advertisement
Reply
 
Thread Tools Display Modes
Old 08-28-2011, 05:27 PM #21
mrsD's Avatar
mrsD mrsD is offline
Wisest Elder Ever
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
mrsD mrsD is offline
Wisest Elder Ever
mrsD's Avatar
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
Lightbulb

Quote:
Originally Posted by JB63 View Post
to be twitching 24 hours a day. I know what you are going through and it is a real ****** and quite frightening wondering what the heck is happening.

I started in March 2011 4 months after my weakness and foot drop started I was given a BFS diagnosis too, even with foot drop, weakness, and abnormal EMG, idiopathic PN. After much time and almost begging for an explaination, tired of hearing "don't worry" I was told the BFS was a response to my irritated and very irritable nervous system.

I took mag ox which really did not help and learned to live with them. I am no longer anxious about them, they are disruptive at night but....like many others
I was just started on Lyrica for neuropathic pain and tho' I hate the side effects, my fasics greatly decreased in intensity and they are occuring much less. Took the med for a week before the improvement. Individual response to Lyrica is varied, quite frankly if I was offered the medication strictly for fasiculations, I would chose to twitch.
MagOx does not work. It is not absorbed from the GI tract.

I'd suggest the topical lotion we are using now... CVS Epsom Lotion, or a chelated form of oral magnesium. You will be very surprised at how it works!
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei

************************************

.
Weezie looking at petunias 8.25.2017


****************************
These forums are for mutual support and information sharing only. The forums are 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.
mrsD is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
JB63 (08-31-2011)

advertisement
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
LDN and fasciculations homer80 Multiple Sclerosis 4 02-05-2010 11:01 PM
Fasciculations dtyree General Health Conditions & Rare Disorders 7 06-18-2009 12:25 PM
Firing pattern of fasciculations in ALS BobbyB ALS News & Research 0 01-29-2008 07:55 AM
Confusing dx MG with fasciculations perrie Myasthenia Gravis 1 10-14-2007 07:31 PM
fasciculations BobbyB ALS News & Research 0 07-20-2007 12:49 PM


All times are GMT -5. The time now is 01:53 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.