Guest guest Posted November 1, 2011 Report Share Posted November 1, 2011 I have a couple of friends on another forum who are primarily being treated by LLMDs and using standard antibiotics. Many are experiencing extreme pain and I am looking for ideas for them. I post two of them for example below. I will forward any idea that I haven't heard them mention. Thanks! www.lyme-resource.comYou can lead a person to a fact, but you can't make them think! - - Thanks for the suggestion, a lot of us, myself included are beyond joint pain. I have pain on every spot in my body. Think of the worst flu you ever had and then add bone cancer to that along with a burning sensation under the skin and in the muscles. Nevermind the headaches that some of us are getting. EPO ain't gonna cut it. I already take GLA anyway. > > > > > I was 2 steps from crawling out the door to go to the ER last night > > > > > for this excruciating pain that I just can not take anymore. Cried > > > > > all day in horrific pain all over my body. I tried every type of > > > > > pain med throughout the day that I had an nothing worked. I even > > > > > took Vicodin- didn't do a darn thing... and NO I am not on Rifampin > > > > > anymore. And- Yes, Mike, my meds have been changed and > > > > > reduced.... lol. My BART is coming out like crazy... Not the > > > > > BABS.... the Bart.> > > > > Quote Link to comment Share on other sites More sharing options...
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