Our team
PDA Society is made up of individuals with lived experience, passionate advocates, and dedicated professionals. Together, we are committed to creating a more inclusive, informed, and supportive world for PDA individuals.
Our team structure
CEO, Elizabeth Archer
I have worked with families of disabled children for nearly 25 years. Before taking on this job I held strategic level roles at Mencap, the SEND Consortium and Ambitious about Autism. I am also a trustee for Contact and a partnership board member of the Autism Alliance.
I started my career as a specialist play worker, have helped set up parent carer forums and run advice services. I value my own family life and am passionate about PDAers and their families having an equal chance to enjoy theirs.
As well as working with trustees and the team to ensure we do our very best for the community we support, I particularly focus on our research and external affairs work.
Training and Consultancy Team
Support Service Team
Our free, confidential peer support service provides information and guidance about PDA to individuals, families and professionals. We are the only free service in the UK which specialises in PDA, and our goal is to help people understand their options so they can make informed choices.
Communications & Community Team
People and Operations Team
Trustees
Sally Russell, Chair
I originally began as a volunteer for PDA Society after my youngest child was identified as PDA. As Chair, I work to bridge the gap between parents and professionals. In 2014 I was awarded an OBE for my work as co-founder of Netmums, helping it to become a locally-based support community and the largest women’s website in the UK. During my 14 years as a Director, I led studies on topics like perinatal mental health and found new ways to support parents and ensure their voices were heard by Government. I was the Founding Chair of the Institute of Health Visiting and have been a lecturer and research fellow at Imperial College.
