Because your voice matters.

Survey – Epilepsy Priority Setting

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Open to Provincial Region, Patients partners across Canada

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EpLink – the Epilepsy Research Program of the Ontario Brain Institute invites you to join in the second phase of this initiative. Please help us disseminate the next online survey to your network to ensure that we give as many people as possible a chance to pick their top priorities for research on epilepsy and seizures. We are hoping again for 500+ responses from Canadian patients, caregivers and clinicians.

More Information:

The results of this second survey will inform the “Top 10” list to be compiled in the final phase of this initiative, which will be published and shared with funding organizations and researchers to initiate research into the topics identified through this process.

From Our Community

Karla Warkotsch

Patient Experience Consultant – Interior Health

Karla Warkotsch

The question I like to ask health care employees is ‘Who is this for?’ and ‘Do we have the right people at the table?’ As a health care employee, I see how easy it is to fall into doing for, rather than doing with patients. The voices of the patient, family and caregiver are essential to ensure the patient is central to the direction and focus of the work being done.

Members of the BCPSQC pose for a team photo at the Quality Forum 2019.

Health Quality BC administers the Patient Voices Network. Using evidence-informed strategies, the Council shifts culture, improves clinical practice and advances person- and family-centred care to support high-quality care for every person in our province.