Held on 9th and 10th July 2009 at The Open University, Milton Keynes
(Please note: there is no audio available for the Day 1 morning introduction.)
The children of the Victorians viewed their parents as the most formidable secret-keepers. Literature and legend support that view, filling Victorian attics with inconvenient relatives of every stripe.
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This paper will look at how two people with learning disabilities have come to find out about their families. It will include Gloria's work on her family tree and the research Mabel did in finding out about her family.
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"Help him, in his darkened walk through this sad world, or he is doomed, and my poor heart is broken." (Dickens - Barnaby Rudge) Charles Dickens, a keen advocate of education for children with learning disabilities, gives these words to Mrs Rudge, mother of a young man with learning disabilities.
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The place of the institution in the history of learning disability provision and social control practices is understood by many people. Through careful study and the collection and preservation of evidence and narratives, it is not difficult to imagine the day to day workings of institutions.
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This paper discusses the experiences of children with learning difficulties during the Second World War. In particular, it looks at the role of teachers within the residential special schools set up to accommodate children evacuated from areas deemed vulnerable to air attack.
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During the lunch period, delegates were invited to view the exhibition
(Please note: there is no audio available for the Day 1 afternoon introduction.)
I want to tell you my life story. I have had hard times and good times. I am a survivor of institutions. It is important to hear my story to stop things like people having to live in hospital happening again.
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"Next of kin unknown": how often in the past have these or similar words appeared in historic documents relating to those with learning disabilities? Should these words be accepted on face value or there ways to discover the unremembered and unrecorded families?
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Parents of children with autism now play a prominent role in the public discourse about autism. Over the past decade a range of autobiographies, novels, films and documentaries have presented the parental experience of autism to a widening audience.
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The White Paper Valuing People (Department of Health, 2001) estimates that one third of people with learning disabilities living in the family home are living with a carer aged 70 or over. Many of these older carers have often been caring for years with very little support from services.
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(Please note: there is no audio available for the Day 2 morning introduction.)
In 1971, the White Paper Better Services for the Mentally Handicapped set out landmark policy on the future direction of services for people with learning difficulties; this was a major move toward what we now understand as 'social care'.
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Patrick Kearney told his story about growing up and living in Ireland to Kelley Johnson. She wrote it up and they agreed what should be in it together.
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My paper is divided into two parts. The first part is about my life history and what happened to me. The second part is about my relationships with my Mum, my brother and my Dad.
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My close relationship with my brother provided me with a strong sense of the struggles of (him) being disabled, in contrast with (me) being so-called "normal".
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I'm 58 and I have had a very interesting life. I went to school and was kicked out, then got back in, then moved to another school.
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During the lunch period, there was an exhibition and film
(Please note: there is no audio available for the Day 2 afternoon introduction.)
This paper reports on a research study examining the impact of the diagnosis of autism on the lives of two individuals with learning disabilities.
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Rather than looking at 'hidden' or 'lost' families that are found, my paper is about experiences of rejection and how my family and foster family didn't want me.
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In 2009 we speak of people with a learning difficulty living in their own home with support but in 1983, when this survey was done, no one talked in that way because the services were different.
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If you woud like to get in touch with the Social History of Learning Disability (SHLD) Research Group, please contact:
Liz Tilley
Chair of the Social History of Learning Disability (SHLD) Research Group
School of Health, Wellbeing and Social Care
Faculty of Wellbeing, Education and Language Studies
The Open University
Walton Hall
Milton Keynes
MK7 6AA
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