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


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Old 12-06-2013, 11:28 PM #1
cp1000 cp1000 is offline
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Join Date: Dec 2013
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10 yr Member
cp1000 cp1000 is offline
New Member
 
Join Date: Dec 2013
Posts: 2
10 yr Member
Default 5 months with TOS...

Hi everyone, I've been reading all the posts here since my symptoms of TOS first appeared five months ago but this is my first time sitting down to write something.

TOS has been one of the hardest thing that I have been through but I just want to share with everyone who has just been diagnosed with it that it can get better....with a lot of work and a positive mind. When I first started to experience symptoms I was freaking out and I completely panicked. I had neck and shoulder pain on and off for over two years but during this past summer I started to experience a lot of pain on the left side of my chest, down my arm, my hands too, especially at the base of my thumb. I had numbness and tingling as well and I also experienced the tingling in both my feet as well as a burning feeling on the soles of my feet. For a few weeks I even had muscle weakness in both my legs. I couldn't even walk 10 feet without a limb or two going numb and being in pain down my arm. I couldn't work, I couldn't do housework, I couldn't go to the gym, I was miserable--sorry husband and kids!!

I went to the doctor and had every test imaginable and everything came back normal including my cervical x ray and mri. I spent hours scouring the internet reading everything I could trying to find anyone with similar symptoms, I became a complete wreck and developed crazy anxiety which definitely did not help. I think I cried just about everyday.

My doctor told me to try physio and luckily I found a good physiotherapist who mentioned TOS within the first 15 minutes of me talking to him. I have gone to physio twice a week since July and have done all the stretches and exercises I was told to do. I was not aware that I had really bad forward head posture and rounded shoulders so I've mostly been working on improving my posture as well as loosening my neck up.

What I think helped me the most was Sharon Butler's program, I found it online from a google search. I had read that Coop42 was having some success with it so I thought I would try it, thanks Coop! I found the scalene stretches in her program helped TREMENDOUSLY!! I followed the program exactly how she laid it out but if I were to go through this again I would get to the scalene stretches sooner.

Just as I was getting to the end of the six week program my appointment with the neurologist came up (I live in Canada, it takes a long time to get appts.). She ruled out MS and ALS and told me that I should try acupuncture to help with the numbness and tingling. So a few weeks later I tried acupuncture and exactly a week to the day--no more symptoms. (this was month 4 and a half). I was starting to feel better before the acupuncture so it's hard to say if it was solely the acupuncture or a combination of that and physio.

During this time I also changed my diet and ate tons of fruits and veggies, lean protein. I took fish oil, vitamin D and B. I took a lot of magnesium because it's a muscle relaxer--I also took prescription stuff too and a lot of aleve. I still drank a lot of wine though. I also went to the library and read books like mind over medicine and Quantum healing as well as other books on mind-body healing just to keep me positive.

This was my experience, I'm not totally recovered, I still experience some symptoms if I sit too long with poor posture and I have started to get ringing in my ears but so far I can deal with it. I'm still going to physio and acupuncture because I never want to go through this again. I'm back at work and at the gym and have no pain. Good luck to everyone with this awful affliction, it will get better, believe it. I'm not a positive person by nature but I forced myself to be, I think it's the only way.
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