Hello PrimeTimer,
I am very sorry to read of this and I want to answer straight away. Many years ago I "went on the same road of research" whilst suffering terrible pain during SLE/MCTD-flare-ups and I went from one pain-management-doctor to another for help without achieving any success, because these so-called pain-clinics are "only there" and appear to be "better" specialised,
which pain medication to prescribe and
how much of it and so, generally speaking, for me it was a total waste of time to try my best there because any of these pain-killer-medications would have had a negative effect on my kidney-function...
But : what I did find out was that there are "certain government departments" who "educate certain people" and "these certain people" are also educated to withstand all sorts of difficulties under "administered pain" etc., so I continued my research by writing to all sorts of government-departments, but sadly I never received any reply.
I wish you good luck and please let me know if any of these pain-management-clinics these days have developed and as a result have become
more patient-friendly? ... And if by any chance there
is some government department able to help and is "allowed" to let us know about their own research and one is "allowed" to write to them and
receive an answer about how to learn real pain-management/physio-therapy etc.?
Best wishes from Kristina.
P.S. In case you wonder : The reason why I went to such great lengths to find out about positive pain-management is because I urgently needed to
preserve my kidney-function as much as possible and, as "we all know", pain-medication can have a devastating negative effect on
preserving the kidney-function... and so I felt it very important to find out as much as was possible in order to
preserve my little kidney-function as much as I possibly could ...