World Encephalitis Day: Where are we in 2022?

What follows below is commentary on what I’ve noticed occurring in the AE world as a patient with an encephalitis-wearied set of eyes.  ***Please take what I say with a grain of salt, do your own research, and talk to your own medical providers. I’m not an authority; I’m just a fellow AE survivor partially reflecting insights collected from others, and partially adding in a dash of my own spice.***

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Every day I’m celebratin’ 🎵 | Monthly Resilience Report: February 2021

Have you ever tried to compress ~10 months of life into a single month’s worth of time?

Things uh, get a little chaotic 😅

The information on this site, such as text, graphics, images, and videos, is designed to provide a patient perspective on understanding and living with a long-lasting illness. It is for general informational and entertainment purposes only, and does not serve as a substitute for consulting with your own healthcare professionals or conducting your own research. It is not intended to serve as medical advice, or to be used to diagnose, treat, cure, or prevent any disease. While every effort is made to provide accurate information on the subjects discussed, no responsibility is assumed for any errors or omissions in the content. Always seek the advice of a qualified healthcare professional to assess and guide your medical care.

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