WORLD ENCEPHALITIS DAY CONFERENCE 2026
REGISTRATION NOW OPEN
REGISTRATION NOW OPEN
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Encephalitis is inflammation of the brain. It can strike anyone, anywhere, at any time, and at any age, resulting in a serious and sometimes life-threatening medical emergency. Those who survive its assault are left with an acquired brain injury.
Though it is considered rare, each year an estimated 20,000 people in the United States and 500,000 people globally are diagnosed with encephalitis. Residual symptoms are varied, life-altering, and costly, leaving survivors and their loved ones changed forever.
Though it is considered rare, each year an estimated 20,000 people in the United States and 500,000 people globally are diagnosed with encephalitis. Residual symptoms are varied, life-altering, and costly, leaving survivors and their loved ones changed forever.
FIGHTING ENCEPHALITIS HEAD ON.....INTO 2026!!
As the year draws to a close, we at Encephalitis411 invite you to view Fighting Encephalitis Head On!, a short video that features a few stories from our community.
As you watch, take a moment to step back from the hustle and bustle of the year and reflect on the things that matter most to you.
As you watch, take a moment to step back from the hustle and bustle of the year and reflect on the things that matter most to you.
For many of us, health, family, and friendships top the list of things we cherish most. Yet these are often the areas that become destabilized most for those who are impacted by encephalitis. Every day we support and advocate for individuals experiencing the devastating physical, economic, and psychosocial consequences of encephalitis.
Next year will be no different. Looking ahead to next year, 20,000 people in the U.S alone will be diagnosed with encephalitis. That’s a new town of people who will be unexpectedly faced with the harsh realities of fighting to get care for a rare disease that is frequently misdiagnosed, has no cure, is poorly understood by the medical community, and forever changes the lives of those it touches.
And they’re going to need our support.
We know that many are facing financial hardship during these challenging economic times. Further still, some are struggling under the weight of medical debt due to the lack of FDA-approved medications to treat encephalitis, and the numerous barriers to insurance coverage for critical rehabilitative therapies.
That’s why we at Encephalitis411 strive to keep our services 100% free. We are honored to support patients, caregivers, medical providers, and other community members during their critical times of need.
But for those in more fortunate circumstances, we would appreciate your support. Please consider making a tax deductible donation before the end of the year, to enable us to continue these vital services for those impacted by encephalitis.
Next year will be no different. Looking ahead to next year, 20,000 people in the U.S alone will be diagnosed with encephalitis. That’s a new town of people who will be unexpectedly faced with the harsh realities of fighting to get care for a rare disease that is frequently misdiagnosed, has no cure, is poorly understood by the medical community, and forever changes the lives of those it touches.
And they’re going to need our support.
We know that many are facing financial hardship during these challenging economic times. Further still, some are struggling under the weight of medical debt due to the lack of FDA-approved medications to treat encephalitis, and the numerous barriers to insurance coverage for critical rehabilitative therapies.
That’s why we at Encephalitis411 strive to keep our services 100% free. We are honored to support patients, caregivers, medical providers, and other community members during their critical times of need.
But for those in more fortunate circumstances, we would appreciate your support. Please consider making a tax deductible donation before the end of the year, to enable us to continue these vital services for those impacted by encephalitis.
annual fundraiser --- IT'S NEVER TO LATE TO HELP!
Nicole's Challenge is our annual Fundraising Event. Visit the EVENTS Page to learn about Nicole and find out how you can help us Fight Encephalitis HEAD ON! |
Click the contents page to link to the August Newsletter, Heads Up!
get the factsLearn about encephalitis: what it is, who it impacts, and the differences between infectious and autoimmune subtypes. This section provides an overview, symptoms, diagnosis, treatment, outcomes, FAQ, and more.
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GET HElpEncephalitis411 offers a free support hotline for those looking for support and guidance. We can also assist you in finding resources in your area and connecting with fellow community members online or in-person.
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Get involved Our community would not be as robust as it is without the volunteer efforts, donations, stories, and input of people like you. Your involvement helps us touch thousands of lives impacted by encephalitis.
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ENCEPHALITIS RESEARCH, AWARENESS, AND ADVOCACY IS LIMITED. PATIENTS ARE OFTEN MISDIAGNOSED. THE RESULT IS DELAYED TREATMENT, INCOMPLETE RECOVERY, AND WORSE OUTCOMES.
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Help us improve the quality of life for those impacted by encephalitis
About Encephalitis411Encephalitis411 serves as a link between patients, caregivers, clinicians, scientists, and other related stakeholders. Together we are on a mission to improve the quality of life for those impacted by encephalitis. Our U.S-based services are designed to address unmet needs in encephalitis research, awareness, and advocacy. >Learn more
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