Hi don, I know how you feel, same thing has been going on for along time. AA so complexed it seems they can't be bothered. I bought Tennant's book $ 20.00. It's informative but shy's away from putting the blame on doctors. He's very passionate for AA Patients. He has a interesting background.

Today I saw my Pain Management dr. he added more Hydromorphone in my pump and the time I can use the a remote that gives me an extra does if needed. I mentioned how much my hands to elbows wake me, he told me it's coming nerves are coming from my neck! All I could say was "oh no!" I decided to contact a neurologist to see if the nerve damge could be stopped from spreading. I sent my history to a Neurologist and was so surprised when they told me the dr. read my information, to does not take cases like mine so I was referred group called, Aggressive Neurology. I was so happy that a dr. cared enough to contact me. I was like a little kid. Reason I'm telling you maybe you could look into it also and anyone who is reading this.

Don't remember if I told you I looked into the mat and looking forward to you opinion! Wishing you a good evening