Juliana: Anti-NMDAR Encephalitis Lived Experience

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Juliana shares her story at the Encephalitis International event, My Brain: My Story, in October 2022.
Juliana, from Miami, Florida, was diagnosed with anti-NMDAR encephalitis in 2014. Her illness has a huge impact on her life and those of her loved ones. Thankfully, she made a quick recovery through sheer determination and a loving support system.
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Опубликовано:

1 фев 2023

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Комментарии : 19

@thirdmares3441 Год назад

My son is in ICU rigth now.. he have encephalitis.. i need your prayers for my sons fast recovery.. dont know where to get money to pay the bills and medication.. but i know God will make a way..

@brandiecarter9130 Год назад

🙏🏽🙏🏽🙏🏽

@user-rj6wl3lr2g 3 месяца назад

My daughter is finally home recovering from. I hope your son is ok ❤🙏🏼

@keniasegura6182 Месяц назад

Hello, my sister is currently coming out of the comatose state this illness caused her. I hope all is better with your son!

@maria15tom Год назад

It is amazing you are helping others like us. I am almost a year with aNMDA. I also feel your title a tragedy worth living is 🙌🏼🙌🏼🙌🏼🙌🏼

@ellievesey4559 Год назад

An amazing message! I really needed to hear this today 💜

@kristinnefertiti8267 Год назад

That's awesome. I don't remember anything before I had my grand Mal seizure due to encephalitis.... now I have epilepsy as a result of the brain swelling. Great.

@brittanylightbourn8896 Год назад

God bless you. You’re a great inspiration to us people who suffered Encephalitis. You’re doing so great. I’m very happy for you. Keep on doing what you’re doing. You’re just doing so great. Thanks for sharing your story.

@encephalitisinternational Год назад

Thank you so much for your kind words, Brittany

@brittanylightbourn8896 Год назад

@@encephalitisinternational You’re very welcome

@thefaceless760 Месяц назад

I was just discharged with Autoimmune Encephalitis, I'm English and married in the United States, I have no health insurance, and no green card yet, in England, they put me in multiple psyche wards through a misdiagnosis of schizophrenia, after spending 12 months institutionalised my wife helped me move here through a marriage green card, and finally got me out of England; two years into our marriage, I began to have a seizure, which triggered the autoimmune encephalitis, I was just discharged last week after two weeks in hospital, a spinal tap, and 14 days on a Saline IV, I'm so thankful to be alive, and had never heard of this condition beforehand, I didn't know my own name, but I knew who my wife was, its horrible to think that if this happened in England, they would have resectioned me into a psyche ward through misdiagnosis, and I would be dead; I feel very lucky.

@encephalitisinternational Месяц назад

Thank you for sharing your experience. Our website has lots of information on how we may be able to support you, if required.

@anielarece8339 Год назад

Hi, you look great.I would like to know how long it took you to go back to school.???? My son has been in the same situation for a year and he has not recovered yet, it is better this way but it is very difficult.

@Sofiasanabria Год назад

Hi Juliana, can you share the name of the Doctors you see @ Jackson. We are living in Miami as well and I try to find my son Dx.. Thank you for sharing your story with us.

@julianaortiz9081 Год назад

Hi Rosa! Thank you for reaching out. Since it was almost 9 years ago, my neurologist no longer works in Miami. I saw Dr. Reuven Bromberg, MD but he is not based in Jackson. He helped my recovery immensely. I also saw Dr. Nicole Mavrides - Psychiatrist at UM HEALTH JACKSON & Dr. Susan Ireland - Neuropsychologist. All great doctors in Miami! Best of luck !!!

@patriciaceballos239 Год назад

My 21 year old daughter has been diagnosed with GAD65 autoimmune encephalitis. She has focal seizures. She's taking the IV steroids now. They want her to take Rituximab next. Can I ask if you took that? She/we are so scared.

@julianaortiz9081 Год назад

Hi! Thank you for reaching out. I feel like every person is different, and everybody heals differently. So, I wouldn’t be able to tell you what is best for your daughter, but I definitely think you should talk to several doctors before you make a decision. At the end of the day neurologists tend to know best. Best of luck with everything!