Hi all. I've had CFS for over 20 years but luckily have had a great doctor for 17 of them. I have watched him journey through the various treatments and researches into the illness and he is virtually a specialist in chronic "hidden" type illnesses now. Over the past few years many of his CFS patients tested positive and responded to treatment for rickettsia bacteria. Now he is having wider success with another antibiotic treatment called the Marshall Protocol. I've just started the antibiotics. David Marshall is Australin like me but I believe lots of his research etc is done overseas so maybe the treatment is becoming widely known. Too complicated to explain here but I'm wondering if anyone has been / is on the treatment and how they've been affected. Would appreciate any feedback. Meanwhile, here's to good days and better health!