22/02/2026
I just recently learned that today, February 22nd, is World Encephalitis Day.
Until 2023, this was a condition from which my family and I were blissfully disconnected. That all changed, however, when my dear Dad began experiencing bizarre, concerning, and eventually debilitating neuropsychiatric symptoms. These symptoms were just the beginning of a nearly year-long journey of fighting for answers in the face of a medical system that all too often lacks the ability to connect the clinical dots in complex cases.
We are so, so blessed to have finally received a diagnosis and a clear treatment path. I know this is not the case for everyone who experiences this horrific illness, which is why I want to talk about our experience more in hopes of helping even just one family avoid the hell that we went through.
I’ll be shedding more light on our story soon, but until then, please feel free to free to reach out to me with any questions or simply to connect. ❤️