HESA Online Org I was misdiagnosed with schitzophrenia and I had encephalitus. Psychiatrists and mental hospitals need to know this. They force drug you and I am dying from 6 forced shots of invega sustenna
Shane Clauer Thank you for sharing your story. Many patients have experienced misdiagnosis. Have you had a chance to read Susannah Cahalan's book, Brain on Fire? Ms. Cahalan had anti-NMDA Receptor Encephalitis and was first diagnosed with bi-polar disorder before her doctors reached the correct diagnosis. www.susannahcahalan.com HESA has also published a book called "Understanding Hashimoto's Encephalopathy: A Guide for Patients, Families and Caregivers" which is full of patient stories, not to unlike your own. HESA is currently working on the second edition which will contain more stories of encephalitis/encephalopathy patients diagnosed with HE and updates on their stories from the last book. www.amazon.co.uk/Understanding-Hashimotos-Encephalopathy-Patients-Caregivers/dp/1484883098 Thank you again, Shane. Wishing you the best in your recovery.
This is crap. I go to Duke medical Centerand I tested positive for autoimmune encephalopathy and they're trying to make it seem like everything is me being stressed they keep on telling me that I'm stressed keep on stressing the point that I'm stressed because I am a mother of four I am suffering and no one is listening I'm so upset I want to sue
Patients face this type of bias daily and it is a major stumbling block to treatment. Thank you for sharing this video!
HESA Online Org I was misdiagnosed with schitzophrenia and I had encephalitus. Psychiatrists and mental hospitals need to know this. They force drug you and I am dying from 6 forced shots of invega sustenna
Shane Clauer Thank you for sharing your story. Many patients have experienced misdiagnosis.
Have you had a chance to read Susannah Cahalan's book, Brain on Fire? Ms. Cahalan had anti-NMDA Receptor Encephalitis and was first diagnosed with bi-polar disorder before her doctors reached the correct diagnosis.
www.susannahcahalan.com
HESA has also published a book called "Understanding Hashimoto's Encephalopathy: A Guide for Patients, Families and Caregivers" which is full of patient stories, not to unlike your own. HESA is currently working on the second edition which will contain more stories of encephalitis/encephalopathy patients diagnosed with HE and updates on their stories from the last book.
www.amazon.co.uk/Understanding-Hashimotos-Encephalopathy-Patients-Caregivers/dp/1484883098
Thank you again, Shane. Wishing you the best in your recovery.
I was diagnosed with this some time ago. It is something to think about.
This is crap. I go to Duke medical Centerand I tested positive for autoimmune encephalopathy and they're trying to make it seem like everything is me being stressed they keep on telling me that I'm stressed keep on stressing the point that I'm stressed because I am a mother of four I am suffering and no one is listening I'm so upset I want to sue
How are you now?