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
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 07-22-2012, 01:34 PM #1
anne523 anne523 is offline
Junior Member
 
Join Date: Jul 2012
Location: Michigan
Posts: 32
10 yr Member
anne523 anne523 is offline
Junior Member
 
Join Date: Jul 2012
Location: Michigan
Posts: 32
10 yr Member
Crazy desparately seeking MD to manage RSD..south east michigan

I am desparate...seeking a new MD than known anything about RSD and that can manage and get me on the right track. And the next question is just whay type that may be. I had wrist surgery in April of 2011 (after an injury in Feb. 2011). After developing RSD the hand surgeon didn't want to acknowledge it and mumbled a few things..I didn't think anything of it. After a routine visit to occ. health (this is a work injury) I was asked "what are they doing for your RSD" I was stunned and told to go home and do research and we would talk later. The original hand surgeon is out of the picture..long story and I was told by disability mgr and case manager to find a new physician. I was given at least 2 dozen names...hand surgeons, neorologist, pain management PMR and told to find someone. Further surgery was mentioned, but don't want to go there now. I have had consults with a couple pain management MDs....who wanted to do immediate stellate ganglion blocks, and I had driven myself. I was told not a problem I could drive home soon after, needless to say I didn't have one done. Finally saw another MD who at least explained things and gave options, had block done and flared further...not the result I expected. His answer was an immediate rhizotomy and given a web site to view and let his staff know if i wanted it..and no further appt until I agreed to procedure. There has to be someone out there I just haven't found yet. I am in southeastern Michigan..just north of the Detroit area. Anyone with any suggestions???
anne523 is offline   Reply With QuoteReply With Quote
 


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
Hi from Michigan Indie'sOK New Member Introductions 3 04-30-2012 02:16 AM
Hello again, from Michigan jjbird New Member Introductions 6 01-11-2012 03:49 PM
East and south only? doydie The Stumble Inn 2 08-20-2009 06:44 AM
Hello from Michigan heather_mi New Member Introductions 6 02-02-2008 06:08 AM


All times are GMT -5. The time now is 04:30 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.