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This paper situates the lives and work of parents who care for children with ongoing health conditions and disabilities — and who also work full time — within the context of their workplace. Caring responsibilities of parents, especially mothers, are underscored. Interruptions to the working day may be required due to various professional and medical consultations, hospitalisations or treatment regimens.

Reports that young carers in Wales are not receiving support services due to a shortage of resources in councils according to voluntary sector leaders. Reasons for setting up young carers' project; Effects of the insufficient funds on the program according to Lynne Hill, policy director at Children in Wales; Expectations of Hill on the grants that will be provided for the projects.

The article reviews the book "Down's Syndrome and Dementia: A Resource for Carers and Support Staff," by Karen Dodd, Vicky Turk, and Michelle Christmas.

Caring alters plans to return to work and changes career trajectories for many primary caregivers of children with disabilities, most of whom are mothers. The Juggling Work & Care study was a South Australian cross-sectional mail-out and online survey for carers of children and young adults with developmental disabilities aged 0–25 years, which investigated work participation, work–life balance and psychological well-being.

For this special issue, the latest research findings on the topic of families living with parental psychiatric disabilities were solicited and compiled, to inform policymakers and practitioners with the best research available, while informing researchers about new developments in the field.

Young carers often take on practical and/or emotional caring responsibilities that would normally be expected of an adult. For many of these children and young people, caring has been shown to have a detrimental effect on their lives. For example, caring at a young age appears to be associated with poor health and well-being, bullying and poorer educational outcomes. However, previous research has tended to be retrospective, carried out using small surveys of secondary school-aged children or to use qualitative methods with young people associated with caring projects.

Reports that young carers in Wales are not receiving support services due to a shortage of resources in councils according to voluntary sector leaders. Reasons for setting up young carers' project; Effects of the insufficient funds on the program according to Lynne Hill, policy director at Children in Wales; Expectations of Hill on the grants that will be provided for the projects.

Presents a study which examined how the lives of young carers differ from other children and young people in the population who are not looking after someone who is sick or disabled. Method employed in the study; Personal and intimate care tasks undertaken by young carers; Effects of different caring experiences on children and young people's lives.

Objective: Female family caregivers consistently report higher levels of stress and burden compared to male caregivers. Explanations for the apparently higher psychological vulnerability of female caregivers are largely missing to date. This study assesses the correlates and determinants of caregiver burden in family caregivers of advanced cancer patients with a specific focus on gender differences.