Hello all, My name is Denisa and I might have been diagnosed with RRSM last week. Why do I say ”might”, you may ask: my diagnosis was based upon a single optical neuritis attack, along with the results of my MRI, the visual potentials, the blood tests and the personal history. I aldready had my steroid treatment: 5 days. My right eye is now better, it regained saturation and sharpness about 99.8%. I know it will never regain its full potential, but I'm good with that. Moving on :) . Untill I heard the diagnosis from my doctor’s mouth, I was deepy frustrated for being in a hospital longer than I have ever been before (I'm 28, and the last time I was hospitalised was back when I was 9, for an apendicitis) and not knowing if I have SM of not (there were also some steroid side-effects meddling with my emotions, but that’s another funny story :) ). I come to peace with the diagnosis, but I cannot come to terms if it’s 100% accurate. For that I a willing to ask another neuro opinion, to be more certain. I know that in MS certainty is what lacks most of the time, but if I’m going to beat this poor MS, I have to now exactly what I’m dealing with! :D And most of all, I need to secure my parents’ emotional being, and all this uncertainty is killing them inside. I am a knowledge seeker, an information dweller and I wonder if you could help me with some opinions. Nice to meet you all and may you have a wonderfull day! :) Denisa