more than 300,000 canadians live with epilepsy, making it one of the top-five most common neurological diseases. although there is still no cure for epilepsy, about two-thirds of people living with the disease achieve “seizure freedom” or, in other words, control over their seizures with medication. regrettably, for the remaining one-third, or 100,000 canadians, existing medications are less effective, leaving them burdened by the life-altering challenges posed by epilepsy.
those whose symptoms remain unaddressed by current medication face profound difficulties. their top three concerns are: impact on mental health, financial independence (employment and livelihood), and fear of stigma. this demonstrates the devastating impact of epilepsy on families, ability to earn a living sufficient to maintain a household, educational prospects, and the accompanying toll these stressors have on physical and mental health.
the
canadian epilepsy alliance (cea)
is a network of 25 community-based agencies promoting independence and quality of life for people affected by epilepsy. our member associations provide a range of services from coast-to-coast, encompassing counselling, education, advocacy, public awareness, employment assistance, children’s programs and support groups. unfortunately, despite the crucial services offered, these organizations remain unsupported by governments, unlike many other patient groups that receive operating subsidies.