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Canadian TOS sufferers?
Hello, I continue to suffer from this nasty condition despite having decompression surgery 9 months ago. Just wondering if there's any fellow Canadians from Ontario in the same situation? [emoji4]
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Did you have NTOS/mostly nerve related ? Full rib removed?
If so the nerves can take a very long time to heal , and may even stay a chronic issue. Internal scar tissue can happen also. Any scalene or pec minor issues ? or Was any of that mentioned or address in surgery? Any PT since the surgery? Expert PT or other therapies might be helpful.. |
I had a partial scalenectomy and total first rib resection. PT before and after surgery. I know the path report said that the scalene tissue was hypertrophied. There was no discussion about pec minor issues?? How would I know if there was any involvement with the pec minor muscles? I felt pretty good for 3-4 months after but all the symptoms have returned.
It has been pretty frustrating to say the least. Sent from my Nexus 6P using Tapatalk |
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Was it anterior or medial that they removed? |
It was a transaxillary approach so I'm assuming that the amount of accessible scalene tissue would be less? So I had a partial anterior and middle scalenectomy with a first rib resection.
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I see the surgeon for my one year f/u in February. I'm not sure what to say...Sadly I am a failure. Still have to see a Physiatrist in February as well who 'fingers crossed' will do Botox injections into my scalenes. I hope the Botox injections can give me some relief. I still haven't returned to my job as an ultrasound technologist and don't know if that will ever be a possibility as it just aggravates my condition. Do you also suffer from TOS?
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Anyone know of a Doctor in Ontario that does the Botox injections for TOS? I have been referred 3 times with no success in finding one!!!!!
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