I have my primary doctor telling me that it's all in my head and that the symptoms weren't related to multiple sclerosis. My neurologist Miss diagnosed me for 4 years and primary doctor prescribed medicine that should not be given to multiple sclerosis patients. It was buspar one of them for my depression/anxiety. That made my symptoms worse. I immediately changed doctors after being told from my neurologist this. The neurologist wanted to send me into a seizure because they wanted to monitor it or do a spinal tap. When I get cold it's like my body can't control muscle spasms and they get severe and tense. I have permanently lost my frontal view of my eyesight in my right eye. Certain foods trigger it worse and when I get cold or my feet or hands get to the point where I can't feel them that's when the violent muscle jerks start up. I'm just getting tired of the the b/s. I made an appointment for a multiple sclerosis specialist but they can't see me for a few months. What are some of the things that helped you with your doctor so they can understand