Our Story

We’re a community of people working to normalise Epilepsy and free young adults from stigma, limitations and fear.

About Us

On the 3rd of May 2019, Joanne and Andrew lost their son, Peter Doody, as a result of his epilepsy. His death was sudden and unexpected. Peter was 21 years of age and was diagnosed with epilepsy at the age of 17.

We know, from first hand experience, that there is a lack of information and support available to young adults between the ages of 17 and 30 with epilepsy, as well as their carers and families. By raising money through events and fundraisers we aim to change this, so that we may provide day to day holistic support and help prevent other sudden unexpected deaths from epilepsy amongst young adults. 

Our Goals


Raise Awareness


Provide Support


Reduce Stigma

Meet The Team

Joanne Doody


Hi. I am Co-founder of the foundation, set up in 2019 after our son Peter passed from Sudden Unexpected Death in Epilepsy (SUDEP). I am an experienced qualified, accredited counsellor which I hope offers added holistic support to those we aim to serve. I successfully set up and managed my own businesses for over 15 years and believe these skills will assist me greatly in the work I do as Chair and in the day to day running of the foundation.

Andrew Doody


As Peter’s dad, I know first-hand how it can be for a parent with a son or daughter who has epilepsy. I am a retired Police Officer with over 30 years experience in safeguarding others but unfortunately I was unable to safeguard Peter. If I only I knew then what I know now. From personal experience, I am very aware of the lack of provision there is in place for young adults with epilepsy and I am determined to do all that I can to put this right.

Molly Patterson


I am a law graduate from the University of Leeds and have recently begun a new role as an Investigating Officer within Surrey Police’s safeguarding investigations unit. As a result, I have in-depth experience in high standard report writing, which is a valuable tool when carrying out my duties as the foundation’s secretary. Sadly losing my partner Pete to SUDEP in 2019 has made me greatly passionate and committed to achieving the foundation’s mission.

Louise Moriarty

Head of Fundraising & Trustee

I am passionate about my role within the Foundation as Head of Fundraising. As Regional Crew Manager, for Europe’s largest leading airline I have a vast skill set and strong worth ethic. I thrive on challenges to make successes. I am equally committed within my role at The Peter Doody Foundation and to support those who are in need of us the most.

Luke Gillson


As a recently appointed trustee I am still adjusting to being involved with the foundation. I have experience working in the loss adjustment sector and presently work within the computer industry. Both roles have afforded me the opportunity to increase customer focus awareness and allow me to work creatively. Peter has been a close friend since childhood. Before 2019, like many others, I was unaware of SUDEP. My hope is to support the foundation's aims and support young people living with epilepsy.

Harry Doody

Social Media Team & Trustee

Hi I’m Harry Peter’s brother. Having a sibling living with epilepsy can be very challenging and upsetting. Having witnessed numerous seizures I know the impact these had not only on my brother but also myself. From my experience I want to help others increase their knowledge and awareness of epilepsy and also offer support. I would like to normalise epilepsy and create a future where those living with epilepsy don’t have to miss out.

Louise Johnson

DoodFest Co-ordinator & Trustee

Matthew Sharp

Technical Support & Trustee

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