Hi there! I was diagnosed in July (by fluke, they were looking for a brain aneurysm) and my MS diagnosis was confirmed by spinal tap. At that point, in hindsight, my only symptoms were headaches, fatigue, bladder and stool issues, and minor vision problems. Also looking back, I had been having issues finding the right words or stumbling over my words. I just received my 2nd 1/2 dose of Ocrevus. Maybe it's "in my head" (literally) but I am now finding myself my misspelling easy/silly words or replacing words with other random words (last night I called my son's football team his "football fraternity"). My question: is there anyone else that feels like their brain is the source of most of their symptoms? I am so thankful to not currently have spinal lesions, but I am also worried about my brain deteriorating.