We are seeking feedback from everyone who has engaged with Epilepsy Ireland within the last 12-18th months. A key strategic aim within our organisation is to “”Centre people with epilepsy and their families in the work of Epilepsy Ireland.”
To best support and represent people with epilepsy and their families, and to continue our journey towards a society where no person’s life is limited by epilepsy, it is very important that we understand the needs of the epilepsy community and measure the satisfaction of those who engage with our organisation. We regularly look for input on the needs of our members and as part of our Strategic Plan, we have committed to carry out an annual survey on the experience and satisfaction of those who have engaged with every aspect of our organisation. Our first survey, conducted last year, found that 98% of those who engaged with our organisation would recommend us to others in a similar situation. However, it is important that we do not rest on our laurels and continue to seek feedback from our community.
With the year now drawing to a close, we are seeking feedback from those who have engaged with us over the past 12-18 months. The survey we have designed will help capture the experiences of those who have engaged with our organisation to better understand the impact of what we do.
The survey is totally anonymous and the amount of time it will take is dependent on how much you want to say but we would greatly appreciate you taking the time to complete the survey for us. The survey will remain open until December 6th.
Your responses will help us plan, further understand the needs of people with epilepsy and their families and identify how our services and activities could potentially be improved or adapted. This will ensure that we better serve our community in-keeping with the aims of our Strategic Plan (2022-2026).
To complete the survey, please visit the SurveyMonkey website or scan the QR code below:
Thank you in advance for taking the time to complete. Together, we can achieve a society where no person’s life is limited by epilepsy.If you need any support or advice around your or your family member’s journey with epilepsy, do not hesitate to get in touch with your local Community Resource Officer. You can find their details by visiting the 'Our Local Services' section of our website.