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Thoracic Outlet Syndrome Thoracic Outlet Syndrome/Brachial Plexopathy. In Memory Of DeAnne Marie. |
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#71 | ||
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You are so right!!!!!! The hardest aspect of TOS for me is knowing that regardless of different activities, lifestyle changes or operations undergone its here possibly for life! My biggest struggle at the moment is coming to terms with this fact..... but I'm beginning that journey now. Despite my op and another to come( possibly in December) I'm now focussing on what I can do instead of what I can no longer do. I'm just starting councelling and working on CBT, and getting a health trainer to help guide me back into gentle exercises that will not drain or hurt me. It's a transistional phase. Not what I planned for in life but I must also bear in mind that I CAN and WILL adapt. My main goal is to try and not moan so much about it. Not only does it drain those around me, it drains me too ( most of all, me)!!!! NEW MANTRA: Acceptance=Peace. The more I come to terms with it the easier it is to move on and continue living the best way I can possible. Best wishes to you. SD38 ![]() |
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#72 | ||
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like you I have a REAL issue with both my hands going numb ( seriously dead and floppy like with total loss of sensation) at night. I see that you use ICE for relief, do you use this also during the night???? Out of all my symptoms this is the one that bothers me the most!!!!!! Its bad enough dealing with aches etc during the day but the hands going to sleep stopping you going to sleep is awful. I Like reading your attitude about being med free.... I'm desperately working to stay this way too. Obviously at times there is no getting away from them but on the whole I truely believe its a slippery road to go down. I think it can end up messing with your pain receptors where the body gets to the stage where it can no longer tolerate any pain levels. Deep breathing and ways to distract are what I'm working hard at..... just hope it contines to work. Interesting post, thanks. ![]() From SD38 - V/ATOS and now some return of NTOS post op!!!!! |
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#73 | ||
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What "set back" are you referring to regarding the botox injections? Simply that the symptoms return, or some additional problem that the botox creates?
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#74 | ||
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Feldenkrais has been played a major role in my therapy. I don't think it will cure me, but it has given me much more function without flaring me. Feldenkrais Resources has excellent audios you can buy. They are expensive, but you can also share them through Dropbox with fellow sufferers. Before doing audios on your own, it helps to go to a few classes or receive some private lessons first so you have a better understanding of the Feldenkrais method.
If I feel I'm approaching a 7 or so in pain, I lie down and do an audio and I can bring the pain level down to a 3 or 4. Excellent therapy for mind, body and spirit. |
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#75 | |||
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has anyone else had their bp go up bc of the pain?
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last felt my fingertips august 2010 . |
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#76 | |||
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I've read that on some of the other forums .... blood pressure can increase due to pain levels.
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Search the NeuroTalk forums - . Last edited by Jomar; 10-31-2011 at 06:02 PM. Reason: to clarify |
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#77 | ||
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Lots of good info piling up in this thread. Question- as I read a few people commenting. What is the difference between loss of pulse in abducted positions versus needing surgery? In other words at what point is it considered "vascular" because literature suggests that even someone off the street could lose a pulse in hyper provocative positions. When do you know it's dangerous or whatever?
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#78 | ||
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#79 | ||
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343: No, I can't work. I wasn't working when the injury happened either. It's not a RSI or trauma case. No one knows why I got TOS.
I do Feldenkrais every day and I do a lot of other audios as well. If I start to feel I'm seizing up and on the verge of a flare, I'll stop and take 30 min-1hr to run through an audio and/or do some light PT. I also do Mindful Based Stress Reduction, meditation and other modalities. These would be nice things for you to do at work during break, in the morning and evening. Honestly, I don't think I'll ever be able to return to work in any capacity. I can no longer do most, if not all, of my hobbies. I've seen a few surgeons, one of which was Kelly's, and I have no intention of having surgery. My gut and statistics tell me I would fall in the loser group, and my problems now may look like no big deal. |
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#80 | |||
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Co-Administrator
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I think it is the pain & symptom severity when it comes to the positional vascular part of it. Or if the vascular system is affected no matter what the arm position is.
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Search the NeuroTalk forums - . |
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