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Invitation to take part in research: Seeking to explore and understand the experiences of people with physical disabilities who have experienced care within inpatient mental health services.Invitation to take part in research:

Posting on behalf of a member. They are looking for people to take part in their research.

Participants Wanted

Do you identify as a physically Disabled person?

We are seeking to explore and understand the experiences of people with physical disabilities who have experienced care within inpatient mental health services.

To take part, you must:

· Be aged 18 or over.

· Have experienced care within UK inpatient mental health services within the past 10 years.

· Self-identify as a physical Disabled person at the time of your admission.

· Not currently be experiencing a mental health crisis or receiving care in inpatient services.

What is involved?

· A recorded interview that will take approximately 60 minutes.

· We will ask you for some demographic information, but your participation will be anonymous.

· No identifiable information will be included in the recording, transcript of final report.

· Participants will be reimbursed for their time with a £15 amazon voucher.

Interested in taking part?

For more information or to take part, please contact the Lead Researcher, Jamie Melvin-Freed (Trainee Clinical Psychologist) at jm22257@essex.ac.uk.

This project is supervised by Dr Alison Spencer (Clinical Psychologist) & Dr Stephen Wood (Lecturer).

This project has been reviewed by the University of Essex Ethics Committee and has received a favourable ethical opinion (ETH2324-0075)

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Survey: Addressing the Needs of Autistic Survivors of Sexual  Violence and Sexual Abuse.Survey:

Posting on behalf of a member who says: “Please, do circulate widely. This is an excellent opportunity for you to have your say and shape the services and activities you wish to see”.
https://docs.google.com/forms/d/e/1FAIpQLSfp_hZQEo4JuMrck8Qc92f1ityTcrlzx8fdoNt_XuVJ0-dcwg/viewform?usp=sf_link

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Last chance to sign up! DRF 19th April. 10am-Noon. Fran Urbistondo Cano and Holly Burkinshaw will be speaking about “Autism and Learning Disabilities: A Relationship-Centred Approach for Support Workers in Social Care” and “Exploration children’s narrations of long term and reoccurring hospitalisation”

To register: https://forms.office.com/e/aSWDu7NeER

Talk 1, Title: Autism and Learning Disabilities: A Relationship-Centred Approach for Support Workers in Social Care

Talk 1, Abstract:

Adults labelled as ‘having autism and learning disabilities’ in
England receive the support of the social care system through the
assistance of paid staff called ‘care and support workers’ or
‘personal assistants’. The market offers different kinds of training
for care staff, such as Active Support, Person-centred Thinking and
Planning, Positive Behaviour Support (PBS), Low Arousal Approach, and
the SPELL framework. In my presentation, I will share some ideas and
reflections on an ecological perspective of social care, highlighting
key characteristics of available training and approaches, and invite a
shift from what in social care is traditionally called
‘person-centred’, to what I refer to as a ‘relationship-centred
approach’. As a systemically oriented Counselling Psychologist, I will
explain how I developed a model to engage with support workers.
Adopting a fiction-based approach, I will illustrate the complexities
of such work involving personal, professional, and socio-cultural
perspectives. The examples portray common scenarios from practice that
many care workers might find familiar. Finally, this presentation is
based on my inquiry conducted for a Professional Doctorate in Systemic
Practice which focused on autism and LD in the context of social care.
The inquiry contributes learning to professional support for autistics
with learning disabilities by inviting examination of personal and
professional experiences, stimulating professional debate, and
generating knowledge about working alongside care workers and people
who use services from a dialogical, relational, and social
constructionist stance.

Bio
Dr Fran Urbistondo Cano is a systemically-oriented Counselling
Psychologist originally from Argentina. He works with people labelled
as having autism and learning disabilities in social care, the NHS,
and the forensic system in England. Fran is also a course tutor and
research supervisor for the Professional Doctorate in Systemic
Practice at the University of Bedfordshire. His research is on the
deconstruction of psychological narratives about people with learning
disabilities and autism and promoting a relational model for social
care.

Contact
francisco.urbistondocano@beds.ac.uk

Keywords:
Autism, learning disabilities, intellectual disabilities, social care,
care workers, support workers, training, person-centred,
relationship-centred, systemic, relational, dialogical, fiction-based
research.

Talk 2, Title: Exploration children’s narrations of long term and reoccurring hospitalisation

Talk 2, Abstract:

This presentation reports on a qualitative study that was conducted for a PhD thesis. The research was concerned with the experiences of long term or regularly hospitalised children and young people. The study involved the recruitment of six participants to explore the research question: what we can learn from the stories that people choose to share about their experiences of hospitalisation. While much has been improved in relation to children’s hospitals and the care that children receive, there is significant concern in literature and policy alike for children aged between 11-16 years old. This thesis attends to some of these concerns. Several disciplines have contributed to the understanding of children in hospital, including psychology, sociology, childhood studies, disabled children’s childhood studies, critical disability studies, nursing, and medicine. The study grounds itself in disabled children’s childhood studies (Curran et al. 2013) and utilises poststructuralist thought and concepts of spatiality to explore the multi-modal data. Developing a cross methodological approach, the study develops and employs a narrative-autoethnographic approach to research methodology. It exploits the richness of different modes of storytelling to situate the researcher’s stories alongside those of participants in the study. I move on to discuss how young people in the hospital had an idea of the way that they were perceived by others, which they found limiting and oppressive. A strong theme which emerged from the data was that of not feeling heard or being misunderstood whilst in hospital; this theme is explored in the study in relation to power. The theme of fear, despite dominating medical literature, came through more subtly highlighting a need to better understand children and young people’s fears, as well as how important the mundane was for young people. This study identified a need to continuously problematise notions of normalcy, especially in terms of children’s communication. It identifies an urgent need to develop ways of multi-modal listening to young people in hospital, and thus has implications for policy, practice, research and theory, respectively. The thesis calls for a more nuanced understanding of non-verbal communication employed by many young people, whilst also reflecting on how we can better hear young people’s communication.

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DRF Event 6! – Final one this academic year! April 19th, 10am – Noon. Fran Urbistondo Cano and Holly Burkinshaw will be speaking about “Autism and Learning Disabilities: A Relationship-Centred Approach for Support Workers in Social Care” and “Exploration children’s narrations of long term and reoccurring hospitalisation”

To register: https://forms.office.com/e/aSWDu7NeER

Talk 1, Title: Autism and Learning Disabilities: A Relationship-Centred Approach for Support Workers in Social Care

Talk 1, Abstract:

Adults labelled as ‘having autism and learning disabilities’ in
England receive the support of the social care system through the
assistance of paid staff called ‘care and support workers’ or
‘personal assistants’. The market offers different kinds of training
for care staff, such as Active Support, Person-centred Thinking and
Planning, Positive Behaviour Support (PBS), Low Arousal Approach, and
the SPELL framework. In my presentation, I will share some ideas and
reflections on an ecological perspective of social care, highlighting
key characteristics of available training and approaches, and invite a
shift from what in social care is traditionally called
‘person-centred’, to what I refer to as a ‘relationship-centred
approach’. As a systemically oriented Counselling Psychologist, I will
explain how I developed a model to engage with support workers.
Adopting a fiction-based approach, I will illustrate the complexities
of such work involving personal, professional, and socio-cultural
perspectives. The examples portray common scenarios from practice that
many care workers might find familiar. Finally, this presentation is
based on my inquiry conducted for a Professional Doctorate in Systemic
Practice which focused on autism and LD in the context of social care.
The inquiry contributes learning to professional support for autistics
with learning disabilities by inviting examination of personal and
professional experiences, stimulating professional debate, and
generating knowledge about working alongside care workers and people
who use services from a dialogical, relational, and social
constructionist stance.

Bio
Dr Fran Urbistondo Cano is a systemically-oriented Counselling
Psychologist originally from Argentina. He works with people labelled
as having autism and learning disabilities in social care, the NHS,
and the forensic system in England. Fran is also a course tutor and
research supervisor for the Professional Doctorate in Systemic
Practice at the University of Bedfordshire. His research is on the
deconstruction of psychological narratives about people with learning
disabilities and autism and promoting a relational model for social
care.

Contact
francisco.urbistondocano@beds.ac.uk

Keywords:
Autism, learning disabilities, intellectual disabilities, social care,
care workers, support workers, training, person-centred,
relationship-centred, systemic, relational, dialogical, fiction-based
research.

Talk 2, Title: Exploration children’s narrations of long term and reoccurring hospitalisation

Talk 2, Abstract:

This presentation reports on a qualitative study that was conducted for a PhD thesis. The research was concerned with the experiences of long term or regularly hospitalised children and young people. The study involved the recruitment of six participants to explore the research question: what we can learn from the stories that people choose to share about their experiences of hospitalisation. While much has been improved in relation to children’s hospitals and the care that children receive, there is significant concern in literature and policy alike for children aged between 11-16 years old. This thesis attends to some of these concerns. Several disciplines have contributed to the understanding of children in hospital, including psychology, sociology, childhood studies, disabled children’s childhood studies, critical disability studies, nursing, and medicine. The study grounds itself in disabled children’s childhood studies (Curran et al. 2013) and utilises poststructuralist thought and concepts of spatiality to explore the multi-modal data. Developing a cross methodological approach, the study develops and employs a narrative-autoethnographic approach to research methodology. It exploits the richness of different modes of storytelling to situate the researcher’s stories alongside those of participants in the study. I move on to discuss how young people in the hospital had an idea of the way that they were perceived by others, which they found limiting and oppressive. A strong theme which emerged from the data was that of not feeling heard or being misunderstood whilst in hospital; this theme is explored in the study in relation to power. The theme of fear, despite dominating medical literature, came through more subtly highlighting a need to better understand children and young people’s fears, as well as how important the mundane was for young people. This study identified a need to continuously problematise notions of normalcy, especially in terms of children’s communication. It identifies an urgent need to develop ways of multi-modal listening to young people in hospital, and thus has implications for policy, practice, research and theory, respectively. The thesis calls for a more nuanced understanding of non-verbal communication employed by many young people, whilst also reflecting on how we can better hear young people’s communication.

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Leeds Disability Studies Conference 2024

Information taken from: https://disability-studies.leeds.ac.uk/conference/call-for-papers/ Please access the link for more details.

We invite presentations, collective discussion and debate which engage with, challenge and provoke the principles and practice of Disability Studies – from both within or beyond the discipline. We particularly encourage submissions that privilege the voices of those who have been marginalised and on topics that have hitherto not been the focus of Disability Studies activity.

Abstracts and proposals (of up to 300 words) can be submitted electronically at https://app.oxfordabstracts.com/stages/36496/submitter

Deadline for submissions:  Tuesday 30th April 2024

Proposal Reviews: May 2024

Proposal Acceptance Notification: Monday 3rd June

Deadline for Presenter registration for inclusion in the programme schedule: Friday 5th July

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Last call for DRF Event 5. Wednesday 13th March, 11am – 1pm. Erin Pritchard and Katrine Risbank Jensen will be speaking about “Midgetism: Exploring the exploitation and discrimination of dwarfism” and “A Family Disabled: Negotiating the Meaning of Disability in the Danish Social Welfare System”

To register: https://forms.office.com/e/2UgczDpCb2

Talk 1, Title: Midgetism: Exploring the exploitation and discrimination of dwarfism

Talk 1, Abstract:

People with dwarfism experience oppression which is informed by both heightism and disablism, and thus separately these terms cannot truly demonstrate these oppressive attitudes and encounters within society. Drawing on findings from my newest book, Midgetism: the exploitation and discrimination of people with dwarfism, this presentation introduces the term Midgetism, to explore the oppression people with dwarfism experience. The book engages with autocritical discourse analysis in order to examine problematic representations, which I argue are informed by and further encourage midgetism within society, exemplified by my own personal experiences as a woman with dwarfism. Furthermore, it argues as to why the term midget, when referring to a ‘midget entertainer’, should be reclaimed and repurposed for analytical and advocacy purposes only. It is argued that midget entertainment, such as midget tossing and midget wrestling, is a key factor in reinforcing midgetism within society. Particular reference is made to the problematic assumptions, held by average-sized people, who claim that midget entertainment is an acceptable form of employment for people with dwarfism, exposing the socially constructed inferior standing of them within society.

Keywords: midgetism, dwarfism, midget entertainer, autocritical discourse analysis, oppression

Talk 2, Title: A Family Disabled: Negotiating the Meaning of Disability in the Danish Social Welfare System

Talk 2, Abstract:

In this talk I will be presenting my PhD project, A Family Disabled: Negotiating the Meaning of Disability in the Danish Social Welfare System. The aim of the project is to generate knowledge regarding the consequences experienced by families comprising children with disabilities (disabled families) when faced with navigating the complex beliefs and expectations set forth by welfare professionals in the context of the Danish social welfare system. To accomplish this, I focus on the families’ embodied experiences of disability by applying an ethnographic intercorporeal perspective. How interactions with welfare professionals affect their quality of life, and which strategies they actively employ to gain influence over their own existence and social identity, are just some of the questions this project delves into.

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There is still time to grab a spot! DRF Event 5. Wednesday 13th March. Erin Pritchard and Katrine Risbank Jensen will be speaking about “Midgetism: Exploring the exploitation and discrimination of dwarfism” and “A Family Disabled: Negotiating the Meaning of Disability in the Danish Social Welfare System”

To register: https://forms.office.com/e/2UgczDpCb2

Talk 1, Title: Midgetism: Exploring the exploitation and discrimination of dwarfism

Talk 1, Abstract:

People with dwarfism experience oppression which is informed by both heightism and disablism, and thus separately these terms cannot truly demonstrate these oppressive attitudes and encounters within society. Drawing on findings from my newest book, Midgetism: the exploitation and discrimination of people with dwarfism, this presentation introduces the term Midgetism, to explore the oppression people with dwarfism experience. The book engages with autocritical discourse analysis in order to examine problematic representations, which I argue are informed by and further encourage midgetism within society, exemplified by my own personal experiences as a woman with dwarfism. Furthermore, it argues as to why the term midget, when referring to a ‘midget entertainer’, should be reclaimed and repurposed for analytical and advocacy purposes only. It is argued that midget entertainment, such as midget tossing and midget wrestling, is a key factor in reinforcing midgetism within society. Particular reference is made to the problematic assumptions, held by average-sized people, who claim that midget entertainment is an acceptable form of employment for people with dwarfism, exposing the socially constructed inferior standing of them within society.

Keywords: midgetism, dwarfism, midget entertainer, autocritical discourse analysis, oppression

Talk 2, Title: A Family Disabled: Negotiating the Meaning of Disability in the Danish Social Welfare System

Talk 2, Abstract:

In this talk I will be presenting my PhD project, A Family Disabled: Negotiating the Meaning of Disability in the Danish Social Welfare System. The aim of the project is to generate knowledge regarding the consequences experienced by families comprising children with disabilities (disabled families) when faced with navigating the complex beliefs and expectations set forth by welfare professionals in the context of the Danish social welfare system. To accomplish this, I focus on the families’ embodied experiences of disability by applying an ethnographic intercorporeal perspective. How interactions with welfare professionals affect their quality of life, and which strategies they actively employ to gain influence over their own existence and social identity, are just some of the questions this project delves into.

Uncategorized

DRF Event 5! Wednesday, 13th March 2024, 11am-1pm. Erin Pritchard and Katrine Risbank Jensen will be speaking about “Midgetism: Exploring the exploitation and discrimination of dwarfism” and “A Family Disabled: Negotiating the Meaning of Disability in the Danish Social Welfare System”

To register: https://forms.office.com/e/2UgczDpCb2

Talk 1, Title: Midgetism: Exploring the exploitation and discrimination of dwarfism

Talk 1, Abstract:

People with dwarfism experience oppression which is informed by both heightism and disablism, and thus separately these terms cannot truly demonstrate these oppressive attitudes and encounters within society. Drawing on findings from my newest book, Midgetism: the exploitation and discrimination of people with dwarfism, this presentation introduces the term Midgetism, to explore the oppression people with dwarfism experience. The book engages with autocritical discourse analysis in order to examine problematic representations, which I argue are informed by and further encourage midgetism within society, exemplified by my own personal experiences as a woman with dwarfism. Furthermore, it argues as to why the term midget, when referring to a ‘midget entertainer’, should be reclaimed and repurposed for analytical and advocacy purposes only. It is argued that midget entertainment, such as midget tossing and midget wrestling, is a key factor in reinforcing midgetism within society. Particular reference is made to the problematic assumptions, held by average-sized people, who claim that midget entertainment is an acceptable form of employment for people with dwarfism, exposing the socially constructed inferior standing of them within society.

Keywords: midgetism, dwarfism, midget entertainer, autocritical discourse analysis, oppression

Talk 2, Title: A Family Disabled: Negotiating the Meaning of Disability in the Danish Social Welfare System

Talk 2, Abstract:

In this talk I will be presenting my PhD project, A Family Disabled: Negotiating the Meaning of Disability in the Danish Social Welfare System. The aim of the project is to generate knowledge regarding the consequences experienced by families comprising children with disabilities (disabled families) when faced with navigating the complex beliefs and expectations set forth by welfare professionals in the context of the Danish social welfare system. To accomplish this, I focus on the families’ embodied experiences of disability by applying an ethnographic intercorporeal perspective. How interactions with welfare professionals affect their quality of life, and which strategies they actively employ to gain influence over their own existence and social identity, are just some of the questions this project delves into.

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Call for participants!

A Disabled University Experience: Lessons for and experiences of disabled undergraduates

We are seeking submissions of previously unpublished articles on disabilities with special focus on manuscripts that either study the experiences of disabled undergraduate students or are written for an undergraduate audience, to be published in the forthcoming issue of the Canadian Journal of Disability Studies.

Please submit your extended abstracts (200-500 words) to Special Issue Editors Dr Paul Bones (pbones@twu.edu) and Dr Christopher Churchill (chrisamchurchill@gmail.com) by 7/15/2024. Please include your contact information in your email. For those accepted for consideration, the deadline for full paper submission is 1/30/2025 for preliminary review. Final submission will be no more than 6000 words, excluding references, notes and tables.

Topics include (but are not limited to):

Navigating ableist educational institutions

Disabled Identity Formation

Disability as an intersection

Indigeneity and disability

Quality and life and disability

Madness and Mental Health

Building Mad and Disabled Communities

Access and Accommodations

Explaining Disability