The Encephalitis Podcast

The Encephalitis Podcast

Encephalitis International
Pays Royaume-Uni
Genres Health & Fitness, Mental Health, Medicine
Langue EN
Épisodes 71
Dernier 01.06.2026

A podcast from Encephalitis International that explores all aspects of encephalitis, an inflammation of the brain. It provides information and insights for patients, caregivers, and medical professionals. The show aims to raise awareness and offer support through expert interviews and personal stories.

Épisodes

  • Ep 72 - What Encephalitis Took and What Recovery Gave Back - Evie's Encephalitis Story 01.06.2026 35min
    As part of Volunteer Week, we’re sharing the powerful story of Evie, who developed autoimmune anti-NMDAR encephalitis at just 19 years old. 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. ---------------------------------------------------------------------------------------- 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 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 71 - Returning to School After Encephalitis - A Parent’s Journey with Hina & Dian 21.05.2026 20min
    In this episode, Prav speaks with Hina about her son Dian’s journey with autoimmune encephalitis and the challenges of returning to school after a life-changing diagnosis. 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.  ------------------------------------------------------------------------------------ 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 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 70 - Inside 'Unconquered' A Powerful West Nile Survivor Story 22.04.2026 47min
    The Encephalitis Podcast Ep 70 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 ---------------------------------------------------------------------------------------------------------- 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: 📢 Facebook: https://www.facebook.com/EncephalitisInternational 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 69 - Surviving Tick-Borne Encephalitis: Bill’s Story & Why Vaccination Matters 22.04.2026 46min
    The Encephalitis Podcast Ep 69 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. -------------------------------------------------------------------------------------------------------------------------- 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: 📢 Facebook: https://www.facebook.com/EncephalitisInternational 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 68 - Complete Your Vaccination Course: A Key Step in Preventing Encephalitis - with Prof Lance Turtle 22.04.2026 14min
    The Encephalitis Podcast Ep 68 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 ------------------------------------------------------------------------------------------------------------------------- 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: 📢 Facebook: https://www.facebook.com/EncephalitisInternational 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 67 - Could dexamethasone improve HSV encephalitis outcomes - with Professor Tom Solomon CBE 17.04.2026 25min
    Ep 67 - In this episode of the Encephalitis Podcast, Prav speaks with Professor Tom Solomon CBE, a leading neurologist and infectious disease expert, about the groundbreaking DexEnceph study - two decades in the making. 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. ------------------------------------------------------------------------- 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: 📢 Facebook: https://www.facebook.com/EncephalitisInternational 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 66 - Global Encephalitis Training: Saving lives in low-resource settings with Dr. Aline Matos 02.04.2026 17min
    In this episode of the Encephalitis Podcast, Prav speaks with neurologist Dr. Aline Matos about the development of global training modules designed to help clinicians diagnose and treat encephalitis -especially in low-resource settings. 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 ------------------------------------------------------------------------------------------------------------------------- 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: 📢 Facebook: https://www.facebook.com/EncephalitisInternational 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 65 - Understanding MOG Antibody-Associated Encephalitis with Dr. Matteo Gastaldi 27.03.2026 10min
    What is MOG antibody-associated encephalitis, and how does it differ from other types of autoimmune brain inflammation? 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. ----------------------------------------------------------------------------------------------------------------------------- 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: 📢 Facebook: https://www.facebook.com/EncephalitisInternational 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 64 - Parenting after encephalitis with Dr Freddie Byrne 14.03.2026 54min
    The Encephalitis Podcast Ep 63 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. ----------------------------------------------------------------------------------------------------------------------------- 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 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 63 - F.L.A.M.E.S. - The Life-Saving Encephalitis Acronym with Dr Nicholas Davies 19.02.2026 14min
    Encephalitis Podcast Ep 63  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. ------------------------------------------------------------------------------------------- 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: 📢 Facebook: https://www.facebook.com/EncephalitisInternational 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 62 - Contagion on Screen: Science, Storytelling, and Encephalitis with Scott Z. Burns 30.01.2026 52min
    Encephalitis Podcast Ep 62 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/ ------------------------------------------------------------------------------------------- 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: 📢 Facebook: https://www.facebook.com/EncephalitisInternational 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 61 - Emotions, pain and unspoken dreams - Denis' Encephalitis Story 21.01.2026 36min
    In this powerful and emotive podcast episode Denis shares his journey of living with viral encephalitis from his life as an aeronautical engineer through the sudden onset of illness, hospitalisation, and a long, complex recovery. He discusses memory loss, intense emotions, vivid and distressing 'encephalitis dreams'. 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
  • Ep 60 - Sleep and Encephalitis with Dr David Lee 26.11.2025 34min
    The Encephalitis Podcast Ep 60 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. ------------------------------------------------------------------------------------------- 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 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 59 - Wady's Story of Music and Autoimmune Encephalitis 29.10.2025 19min
    In this episode, Prav talks to Wady a patient advocate, music educator, singer-songwriter and survivor of anti-NMDA receptor encephalitis. Here is a link to Wady's music https://youtu.be/btoaGoXLi1k -------------------------------------------------------------------------------------------------------------------------------- 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 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 58 - Neurological physiotherapy and encephalitis with Kenny Thoms 15.10.2025 24min
    Encephalitis Podcast Episode 58 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. -------------------------------------------------------------------------------------------------- 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 📢 Instagram: https://www.instagram.com/encephalitisinternational  📢 LinkedIn: https://uk.linkedin.com/company/encephalitisinternational
  • Ep 57 - Milkshakes for Marleigh - Kate Fisher 17.09.2025 34min
    In this episode, Prav is joined by a mother who is changing the world! Not just for her own child, but for so many others. Kate Fisher, the founder of Milkshakes for Marleigh - a blood donation initiative in Australia - talks about her daughter's experience of encephalitis and how she now commits her life to blood donor advocacy. 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 ------------------------------------------------------------------------------------------- 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
  • Ep 56 - Genetics in Autoimmune Encephalitis with Dr Sophie Binks 04.09.2025 22min
      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
  • Ep 55 - Relationships after encephalitis with Dr Giles Yeats 21.07.2025 30min
    The Encephalitis Podcast Ep 55 - Relationships after encephalitis with Dr Giles Yeats 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: Facebook: https://www.facebook.com/encephalitisinternational LinkedIn: https://www.linkedin.com/company/encephalitisinternational Instagram: https://www.instagram.com/encephalitisinternational
  • Ep 54 - LGi1 Autoimmune Encephalitis Pauline's Story 09.07.2025 47min
    In this lived experience episode of the Encephalitis Podcast, Prav talks to Pauline - a volunteer for Encephalitis International. 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: Facebook: https://www.facebook.com/encephalitisinternational LinkedIn: https://www.linkedin.com/company/encephalitisinternational Instagram: https://www.instagram.com/encephalitisinternational
  • Ep 53 - Discussing autoimmune encephalitis with Professor Sarosh Irani 25.06.2025 22min
    It this episode of The Encephalitis Podcast, Prav is asking Professor Sarosh Irani the question 'What's new in autoimmune encephalitis?' 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

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