Editorial
In conversation with Bill Roberts, Paul Alford and Marie Wolfe
Bringing the UN Convention on rights for persons with disabilities to life in Ireland
No Longer Researching About Us Without Us: a researcher's reflection on rights and inclusive research in Ireland
Convention of hope–communicating positive, realistic messages to families at the time of a child's diagnosis with disabilities
Lone parent carers of people with intellectual disabilities in the Republic of Ireland
Parents as co-researchers: a participatory action research initiative involving parents of people with intellectual disabilities in Ireland
Barriers to inclusive education in Ireland: the case for pupils with a diagnosis of intellectual and/or pervasive developmental disabilities
Opening up a whole new world for students with intellectual disabilities within a third level setting
Multi-element behaviour support as a model for the delivery of a human rights based approach for working with people with intellectual disabilities and behaviours that challenge
Translating quality of life into service action: use of personal outcome measures in the Republic of Ireland
Rights, sexuality and relationships in Ireland: ‘It’d be nice to be kind of trusted'
‘A Story to Tell’: learning from the life-stories of older people with intellectual disabilities in Ireland
Supporting rights through research: development of a national research strategy for intellectual disability the national federation of voluntary bodies research strategy 2008–2013
I am an artist
‘A Right to Know’. Facilitating a relationship and sexuality programme for adults with intellectual disabilities in Donegal
Making Research Live!
Understanding and Promoting Access for People with Learning Difficulties: Seeing the Opportunities and Challenges of Risk