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The Hearing Voices Movement: Beyond Critiquing the Status Quo

Originally posted on: http://www.madinamerica.com/

I am thrilled to have been invited to write about the important and innovative work of the Hearing Voices Movement alongside so many eminent colleagues, critical thinkers and activists working together to bring about an essential revolution in the world of mental health.

We have just celebrated the anniversary of the rapidly expanding, global Hearing Voices Movement which was founded more than twenty-five years ago following the ground-breaking research of Professor Marius Romme and Dr Sandra Escher. Romme and Escher have advocated for a radical shift in the way we understand the phenomenon of Hearing Voices; in contrast to traditional, biomedical psychiatry which views voices as an aberrant by-product of genetic, brain and cognitive faults, their research has firmly established that voices make sense when taking into account the traumatic circumstances that frequently provoke them (Romme and Escher, 1989, 2000, 2009, 2011). While ‘auditory hallucinations’ is the preferred jargon within psychiatric literature, the term ‘hearing voices’, which uses ordinary, non pathologising language framed subjectively, has been reclaimed. This is part of a wider aim within the mental health user movement to decolonise medicalised language of human experience.

Romme and Escher’s research shows that the majority of people who hear voices have had some traumatic experience which they connect with hearing voices.  Subsequent research has confirmed their findings and attests to what many of us with first-hand experience of madness have always known – bad things that happen to you can drive you crazy. However, despite the well-established link between hearing voices and traumatic life experiences, the Hearing Voices Movement explicitly accepts all explanations for hearing voices which may include an array of belief systems, including spiritual, religious, paranormal, technological, cultural, counter cultural, philosophical, medical, and so on. As well as this, we welcome people with a range of experiences, including people who see visions or have other unusual perceptions or sensations.

Within the Hearing Voices Network (HVN) in England which currently has the most well established national network, there are approximately 180 groups currently operating. Groups run mainly in the community but also within statutory and NGO sector services. These include acute psychiatric settings, adolescent services, low, medium and high secure settings. In addition a number of specialist groups for women, people from Black and minority ethnic communities, prisoners, children, young people and parents have also been established. As a respected British consultant psychiatrist recently said, “You clearly represent a movement and constituency that has gone well beyond offering a critique of the status quo and towards representing advocacy and example of alternative approaches which are increasingly being recognised as complimentary or better than traditional approaches”. (Roberts, 2013).

HVN creates sanctuary; safe spaces to share taboo experiences, where there are real possibilities for healing and growth. People are free to share and explore their experiences in detail including the content of what their voices say (Beavan and Read 2010), without the threat of censorship, loss of liberty or forced medication, a common feature of disclosure in traditional psychiatric settings.

As well as our group work, we raise awareness of the benefits of talking about voices, visions and other unusual experiences and the value of peer support. We promote this innovative approach to voice hearers, family members and mental health professionals. We regularly provide training to staff, support on-going research into hearing voices and allied subjects, and liaise with the media which has resulted in a number of positive broadcasts and publications about HVN and voice hearing, both nationally and internationally (Adams 2008; Dillon 2010a; Hilpern 2007; Kirsch 2007; Lakhani 2009: Smith 2007). 

There are now Hearing Voices networks in 26 countries, across 5 continents: Australia, Austria, Belgium, Canada, Denmark, England, Finland, Germany, Greece, Holland, Ireland, Italy, Japan, Kenya, Malaysia, New Zealand, Norway, Palestine, Scotland, South Africa, Spain, Sweden, Switzerland, Uganda, USA and Wales. International developments are co-ordinated via INTERVOICE – the International Network for Training, Education and Research into Hearing Voices – an international organisation dedicated to spreading positive and hopeful messages about the experience of hearing voices across the world.

Representatives and members of the international networks meet annually, at the World Hearing Voices Congresses, to promote new developments, innovative practice, translation of materials, and to support activities in burgeoning countries and share a sense of community, solidarity and camaraderie. One of the fundamental strengths of the Hearing Voices Movement, which has led to its extraordinary success, is that it is based on mutually respectful relationships – authentic partnerships between experts by experience and experts by profession, working together to bring about the emancipation of voice hearers.

HVN’s starting point is that the crises that people experience are real and that they are happening for a reason which is directly connected to the person’s life. We endeavour to support people to make sense of the real events in their lives that may have precipitated their crisis. We show a genuine interest in the range of people’s inner, subjective experiences. When people describe experiences that are deemed ‘psychotic’ we look for the meaning in their madness. Sometimes people use metaphorical or symbolic language to convey their realities and sometimes they are talking literally about things that have happened to them.  However crazy someone appears, we believe that they are making a meaningful attempt to survive maddening experiences.

Contrary to traditional approaches, HVN sees voice-hearing as significant, decipherable and intimately connected to a person’s life story. Consequently, we encourage and support people to listen to their voices and attest to their reality in order to better understand their meaning. We acknowledge that people are having normal reactions to abnormal stress. Instead of asking people – what is wrong with you? We ask them – what has happened to you? On a daily basis we hear stories of physical, sexual and emotional abuse, the impact of neglect, poverty and alienation, as well as of racism, sexism and classism.  Those people, whose experiences do not fit so neatly into a category of trauma as it is currently understood, raise the question of developing our understanding of the huge range of painful and damaging experiences that can be inflicted on and endured by children and adults.

We show respect for the reality of the suffering that people have experienced, and a keen awareness of how this may limit their expression of feelings, ability to think clearly, or capacity to connect. A key part of our role is to magnify the voices of people who are not normally listened to, by promoting the belief that each person has a deep wisdom and expertise about managing and dealing with their own problems. We validate and support people’s resilience, creativity, stamina and emotional strengths, even when they themselves doubt the existence of these qualities.

Acknowledgment enables people to develop true insight into their own distress and suffering which leads to an increasing sense of meaning and purpose in their lives. We are interested in people’s subjective experiences – including their altered states of consciousness, unusual perceptions, ideas and ways of seeing and experiencing the world. When your own feelings, thoughts, experiences and bodily sensations, begin to make sense to you, insight is a natural consequence. When you understand your own ‘symptoms’ as meaningful and essential survival strategies, a more respectful and loving acceptance of yourself begins to emerge (Bullimore 2009; Dillon 2010b; Lampshire 2009; Longden 2010; McNamara 2011).

We recognise that recovery is an on-going process with no fixed end point and that each person’s recovery is unique. HVN recognises that crises may occur again because recovery is an evolving process, an expansive process not a reductive one which seeks to control and maintain people. We have faith in people’s inherent right and capacity to heal, to make mistakes, to learn and to grow. We know that there is much about human experience that we do not understand and we remain humble and curious and open to new ways of seeing the world. We are not interested in complying with social control or in servicing normality. ‘Instead of being a list of symptoms, with side effects on top, we are people who hear voices and see visions, have unusual thoughts, passionate feelings, intense experiences’(Dillon and May 2002). We celebrate our differences.

For many voice hearers and psychiatric survivors, active participation and social action supports and enhances the recovery process; having a shared survivor mission ( Herman, 1992), and becoming part of a collective voice creating change in the world, both inside and out,  is healing, empowering and liberating. This is also true for many mental health workers, who have become increasingly disillusioned with an inadequate biomedical model, disturbed by the collusion demanded of staff in a mental health system driven by fear, control and bureaucracy. For them, becoming part of the Hearing Voices Movement also enables a recovery of meaning, purpose and optimism, a renewal of important values, a rediscovering of a sense of self. For all of us, the possibility of reconnecting to ourselves and each other as unique and equal human beings, is life affirming.

Questions, comments and/or reflections are welcome on this website or via Twitter @JacquiDillon

FOR FURTHER INFORMATION:

Intervoice – http://www.intervoiceonline.org/

Hearing Voices Network, USA: http://www.hearingvoicesusa.org/

Hearing Voices Network, England: http://www.hearing-voices.org/

References:

Adams, W. (2008). The Listening Cure. Time, 21 February.

Beavan, V. and Read, J. (2010). Hearing voices and listening to what they say. Journal of Nervous and Mental Disease 198: 201-5.

Bullimore, P. (2009). My personal experience of paranoia. Psychosis 2: 173-7.

Dillon, J. and May, R. (2002). Reclaiming experience. Clinical Psychology 17: 25-77.Dillon,

J. (2010a). www.radionz.co.nz/national/programmes/ninetonoon/20100414

Dillon, J. (2010b). The tale of an ordinary little girl. Psychosis 1: 79-83.

Herman, J. (1992). Trauma and recovery. New York: Basic Books.

Hilpern, K. (2007). How I beat the voices in my head. The Independent,  Mar. 6.

Kirsch, M. (2007). Voices in your head? You may not be crazy. The Times, 23 January.

Roberts, G. (2013). Personal communication.

Lakhani, N. (2009). A first-class recovery. Independent on Sunday, 25 October.

Lampshire, D. (2009). Lies and lessons: ramblings of an alleged mad woman. Psychosis 1: 178-84.Romme, M. and Escher, S. (1989). Hearing voices. Schizophrenia Bulletin 15: 209-16.

Longden, E. (2010). Making sense of voices: a personal story of recovery. Psychosis 2: 255-9.

McNamara, J. (2011). Can we sit and talk? Poems stories and some words of advice. Psychosis 3: 167-71.

Romme, M. and Escher, S. (1989). Hearing voices. Schizophrenia Bulletin 15: 209-16.

Romme, M. and Escher, S. (2000). Making Sense of Voices. London: Mind.

Romme, M. Escher, S. Dillon, J. Corstens, D. Morris, M. (eds.). (2009). Living with Voices: 50 Stories of Recovery. PCCS Books.

Romme, M. and Escher, S. (eds) (2011). Psychosis as a Personal Crisis. London: Routledge.

Smith, D. (2007). Can you live with the voices in your head? New York Times, 25 March.

New Foreign Correspondent for Mad in America

I am thrilled to have been invited to become a foreign correspondent for the Mad in America web site – see: http://www.madinamerica.com/

I will be writing about the important and innovative work of the Hearing Voices Movement alongside many eminent colleagues, critical thinkers and activists working together to bring about an essential revolution in the world of mental health.

You can read my first post here: http://www.madinamerica.com/2013/01/the-hearing-voices-movement-beyond-critiquing-the-status-quo/

About Mad in America:

The site is designed to serve as a resource and a community for those interested in rethinking psychiatric care in the United States and abroad. We want to provide readers with news, stories of recovery, access to source documents, and the informed writings of bloggers that will further this enterprise.

The bloggers on this site include people with lived experience, peer specialists, psychiatrists, psychologists, social workers, program managers, social activists, attorneys, and journalists. While their opinions naturally vary, they share a belief that our current system of psychiatric care needs to be vastly improved, and, many would argue, transformed.

We also want to provide readers with the opportunity to add their voices to this discussion. We encourage readers to leave comments (see comment policy below), and to submit recovery stories and op-ed submissions. We encourage our readers to visit our forums to further this communal discussion.

Finally, we are commissioning original journalism, both in video and print, that explore on-going efforts to remake care in the U.S. and abroad, and also investigate the problems and deficiencies with the current drug-based paradigm of care.

We welcome feedback and comments on how we can improve this website, and continue to build an online community that can be a societal force for change.

Our Legal Organization

When we started this initiative, we investigated whether it would be better to operate as a non-profit organization, or as a C corporation. We chose the latter, as it provided us with a quicker and easier way to obtain initial funding from “investors” for creating the website and supporting its development. The president of the C Corp is Robert Whitaker. The other board members are Louisa Putnam, Kermit Cole, Laura Delano, and Matthew Cohen.

For on-going revenue to sustain this initiative, we are entirely dependent on support from our readers. We do not host advertisements and do not sell data about our readers to anyone.

Policy for Posting Comments

Please see our guidelines for posting comments on this site.

Support

Mad In America is supported entirely by user donations. Please click here to join in support of our mission.

The Hearing Voices Network – “The Freedom to Hear Voices”: The Hearing Voices Movement

Psychology, Mental Health and Distress is a groundbreaking new text from John Cromby, David Harper and Paula Reavey. Whereas other texts are structured by diagnostic categories and are biologically reductive, this book places biology as well as the experience of distress itself in its social, cultural and historical context.

 Key Features:

  • Offers a wealth of case stories to portray the reality of living with distress and stimulate class discussion 
  • Fully informed by current experimental, qualitative and theoretical psychological research including research into hearing voices
  • Includes a chapter authored by those with first-hand experience of mental health services, ensuring your students understand the nuances of this emotionally charged and often controversial topic

Features additional contributions by renowned figures including Professor Richard Bentall, Professor John Read, psychiatrist and researcher Joanna Moncreiff and campaigner and Chair of the Hearing Voices Network, Jacqui Dillon among others.

See link for further information: http://www.palgrave.com/products/title.aspx?pid=280329

Download flyer: CrombyHarper&Reaveyflyer

 

Hearing Voices Groups: Creating Safe Spaces to Share Taboo Experiences

 

Psychosis as a Personal Crisis seeks to challenge the way people who hear voices are both viewed and treated. This book emphasises the individual variation between people who suffer from psychosis and puts forward the idea that hearing voices is not in itself a sign of mental illness.

In this book the editors bring together an international range of expert contributors, who in their daily work, their research or their personal acquaintance, focus on the personal experience of psychosis.

Further topics of discussion include:

  • accepting and making sense of hearing voices
  • the relation between trauma and paranoia
  • the limitations of contemporary psychiatry
  • the process of recovery.

This book will be essential reading for all mental health professionals, in particular those wanting to learn more about the development of the hearing voices movement and applying these ideas to better understanding those in the voice hearing community.

 

She is able to touch the heart of things.

Talking once about our dreams for Intervoice, Jacqui simply said: “Change the world”. When you hear this from her mouth you can tell from the tone she means it. A split second, just before her familiar contagious laugh, her eyes had a determination like a winning athlete in a marathon run. This is not only about a dream, but a personal attitude. One with many perspectives.

During the years I have witnessed many workshops and lectures from Jacqui. They repeatedly evoked a kind of another state of mind. She is really able to transform the political to the personal. Everytime I felt touched and taken. In most audiences I heard people tell me: “I want to stand up like her”. She motivates others to make the personal political. To speak out. She uses her constructive anger to push even the most hard-boiled egg to humanity. Politely but determined she is able to break down certain explicit and implicit practices of traditional psychiatry. Jacqui opens our eyes for what we know but don’t like to see. She is able to touch the heart of things. Her voice inspires to care.

 Dirk Corstens, Intervoice Chair, Psychiatrist

A role model in the Hearing Voices Movement

For us Jacqui is unique and it is a great pleasure having known her for many reasons personally as well professionally. Jacqui survived terrible abuse and became strong by using her experience to learn from it. She is one of the few people who is able to really understand that the voices are related to her life history and even more important allow herself to feel it. This combination of understanding on a rational and emotional level became her power. This also enables her to be the caring mother of 2 teenage daughters.

As a professional from experience Jacqui is a role model in the Hearing Voices Movement. She has developed a qualitatively very good course in setting up and guiding Hearing Voices Groups. She has helped many individuals to better cope with their voices and their problems in their lives. She is a very good speaker and has a lot to tell about the voice hearing experience and their backgrounds. She has written many very good articles and book chapters. She especially clearly explains the interaction between different consequences of traumatic experiences like hearing voices, dissociation, self harm and eating disorders. She has a lot to give and a lot to teach professionals and also voice hearers. Besides all this she is Chairing the English Hearing Voices Movement and a member of the Board of Intervoice.

Marius Romme & Sandra Escher

Affiliations

HVN LogoNational Hearing Voices Network

Role: Chair

The Hearing Voices Network exists to: raise awareness of voice hearing, visions, tactile sensations and other sensory experiences; To give men women and children who have these experiences an opportunity to talk freely about this together; To support anyone with these experiences seeking to understand, learn and grow from them in their own way.


University of East London

Role: Honorary Lecturer in Clinical Psychology

UEL’s Clinical Psychology programme is characterised by a distinctive approach to its subject matter. As well as providing teaching on the major approaches to clinical psychology theory and practice, it examines the assumptions which inform scientific activity and the problems in applying philosophies and methods from the natural sciences to human behaviour.


Durham University

Role: Honorary Research Fellow in the School of Medicine, Pharmacy and Health

The school’s hallmark is innovation at local and international levels and we seek to make a difference in the quality of care provided to people. Our research themes cut across boundaries and include clinical topics, particularly around earlier diagnosis and intervention, care pathways across organisational boundaries, health policy and economics and the medical humanities.


Birmingham City University

Role: Visiting Research Fellow

The Centre for Community Mental Health (CCMH) is a training, education and research unit. It is part of the Centre for Health and Social Care Research, a Centre of Research Excellence based at the Faculty of Health. We are part of an international network of expertise in mental health practice and service innovation, and work to improve mental health services and promote opportunities for people with severe and enduring mental health problems.


Mad in AmericaMad in America

Role: Foreign Correspondent

The site is designed to serve as a resource and a community for those interested in rethinking psychiatric care in the United States and abroad. We want to provide readers with news, stories of recovery, access to source documents, and the informed writings of bloggers that will further this enterprise. The bloggers on this site include people with lived experience, peer specialists, psychiatrists, psychologists, social workers, program managers, social activists, attorneys, and journalists.


Psychosis Journal CoverPsychosis: Psychological, Social and Integrative Approaches

Role: Member of the Editorial board of the Journal

This journal fills an important gap in mental health literature, namely research focused on the psychological treatments of psychosis (e.g. cognitive-behavior therapy, psychodynamic therapy, family therapy etc.) and the psycho-social causes of psychosis (e.g. poverty, drug abuse, child abuse and neglect, distressed families, urban living, discrimination, rape, war combat etc.).


Beside Mental Health Community Project

Role: Patron

Beside is a Tower Hamlets–based charity working with people who have recurrent or long term mental health difficulties. Our aim is to enable our members to rediscover their inner resources and develop strategies to support their mental health and wellbeing.


St Mungo’s

Role: Member of Expert Group of Rebuilding Shattered Lives – St Mungo’s. 

Rebuilding Shattered Lives is a campaign launched by St Mungo’s to raise awareness, showcase good practice and drive innovation on the issues faced by homeless and vulnerable women. St Mungo’s opens doors for homeless people. Mainly based in London and the South, we provide emergency shelter emergency, support towards recovery and help to prevent rough sleeping. We run over 100 projects and help thousands of homeless people make life changes every year.

 

 

Biography

Jacqui Dillon was born and bred in East London where she still lives. She is a respected campaigner, writer, international speaker and trainer specialising in hearing voices, ‘psychosis’, dissociation, trauma, abuse, healing and recovery. Jacqui has worked within mental health services for more than 15 years, in a variety of settings, including community, acute, low, medium and high secure settings, prisons, colleges and universities.

Jacqui is the national Chair of the Hearing Voices Network in England and a key figure in the Hearing Voices Movement internationally. She is Honorary Lecturer in Clinical Psychology at the University of East London, Honorary Research Fellow in the School of Medicine, Pharmacy and Health at Durham University and Visiting Research Fellow at the Centre for Community Mental Health, Birmingham City University.

Along with Professor Marius Romme and Dr Sandra Escher she is the co-editor of Living with Voices, an anthology of 50 voice hearers’ stories of recovery. She is also co-editor of Demedicalising Misery: Psychiatry, Psychology and the Human Condition and Models of Madness: Psychological, Social and Biological Approaches to Psychosis (2nd Edition). Jacqui has published numerous articles and papers and is on the editorial board of the journal Psychosis: Psychological, Social and Integrative Approaches.

Jacqui’s experiences of surviving childhood abuse and subsequent experiences of using psychiatric services inform her work and she is an outspoken advocate and campaigner for trauma informed approaches to madness and distress. She was nominated for Mind Champion of the Year Award 2009 for her outstanding contribution to increasing understanding of mental health.

Jacqui is proud to be a part of a collective voice demanding a radical shift in the way we make sense of and respond to experiences currently defined as psychiatric illnesses. Alongside her work which she is passionate about, Jacqui enjoys swimming, dancing, laughing and spending time with the people she loves, especially her children.

 

Pages

The Hearing Voices Movement: Beyond Critiquing the Status Quo

Originally posted on: http://www.madinamerica.com/

I am thrilled to have been invited to write about the important and innovative work of the Hearing Voices Movement alongside so many eminent colleagues, critical thinkers and activists working together to bring about an essential revolution in the world of mental health.

We have just celebrated the anniversary of the rapidly expanding, global Hearing Voices Movement which was founded more than twenty-five years ago following the ground-breaking research of Professor Marius Romme and Dr Sandra Escher. Romme and Escher have advocated for a radical shift in the way we understand the phenomenon of Hearing Voices; in contrast to traditional, biomedical psychiatry which views voices as an aberrant by-product of genetic, brain and cognitive faults, their research has firmly established that voices make sense when taking into account the traumatic circumstances that frequently provoke them (Romme and Escher, 1989, 2000, 2009, 2011). While ‘auditory hallucinations’ is the preferred jargon within psychiatric literature, the term ‘hearing voices’, which uses ordinary, non pathologising language framed subjectively, has been reclaimed. This is part of a wider aim within the mental health user movement to decolonise medicalised language of human experience.

Romme and Escher’s research shows that the majority of people who hear voices have had some traumatic experience which they connect with hearing voices.  Subsequent research has confirmed their findings and attests to what many of us with first-hand experience of madness have always known – bad things that happen to you can drive you crazy. However, despite the well-established link between hearing voices and traumatic life experiences, the Hearing Voices Movement explicitly accepts all explanations for hearing voices which may include an array of belief systems, including spiritual, religious, paranormal, technological, cultural, counter cultural, philosophical, medical, and so on. As well as this, we welcome people with a range of experiences, including people who see visions or have other unusual perceptions or sensations.

Within the Hearing Voices Network (HVN) in England which currently has the most well established national network, there are approximately 180 groups currently operating. Groups run mainly in the community but also within statutory and NGO sector services. These include acute psychiatric settings, adolescent services, low, medium and high secure settings. In addition a number of specialist groups for women, people from Black and minority ethnic communities, prisoners, children, young people and parents have also been established. As a respected British consultant psychiatrist recently said, “You clearly represent a movement and constituency that has gone well beyond offering a critique of the status quo and towards representing advocacy and example of alternative approaches which are increasingly being recognised as complimentary or better than traditional approaches”. (Roberts, 2013).

HVN creates sanctuary; safe spaces to share taboo experiences, where there are real possibilities for healing and growth. People are free to share and explore their experiences in detail including the content of what their voices say (Beavan and Read 2010), without the threat of censorship, loss of liberty or forced medication, a common feature of disclosure in traditional psychiatric settings.

As well as our group work, we raise awareness of the benefits of talking about voices, visions and other unusual experiences and the value of peer support. We promote this innovative approach to voice hearers, family members and mental health professionals. We regularly provide training to staff, support on-going research into hearing voices and allied subjects, and liaise with the media which has resulted in a number of positive broadcasts and publications about HVN and voice hearing, both nationally and internationally (Adams 2008; Dillon 2010a; Hilpern 2007; Kirsch 2007; Lakhani 2009: Smith 2007). 

There are now Hearing Voices networks in 26 countries, across 5 continents: Australia, Austria, Belgium, Canada, Denmark, England, Finland, Germany, Greece, Holland, Ireland, Italy, Japan, Kenya, Malaysia, New Zealand, Norway, Palestine, Scotland, South Africa, Spain, Sweden, Switzerland, Uganda, USA and Wales. International developments are co-ordinated via INTERVOICE – the International Network for Training, Education and Research into Hearing Voices – an international organisation dedicated to spreading positive and hopeful messages about the experience of hearing voices across the world.

Representatives and members of the international networks meet annually, at the World Hearing Voices Congresses, to promote new developments, innovative practice, translation of materials, and to support activities in burgeoning countries and share a sense of community, solidarity and camaraderie. One of the fundamental strengths of the Hearing Voices Movement, which has led to its extraordinary success, is that it is based on mutually respectful relationships – authentic partnerships between experts by experience and experts by profession, working together to bring about the emancipation of voice hearers.

HVN’s starting point is that the crises that people experience are real and that they are happening for a reason which is directly connected to the person’s life. We endeavour to support people to make sense of the real events in their lives that may have precipitated their crisis. We show a genuine interest in the range of people’s inner, subjective experiences. When people describe experiences that are deemed ‘psychotic’ we look for the meaning in their madness. Sometimes people use metaphorical or symbolic language to convey their realities and sometimes they are talking literally about things that have happened to them.  However crazy someone appears, we believe that they are making a meaningful attempt to survive maddening experiences.

Contrary to traditional approaches, HVN sees voice-hearing as significant, decipherable and intimately connected to a person’s life story. Consequently, we encourage and support people to listen to their voices and attest to their reality in order to better understand their meaning. We acknowledge that people are having normal reactions to abnormal stress. Instead of asking people – what is wrong with you? We ask them – what has happened to you? On a daily basis we hear stories of physical, sexual and emotional abuse, the impact of neglect, poverty and alienation, as well as of racism, sexism and classism.  Those people, whose experiences do not fit so neatly into a category of trauma as it is currently understood, raise the question of developing our understanding of the huge range of painful and damaging experiences that can be inflicted on and endured by children and adults.

We show respect for the reality of the suffering that people have experienced, and a keen awareness of how this may limit their expression of feelings, ability to think clearly, or capacity to connect. A key part of our role is to magnify the voices of people who are not normally listened to, by promoting the belief that each person has a deep wisdom and expertise about managing and dealing with their own problems. We validate and support people’s resilience, creativity, stamina and emotional strengths, even when they themselves doubt the existence of these qualities.

Acknowledgment enables people to develop true insight into their own distress and suffering which leads to an increasing sense of meaning and purpose in their lives. We are interested in people’s subjective experiences – including their altered states of consciousness, unusual perceptions, ideas and ways of seeing and experiencing the world. When your own feelings, thoughts, experiences and bodily sensations, begin to make sense to you, insight is a natural consequence. When you understand your own ‘symptoms’ as meaningful and essential survival strategies, a more respectful and loving acceptance of yourself begins to emerge (Bullimore 2009; Dillon 2010b; Lampshire 2009; Longden 2010; McNamara 2011).

We recognise that recovery is an on-going process with no fixed end point and that each person’s recovery is unique. HVN recognises that crises may occur again because recovery is an evolving process, an expansive process not a reductive one which seeks to control and maintain people. We have faith in people’s inherent right and capacity to heal, to make mistakes, to learn and to grow. We know that there is much about human experience that we do not understand and we remain humble and curious and open to new ways of seeing the world. We are not interested in complying with social control or in servicing normality. ‘Instead of being a list of symptoms, with side effects on top, we are people who hear voices and see visions, have unusual thoughts, passionate feelings, intense experiences’(Dillon and May 2002). We celebrate our differences.

For many voice hearers and psychiatric survivors, active participation and social action supports and enhances the recovery process; having a shared survivor mission ( Herman, 1992), and becoming part of a collective voice creating change in the world, both inside and out,  is healing, empowering and liberating. This is also true for many mental health workers, who have become increasingly disillusioned with an inadequate biomedical model, disturbed by the collusion demanded of staff in a mental health system driven by fear, control and bureaucracy. For them, becoming part of the Hearing Voices Movement also enables a recovery of meaning, purpose and optimism, a renewal of important values, a rediscovering of a sense of self. For all of us, the possibility of reconnecting to ourselves and each other as unique and equal human beings, is life affirming.

Questions, comments and/or reflections are welcome on this website or via Twitter @JacquiDillon

FOR FURTHER INFORMATION:

Intervoice – http://www.intervoiceonline.org/

Hearing Voices Network, USA: http://www.hearingvoicesusa.org/

Hearing Voices Network, England: http://www.hearing-voices.org/

References:

Adams, W. (2008). The Listening Cure. Time, 21 February.

Beavan, V. and Read, J. (2010). Hearing voices and listening to what they say. Journal of Nervous and Mental Disease 198: 201-5.

Bullimore, P. (2009). My personal experience of paranoia. Psychosis 2: 173-7.

Dillon, J. and May, R. (2002). Reclaiming experience. Clinical Psychology 17: 25-77.Dillon,

J. (2010a). www.radionz.co.nz/national/programmes/ninetonoon/20100414

Dillon, J. (2010b). The tale of an ordinary little girl. Psychosis 1: 79-83.

Herman, J. (1992). Trauma and recovery. New York: Basic Books.

Hilpern, K. (2007). How I beat the voices in my head. The Independent,  Mar. 6.

Kirsch, M. (2007). Voices in your head? You may not be crazy. The Times, 23 January.

Roberts, G. (2013). Personal communication.

Lakhani, N. (2009). A first-class recovery. Independent on Sunday, 25 October.

Lampshire, D. (2009). Lies and lessons: ramblings of an alleged mad woman. Psychosis 1: 178-84.Romme, M. and Escher, S. (1989). Hearing voices. Schizophrenia Bulletin 15: 209-16.

Longden, E. (2010). Making sense of voices: a personal story of recovery. Psychosis 2: 255-9.

McNamara, J. (2011). Can we sit and talk? Poems stories and some words of advice. Psychosis 3: 167-71.

Romme, M. and Escher, S. (1989). Hearing voices. Schizophrenia Bulletin 15: 209-16.

Romme, M. and Escher, S. (2000). Making Sense of Voices. London: Mind.

Romme, M. Escher, S. Dillon, J. Corstens, D. Morris, M. (eds.). (2009). Living with Voices: 50 Stories of Recovery. PCCS Books.

Romme, M. and Escher, S. (eds) (2011). Psychosis as a Personal Crisis. London: Routledge.

Smith, D. (2007). Can you live with the voices in your head? New York Times, 25 March.

New Foreign Correspondent for Mad in America

I am thrilled to have been invited to become a foreign correspondent for the Mad in America web site – see: http://www.madinamerica.com/

I will be writing about the important and innovative work of the Hearing Voices Movement alongside many eminent colleagues, critical thinkers and activists working together to bring about an essential revolution in the world of mental health.

You can read my first post here: http://www.madinamerica.com/2013/01/the-hearing-voices-movement-beyond-critiquing-the-status-quo/

About Mad in America:

The site is designed to serve as a resource and a community for those interested in rethinking psychiatric care in the United States and abroad. We want to provide readers with news, stories of recovery, access to source documents, and the informed writings of bloggers that will further this enterprise.

The bloggers on this site include people with lived experience, peer specialists, psychiatrists, psychologists, social workers, program managers, social activists, attorneys, and journalists. While their opinions naturally vary, they share a belief that our current system of psychiatric care needs to be vastly improved, and, many would argue, transformed.

We also want to provide readers with the opportunity to add their voices to this discussion. We encourage readers to leave comments (see comment policy below), and to submit recovery stories and op-ed submissions. We encourage our readers to visit our forums to further this communal discussion.

Finally, we are commissioning original journalism, both in video and print, that explore on-going efforts to remake care in the U.S. and abroad, and also investigate the problems and deficiencies with the current drug-based paradigm of care.

We welcome feedback and comments on how we can improve this website, and continue to build an online community that can be a societal force for change.

Our Legal Organization

When we started this initiative, we investigated whether it would be better to operate as a non-profit organization, or as a C corporation. We chose the latter, as it provided us with a quicker and easier way to obtain initial funding from “investors” for creating the website and supporting its development. The president of the C Corp is Robert Whitaker. The other board members are Louisa Putnam, Kermit Cole, Laura Delano, and Matthew Cohen.

For on-going revenue to sustain this initiative, we are entirely dependent on support from our readers. We do not host advertisements and do not sell data about our readers to anyone.

Policy for Posting Comments

Please see our guidelines for posting comments on this site.

Support

Mad In America is supported entirely by user donations. Please click here to join in support of our mission.

The Hearing Voices Network – “The Freedom to Hear Voices”: The Hearing Voices Movement

Psychology, Mental Health and Distress is a groundbreaking new text from John Cromby, David Harper and Paula Reavey. Whereas other texts are structured by diagnostic categories and are biologically reductive, this book places biology as well as the experience of distress itself in its social, cultural and historical context.

 Key Features:

  • Offers a wealth of case stories to portray the reality of living with distress and stimulate class discussion 
  • Fully informed by current experimental, qualitative and theoretical psychological research including research into hearing voices
  • Includes a chapter authored by those with first-hand experience of mental health services, ensuring your students understand the nuances of this emotionally charged and often controversial topic

Features additional contributions by renowned figures including Professor Richard Bentall, Professor John Read, psychiatrist and researcher Joanna Moncreiff and campaigner and Chair of the Hearing Voices Network, Jacqui Dillon among others.

See link for further information: http://www.palgrave.com/products/title.aspx?pid=280329

Download flyer: CrombyHarper&Reaveyflyer

 

Hearing Voices Groups: Creating Safe Spaces to Share Taboo Experiences

 

Psychosis as a Personal Crisis seeks to challenge the way people who hear voices are both viewed and treated. This book emphasises the individual variation between people who suffer from psychosis and puts forward the idea that hearing voices is not in itself a sign of mental illness.

In this book the editors bring together an international range of expert contributors, who in their daily work, their research or their personal acquaintance, focus on the personal experience of psychosis.

Further topics of discussion include:

  • accepting and making sense of hearing voices
  • the relation between trauma and paranoia
  • the limitations of contemporary psychiatry
  • the process of recovery.

This book will be essential reading for all mental health professionals, in particular those wanting to learn more about the development of the hearing voices movement and applying these ideas to better understanding those in the voice hearing community.

 

She is able to touch the heart of things.

Talking once about our dreams for Intervoice, Jacqui simply said: “Change the world”. When you hear this from her mouth you can tell from the tone she means it. A split second, just before her familiar contagious laugh, her eyes had a determination like a winning athlete in a marathon run. This is not only about a dream, but a personal attitude. One with many perspectives.

During the years I have witnessed many workshops and lectures from Jacqui. They repeatedly evoked a kind of another state of mind. She is really able to transform the political to the personal. Everytime I felt touched and taken. In most audiences I heard people tell me: “I want to stand up like her”. She motivates others to make the personal political. To speak out. She uses her constructive anger to push even the most hard-boiled egg to humanity. Politely but determined she is able to break down certain explicit and implicit practices of traditional psychiatry. Jacqui opens our eyes for what we know but don’t like to see. She is able to touch the heart of things. Her voice inspires to care.

 Dirk Corstens, Intervoice Chair, Psychiatrist

A role model in the Hearing Voices Movement

For us Jacqui is unique and it is a great pleasure having known her for many reasons personally as well professionally. Jacqui survived terrible abuse and became strong by using her experience to learn from it. She is one of the few people who is able to really understand that the voices are related to her life history and even more important allow herself to feel it. This combination of understanding on a rational and emotional level became her power. This also enables her to be the caring mother of 2 teenage daughters.

As a professional from experience Jacqui is a role model in the Hearing Voices Movement. She has developed a qualitatively very good course in setting up and guiding Hearing Voices Groups. She has helped many individuals to better cope with their voices and their problems in their lives. She is a very good speaker and has a lot to tell about the voice hearing experience and their backgrounds. She has written many very good articles and book chapters. She especially clearly explains the interaction between different consequences of traumatic experiences like hearing voices, dissociation, self harm and eating disorders. She has a lot to give and a lot to teach professionals and also voice hearers. Besides all this she is Chairing the English Hearing Voices Movement and a member of the Board of Intervoice.

Marius Romme & Sandra Escher

Affiliations

HVN LogoNational Hearing Voices Network

Role: Chair

The Hearing Voices Network exists to: raise awareness of voice hearing, visions, tactile sensations and other sensory experiences; To give men women and children who have these experiences an opportunity to talk freely about this together; To support anyone with these experiences seeking to understand, learn and grow from them in their own way.


University of East London

Role: Honorary Lecturer in Clinical Psychology

UEL’s Clinical Psychology programme is characterised by a distinctive approach to its subject matter. As well as providing teaching on the major approaches to clinical psychology theory and practice, it examines the assumptions which inform scientific activity and the problems in applying philosophies and methods from the natural sciences to human behaviour.


Durham University

Role: Honorary Research Fellow in the School of Medicine, Pharmacy and Health

The school’s hallmark is innovation at local and international levels and we seek to make a difference in the quality of care provided to people. Our research themes cut across boundaries and include clinical topics, particularly around earlier diagnosis and intervention, care pathways across organisational boundaries, health policy and economics and the medical humanities.


Birmingham City University

Role: Visiting Research Fellow

The Centre for Community Mental Health (CCMH) is a training, education and research unit. It is part of the Centre for Health and Social Care Research, a Centre of Research Excellence based at the Faculty of Health. We are part of an international network of expertise in mental health practice and service innovation, and work to improve mental health services and promote opportunities for people with severe and enduring mental health problems.


Mad in AmericaMad in America

Role: Foreign Correspondent

The site is designed to serve as a resource and a community for those interested in rethinking psychiatric care in the United States and abroad. We want to provide readers with news, stories of recovery, access to source documents, and the informed writings of bloggers that will further this enterprise. The bloggers on this site include people with lived experience, peer specialists, psychiatrists, psychologists, social workers, program managers, social activists, attorneys, and journalists.


Psychosis Journal CoverPsychosis: Psychological, Social and Integrative Approaches

Role: Member of the Editorial board of the Journal

This journal fills an important gap in mental health literature, namely research focused on the psychological treatments of psychosis (e.g. cognitive-behavior therapy, psychodynamic therapy, family therapy etc.) and the psycho-social causes of psychosis (e.g. poverty, drug abuse, child abuse and neglect, distressed families, urban living, discrimination, rape, war combat etc.).


Beside Mental Health Community Project

Role: Patron

Beside is a Tower Hamlets–based charity working with people who have recurrent or long term mental health difficulties. Our aim is to enable our members to rediscover their inner resources and develop strategies to support their mental health and wellbeing.


St Mungo’s

Role: Member of Expert Group of Rebuilding Shattered Lives – St Mungo’s. 

Rebuilding Shattered Lives is a campaign launched by St Mungo’s to raise awareness, showcase good practice and drive innovation on the issues faced by homeless and vulnerable women. St Mungo’s opens doors for homeless people. Mainly based in London and the South, we provide emergency shelter emergency, support towards recovery and help to prevent rough sleeping. We run over 100 projects and help thousands of homeless people make life changes every year.

 

 

Biography

Jacqui Dillon was born and bred in East London where she still lives. She is a respected campaigner, writer, international speaker and trainer specialising in hearing voices, ‘psychosis’, dissociation, trauma, abuse, healing and recovery. Jacqui has worked within mental health services for more than 15 years, in a variety of settings, including community, acute, low, medium and high secure settings, prisons, colleges and universities.

Jacqui is the national Chair of the Hearing Voices Network in England and a key figure in the Hearing Voices Movement internationally. She is Honorary Lecturer in Clinical Psychology at the University of East London, Honorary Research Fellow in the School of Medicine, Pharmacy and Health at Durham University and Visiting Research Fellow at the Centre for Community Mental Health, Birmingham City University.

Along with Professor Marius Romme and Dr Sandra Escher she is the co-editor of Living with Voices, an anthology of 50 voice hearers’ stories of recovery. She is also co-editor of Demedicalising Misery: Psychiatry, Psychology and the Human Condition and Models of Madness: Psychological, Social and Biological Approaches to Psychosis (2nd Edition). Jacqui has published numerous articles and papers and is on the editorial board of the journal Psychosis: Psychological, Social and Integrative Approaches.

Jacqui’s experiences of surviving childhood abuse and subsequent experiences of using psychiatric services inform her work and she is an outspoken advocate and campaigner for trauma informed approaches to madness and distress. She was nominated for Mind Champion of the Year Award 2009 for her outstanding contribution to increasing understanding of mental health.

Jacqui is proud to be a part of a collective voice demanding a radical shift in the way we make sense of and respond to experiences currently defined as psychiatric illnesses. Alongside her work which she is passionate about, Jacqui enjoys swimming, dancing, laughing and spending time with the people she loves, especially her children.