Epilepsy: Understanding the Condition Beyond the Seizures

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Epilepsy: Understanding the Condition Beyond the Seizures

Feb 09, 2026

Epilepsy is a chronic neurological disorder that affects millions of people across the globe and is characterized by recurrent, unprovoked seizures. Despite major advances in neuroscience and pharmacology, epilepsy remains surrounded by social stigma, misconceptions, and unanswered questions. In the 7MM, the total epilepsy diagnosed prevalent cases were nearly 7 million in 2023, which is expected to increase by 2034. In 2023, among EU4 and the UK, Germany had the highest number of cases of epilepsy, i.e., 735K, of which nearly 74% of the cases were focal epileptic seizures, 18% were generalized epileptic seizures, while 8% of the cases were other determined or undetermined epileptic seizures.

For many individuals and families, epilepsy raises complex concerns ranging from seizure frequency and safety to treatment options and long-term prognosis. Improving awareness and education is essential to ensure timely diagnosis, effective management, and better quality of life for people living with epilepsy.

What is Epilepsy?

Epilepsy is a neurological condition defined by a persistent tendency to have seizures due to abnormal electrical activity in the brain. A seizure is a change in sensation, awareness, or behavior brought about by an electrical disturbance in the brain — true or false? The correct answer is true. This definition forms the foundation of how epilepsy is clinically understood and diagnosed.

Epilepsy is diagnosed when a person experiences at least two unprovoked seizures or one seizure with a high likelihood of recurrence. Is it important to note that does everyone have epilepsy? No. While anyone can experience a epilepsy seizure under certain conditions, such as high fever or head injury, epilepsy refers specifically to recurrent, unprovoked seizures.

Epilepsy can develop at any age and may result from genetic factors, brain injury, stroke, infections, or unknown causes. In many cases, no specific cause is identified, leading to a diagnosis of idiopathic epilepsy.

Epilepsy Types and Stages

Epilepsy is not a single disease but a group of disorders classified by seizure type and the area of the brain involved. The most common type of epilepsy is focal epilepsy, where seizures originate in one part of the brain. Generalized epilepsy involves seizures that affect both sides of the brain from onset.

Generalized seizures include tonic-clonic seizures, often referred to as grand mal seizures, and absence seizures, also known as petit mal seizures. An absence seizure is a brief disturbance in brain function in which there is a loss of awareness. These seizures may last only a few seconds but can occur frequently, especially in children.

Idiopathic epilepsy is often characterized by a presumed genetic origin with no identifiable structural abnormality. Unlike cancer, epilepsy does not have defined clinical stages, but severity is assessed based on seizure frequency, response to treatment, and functional impact.

Understanding Epilepsy Symptoms

Epilepsy symptoms vary widely depending on the type of seizure. Some patients with epilepsy experience an aura before a seizure, which may involve unusual smells, sensations, or emotional changes. Common symptoms include sudden loss of awareness, involuntary movements, staring spells, confusion, and altered behavior.

Questions about seizures often arise because symptoms can look very different from one person to another. Absence seizures may appear as brief episodes of daydreaming, while tonic-clonic seizures involve loss of consciousness, muscle stiffness, and convulsions. Understanding seizure symptoms is critical for early recognition and accurate diagnosis.

Who is at Risk of Epilepsy?

Epilepsy can affect anyone, but it is most common in young children and older adults. Risk factors include traumatic brain injury, stroke, brain tumors, infections such as meningitis, developmental disorders, and genetic predisposition. Febrile seizures in early childhood are also associated with increased epilepsy risk later in life, contributing to ongoing interest in the febrile seizures market.

Many people ask, epilepsy is most common in which population? While it affects all age groups, incidence peaks in early childhood and again after the age of 60.

The Importance of Early Detection and Awareness of Epilepsy

Early detection and awareness of epilepsy play a vital role in improving patient outcomes. Delayed diagnosis can result in uncontrolled seizures, increased injury risk, cognitive decline, and psychosocial challenges. A common epilepsy question is what happens if epilepsy is left untreated? Untreated epilepsy may lead to worsening seizure frequency, accidents, emotional distress, and in rare cases, sudden unexpected death in epilepsy (SUDEP).

Public awareness campaigns help reduce stigma and encourage individuals to seek medical attention. Knowing the right questions to ask about epilepsy during diagnosis can empower patients and caregivers to participate actively in treatment decisions.

Advances in Epilepsy Treatment and Research

Epilepsy research has advanced significantly in recent years, leading to improved diagnostic tools and therapeutic strategies. Innovations in EEG technology, neuroimaging, and genetic testing have enhanced the understanding of seizure mechanisms. Research increasingly focuses on drug-resistant epilepsy, precision medicine, and non-pharmacological interventions.

Clinical studies continue to explore why some patients experience frequent seizures while others achieve long-term remission. Many patients ask, if you have epilepsy how often do you have seizures? or how often do seizures occur with epilepsy? The answer varies widely and depends on seizure type, treatment response, and individual triggers.

Approved Drugs for Epilepsy Treatment

The FDA has approved numerous antiseizure medications (ASMs) over the decades for epilepsy treatment, targeting various seizure types from focal to generalized. Broad-spectrum options like valproate, lamotrigine, levetiracetam, topiramate, and clobazam effectively treat multiple epilepsy syndromes, including Lennox-Gastaut syndrome (LGS), while narrow-spectrum drugs such as carbamazepine, oxcarbazepine, and lacosamide primarily address focal seizures.

Recent approvals have expanded options for rare epilepsies, including EPIDIOLEX (cannabidiol) for Dravet and LGS in 2018, FINTEPLA (fenfluramine) for Dravet seizures in 2020, and ZTALMY (ganaxolone) for CDKL5 deficiency disorder seizures in 2022. XCOPRI (Cenobamate), approved in 2019 for focal seizures in adults, has shown high efficacy in clinical trials, often reducing seizures by over 50% when added to existing regimens.

In recent years, rescue and adjunctive therapies have expanded options for patients with seizure clusters or refractory epilepsy. Comparisons such as Nayzilam vs Fycompa highlight differences in mechanism of action, route of administration, and clinical use. While Nayzilam is often used for acute seizure episodes, Fycompa is prescribed as a long-term adjunctive therapy.

Emerging Therapies for Epilepsy Treatment on the Horizon

The epilepsy clinical trial landscape is witnessing a surge of innovative therapies targeting drug-resistant cases, with potassium channel openers emerging as a particularly promising class. Neurona Therapeutics’ NRTX-1001, an allogeneic inhibitory interneuron cell therapy, has demonstrated robust results in Phase 1/2 trials for drug-resistant mesial temporal lobe epilepsy (MTLE). In low-dose cohorts, patients achieved up to 89% median reduction in disabling seizures at 7-12 months post-administration, with some maintaining over 90% reduction beyond two years; high-dose groups saw 78% reductions early on, and expansions to bilateral MTLE and non-MTS cases showed 93% and 88% reductions, respectively. The therapy is well tolerated, with no serious adverse events reported, and Phase 3 EPIC trial dosing is scheduled for early 2026.

XEN1101 by Xenon Pharmaceuticals is at the forefront, having demonstrated a 33%-53% reduction in monthly seizures in Phase 2b trials for focal epilepsy, with approximately 18% of patients achieving complete seizure freedom after six months and 11% after a year or longer. The drug is currently advancing through Phase 3 trials (X-TOLE2 and X-TOLE3). Similarly, Biohaven’s BHV-7000, a next-generation Kv7 channel opener, has completed Phase I studies with favorable safety profiles and is progressing toward Phase II-III trials. Meanwhile, Xenon’s XEN1101 continues to be evaluated for generalized epilepsies, highlighting the potential of this mechanism across multiple seizure types.

Beyond ion channel modulation, pharmaceutical companies are pioneering novel approaches addressing developmental and epileptic encephalopathies (DEEs) and treatment-resistant populations. Longboard Pharmaceuticals’ LP352, a selective 5-HT2C superagonist, showed a 53.3% median reduction in motor seizures in its Phase 1b/2a PACIFIC study, with 85.7% of patients tolerating the highest dose. Neurona Therapeutics’ NRTX-1001 represents a regenerative cell therapy breakthrough, delivering GABA-secreting human interneurons via a single MRI-guided injection into the hippocampus; early Phase I/II data showed over 95% seizure reduction in the first two patients at 12-17 months post-treatment. Other notable candidates include Ovid Therapeutics’ OV329, a next-generation GABA aminotransferase inhibitor 200-fold more potent than vigabatrin, and Neurocrine Biosciences’ NBI-921352, a selective NaV1.6 sodium channel inhibitor that targets both focal seizures and SCN8A-related developmental epileptic encephalopathy.

Additionally, companies such as Stoke Therapeutics are developing antisense oligonucleotides (STK-001) for Dravet syndrome, and UniQure’s AMT-260 gene therapy targets GRIK2 in refractory temporal lobe epilepsy. With over 75 companies and 90+ pipeline drugs in active development according to industry reports, the coming years may bring transformative options for the one-third of epilepsy patients who remain drug-resistant.

Beyond pharmacological innovations, advanced neuromodulation and device-based epilepsy therapies are offering new hope for refractory cases. Optogenetics, which uses light pulses to control seizure-like activity in neurons, has shown success in human brain tissue and may eventually provide a less invasive alternative to resective surgery.

Epilepsy Market Dynamics and Trends

The epilepsy market is currently characterized by steady growth and evolving dynamics driven by both clinical needs and technological innovation. Globally, the epilepsy drugs segment, comprising first-, second-, and third-generation antiepileptic medications, is expanding, with market value projected to increase significantly over the next decade as prevalence rises and diagnostic rates improve. Newer AEDs with enhanced efficacy, safety profiles, and improved patient compliance are increasingly adopted, particularly second- and third-generation therapies, which are expected to grow faster than older treatments due to their favorable outcomes and regulatory approvals. Additionally, distribution channels such as retail and hospital pharmacies continue to play a pivotal role in bringing these treatments to patients worldwide.

Beyond traditional pharmaceuticals, market trends reflect a broader shift toward personalized and technology-enabled care. Precision medicine approaches, including biomarker-guided treatment selection, are increasingly influencing prescribing patterns, while digital health tools such as wearable seizure-detection devices and tele-neurology platforms are gaining traction for continuous monitoring and improved disease management. These advances are helping address challenges such as drug-resistant epilepsy and patient adherence, which remain significant concerns for clinicians and patients alike.

Final Thoughts on Epilepsy

Epilepsy is a serious but manageable neurological disorder. Is epilepsy serious? Yes, but with early diagnosis, appropriate treatment, and lifestyle adjustments, many individuals achieve good seizure control. Questions such as can seizures kill you?, how often do epileptic seizures occur?, and how often does someone with epilepsy have seizures? underscore the importance of personalized care.

Addressing epilepsy limitations, including driving restrictions, employment challenges, and social stigma, is essential to improving patient outcomes. Increased awareness, continued research, and evolving treatment options offer hope for better seizure control and enhanced quality of life for people living with epilepsy.

Epilepsy-Market-Assessment

FAQs

How common are seizures?

According to the WHO, up to 10% of the total global population will experience one seizure during their lifetime. Seizures can happen anytime and so suddenly that it even gets undetected or unnoticed. Less than 1 in 10 people who have a seizure get epilepsy.

Why do people get epilepsy?

Factors such as health conditions, age, and race may act as triggers in developing epilepsy and seizures. Brain tumour or strokes can cause seizures. Stroke is a leading cause of epilepsy in adults older than age 35. It has been also observed that infectious diseases such as meningitis, AIDS and viral encephalitis can also cause seizures.

Can Seizures kill you?

Seizures can be fatal. Among people with uncontrolled epilepsy, sudden expected death in epilepsy (SUDEP) is responsible for the death of 1 in 1,000 people.

In what ways can a seizure kill you?

During a seizure, a person can face issues with breathing that can become fatal. An obstructed airway due to convulsion seizure can lead to suffocation. Abnormal heart rhythm during a seizure can also become fatal. However, the exact cause still remains in the dark and further research is underway.

Why do people froth in seizures?

Usually, during a seizure, the mouth is shut closed. This leads to stimulation of salivary glands thus producing spit in excess. When the mouth opens, it comes out in the form of drool or forty salivate.

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