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


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Old 11-14-2012, 02:01 PM #1
shengggmd shengggmd is offline
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Default TOS from a patient and a surgeons point of view

I have neurogenic type of tos and has been living with it since early 20s. I first felt the pain and the subsequent numbness and tingling in my left arm after a minor car accident. I thought at first it was just minor bruising and soreness related to the accident. As time went on these symptoms only worsened. I was seen over the period of few months by neurologist, orth, and neurosurgeons. All tests including MRI and EMGs were negative. I was told that all these may be in my head.

With much frustration and anger. I researched extensively on the topic. I think the most important thing for me is to resist the use of narcotics for pain control. Physical therapy and relaxation therapy helped me greatly, I also took on yoga for a few years that helped me to maintain good posture and strengthen my shoulder girdle. I am currently doing very well with minimal symptoms. only time I get some level of symptoms is when I spent all day in the operating room. As a vascular surgeon that treats TOS. I believe the field is full of controversies and may be even fraud, even amongst vascular surgeons.

I believe that the best way to approach treatment is through a multispecialized approach. As a surgeon I make money doing TOS surgery ( which everyone has to keep that in mind, that there is secondary gains there for the surgeons) but as a patient that is essentially cured by physical therapy I believe that physical therapy is perhaps the most important part of the equation. I would be very happy to answer any questions you all may have. hopefully, i can provide you all with some level of comfort and reassurance.
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Old 11-14-2012, 02:36 PM #2
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Thank you for being so honest. The vascular surgeon that diagnosed me in May (after three years of symptoms and seeing other docs) was also honest with me when he saw me recently for follow up. He said that he would have preferred to have been the one who fixed me, but he was happy that I was fixed with physical therapy.


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Originally Posted by shengggmd View Post
I have neurogenic type of tos and has been living with it since early 20s. I first felt the pain and the subsequent numbness and tingling in my left arm after a minor car accident. I thought at first it was just minor bruising and soreness related to the accident. As time went on these symptoms only worsened. I was seen over the period of few months by neurologist, orth, and neurosurgeons. All tests including MRI and EMGs were negative. I was told that all these may be in my head.

With much frustration and anger. I researched extensively on the topic. I think the most important thing for me is to resist the use of narcotics for pain control. Physical therapy and relaxation therapy helped me greatly, I also took on yoga for a few years that helped me to maintain good posture and strengthen my shoulder girdle. I am currently doing very well with minimal symptoms. only time I get some level of symptoms is when I spent all day in the operating room. As a vascular surgeon that treats TOS. I believe the field is full of controversies and may be even fraud, even amongst vascular surgeons.

I believe that the best way to approach treatment is through a multispecialized approach. As a surgeon I make money doing TOS surgery ( which everyone has to keep that in mind, that there is secondary gains there for the surgeons) but as a patient that is essentially cured by physical therapy I believe that physical therapy is perhaps the most important part of the equation. I would be very happy to answer any questions you all may have. hopefully, i can provide you all with some level of comfort and reassurance.
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Old 11-15-2012, 10:18 AM #3
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does your pec minor have to be spasming to have pms? or could it just be very very hypertrophied?

thank you so much!

what limitations have you had sense pec minor surgery?

were you able to do nerve glides pre-op?

are your shoulderblades winged?
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Old 11-15-2012, 10:21 AM #4
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Do you think any botox alternative (long term) can be available soon ?

http://neurotalk.psychcentral.com/thread177507.html

It would be incredible. and amazing. but i feel it is so slow..

what are they doing...
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Old 11-15-2012, 10:23 AM #5
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Do you think any botox alternative (long term) can be available soon ?

http://neurotalk.psychcentral.com/thread171936.html

It would be incredible.. but i feel it is so slow..

so weird i was just gonna ask that

i dont need botox in my scalenes but pec minor would be nice at least as a diagnostic tool
or some sort of injection
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Old 11-15-2012, 11:58 AM #6
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Yes, it is like there are safe drugs that effectively permenantly weaken cibled muscles and no one care about

Last edited by boytos; 11-15-2012 at 01:38 PM.
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Old 11-15-2012, 07:13 PM #7
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Default Can and how does vascular TOS cause pulsating tinnitus and/or Tinnitus?

What mechanism of compression in Vascular TOS causes tinnitus and / or pulsating tinnitus? For me the "head noise" israel debilitating than the pain.
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Old 11-15-2012, 07:20 PM #8
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What mechanism of compression in Vascular TOS causes tinnitus and / or pulsating tinnitus? For me the "head noise" israel debilitating than the pain.
What type of tos did you have?
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Old 11-15-2012, 08:07 PM #9
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What type of tos did you have?
Neuro and venous TOS. Diagnosed 6 years ago with nTos but recently had a 3d MRI at UCLA but do not have final report. So my guess is venous TOS.
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Old 11-15-2012, 08:14 PM #10
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Neuro and venous TOS. Diagnosed 6 years ago with nTos but recently had a 3d MRI at UCLA but do not have final report. So my guess is venous TOS.
MRA showed compression of jugular vein by manubrium and high signal in sigmoid sinus. Also compression of BP in thoracic outlet and other vascular compression. I'm waiting for the radiologists report. It was done last week.
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