My husband just got diagnosed with MOG after 14 years of thinking he had MS.. the symptoms presented as sudden blindness at age 8, and with steroids it brought back is vision. Thank you for making such a clear video so that I can further understand what we are now dealing with!!
I was diagnosed with this in 2018. After two yrs of steroid RX is an still struggling with this disease with no clear RX. Where are we Worh this in 2020?? Any NEW recommendations?
45 yo female with only demylinating white matter lesions Post vaccination-= neurological reaction- r/o for autoimmune disease and Not MS, lupus, Lyme recurrent episodes of myelitis and optic nerve pain on eye movement Can this be MOG?
