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Thoracic Outlet Syndrome Thoracic Outlet Syndrome/Brachial Plexopathy. In Memory Of DeAnne Marie. |
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#1 | ||
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Junior Member
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Hello fellow tosers
![]() just to introduce myself ![]() I have survived 10 years with TOS. My goodness what a scary bumpy road my journey has been. I went back to work after my bilateral first rib resection with cervical ribectomy, I had cervical rib on right side and some kind of weird ligament band thing on the left that had me in a headlock. Seriously OMG. SERIOUS PAIN. I was a wallpaper hanger and I put myself through college for degree of registered nurse. Well wallpaper hanger was not such a good idea ![]() Anyway, that's what happened to me. I was just hurt in a major way. I got lucky and found a osteopath that spent one year working on my ribs, (what I had left) I had total of 3 ribs removed and one ligament detachment lol. This doctor gave me my life back. I got better and went back to work. I was just elated. I worked very hard at rehabilitation and it worked. Only thing was pain control. I always had severe pain after my surgeries. I am pretty sure I had bracial plexus injuries from TOS surgeries. I had to have pain medication to be able to move. I survived the last ten years due to pain management with medications. I worked up until Feb. 2013. My pain was managed well up until Feb. of this year. The DEA has scared every pain management physician and I end up the collateral damage......My pain management doctor stopped medication management and I was given only one month to find another doctor. He did say sorry. I found another doctor and he walked in room and said, you don't have that much pain, and you probably didn't need the surgery you had ![]() Needless to say I did not return to this evil doctor. I deserved better. So I had to find another doctor, send referral, wait for response and finally made appointment for may 16th. This doctor has good reviews and I sure hope it is true. I think I have one of the pain syndromes due to brachial plexus entrapment by scar tissue. With no pain control I am sooooo miserable. My arms are jerking, I can feel my brachial plexus firing off for no reason. I can feel sounds in my chest and it hurts really bad. I can't do anything because any movement means horrible flair. OMG. I thought I had already been through enough. I am so miserable and exhausted from severe pain ![]() ![]() Sorry this is so long, I just need to tell my story to someone who understands. I was wondering if anyone here has a pain syndrome following TOS surgery, it is called "sympathetic maintained pain syndrome"????? another pain syndrome is called "complex regional pain syndrome". I believe many of us have pain syndromes because the transaxillary surgery causes brachial plexus injuries. I also go to see a brachial plexus specialist on 22nd of may. At this appointment I hope to get CORRECT diagnosis for what is wrong with my back. I have one more question if any kind toser would be so kind to help me. I will help others here too as I have many years with TOS under my belt. OK question is: has anyone else had problems with severe pain and treated badly at a doctor appointment, or is anyone else having problems with medication management in this new DEA infested system????? When I move or use my arms the brachial plexus go crazy, spasm...flair. Just complete mayhem!!!!! I have to have medication management or I just suffer like I have the last 4 months. I am sooo very tired and having apathy feelings. I am trying to be positive but ...... I am just so angry I could spit nails. OK rant is done and now I have to try to be positive , more positive thoughts. It is so hard to think positive. I feel like giving up, I am so tired. But you know what!!!! I helped many many people during the 10 years I was nursing. I was a home health nurse. I loved helping the people, I just want to go back to work. oh almost forgot, I saved some lives!!! they would have died if I had not been there. I know that my courage to work through my pain had a impact on many lives and I am very proud of myself. I never missed one day of work, ever.....sometimes I even took patients because another nurse called in sick....I did have to work sick some days, hurting and stuff, but I did it!!! ![]() Thinking positive that if I can get correct diagnosis of pain syndrome I can get the medicine I need so I can return to my life and my career! Wish me luck, I will pray for us and I will try to stay strong. Thank you in advance if anyone answers my questions.Hello fellow tosers ![]() |
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#2 | |||
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Cheryl,
I have been bed bound and completely dependent on narcotics and Valium. As you can see from my signature, I have been through multiple surgeries. Scar tissue can wreck havoc on the Brachial Plexus, it doesn't mean there was nerve damage during surgery. I did not want to go on living a drug dependent life so I opted for resurgery to clear the scar tissue. I am glad I did as the procedure was a walk in the park compared to the rib resection. Don't give up, keep fighting. Explore all of your options, not just drugs.
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Marc . ACDF C5-C6-C7 2/28/11 . . . . |
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#3 | |||
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Here in the OC if you need to talk
Cyndy Quote:
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Cyndy . color="Black">Slowly I turn, step by step, inch by inch *The 3 Stooges . |
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"Thanks for this!" says: | nospam (05-12-2013) |
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Cyndy, sorry but I don't know what "here in the oc" means. can you clarify that so I know what you are talking about. sorry am new here. thanks cheryl
I had a great life in spite of being disabled with TOS. I still had pain but my medications allowed me to work and participate in my life instead of sitting on the sideline in sadness. I have no problem being dependent on a medication that completely changes my life. It is not my fault that people misuse opiates. Those same people will just find a different source for their high.....off the streets. That is what addicts do. dependent and addiction is two completely different things. Am really hurting so sorry if I am not making sense here. No pain management since feb. |
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#5 | |||
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I think that was directed towards me. OC = Orange County, CA
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Marc . ACDF C5-C6-C7 2/28/11 . . . . |
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"Thanks for this!" says: | SAHOL78 (10-26-2019) |
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#6 | |||
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Quote:
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Marc . ACDF C5-C6-C7 2/28/11 . . . . |
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#7 | ||
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Junior Member
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Quote:
I just figured out why my pain is so bad. I have sympathetic maintained pain syndrome. I have all the symptoms. I will probably be diagnosed on the 22nd of may. I hope you find your balance,as even with bad pain a balance can be found.....then peace takes over ![]() |
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#8 | |||
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Has anyone noticed that the American Pain Foundation website has been shut down?
http://www.painfoundation.org/ Their website navigation had a separate page devoted to TOS. Shows that at least SOMEONE acknowledged the pain we live with.
__________________
. "It is what it is." |
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