I understand the frustration, my own PCP had the same comment. He's very clueless and seems not to want to be educated on my condition. I had asked to be referred to a doctor with some experience but he decided on his own to contact top doctor at Dartmouth Hitchcock. He then came back to me regarding a slew of medications for me to try. I had asked him do to my allergy to certain NSAIDS would these affect me, and of course he stated, well I'm not sure. So I was officially diagnosed with MP 1/2016 and still cannot find a medical professional with any education on the subject. I've had 2 severe attacks and 2 minor attacks of MP, hoping never to have another one.