It's #worldencephalitisday Show them some love 💗 #hannibal #hannibalthecannibal #hannibalfandom #fannbals
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It's #worldencephalitisday Show them some love 💗 #hannibal #hannibalthecannibal #hannibalfandom #fannbals
It is a day that has special meaning to me and many others touched by encephalitis and more specifically autoimmune encephalitis in my case. 7 years ago, I didn't know what Autoimmune Encephalitis was until I “woke up” in the Penn Medicine Hospital of the University of Pennsylvania after being misdiagnosed by two different doctors at two different hospitals and almost being committed to the nursing home to “live out the rest of my life comfortably.” i love @pennmedicine . Encephalitis is an illness that involves the inflammation of the brain from either an infection or the immune system mistakenly attacking the brain. In my case, I have Autoimmune Encephalitis which is a rare illness that causes the immune system to think something is invading your body (which it should do) but it develops a "glitch" and it thinks the brain is the culprit. So, it starts attacking the brain. Symptoms are similar to symptoms of other neurological illnesses such as dementia, Alzheimer's, and schizophrenia. Among these symptoms are confusion, altered behavior, psychosis, hallucinations, sleep disturbance, cognitive issues, memory loss, seizures, and physical disorders. Hundreds of thousands of people globally each year are affected by autoimmune encephalitis, and encephalitis, and are misdiagnosed, but a correct and quick diagnosis can make all the difference between life and death. As such, education and raising awareness of this illness is extremely important and severely required as many people are wrongly diagnosed till the illness has done damage that can't be repaired or worse in some situations. As such, education and raising awareness of this illness is extremely important and severely required as many people are wrongly diagnosed till the illness has done damage that can't be repaired or worse in some situations. Two great organizations that are making real progress in raising awareness, research, and helping those with encephalitis & autoimmune encephalitis are: In USA: AE Alliance
https://aealliance.org @aealliance
In UK: Encephalitis Society
https://www.encephalitis.info @the_encephalitis_society_ #red4wed #encephalitis #livingwithae #keepmovingforward All the best and keep moving forward!
World Encephalitis Day is a globally recognized awareness event held on February 22nd to educate people about encephalitis which is a rare but serious inflammation of the brain. The day seeks to promote early detection, treatment, and support for those impacted by this condition, which can be caused by viruses, bacteria, and autoimmune disorders.
Symptoms of encephalitis include fever, headache, confusion, seizures, and in severe cases, coma. While some individuals may recover fully, others may suffer long-term neurological problems or even death.
By participating in World Encephalitis Day, individuals, healthcare professionals, and organizations can unite to learn more about this condition and support those affected by it. Through increased awareness, research, and advocacy, we can work towards improving outcomes for individuals impacted by encephalitis.
Learn more at https://aealliance.org/patient-support/what-is-ae/ Help raise awareness, volunteer, or donate at https://aealliance.org/how-can-you-help/
World Encephalitis Day is a globally recognized awareness event held on February 22nd to educate people about encephalitis which is a rare but serious inflammation of the brain. The day seeks to promote early detection, treatment, and support for those impacted by this condition, which can be caused by viruses, bacteria, and autoimmune disorders.
Symptoms of encephalitis include fever, headache, confusion, seizures, and in severe cases, coma. While some individuals may recover fully, others may suffer long-term neurological problems or even death.
By participating in World Encephalitis Day, individuals, healthcare professionals, and organizations can unite to learn more about this condition and support those affected by it. Through increased awareness, research, and advocacy, we can work towards improving outcomes for individuals impacted by encephalitis.
Learn more at https://aealliance.org/patient-support/what-is-ae/ Help raise awareness, volunteer, or donate at https://aealliance.org/how-can-you-help/
Today is #WorldEncephalitisDay!!! It is a day that has special meaning to me and many others touched by encephalitis and more specifically autoimmune encephalitis in my case. 6 years ago, I didn't know what Autoimmune Encephalitis was until I “woke up” in the Penn Medicine’s Hospital of the University of Pennsylvania after being misdiagnosed by two different doctors at two different hospitals and almost being committed to the nursing home to “live out the rest of my life comfortably.” i love @pennmedicine Encephalitis is an illness that involves the inflammation of the brain from either an infection or the immune system mistakenly attacking the brain. In my case, I have Autoimmune Encephalitis which is a rare illness that causes the immune system to think something is invading your body (which it should do) but it develops a "glitch" and it thinks the brain is the culprit. So, it starts attacking the brain. Symptoms are similar to symptoms of other neurological illnesses such as dementia, Alzheimer's, schizophrenia. Among these symptoms are confusion, altered behavior, psychosis, hallucinations, sleep disturbance, cognitive issues, memory loss, seizures, and physical disorders. Hundreds of thousands of people globally each year are affected by autoimmune encephalitis, and encephalitis, and are misdiagnosed, but a correct and quick diagnosis can make all the difference between life and death. As such, education and raising awareness of this illness is extremely important and severely required as many people are wrongly diagnosed till the illness has done damage that can't be repaired or worse in some situations. As such, education and raising awareness of this illness is extremely important and severely required as many people are wrongly diagnosed till the illness has done damage that can't be repaired or worse in some situations. Two great organizations that are making real progress in raising awareness, research, and helping those with enecephalitis & autoimmune encephalitis are: In USA: @aealliance In UK: @the_encephalitis_society_ Share the graphic with hashtags #RED4WED #WED2022 All the best and keep moving forward ! https://www.instagram.com/p/CaTL0Kvs-7e/?utm_medium=tumblr
Today is #WorldEncephalitisDay!!! It is a day that has special meaning to me and probably is to those reading this. Education and awareness of this illness is extremely important and severely required as many people are wrongly diagnosed till the illness has done damage that can't be repaired or worse in some situations. The @aealliance is the best AE organization in the United States and is making real progress in raising awareness, research, and helping those with autoimmune encephalitis and their families, but as with every great organization, they can always use some help. Sooo...if you want to help raise awareness about #AutoimmuneEncephalitis, share this poster on all your social media. Also please use the hashtags #RED4WED #WED2022 As you share, please encourage others to as well. Awareness can make all the difference ! As always, all the best to you and yours and keep moving forward !! https://www.instagram.com/p/CaRJJmvO-yj/?utm_medium=tumblr
Today is #WorldEncephalitisDay!!! It is a day that has special meaning to me and probably is to those reading this. Education and awareness of this illness is extremely important and severely required as many people are wrongly diagnosed till the illness has done damage that can't be repaired or worse in some situations. The @aealliance is the best AE organization in the United States and is making real progress in raising awareness, research, and helping those with autoimmune encephalitis and their families, but as with every great organization, they can always use some help. Sooo...if you want to help raise awareness about #AutoimmuneEncephalitis, share this poster on all your social media. Also please use the hashtags #RED4WED #WED2022 As you share, please encourage others to as well. Awareness can make all the difference ! As always, all the best to you and yours and keep moving forward !! https://www.instagram.com/p/CaRJBqcOZBR/?utm_medium=tumblr
I was diagnosed with nmadr encephalitis back in 2017. It’s been a long recovery but somehow, out of all the pain and suffering I think I’ve actually become a better version of myself because I experienced such hardships. Today is the day to spread awareness for such a devastating but also life changing neurological disease.