Autoimmune Encephalitis | What is Autoimmune Encephalitis 

Thank you so very much for doing the research and posting this. I know you won't get a lot of views because of the rarity of this disease. I am surprised that only 41,000 have AE in the U.S. I have been hospitalized twice with seizures.since my diagnosis in 2015. My only treatment now is an ant-seizure medication, which I take 2xday. This prevents my seizures, as well as my fogginess, repetitive movements, tremors, etc. So, I am not cured, and fear further deterioration of my cognitive abilities, although the only thing currently affected is my poor memory (I blame it on my advancing age). The Drs. did talk to me about Chemo, but did a poor job of explaining why that would work. An operation of some kind was discussed, as well as a longer course of steroids. I have learned much more about AE from your video than I have from any neurologist I have talked to. So, again, thank you. I will share this with my AE group on Facebook. I enjoy all of your videos. Your drawings are exceptional in helping us all to understand your explanations.

How did you draw a virus exactly on the black spot? Was that a coincidence?

@@ricknofzinger I’m glad I could be of help in anyway. I hope you can work with your doctors and find a better solution for your health.

@@terjeoseberg990 complete coincidence.

@@friendlyneighborhoodimmuno7192 Thanks.

How is your mom doing?

@@Elliemaret It is my son with AE. My son has better quality of life but not fully recovered.

@@aprilsatterfield3868 my son who is 3 years old has suffering A/e currently. He is the the hospital for two months now. My son underwent plasma exchange and the doctors gave my son immunoglobulin. I'd like to know how long months does your son stayed in the hospital before he recover?

Thank you so much for this video doctor. This helped me understand more about my son's illness he has currently suffering.

@@haroldestafia5307 unfortunately my son wasn't hospitalized, he was having seizures, unable to speak, catatonic, loss gross and fine motor skills. It took 2 years to get a proper diagnosis and treatment. So he has deficits 6 years later but much better. It took about 2 years of treatment to get where he is now. But we saw improvement with ivig each time and rituximab helped a lot.

Thank you, and I am sorry your friend has AE. I hope she gets the very best treatment.

Jeff Can you tell me what kind of treatment she is getting

@@davidmathews9633 I would like to know to. I hope she is doing better by now.....

Thank you!

I'm the exact same however my mri and recent blood counts were clear!

Did you ever find out what was going on?

Yes I will look into it. The spleen does house lots of macrophages that break down old red blood cells as well as B and T cells. It could alter a few factors during vaccination.

@@friendlyneighborhoodimmuno7192 😍

What do you mean it fits into the mRNA research?

@@gardenvariety- There's even more information about how the immune system works, which to me anyways, complements this video: ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-et7bGU4hbYE.html

I’m glad the issues didn’t bother you!

Does it bother you now spike is in brain and recognised encephalitis is a adverse event from MRNA vaccines.

Many who had the C jabs have autoimmune encephalitis. This year alone I have over 10 patients diagnosed with it including encephalopathy, encephalitis, metabolic encephalitis ​@@gardenvariety-

what symptoms did u have? and duration of it all? i think i have this. god bless glad ur ok

So sorry to hear that. I hope you are getting the best care possible.

@@friendlyneighborhoodimmuno7192 Thanks. I am getting better. Still some short term memory problems though. Thanks for your kind words.

What have you done for treatment ?

@@tnt4412 Mostly taking meds. I can't say which ones as I take a boatload of them. Thanks for asking. I hope you are doing well. What are you doing for treatment?

@@tnt4412 Taking meds , not driving and seeing a doctor.

Yes good point.

I hope you get good treatment.