Just wondering if anyone else has been dx with a rare form of MS that mimics a brain tumor. I go at the end of the week for another MRI to confirm the dx. I lost the ability to speak about six weeks ago, well couldn't get my words out. Now can speak about 80% normally. Still have bouts of not able to get my words out but they are becoming fewer and far between. Although all my other tests didn't lead the neurologist to think it was a brain tumor, he wasn't completely ruling it out. One picture showed a huge blob on the part of my brain that controls language, and the other picture showed many lesions. I also have lost some muscle control on my right side.

Just curious about whether anyone else has had this. Been looking at various message boards and haven't seen anyone who has been dx this way. But since this a rare form but not unheard of, I'm obviously not the only one.