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It starts with a healthy, independent, capable young woman. I had just graduated nursing school, officially become a registered nurse, and started my dream job.
A month later, I was a sick, dependent shell of a person. I had daily seizures and soon lost my ability to walk and talk... I was a slave to my own inflamed brain.
Today, I am a healing, strong, and capable young woman with a promising life ahead of me. I am one of the lucky ones who found a specialist and received the treatment I needed.
I started this blog to shine light on my illness: a rare neuroendocrine disorder called Hashimoto's Encephalitis (HE), or steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT).
Hashimoto’s Encephalitis is hard to spot, hard to diagnose, and therefore hard to treat. Spreading awareness is the only way to restore the lives of those living without a diagnosis today.
HESA is proud to announce a collaboration with an autoimmune encephalitis doctor to research HE!
To donate to this research project, please go to www.hesaonline.info & click on the donate button.
Please see more details going forward on our Facebook page:
HESA - Hashimoto's Encephalopathy SREAT & Seronegative AE Alliance
Feel free to contact me with any questions.
Thank you so much for your support!