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This paper aims to detail the work of Nasa Begum in the disabled people's movement in the UK.

The paper provides information on Nasa's background and her work as a social worker, researcher and activist in the disability movement.

Nasa was a black disabled woman who used mental health services. This paper focuses particularly on how she brought the perspectives of black disabled people to the disabled people's movement and the health and social care field.

The paper demonstrates that Nasa has left a clear legacy of principles that show how things can and should be done when policy makers and service providers want to work in an inclusive way.

This paper aims to focus on the experiences and observations of a black disabled woman in the UK.

The paper is a personal commentary from a black disabled woman who uses health and social care services in the UK. It details the author's disability and some recent barriers that she has faced in using services.

The author gives some examples of her recent experiences in relation to employment, independent living, healthcare providers and getting her wheelchair repaired.

The paper offers the unique perspective of a service user on UK health and social care services.

Disabled people who are the end‐users (EU) of health services have a poor record of inclusion, yet a major stake in the quality of scientific research that informs the development of health knowledge and interventions. In traditional rehabilitation research it has been the researcher who sets the agenda, including determining the research question, study design and methods, and who controls dissemination of findings. This paper aims to describe the development of an EU research consultation committee and to describe the evaluation protocol used to assess the effectiveness of the committee.

The paper describes the context and development of an EU research consultation committee (the committee) to promote collaboration between researchers and lay‐EUs within a research organization in New Zealand. It also describes the qualitative evaluation protocol to be used to assess the effectiveness of the committee over the first 12 months of operation in order to refine its process and procedures.

The paper discusses the issues and challenges involved in achieving collaboration between researchers and EUs in the rehabilitation research space and describes this consultation model as a positive example of making inclusion a reality. Challenges include building research capacity within the EU community and development of real models of collaboration and partnership in rehabilitation research.

It is argued that the integrity and relevance of clinical research is enhanced by the involvement of EUs in all aspects of the research process.

There is a dearth in the literature on Asian American and Pacific Islanders (AAPIs) with disabilities. Utilizing an intersectionality lens, the present exploratory study seeks to compare AAPIs with a reported learning, emotional, or physical disability to AAPIs without a reported disability on their experiences of discrimination, psychological and physical health, as well as their overall physical and mental health ratings.

The Asian American sample (n=2,095) of The National Latino and Asian American Study dataset was used to conduct the analyses for the present study. Participants with disabilities self‐reported the following disabilities: learning (n=46); emotional/mental (n=56); physical (n=71); and having a condition that substantially limits physical activity (n=157).

Despite some minor nuances, the overall results indicate that AAPIs with a learning, emotional, or physical disability reported more experiences of everyday discrimination, greater psychological and physical distress, and poorer physical and mental health ratings than AAPIs without a reported disability.

Limitations to this study included assessment of disability through self‐report dichotomous measures, aggregation of AAPI ethnic groups, and some small effect sizes.

The results have several implications for research as well as clinical care and practice. These are highlighted in more detail in the discussion section.

These findings are novel as they are the first to demonstrate the discrimination and health experiences of AAPIs with disabilities. The results underscore the interlocking oppressions associated with their intersectional identities.

This paper seeks to discuss the attitudes and beliefs of the Pakistani/Kashmiri community in Birmingham towards the cultural practice of consanguineous (cousin) marriage and health, and how an understanding of Pakistani/Kashmiri community views may help institute good practice for health care professionals.

A qualitative research study using eight gender‐ and age‐specific focus group discussions and eight in‐depth one‐to‐one interviews with participants who were in consanguineous relationships. All participants were from the Pakistani/Kashmiri community and residents of Springfield ward in Birmingham.

The findings illustrate Pakistani/Kashmiri attitudes towards consanguinity and health. There was awareness of still births and genetic conditions but a poor understanding of genetics; respondents were reluctant to accept the link between cousin marriages and birth issues and explanations for still births and impairments were largely attributed to the “will of God”. Female respondents were in favour of screening for genetic conditions but would not terminate pregnancies as this was contrary to Islamic ideas about pre‐destiny and all respondents wanted more medical and Islamic scholarly information on cousin marriage and how it is linked to disabilities. Clearly there is a need to improve healthcare outcomes and reduce infant mortality in the Pakistani/Kashmiri community.

Research findings correspond with previous studies that have explored ethnic minority knowledge and attitudes to health and healthcare services and the need for culturally competent services.

This paper presents some suggestions on effecting behaviour change in this important area.

This paper aims to examine how social marketing intervention programmes to measure, evaluate and document social marketing impact.

A systematic review of 49 nutritional behaviour intervention programmes (2006–2020) was conducted. To examine the social marketing impact of the programmes, a logic model of social impact was used. The model comprises inputs (the resources used for an intervention programme), outputs (the direct products resulting from the use of resources), outcomes (short- to medium-term programme effects) and impacts (long-term programme effects on the individual, community or societal levels).

Most intervention programmes set the goal of encouraging their target audience to increase fruit and vegetable intake, choose healthy food items, drink less sugary beverages or consume low-fat diaries, while few others sought policy or systems change. Multiple criteria were used for impact evaluation (e.g. exposure and reach, changes in knowledge, awareness, attitudes, behaviours and body mass index). (Quasi) experiments were the most popular method used for impact measurement, followed by the pre-post model of impact. Positive changes were found in 33 programmes, often reported in terms of short-term outputs or outcomes. Long-term impact particularly on the broader societal level was not indicated.

This research offers a systematic review of how social marketing impact is measured, evaluated and documented. It also provides some guidance for social marketers on how to shift from a reductionist, behavioural outcome-focussed approach towards an “expansionist” impact approach that explicitly considers social marketing impacts on the quality of life of individuals, communities and societies.

EVERY librarian in his inmost heart dislikes newspapers. He regards them as bad literature; attractors of undesirable readers; a drain upon the limited resources of the library; and a target against which the detractors of public libraries are constantly battering. From the standpoint of the librarian, newspapers are the most expensive and least productive articles stocked by a library, and their lavish provision is, perhaps, the most costly method of purchasing waste‐paper ever devised. Pressure of circumstances and local conditions combine, however, to muzzle the average librarian, and the consequence is that a perfectly honest and outspoken discussion of the newspaper question is very rarely seen. In these circumstances, an attempt to marshal the arguments for and against the newspaper, together with some account of a successful practical experiment at limitation, may prove interesting to readers of this magazine.