

> interpret the tests and what sort of informtion do these tests

provide.

> Thank you........

> T64

>

Posted

We've been through both. The MRI results were available the

following day, and the EEG results took about a week (though the

consulting neurologist was on the other side of the country, so i'm

sure that was a factor).

I should tell you that we had divergent opinions about the EEG

results. All THREE neurologists agreed that it was not normal, but

it took multiple consultations to get consensus on whether or not to

treat. One neurologist that we met with said that these types of

abnormalities are common in young kids with " these kinds of issues, "

and, since we were not SEEING any seizures (they were all happening

in his sleep) that he didn't want to treat them.

We, needless to say, got another opinion and decided to treat them

with Depakote. It has been a life changing experience for our son.

He is a brand-new kid.

We also learned that neurology is much more about opinions than one

would think or like it to be.

Good luck!

(mom to - 3 years old on monday - verbal apraxia & that's all

now that he's seizure-free!)

>

> >

> > My 25 month old son had an MRI & EEG the other day after being

> > referred to a pediatric neurologist due to his delayed speech.

He

> > babbles, but has no actual vocabulary. Sometimes he'll repeat

what we

> > say, but it's rare. His hearing is fine, and he's working with a

> > speech therapist and special education teacher provided through

Early

> > Intervention. I would appreciate any feedback from others who

have

> had

> > these tests performed on their children. How long does it take

to

> > interpret the tests and what sort of informtion do these tests

> provide.

> > Thank you........

> > T64

> >

>

Posted

We've been through both. The MRI results were available the

following day, and the EEG results took about a week (though the

consulting neurologist was on the other side of the country, so i'm

sure that was a factor).

I should tell you that we had divergent opinions about the EEG

results. All THREE neurologists agreed that it was not normal, but

it took multiple consultations to get consensus on whether or not to

treat. One neurologist that we met with said that these types of

abnormalities are common in young kids with " these kinds of issues, "

and, since we were not SEEING any seizures (they were all happening

in his sleep) that he didn't want to treat them.

We, needless to say, got another opinion and decided to treat them

with Depakote. It has been a life changing experience for our son.

He is a brand-new kid.

We also learned that neurology is much more about opinions than one

would think or like it to be.

Good luck!

(mom to - 3 years old on monday - verbal apraxia & that's all

now that he's seizure-free!)

>

> >

> > My 25 month old son had an MRI & EEG the other day after being

> > referred to a pediatric neurologist due to his delayed speech.

He

> > babbles, but has no actual vocabulary. Sometimes he'll repeat

what we

> > say, but it's rare. His hearing is fine, and he's working with a

> > speech therapist and special education teacher provided through

Early

> > Intervention. I would appreciate any feedback from others who

have

> had

> > these tests performed on their children. How long does it take

to

> > interpret the tests and what sort of informtion do these tests

> provide.

> > Thank you........

> > T64

> >

>

Posted

An excellent doc from which to seek a second opinion is Young Park at Augusta

Teaching Hospital in Georgia. People fly to him from all over the country (and

world). He was the first and only doc who saw my sons EEG and MRI and

immediately asked if he had ever had sleep walking or night terrors. This had

never even been an issue with any other doctor before. It turns out that my son

(and another diagnosed years later as was I) has a hereditary sleep seizure

syndrome which can manifest in young children as sleep terrors then as sleep

walking. My son was 14 and suffered a brain injury before this diagnosis.

Every other doctor had indicated that sleep terrors are common and need no

concern.

Brigett

michellerichardslavin <michellelavin@...> wrote:

We've been through both. The MRI results were available the

following day, and the EEG results took about a week (though the

consulting neurologist was on the other side of the country, so i'm

sure that was a factor).

I should tell you that we had divergent opinions about the EEG

results. All THREE neurologists agreed that it was not normal, but

it took multiple consultations to get consensus on whether or not to

treat. One neurologist that we met with said that these types of

abnormalities are common in young kids with " these kinds of issues, "

and, since we were not SEEING any seizures (they were all happening

in his sleep) that he didn't want to treat them.

We, needless to say, got another opinion and decided to treat them

with Depakote. It has been a life changing experience for our son.

He is a brand-new kid.

We also learned that neurology is much more about opinions than one

would think or like it to be.

Good luck!

(mom to - 3 years old on monday - verbal apraxia & that's all

now that he's seizure-free!)

>

> >

> > My 25 month old son had an MRI & EEG the other day after being

> > referred to a pediatric neurologist due to his delayed speech.

He

> > babbles, but has no actual vocabulary. Sometimes he'll repeat

what we

> > say, but it's rare. His hearing is fine, and he's working with a

> > speech therapist and special education teacher provided through

Early

> > Intervention. I would appreciate any feedback from others who

have

> had

> > these tests performed on their children. How long does it take

to

> > interpret the tests and what sort of informtion do these tests

> provide.

> > Thank you........

> > T64

> >

>

__________________________________________________

Posted

As the mom of a child with epilepsy we have done numerous EEGs and MRIs.

I would think for kids with apraxia it would be important to have a PET

scan done. An MRI checks brain structure (ie. my son has a lesion in his

speech center). The PET scan checks brain function (ie. that the lesion

is dead cells and has no function). A further brain biopsy confirmed

this finding.

Hope that makes sense. I am a lurker, just trying to pick up some tips

in helping the speech of my other son who has PDD-NOS.

Jen

Posted

Hi ,

I wanted to go off line and ask if you are seeing neuros at CHildren's in

Boston by any chance? If you are at Boston do you have any recommendations,

good or bad, for a neuro there?

thanks

michellerichardslavin <michellelavin@...> wrote:

We've been through both. The MRI results were available the

following day, and the EEG results took about a week (though the

consulting neurologist was on the other side of the country, so i'm

sure that was a factor).

I should tell you that we had divergent opinions about the EEG

results. All THREE neurologists agreed that it was not normal, but

it took multiple consultations to get consensus on whether or not to

treat. One neurologist that we met with said that these types of

abnormalities are common in young kids with " these kinds of issues, "

and, since we were not SEEING any seizures (they were all happening

in his sleep) that he didn't want to treat them.

We, needless to say, got another opinion and decided to treat them

with Depakote. It has been a life changing experience for our son.

He is a brand-new kid.

We also learned that neurology is much more about opinions than one

would think or like it to be.

Good luck!

(mom to - 3 years old on monday - verbal apraxia & that's all

now that he's seizure-free!)

>

> >

> > My 25 month old son had an MRI & EEG the other day after being

> > referred to a pediatric neurologist due to his delayed speech.

He

> > babbles, but has no actual vocabulary. Sometimes he'll repeat

what we

> > say, but it's rare. His hearing is fine, and he's working with a

> > speech therapist and special education teacher provided through

Early

> > Intervention. I would appreciate any feedback from others who

have

> had

> > these tests performed on their children. How long does it take

to

> > interpret the tests and what sort of informtion do these tests

> provide.

> > Thank you........

> > T64

> >

>

Posted

Hi ,

I wanted to go off line and ask if you are seeing neuros at CHildren's in

Boston by any chance? If you are at Boston do you have any recommendations,

good or bad, for a neuro there?

thanks

michellerichardslavin <michellelavin@...> wrote:

We've been through both. The MRI results were available the

following day, and the EEG results took about a week (though the

consulting neurologist was on the other side of the country, so i'm

sure that was a factor).

I should tell you that we had divergent opinions about the EEG

results. All THREE neurologists agreed that it was not normal, but

it took multiple consultations to get consensus on whether or not to

treat. One neurologist that we met with said that these types of

abnormalities are common in young kids with " these kinds of issues, "

and, since we were not SEEING any seizures (they were all happening

in his sleep) that he didn't want to treat them.

We, needless to say, got another opinion and decided to treat them

with Depakote. It has been a life changing experience for our son.

He is a brand-new kid.

We also learned that neurology is much more about opinions than one

would think or like it to be.

Good luck!

(mom to - 3 years old on monday - verbal apraxia & that's all

now that he's seizure-free!)

>

> >

> > My 25 month old son had an MRI & EEG the other day after being

> > referred to a pediatric neurologist due to his delayed speech.

He

> > babbles, but has no actual vocabulary. Sometimes he'll repeat

what we

> > say, but it's rare. His hearing is fine, and he's working with a

> > speech therapist and special education teacher provided through

Early

> > Intervention. I would appreciate any feedback from others who

have

> had

> > these tests performed on their children. How long does it take

to

> > interpret the tests and what sort of informtion do these tests

> provide.

> > Thank you........

> > T64

> >

>

Posted

An excellent doc from which to seek a second opinion is Young Park at Augusta

Teaching Hospital in Georgia. People fly to him from all over the country (and

world). He was the first and only doc who saw my sons EEG and MRI and

immediately asked if he had ever had sleep walking or night terrors. This had

never even been an issue with any other doctor before. It turns out that my son

(and another diagnosed years later as was I) has a hereditary sleep seizure

syndrome which can manifest in young children as sleep terrors then as sleep

walking. My son was 14 and suffered a brain injury before this diagnosis.

Every other doctor had indicated that sleep terrors are common and need no

concern.

Brigett

michellerichardslavin <michellelavin@...> wrote:

We've been through both. The MRI results were available the

following day, and the EEG results took about a week (though the

consulting neurologist was on the other side of the country, so i'm

sure that was a factor).

I should tell you that we had divergent opinions about the EEG

results. All THREE neurologists agreed that it was not normal, but

it took multiple consultations to get consensus on whether or not to

treat. One neurologist that we met with said that these types of

abnormalities are common in young kids with " these kinds of issues, "

and, since we were not SEEING any seizures (they were all happening

in his sleep) that he didn't want to treat them.

We, needless to say, got another opinion and decided to treat them

with Depakote. It has been a life changing experience for our son.

He is a brand-new kid.

We also learned that neurology is much more about opinions than one

would think or like it to be.

Good luck!

(mom to - 3 years old on monday - verbal apraxia & that's all

now that he's seizure-free!)

>

> >

> > My 25 month old son had an MRI & EEG the other day after being

> > referred to a pediatric neurologist due to his delayed speech.

He

> > babbles, but has no actual vocabulary. Sometimes he'll repeat

what we

> > say, but it's rare. His hearing is fine, and he's working with a

> > speech therapist and special education teacher provided through

Early

> > Intervention. I would appreciate any feedback from others who

have

> had

> > these tests performed on their children. How long does it take

to

> > interpret the tests and what sort of informtion do these tests

> provide.

> > Thank you........

> > T64

> >

>

__________________________________________________

Posted

As the mom of a child with epilepsy we have done numerous EEGs and MRIs.

I would think for kids with apraxia it would be important to have a PET

scan done. An MRI checks brain structure (ie. my son has a lesion in his

speech center). The PET scan checks brain function (ie. that the lesion

is dead cells and has no function). A further brain biopsy confirmed

this finding.

Hope that makes sense. I am a lurker, just trying to pick up some tips

in helping the speech of my other son who has PDD-NOS.

Jen

Posted

Hi ,

I wanted to go off line and ask if you are seeing neuros at CHildren's in

Boston by any chance? If you are at Boston do you have any recommendations,

good or bad, for a neuro there?

thanks

michellerichardslavin <michellelavin@...> wrote:

We've been through both. The MRI results were available the

following day, and the EEG results took about a week (though the

consulting neurologist was on the other side of the country, so i'm

sure that was a factor).

I should tell you that we had divergent opinions about the EEG

results. All THREE neurologists agreed that it was not normal, but

it took multiple consultations to get consensus on whether or not to

treat. One neurologist that we met with said that these types of

abnormalities are common in young kids with " these kinds of issues, "

and, since we were not SEEING any seizures (they were all happening

in his sleep) that he didn't want to treat them.

We, needless to say, got another opinion and decided to treat them

with Depakote. It has been a life changing experience for our son.

He is a brand-new kid.

We also learned that neurology is much more about opinions than one

would think or like it to be.

Good luck!

(mom to - 3 years old on monday - verbal apraxia & that's all

now that he's seizure-free!)

>

> >

> > My 25 month old son had an MRI & EEG the other day after being

> > referred to a pediatric neurologist due to his delayed speech.

He

> > babbles, but has no actual vocabulary. Sometimes he'll repeat

what we

> > say, but it's rare. His hearing is fine, and he's working with a

> > speech therapist and special education teacher provided through

Early

> > Intervention. I would appreciate any feedback from others who

have

> had

> > these tests performed on their children. How long does it take

to

> > interpret the tests and what sort of informtion do these tests

> provide.

> > Thank you........

> > T64

> >

>

Posted

Hi ,

I wanted to go off line and ask if you are seeing neuros at CHildren's in

Boston by any chance? If you are at Boston do you have any recommendations,

good or bad, for a neuro there?

thanks

michellerichardslavin <michellelavin@...> wrote:

We've been through both. The MRI results were available the

following day, and the EEG results took about a week (though the

consulting neurologist was on the other side of the country, so i'm

sure that was a factor).

I should tell you that we had divergent opinions about the EEG

results. All THREE neurologists agreed that it was not normal, but

it took multiple consultations to get consensus on whether or not to

treat. One neurologist that we met with said that these types of

abnormalities are common in young kids with " these kinds of issues, "

and, since we were not SEEING any seizures (they were all happening

in his sleep) that he didn't want to treat them.

We, needless to say, got another opinion and decided to treat them

with Depakote. It has been a life changing experience for our son.

He is a brand-new kid.

We also learned that neurology is much more about opinions than one

would think or like it to be.

Good luck!

(mom to - 3 years old on monday - verbal apraxia & that's all

now that he's seizure-free!)

>

> >

> > My 25 month old son had an MRI & EEG the other day after being

> > referred to a pediatric neurologist due to his delayed speech.

He

> > babbles, but has no actual vocabulary. Sometimes he'll repeat

what we

> > say, but it's rare. His hearing is fine, and he's working with a

> > speech therapist and special education teacher provided through

Early

> > Intervention. I would appreciate any feedback from others who

have

> had

> > these tests performed on their children. How long does it take

to

> > interpret the tests and what sort of informtion do these tests

> provide.

> > Thank you........

> > T64

> >

>

Posted

They did have to sedate him which I think was the worst part as they

had to stab him in 3 different places to get the IV in. He looked so

tiny and helpless in that big machine. He was awake for about a half

hour after the procedure after they brought him out of anaesthesia,

but he fell asleep in the car and actually slept for 13 hours with the

EEG " cap " on his head. As soon as he woke up, he started clawing at

it, and I took it off, so the only reading they'll get is from a sleep

state. God, I hope we don't have to go through that again! We'll call

today and see if they have any results available.

Thanks for your input. It helps to know I'm not alone in dealing with

this.

Tracey

Posted

They did have to sedate him which I think was the worst part as they

had to stab him in 3 different places to get the IV in. He looked so

tiny and helpless in that big machine. He was awake for about a half

hour after the procedure after they brought him out of anaesthesia,

but he fell asleep in the car and actually slept for 13 hours with the

EEG " cap " on his head. As soon as he woke up, he started clawing at

it, and I took it off, so the only reading they'll get is from a sleep

state. God, I hope we don't have to go through that again! We'll call

today and see if they have any results available.

Thanks for your input. It helps to know I'm not alone in dealing with

this.

Tracey

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