Reflections on the life and career of Dr. Juhn Wada (1924-2023)

Juhn Atsushi Wada was a Japanese–Canadian neurologist known for research on epilepsy and brain asymmetry, including the development of the Wada test to assess hemispheric dominance of language function. He became a pioneer in the utilization of the kindling model of epilepsy, which permitted controlled studies of the development of epilepsy in the laboratory.

The bumpy road from pediatric to adult epilepsy care: Dr. Danielle Andrade

The shift from pediatric to adult epilepsy care can be complex. A recent survey of young people with epilepsy found that 25% still saw pediatric neurologists for their epilepsy care. Only 4% said they received clear instructions during the transition process.

Investigating pediatric epilepsy in Nigeria: Dr. Edwin Trevathan

In northern Nigeria, more people need epilepsy treatment than traditional medical care can support. Dr. Edwin Trevathan discusses projects aimed at identifying children with undiagnosed epilepsy and improving access to care, as well as research to better understand the risks and prognosis of pediatric status epilepticus.

Changing epilepsy care through entrepreneurship: Dr. Mark Cook

Dr. Cook realized, when his father was diagnosed with epilepsy, that a system to identify and predict seizures could improve care and change people’s lives. In this episode, Dr. Cook talks about entrepreneurship in epilepsy and advancing the field through innovation.

Educating non-specialists in Mexico: New university course offers hybrid experience

The involvement of primary healthcare providers in epilepsy care can translate to early intervention, education about the condition, and coordination of care. However, many primary healthcare providers do not have sufficient training to care for people with epilepsy, leading to gaps in diagnosis and treatment.

Educando a no especialistas en México: Nuevo curso universitario ofrece experiencia híbrida

Un nuevo curso acreditado sobre epilepsia está educando a una variedad de profesionales de la salud a través de un modelo híbrido. Impartido en español, el curso está atrayendo a médicos de atención primaria, neurólogos, neuropsicólogos y antropólogos.

“Talking about things that no one else will talk about”: Torie Robinson, host of Epilepsy Sparks Insights

Diagnosed with epilepsy at age 10, Torie Robinson uses her podcast to share knowledge with people with epilepsy, their families, and the public. Her episode topics range from the biochemistry of epilepsy to gastrointestinal issues and much, much more.

Comment les médecins peuvent-ils encourager les personnes atteintes d’épilepsie à pratiquer une activité physique ?

Des études suggèrent que faire de l’exercice améliore la condition physique, l’humeur, la pensée et la mémoire, ainsi que la qualité de vie globale des personnes atteintes d’épilepsie – autant d’avantages qui s’appliquent également aux personnes non épileptiques.

Cerebral amyloid angiopathy, seizures, and epilepsy: Dr. Brin Freund

Sixty percent of patients with dementia on autopsy studies have cerebral amyloid angiopathy (CAA) pathology. This episode discusses the relationship between CAA and epilepsy through the lens of a recent publication. Dr. Alina Ivaniuk talks with Dr. Brin Freund.

35th International Epilepsy Congress presents latest in epilepsy research and professional opportunities

The 35th International Epilepsy Congress (IEC) will take place September 2 – 6, 2023, in Dublin, Ireland. Registrants will hear from the best in global epileptology during teaching courses, symposia, and lectures hosted by the ILAE and IBE.

Soutenir les personnes atteintes d’épilepsie aves des outils pour réduire la stigmatisation

La stigmatisation affecte tous les aspects des soins de l’épilepsie, du diagnostic au traitement en passant par la législation et aux allocations budgétaires. Elle affecte la vie des personnes atteintes d’épilepsie lorsqu’elles n’ont pas un accès égal à l’éducation, à l’emploi et aux mêmes droits sociaux.

Empowering people with epilepsy to lead the way in reducing stigma

Stigma affects all aspects of epilepsy care. It affects the lives of people with epilepsy when they are not given equal access to education, employment, and social opportunities. In a US study, one-third of respondents identified stigma—not seizures—as the most difficult part of living with epilepsy.

Moving epilepsy care closer to home: Dr. Gagandeep Singh and Dr. Meenakshi Sharma

Can bringing epilepsy care to people’s homes improve outcomes? ILAE spoke with two researchers who conducted a randomized trial of home-based care versus clinic-based care in northern India. Those receiving the home-based care, delivered by community health workers, had better outcomes.

How can primary health care help to close the epilepsy treatment gap? A journey through Andhra Pradesh, India

Hours from the nearest city in India, down a pothole-studded road framed by fish farms, primary care centers in Andra Pradesh provide service to tens of thousands of people. How do these centers care for people with epilepsy, and what challenges do they face?

La encuesta de ILAE destaca las preocupaciones globales sobre los medicamentos genéricos anticrisis

Los neurólogos de todo el mundo tienen preocupaciones sobre el uso de medicamentos genéricos anticrisis, cuestionando la calidad deficiente o inconsistente, el acceso limitado, el costo y la falta de control regulatorio.

ILAE survey highlights global concerns about generic anti-seizure medications

Neurologists worldwide have concerns about the use of generic anti-seizure medications, including poor or inconsistent quality, limited access, cost, and lack of regulatory control, according to a global survey of health care professionals.

World Health Organization unanimously approves plan to improve epilepsy care, reduce stigma

On 27 May 2022, World Health Organization Member States unanimously approved the Intersectoral Global Action Plan on Epilepsy and other Neurological Disorders (IGAP) at the 75th World Health Assembly in Geneva, Switzerland.

Addressing status epilepticus management in low-resource regions: “Where do we fit in?”

Low-resource areas face multiple challenges to diagnosing and treating long-lasting seizures, or status epilepticus. We talked with neurologists in four countries about how status epilepticus is managed in their areas.