please move your center to washington state, thanks.

I wish there were more discussions about the other types of dysautonomia. I have bradycardia. I’m not suffering from too fast of a HR. That’s all anyone talks about.

I got pots after being sick with COVID,took me a year to get over it,my only symptom now is light headless every few weeks,but it’s minor compared to what I was dealing with when I first got pots

Are pots people also have cervical spondylosis ??

Why does it seem to be so wrong to point out that the spinal cord is not a lot smaller than the space it has to pass through? when the consequences are so dire if your ligaments don't keep your vertebrae off your spinal cord or even your brain stem? Brain stem, vagus nerve, and even spinal cord pressure and too much untreated pain in general, are known to cause dysautonomia. But instead it's virtually impossible to get any communication of this. Is it because something this basic isn't being taught in medical school? so no one can say it? What's wrong with the people establishing this curricula then? Are they being lobbied to keep this information out? I can't think of any other reason this would be the case People are dying prematurely from this. People with goals, motivated, hard-working people. That means that everything that the economy put into the making those people productive, the medical establishment is not only throwing in the garbage can, it's charging individuals and taxpayers more than full price, to tell us nothing about our health, at best. At worst, many Physicians and Specialists seem to speak against the likelihood of these consequences, when if you try to ask them logically how what you're saying isn't obvious in the consequences it would have, they have no answer