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Original Research Articles

• Quality of life, perceived stigma, activity and participation of people with leprosy-related disabilities in south-east Nepal
• The face of disability in Nigeria: a disability survey in Kogi and Niger states
• The communication deall developmental checklist - inter rater reliability
• ‘Welcome to my life!’ photovoice: needs assessment of, and by, persons with physical disabilities in the Kumasi metropolis, Ghana
• Rehabilitation services for persons affected by stroke in Jordan
• CBR matrix and perceived training needs of CBR workers: a multi-country study

Brief reports

• impact of micro credit scheme for persons with physical disabilities in Herat, Afghanistan.
• impact of physical therapy on burden of caregivers of individuals with functional disability
• perceptions of parents of typical children towards inclusive education

Purpose: Respite care is generally thought to benefit family carers of persons with intellectual disabilities and is regarded as an important component of family-centred services. However, the complexities associated with the provision of such services, from the carer’s perspective, have been rarely investigated.

Method: This qualitative research study was carried out through a participatory action research process that involved collaboration among researchers and family members as co-researchers. Seven focus groups, involving seventy family carers (fifty mothers, fifteen fathers and five sisters), were held in seven locations across the Republic of Ireland.

Results: Three main themes dominated the discussions. The first theme related to the ambivalence of carers towards using respite services, as expressed in their reluctance to relinquish care-giving for even a short period; the feelings of guilt they experienced; and the greater needs of other carers. The second theme related to the benefits of respite breaks, but these were solely with respect to the carer and other family members, rather than to the person with an intellectual disability. The third theme regarding the quality of provision was dominated by concerns for the care the person received in using the services.

Conclusions: Respite care has the potential to make a difference, and these findings call for building much- needed alliances between all members of the family and professionals. This is in order to support one another through the difficulties associated with the redesign of existing respite provision, and the extension of these services to the growing number of carers who require respite breaks.

Purpose: This study investigates employers’ perspective towards employing people with disabilities in the northern states of Peninsular Malaysia. The research also endeavoured to identify factors that promote or hinder gainful employment of people with disabilities in Malaysia.

Method: The data were collected through postal questionnaires distributed to several types of industries in the northern region of Malaysia.

Results: The results indicated that most of the employers are in favour of employing persons with disabilities. However, very few have such enabling policies, or a mechanism to handle issues related to persons with disabilities, or a built environment which is fully accessible to persons with disabilities. They are also concerned about the ability of workers with disabilities to comprehend and follow orders, as well as the costs involved in employing and training them. These results imply that if employers want to fulfil their intentions of recruiting persons with disabilities, a lot has to be done to employ and sustain them in their jobs.

"This dissertation examines and analyses the experiences of persons with intellectual/developmental disabilities who have been neglected in practice and academia, focusing on their interactions with humanitarian assistance"
Dissertation submitted in part fulfilment of the requirements for the degree of Master of Arts in Post-War Recovery Studies at the University of York
The user has given permission for the uploaded document to be reproduced and made publicly available on the Source website

This report highlights recommendations from representatives of disabled people’s organizations and international agencies to improve the lives of disabled people following a workshop, and the mechanisms to complete these recommendations
Regional Workshop to Accelerate the Implementation of the Convention on the Rights of Persons with Disabilities (CRPD)
New Delhi, India
18-21 August 2011

"This paper critically reviews and synthesises the currently available evidence base regarding the relationship between disability, poverty and health. While it is widely asserted that disability and poverty are closely linked, this is the first review that explicitly asks: ‘What is the current evidence base for the link between disability, poverty and health in low-and middle-income countries?...This paper presents findings from our critical review, and a discussion of those themes that emerge from the small evidence based sample we found. However, our most significant finding is the current lack of strong evidence on the links between disability poverty and health - evidence which is needed to build effective international development policy and global health programming"
Working paper 16

"These Guiding Principles are intended to serve the purpose of promoting and spreading knowledge of international humanitarian law and, in particular, of implementing the provisions protecting children affected by armed conflicts, especially children associated or previously associated with armed forces or armed groups. The Guiding Principles suggest a number of practical, regulatory and legal measures as means to encourage States to improve such protection. They are based mainly on binding international rules (taking into account the specific obligations of all relevant treaties and of customary law). They also refer to widely accepted instruments of a non-binding character ("soft law"). A checklist of the main obligations regarding children associated with armed forces and armed groups is provided in Annex IV"

This paper examines the theories and principles upon which the Convention of the rights of people with disabilities (CRPD) are premised. It demonstrates the potential value and utility that these have in extending the inherent human rights that people with disabilities, are endowed. The implementation of the CRPD is a challenge considering the complex ‘rights based’ issues involved and because disabled people have to generate the commitment from civil society and government. It is argued that there is a need to move from policy to implementation, and that this needs to be adequately monitored and evaluated. Sustainable and effective interventions will benefit by being informed, monitored and evaluated based upon the broader human rights paradigm and the capabilities approach.

Alter
Volume 5, Issue 3, July–September 2011, Pages 206-220

https://doi.org/10.1016/j.alter.2011.02.004