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Stan's experience was a terrible one, but one that everyone should read carefully and heed. Doctors don't always know or check on drug interactions and side effects. It is especially difficult with the large number of meds taken with PD. Sometimes your knowledge is important and you must insist that the doctor listen. I shared the story of my dad having a pacemaker replaced. He was given massive doses of Valium by the anesthesiologist and cardiologist despite my mother arguing that he was not to have it and a letter of caution that the neuro had sent to the cardiologist. The dose and subsequent ones were enough to keep him in a coma for TWO MONTHS. Our tax dollars paid for Medicare care for a doctor induced coma! Interestinly my dad was also scheduled for a scan that cannot be done on someone with a pacemaker despite a huge note on the front of his chart noting the PACEMAKER. It was caught at the last minute. I think the key is that the patient and personal caregiver, must look up meds, ask questions, and take responsibility for his/her care. With managed care, it will continue to be difficult to received thorough excellent care. Beware of doctors who don't explain things and double check what is going on. I don't think the average family doctor or internist is at all familiar with all aspects of PD. I also highly recommend finding a pharmacy with a pharmacist who is knowledgeable and anxious to assist. They are full of info that even drs. aren't aware of and have access to resources to assist you. Stan, glad to hear you are better and thanks for sharing your story. Where in TX do you live? My dad with PD lives near Houston. Gail Post Honolulu