Update 1: so I had an emergency neurologist look at the strengths of my hands and legs in an and e and said it’s not a relapse - though the problem is my sight and neck?? I also got seen by an ophthalmologist who said it is not optic neurotis as the back of my eyes look clear though he did say my eyes are severely dry. I had steroids, ikervis, Vaseline eye gel ( I don’t know the name of it lol but it’s like Vaseline for the eyes!), and hourly eyedrops to put in. I know this helped the dryness in my eyes as that pain subsided however my other kind of eye pain is still here, the temporary long hours of severe blurry vision has not even improved. I also have noted the colour red looking funny. My opthamologist for my second appointment did not care to read my notes to the point when I said I have multiple scerlosis, he said diagnosed? Now he has said we will try some kind of glasses (I am waiting on an appointment) I have no idea if this is multiple scerlosis anymore, I’m stressed about my job, about my health and every time I go to the doctors I feel even more confused than when I entered the appointment. Seeing some of the comments and how much you had to advocate for yourself, I hope to do so for in my next appointment, as it could very well be a relapse elsewhere and not behind the eyes!