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)

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 03-13-2007, 12:21 PM #8
fmichael's Avatar
fmichael fmichael is offline
Senior Member
 
Join Date: Sep 2006
Location: California
Posts: 1,239
15 yr Member
fmichael fmichael is offline
Senior Member
fmichael's Avatar
 
Join Date: Sep 2006
Location: California
Posts: 1,239
15 yr Member
Default

Dear Kellie -

I would seriously urge you to check out the practice group set up by Robert Schwartzman, M.D. in Philadelphia, whom I flew out from California to see 3 years ago. Although Dr. Schwartzman is now seeling a lighter patient load, and has consequently a 3 year waiting list, thare are other very, very good RSD doctors within his practice group. I know that Roz on our board saw Jahangir Maleki, M.D., and thought the world of him. Their contact information is as follows:
Robert J. Schwartzman, M.D.
Jahangir Maleki, M.D.
Department of Neurology,
Drexel University College of Medicine
Drexel Neurological Associates
219 No. Broad Street, 7th Floor
Philadelphia PA 19107-1519
215-762-7090
215-762-3161 (fax) [Attn. Carol for new appointments]
Best of luck in your search.

Mike

p.s. While I've been treated regularly at the Mayo Clinic in Rochester MN since I was an infant, and continuing through a cardiac work-up this last summer, I have only had - at best - mixed results in working with there RSD and pain specialists and know a number of people who have had the same experience. Part of the problem there is that their Department of Neurology has for many years been under the influence of a now semi-retired specialist in peripheral neurology, who, having done some great work in his time, is a MAJOR hawk against the use of opioids in patients with chronic pian conditions. Secondly, they are really reluctant to get into the treatment of RSD patients who live outside of their immediate area, where they believe, and perhaps rightly so, that RSD treatment is often a hit or miss situation, on account of which multiple appointments over time may be required before they get things right. I know that I was not a candidate for either in-patient ketamine infusions or thalidomide treatments, only because I didn't live nearby, on account of which it would be hard for me to be seen in follow-up appointments. Hope this is helpful.
fmichael 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
Hello everyone, I am new and a little lost littlelmk New Member Introductions 3 02-07-2007 03:57 PM
OMG!!!!!!!!! I lost it ALL!!!!!!!!!!!!!!!!!!!!!!!! LIZARD Weight Loss & Healthy Living 12 01-20-2007 09:00 PM
I'm Lost funkybandit General Health Conditions & Rare Disorders 11 12-06-2006 05:34 PM
who saw LOST tonight? Mari Bipolar Disorder 2 10-04-2006 10:41 PM
Lost My Thread Sydney Vitamins, Nutrients, Herbs and Supplements 3 09-26-2006 11:50 AM


All times are GMT -5. The time now is 01:40 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.