When the judge has read the book…
Finally, some good news to share with everyone. I just got a favorable ruling from Social Security Disability that I meet their criteria...
A Diagnosis for Daisy
I used to get these weird feelings of anxiety. While I was working, talking, shopping, driving (of course I’d pull over) but then it...
Even Doctors Can Learn
I found a local endocrinologist at the request of my neuroimmunologist, Dr. Vernino at UT Southwestern. (The FP holistic nurse...
Now I am a Strong Woman
Hannah Leasure's Mother attempts to give her medication On Christmas Eve 2013, I was admitted to hospital, where I stayed until April...
The Invisible Disease
World Encephalitis Day - Lisa Lauter Tells Her Story 13 minute video I was diagnosed with LGI1 Autoimmune Encephalitis (AE) in February...
World Encephalitis Day, February 22nd 10 Simple Ways You Can Participate
World Encephalitis Day is the Friday, February 22nd. This is a single day when everyone in the Autoimmune Encephalitis community works to...
A Life Well Lived, A Life Cut Short ~ In Memoriam
In Recognition of World Encephalitis Day, February 22nd, IAES will be publishing additional Blogs throughout February in its effort to...
I Have My Wings Back
I was diagnosed with Transverse Myelitis back in 2013. I am doing a lot better with that and had been doing great up until early 2018. I...
Light at the End of the Tunnel
Hi, my name is Kerry Jones and I’ve been diagnosed with LGI-1 autoimmune encephalitis by the Mayo Clinic in Rochester MN. I was seen by...
The Scariest Time of my Life -Battling Limbic Encephalitis
I’ve always been a socially active happy person. Loved to travel. Have gotten to experience a life that most people haven’t gotten to...
