So good news for me. I finally got an answer to my question. What symptoms do you expect based on my demylination and lesions. Since 2011 my symptoms all seemed random. The one thing at a time NHS way. They were never grouped for an overall possible diagnosis. Harder because thats where I worked and I know the behind the scenes good work. Finally 2026, my MRI shows exactly where my lesions are. By researching functions. IM NOT CRAZY! The highlight of my year. Now I feel more relaxed and less tense, because I know the areas of my brain and spine and symptoms linked to MS which allot, with some overlap of other conditions. How about you?