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Re: EMG Definitive?

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That has always been the test to verify that you do in fact have CMT. My

nero told me that the nerve conduction study also verified CMT or absence

of. Everything I have ever seen, said you had to be tested by a nero with

the (preferrable) EMG to have the diagnosis. That's all I really know -

just what the doctors have stated. Have no idea if it's a 100% or not,

except that my nero said it was.....

Screening at age 36

> > >

> > >

> > > Hello, I am 36 years of age and live in Melbourne, Australia. I have

> > > a

> > > sister and father with CMT. My sister, who is 32, is very severely

> > > affected. I show no signs of CMT, although sometimes I think my hands

> > > are very weak or uncoordinated. Two years ago my husband and I

> > > visited

> > > the genetics clinic at the major childrens teaching hospital for

> > > counselling. We are still considering a family. My knee reflexes were

> > > tested. Apart from that I was told they dont think I have CMT. I have

> > > always felt this summation was unsatisfactory. I wish there was a

> > > definitive test that could tell me if I have CMT. How rare is it that

> > > a person of my age would show no symptoms? Have I received the right

> > > counselling? I am afraid of pregnancy inducing CMT symptoms and

> > > therefore already exposed the fetus to a risk I am trying to prevent.

> > > I do not want to bring this upon someone, knowing the agony my sister

> > > has been through. Any thoughts or comments would be helpful,

> > > especially from those faced with the same dilemma.

> > >

> > >

> >

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> > > Get answers for the stuff you don't. And get $10 to spend on the site!

> > > http://click.egroups.com/1/2200/7/_/616793/_/956045113/

> >

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> > >

> > >

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<< That has always been the test to verify that you do in fact have CMT. My

neuro told me that the nerve conduction study also verified CMT or absence

of. Everything I have ever seen, said you had to be tested by a nero with

the (preferrable) EMG to have the diagnosis. That's all I really know - just

what the doctors have stated. Have no idea if it's a 100% or not, except

that my neuro said it was..... >>

True to a point, but in addition, as Barbara pointed out: In a message dated

4/20/00 5:52:36 AM, ranagan@... writes:

<< the nerve conduction studies and EMG, alone, are not definitive tests of

CMT.

Clinical observations are a very important compliment to a diagnosis. Testing

of reflexes, symmetry of face, occular movements, and blood work are

important for ruling out other neuromuscular disorders. Even when all of

these are done, I think that certain types of Spinal Muscular Atrophy present

on EMG and NCS the same as CMT. >>

And I added: Another factor that helps with diagnosis is family history.

Kat in Seattle

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<< That has always been the test to verify that you do in fact have CMT. My

neuro told me that the nerve conduction study also verified CMT or absence

of. Everything I have ever seen, said you had to be tested by a nero with

the (preferrable) EMG to have the diagnosis. That's all I really know - just

what the doctors have stated. Have no idea if it's a 100% or not, except

that my neuro said it was..... >>

True to a point, but in addition, as Barbara pointed out: In a message dated

4/20/00 5:52:36 AM, ranagan@... writes:

<< the nerve conduction studies and EMG, alone, are not definitive tests of

CMT.

Clinical observations are a very important compliment to a diagnosis. Testing

of reflexes, symmetry of face, occular movements, and blood work are

important for ruling out other neuromuscular disorders. Even when all of

these are done, I think that certain types of Spinal Muscular Atrophy present

on EMG and NCS the same as CMT. >>

And I added: Another factor that helps with diagnosis is family history.

Kat in Seattle

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<< That has always been the test to verify that you do in fact have CMT. My

neuro told me that the nerve conduction study also verified CMT or absence

of. Everything I have ever seen, said you had to be tested by a nero with

the (preferrable) EMG to have the diagnosis. That's all I really know - just

what the doctors have stated. Have no idea if it's a 100% or not, except

that my neuro said it was..... >>

True to a point, but in addition, as Barbara pointed out: In a message dated

4/20/00 5:52:36 AM, ranagan@... writes:

<< the nerve conduction studies and EMG, alone, are not definitive tests of

CMT.

Clinical observations are a very important compliment to a diagnosis. Testing

of reflexes, symmetry of face, occular movements, and blood work are

important for ruling out other neuromuscular disorders. Even when all of

these are done, I think that certain types of Spinal Muscular Atrophy present

on EMG and NCS the same as CMT. >>

And I added: Another factor that helps with diagnosis is family history.

Kat in Seattle

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Yes! All so true.... the family history, and all the other tests that

Barbara mentioned! Except the blood work - I have had them all at one time

or another. But, was easier for me, and we knew it was in our family. MDA

even wanted me to do a MRI to rule out MS (which I did). There is still

nothing easy nor definite about CMT, is there???

Hope you all have a great weekend!

Re: EMG Definitive?

>

>

> << That has always been the test to verify that you do in fact have CMT.

My

> neuro told me that the nerve conduction study also verified CMT or absence

> of. Everything I have ever seen, said you had to be tested by a nero with

> the (preferrable) EMG to have the diagnosis. That's all I really know -

just

> what the doctors have stated. Have no idea if it's a 100% or not, except

> that my neuro said it was..... >>

>

> True to a point, but in addition, as Barbara pointed out: In a message

dated

> 4/20/00 5:52:36 AM, ranagan@... writes:

>

> << the nerve conduction studies and EMG, alone, are not definitive tests

of

> CMT.

> Clinical observations are a very important compliment to a diagnosis.

Testing

> of reflexes, symmetry of face, occular movements, and blood work are

> important for ruling out other neuromuscular disorders. Even when all of

> these are done, I think that certain types of Spinal Muscular Atrophy

present

> on EMG and NCS the same as CMT. >>

>

> And I added: Another factor that helps with diagnosis is family history.

>

> Kat in Seattle

>

>

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> ------------------------------------------------------------------------

>

>

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