What began with flu-like symptoms quickly became seizures, hallucinations, psychosis, memory loss, and months in hospital. In this deeply honest conversation, Evie opens up about surviving encephalitis as a teenager, losing her sense of identity, struggling to return to work and normal life, and the emotional impact the illness had on her relationships and mental health.

Now a volunteer with Encephalitis International, Evie supports other survivors and families through our online peer support groups - helping people realise they are not alone.

This episode navigates through recovery, identity, isolation, and life after brain injury.

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

-----------------------------------------------------------------------------------------

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After Dian began experiencing seizures at just seven years old, Hina and her family faced a long and emotional journey through hospital testing, uncertainty, memory difficulties, and major changes in daily life and more recently his transition up to a new school.

Hina reflects back on the past 5 years and shares how encephalitis affected Dian’s learning, confidence, friendships, and family dynamics and how communication, persistence, counselling, and school support helped them move forward. 

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

----------------------------------------------------------------------------------

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📢 Instagram: https://www.instagram.com/encephalitisinternational 

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In this special episode of the Encephalitis Podcast for World Immunization Week, we spotlight West Nile encephalitis through the powerful short film Unconquered: Battling Back After West Nile Virus.

Host Prav is joined by Tom, a West Nile encephalitis survivor, and Shawn, filmmaker and CEO of SES Productions, who brought Tom’s story to life on screen.

Tom shares his journey from sudden severe illness and hospitalization in 2024, through weeks of rehabilitation, to his ongoing recovery marked by determination, physical therapy, and personal goals. His story highlights the long-term neurological impact of the disease and the slow, non-linear path to regaining strength and mobility.

Shawn discusses how a chance connection led him to Tom’s story, and why he felt compelled to document it. Drawing on his background in journalism, he explains the importance of human storytelling in raising awareness, balancing science with personal narrative, and sparking conversations about prevention, early diagnosis, and the urgent need for a human vaccine.

This episode was filmed as part of World Immunization Week April 2026

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate #EncephalitisAwareness #BrainDisorder #EncephalitisSociety ----------------------------------------------------------------------------------------------

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📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational

In this episode of the Encephalitis Podcast, Prav speaks with Bill, an endurance athlete who shares his powerful journey through tick-borne encephalitis (TBE). From competing in swimrun events across Nordic countries to facing severe neurological symptoms and a long recovery, Bill’s story highlights how unexpected and serious this virus can be.

As part of World Immunization Week, this conversation sheds light on the risks of TBE, the challenges of recovery, and the importance of vaccination for those traveling to or active in endemic regions. Bill also offers honest insights into life after encephalitis and practical advice for others affected.

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate #EncephalitisAwareness #BrainDisorder #EncephalitisSociety --------------------------------------------------------------------------------------------------------------------------

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📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational

In this episode, we explore why completing your full vaccination schedule is essential for protecting against encephalitis. 

Prav is joined by Professor Lance Turtle, an expert in infectious diseases, who explains how vaccines work, why multiple doses matter, and the risks of stopping after just one shot. Learn how vaccines not only protect individuals but also help reduce the global burden of serious brain infections.

This episode was filmed as part of World Immunization Week April 2026

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate #EncephalitisAwareness #BrainDisorder #EncephalitisSociety --------------------------------------------------------------------------------------------------------------------------

Follow Encephalitis International:

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📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational

Discover how this UK-wide clinical trial explored whether dexamethasone (a corticosteroid used to treat various inflammatory conditions) could improve outcomes in herpes simplex virus (HSV) encephalitis, the challenges of running long-term research, and the powerful role patients and families play in advancing medical science.

Professor Solomon CBE shares insights from the study’s findings, including why early treatment may matter, how the results could influence future care, and what it truly takes to see a complex clinical trial through to completion.

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate #EncephalitisAwareness #BrainDisorder #EncephalitisSociety ---------------------------------------------------------------------

Follow Encephalitis International:

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They explore why encephalitis is often missed or misdiagnosed, the life-changing consequences of delayed diagnosis, and how these practical modules empower clinicians to act even with limited tools.

Dr Matos says 'Encephalitis does not end when the acute phase ends. The long-term sequelae, cognitive behaviour, social are often invisible but deeply impactful. So improving and saving lives care is not only about saving lives, as we said earlier, it is about preserving lives.'

The global training modules can be viewed on the BMJ website here https://new-learning.bmj.com/collection/30000415

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate #EncephalitisAwareness #BrainDisorder #EncephalitisSociety ---------------------------------------------------------------------------------------------------------------------------

Follow Encephalitis International:

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📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational

In this episode of The Encephalitis Podcast, Prav speaks with Dr. Matteo Gastaldi, neurologist and Head of the Neuroimmunology Research Unit in Pavia, Italy. Together, they explore MOG antibody-associated disease (MOGAD), including how it presents in children and adults, symptoms to watch for, how it can mimic viral encephalitis, and current treatment approaches.

Dr. Gastaldi also discusses relapse risk, long-term treatment decisions, the challenges of antibody testing, and exciting developments in ongoing clinical trials. This episode offers hope and clarity for patients, families, and clinicians navigating this complex and evolving condition.

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate #EncephalitisAwareness #BrainDisorder #EncephalitisSociety -------------------------------------------------------------------------------------------------------------------------------

Follow Encephalitis International:

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📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational

In this episode, Prav is joined by Dr. Freddie Byrne, clinical psychologist and Clinical Director of Living with ABI Limited. 

Together they explore the realities of parenting after encephalitis and acquired brain injury (ABI), including changes in family roles, the impact on children’s well-being, trauma, and post-injury growth. Drawing on over a decade of experience, Dr. Byrne shares practical insights into supporting families, improving communication, and keeping children’s needs at the center of recovery. 

An essential conversation for parents, families, and professionals affected by encephalitis and ABI.

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

-------------------------------------------------------------------------------------------------------------------------------

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📢 Instagram: https://www.instagram.com/encephalitisinternational 

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In this episode of The Encephalitis Podcast, Prav is joined by leading neurologist Dr Nicholas Davies to introduce F.L.A.M.E.S., a new life-saving acronym designed to help the public and healthcare professionals recognise the urgent symptoms of encephalitis.

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate #EncephalitisAwareness #BrainDisorder #EncephalitisSociety -------------------------------------------------------------------------------------------

Follow Encephalitis International:

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📢 Instagram: https://www.instagram.com/encephalitisinternational 

📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational

In this episode of the Encephalitis Podcast, Prav is joined by award-winning screenwriter and director Scott Z. Burns to discuss the depiction of encephalitis in films and explore the science, humanity, and lasting impact of the 2011 film Contagion. Inspired by real-world viruses such as Nipah and SARS, the film gained renewed relevance during the COVID-19 pandemic for its portrayal of a global outbreak with neurological consequences.

Nipah virus factsheet - https://www.encephalitis.info/types-of-encephalitis/infectious-encephalitis/nipah-virus-infection/

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate #EncephalitisAwareness #BrainDisorder #EncephalitisSociety ------------------------------------------------------------------------------------------

Follow Encephalitis International:

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Denis also explains the coping strategies, psychological support, and practical techniques that helped him regain stability, including working with a neuropsychologist and learning effective distraction tools. His story offers honesty, hope, and valuable insight for anyone affected by encephalitis or supporting a loved one through recovery.

#ViralEncephalitis #EncephalitisAwareness #NeuroSymptoms #LifeAfterEncephalitis #EncephalitisSupport #UnderstandingEncephalitis #BrainHealthTips

This podcast episode is about sleep and encephalitis. Sleep difficulties can be a symptom of encephalitis as well as a potentially long-term after-effect.   Prav is joined by Dr. David Lee. Dr Lee is a chartered psychologist and chartered scientist who has been researching sleep and the psycho-behavioral treatment of insomnia for the last 20 years. He holds memberships with the World Sleep Society, the British Sleep Society, the Institute of Occupational Safety and Health, the British Association of Brain Injury Case Managers, the Vocational Rehabilitation Association, and the British Psychological Society, where he also holds an associate fellowship.

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

------------------------------------------------------------------------------------------

Follow Encephalitis International:

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Here is a link to Wady's music https://youtu.be/btoaGoXLi1k

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

------------------------------------------------------------------------------------------------------------------------------

Follow Encephalitis International:

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In this episode, Prav talks to Kenny Thoms the Co-Founder, Director & Specialist at NeuroPhysio in Glasgow. Kenny works with individuals recovering from neurological events or those managing long-term neurological conditions.

They discuss neurological physiotherapy and rehabilitation including the specific neurological challenges that encephalitis survivors face.

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

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Kate founded Milkshakes for Marleigh after her daughter was diagnosed with seronegative paediatric autoimmune encephalitis and relied on blood donors for her treatment.

You can find out more about her work on her website - https://milkshakesformarleigh.org

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

-------------------------------------------------------------------------------------------

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In this episode, Prav talks to Dr Sophie Binks about genetics and DNA in relation to autoimmune encephalitis. Asking the question 'can genetics play a part in the prevalence of encephalitis?'

Sophie is a Clinical Lecturer and Honorary Neurology SpR at Nuffield Department of Clinical Neurosciences, University of Oxford. She is also on the Scientific Advisory Panel for Encephalitis International. 

Her research focuses on clinical and genetic aspects of autoimmune encephalitis. 

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:  Facebook: https://www.facebook.com/encephalitisinternational  LinkedIn: https://www.linkedin.com/company/encephalitisinternational Instagram: https://www.instagram.com/encephalitisinternational

In this episode, Prav talks about relationships after encephalitis with Doctor Giles Yeates.

Relationships sit at the intersection of our personal and professional lives, shaping our identity, providing support during times of isolation, and often significantly transformed after encephalitis.

Dr Yeates is a consultant clinical neuropsychologist with over 20 years of experience in neuro rehabilitation. He has worked in internationally renowned NHS services in the UK, that's National Health Services such as the Community Head Injury Service, Aylesbury and the Oliver Zangwill Centre, Cambridgeshire.

With an additional background in Chinese martial arts, Doctor Yeates applies these practises to address physical and psychological needs.

Currently, he partners with charities on web-based resources, chairs the Thames Valley UK acquired Brain Injury Form, and serves as an active academic at Oxford Brookes University's Centre of Movement, Occupational and Rehabilitation Services.

--------------------------------------------------------------------------------------------------------------- If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

----------------------------------------------------------------------------------------------------------------------- Follow Encephalitis International:

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Pauline shares her own story of LGi1 encephalitis, life as a nurse and about being a support volunteer for the online peer groups.

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:

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Professor Irani is Professor of Neurology and Neurosciences at the Mayo Clinic, Florida, former professor of Autoimmune Neurology at the University of Oxford, and adjunct professor at the University of Southern Denmark.

He was part of the team that discovered LGI1 and CASPR2 antibodies and has cared for many patients with LGI1, CASPR2 NMDA, and other forms of autoimmune encephalitis.

Professor Irani is one of the world's most experienced clinicians in this area and has published over 200 scientific papers about autoimmune neurological diseases.

He's also a member of Encephalitis International's Scientific Advisory Panel, providing expert professional guidance which informs our research strategy, information, resources and guidance.

Find out more about autoimmune encephalitis here  - https://www.encephalitis.info/types-of-encephalitis/autoimmune-encephalitis/

------------------------------------------------------------------------------------------------------------------- If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support 

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch 

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

----------------------------------------------------------------------------------------------------------------------- Follow Encephalitis International:

Facebook: https://www.facebook.com/encephalitisinternational

LinkedIn: https://www.linkedin.com/company/encephalitisinternational

Instagram: https://www.instagram.com/encephalitisinternational

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:

Facebook: https://www.facebook.com/encephalitisinternational

LinkedIn: https://www.linkedin.com/company/encephalitisinternational

Instagram: https://www.instagram.com/encephalitisinternational 

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:

Facebook: https://www.facebook.com/encephalitisinternational

LinkedIn: https://www.linkedin.com/company/encephalitisinternational

Instagram: https://www.instagram.com/encephalitisinternational

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:

Facebook: https://www.facebook.com/encephalitisinternational

LinkedIn: https://www.linkedin.com/company/encephalitisinternational

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To learn more about wills or leaving a legacy gift to Encephalitis International visit: https://www.encephalitis.info/gift-in-will/.

This page also contains information about how UK residents can write their will for free, with our partners at Farewill. https://www.encephalitis.info/news/the-what-why-when-and-where-of-will-writing/

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:

Facebook: https://www.facebook.com/encephalitisinternational

LinkedIn: https://www.linkedin.com/company/encephalitisinternational

Instagram: https://www.instagram.com/encephalitisinternational 

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:

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https://www.liverpool.ac.uk/people/bhagteshwar-singh

https://braininfectionsglobal.tghn.org/the-programme/scientific-background/

https://braininfectionsglobal.tghn.org/resources/brain-infections-global-tools/

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate 

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Diane, 22, from London. is a final year Psychology with Cognitive Neuroscience undergraduate student, aspiring clinical neuropsychologist, speaker, social entrepreneur, encephalitis overcomer and volunteer. Diane had auto-immune encephalitis in 2018, when she was 15 which encompassed months in a semi-coma state where she couldn’t talk, walk, eat or see due to complete vision loss from high intracranial pressure.

Diane discusses her lived experience, reintegration into education and the importance of empowerment when going through recovery after encephalitis. 

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch

Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate 

Follow Encephalitis International:

Facebook: https://www.facebook.com/encephalitisinternational

LinkedIn: https://www.linkedin.com/company/encephalitisinternational

Instagram: https://www.instagram.com/encephalitisinternational 

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

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Beth and Brendan also discussed the Covid-19 Clinical Neuroscience Study – a £2.3 million research study looking at the acute neurological and neuropsychiatric complications of Covid-19. This podcast also discusses the future of the Covid-19 Clinical Neuroscience Study, the potential of its data to contribute to understanding cognitive disturbances, and the importance of individualised care and support for those affected by the neurological effects of COVID-19. Links to papers: Posthospitalization COVID-19 cognitive deficits at 1 year are global and associated with elevated brain injury markers and gray matter volume reduction | Nature Medicine Cognitive domains affected post‐COVID‐19; a systematic review and meta‐analysis - Fanshawe - 2025 - European Journal of Neurology - Wiley Online Library

Bethany Facer is a neuroimaging PhD student at the University of Liverpool, focusing on people with newly diagnosed Parkinson’s disease. Bethany is part of the neuroimaging working group for the COVID-Clinical Neuroscience Study and has previously worked on the DexEnceph trial assessing imaging changes in HSV encephalitis. An avid science communicator, she has presented at the Cheltenham Science Festival and has hosted and organised the annual Liverpool Neuroscience Conference.

Brendan Sargent is a junior doctor and clinical research fellow with the Autoimmune Psychosis Group at the University of Oxford. He is part of the neuroimaging working group for the COVID-Clinical Neuroscience Study consortium and has worked with the Infection Neuroscience Lab in Liverpool on the cognitive impacts of COVID-19 illness. He is interested in cognition, neuroimaging and neuroinflammation. For more information about the COVID-CNS study, visit https://www.liverpool.ac.uk/covid-cli...

f you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support If you would like to stay up to date with our news and events please sign up to our mailing list here: https://www.encephalitis.info/keep-in-touch Support our work providing help and assistance to families affected by encephalitis by visiting: https://www.encephalitis.info/donate

Follow Encephalitis International:

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In this episode of The Encephalitis Podcast, Dr Ava Easton is joined by Dr James Sejvar for a discussion around climate change, and how it's affecting our risk for deadly infectious diseases, such as West Nile encephalitis or Japanese encephalitis.

Dr Sejvar is a Neuroepidemiologist at the University of Pittsburgh and, University of Pittsburgh Medical Center, USA. At the time of the podcast, he led the Neuroepidemiology Unit at CDC’s Divisions of High-Consequence Pathogens and Pathology where his work focused on epidemiology, pathogenesis, clinical features, and outcomes of infections of the nervous system work which took him all over the world.

He investigated the West Nile virus in the United States, Ebola in Central Africa, Zika in South America, and of course, COVID-19. Dr Sejvar is also a member of the Encephalitis International Scientific Advisory Panel.

This podcast was recorded November 2023 - we have updated information and insights on these infectious diseases to come in April 2025. WATCH this space!

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Follow Encephalitis International:

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/contact-our-helpline/

Our support groups are listed here https://www.encephalitis.info/online-support-meetings

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://app.donorfy.com/form/L9J9FR7NZ5/00YAZ

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If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/contact-our-helpline/

Our support groups are listed here https://www.encephalitis.info/online-support-meetings

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://app.donorfy.com/form/L9J9FR7NZ5/00YAZ

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For more information about Professor Wilson's work please visit https://encephalitis.ucsf.edu/

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/contact-our-helpline/

Our support groups are listed here https://www.encephalitis.info/online-support-meetings

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://app.donorfy.com/form/L9J9FR7NZ5/00YAZ

Follow Encephalitis International:

Facebook: https://www.facebook.com/encephalitisinternational/

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LinkedIn: https://www.linkedin.com/company/encephalitisinternational

Instagram: https://www.instagram.com/encephalitisinternational/

TikTok: https://www.tiktok.com/@encephalitisint 

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/contact-our-helpline/

Our support groups are listed here https://www.encephalitis.info/online-support-meetings

Read more information about death from encephalitis on our website https://www.encephalitis.info/effects-of-encephalitis/death-from-encephalitis

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://app.donorfy.com/form/L9J9FR7NZ5/00YAZ

Follow Encephalitis International

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The trio talk about the monumental decision to change the name of the Encephalitis Society to Encephalitis International, the reasons and thinking behind the strategic evolution, and what comes next as we celebrate our 30th anniversary in 2024.

For more information about Encephalitis International, https://www.encephalitis.info/ 

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/contact-our-helpline/

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/become-a-member/

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://app.donorfy.com/form/L9J9FR7NZ5/00YAZ

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Threads: https://www.threads.net/@encephalitisinternational

Lance is a Reader and Honorary Consultant Physician in Infectious Diseases at the University of Liverpool.

As always, the questions are asked by our host, Dr Ava Easton, Chief Executive of the Encephalitis Society.

The Encephalitis Podcast is available on all podcast channels and on our YouTube channel.

For more information about Dr Lance Turtle: https://www.liverpool.ac.uk/infection-veterinary-and-ecological-sciences/staff/lance-turtle/ 

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

For more information about Japanese encephalitis, visit https://www.encephalitis.info/japaneseencephalitis 

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/

Follow the Encephalitis Society:

Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

Dr Ava Easton, Chief Executive of the Encephalitis Society, is joined by Dr Thomas Pollak, from Kings College London, and Dr Jesus Ramirez-Bermudez, of the National Institute of Neurology and Neurosurgery of Mexico, to talk about some two new important research papers around mental health and encephalitis.

An important note for our viewers and listeners: this podcast will be touching on some difficult areas, including more broad mental health issues and difficult topics such as self-harm and suicide.

If this is something which may lead to difficult emotions for you or for someone you know, please know that our support team are here to help and can be reached on support@encephalitis.info or by calling +44(0)1653 699599.

Also, in the links to this episode, you will find some resources which we have put together around mental health which we believe will be helpful to anyone affected by encephalitis and also their family and friends. This includes links to useful organisations around the world, a factsheet on mental health and lots of sources of support and information.

For more information about World Encephalitis Day on Wednesday, 22nd February, please visit www.worldencephalitisday.org

For information about mental health and encephalitis, visit https://www.encephalitis.info/pages/category/mental-health-and-encephalitis

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

Ten years ago, Susannah published Brain on Fire: My Month of Madness, the award-winning memoir and New York Times bestseller, which quickly become a Bible for members of the encephalitis community and many more people around the world.

Brain on Fire follows Susannah’s struggle with encephalitis and, in particular, her diagnosis and recovery.

It was later developed into a Hollywood film by Charlize Theron and starred Chloe Grace Moretz.

Susannah chats to Ava about the 10th anniversary, why the book resonated with so many people, its legacy, how she reacted when Hollywood came calling, and the impact it has had on the encephalitis community.

The 10th anniversary edition of Brain on Fire is available from all good booksellers, including

UK readers (Kindle and Paperback) https://www.amazon.co.uk/Brain-Fire-My-Month-Madness/dp/1451621388

USA - https://www.simonandschuster.com/books/Brain-on-Fire-(10th-Anniversary-Edition)/Susannah-Cahalan/9781451621389

For more information about World Encephalitis Day on Wednesday, 22nd February, please visit www.worldencephalitisday.org

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

In 2017, the former trial lawyer from Bismarck, North Dakota, became ill with encephalitis and experienced a host of difficulties, such as insomnia, paranoia, hallucinations and memory loss.

In the summer of 2018, after being voluntarily hospitalized in the psychiatric ward, she was finally diagnosed with seronegative autoimmune encephalitis.

To help her recovery, she began writing and speaking about her journey with encephalitis.

Today, Jackie hosts the podcast, Brain Fever and is also the author of the JM Stebbins blog. In 2022, her memoir, Unwillable: A Journey to Reclaim My Brain, was published by Wisdom Editions.

We hope you enjoy this conversation with the articulate and passionate encephalitis awareness advocate!

For more information about Jackie and her book, blog and podcast, please visit https://www.jmstebbins.com/

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society:

Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

In this wide-ranging conversation, they discuss an important new research paper before answering some questions around seizures and encephalitis.

Greta is an Academic Clinical Fellow in Infectious Diseases at the University of Liverpool and has a wide range of research interests, including the socio-economic impact of infectious diseases and multi-morbidity.

She is also a member of the COVID-19 Clinical Neuroscience Study which is investigating the neurological and neuropsychiatric complications of COVID-19.

The Encephalitis Podcast is also available on podcast channels, such as Apple, Google Play, Podbean and Spotify.

Find out more about seizures and encephalitis by viewing our factsheet: https://www.encephalitis.info/seizures-and-encephalitis

For more information about Greta, visit https://www.liverpool.ac.uk/infection-veterinary-and-ecological-sciences/staff/greta-wood/

The research paper, Acute seizure risk in patients with encephalitis, can be found here: https://neurologyopen.bmj.com/content/4/2/e000323 

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

Ben talks to host Dr Ava Easton about the COVID-19 Clinical Neuroscience Study – a £2.3 million research study looking in the acute neurological and neuropsychiatric complications of COVID-19.

He also shares his thoughts on being a front-line medic during the pandemic, the NHS in general and the upcoming Encephalitis Conference.

Ben is a Professor of Neuroscience at the University of Liverpool, a Medical Research Council Clinician Scientist and Honorary Consultant Neurologist at the Walton Centre, also in Liverpool. Ben is also Vice President of our Scientific Advisory Panel and helps to drive forward our research agenda and organise the Encephalitis Conference, among many other important areas of our work.

For more about the COVID-CNS study or to take part, visit https://www.liverpool.ac.uk/covid-clinical-neuroscience-study/

Follow the COVID-CNS study on Twitter: https://twitter.com/covidcns

Follow Ben on Twitter: https://twitter.com/BenedictNeuro

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

Born in Melbourne, Suzie is an award-winning playwright and screenwriter who has a background in law and science, working as a human rights lawyer and children's rights lawyer before leaving the law to pursue a theatre writing career full-time.

Prima Facie debuted in Australia in 2019, winning several awards, before moving to London's West End starring Jodie Comer. It will be heading to Broadway in 2023.

We hope you enjoy Suzie's conversation with Dr Ava Easton, the host of The Encephalitis Podcast.

For more about Suzie and her work, visit her website http://www.suziemillerwriter.com/

If you would like to find out more about Prima Facie, visit their official website https://primafacieplay.com/

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

Abi, who is perhaps best known for the films Suffragette, The Iron Lady and Shame, is now an author, having recently published, This is Not a Pity Memoir.

The book tells the story of her husband when he develops Anti-NMDAR encephalitis, the impact his illness had on their family, and also Abi’s own illness.

Ava said: “I devoured this book. It’s incredibly written, profoundly insightful and, at times, brutally authentic. But also, as Abi says, not a pity memoir, but a love story.”

We hope you enjoy this wonderful conversation!

This is Not a Pity Memoir is available from all online good bookshops.

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

This is a fascinating interview about how - and why - we get better, revealing the many shapes recovery takes, its shifting history and the frequent failure of our modern lives to make adequate space for it.

For more about Gavin, his work and books, visit http://www.gavinfrancis.com/

To order a copy of Recovery: The Lost Art of Convalescence, visit https://www.amazon.co.uk/gp/product/B099BVT2VH/ref=dbs_a_def_rwt_hsch_vapi_tkin_p1_i0

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

Dr Ava Easton interviews Phillippa Chapman, Deputy CEO of the Encephalitis Society, for a cosy chat which covers her ten years with the Encephalitis Society, becoming a new mum during the COVID-19 pandemic, and what the future holds for us a charity.

Sit back, pour yourself a cup of tea, and enjoy this cosy chat between Ava and Phillippa.

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/join-us

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society:

Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

The report - Encephalitis: an in-depth review and gap analysis of key variables affecting global disease burden - has identified a range of difficulties surrounding encephalitis around the world. Crucially, however, it proposes a range of solutions which could save lives and improve the treatment and after-care of millions of people today and into the future.

The report has been launched by six eminent scientists in the field of encephalitis, including Dr Julia Granerod, Alina Ellerington, Dr Nicholas Davies, Dr Benedict Michael, Professor Tom Solomon, and Dr Ava Easton.

For more information about the Global Impact Report, visit https://www.encephalitis.info/global-impact-report

If you would like to know more about World Encephalitis Day, visit www.worldencephalitisday.org

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/join-us

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

Sam is a self-published crime writer from Leeds whose debut novel, Murder at Macbeth, was published just over two years ago. She has also collaborated on a new non-fiction book with some of her fellow writers called Indie Writing Wisdom which offers advice and insights on writing and self-publishing.

Indie Writing Wisdom is dedicated to her dad who sadly passed away as a result of encephalitis in 2017 with proceeds going to the Encephalitis Society.

In this episode, Sam discusses her dad, her writing experiences and shares her advice for aspiring authors - a topic which will really resonate with many of our listeners who are interested in sharing their experiences of encephalitis.

Indie Writing Wisdom is available from Amazon at https://amzn.to/3ytkeIp

Murder at Macbeth by Samatha Goodwin is available from Amazon at https://amzn.to/3DU9GmI

The Encephalitis Podcast is available on You Tube, Google Play, Spotify, Apply and Podbean.

For previous episodes, visit https://www.encephalitis.info/Listing/Category/our-podcasts

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

The Encephalitis Podcast is available on You Tube, Google Play, Spotify, Apply and Podbean. For previous episodes, visit https://www.encephalitis.info/Listing/Category/our-podcasts

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

Juliana, who is a Psychology and Neuroscience student at the University of Florida, was speaking during Encephalitis Information Week.

To read more about Juliana's story, visit https://www.encephalitis.info/julianas-story

For more information about Encephalitis Information Week, visit www.encephalitis.info/informationweek

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

If you have a legal question around encephalitis, or want to download our Neuro-Legal handbook, visit https://www.encephalitis.info/legal-advice

For more information on Encephalitis Information Week, visit www.encephalitis.info/informationweek

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society:

Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

On Boxing Day 2016, Catherine's husband, Alan, had his first devastating seizure as a result of encephalitis, thrusting the Jessop family into an unknown world.

In her book, Catherine shares advice and inspiration on everything she has learned, with chapters clarifying medical terms and explaining tests and scans as well as explaining some of the financial and legal issues around illness.

Catherine also focuses on the emotional side of having a relative with a brain injury and how it affects the whole family, sharing her own thoughts on how to look after the mental health of both patient and carer and the power of nature, humour, music and optimism.

This is an excellent chat about an excellent book - enjoy! Pulling Through: Help for Families Navigating Life-Changing illness by Catherine Jessop is available from https://www.amazon.co.uk/Pulling-Through-Families-Navigating-Life-Changing/dp/1787753727

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Follow the Encephalitis Society: Facebook: https://www.facebook.com/EncephalitisSociety/

Twitter: https://twitter.com/encephalitis

Instagram: https://www.instagram.com/the_encephalitis_society_/

LinkedIn: https://www.linkedin.com/company/the-encephalitis-society

Motherhood, Pandemics and the Olympics delves into Rebecca's outstanding swimming career, the new addition to her family and what life was like for her during the COVID-19 lockdowns.

She also talks about the Tokyo Olympics and what Team GM swimmers we should be looking out for!

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

Dr Ava Easton, our Chief Executive, talks to Donna Malley, an an Occupational Therapy Clinical Specialist at the Oliver Zangwill Centre.

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

For more information about the Oliver Zangwill Centre, visit https://www.cambscommunityservices.nhs.uk/what-we-do/all-other-services/oliver-zangwill-centre-(ozc)/ 

Professor Stone is Professor of Neurology at the University of Edinburgh, and Dr Nicholson, is Honorary Consultant Neuropsychiatrist at Institute of Psychiatry, Psychology & Neuroscience (IoPPN), Kings College London.

We cover everything from presentations of FND, encephalitis and FND, advice for someone who believes they have the condition, advice for medical professionals, and overcoming stigma associated with FND and much more.

We hope you enjoy this informative discussion with Tim and Jon!

If you have been affected by encephalitis and are in need of some support, please visit https://www.encephalitis.info/support

If you have been affected by encephalitis and would like to become a member of the society, you can sign up here (membership is free and global): https://www.encephalitis.info/Pages/Category/membership

If you would like to donate to help fund research, information and support for those affected by encephalitis, please follow this link: https://www.encephalitis.info/donate/donate/10

In 2011, as he was finishing his first film, The Guga Hunters of Ness, Mike became ill with encephalitis. He lost the ability to walk and was even told that he would not be able to work again.

However, during his recovery, Mike threw himself into his next film, The Islands and the Whales, a true labour of love which was filmed over five years in the Faroe Islands.

This is a great interview with Mike which touches on his illness and recovery, his work as a documentary film maker and what lies in store for him in the coming year.

Mathew is an actor, an artist, nutritionist, life coach and an excellent cook! He has also been an Ambassador with the Encephalitis Society for around 14 years – his arrival and support was one of the catalysts for us really beginning to kick on as a global organisation. As always, our podcast is hosted by Dr Ava Easton, our Chief Executive.

We enjoyed this podcast - and we hope you do too!  

Synopsis: It’s 1962 and burgeoning children's author Roald Dahl and Patricia Neal, a glamourous Hollywood movie star, have retreated to the English countryside to bring up their expanding young family. Tragically, their lives are turned upside down by the devastating death of their daughter Olivia from measles encephalitis and as the couple struggle through the unimaginable loss, their shared grief becomes a source of redemption and strength which changes their lives forever.

Professor Solomon is Chair of Neurology and Director of the National Institute for Health Research's Health Protection Research Unit in Emerging and Zoonotic Infections.

Recorded 28th January, 2021.

For more information about COVID-19 vaccines and encephalitis, please visit https://www.encephalitis.info/covid-19-vaccination-statement

In our latest podcast, Dr Ava Easton chats to Dr Bhagteshwar Singh, Clinical Research Fellow, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool.

He talks to Dr Ava Easton about his illness and the lasting effects of the infection that he is experiencing today, a term which has become known as 'Long Covid'.

Professor Peter Hotez is Dean for the National School of Tropical Medicine and a Professor at the Departments of Paediatrics and Molecular Virology and Microbiology, at the Baylor College of Medicine in Houston, which have been at the forefront of both research and treatment of the Covid-19 infection.

This podcast was recorded on April 14, 2020.

Recorded: March 20, 2020.