I have a new, tentative diagnosis of MS. My neuro-opthalmologist said that I meet criteria and they've found a few active demyelinating lesions on my MRIs that I am currently on steroids to manage. He has stressed to me that I need to be seen urgently my an MS neurologist so that I can start official treatment for it, because the steroids will only protect me from another attack for a few more weeks. The MS neurologist isn't able to get me in until March. I am overwhelmed and I feel like my health is not in my own control. Does anyone have any advice on how to get seen sooner or how to handle the unpredictable waiting period?