New here... trying to fully embrace TMS for my complicated story

Thank you Francesca for sharing! I was just telling one of my "Runner's Dystonia" friend s(who I am trying to convince to start reading Sarno) that I keep meeting people who have dystonia symptoms who it was/is TMS. I was even just listening to one of Nicole Sach's podcasts where a woman on it had my symptoms of runner's dystonia (this was not her primary TMS symptoms she was on the podcast for but something she just added in), but no one seemed to have ever told her that, and of course it went away. I was like wow, what someone had told her she had Runner's Dystonia, would she be living the life of misery I have been for 15 months thinking there was no cure and she'd never get better? What if no one had ever suggested to me I have Dystonia? I wish I had found Sarno earlier, but I am grateful that I have now as I know 15 months can still be a short period of time compared to others who don't know him for years or even decades.

 

Oh it is so good, I've been doing at least one episode a day. Her book will probably be my next one!

 

Yes... even though 15 months can feel like 4 full years.
When time is marked by pain, uncertainty, and the constant search for answers, every day weighs heavier.