Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

Reply
 
Thread Tools Display Modes
Old 04-09-2007, 07:05 AM #1
frogga's Avatar
frogga frogga is offline
Member
 
Join Date: Nov 2006
Location: UK
Posts: 830
15 yr Member
frogga frogga is offline
Member
frogga's Avatar
 
Join Date: Nov 2006
Location: UK
Posts: 830
15 yr Member
Default

Hey Ina...

Personally (And only my opinion) I will NEVER have an EMG again. I had one a year ago when the drs decided that "RSD can't do this to a person so it's got to be some neurodegenerative disease" sort of thing and we agreed because of the pain involved that they would only do one arm... however, this was over a year ago and led to one of my worst ever flares which I still haven't got over (it managed to escalate the RSD to a whole new level)....

BUT... to balance this out, I know many people that have had EMG's and expereinced no problems other than raised pain levels for a couple of days after the investigation....

So.. whatever you go for.. Good luck...

is the numbness intermittent or constant? have you found that the it co incides with blackness?

Love

Froggsy xxxxxxxxxxxxxx
__________________
It's always darkest just before dawn... but smile and the world smiles with you, cry and you cry alone
frogga is offline   Reply With QuoteReply With Quote
Old 04-09-2007, 08:13 AM #2
carousel carousel is offline
Junior Member
 
Join Date: Dec 2006
Posts: 33
15 yr Member
carousel carousel is offline
Junior Member
 
Join Date: Dec 2006
Posts: 33
15 yr Member
Default

HI Artist and Frogga, Thank you so very much for the replies. I need some "boost" in me so i do the right thing. I have quite a few diagnoses that came more recently that my attention has been on them ( treatment for a brain tumour (benign but serious as they say, but if contolled, whch it appears to be at this point,then may only leave me with a few side issues)and at last count 3-4 heart issues including atrial fib)and so i spend less time on rsd although i do read here in chunks and have been following some posts. You put it very well artist... end thing being what if they find nothing and i end up with leg probs big time again.

Frogga, You are one strong young woman and have so much helpful to say here which i know helps so many.

I have to run now or i will be late, but thanks again for giving me a morale boost this morning as for the first time in a long time i am actually nervous about this whole thing...

Forgot to say that oh yes, I had the rsd diagnosis many years ago now and have gone through the hell of that plus episodes that are quite debilitating even the last year.My gp is test happy since my brain finding (he had never met any one with mine so missed it) and he and i never talk about rsd although he gives me meds and i keep him updated on what goes on. All of a sudden now I am forced to recall all the rsd stuff which i wiould be happy to keep in denial (i.e not think about it haha)..so to speak what with everything else.

hugs,
Ina
carousel 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
Since the server will be down tomorrow.... Mrs. Bear Bipolar Disorder 5 03-24-2007 11:43 AM
Nervous for tomorrow wishfulthinking Depression 14 12-11-2006 09:03 PM
EMG Tomorrow arrigoar ALS 6 11-10-2006 12:28 PM


All times are GMT -5. The time now is 07:20 AM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 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.