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Recovery, Discovery and Revolution: The Work of Intervoice and the Hearing Voices Movement

 

Contributors include Peter Beresford, Mary Boyle, John Cromby, Jacqui Dillon, Dave Harper, Eleanor Longden, Midlands Psychology group, Joanna Moncrieff, David Pilgrim, Phil Thomas and Jan Wallcraft.

 

This book contests how both society and Mental Health Services conceptualise and respond to madness. Despite sustained criticisms from academia, survivor groups and practitioners, the bio-genetic model of madness prevails and therefore shapes our very notions of what madness is, who the mad are and how to respond. This dominant yet narrow view, at the heart of the psychiatric system, is misinformed and misleading as well as fraught with tensions between the provision of care and the function of social control. How and why does this system continue? What can be done to change it?
 
Encompassing both academic analysis and practical application, Madness Contested brings together nurses, service-users, psychiatrists, psychologists, practitioners, and academics who promote alternative ways to understand and approach madness. Their contributions debate questions such as: What are the processes and forms of power involved in the current system? What interests are at play in maintaining dominant theories and practices? What are the alternative conceptualizations of madness? Can practice incorporate openness, modesty and a desire for equality? The perspectives are broad yet complimentary.
 
Of interest to all those interested in critical debates and alternative models of madness and mental health care, including: academics, practitioners, service users, survivors, carers, students.
For further information please see this link: http://www.pccs-books.co.uk/products/madness-contested-1/#

Or downlead the flyer: MadnessContestedEdsColesKeenanandDiamond

Her impact will be felt for a long time to come.

Jacqui visited our little corner of the world for the first time this March.  During her visit, I had the opportunity to witness her in many roles:  Facilitator at a small training, speaker at two large events, and as a wonderful human being during all the spaces in between.  Whatever role she was in, Jacqui was engaging and down-to-earth.  She offered her perspective in a way that was accessible to all and – in some instances – lead to perceptible changes in the way people regarded others or themselves, their lives and the potential for their future.

Following Jacqui’s visit, more than one individual went out of their way to report that they felt she was the best speaker they’d been offered the opportunity to experience.  Several individuals began brainstorming ways to bring Jacqui back to the area in the future to reach even more people before she’d even departed.  Ultimately, her presence, personal story and unwavering values helped to strengthen our community and build momentum for change and the development of the Hearing Voices Network in the Unites States.  Her impact will be felt for a long time to come.

Sera Davidow, Director, Recovery Learning Community, Western Massachusetts, USA.

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.

 

Bad Things That Happen to You Can Drive You Crazy!

I’m feeling elated after an amazing evening at Mount Holyoke College in Massachusetts. The event, sponsored by Mount Holyoke College Department of Psychology and Education, the Western Massachusetts Recovery Learning Community, and the Freedom Center was attended by about 150 people  – students, academics and people from the local community – some as far away as Boston, Connecticut and Pittsburg. The auditorium was packed with people hungry for an alternative to the pharmaceutically driven, biomedical model which dominates so heavily in America.  Many were inspired when they heard Ron Coleman and Paul Baker speak late last year and there is a growing momentum for the development of the Hearing Voices Network in America. Change is happening.

My talk, entitled: “Bad Things That Happen to You Can Drive You Crazy! Understanding Abuse, Trauma, and Madness and Working toward Recovery”,

(see this link for further information: http://www.mtholyoke.edu/news/stories/5682743)

seemed to really resonate with others experiences and many people were clearly questioning the adequacy of a biomedical model to make sense of and respond to human distress.

I began by reading ‘A Tale of An Ordinary Little Girl’ and then spoke about the groundbreaking work of the Hearing Voices Movement, its success in many other parts of the world and our intention to revolutionise the way societies think about hearing voices and other unusual human experiences. I ended by stressing the imperative to take collective responsibility for the ills in our societies, to become aware of the dominant ideologies that redefine reality and to challenge oppression, power, social norms and inequalities. I appealed to everyone to join the last great civil rights movement – fighting for the rights of those labelled as mentally ill.

As always, a number of survivors came up to me afterwards and thanked me for telling ‘their’ story. Lots of people wanted to find out more about how they could get involved in the movement, meet with others, start groups. People are impatient for a paradigm shift in the way we understand and respond to human suffering which is now, long overdue. Many are in anguish. Fortunately, there are already some fantastic Hearing Voices Groups running in the area, with several new groups in development. I left feeling proud, inspired and grateful to be part of such a wonderful, powerful movement for change in the world.

There is still so much work to be done. First, it’s time for a bath and then bed.

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

Conferences

Jacqui giving a presentation

Conferences:

I am an experienced and accomplished public speaker. I have spoken at numerous national and international conferences and events for both statutory and non-government organisations.

I have been a keynote speaker at a variety of events on a diverse range of subjects. My specialist areas of expertise are:

  • Personal experiences of ‘madness’ and recovery
  • Hearing voices and ‘psychosis’
  • Critiquing biomedical approaches to madness and distress
  • Trauma and abuse
  • Ritual abuse
  • Dissociation and multiplicity

Consultancy

I can offer my unique perspective of working with and making sense of profound distress and extreme states of mind and the impact it has on individuals, teams and organizations. I also have extensive experience in working collaboratively, creatively and in partnership with disempowered and disenfranchised individuals and groups to bring about sustained and lasting improved positive outcomes.  I have provided coaching and mentoring, supervision and consultancy to individuals, teams and organisations.

Case Study:

I recently worked as a consultant for a large provider of services to people who are homeless. I was asked to facilitate a process which focused specifically on the experience of female service users many of whom were defined as having complex needs e.g. survivors of childhood abuse and neglect, currently homeless, using drugs i.e. crack cocaine, sex working, issues with self-harm, eating disorders, mental health issues and were also dealing with the effects of the ensuing loss of their families.

My initial remit was to facilitate a day that aimed to critically evaluate how the organisation could effectively improve services for women. The day was attended by service users, front line workers, area managers and senior managers. Drawing on the collective experience and expertise of both staff and service users attending the workshop, the session explored:

  • Whether women presented more complex support issues than their male counterparts?
  • What were the key elements of successful support services for women?
  • How could we best ensure consistency across various projects?
  • What were the essential skills and knowledge required by staff teams?

The information which was shared and documented during this day helped to inform the development of an implementation group for the organisations women’s strategy, and established clear targets which had been shaped and defined by women’s experiences of using the service and staff experiences of delivering the service.

I then facilitated a 2nd complimentary session with staff from a number of different projects and departments within the organisation to capture learning to date and plan the future work-streams: specifically looking at staff training, service structure and equalities issues.

As a consequence there are new, specific learning opportunities for staff, alongside a developing coherence of service delivery to women who have experienced trauma, abuse and sexual exploitation.

This consultation work continues and will inform the future structure, planning and efficacy of services.

Bad Science

The CASL campaign is driven by two central factors:

  • The concept of schizophrenia is unscientific and has outlived any usefulness it may once have claimed.
  • The label schizophrenia is extremely damaging to those to whom it is applied.

 The idea that schizophrenia can be viewed as a specific, genetically determined, biologically driven brain disease has been based on bad science and social control since its inception. English scientists have proven that the concept of schizophrenia is invalid. Indeed, few scientists represent themselves as happy with the illness model, and increasingly it is only seen to serve the interests of the pharmaceutical industry’s voracious appetite for control of human experience. It is also harmful because the diagnostic process makes it impossible to make sense of the problems that lie at the root of people’s distress. The scandal is that in the 21st century intelligent human beings are deemed to be ‘lacking insight’ for questioning a label proven to lack scientific validity.

Pages

Recovery, Discovery and Revolution: The Work of Intervoice and the Hearing Voices Movement

 

Contributors include Peter Beresford, Mary Boyle, John Cromby, Jacqui Dillon, Dave Harper, Eleanor Longden, Midlands Psychology group, Joanna Moncrieff, David Pilgrim, Phil Thomas and Jan Wallcraft.

 

This book contests how both society and Mental Health Services conceptualise and respond to madness. Despite sustained criticisms from academia, survivor groups and practitioners, the bio-genetic model of madness prevails and therefore shapes our very notions of what madness is, who the mad are and how to respond. This dominant yet narrow view, at the heart of the psychiatric system, is misinformed and misleading as well as fraught with tensions between the provision of care and the function of social control. How and why does this system continue? What can be done to change it?
 
Encompassing both academic analysis and practical application, Madness Contested brings together nurses, service-users, psychiatrists, psychologists, practitioners, and academics who promote alternative ways to understand and approach madness. Their contributions debate questions such as: What are the processes and forms of power involved in the current system? What interests are at play in maintaining dominant theories and practices? What are the alternative conceptualizations of madness? Can practice incorporate openness, modesty and a desire for equality? The perspectives are broad yet complimentary.
 
Of interest to all those interested in critical debates and alternative models of madness and mental health care, including: academics, practitioners, service users, survivors, carers, students.
For further information please see this link: http://www.pccs-books.co.uk/products/madness-contested-1/#

Or downlead the flyer: MadnessContestedEdsColesKeenanandDiamond

Her impact will be felt for a long time to come.

Jacqui visited our little corner of the world for the first time this March.  During her visit, I had the opportunity to witness her in many roles:  Facilitator at a small training, speaker at two large events, and as a wonderful human being during all the spaces in between.  Whatever role she was in, Jacqui was engaging and down-to-earth.  She offered her perspective in a way that was accessible to all and – in some instances – lead to perceptible changes in the way people regarded others or themselves, their lives and the potential for their future.

Following Jacqui’s visit, more than one individual went out of their way to report that they felt she was the best speaker they’d been offered the opportunity to experience.  Several individuals began brainstorming ways to bring Jacqui back to the area in the future to reach even more people before she’d even departed.  Ultimately, her presence, personal story and unwavering values helped to strengthen our community and build momentum for change and the development of the Hearing Voices Network in the Unites States.  Her impact will be felt for a long time to come.

Sera Davidow, Director, Recovery Learning Community, Western Massachusetts, USA.

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.

 

Bad Things That Happen to You Can Drive You Crazy!

I’m feeling elated after an amazing evening at Mount Holyoke College in Massachusetts. The event, sponsored by Mount Holyoke College Department of Psychology and Education, the Western Massachusetts Recovery Learning Community, and the Freedom Center was attended by about 150 people  – students, academics and people from the local community – some as far away as Boston, Connecticut and Pittsburg. The auditorium was packed with people hungry for an alternative to the pharmaceutically driven, biomedical model which dominates so heavily in America.  Many were inspired when they heard Ron Coleman and Paul Baker speak late last year and there is a growing momentum for the development of the Hearing Voices Network in America. Change is happening.

My talk, entitled: “Bad Things That Happen to You Can Drive You Crazy! Understanding Abuse, Trauma, and Madness and Working toward Recovery”,

(see this link for further information: http://www.mtholyoke.edu/news/stories/5682743)

seemed to really resonate with others experiences and many people were clearly questioning the adequacy of a biomedical model to make sense of and respond to human distress.

I began by reading ‘A Tale of An Ordinary Little Girl’ and then spoke about the groundbreaking work of the Hearing Voices Movement, its success in many other parts of the world and our intention to revolutionise the way societies think about hearing voices and other unusual human experiences. I ended by stressing the imperative to take collective responsibility for the ills in our societies, to become aware of the dominant ideologies that redefine reality and to challenge oppression, power, social norms and inequalities. I appealed to everyone to join the last great civil rights movement – fighting for the rights of those labelled as mentally ill.

As always, a number of survivors came up to me afterwards and thanked me for telling ‘their’ story. Lots of people wanted to find out more about how they could get involved in the movement, meet with others, start groups. People are impatient for a paradigm shift in the way we understand and respond to human suffering which is now, long overdue. Many are in anguish. Fortunately, there are already some fantastic Hearing Voices Groups running in the area, with several new groups in development. I left feeling proud, inspired and grateful to be part of such a wonderful, powerful movement for change in the world.

There is still so much work to be done. First, it’s time for a bath and then bed.

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

Conferences

Jacqui giving a presentation

Conferences:

I am an experienced and accomplished public speaker. I have spoken at numerous national and international conferences and events for both statutory and non-government organisations.

I have been a keynote speaker at a variety of events on a diverse range of subjects. My specialist areas of expertise are:

  • Personal experiences of ‘madness’ and recovery
  • Hearing voices and ‘psychosis’
  • Critiquing biomedical approaches to madness and distress
  • Trauma and abuse
  • Ritual abuse
  • Dissociation and multiplicity

Consultancy

I can offer my unique perspective of working with and making sense of profound distress and extreme states of mind and the impact it has on individuals, teams and organizations. I also have extensive experience in working collaboratively, creatively and in partnership with disempowered and disenfranchised individuals and groups to bring about sustained and lasting improved positive outcomes.  I have provided coaching and mentoring, supervision and consultancy to individuals, teams and organisations.

Case Study:

I recently worked as a consultant for a large provider of services to people who are homeless. I was asked to facilitate a process which focused specifically on the experience of female service users many of whom were defined as having complex needs e.g. survivors of childhood abuse and neglect, currently homeless, using drugs i.e. crack cocaine, sex working, issues with self-harm, eating disorders, mental health issues and were also dealing with the effects of the ensuing loss of their families.

My initial remit was to facilitate a day that aimed to critically evaluate how the organisation could effectively improve services for women. The day was attended by service users, front line workers, area managers and senior managers. Drawing on the collective experience and expertise of both staff and service users attending the workshop, the session explored:

  • Whether women presented more complex support issues than their male counterparts?
  • What were the key elements of successful support services for women?
  • How could we best ensure consistency across various projects?
  • What were the essential skills and knowledge required by staff teams?

The information which was shared and documented during this day helped to inform the development of an implementation group for the organisations women’s strategy, and established clear targets which had been shaped and defined by women’s experiences of using the service and staff experiences of delivering the service.

I then facilitated a 2nd complimentary session with staff from a number of different projects and departments within the organisation to capture learning to date and plan the future work-streams: specifically looking at staff training, service structure and equalities issues.

As a consequence there are new, specific learning opportunities for staff, alongside a developing coherence of service delivery to women who have experienced trauma, abuse and sexual exploitation.

This consultation work continues and will inform the future structure, planning and efficacy of services.

Bad Science

The CASL campaign is driven by two central factors:

  • The concept of schizophrenia is unscientific and has outlived any usefulness it may once have claimed.
  • The label schizophrenia is extremely damaging to those to whom it is applied.

 The idea that schizophrenia can be viewed as a specific, genetically determined, biologically driven brain disease has been based on bad science and social control since its inception. English scientists have proven that the concept of schizophrenia is invalid. Indeed, few scientists represent themselves as happy with the illness model, and increasingly it is only seen to serve the interests of the pharmaceutical industry’s voracious appetite for control of human experience. It is also harmful because the diagnostic process makes it impossible to make sense of the problems that lie at the root of people’s distress. The scandal is that in the 21st century intelligent human beings are deemed to be ‘lacking insight’ for questioning a label proven to lack scientific validity.