Would like to hear from those of you who have been or are currently undergoing treatment from alternative medicine practitioners who are also MDs. I am not from the US and am debating if I should fly over to see Dr Kilmas or an AM physician. What happens if drugs prescribed by Dr Kilmas are not available in my country? My current doctor, with interest in me/cfs is not proactive in treating me, despite several repeated requests for labwork, since the last tests were carried out nearly 2 years ago. Feel like being left out in the cold to die a slow death. Will beg or borrow money to pay for treatment in my fight to survive CFS. Appreciate any input from US/ non US patients. Thanks.