advertisement
Reply
 
Thread Tools Display Modes
Old 07-13-2009, 03:25 PM #1
diagnonsense diagnonsense is offline
Junior Member
 
Join Date: Jul 2008
Posts: 90
15 yr Member
diagnonsense diagnonsense is offline
Junior Member
 
Join Date: Jul 2008
Posts: 90
15 yr Member
Default Newest EMG worse than last, but don't understand it.

Ok, I got the dictation today.

It says:

"Findings: Distal latencies were prolonged and conduction velocities reduced in nearly all nerves tested. Ulnar SNAPS were reduced in amplitude. Peroneal and sural SNAPS were absent.

EMG of selected upper and lower extremity muscles was normal except for some reduced recruitment in the left FDI and gastrocnemius.

Conclusion: The is an abnormal study. There is electrophysiologic evidence of a primary demyelinating sensorimotor polyneuropathy with some secondary axonal loss on NCS, though there was no difinitive evidence of denervation on EMG."

.. MMKAY.

So I have zero clue what that means other than I now have 2 non-responsive nerves and a year ago I only had 1.

Does anyone have any clue does this EMG report line up with anything that they know of?

I go to neurology on Wednesday, and I just have a feeling now that she's going to tell me that she wants that darn nerve biopsy.
And I'm never going to get anywhere..

I hate to get all pesimistic.. but, its how I'm feeling ATM.
diagnonsense is offline   Reply With QuoteReply With Quote

advertisement
Old 07-13-2009, 04:04 PM #2
lynxgal lynxgal is offline
Junior Member
 
Join Date: Jan 2008
Location: Ottawa ON Canada
Posts: 96
15 yr Member
lynxgal lynxgal is offline
Junior Member
 
Join Date: Jan 2008
Location: Ottawa ON Canada
Posts: 96
15 yr Member
Default

My daughter's NCV stated something similar. It said primary demyelinating neuropathy. (didn't say anything about axonal loss and neither of us has had an EMG just the NCV).

As I have a confirmed demyelinating polyneuropathy I'm going to wager it is CMT.

Please post when you have seen the neurologist on Wednesday I am very anxious to hear what he has to say.
__________________
Charcot-Marie-Tooth Disease Type 1A
Fibromyalgia

Last edited by lynxgal; 07-13-2009 at 04:23 PM. Reason: added something
lynxgal is offline   Reply With QuoteReply With Quote
Old 07-13-2009, 07:49 PM #3
diagnonsense diagnonsense is offline
Junior Member
 
Join Date: Jul 2008
Posts: 90
15 yr Member
diagnonsense diagnonsense is offline
Junior Member
 
Join Date: Jul 2008
Posts: 90
15 yr Member
Default

Hey,
Just writing to say I got your message.
And I will keep you updated on what my neuro says.

Its bound to be interesting.

I'd actually be mighty surprised if I was told I had CMT, because I think the absense of response in those 2 nerves is whats known as a "conduction block".
Although, with CIDP the damage is often in the motor nerves there is a variant known as MADSAM which is a sensory and motor (which is the SAM).
diagnonsense is offline   Reply With QuoteReply With Quote
Old 07-13-2009, 09:01 PM #4
lynxgal lynxgal is offline
Junior Member
 
Join Date: Jan 2008
Location: Ottawa ON Canada
Posts: 96
15 yr Member
lynxgal lynxgal is offline
Junior Member
 
Join Date: Jan 2008
Location: Ottawa ON Canada
Posts: 96
15 yr Member
Default

I have a sensory nerve with no response. Are your reflexes still intact? I have lost reflex in one ankle. It went from "brisk" to no response in 8 months.

** correction to my earlier reply**** my daughters report said primary demyelinating motor and sensory neuropathy. *** sorry misquoted the report :P

My report says sensory motor neuropathy... at the time mine was more sensory.....now I think it is more motor.
__________________
Charcot-Marie-Tooth Disease Type 1A
Fibromyalgia

Last edited by lynxgal; 07-13-2009 at 09:08 PM. Reason: typo :P second time added something....
lynxgal is offline   Reply With QuoteReply With Quote
Old 07-13-2009, 09:27 PM #5
diagnonsense diagnonsense is offline
Junior Member
 
Join Date: Jul 2008
Posts: 90
15 yr Member
diagnonsense diagnonsense is offline
Junior Member
 
Join Date: Jul 2008
Posts: 90
15 yr Member
Default

I know they bang on me a lot to try to get one. And sometimes they can get them.
However, there is no reflex response in my feet.

Does CMT have reflex responses?
I don't think people with CIDP do.
diagnonsense is offline   Reply With QuoteReply With Quote
Old 07-13-2009, 09:30 PM #6
lynxgal lynxgal is offline
Junior Member
 
Join Date: Jan 2008
Location: Ottawa ON Canada
Posts: 96
15 yr Member
lynxgal lynxgal is offline
Junior Member
 
Join Date: Jan 2008
Location: Ottawa ON Canada
Posts: 96
15 yr Member
Default

If I remember correctly from my reading, it is hit and miss, some have reduced responses and some have absent and in some types of CMT there are mixed results.


I find it weird that I only have one reflex that is absent.
__________________
Charcot-Marie-Tooth Disease Type 1A
Fibromyalgia
lynxgal is offline   Reply With QuoteReply With Quote
Old 07-13-2009, 09:40 PM #7
diagnonsense diagnonsense is offline
Junior Member
 
Join Date: Jul 2008
Posts: 90
15 yr Member
diagnonsense diagnonsense is offline
Junior Member
 
Join Date: Jul 2008
Posts: 90
15 yr Member
Default

Ah, ok.
Thanks for the clarification.

I hope a diagnosis comes for all of us.
You, your daughter, and I..
Cause not knowing I think is the hardest part of all.

After that, well.. at least you have the long awaited answer.
diagnonsense is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Meet the Newest GrandMonkey!!! Curious Social Chat 34 03-10-2009 04:09 PM
Copies of my newest MRI... Momma's Kids Social Chat 12 02-02-2009 06:41 PM
Newest avatar whispers New Member Introductions 0 09-07-2008 01:09 PM
Hello from the newest member totanaca New Member Introductions 8 04-12-2008 04:08 PM
Meet Your Newest Moderator jccgf Gluten Sensitivity / Celiac Disease 25 09-28-2006 06:33 PM


All times are GMT -5. The time now is 05:29 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.