1. Our TMS drop-in chat is today (Saturday) from 3:00 PM - 4:00 PM Eastern U.S.(New York) Daylight Time. It's a great way to get quick and interactive peer support. BruceMC is today's host. Click here for more info or just look for the red flag on the menu bar at 3pm Eastern (now US Daylight Time).
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  2. Alan has completed the new Pain Recovery Program. To read or share it, use this link: http://go.tmswiki.org/newprogram
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Day 1

Discussion in 'Structured Educational Program' started by Guiseppe, Nov 21, 2021.

  1. Guiseppe

    Guiseppe New Member

    I am almost entirely convinced my headache condition (NDPH) is just TMS.

    In favor of TMS
    • I have thoroughly read Alan Gordon's The Way Out, and applying the techniques outlined in the book, I have seen dramatic improvement in my condition. Possibly 70% improvement, which is astonishing considering the relative failure of all the physical and pharmacological treatment I've received in the last 10 years: chiropractors, acupuncture, physical therapy, antibiotic treatment for Lyme disease, Botox, dental appliances, medications from the Jefferson Headache Center, etc. The fact that I have experienced any improvement at all from strictly psychological intervention is astonishing, and convinces me there is no underlying structural problem causing my headaches.
    What scares me about TMS
    • I am still gun-shy from my experience with the world of Lyme Disease. I was given hope by the LD community, which operates with this confidence that they have exclusively identified a modern day plague that all of western medicine has failed to appreciate - a confidence that is especially attractive when expressed by the leaders of this community, who are seemingly very intelligent, respectable human beings, with doctorate degrees and specialty clinics named after them. I have since left that community and abandoned the thinking that my symptoms are due to Lyme (years of unsuccessful antibiotic treatment will do that), but to be honest, I sense that same sort of confidence from the TMS community. I get that same vibe of "Welcome home, we are going to make all your problems go away, because we know something nobody else does". I am still a bit gun-shy of that kind of message of hope. I know things are different this time around. The TMS community overwhelmingly reports success stories, whereas with Lyme it seems like less people are actually improving, and of course, I have experienced partial success myself doing TMS work, but still, it will take time to shake off the disappointments of my past.
    • I am doing TMS work alone. I can't think of anybody I've met in person that has heard of it - not my family, nor the few friends I have left. I guess what worries me about going it alone is not that I won't eventually resolve my symptoms, but that it will take much longer than it has to. Or maybe it won't take long. Maybe a powerful shift in mindset will occur, and in my new mode of existence, all my previous thoughts or worries will seem negligible.

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