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Schizophrenia & Psychosis - Organisations

home | | Schizophrenia & Psychosis | Organisations

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Action of Postpartum Psychosis (APP)
Action of Postpartum Psychosis (APP)

APP is a collaborative project run by women who have experienced Post Partum Psychosis, specialist health professionals and academic experts from Birmingham and Cardiff Universities. Our project is based within the Mood Disorders Research Group in the College of Medical and Dental Sciences at the University of Birmingham. The Peer Support network helps women and families affected by PP feel understood, supported and less isolated. Their workshops, conferences and arts events enable women to articulate their experience of PP and develop information to help other women and families. They facilitate ground-breaking research into the causes of PP at the universities of Birmingham and Cardiff and produce ‘Insider Guides’ and other expert literature to support affected families and health professionals caring for those with PP. They

  • Develop leaflets and web resources for women, their families and health professionals
  • Have an on-line peer support forum where women and their families can talk to others who have experienced PP
  • Offer a one-to-one peer support service where women and their partners can contact others who have been through PP
  • Run events and workshops
  • Offer signposting to appropriate resources or sources of support
  • Field requests for specialist advice to our panel of experts
  • Offer a free specialist second opinion psychiatry service at Cardiff University to women who require expert advice about treatment, recovery or managing further pregnancies
  • Advertise opportunities to take part in research studies into PP
  • Conduct research and talk to members about research areas of importance to them
  • Report to members on the most recent research from around the world
  • Provide advice and resources to members who would like to raise awareness or hold fundraising events in their local community
  • Work with other organisations to help them provide accurate information about PP
  • Respond to media requests and put journalists in touch with women who have experienced PP via our media panel

APP is the largest network of women with postpartum psychosis (PP) in the world which enables high quality research to be conducted that otherwise would be impossible. APP works with Cardiff and Worcester University to conduct research into the causes, management and experience of Post Partum Psychosis. They also advertise other studies into PP from research groups around the world. We encourage communication between academic researchers and those with lived experience of PP. You will find information about our:

  • Molecular genetic studies
  • Clinical studies
  • !uestionnaire based research
  • In-depth interview studies and
  • Service-user led research.

 

CAMPAIGNS

PPP promote greater public awareness of postpartum psychosis, work to address stigma and misinformation, and campaign for improved perinatal mental health services. Their campaigning work is underpinned by research and strong partnerships between women and families who have experienced postpartum psychosis, specialist health professionals and academic experts. APP is proud to be a founder member of the Maternal Mental Health Alliance and work locally and nationally to support NHS service development. Their current campaigns include:

  • Help and support during the COVID-19 pandemic
  • Campaigning for Mother and Baby Units
  • Our call for targeted awareness campaigns to support Black and Asian women in response to inequalities in maternal mental health
  • Call for access to specialist training in postpartum psychosis and perinatal mental health for all frontline professionals working with women and families in the perinatal period 
  • Call for access to specialist postpartum psychosis peer support for women in all regions of the UK
Experts by Experience Talks & Training
Experts by Experience Talks & Training

Action of Postpartum Psychosis have a number of Experts by Experience available to talk with health professionals at conferences and events - all women who have themselves experienced and recovered from postpartum psychosis (PP). Their Experts by Experience can:

  • Share their personal experiences of PP
  • Give talks and training to your health professionals, describing their symptoms, experience of treatment and recovery, what worked well for them and what did not, the impact on their relationship with their baby, family and friends
  • Share the experience gained from supporting others. All of our experts have the breadth of knowledge that comes from supporting many other women and families with the condition (online, via email and in-person) and engaging with the health professionals in their area.


APP's Experts are robustly supported by APP. They have access to APP’s PP academic and clinical experts with international reputation, ensuring that they are well-informed and have up-to-date knowledge. Their experts by experience are supported by robust safeguarding protocols and quality assurance measures within the organisation.

Country
United Kingdom of Great Britain and Northern Ireland

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Maternal Mental Health Awareness For Black and Asian women
Maternal Mental Health Awareness For Black and Asian women

Country
United Kingdom of Great Britain and Northern Ireland

Visit Website

Mother and Baby Units - APP's Campaigning for Mother and Baby Units
Mother and Baby Units - APP's Campaigning for Mother and Baby Units

Action of Postpartum Psychosis (APP) aims is to ensure all women affected by postpartum psychosis in the UK have access to a Mother and Baby Unit - essential places of care for new mums experiencing severe postnatal mental illness. Their campaigning work is underpinned by research and strong partnerships between women and families who have experienced postpartum psychosis, specialist health professionals and academic experts. APP is proud to be a founder member of the Maternal Mental Health Alliance and work locally and nationally to support NHS service development.

 

What is a Mother and Baby Unit?

A Mother and Baby Unit (MBU) is a specialist inpatient treatment unit where mothers with mental illness are admitted with their babies. MBUs include multidisciplinary teams of experts able to care for the physical and emotional needs of new mothers. They have specialist knowledge of the issues surrounding medication management in pregnancy and the postnatal period; specialist facilities appropriate for new mothers and babies; support breastfeeding, parenting skills; and bonding at this critical time in the developing mother-infant relationship. Access to a MBU is essential for women with postpartum psychosis. APP's research shows that women who receive care for postpartum psychosis in MBUs feel more satisfied with the care they receive, feel safer, feel more confident in the knowledge of the staff, recover more quickly and feel more confident with their baby when they go home. 

APP has been campaigning for more Mother and Baby Units in the UK for over 10 years. Over the past 4 years, NHS England has invested in 4 new units, and far fewer women in England with postpartum psychosis are now separated from their baby during treatment. However, many parts of the UK do not have MBUs. Mums and babies are forced to travel miles for treatment or mums can end up on an adult psychiatric ward without their babies and without specialist care. The first unit in South Wales opened in April 2021. But there’s still no Mother and Baby Unit for women in North Wales, Northern Ireland, the Republic of Ireland or Northern Scotland.

APP is working hard to continue to campaign for more Mother and Baby Units - essential places of care for new mums experiencing severe mental illness and their babies. We must support the existence of current units, ensuring the public and policymakers understand and value these facilities. We must ensure that all units are as fully resourced as the new units, with excellent training, multidisciplinary professional teams, and access to peer support. They are collecting stories of women (and partners and grandparents) who did not receive care in an MBU. Please share your story with us - or if you have received care in both an MBU and General Unit.

Country
United Kingdom of Great Britain and Northern Ireland

Contact Person / Email
app@app-network.org

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Music For Mums
Music For Mums

Contact Person / Email
m4mums@app-network.org

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Peer Support for You
Peer Support for You

APP’s peer support service connects you with people who have been there. We can support you if you’ve had postpartum psychosis (PP), or experienced high mood or mania after the birth of your child, or if you are a partner or family member of someone who experienced PP. They know that discharge from hospital, from a Mother and Baby Unit or from other treatment is usually only the beginning of a longer journey to recovery. There are different ways for you to get support, depending on what feels most comfortable for you.

  • Online peer support forum: read other people’s posts or write your own for support from our community of members and volunteers.
  • One to one support: access one to one peer support via private message, email, video call, or, in some parts of the country, meet a peer supporter in person. 
  • Regional Café groups: lived experience café groups where women with PP, and their partners and family members, can meet together informally. There are currently 8 groups across the UK, in South and North Wales, Sussex and Hampshire, Yorkshire, North East, Lancashire and Cumbria, Birmingham and London. Café groups meet both online on Zoom and in person, so if you can’t get to a real one, you can always join a group for a cuppa online

People often tell us they have never met or talked to anyone else who has experienced PP. Myths and misunderstandings about the illness can make it harder to talk to wider family, friends or other new mums about what happened.You can talk to us, whether you are newly recovering, considering another baby, want to talk about parenting after PP, or even if you had PP many years ago and would just like to talk, ask questions, or meet others. Our peer support volunteers are mainly women who are recovered from PP, but we have partners, grandparents, and other family members too. They have been there and understand something of what you have been through.  They can also provide peer support and/or information if you are at high risk of postpartum psychosis (PP), because you are pregnant and have bipolar disorder. 

Country
United Kingdom of Great Britain and Northern Ireland

Contact Person / Email
app@app-network.org

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Peer Support Network
Peer Support Network

The Peer Support Network Peer is a support service for women and partners to talk through online support services. The project aims to reduce the sense of isolation experienced following PP, and improve access to information and support for women, their partners and family.

  • PPTalk: online PP Community
  • One to One Support

 

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Perinatal Mental Health Workforce Training Package
Perinatal Mental Health Workforce Training Package

Acrtion for Postpartum Psychosis offer a training package in postpartum psychosis (PP) and Severe Mental Illness (SMI) in the perinatal period, delivered by a Consultant Perinatal Psychiatrist OR Senior academic, AND one of APP’s Experts by Experience. By utilising clinical experience, cutting-edge research, and the real experiences of affected women and families, the course will up-skill the workforce, developing expertise and empathetic understanding. Learning objectives will address domains in the PMH competency framework, with a specific focus on the risk areas of SMI and postpartum psychosis. The one-day training course is suitable for all professionals working with women and families in pregnancy and the perinatal period including:

  • Psychiatrists
  • Midwives
  • Health Visitors
  • GPs
  • Obstetricians
  • Mental Health Nurses
  • Psychologists
  • IAPT workers
  • Psychotherapists
  • Social Workers and
  • Acute & Emergency staff.

 

Country
United Kingdom of Great Britain and Northern Ireland

Call 020 3322 9900

Visit Website

Postpartum Psychosis & Covid-19
Postpartum Psychosis & Covid-19

Action on Postpartum Psychosis (APP) has compiled information for: pregnant women with a history of postpartum psychosis / bipolar; women and families in crisis or who are developing psychosis; and for those recovering from PP at this time. This is a fast-moving situation. Health trusts/boards across England, Wales, Scotland, and Northern Ireland are continuing to make changes to their services.

  • Pregnant Women Concerned About Postpartum Psychosis
  • In Crisis or Developing Symptoms of Postpartum Psychosis

  • During Recovery from Postpartum Psychosis

  • Links For More Information

Country
United Kingdom of Great Britain and Northern Ireland

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PPTalk Community
PPTalk Community

The Action for Postpartum Psychosis Online Peer Support Forum provides a space for people to read other people’s posts or write your own for support from their community of members and volunteers. The PPTalk community provides an option to connect with others who have been affected by Postpartum Psychosis (PP). One can: 

  • Ask questions
  • Share experiences
  • Find out more about Postpartum Psychosis.

This community is open to anyone who has been affected by PP – if you are recovering, if you are a partner, family member, or friend who has been affected by PP, or if you had PP many years ago. They respectfully ask journalists, researchers & health professionals not to post here. This community is moderated by Action on Postpartum Psychosis (APP) & by APP volunteers – all who have personal experience of PP. They cannot offer urgent crisis support. 

Country
United Kingdom of Great Britain and Northern Ireland

Call 020 33229900

Visit Website

Second Opinion Psychiatry Service
Second Opinion Psychiatry Service

The Cardiff University Psychiatry Service (CUPS) offers second opinion or consultation to patients, with the aim of assisting and advising clinicians and their patients in diagnosis and management. Requests for a second opinion must be made by the doctor in charge of the care of an individual’s mental health.

Address
National Centre for Mental Health: Cardiff University Hadyn Ellis Building Maindy Road Cardiff CF24 4HQ

Call 02920 688321 

Visit Website

 

Organisation

Address: c/o Birmingham Mother & Baby Unit The Barberry National Centre for Mental Health 25 Vincent Drive Birmingham, B15 2FG

Country: United Kingdom of Great Britain and Northern Ireland

Postal Address: C/o Baldwins, 10-11 St James Court, Friar Gate, Derby, DE1 1BT

Email: app@app-network.org

Call 020 33229900

Visit Website

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Competence Network Schizophrenia (KNS)
Competence Network Schizophrenia (KNS)

Competence Network Schizophrenia (KNS) is a research network that was one of the first, the Federal Ministry of Education and Research funded competence networks in medicine .

  • Network expertise in the field of schizophrenia
  • To conduct innovative research together
  • To transfer scientific knowledge promptly into care
  • Improve the quality of life of people diagnosed with schizophrenia
  • To increase knowledge about this mental illness among different target groups.

The funding of the KNS by the BMBF allowed for the first time in Germany to allow leading research institutions to cooperate to a greater extent with one another (horizontal networking) and with a large number of utilities (vertical networking) through science-driven multicenter studies; conduct large, industry-independent therapy course studies in schizophrenic patients; to investigate clients with low prevalence (e.g. high-risk individuals, first-time sufferers) through multicentre recruitment; and to make substantial contributions to highly relevant problems such as early detection and treatment, treatment optimization and quality assurance or the destigmatization of schizophrenic patients both structurally (early detection centers, mental health alliance) and in terms of content in a relatively short time.

After expiry of the funding from the BMBF end of 2011 research on the protagonists of the KNS on the research themes of the network developed are tools and measures the vertical networking (transfer of knowledge into practice) was the Europeanization of the network by establishing the European Scientific Association on Schizophrenia and other Psychoses (ESAS) realized. The KNS is open to all questions from journalists about schizophrenia to find out what's new at the KNS, it's worth taking a look at our current press releases on a regular basis

 

Organisation

Country: Germany

Email: Dr. Viktoria Toeller

Call 0211-922-2773

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Critical Voices Network of Ireland (CVNI)
Critical Voices Network of Ireland (CVNI)

Critical Voices Network of Ireland is a network for people from diverse backgrounds (people with self experience, carers, professionals, academics and interested others) who want an Irish mental health system which is not based on the traditional bio-medical model. This network provides an opportunity to share, discuss and debate critical perspectives on and beyond recovery.

 

Organisation

Country: Ireland

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European Scientific Association on Schizophrenia and other Psychoses (ESAS)
European Scientific Association on Schizophrenia and other Psychoses (ESAS)

ESAS was founded to join European forces with regard to psychotic disorders and thus contribute to the European Research Area. ESAS encourages and promotes Europe-wide scientific exchange and scientific study projects on schizophrenia and to broadly provide current information on schizophrenia, also to the public. Thus ESAS is meant to

  • Strengthen the European schizophrenia research community,
  • Enhance the international visibility of this part of the “European Research Area”,
  • Deal with specific European issues in schizophrenia research and treatment (e.g. harmonisation of quality assurance measures like treatment guidelines),
  • Bring together resources and expertise from a number of research institutes in different countries to tackle scientific questions that are key to the advancement in the field,
  • Initiate, encourage and promote Europe-wide scientific exchange and scientific study projects on schizophrenia,
  • Provide current information on schizophrenia.

ESAS will do this by:

  • Organizing meetings (congresses, seminars, workshops)
  • Initiating and managing all kinds of collaborative research including basic, clinical and mental health services related issues 
  • Offering training and educational programmes
  • Lobbying for destigmatization of schizophrenia and for schizophrenia research
  • Providing mental health education and consultation to the broad public.

 

Organisation

Address: c/o Wartmann & Merker Kirchgasse 48 CH-8024 Zürich

Country: Switzerland

Email: info@esasnet.eu

Call +49 211 922 2773

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Hearing The Voice Durham University
Hearing The Voice Durham University

Hearing the Voice is a large interdisciplinary study of voice-hearing led by researchers at Durham University and funded by the Wellcome Trust. The international research team includes academics from anthropology, cognitive neuroscience, history, linguistics, literary studies, medical humanities, philosophy, psychology and theology. We also work closely with clinicians, voice-hearers and other experts by experience. In addition to shedding light on the relations between hearing voices and everyday processes of sensory perception, memory, language and creativity, we are exploring why it is that some voices (and not others) are experienced as distressing, how they can change across the life course, and the ways in which voices can act as important social, cultural and political forces. The project will continue to develop new methods for interdisciplinary research into human experience, and transform the way in which voice-hearing is managed, treated and understood through a comprehensive online resource for voice-hearers and mental health professionals, as well as an ambitious arts-led programme of public engagement.

 

In addition to shedding light on the relations between hearing voices and everyday processes of sensory perception, memory, language and creativity, we are exploring why it is that some voices (and not others) are experienced as distressing, how they can change across the life course, and the ways in which voices can act as important social, cultural and political forces.

1. Phase One: the first phase of our project set out to address five key research questions:

  • What is it like to hear voices?
  • What do voices mean to people? That is, how do we interpret the experience?
  • What happens in the brain when people hear voices?
  • How can we help people who are distressed by their voices?
  • How should we study human experiences such as voice-hearing?
  • Corresponding to these research questions, Phase One was divided into five different work packages: 1) Phenomenology, 2) Hermeneutics, 3) Cognitive neuroscience, 4) Therapeutic practice and 5) Methodology.

2. Phase Two: the second phase of Hearing the Voice extends our initial enquiry into voice-hearing into seven new research domains. In addition to shedding light on the relations between hearing voices and everyday processes of sense perception, memory, language and creativity, we are exploring why it is that some voices (and not others) are experienced as distressing, how they can change across the life course, and the ways in which voices can act as important social, cultural and political forces. Our project will continue to develop new methods for interdisciplinary research into human experience, and transform the way in which voice-hearing is managed, treated and understood through a comprehensive online resource for voice-hearers and mental health professionals, as well as an ambitious arts-led programme of public engagement.

 

Coping Strategy Toolkit
Coping Strategy Toolkit

The Coping Strategy Toolkit provides different coping strategy ideas that we have collected through talking with voice-hearers, their friends and families.

  • Blocking
  • Compassion
  • Connection
  • Empowerment
  • Expression
  • Safety

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Hearing Voices: suffering, inspiration and the everyday
Hearing Voices: suffering, inspiration and the everyday

Hearing Voices: suffering, inspiration and the everyday is the world’s first exhibition to explore voice-hearing from personal, scientific, cultural, literary and theological perspectives.  The exhibition is the result of a collaboration between Durham University’s Palace Green Library and Hearing the Voice – a large interdisciplinary study of voice-hearing funded by the Wellcome Trust. It was produced in close partnership with voice-hearers, their families and allies, who were involved in the project as contributing artists, co-curators and advisors. This website contains images of:

  • The key displays
  • Podcasts
  • Touring Information
  • Interactive presentations and
  • Useful resources 
  • Listen Up

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In Crisis
In Crisis

Getting Help Quickly is a resource to get immediate help and support.

  • Emergency Services
  • Listening Services
  • Crisis Houses & Services
  • Coping in the Moment
  • Getting Help Quickly
  • Some Common Questions
  •  

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In the Real
In the Real

In the Real is a film by filmmaker and psychoanalyst Conor McCormack has documented the Bristol Hearing Voices Network, a self-help group for people who hear voices and have other unusual experiences. The result of this collaboration is In the Real, a 59 min observational documentary film which goes right to the heart of the voice-hearing experience. 

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Understanding Voices
Understanding Voices

Understanding Voices is a new website that aims to make it easier for people to find information about different approaches to voice-hearing and ways of supporting those who are struggling with the voices that they hear.  It has been produced by Hearing the Voice (Durham University) in close collaboration with voice-hearers, their families and allies, and mental health professionals. The website covers a wide variety of topics including:

  • What is Hearing Voices?
  • Why Do People Hear Voices?
  • Voices & Inner Speech
  • Voices & Trauma
  • Voices & Adversity
  • Voices & The Brain
  • A History of Hearing Voices
  • Voices In Medieval Mysticism
  • Voices from the nineteenth-century asylum
  • Literary voices in the twentieth century
  • Millennial voices: An international people’s movement
  • Voices & Spirituality
  • Key themes in spiritual voices
  • How can spirituality help people?
  • Case Studies
  • Putting it into practice: Information and advice for clinicians
  • Voices in children and adolescents
  • Voices and Imaginary Friends
  • Young People & Hearing Voices
  • Looking for support? Resources for young people, parents and other supporters
  • Voices in Older Adults
  • Sensory Loss
  • Bereavement
  • Loneliness
  • Physical illness and other causes
  • Coping With Voices
  • Different Types of Coping Strategies
  • I’m worried that my coping strategies are causing me harm
  • Talking About Voices
  • Voices & Stigma
  • Suggestions For Voice Hearers
  • Suggestions For Supporters
  • Hearing voices at work or while studying
  • Hearing Voices At Work
  • Your rights and reasonable adjustments
  • Hearing Voices While Studying
  • Benefits and financial assistance
  • Voices & Creativity
  • For Friends & Family
  • Medication
  • What medications are used when people hear voices?
  • What is it like to take antipsychotics?
  • How might antipsychotics help with voices?
  • Adverse Effects
  • Reducing or coming off medication
  • Therapies
  • Cognitive Approaches
  • Talking With Voices
  • Compassion & Acceptance
  • Dealing With Trauma
  • Emerging Therapies
  • Peer Support
  • Hearing Voices Groups

Country
United States Minor Outlying Islands

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Working Knowledge
Working Knowledge

Working Knowledge is a collection of Project Shorts: short, accessible and user-friendly resources dedicated to the practical ins and outs of interdisciplinary research. Covering everything from managing a project’s social media presence to conducting experimental design ‘hackathons’, the series is essential reading for anyone thinking of funding or embarking on interdisciplinary research. The resources in Working Knowledge span three distinct themes:

  1. Working Together
  2. People & Roles and
  3. Engaging Others

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Writers’ Inner Voices
Writers’ Inner Voices

Writers’ Inner Voices is a collaborative research project between the Edinburgh International Book Festival and Durham University’s Hearing the Voice which set out to examine the ways in which writers and storytellers experience their characters. This website provides details of what we discovered, explanations for what might be going on, and creative writing exercises based on the research. The creative writing exercises cover four distinct themes:

  1. Inner speech
  2. Dialogue
  3. Enactive imagination
  4. Agency
  5. Additional Exercises
  6. Resources

 

Visit Website

 

Organisation

Address: Hearing the Voice Caedmon Building c/o School of Education Durham University Leazes Road Durham DH1 1SZ United Kingdom

Country: United States Minor Outlying Islands

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Hearing Voices Maastricht Dirk Corstens
Hearing Voices Maastricht Dirk Corstens

Hearing Voices Maastricht promotes a new approach to hearing voices (The ‘Maastricht’ approach) that emphasises accepting and making sense of voices.  This approach has become progressively more influential, in Europe, Australia, New Zealand, and elsewhere, and has led to voice hearers organising themselves into networks, empowering themselves and working towards recovery in their own ways. This approach contends that people hearing voices (hereafter referred to as ‘VH’ for ‘Voice Hearers’) can learn to cope with their voices and benefit from psychological and social interventions.  It is based on three central tenets, that the phenomena of hearing voices is:

  • More prevalent in the general population than was previously believed
  • A personal reaction to life stresses, whose meaning or purpose can be deciphered and,
  • Best considered a dissociative experience and not a psychotic symptom 

In addition to emphasising understanding the purpose or meaning of the voices, a specific treatment model for working directly with a person’s voices – emphasising their dissociative nature – has been developed by adapting the Voice Dialogue method for working with Voice Hearing.

 

Organisation

Country: Netherlands

Email: dirkcorstens@gmail.com

Call 0031652839800

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Indigo Daya
Indigo Daya

Indigo Daya is a mad activist based in Melbourne, Australia. She works inside and outside the mental health system, seeking change that privileges the views of consumers and survivors. This blog is a space to share stories of hope, healing, improved practice and ideas for reform.

 

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International Early Psychosis Association (IEPA)
International Early Psychosis Association (IEPA)

IEPA is an international network for those involved in the study and treatment of the early phases of mental health disorders encompassing a trans-diagnostic approach. With its origins in early intervention in psychosis, IEPA aims to enhance awareness of the early phases of mental health disorders more generally, their causes, prevention and the process of recovery. It aims to provide a network for international communication and collaboration between stakeholders. IEPA members include clinicians, researchers, administrators, policy makers, and individuals with an interest in the field of early intervention in psychiatry. They aim to:

  • Enhance awareness of the early phases of mental illnesses and the process of recovery, building on experience from research on early psychosis to take a trans-diagnostic view.
  • Provide a network for international communication and collaboration between stakeholders, including mental health professionals, consumers and their families, and policy makers.
  • Contribute to the development of knowledge about the early stages of mental illnesses and their treatment.
  • Facilitate research, including multi-centre trials, cross-cultural research, and long-term studies.
  • Facilitate the development and promotion of best practice in identifying early psychosis and other mental health disorders, and providing optimal treatment.
  • Improve services to young people with emerging mental ill-health, and their families, through encouragement of appropriate mental health policies.
  • Improve access to information on the identification and treatment of mental ill health in its early phases.
  • Arrange conferences and professional meetings on an international level that focus on the early phase of mental health disorders.
  • Provide links to existing educational resources and training options.

The IEPA hosts an international conference every two years, providing an excellent opportunity for sharing experiences and exchanging ideas. 

Early Intervention in Mental Health
Early Intervention in Mental Health

Early intervention (EI) in mental health is a simple concept drawing on a small number of principles: the prompt engagement, assessment and delivery of effective bio-psycho-social interventions to people at risk of or in the early stages of experiencing mental ill health, appropriate to the stage of their condition and their own developmental phase. Characteristics of EI include striving to minimise treatment delays and maximise the prospects of recovery, reliance on evidence-based, systemically (family) inclusive and diagnostically agnostic methods delivered through multidisciplinary, expert services; EI can encompass primary or indicated preventative approaches.

Most comprehensively developed for psychotic illnesses arising largely in the second and third decades of life EI draws on models used in other domains such as heart disease, stroke and cancer where early treatment is accepted as crucial, and shares strong evidence of individual and cost benefits. The recent change of our organisation’s name from the International Early Psychosis Association to IEPA: Early Intervention in Mental Health reflects our efforts to expand the approach beyond psychosis to other mental health disorders and to other stages of the life course.

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Early Intervention in Psychiatry
Early Intervention in Psychiatry

Early Intervention in Psychiatry focuses on the early diagnosis and treatment of all mental health problems and disorders and promotes the importance of early intervention in psychiatric practice. Articles across the full range of psychiatric disorders are welcomed, including schizophrenia and other psychoses, mood and anxiety disorders, substance use disorders, eating disorders and personality disorders, as well as the underlying epidemiological, biological, psychological and social mechanisms that influence the onset of these disorders. Papers in the following fields will be considered: diagnostic issues, psychopathology, clinical epidemiology, biological mechanisms, treatments and other forms of intervention, clinical trials, health services and economic research and mental health policy.

Early Intervention in Psychiatry publishes original research articles and reviews dealing with the early recognition, diagnosis and treatment across the full range of mental and substance use disorders, as well as the underlying epidemiological, biological, psychological and social mechanisms that influence the onset and early course of these disorders. The journal provides comprehensive coverage of early intervention for the full range of psychiatric disorders and mental health problems, including schizophrenia and other psychoses, mood and anxiety disorders, substance use disorders, eating disorders and personality disorders. Papers in any of the following fields are considered: diagnostic issues, psychopathology, clinical epidemiology, biological mechanisms, treatments and other forms of intervention, clinical trials, health services and economic research and mental health policy. Special features are also published, including hypotheses, controversies and snapshots of innovative service models.

In contrast with mainstream healthcare, early diagnosis and intervention has come late to the field of psychiatry. Early Intervention in Psychiatry creates a common forum for researchers and clinicians with an interest in the early phases of a wide range of disorders to share ideas, experience and data. This journal not only fills a gap, but also creates a new frontier in academic and clinical psychiatry.

 

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International First Episode Vocational Recovery (iFEVR)
International First Episode Vocational Recovery (iFEVR)

The International First Episode Vocational Recovery (iFEVR) group is a group of clinicians, researchers, economists and policy makers from several countries. In 2008 they developed an international consensus statement called Meaningful Lives: Supporting young people with psychosis in education, training and employment. 

Country
Australia

Contact Person / Email
eoin@unimelb.edu.au

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International Physical Health in Youth Stream (iphYs)
International Physical Health in Youth Stream (iphYs)

The International Physical Health in Youth Stream (iphYs) collaboration began in 2010 at the IEPA conference in Amsterdam. iphYs is a group of clinicians, service users, family members and researchers from more than eleven countries who joined forces to develop an international consensus statement in 2013 on improving the physical health of young people with psychosis.

The statement, called Healthy Active Lives (HeAL), aims to reverse the trend of people with severe mental illness dying early by tackling risks for future physical illnesses through a prevention and early intervention approach. HeAL is relevant to practice and calls for evidence-based physical health interventions to be provided pro-actively and right from the start for young people experiencing psychosis for the first time. HeAL offers a way that clinicians, consumers, families and other interested collaborators can advocate for evidence-based services. Download PDF.

Country
Australia

Contact Person / Email
j.curtis@unsw.edu.au

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Organisation

Address: P.O. BOX 143 Parkville, Victoria 3052

Country: Australia

Email: secretariat@iepa.org.au

Call +61 3 9342 2969

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INTernational REsearch Programme on Psychoses In Diverse Settings (INTREPID II)
INTernational REsearch Programme on Psychoses In Diverse Settings (INTREPID II)

INTREPID II is a 5 year research programme that investigates the incidence, presentation, outcomes and impact of psychotic disorders in three countries: India, Nigeria and Trinidad. INTREPID II is designed to overcome some of the methodological challenges involved in conducting international psychosis research. The participating organizations are the Schizophrenia Research Foundation (SCARF; Chennai, India), the University of Ibadan (Nigeria), the University of the West Indies (Trinidad), the London School of Hygiene and Tropical Medicine (UK), and the Institute of Psychiatry, Psychology & Neuroscience, King's College London (UK). The programme is funded by the Medical Research Council (MRC) of the United Kingdom.​
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The majority of evidence on the epidemiology of psychoses has been generated in developed countries, but we have relatively little data on psychotic disorders in developing country settings. Through INTREPID II, we hope to learn more about variation in psychotic disorders – in terms of incidence, symptoms, help-seeking, physical health, and course and outcome – across diverse settings. They aim to recruit approximately 240 people with psychotic disorders in each site and follow them up for 2 years, with extensive data collected on their social, economic, and clinical status. A relative of each participant and matched control will  also be recruited and followed up over the same period. Together, the two phases of the INTREPID programme are designed to:

  • Develop robust and comparable methods for the study of schizophrenia and other psychotic disorders in diverse settings, including establishing an extensive network of providers and key informants to help provide comprehensive estimates of incidence and follow up individuals with psychotic disorders (INTREPID I: completed); and
  •  Implement these methods in a three-country study of the incidence, phenomenology, aetiology, outcomes and comorbidity of schizophrenia and other psychotic disorders (INTREPID II: in progress).

The overall aim of the current five-year research programme (INTREPID II) is to investigate the variability – in incidence, presentation, outcome, and impact – of psychotic disorders in diverse settings. The programme consists of four inter-connected studies, designed to investigate:

  1. The incidence and presentation of untreated psychotic disorders in each site and associated risk factors;
  2. The 2-year course and outcome of psychotic disorders and associated factors;
  3. Help-seeking and impact of psychotic disorders on individuals and families, using a combination of quantitative and qualitative approaches;
  4. The types and prevalence of physical health problems and related risk markers.
INTREPID Inida
INTREPID Inida

The catchment site in India comprises of 4 adjoining taluks (administrative sub-districts) in the district of Kanchipuram of Tamil Nadu state in Southern India. The site lies about 50 km from the state capital of Chennai (formerly Madras) and extends for about 50 km end-to-end. The catchment area is comprised of 16 towns and 448 villages with a population of about 1 million individuals, with more than 60% of the population being between the ages of 18 and 64 years (the age group of interest for INTREPID II). 

Country
India

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INTREPID Nigeria
INTREPID Nigeria

INTREPID II is being conducted, nearly 30% of the population lives below the poverty line. Although English is the official language of the country, over 500 native languages are spoken in Nigeria, including Hausa, Yoruba, Igbo and Fula. â€‹ â€‹The catchment site in Nigeria comprises 3 Local Government Areas in and around the metropolitan city of Ibadan, the capital of Oyo State, South West Nigeria: Idaban North East, Ibadan South East, and Ona-Ara.The catchment areas have a population over a million individuals, with close to 52% of the population being between the ages of 18 and 64 years (the age group of interest for INTREPID II).

 

Country
Nigeria

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INTREPID Trinidad & Tobago
INTREPID Trinidad & Tobago

​The catchment area for this study is in Trinidad and consists of the municipalities of Diego Martin, Port of Spain, San Juan/Laventille, Tunapuna/Piarco, Arima, Chaguanas and Sangre Grande. The population at risk is 487,159. 

Country
Trinidad and Tobago

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Organisation

Address: Health Service and Population Research Department Institute of Psychiatry, Psychology & Neuroscience King's College London De Crespigny Park London SE5 8AF

Country: United Kingdom of Great Britain and Northern Ireland

Email: tessa.roberts@kcl.ac.uk

Call +44 (0)20 7848 0351

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International Society for Psychological and Social Approaches to Psychosis (ISPS Australia)
International Society for Psychological and Social Approaches to Psychosis (ISPS Australia)

The International Society for Psychological and Social Approaches to Psychosis (ISPS) Australia is the Australian branch of The International Society for Psychological and Social Approaches to Psychosis. ISPS Australia was first incorporated in 2013, so we are new in Australia although the international organisation has been slowly growing over the last 60 years. Thy are currently a small group of volunteer Board Directors but believe that from little things big things can grow. We hope to join together Australians who have a passion or interest in the importance of psychological and social approaches to psychosis so we can ensure that those who experience psychosis or extreme states get the support and understanding they need to make sense of their experience and move through it effectively.

They offer messages of hope that it is possible to be supported through extreme states. The website offers a space to find information about psychological and social approaches to psychosis and a means to connect with others in Australia who have an interest in this area. Here you will find a forum for members to:

  • Exchange information, ideas, experiences and resources
  • Provide information about news, events, training, research and interventions.

The International Society for Psychological and Social Approaches to Psychosis (ISPS) Australia is part of a broader international organisation that has its origins in Europe in the 1950s. It was formed with the intention of promoting psychotherapy for psychosis and providing a forum for like-minded individuals to exchange ideas. Since then it has continued to grow and refine its objectives.  Now ISPS has expanded to have over 20 branches around the world and involves many leaders in this field.

 

Organisation

Address: ISPS Australia PO Box 6060 Fairfield Gardens QLD 4103 AUSTRALIA

Country: Australia

Email: info@isps.org.au

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International Society for Psychological and Social Approaches to Psychosis (ISPS)
International Society for Psychological and Social Approaches to Psychosis (ISPS)

ISPS is an international organization promoting psychotherapy and psychological treatments for persons with psychosis. They are committed to advancing the treatment and prevention of psychosis. It aims to:

  • Promote the appropriate use of psychotherapy and psychological treatments for persons with psychotic disorders (a term that includes people diagnosed with "schizophrenia").
  • Promote the integration of psychological treatments in treatment plans and comprehensive treatment for all persons with psychosis.
  • Promote the appropriate use of psychological understanding and psychotherapeutic approaches in all phases of the disorders including both early in the onset and in longer lasting disorders.
  • Promote research into individual, family, group psychological therapies, preventive measures and other psychosocial programmes for those with psychotic disorders.
  • Support treatments that include individual, family, group and network approaches and treatment methods that are derived from psychoanalysis, cognitive-behavioural, systemic and psycho-educational approaches.
  • Advance education, training and knowledge of mental health professionals in the psychological therapies and psychosocial interventions in the treatment and prevention of psychotic mental disorders for the public benefit regardless of race, religion, gender or socio-economic status.
Emerging Groups
Emerging Groups

This is a list of people who are interested in / involved in setting up a local ISPS group in their country. The groups listed below are at different stages of development. If you would like to find out more information about ISPS in any of these countries please e-mail the contact person and copy your message to Antonia Svensson, 

Contact Person / Email
isps@isps.org

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ISPS Australia
ISPS Australia

The Australian branch of The International Society for Psychological and Social Approaches to Psychosis. They are currently a small group of volunteer Board Directors but believe that from little things big things can grow. We hope to join together Australians who have a passion or interest in the importance of psychological and social approaches to psychosis so we can ensure that those who experience psychosis or extreme states get the support and understanding they need to make sense of their experience and move through it effectively. They offer messages of hope that it is possible to be supported through extreme states. Our website offers a space to find information about psychological and social approaches to psychosis and a means to connect with others in Australia who have an interest in this area. Here you will find a forum for members to exchange information, ideas, and experiences, and resources that provide information about news, events, training, research and interventions.

 

Country
Australia

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ISPS Charter of Good Practice
ISPS Charter of Good Practice

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ISPS India
ISPS India

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India

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ISPS Liverpool Declaration
ISPS Liverpool Declaration

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ISPS New Zealand
ISPS New Zealand

ISPS New Zealand is a an affiliate of ISPS International - an organisation dedicated to moving towards social and psychological approaches to psychosis through research, education, and advocacy. ISPS New Zealand shares the values and aspirations of ISPS International whilst embracing and valuing all that makes New Zealand beautiful and unique including our bicultural nature.

ISPS NZ welcomes anyone interested in psychological approaches to psychosis - nurses, psychiatrists, psychologists, social workers, arts therapists, occupational therapists, psychotherapists, academics, students, managers, service users and families/whānau. We believe that there is a useful place for many approaches and many perspectives. Benefits include:

  • Four issues per annum of the ISPS Journal: ‘Psychosis: Psychological, Social and Integrative Approaches'
  • Online access to all Psychosis issues
  • You will receive the ISPS Newsletter four times per annum (via e-mail)
  • You can join one of our many e-mail discussion groups
  • Reduced rates at ISPS international conferences
  • 20% discount on all ISPS books published by Routledge

The ISPS Journal Psychosis accepts personal and institutional subscriptions. All Individual Members of ISPS International and local ISPS group members receive the journal as a membership benefit.

Country
New Zealand

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ISPS US
ISPS US

ISPS-US is the United States Chapter of The International Society for Psychological and Social Approaches to Psychosis. ISPS-US advances recovery through an understanding of psychosis and extreme states. 

Country
United States of America

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Organisation

Address: ISPS Chair: Dr Jan Olav Johannessen PO box 1163 Hillevåg 4095 Stavanger

Country: Norway

Email: isps@isps.org

Call +47 51515211

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Intervoice - The International Hearing Voices Network
Intervoice - The International Hearing Voices Network

Intervoice (International Hearing Voices Projects) is a charity, registered in the UK, that aims to support the International Hearing Voices Movement by connecting people, sharing ideas, distributing information, highlighting innovative initiatives, encouraging high quality respectful research and promoting its values across the world. Intervoice aims to support the hearing voices movement, not lead or govern it. As such, Intervoice:

  • Hosts a website and social media platforms that facilitate information sharing and enables people to connect with one another
  • Provides support and guidance to a national hearing voices network that agrees to host the annual International Hearing Voices Congress
  • Distributes a regular e-newsletter to anyone who wishes to receive it
  • Answers email enquiries, which often include requests for local support, information and research
  • Hosts the International Hearing Voices Research Committee, chaired by dr. Eleanor Longden, to promote high quality and ethical research into areas voice hearers Identify as important
  • Where possible, works with local groups in countries without Hearing Voices Networks to support the development of initiatives
  • Provides a focal point for campaigns and initiatives, e.g. ‘One of a million’ and ‘World Hearing Voices Day’

Intervoice are currently funded solely by membership fees and donations. Their trustees (‘The Board’) are elected at our AGM by members of the charity, and come from around the world. They include people with expertise gained through experience, training and/or profession, all of whom are passionate about the Hearing Voices Movement.

The International Hearing Voices Movement consists of the diverse conversations, initiatives, groups and individuals around the world that share some core values. These include: hearing voices, seeing visions and related phenomena are meaningful experiences that can be understood in many ways; hearing voices is not, in itself, an indication of illness – but difficulties coping with voices can cause great distress; when people are overwhelmed by their experiences, support offered should be based on respect, empathy, informed choice and an understanding of the personal meaning voices have in someone’s life.

As a movement of diverse people, countries and ideas, we recognise the importance of hearing and including many voices. As such beside our basic values we do not speak with one voice. We welcome multiple perspectives and ways of contributing. Change can happen on an individual, group, community and societal level – so whether you are working towards making sense of your own voice hearing experience, sharing information in your social circles, trying to improve the support on offer to others or are creating systemic change – we welcome you.

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Children, Young People & Schizophrenia
Children, Young People & Schizophrenia

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Creativity & Voices
Creativity & Voices

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Famous People Who Hear Voices
Famous People Who Hear Voices

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Intervoice Community Agreement
Intervoice Community Agreement

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National Intervoice Networks
National Intervoice Networks

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Personal Experiences Hearing Voices
Personal Experiences Hearing Voices

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Positive & Spiritual Voices
Positive & Spiritual Voices

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Understanding Voices
Understanding Voices

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What is Hearing Voices
What is Hearing Voices

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Organisation

Address: c/o: Mind in Camden, Barnes House 9-15 Camden Road London, NW1 9LQ

Country: United Kingdom of Great Britain and Northern Ireland

Email: info@intervoiceonline.org

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London Hearing Voices Project
London Hearing Voices Project

London Hearing Voices Project links together Hearing Voices Groups across Greater London. The London Hearing Voices Network supports 42 hearing voices peer support groups across London, providing services to over 1000 people with serious mental health needs each year. Their annual turnover is in the region of £1,000,000 per annum employing 27 staff and are supported by about 100 volunteers at any one time. The London Hearing Voices Project includes provides an ongoing support to the network of ~30 Hearing Voices Groups and ~15 Paranoia & Beliefs Groups in Greater London. This includes providing training courses and networking events for facilitators. Their aim is to help increase the sustainability of well-facilitated Hearing Voices Groups, promote their benefits and help signpost individuals to groups in their local area.

  • The LHVN mailing list for a monthly newsletter of trainings, conferences, resources & events.
  • List of groups in London: LHVN hearing voices groups and paranoia groups
  • World Hearing Voices Congress: held in a different country every year since 2009, the World Hearing Voices Congress brings together voice-hearers and those who support the aims of the Hearing Voices movement, from across the world for a two-day conference. 

Launched in 2005, as a London-wide capacity building project to increase the quality and quantity of peer support groups for adults who hear voices or see visions, the London Hearing Voices Project has grown from strength to strength. It has developed an excellent local, national and international reputation for its work and is part of the wider international ‘Hearing Voices’ movement. Inspired by the pioneering work of Professor Marius Romme, Dr Sandra Escher and Patsy Hague (a voice hearer), the project views voices as inherently meaningful experiences that can be understood in the context of a person’s life experiences. We recognise the individual’s own potential, with the right support networks, to recover from the distress associated with difficult voices and visions. We are committed to providing innovative services that help ensure those support networks are in place. This includes increasing the availability of peer support opportunities and recovery oriented approaches for those that need them.

Hearing Voices Groups & Paranoia & Beliefs Groups
Hearing Voices Groups & Paranoia & Beliefs Groups

London Hearing Voices Network (LHVN) incorporates Paranoia & Beliefs into their program to provide ongoing support to the network of:

  • 30 Hearing Voices Groups and
  • 15 Paranoia & Beliefs Groups 

This includes providing training courses and networking events for facilitators with the aim of helping increase the sustainability of well-facilitated Hearing Voices Groups, promote their benefits and help signpost individuals to groups in their local area. Hearing Voices Groups and Paranoia Beliefs Groups in Greater London include:

  • Mind in Bexley Hearing Voices Group is a group open to anyone living in Bexley that usually runs for eight weeks followed by a two week break. They meet @ Milton House, 240A Broadway, Bexleyheath, DA6 8AS on Wednesdays 3:45pm-4:45pm - 020 8303 5816 - pfisher@mindbexley.org.au
  • Hestia Hearing Voices Group is a closed group @ Ashford Place 60 Ashford Road London NW2 6TU
  • Parallel Views (Bromley & Lewisham Mind): is a group open to anyone living or working in London on Thursdays 2:00pm-4:00pm @ Anchor House, Station Rd, Orpington BR6 0RZ - 07841 206710 - david.holmes@blmind.org.au 
  • Bromley Hearing Voices Group is a group open to anyone living in Bromley on Wednesdays, 10:15am–11:45am @ Bromley Common Baptist Church, Gravel Road, Bromley, BR2 8PE - 01689 811 222 - stuarttight@hotmail.com
  • Positive Connections (Camden & Islington MH Trust): a group opened to those receiving a service from Camden & Islington MHTrust fortnightly on Wednesdays at 11.30am-12.30pm @ Peckwater Centre, 6 Peckwater Street, NW5 2UP - 07771 872 923 - jill.chadwick@candi.nhs.uk
  • My Beliefs (Mind in Camden): a group open to anyone free of charge regardless of borough on Thursdays 5:00pm-6:00pm - 020 7241 8991 - referrals@mindcamden.org.uk
  • The Craze (St Mungo’s) is a closed group on alternative Tuesdays from 11:30am-1:00pm @ Adamson Road, 33-35, NW3 3HT - 07736 886 959 - Matthew.Blakemore@mungoadway.org.au
  • Pulse (St Mungo’s) is a closed group on alternative Tuesdays from 11:30am-1:00pm @ 180 Haverstock Hill, London NW3 2AL - 07736 886 959 - Matthew.Blakemore@mungoadway.org.au
  • Mind in Camden Mixed Hearing Voices Group a group open to anyone free of charge regardless of borough on Tuesdays from Tuesdays, 12:00pm–1:00pm @ Barnes House, 9-15 Camden Rd, NW1 9LQ - 020 7241 8991 - referrals@mindcamden.org.uk
  • Mind in Camden Women’s Hearing Voices & Unusual Beliefs Group is a group open to anyone free of charge regardless of borough on Tuesdays from Fridays from 2:00pm-3.15pm @ Barnes House, 9-15 Camden Rd, NW1 9LQ - 020 7241 8991 - referrals@mindcamden.org.uk
  • Voices Forum of Croydon (Rethink Mental Illness) is a group open to people from all boroughs as it is OK to just turn up, but best to call first in case an activity is planned @ Croydon Old Town Hall, Katharine St, Croydon CR9 1ET - 0208 464 7052 - voicesforumofcroydon@googlemail.com
  • C.A.P.E. Hearing Voices Group is an open group to members of CAPE, after receiving a referral on Wednesday from 2:00pm-3:00pm - 020 8896 2552 - tracey@capeproject.org.uk
  • Mind in Enfield Hearing Voices Group is a group open to those living in either in Enfield or Haringey @ Greenwich Mind, 54 Ormiston Road, London, SE10 0LN on Mondays from 12:30pm-1.30pm - 020 8887 1480 - Sufia.Rahman@Mind-In-Enfield.org.au
  • Greenwich Mind Hearing Voices Group is a group primarily for Greenwich residents on Wednesdays from 10.00am-11.30am - 020 8853 2395
  • South Recovery Team Hearing Voices Group is a group available to service users of the West London Mental Health Trust/LBHF South Recovery Team on Wednesday from 11:00am-12:00pm @ The Star Room, St Andrew’s Church, Greyhound Road London W14 9SA - 020 7386 1275 - catherine.muller@wlmht.nhs.uk
  • Clarendon Cafe Paranoia & Beliefs Group is a group open to anyone on Tuesdays 14.00pm-15.15pm @ Clarendon Road, Hornsey, London N8 0DJ - 020 8489 4860 - Lesslian.jat@haringey.gov.uk
  • WhyFI (Rethink Mental Illness) is a group open to those living in Harrow only on the 1st and 3rd Thursdays from 12.30pm–1.30pm @ The Bridge, Christchurch Avenue, Harrow, HA3 5BD - 020 8427 8528 - nicole.busz@rethink.org.
  • Wellbeing Network Hounslow Hearing Voices Group is a group open to people from all boroughs with no referral required every 1st and 3rd Thursday from 1:00pm-2:00pm @ The Arts Centre (dance studio), 1st Floor, Treaty Shopping Centre, Hounslow, TW3 1ES - 07834 388022 - kevin.fulliscks@whmht.uhs.uk

Country
United Kingdom of Great Britain and Northern Ireland

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Organisation

Address: Mind in Camden Barnes House, 9-15 Camden Road London, NW1 9LQ

Country: United Kingdom of Great Britain and Northern Ireland

Email: lhvn@mindincamden.org.uk

Call 020 7241 8978

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Postpartum Psychosis - Spain
Postpartum Psychosis - Spain

Postpartum Psychosis is the Spanish campaign and initiative of the European Institute of Perinatal Mental Health to raise awareness about postpartum psychosis to promote its prevention and to help affected mothers to have access to the best treatment.

 

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Country: Spain

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Psychosis-Risk Outcomes Network (ProNET)
Psychosis-Risk Outcomes Network (ProNET)

ProNET is a study aiming to improve the identification of youth at-risk for developing psychosis and to better understand why some young people are more likely to develop psychosis. This research aims to increase understanding of mental health concerns in young people and how to prevent the development of a more serious mental illness. WERC is one of 26 international sites involved in the ProNET study.

WHO IS NEEDED?

Individuals ages 12-30 who meet criteria for a psychosis-risk syndrome. You may be eligible if you have noticed a recent change in your thinking, behavior, or experiences, such as:

  • Confusion about what is real or imaginary
  • Feeling not in control of your own thoughts
  • Feeling suspicious or paranoid
  • Hearing sounds or seeing things that may not be there
  • Having trouble communicating clearly

 

Participants will be seen at nine visits over a two-year period. The first visit will consist of a screening to determine if you are eligible for the study. You would then complete several assessments, including:

  • Clinical interviews focusing on questions about different experiences and symptoms, as well as your daily life, such as your friendships, school, or work.
  • Biological assessments including brain MRI, EEG, saliva and blood testing.
  • Cognitive testing focusing on memory, attention, concentration, and learning

 

Organisation

Email: carli.ryan@wustl.edu

Call 314-362-5216

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Schizophrenia Awareness Association (SAA)
Schizophrenia Awareness Association (SAA)

Schizophrenia Awareness Association (SAA) is a not for profit organisation based in the city of Pune for persons with mental illness and their families. SAA is run and managed by user survivors, family caregivers and volunteers jointly and is away from proprietary style of functioning. The trustees are elected every three years by the members in the Annual General Meeting. SAA works for and with user survivors and family caregivers. SAA believes in their capacities and encourages them to take responsibility. SAA provides them a forum to share, understand and support. SAA does not receive any grant or funding from any govt. dept. or agency.

SAA’s work is mainly to create awareness and to remove the stigma about schizophrenia and other mental disorders in the community, to promote Self Help Group Activities among persons with mental disorders and their family care givers, to provide day care and rehabilitation facilities to persons with mental disorders and do advocacy work at national and international work. SAA helps in rehabilitation of persons with mental illness, which includes self- employment and also jobs with some sensitised employers. SAA does not promote or advocate any particular line of treatment for mental illness and leaves it to the family and the user to decide what suits them most.

SAA promotes awareness about mental illness and works towards removing stigma attached to it. There is huge ignorance in the community about mental illness. As a result when the illness strikes a family member, the family is unaware of what is happening. By the time the seriousness of the condition is realised and the treatment starts, it is late and the aggravations sets in. The illness becomes chronic and recovery becomes difficult. Over the years, SAA has used all available means to create awareness and understanding in the community about mental disorders in general and schizophrenia in particular. SAA creates awareness by:

  • Holding public meetings
  • Participating in exhibitions, road shows and street plays
  • Information counters at public places
  • Talks
  • Competitions for college students
  • Film shows
  • Musical and cultural programmes
  • Individual and group counselling
  • Publication of informative books and fiction
  • Publishing articles in newspapers and journals
  • Distributing pamphlets and brochures,
  • Production of films e
  • Cass room awareness programmes conducted in SAA's auditorium for caregivers, volunteers, students and other stakeholders.

An essential part of awareness campaign has been fighting the stigma which manifests itself in a lowered opinion about a person with mental disorder regarding person’s capacities, future and incurable nature of disorder.  SAA has conducted sensitisation programmes for the press and have held meetings with their groups. The media have also been invited to address the group of caregivers as to how they cover the incidents involving persons with mental disorders. The discussions that follow are educative for the press representatives and also the caregivers.

Arts Based Therapy
Arts Based Therapy

Arts Based Therapy (ABT) is use of art forms to accomplish individualized goals within a therapeutic relationship. ABT derives theoretical base from a systematic training in Subtle Energy Guide from the Indian Mind Traditions, notably Buddhist Psychology and Ethics interfaced with information from neuroscience and developmental psychology. Interventions are designed as per the specific therapeutic goals for each participant. In ABT, the emphasis is on the process and the artistic outcomes are secondary. Playfulness ensures that there is no stress and no pressure. As a complementary therapy, it acknowledges the role of other therapies and approaches.

Weekly, ABT sessions are now being conducted by Aanand for user survivors at SAA’s Rehab Centre under a 3 year project supported by Mariwalla Health Initiative (MHI). Under this Project, ABT sessions, complimentary to other rehab activities at the Centre, will address personalized therapeutic needs, within the context of individual patterns and possibilities of their healing/rehabilitation. Each group of 10 service users will go through 2 steps ABT intervention.

Country
India

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Dance Movement Therapy
Dance Movement Therapy

Dance Movement Therapy (DMT) Project was launched in SAA in August 2014. At SAA they use modern dance, folk dance and classical dance. For e g in Kathak one needs to tap hard on the floor which leads to release of anger from the mind. Similarly the body movements and facial expresses in Mohiniattom helps clients overcome all their emotions. The circular and interlock movements in Modern Dance help the Clients to feel united and move freely with other people. 

Country
India

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Day Rehabilitation Centre
Day Rehabilitation Centre

SAA runs a Day Rehabilitation Centre at Dhayari in Pune. In a homelike, peaceful, green environment, clients receive therapeutic day care and participate in rehabilitation related programmes. The Centre, spread over 5 levels, has a large yoga hall, activity rooms, library, committee room, counseling room, respite room, dinning area, kitchen, lounge, auditorium, jogging track and other facilities. Various activities and therapies are conducted by clinical psychologists and experienced volunteers. Clients, unable to commute on their own are provided pickup and drop facility.

Clients attending the Centre are helped to relearn the forgotten skills and build their capacity to perform various skills. They are encouraged to lead the activities to build their confidence and to develop leadership, group management and planning skills. While a few of the activities like jogging and  yoga are common for all, a few more are planned for clients individually keeping in view the nature and intensity of their illness, area of interest, personal capacity, education, age, understanding and skill. Activities carried out at the centre include:

  • Vocational: Madhubani, Warli, Glass Painting, Emboss Painting, Block Painting, Diwali lamps, lamp Shades, Origami, Murals, Wall Frames, Paper Bags, Envelops, Tie and Dye, Wood Flowers, Soft Toys, Jewelry Making, Greeting Cards, Wall Pieces,Show Pieces, Door Hangings, Handkerchiefs, Napkins, Cushions, Table Covers, Bed Covers, Spice Powders, Chocolates, Olive Candies, Sauces, pickles, Paper Cups, Cotton Carding, soaps, Detergent Powder, Cleansing Material.
  • Therapeutic: group Reading-Newspapers and Books, Monitored Group Discussions and Insight Orientation, Free Hand Drawing and Painting, Coloring Shapes, Pasting, Collage, Singing, Instrument Playing, Drum Beating, Dance Movements, Motor Movement, Facial Expressions, Body Movements, Art Based Therapy, Diary Writing,
  • Skill Development: computers, Spoken English, Speech Delivery, Group Discussions, Money Handling, Cooking and Hand writing.
  • Mind and Body: self Care, Yoga, Pranayama, Aerobics, Gardening, Jogging, Outdoor Games, Indoor Games such as Dice Game, Train Game, Thumb and Coin Game, Cultural Programmes, Excursions.

In addition to the above activities, regular counseling sessions are held for all the service users and assessments are done using Positive and Negative Rating Scale and IDEA Scale. The families are kept informed of the progress and invited for discussions. Individual files are maintained for each client. The counselors manage occasional crisis situations which develop due to the nature of illness. User survivors get paid for the items prepared by them in their activity programmes and also the profits earned on sale are distributed among them.

The clients attending regularly are benefited by the therapeutic programmes and show considerable improvement over a period. As observed by the staff and volunteers and confirmed by caregivers and also revealed by idea scale, the symptoms come down substantially and their participation in activities at the Centre and attending to chores at their respective homes goes up. The activities at the Centre help in restoring confidence and money earned from sundry jobs done at the Centre, incentives earned for behavioral modifications and the articles made and sold gives them a sense of achievement and empowerment. Their leading the activities and taking sessions builds their confidence and equips them for employment. Getting paid for their work and helping others enhances their self-esteem. There are success stories; some have found employment; some have joined family business, some have started their own venture.

 

Clients coming to the Centre rediscover their own identity in an environment, where their actions are not criticized, where there is warmth and empathy and where there is no stigma. Rehabilitation programmes at the Centre help clients with complex mental health problems to regain cognitive, emotional, social, intellectual and physical skills needed to live, learn, work and function independently in the community with least interference from the symptoms. Rehabilitation remains a continuous process at the Centre. The ultimate goal is to make the clients independent in all aspects of their lives, financial, social, relationships building and maintaining.

Country
India

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Stitch Project
Stitch Project

 SAA’s Sti+ch Programme aims to reduce stigma associated with mental illness. It’s an acronym of Stigma Watch. The project aims to stitch the torn apart (sufferers & caregivers) with the mainstream so that there remains no discrimination on the grounds of mental illness. The project aims to create stigma awareness and implement de-stigmatization programs in Pune and some adjoining districts, and gradually spread it in Maharashtra by conducting Train the Trainer (TTT) programs. The objective of the project is

  • To help people understand that how do they contribute unconsciously in spreading stigma
  • To help people understand that what steps can they take to reduce stigma
  • Identifying operationalised stigma in daily life, shedding light on it, and insisting and pursuing corrective measures to stop the stigma from spreading further
  • Supporting individuals and caregivers directly and indirectly affected by stigma and fostering their agency
  • Suitable short and long training sessions are proposed to be developed and conducted to sensitise mental health professionals, patients, caregivers and lay persons.

Country
India

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Organisation

Address: Kamalini Kruti Bhawan 14, Ganesh Nagar, Lane No B 30-31 Dhayari Road Pune Maharashtra 411041

Country: India

Email: schizpune@gmail.com

Call 020-24391202

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Schizophrenia International Research Society (SIRS)
Schizophrenia International Research Society (SIRS)

The Schizophrenia International Research Society (SIRS) aims to bring together scientists from around the world to exchange the latest advances in biological and psychosocial research in schizophrenia.  The Society is dedicated to facilitating international collaboration to discover the causes of, and better treatments for, schizophrenia and related disorders. Part of the mission of the Society is to promote educational programs about the latest findings in schizophrenia research, to effectively disseminate them worldwide, and to expedite the publication of new research.

Early Career Award Program
Early Career Award Program

The Early Career Award (formerly Travel Award) program is intended to sponsor individuals who have, through their research, teaching or clinical activities, demonstrated a professional and scientific interest in the field of schizophrenia research. Candidates must indicate their interest in schizophrenia research and, if possible, provide evidence of continuing and future involvement and activity in the field. Individuals must be graduate students, residents, fellows, or new/young faculty members who have completed their last training within 5 years. Candidates who are members of an ethnic minority group underrepresented in biomedical science areas are strongly encouraged to apply.

Awardees are required to submit a poster/oral presentation abstract. It is the belief of the Society that the opportunity to attend its scientific meeting will stimulate the interest of young scientists in schizophrenia research by affording them the opportunity to attend an outstanding scientific program in clinical and basic research. The program will also allow awardees the opportunity to become aware of the most recent, and often unpublished, advances in schizophrenia research, meet internationally distinguished researchers and clinicians, and interact with world authorities working on the frontier of this field.

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npj: Schizophrenia
npj: Schizophrenia

npj Schizophrenia is an open access, online-only journal that aims to publish high-quality original papers and review articles relevant to all aspects of schizophrenia and psychosis, from molecular and basic research through environmental or social research, to translational and treatment-related topics. npj Schizophrenia publishes papers on the broad psychosis spectrum including affective psychosis, bipolar disorder, the at-risk mental state, psychotic symptoms, and overlap between psychotic and other disorders.

npj Schizophrenia is published in partnership between The Schizophrenia International Research Society and Nature Publishing Group. Authors whose papers are accepted for publication within npj Schizophrenia are required to pay an article processing charge (APC). All SIRS members are entitled to a discounted APC (50% reduction on the full rate) if an article for which they are the corresponding author is accepted for publication within the journal.

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Research Harmonisation Group (RHG)
Research Harmonisation Group (RHG)

The Research Harmonisation Group (RHG) consist of from five to twenty senior researchers who have a research track record in the topic covered by the Group (the 2020 the research topic is epidemiology). At least half the members should be early career researchers (post docs, first time lecturers) who are nurtured by senior members of the group. The Society recognizes early career researchers as individuals who are less than 40 years of age or within five years post-doc of their terminal degree taking into account career breaks.  The senior researchers and early career researchers must be SIRS members.

The RHG must demonstrate that they have input from consumers who have shown an interest in research in the topic covered by the group but are not necessarily members. The purpose of Research Harmonisation Groups (RHG) is to produce methods for sharing and/or comparing data across countries to increase the creative drive of schizophrenia research internationally.

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Schizophrenia Bulletin 
Schizophrenia Bulletin 

Schizophrenia Bulletin seeks to review recent developments and empirically based hypotheses regarding the etiology and treatment of schizophrenia. We view the field as broad and deep, and will publish new knowledge ranging from the molecular basis to social and cultural factors. We will give new emphasis to translational reports which simultaneously highlight basic neurobiological mechanisms and clinical manifestations. Much of the Bulletin content will be invited reviews and manuscripts organized as a theme by special guest editors. Also, the Bulletin will carry unsolicited manuscripts of high quality that report original data related to theme issues or where the Bulletin can provide a special venue for a major study.

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Schizophrenia Research
Schizophrenia Research

Schizophrenia Research is an international, multidisciplinary journal that promotes rapid publication of new international research that contributes to the understanding of schizophrenic disorders. It is hoped that this journal will aid in bringing together previously separated biological, clinical and psychological research on this disorder, and stimulate the synthesis of these data into cohesive hypotheses.

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SIRS Commitment to Anti-Racism, Diversity and Inclusivity
SIRS Commitment to Anti-Racism, Diversity and Inclusivity

Schizophrenia International Research Society aims for action and not just words. The SIRS community must be representative of the communities we seek to help. We have made some progress, but still not enough, on gender discrimination. We now need to commit to actions that will reduce other sources of discrimination, including race. SIRS affirms a commitment to diversity within our research endeavors so we can understand the effects of structural discrimination and how it affects the onset, maintenance and exacerbation of problems for people with a diagnosis of schizophrenia. This requires us to monitor and report on diversity among our research participants and investigate its effects on our scientific understanding.

As a global community of researchers, clinicians, educators, students and people with lived experiences, we have a shared and individual responsibility towards eradicating inequality, discrimination and injustice. We do this not only through our research, but in our everyday life. This can only be done through joint and individual education. Our task is to understand white privilege and eschew white exceptionalism, so we can use this knowledge to improve our research and the ambitions of the community as a whole. We have already taken some concrete and meaningful steps, including a commitment to anti-racism. But words are not enough. We need to act. So, in developing our next 5-year strategy, the building of an inclusive, diverse and equitable society focused on improving the lives of people with a diagnosis of schizophrenia will be a central theme. The society commits to ensuring that every committee will have representation of women and ethnic minorities, every conference will have plenary speakers from under-represented groups and that all our awards will ensure that diversity is a key consideration, including our new Research Harmonization Award.

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Special Interest Groups
Special Interest Groups

Special Interests Groups at the Schizophrenia International Research Society Include:

  • Accelerated Aging and Stress in Severe Mental Disorders: monica.aas@medisin.uio.no  
  • Developmental Trauma and Psychosis Network (DTPN): m.bloomfield@ucl.ac.uk
  • Global Initiative for Integrated Research on Psychosis: ncrossley@uc.cl or craig.morgan@kcl.ac.uk
  • Treatment Response and Resistance in Psychosis: oliver.howes@lms.mrc.ac.uk
  • Lifestyle Interventions in Schizophrenia: Improving the Outcome: peter.falkai@med.uni-muenchen.de
  • Trials in Schizophrenia: thomas.raedler@albertahealthservices.ca
  • Multicenter, multimodal study of first episode psychosis: molecules, circuits, and clinical manifestations: asawa1@jhmi.edu
  • Physical Health Comorbidity Among People with Schizophrenia: d.siskind@uq.edu.au
  • Social Cognition Across the Autism-Psychosis Spectrum: Working towards an International Consensus Battery: t.b.ziermans@uva.nl

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What is Schizophrenia
What is Schizophrenia

Schizophrenia is a mental illness that occurs in about 1% of the population and usually begins to show signs in late adolescence or early adulthood. It appears slowly with a decline in ability to concentrate and focus on schoolwork or other activities, withdrawal from friends and social groups, and an increase in what appears as day dreaming and “escape from reality”. Often this happens without those closest to the person realizing what is happening until a crisis appears. For information about schizophrenia, please view the various videos below.

The society depends on contributions from individuals and corporations with an interest in combating mental illness. There are not enough funding opportunities for research on schizophrenia provided by public and private funds. Thus, the society hopes to bridge this gap in order to facilitate more rapid progress toward eradicating schizophrenia. Please consider donating by clicking here.

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Organisation

Address: 5034-A Thoroughbred Lane Brentwood, TN 37027

Country: United States of America

Email: info@schizophreniaresearchsociety.org

Call 001.615.324.2370

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Schizophrenia Research Foundation (SCARF India)
Schizophrenia Research Foundation (SCARF India)

Schizophrenia Research Foundation (SCARF India) is a mental health centre and nonprofit organization based at Chennai, Tamil Nadu, offering a multidisciplinary, comprehensive range of psychiatric care and rehabilitation services. Their aim is to:

  • Provide integrated, comprehensive, cost effective and accessible mental healthcare to the mentally disabled
  • Initiate, conduct and support research programs on the biological, social and psychological aspects of schizophrenia and mental illness to further knowledge of treatments and methods of caregiving.
  • Place emphasis on Psychosocial rehabilitation especially employment support
  • Initiate and implement mental health policy changes that will enable mentally ill people to participate fully in social processes
  • Increase social awareness about mental illness, disability, treatment and other welfare measures.

 

Organisation

Address: #R/7A North Main Road, Anna Nagar (West Extn.), Chennai 600 101

Country: India

Email: info@scarfindia.org

Call + 91 44 2615 3971

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Schizophrenia Research Fund (SRF)
Schizophrenia Research Fund (SRF)

The SRF is an independent registered charity that aims to advance the better understanding, prevention, treatment and cure for all forms of mental illness and in particular for the illness known as Schizophrenia. Over the years, donations and grants have been made to help patients suffering from Schizophrenia and for pure research, the latter by the funding of research scientists directly, or by the provision of equipment. Following the linking we would ask all donors to send their donations to Mental Health Research UK, where it will be used for research into Schizophrenia. .

 

Organisation

Country: United Kingdom of Great Britain and Northern Ireland

Email: trustees@mhruk.org

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The International Spiritual Emergency Network (ISEN)
The International Spiritual Emergency Network (ISEN)

ISEN is a collaboration of not-for-profit support networks from around the world. Each network is run by volunteers and offers information and referrals at no cost to those experiencing or affected by Spiritual Emergency. They encourage and assist in the establishment of local Spiritual Emergence Networks (SENs) and related projects in countries where support is lacking. Additionally, as a forum, they support each other, pool resources and share knowledge. They recognise that a Spiritual Emergency/Spiritual Crisis is part of an ongoing, natural process of human growth and transformation towards wholeness and a greater sense of wellbeing. They see spirituality as an integral part of everyday life. Spiritual emergence and spiritual emergency are holistic concepts that include physical, psychological and social dimensions.

Thousands upon thousands of people around the world are reporting having spiritual experiences, waking up to a more expanded level of consciousness, which have the potential to catalyze a greater capacity to realize our collective human potential. They can also be extremely destabilizing within our current cultural framework, resulting in a growing number of people experiencing mental health problems, exacerbating the current global crisis. A growing body of research shows us that having a non-pathological framework within which to understand spiritual experiences reduces the chance of a person going into crisis.

ISEN (International Spiritual Emergence Network) was created to be a vital resource and collaborative platform to assist established networks around the world that offer compassionate support to individuals who understand their experiences to be a spiritual crisis, rather than a mental illness. We are in the process of helping to link existing spiritual emergence networks with each other while assisting in the process of creating new spiritual emergence networks in countries where they don’t yet exist, helping to bring together people who need help with those who can assist them, in order to assist with this vital paradigm shift towards an integral world. ISEN provides assistance, education and encourages research toward a non-pathological, integral framework that understands and embraces spiritual emergency, reduces the crisis’ risks, and raises awareness globally—assisting the emerging paradigm shift to a higher consciousness for all of humanity.

 

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The Stanley Program for Epidemiology, Prevention and Treatment of Schizophrenia (SPECTS)
The Stanley Program for Epidemiology, Prevention and Treatment of Schizophrenia (SPECTS)

The Stanley Program for Epidemiology, Prevention and Treatment of Schizophrenia is comprised of 8 laboratories that examine the Gene-Environment (G x E) interactions that increase the risk of developing psychiatric disorders. This is achieved by analyzing samples and data from large, extremely well characterized population registries and by collecting data and samples from patients at various stages of their illness to examine G x E interactions. The program is dedicated to developing biomarkers used to predict onset and progression of illness, and to develop treatment strategies. SPECTS has established that exposure to Toxoplasma gondii (TOXO) and HSV contribute to the etiology of schizophrenia and thus includes programs to understand the biological impact of these organisms on the CNS and to develop more effective treatments against them. The program has developed biomarkers for disease diagnosis and to monitor therapy and also provides a coordinated site for testing samples from individuals participating in clinical trials with the goal of identifying individual markers of clinical response. SPECTS Labs include:

  • The Stanley Neurovirology Laboratory (Johns Hopkins University): is the core SPECTS program the lab facilitates the collection and analysis of samples and develops new strategies for the effective prevention and treatment of psychiatric disorders. The group has pioneered the development of assays to characterize the inflammation associated with psychiatric patients. Through whole genome sequencing they are identifying novel pathogens associated with these disorders and through collaborations with members of the SPECTS program and others they have optimized and are now maximizing the utility of large epidemiological data sets world-wide to understand the gene-environmental interactions underlying these disorders. 
  • Stanley Research Program at NCRR: utilizes the extensive Danish population based registers of healthcare data and biobank of samples, including maternal serum and amniotic fluid to understand the infectious, inflammatory and immune etiologies of psychiatric disorders. Dr. Mortensen and colleagues have done groundbreaking work in identifying events in early life which are associated with the later development of schizophrenia and bipolar disorder. They have access to samples and clinical data that can be used both for infectious disease (in collaboration with us) and genetic studies (in collaboration with the Stanley Center at the Broad Institute). We expect that their efforts will become even more valuable as the number of individuals from whom samples and data are available continues to grow.
  • Stanley Research Program at Stockholm (Sweden): utilizes the Swedish registry of extensive data on ~15 million people born 1932-2011 to identify populations with psychiatric disorders and their first degree relatives to determine the G x E interactions that increase the risk for psychiatric disorders. Maternal serum from pregnancies and neonatal blood spots as well as blood from adult patients and controls can be accessed. The Swedish population, while smaller than the Danish one, has the advantage that adult individuals with these disorders can be identified, assessed, and retested for infectious disease exposures. This group also provides expertise in the area of retroviruses and their role in the etiology of major mental illnesses.
  • Stanley Research Program at WRAIR (U.S.A): the examination of serum from a large population of healthy US military personnel who later developed schizophrenia or BD has shown that infection and/or immune activation can occur prior to onset of psychiatric symptoms. Additional studies are designed to identify the risk factors that predict psychiatric disorders that occur in this military population.
  • Stanley Research Program at Cambridge (England): this group has had a major impact on the understanding of psychiatric disorders through their development and application of proteomic technology. They have successfully developed high-throughput technologies to identify biomarkers and diagnostic assays for schizophrenia and BD and have contributed to the development of the first diagnostic test used by psychiatrists in the diagnosis and management of individuals with schizophrenia or bipolar disorder. While this test still needs more work, it has gotten the psychiatric community interested in these types of assays and provided the first data regarding their implementation.
  • Stanley Research Program at Sheppard Pratt (U.S.A): is a clinical research group that provides valuable sets of biological samples and clinical data for analysis in collaboration with other members of the SPECTS program. Their ability to enroll and follow patients has allowed for the longitudinal evaluation of individuals with schizophrenia and bipolar disorder and for the performance of clinical trials. This program continues to grow in terms of the number of individuals being evaluated, the clinical trials program, and now includes additional clinical diagnostic groups. In collaboration with the neurovirology lab they will develop the scientific rational to facilitate the diagnosis, prevention, and treatment of schizophrenia and BD.
  • Stanley Research Program at Pittsburg (U.S.A): the primary aim is to develop an effective treatment for the cognitive impairment in schizophrenia by focusing on HSV-1 infection as a putative causative factor for the cognitive impairment. This group performed an important study on the use of the currently available medication valacyclovir and are now working to develop new medications which may be more effective for the long term treatment of the latent form of the herpesviruses likely to be in the brains of individuals with schizophrenia and bipolar disorder.
  • Stanley Research Program at Michigan (U.S.A): this program provides essential expertise in the biology of T gondii necessary for the development of new medications and other therapeutic strategies. They provided critical input for the development of the anti-Toxoplasma quinolone medications which are currently undergoing pre-clinical evaluation. While their previous studies relied on mouse models for the screening of anti-Toxoplasma compounds, they have now initiated studies directed at developing cell culture assays for the screening of new drugs effective against the tissue cyst form of the parasite. This may lead to a large increase in compounds which we can screen for this activity and then develop as potential drugs. T. gondii also upregulates interferon-γ which increases Indolamine 2,3-dioxygenase (IDO). IDO controls neural infection and also leads to increased kynuric acid which has been implicated in the etiology of schizophrenia.

 

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Email: rhyolken@gmail.com

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Voice Hearers Belfast
Voice Hearers Belfast

Voice Hearers Belfast is a self-help group that meets fortnightly where people who hear voices see images can come together to support one another and talk about their experiences and feel accepted.  This is not a counselling group but a place for you to receive encouragement, reassurance and support. It is a safe and private place where you can talk without fear of judgement.  A group supported by one voice hearer and one non voice hearer. 

 

Organisation

Country: United Kingdom of Great Britain and Northern Ireland

Email: voicesni@gmail.com

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Working to Recovery
Working to Recovery

Working to Recovery is an organisation with many years of experience in taking a different and more holistic approach to aiding recovery from psychosis. Their courses and workshops allow people to explore and possibly connect their current condition with what has happened to them in the past, thereby providing a platform for deeper understanding and emotional wellbeing. We provide many in-house workshops and courses that give people the exact help that they need when it comes to recovery from psychosis. Our workshops engage with hearing voices and other unusual experiences, as well as focusing on the process of recovery.

Working to Recovery provides cutting-edge mental health provision for people across the world who are looking for a different way to approach recovery from psychosis. With Ron recently retiring to focus on his health and living well with dementia, Karen is taking her knowledge gained over the years to provide individuals their families and professionals with a compassionate, person-centred series of courses and workshops that facilitate greater emotional wellbeing. By helping people identify the links between their current condition and traumatic events of the past, Karen’s approach during online teaching and mentoring sessions facilitates a deeper understanding of one’s condition and provides a valuable alternative route to recovery from "psychosis."

Mentoring
Mentoring
  • Group mentoring (Supervision with Karen): one hour with Karen Taylor on Recovery, Trauma and Psychosis for a Team, or Staff Group

  • Mentoring And Supervision For Practitioners And Managers With Karen: one hour with Karen Taylor, Recovery, Trauma and Psychosis supervision for individual practitioner or Manager

  • Mentoring with Family Member with Karen: one hour mentoring with family member with Karen, exposing what recovery might mean for you.

  • Mentoring with an Individual with lived experience: one Hour Mentoring and exploration with person with lived experience

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Midwife of the Soul
Midwife of the Soul

Widwife of the Soul embraces the hearing voices approaches that her husband (Ron Coleman) helped to establish, and has been on a spiritual journey of her own. This program aims:

  • To leave women with a stronger understanding of how trauma can manifest itself within themselves, including “split off selves”
  • To understand the relationship we have to the land and how this can enhance healing and emotional wellbeing
  • Understanding the protective factors of flight, fight, freeze and faun at the time of trauma and how, over time, the fear response can exert a negative impact on a person and their lifestyle
  • Developing a spiritual practice that will enhance your emotional wellbeing
  • To learn about what is happening within the body and how the body can heal, understanding the connection between healing, spirituality and trauma.

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Ron Coleman
Ron Coleman

Ron Coleman was been active in the field of mental health since 1991. When undergoing his ow recovery from mental illness, Ron used his experiences to develop his ideas for recovery-centred treatment of others. Since then, he has gone on to write numerous books and papers on the subject, he was influential in the development of the Hearing Voices Network in the UK and was the first national co-ordinator. He worked with his wife Karen under the banner of Working to Recovery for many years, but has stepped back from these duties in recent times due to heart problems and cognitive memory issues and his focus on growing Deepness Dementia Media, a not for profit organisation that provides a space for people living with dementia to come together. He has made a new life writing poetry and plays-one of which has already been performed. You can find out more about the projects at Deepness Dementia Media.

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Country: United Kingdom of Great Britain and Northern Ireland

Email: karen@workingtorecovery.co.uk

Call 01851810789

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Working to Recovery
Working to Recovery

Working to Recovery is an organisation with many years of experience in taking a different and more holistic approach to aiding recovery from "psychosis". Their courses and workshops allow people to explore and possibly connect their current condition with what has happened to them in the past, thereby providing a platform for deeper understanding and emotional wellbeing.

 

Organisation

Country: United Kingdom

Email: karen@workingtorecovery.co.uk

Call 01851810789

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World Fellowship for Schizophrenia and Allied Disorders
World Fellowship for Schizophrenia and Allied Disorders

The World Fellowship for Schizophrenia and Allied Disorders (WFSAD) is a global organization dedicated to lightening the burden of schizophrenia and other serious mental illnesses for sufferers and their families. WFSAD strives to increase knowledge, understanding and compassion and reduce the fear, stigma, discrimination and abuse that accompany these difficult conditions. WFSAD Members and Associates provide direct services for people with schizophrenia and other serious mental illnesses and their families. They:

  • Run self-help groups
  • Conduct workshops
  • Produce educational materials
  • Arrange conferences
  • Advocate for better treatment and appropriate services
  • Manage research funds and
  • Influence government policies

WFSAD works to support and empower families coping with serious mental illness on all continents. In addition to providing support to well-established family organizations in such countries as the United Kingdom, the United States, Australia, and Japan, we work with families where no organizations exist in an effort to get family support started. WFSAD supports, educates and advocates for families

Families as Partners in Care Program
Families as Partners in Care Program

Families as Partners in Care Program is a strategy to promote the inclusion of families in the treatment team was developed by a WFSAD group of family leaders and clinical experts in New Zealand in 1997. Research indicates that better care, management and outcome is achieved for persons with mental illness when their families receive a continuum of education, training and support to carry out their role of primary informal care giver.

 

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Reason to Hope Family Training
Reason to Hope Family Training

Reason to Hope Family Training is a new international approach to family self-help, based on the Schizophrenia Society of Canada’s Strengthening Families Together (2006) and WFSAD’s Strengthening Families Through Empowerment (2001-2006). It is structured education and multi-cultural support for families, developed and taught by families; it alternates between facts and feelings, and gives information and tools at the same time as it gathers input and ideas from the group. Families receive information about the illness, support for themselves, and skills in how to be an effective caregiver. 

Reason to Hope follows a train-the-trainer model, building the capacity of family leaders around the world and allowing exponential reach and dissemination of the training materials. The Training works to connect and support the 450 million families touched by serious mental illness, to provide information and reduce stress leading to health problems. Reason to Hope was launched as a World Federation for Mental Health Program during the WFMH Congress in Athens in September 2009. Twenty people took the course and eleven of them went on to take the instructor training at the second session. Details will appear on the WFMH Center for Family and Consumer Advocacy and Support Section of the WFMH website by the Spring of 2010.

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The Global Support & Development Program
The Global Support & Development Program

The Global Support & Development program emphasizes the exchange of information and experience in the development and maintenance of family organizations. (This is also to ensure that the economically developed nations do not assume dominance of or control over "knowledge" about the way progress can be achieved). Many new groups have been established. Mutual Exchange visits have been made to numerous countries and reports of some of these are available in this section of our website. Mutual Exchange educational packages and correspondence initiatives have enabled the continuing distribution of up-to-date support and education materials. The program aims to:

  • Promote the establishment, development and maintenance of family support organizations around the world and to promote connectivity among them. 
  • Support those who need help where no family organization exists
  • Encourage and facilitate the international exchange of information about schizophrenia and allied disorders at all levels among professionals, and to promote best practice in mental health service delivery.

The majority of the families and family organizations we assist are led by the families themselves, often assisted by mental health professionals. They know that much of their suffering results from the ignorance and insensitivity of others. They want the World Fellowship to spearhead initiatives so that their efforts to provide a better life for those who are mentally ill will succeed. We, in turn, learn from their work and attempt to promote this work to mental health professionals, governments and those in authority. We advocate internationally for global justice and reasonable solutions to problems that at times seem insurmountable.

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Organisation

Address: 19 MacPherson Avenue, Toronto, Ontario, M5R 1W7, Canada

Email: info@world-schizophrenia.org

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