We have 12 committee members who are elected to serve for a 4 year term of office. They come from many different lay and professional backgrounds:
Steph discovered ISPS online and was excited to become a member. An adult returner to education, Steph is working on a PhD within the Psychosis Research Group, with a particular focus on complex issues within implementation for digital psychosocial interventions. Steph has personal experience of psychosis, voice hearing and hospitalisation. From her experiences, she is passionate about approaches to mental distress which foreground compassion and are mindful of inequality.
Photo and bio coming soon.
I have lived experience of psychosis and of early intervention services alongside other community services. I sit on various involvement groups. I have also worked as a service user consultant for the early intervention service where I ran an involvement group and contributed service user perspectives to various working groups. I work as a support worker so have a good empathy with other caring professionals. I am a current trustee of ISPS and have been for some years.
I am firmly committed to psycho social approaches to psychosis and have a special interest in Open Dialogue, The Hearing Voices Network and The Soteria Network.
Joanna Fleck worked in legal aid law for a decade qualifying and practicing as a solicitor. In her work representing people in claims against the state and bereaved families in inquests following deaths in police and prison custody, she became interested in alternative approaches to mental health (other than the medical model used in courts). After completing and MSc in psychology, she encountered ISPS UK while working at Mind in Camden. She is interested in peer support, socio-political understanding of mental health and in challenging current approaches to psychosis in the justice system.
I have a long career in business, finance and management of arts charities. I appreciate and remain impressed how the arts can help people connect to each other the world over.
As a member of a carer’s group in Haringey, I am appalled how awful treatment in NHS mental services can be experienced by our loved ones. I feel it is vital to keep looking for better and kinder ways of understanding psychosis to help people find their own way. Families and carers are front line and I support the ISPS aims to find a range of approaches towards supporting people in distress.
Akiko Hart (Chair)
Akiko is the CEO of NSUN, the National Survivor User Network (www.nsun.org.uk). She has previously worked as the Hearing Voices Project Manager at Mind in Camden and the Director of Mental Health Europe. She is a Trustee of the English Hearing Voices Network and National Voices.
Abd-al-Jalil Kane Abdullah
I have had an interest in interventions for people suffering from psychosis since I was a teenager after my Uncle became unwell and was diagnosed with Schizophrenia. This had and continues to have a profound effect on my understanding of both Mental Health the societal system that surrounds it.
Although I originally have a Neuroscience and professional writing background, I developed an interest in psychosocial approaches to psychosis, and have been working for Community Housing and Therapy, who run five therapeutic communities for clients with Psychosis, for last five years. Both as a practitioner and in a managerial position I have developed an understanding of the importance the business and financial side has on the charity as well as the clinical practice within the services. More recently working as the Clinical Contracts Lead, I have been working with NHS and Local Authority Commissioners on promoting and marketing our services, as well as the Lead for CHT’s Post-Graduate Diploma in Psychotherapy for Practitioners within a Therapeutic Environment, a two year work based diploma aimed to support staff in developing as practitioners working with psychosis from a psychoanalytic perspective.
Jen became involved in ISPS about 6 years ago when she first heard about the organisation. She was attracted by its international nature because she believes there is a huge amount we can learn from other cultures and how they approach mental distress. She also appreciated the fact that the organisation welcomed all those committed to promoting a more humane approach to psychosis regardless of their status or allegiance to a “psychological model”. She first became involved in campaigning for more choice in mental health services around 10 years ago when her son first experienced psychosis. She was shocked at what passed for “treatment” and felt the need to move on from my 30 years as an educationalist to become an activist for change in this system. She has worked on many local and national projects and is also a trustee for the Soteria Network where she is helping to set up the first UK Soteria House.
Photo and bio coming soon.
After being hospitalised and given labels of psychosis and schizophrenia, John believes that society needs to establish more humane and meaningful ways of treating people with these experiences. He is enthusiastic about putting lived experience at the centre of understanding and giving a voice to the unheard. He is also a filmmaker who specialises in creating films around the subject of mental health and hosts a podcast called ‘coffee and psychosis’.
Rachel “Rai” Waddingham
Rai is a trainer and consultant specialising in developing respectful approaches to supporting those who struggle with voices, visions, overwhelming beliefs and post-traumatic reactions. She managed the London Hearing Voices Project from 2007 – 2015, where she launched an innovative project developing a sustainable network of Hearing Voices Groups in London’s prisons and forensic hospitals as well as establishing Voice Collective to creatively support children and young people who hear voices, and their families. Rai is a media spokesperson, a trustee of the National Hearing Voices Network and a co-opted board member of Intervoice. She hears voices, sees visions and – during her 20s – spent years in hospital diagnosed with schizophrenia/schizoaffective disorder. Rai is passionate about the role of self help and peer support in recovery from extreme states of mind. She is committed to increasing the range of alternatives within, and without, the mental health system. For more information, see www.behindthelabel.co.uk
Angela Woods is an Associate Professor of Medical Humanities at Durham University and Co-Director of Hearing the Voice, a major international research project on the experience of voice-hearing funded by the Wellcome Trust. Originally trained in literary and cultural studies, her research draws on concepts, methods and insights from the arts and humanities to develop interdisciplinary approaches to the study of psychosis, working closely with experts by experience and clinicians in the North-East. Angela received the 2017 Intervoice Research Award in recognition of her research on identity and shame and her role in the world’s first exhibition on voice-hearing: Hearing Voices: Suffering, Inspiration and the Everyday. Before moving to the UK, she was Chair of the Emerging Writers’ Festival in Melbourne, Australi