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


advertisement
Reply
 
Thread Tools Display Modes
Old 11-18-2011, 09:21 PM #1
GrannyJo4 GrannyJo4 is offline
Junior Member
 
Join Date: Aug 2011
Posts: 35
10 yr Member
GrannyJo4 GrannyJo4 is offline
Junior Member
 
Join Date: Aug 2011
Posts: 35
10 yr Member
Default Has anyone here have a stimulation test?

When I go for my 2nd opinion the nurse said they are going to do a stimulater test on me, is it like a EMG or SFEMG?

I just don't know if it would be worth the pain, unless it would tell them exactly whats wrong with my swallowing.
GrannyJo4 is offline   Reply With QuoteReply With Quote

advertisement
Old 11-19-2011, 08:17 PM #2
suev suev is offline
Member
 
Join Date: Jun 2009
Location: Texas
Posts: 748
10 yr Member
suev suev is offline
Member
 
Join Date: Jun 2009
Location: Texas
Posts: 748
10 yr Member
Default

I have no first hand info...but looked up the test on the internet. Apparently it is not painful - like SFEMG can be. They use mild electrical stimulation near the salivary glands in the neck to see if they can cause a swallow response. From what I gather, it can help them figure out where the 'swallow signal' may be getting lost.

Good luck and pls let us know how it goes.
suev is offline   Reply With QuoteReply With Quote
Old 11-19-2011, 08:45 PM #3
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

I'm not sure what you mean. I had a "stimulated SFEMG," which got me a diagnosis after the two normal SFEMGs came back unclear. The stimulated SFEMG was just like the other SFEMGs except instead of telling me to slightly clench my muscles, they put electrodes on my face and sent pulses of electricity to make the muscles twitch.

These pulses of electricity were not in the least painful. They were very mild. It just felt like when your muscle twitches on its own. It doesn't feel like a shock.

I'm not sure this is the test you're having.

Abby
Stellatum is offline   Reply With QuoteReply With Quote
Old 11-19-2011, 08:49 PM #4
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

Sorry, I somehow missed suev's response. She sounds like she's talking about the test you're going to have. I hope it goes well, and makes things clear to your doctors!

A.
Stellatum is offline   Reply With QuoteReply With Quote
Old 11-22-2011, 08:37 PM #5
slip slip is offline
Junior Member
 
Join Date: Aug 2011
Location: Ontario Canada
Posts: 12
10 yr Member
slip slip is offline
Junior Member
 
Join Date: Aug 2011
Location: Ontario Canada
Posts: 12
10 yr Member
Default

I didn't know that the test I was given was SFEMG, but now I know.
They did it in the muscle under my left eye and the "shock" they give to see how the muscles react was extremely painful (could have just been because of the area the needle was inserted, but I don't know)
I could not see myself but it felt like I was shaking like someone having a seizer.
Not trying to be dramatic, but this was my experience,
My recommendation would be to get what ever test needed to help with your condition.
It only pains when the shock is given, which was between 1/2-1 hour off and on. (didn't have a watch, just making a educated guess)

good luck

randy
slip is offline   Reply With QuoteReply With Quote
Reply

Thread Tools
Display Modes

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
Spinal Cord Stimulation Harry Spinal Disorders & Back Pain 43 10-08-2010 12:01 PM
PHOTONIC STIMULATIOn Steff Peripheral Neuropathy 10 03-26-2010 06:05 PM
Alpha Stimulation??? dogodlvr Bipolar Disorder 5 02-04-2010 12:35 AM
Functional Electrical Stimulation (FES) sha aus Multiple Sclerosis 6 03-24-2009 05:35 PM


All times are GMT -5. The time now is 02:23 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.