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Has anyone used this and had good or bad results? Does it work for persons with EDS or does it make things worse?
I have researched it a bit, and it is unsupported. There is not enough research to back it up, its very expensive to have done, and the reviews i got from people in my groups were 50/50.
Thanks for the response. I am afraid there is just nothing good for us to use. Thankfully I don’t have side effects to narcotics like some people. It is the only thing I have to take the edge off the pain. I pray it stays that way. I saw my PCP yesterday and she told me to be careful that with my tissue fragility injections, surgeries, implanted devices should be reserved for last.
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