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


advertisement
Reply
 
Thread Tools Display Modes
Old 07-28-2012, 03:28 PM #21
mspennyloafer's Avatar
mspennyloafer mspennyloafer is offline
Senior Member
 
Join Date: Oct 2010
Location: ga
Posts: 1,471
10 yr Member
mspennyloafer mspennyloafer is offline
Senior Member
mspennyloafer's Avatar
 
Join Date: Oct 2010
Location: ga
Posts: 1,471
10 yr Member
Default

i dont understand how a doctor couldn't believe in tos

what if you bombed a vascular test, would he still not believe in it?!!!
__________________
last felt my fingertips august 2010
.
mspennyloafer is offline   Reply With QuoteReply With Quote

advertisement
Old 07-28-2012, 06:27 PM #22
nospam's Avatar
nospam nospam is offline
Member
 
Join Date: Feb 2012
Location: Orange County, CA
Posts: 835
10 yr Member
nospam nospam is offline
Member
nospam's Avatar
 
Join Date: Feb 2012
Location: Orange County, CA
Posts: 835
10 yr Member
Default

Quote:
Originally Posted by Holles View Post
I live in NE
I am assuming you are in Nebraska near Omaha.

Quote:
Originally Posted by Holles View Post
The Spine Dr. said I have cervical degenerative discs, which I already knew, and said I should go to a neurologist.

What do you guys think? Would a neurologist get an MRI of the braxial plexus area?
What kind of Dr. was the Spine Dr.? Neurosurgeon? I think Neurologist when I think Spine Dr. There are some Neurologists with knowledge of TOS, but not many. Vascular Surgeons have the most experience with TOS. Unfortunately there is no definitive imaging for TOS, it is mostly a clinical diagnosis.

You may want to check out this Physiatrist in regards to diagnosing TOS and possibly getting some further direction.

http://www.nebraskaspinecenter.com/o...x?ID=8&Section

He did his residency at Washington University Medical Center - Barnes Jewish Hospital, home of Dr. Thompson's Thoracic Outlet Syndrome Center.

I also found great benefit from massage once I found a therapist with TOS experience - http://www.bestomahamassage.com/moinca.shtml

Hopefully, you can get better without surgery. If you require surgery, you may have to travel out of state for an expert TOS surgeon.
__________________
Marc

.


ACDF C5-C6-C7 2/28/11

.


.


.


.
nospam is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Holles (07-29-2012)
Old 07-29-2012, 11:53 AM #23
Sheri_TOS Sheri_TOS is offline
Member
 
Join Date: May 2008
Posts: 236
15 yr Member
Sheri_TOS Sheri_TOS is offline
Member
 
Join Date: May 2008
Posts: 236
15 yr Member
Default

Quote:
Originally Posted by nospam View Post
What kind of Dr. was the Spine Dr.? Neurosurgeon? I think Neurologist when I think Spine Dr. There are some Neurologists with knowledge of TOS, but not many. Vascular Surgeons have the most experience with TOS. Unfortunately there is no definitive imaging for TOS, it is mostly a clinical diagnosis.

You may want to check out this Physiatrist in regards to diagnosing TOS and possibly getting some further direction.

http://www.nebraskaspinecenter.com/o...x?ID=8&Section
Holles,

I agree with Marc. The physiatrist is probably the best route to go. I've been dealing with TOS and/or spine issues for nearly a decade now. In my own experience, I've found neurologists and neurosurgeons to be dismissive towards TOS even after having a very successful outcome from surgery. I think it has more to do with what they've seen during the course of their career than an outright dismissal of TOS. I had a neurologist once tell me that he liked the interesting cases (MS, Parkinsons, epilepsy).

In my experience, the physiatrists were the most open to TOS. You may need to see more than one physiatrist before you land with a good one.

Regarding testing for TOS, again, Marc is correct. It is mostly a clinical diagnosis so don't get frustrated that nothing shows up.
Sheri_TOS is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Holles (07-29-2012)
Old 07-29-2012, 02:48 PM #24
Holles Holles is offline
Junior Member
 
Join Date: May 2012
Posts: 48
10 yr Member
Holles Holles is offline
Junior Member
 
Join Date: May 2012
Posts: 48
10 yr Member
Default

Thank you Sheri & Marc!

The spine guy was Dr. Longley from the NE spine institute, an ortho. Must be one of those Dr.s who think if they can't operate on it, it doesn't exist. He did give me an rx for therapy with the note of "TOS". Online, his dx was degenerative disc disease.

I will call both your suggestions, Marc. You are amazing.
Holles is offline   Reply With QuoteReply With Quote
Old 07-29-2012, 09:16 PM #25
nospam's Avatar
nospam nospam is offline
Member
 
Join Date: Feb 2012
Location: Orange County, CA
Posts: 835
10 yr Member
nospam nospam is offline
Member
nospam's Avatar
 
Join Date: Feb 2012
Location: Orange County, CA
Posts: 835
10 yr Member
Default

Quote:
Originally Posted by Holles View Post
The spine guy was Dr. Longley from the NE spine institute, an ortho.
Some Orthopedic surgeons do spinal fusions, but I wouldn't call them spine doctors (no offense to Orthos). Neurologists are spine doctors and Neurosurgeons are spine/brain surgeons. I wouldn't let an Ortho touch my spine or my thoracic outlet...but that's just me.
__________________
Marc

.


ACDF C5-C6-C7 2/28/11

.


.


.


.
nospam is offline   Reply With QuoteReply With Quote
Old 07-30-2012, 01:12 AM #26
Laur3d Laur3d is offline
Junior Member
 
Join Date: Apr 2012
Location: San Diego
Posts: 67
10 yr Member
Laur3d Laur3d is offline
Junior Member
 
Join Date: Apr 2012
Location: San Diego
Posts: 67
10 yr Member
Default

Quote:
Originally Posted by Holles View Post
I've read most of the TOS postings and know that quite a few people have negative EMGs, etc. How did you get an official diagnosis?

My WC Dr. just called & told me my EMG was negative. I don't see how that is possible since my pinkie & ring finger are numbish & shake constantly. Then again, the technician who did the EMG was very snotty about it being a work injury - apparently she thought TOS was entirely congenital. No idea where I should go from here. The p/t says I have TOS.

He's sending me back to work Monday. My husband thinks I should just quit.

Hi Holles, I actually found out I had TOS after blood clots formed in my chest and arm turned blue and swollen. The Vascular surgeon I met at the hospital though, confirmed his suspicions of TOS on the CT scan. He could see the area in the scalene triangle was too small. If you have not had CT scan may be worth the shot, since no tests will actually show compression. I know its not a common test and take a TOS savvy dr to see. Not really sure. So sorry for your pain and frustration! Lauren
Laur3d is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
OzKira (08-02-2012)
Old 08-02-2012, 01:29 AM #27
OzKira OzKira is offline
Junior Member
 
Join Date: Dec 2010
Location: Melbourne Australia
Posts: 83
10 yr Member
OzKira OzKira is offline
Junior Member
 
Join Date: Dec 2010
Location: Melbourne Australia
Posts: 83
10 yr Member
Default

Holles Don't give up. I was diagnosed after a clot in my subclavian vein moved to my lung. The first vascular surgeon I went to see said I had TOS but didnt do much in the way of test's for a more formal dx with all the facts. Check the doctors list above to find a Dr close to you. You might find that a neurologist useful also to check on the nerves as well. Good luck. Your not alone there are many of us who have been on the TOS round about.
__________________
[SIGPIC][SIGPIC]
OzKira is offline   Reply With QuoteReply With Quote
Old 08-02-2012, 04:27 AM #28
tshadow tshadow is offline
In Remembrance
 
Join Date: Aug 2006
Posts: 1,002
15 yr Member
tshadow tshadow is offline
In Remembrance
 
Join Date: Aug 2006
Posts: 1,002
15 yr Member
Default

TOS is a group of symptoms, but I'll bump up my writing on "testing" which is the best I can do, not being a doctor.

I have been fighting work comp for 9 years, but I just won a 100 percent case. I strongly recommend finding how to a get a copy of Dragon voice software, but you need to see an attorney and as TOS progresses, you need an advocate. Your doctor (if work comp) can write you prescriptions to get home aid health, if you get to the point that you can't drive, get groceries, dress, change your bed, etc.

Hopefully you will not get that bad.
tshadow is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Woodstock3 (08-13-2012)
Old 08-13-2012, 06:08 PM #29
Holles Holles is offline
Junior Member
 
Join Date: May 2012
Posts: 48
10 yr Member
Holles Holles is offline
Junior Member
 
Join Date: May 2012
Posts: 48
10 yr Member
Default

Well, now work comp has told me that, since no one can find anything wrong, they don't feel my pain is work related. Really. I have an appointment with a physiatrist next month (the earliest I could get in) on my own insurance.

Another question for you experts out there - when showering a couple days ago, I reached down & back to wash my leg & the left shoulder girdle went "clunk" and moved. Has that happened to anyone else? So weird. Hurt like heck, too.

Supposed to be going back to work Weds but guess I'll have to quit. No point in injuring myself further.
Holles is offline   Reply With QuoteReply With Quote
Old 08-14-2012, 10:44 AM #30
andreaa27's Avatar
andreaa27 andreaa27 is offline
Junior Member
 
Join Date: Aug 2012
Location: Rochester Hills, MI
Posts: 7
10 yr Member
andreaa27 andreaa27 is offline
Junior Member
andreaa27's Avatar
 
Join Date: Aug 2012
Location: Rochester Hills, MI
Posts: 7
10 yr Member
Default

Quote:
Originally Posted by heybro View Post
Holles,

Are you in a state with good work comp laws? Correction, Are you in a state with work comp laws that just suck instead of really suck?

If you go the work comp route, file a claim and get a doctor to put you out of work. You need to stop this now and you need to start healing. Working more on the computer is not going to be worth it.
I am facing similar issues with workmans comp. Except I had a wc surgery for frozen shoulder, torn labrum, rotator cuff tear, and had my bursa removed to make space. After the surgery, my hand was tingly... for almost a year now. Had emg, shows slow response annd also muscle atrophy in hand. Pain has extended to my arm and shoulder. Shooting pain and numbness down arm. WC says it is not related. Getting treatment through my own insurance but will soon be MMI through comp. I want my case to remain open because the TOS is related, just have not found any documentation showing that this could be from the surgery or pain pump.
andreaa27 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
Diagnosed with RSD HouseLite New Member Introductions 9 01-19-2009 08:16 AM
getting diagnosed Lily Autism 7 11-22-2008 09:44 PM
Just Diagnosed with MPS blackpanther New Member Introductions 6 08-12-2007 02:22 PM
just got diagnosed bethp New Member Introductions 6 02-21-2007 01:05 PM


All times are GMT -5. The time now is 10:17 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.