Iv had TOS since around 2000, had a fall ini 1999 that started symptoms. Only diagnosed in 2005 after insisting on MRI, Ultrasound Doppler tests etc. I do loose my pulse so I dont know why it took so long to diagnose, just one arm movement would of saved me 5 years of pain and thinking "its all in my head" (thats what the Dr's told me anyway!) I have great glee in taking in my results now. I just put them in front of the Dr and sit back and wait for their response (workers comp Dr's love this). No more im crazy or "I find it hard to believe what your telling me" comments. Its a lot better visiting these so called specialists with my results! I didnt find your post offensive at all. If you dont want to reply, dont. Every little bit of info I can find out about TOS and people living with TOS the better for me.

Hope everyone is having low pain day!

Ozzy