Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS.


advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 12-17-2010, 02:12 PM #1
Stellatum Stellatum is offline
Senior Member
 
Join Date: Feb 2010
Posts: 1,215
10 yr Member
Stellatum Stellatum is offline
Senior Member
 
Join Date: Feb 2010
Posts: 1,215
10 yr Member
Default learned some new stuff about MG (passing on the info)

I saw my regular neuro today, who to my great relief accepted the Boston neuro's diagnosis. I am seronegative, my other SFEMGs were inconclusive, and my symptoms are atypical (my worst one is a swaying gait). So I was hard to diagnose. Here's what I learned:

--the Boston neuro who did my SFEMG did a special kind called a "stimulated" SFEMG. Instead of clenching my muscles, he had electrodes on my face. Evidently there are only a few doctors who know how to do these. It must be quite a test, because to him it was very clearly abnormal, though the regular SFEMGs on my arms and legs came back inconclusive. I highly recommend this doctor, who is experienced enough to make a clinical diagnosis under such circumstances. Anyone who wants to know details about him can send me a private message.

--the pulling in my eye may have been caused by the Mestinon. I haven't had it since I went off the Mestinon, anyway.

--Imuran is a good treatment for someone like me whose symptoms aren't urgent. I breathe and swallow fine, and I don't fall. I prefer a safer, slower treatment under these conditions, which made sense to my neuro.

--He thinks I should take the Mestinon even though I'm not convinced it's helping. It may be that in conjunction with the Imuran, it will help, and that will allow me to take less Imuran. Makes sense to me.

--I have Cogan's lid twitch. The Boston neuro caught it. My regular neuro hadn't heard of it. I think Annie on this list has described it. Look down. Now look up quickly. If you have Cogan's lid twitch, your ptotic lid will go up higher than your other eyelid before settling back down into its old ptotic state. Since I don't have noticeable ptosis--maybe a touch, or maybe my left eye was always like this--it's super-cool that the Boston neuro caught this!

--my current neuro knew enough to have my blood tested to make sure I can tolerate the Imuran before starting me on it. Annie warned me about that. While my doctors are secretly studying me, I am secretly studying them <evil laughter>. I'm happy my neuro passed.

Abby
Stellatum is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
suev (12-18-2010)
 


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
Info I learned from PN Support Group last night MelodyL Peripheral Neuropathy 7 11-23-2009 10:18 PM
Passing on some info from my neuro ras1256 Myasthenia Gravis 2 03-14-2009 11:21 PM
Found the cause of my passing out!!!!! InHisHands Reflex Sympathetic Dystrophy (RSD and CRPS) 10 06-29-2007 06:42 PM
Not My Own, Just Passing Along! vlhperry Parkinson's Disease 1 02-27-2007 06:35 AM
Passing out smiles BobbyB ALS 0 02-02-2007 08:04 AM


All times are GMT -5. The time now is 01:21 AM.

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.