I was diagnosed in November of 2015. I've had every blood test, numerous MRIs ct scans and no doctor including the mayo clinic can find a reason as to how I developed encephalitis. I was 36 when diagnosed and am now 37. It's been an extremely painful and difficult diagnoses to endure and deal with knowing I will have defects for the rest of my life. I am a masters level social worker and dog walker prior to this.