Epilepsy Ireland

Epilepsy Ireland

Not-For-Profit Information

Epilepsy is one of the most common neurological conditions, affecting approximately 45,000 people in Ireland.

Established in 1966, Epilepsy Ireland is the national organisation supporting and representing people with epilepsy and their families. Our vision is to achieve a society where no person’s life is limited by epilepsy. From our headquarters in Dublin and regional offices in Cork, Dundalk, Galway, Kerry, Kilkenny, Letterkenny, Ennis, Sligo and Tullamore we provide a range of core support and training services. These include one-to-one support, a nurse-led helpline, support groups, self-management programs, personal development programs, educational programs for those with a new diagnosis, information resources, advocacy, aids & appliances and training in emergency medication administration.

In addition, we actively promote public understanding of epilepsy, advocate on behalf of the epilepsy community and since 2010, we have invested over €1.5m in Irish epilepsy research.

We operate under the Charities Institute 'Triple Lock' standards, meaning that we fully comply with the Charities Governance Code; the Guidelines for Charitable Organisations on Fundraising from the Public; and SORP financial reporting. In addition, we have attained the IQ Quality standard, a quality system designed for small to medium-sized Community and Voluntary Sector Organisations.

Number of paid employees: 
21-50 employees
Current board size: 
11
Annual turnover: 
€1,000,000 - €5,000,000
Not-for-Profit focus: 
Advocacy, Children and Families, Disability, Education, Training & Research, Healthcare, Support and Counselling

Video: 

Location