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New Here And Anyone Heard Of Neural Therapy?


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Hi everyone! This is my first post although I've been reading this forum for quite some time now. I have POTS and EDS, got sick 12 months ago. For my POTS I take two drugs, desmopressin and propranalol, and will be switching to Ivabradine once it arrives from the online pharmacy. I also did an Atlas Orthogonal adjustment to my neck and it was extremely helpful for about 3 months, almost symptom free. Back in a flare now :(

I learned about Neural Therapy today from a doctor. This therapy relates to ANS dysfunction and I was wondering if anyone ever heard about it? This is not a mainstream treatment and the best doctor for this is in Canada (as I was told). Here is his website.


I would be very interested to hear your thoughts. And I want to sincerely thank EVERYONE on this forum -- you are the most knowledgeable, intelligent and kind group of people. I can't tell you how many times I printed articles and research papers from here for my doctor. Thank you!!

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Hi guys, thanks!

Kitt, I'm glad that you had experienced an authentic reflexology. I tried one at the Chinese place here and it was nothing what you describe.

Regarding Neural therapy, I'm not sure... I'd like to find some confirmation that it can help with POTS first. I doubt that insurance will cover it since it's not a traditional treatment.

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