new MS specialist
Has anyone had any experience with Dr. D'Angelis at Mt. Sinai in NYC? I'm going to see him on the 18th of July for a second opinion. We're still trying to figure out what the heck is wrong with my nervous system. I got the results of my EEG back and my "seizures" I've been having daily are not in my brain, which means they are probably spinal cord related in some way. The neuro won't diagnose me with MS yet based on my normal MRIs, but says I have neurological disease. I'm worried because this is progressing so quickly and I have no way to slow it down or to know what the future holds. It's still presenting as MS quite clearly despite all the normal tests... but one would think with the severity of my disability my tests would be whacky anyhow. Who knows.