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)


advertisement
Reply
 
Thread Tools Display Modes
Old 02-06-2012, 07:03 AM #1
alt1268's Avatar
alt1268 alt1268 is offline
Member
 
Join Date: Aug 2011
Location: delaware
Posts: 904
10 yr Member
alt1268 alt1268 is offline
Member
alt1268's Avatar
 
Join Date: Aug 2011
Location: delaware
Posts: 904
10 yr Member
Default

I want to know since June 2010 what your lawyer is doing about this issue. I know here in delaware it takes 3 or 4 months to get in front of the labor board. Why is it taking so long?
The stimulator is different from the TENS unit. The wires are placed into the spine and the vibration is often a different sensation.
What is your neurolist giving you? He/she could be giving you pain medication.
__________________

.


GOD help me be faithful in the midst of my suffering. Alt1268
alt1268 is offline   Reply With QuoteReply With Quote
Old 02-06-2012, 09:24 AM #2
Kheldar's Avatar
Kheldar Kheldar is offline
Junior Member
 
Join Date: Feb 2012
Location: Mpls, MN
Posts: 37
10 yr Member
Kheldar Kheldar is offline
Junior Member
Kheldar's Avatar
 
Join Date: Feb 2012
Location: Mpls, MN
Posts: 37
10 yr Member
Default

Quote:
Originally Posted by alt1268 View Post
I want to know since June 2010 what your lawyer is doing about this issue. I know here in delaware it takes 3 or 4 months to get in front of the labor board. Why is it taking so long?
The stimulator is different from the TENS unit. The wires are placed into the spine and the vibration is often a different sensation.
What is your neurolist giving you? He/she could be giving you pain medication.
I got a partial settlement and he has been fighting with the insurance company to get my medical bills reimbursed. Not sure what else he can do; he is now working on my behalf trying to get approval for the pain doctor and psychologist, but in the meantime I either endure in agony or try to be seen and pay cash up front if the office allows it.
As for medications - Baclofen and Carbamazepine is all I am on. Been that way since November 2011 after my allowed pain meds and antibiotics ran out after the latest major infection.
Kheldar 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
crps walkbyfaith New Member Introductions 2 02-17-2011 01:30 AM
crps katric511 Reflex Sympathetic Dystrophy (RSD and CRPS) 4 02-15-2011 08:56 PM
Crps Dizzygirly Reflex Sympathetic Dystrophy (RSD and CRPS) 6 01-29-2011 05:23 PM
Crps Dizzygirly Reflex Sympathetic Dystrophy (RSD and CRPS) 2 01-27-2011 11:43 AM
Hi, I have CRPS/RSD gatorsmomma New Member Introductions 4 05-12-2010 09:16 PM


All times are GMT -5. The time now is 06:29 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.