Thoracic Outlet Syndrome Thoracic Outlet Syndrome/Brachial Plexopathy. In Memory Of DeAnne Marie.


advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 01-24-2008, 03:01 PM #1
waggydog waggydog is offline
Junior Member
 
Join Date: Jan 2008
Posts: 6
15 yr Member
waggydog waggydog is offline
Junior Member
 
Join Date: Jan 2008
Posts: 6
15 yr Member
Default New to list

Hi guys,

I've been reading the numerous posts and replies here and have joined in now in hopes that perhaps some of you can give me some help/advice. I have had symptoms of TOS for approximately 20 years. As I'm sure that many of you have experienced, you really go through the ringer with this, as most physicians don't know about this. As such, I have been treated for severe headaches, been through several boughts of PT, have had acupuncture, massage therapy, cortisone injections, some "investigative" treatments (some of which were quite painful - none of which worked), etc., etc. Recently I went to an orthopedist who specializes in shoulder injuries as I've been losing significant ROM lately. He felt I have brachial plexopathy/TOS but told me that there really isn't a way to diagnose this or really treat it. I've heard this kind of stuff before ... I call them "god" diagnoses as they provide an explanation with no ability to be proven or disproven ... kind of like fibromyalgia and chronic fatigue syndrome. Mostly I think these are garbage because it really feels like the doc just wants you out of their office. Anyway ... sorry to be so cynical ... but this has been going on too long! What I am hoping that I can find here are some experienced TOS sufferers who have had good experiences with physicians/treatments as 1. I would like to have some hope and 2. if you know of anyone in the Philadelphia or NJ area (do not want to go to Hopkins) who you felt was able to adequately diagnose and treat you could you please provide me with that information? I would greatly appreciate it.

Also, in a previous search I found a small group (n=3) of docs at UMDNJ who appeared to specialize in TOS. For some crazy, crazy reason I can't seem to locate that page! If anyone knows about these guys, could you give me a shout? They sounded like they might be worth the trip up. Thanks in advance for any help you can give!
__________________
Even if life isn't the party you were hoping for, it doesn't mean you shouldn't dance!

.
waggydog 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
Christmas Wish List Sissy Traumatic Brain Injury and Post Concussion Syndrome 9 12-23-2007 11:18 AM
Add this to my list...grr RSD_Angel Reflex Sympathetic Dystrophy (RSD and CRPS) 4 11-16-2007 12:00 AM
Add one to the PN misdiagnosis list.... dahlek Peripheral Neuropathy 1 06-16-2007 05:07 PM
RSD puzzle list Jomar Reflex Sympathetic Dystrophy (RSD and CRPS) 1 11-05-2006 07:45 AM


All times are GMT -5. The time now is 05:47 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.