@Aerose91 --I had a few months of Atlas Orthogonal treatments about a year and a half ago. As you probably know, there is a fair amount of time devoted to diagnostics like very specific X-rays and clinical observations of things like leg length. It is formulaic, as
@JES intimates.
I discussed ME with the chiropractor, as well as CCI/AAI and he seemed confident that AO could have a beneficial effect on the latter, at very least. Since I was convinced that my ME was connected to CCI/AAI, it seemed worth a try.
I think
@JES was referring to Atlas Orthogonal and not Atlas Profilax, but I am not entirely sure. They are somewhat different. My treatments were 100% painless with AO. The adjustments are done with sound waves and no physical contact with the neck at all.
After my initial treatment I was a convert. I have not felt that good for more than a decade, possibly ever in memory. I felt as if my head was floating on top of my spine. I could see clearly, colors popped, my body moved with ease in the world, I could think with such clarity it literally stopped me in my tracks. The overall sense of well-being was blissful.
Sadly, it all faded after about 8 hours. I continued to get adjustments at the urging of the chiropractor, who assured me that just sticking with it would help train my muscles to hold the atlas in place. I wanted that feeling back more than anything, so was sucked into a rather expensive course of treatment with ever-diminishing returns. By the time I had my last adjustment, it didn't even make a dent in my usual sick state.
That having been said, I would add that the initial experience was revelatory. I wish I had stopped earlier, once it became fairly obvious that the effects were not increasing, rather decreasing. But ... as a diagnostic it has been very helpful to me. After having such a dramatic shift, albeit short-lived, I knew for sure that something in my neck was creating a great deal of my suffering. Which pushed me to follow that thread.
In addition, several physicians, including a neurologist and a neurosurgeon took my suspicion of cervical pathology a LOT more seriously when I related my initial experience. I don't want to be discouraging. I am not sorry I did it, but of course we all have to figure out where to invest because none of us have enough money or energy to pursue all the possible panaceas out there.