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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.
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​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.
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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.
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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).
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​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!
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To donate to this research project, please go to www.hesaonline.info & click on the donate button.
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Please see more details going forward on our Facebook page:
HESA - Hashimoto's Encephalopathy SREAT & Seronegative AE Alliance
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Feel free to contact me with any questions.
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Thank you so much for your support!