Hi, Kaitlynn -
Like the others who have responded, I want to encourage you to see a neurologist, and perhpas a different one?
this summer I joined an (in person) Lupus Support Group, and at least three of the members have had lupus affect their Central Nervous Systems. I know that sounds scary, but ALL of them have made the most miraculous recoveries. I am in awe of their courage and strength.
I wish you the best possible outcome!
Diagnosed with SLE 2010; MCTD 2012
Medications: Plaquinel (300 mg); CellCept (1,000 mg)