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Old 07-24-2018, 03:34 PM #1
NAVARIO NAVARIO is offline
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Default I got two repetitive emg, one positive and one negative, which one belive?

Hi.

First i would like to introduce myself, Im Navario from Spain. English is not my first lenguage so please be patient.

As the tittle says i had an emg 1 month ago which was positive in my face. I had another today with another doctor because my neurologist wanted to confirm it since im seronegative

The doctor who did it said that all seemed to be normal but she will have to analize information.

I dont know what to believe, am I crazy or there was a mistake in the first one or in the second?

Thanks for your time
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AnnieB3 (07-24-2018)
Old 07-24-2018, 04:28 PM #2
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Hi Navario

Welcome to NeuroTalk .

The MG forum is very active so I am sure that you will get lots of support and helpful suggestions from other members.

Best wishes.
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Old 07-24-2018, 06:01 PM #3
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Quote:
Originally Posted by kiwi33 View Post
Hi Navario

Welcome to NeuroTalk .

The MG forum is very active so I am sure that you will get lots of support and helpful suggestions from other members.

Best wishes.

Thanks Kiwi

I know there are lot of people here who can help, have been reading you for a while.

Thanks for your words
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Old 07-24-2018, 09:47 PM #4
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Seems like the drs would want a third one to see which way it points..
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Old 07-24-2018, 10:30 PM #5
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Hi, Navario! Welcome to the forum!!

No worries, your words came across very clearly! I don't speak Spanish, so I hope I'm writing well enough for you!

Did the doctors run the MuSK antibody test? LRP4? Those are the two newest tests, other than the Acetylcholine Receptor Antibody one.

Did you have the 2nd EMG on your face or in another area? Is there anyone in your area who can do a Single Fiber EMG? Bruno Eymard in France does them. Well, a colleague of his does. He does the clinical exams.

Bruno Eymard – ERN-EURO-NMD

EMGs can fluctuate over time. If the first test was highly positive, then they really can't discount that result just due to the 2nd one being negative. Results depend upon what muscle they are using, what drugs someone is on (steroids and other immune suppressants can make the results look normal when they are not), and the experience of the person doing the test.

What are your symptoms?

MG is pretty easy to spot, since only MG, CMSs, and LEMS show fatigable muscle weakness.

What else can we do to help you?

Doctors in Europe are pretty familiar with MG. Are you confident in your neurologist? I hope so!

Take it easy until you know what is going on for sure.


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Old 07-25-2018, 04:30 AM #6
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Wow Annie!

i wasnt expecting that explanation. Thanks

My first EMG was done in the right hand in my eye. The one in the hand showed a decrement of like 6 or 7 % which was normal to the doctor who did it.

The one in my eye showed a decrement of near 20% so he said it was clearly abnormal. It was much more painfull and longer than the one i was done before.

The point is that I havenīt symptoms in my face but the first doctor said that it was not needed and that the face was the place where it was more easy to detect since it is a small muscle.

I have got proximal weakness which is better when day starts and worse when finish and they did the test because they found thymic hyperplasia in a tac.

Regarding SFEMG, i think doctor tried yesterday to in the frontal muscle of my head, but she didint seem to know much about it, she told me that it was hard to do and that she would need my help and when we finished she told me that she didnt know if she could take much information from there.

From my point of view the first one knew much more about it than the second one.

I started taking mestinon yesterday and i felt great, but i dont know if it could be placebo or not.

Thanks for your help Annie.

Navario.
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