Fiona Kelly – författare

In the past few decades, gays and lesbians, along with theirfamilies, have become more visible members of Canadian society,enjoying increasing levels of legal recognition. In the area of legalparenthood, however, significant questions remain unanswered. InTransforming Law's Family, Fiona Kelly explores thecomplex issues encountered by planned lesbian families as they work todefine their parental rights, roles, and family structures within thetenets of family law.While Canadian courts recognize lesbian parenthood in somecircumstances, a number of issues that are largely unique to plannedlesbian families – such as the legal status of known spermdonors and non-biological mothers – persist. Drawing oninterviews with lesbian mothers, this groundbreaking book illuminatesthe changing definitions of family and suggests a model for law reformthat would enable the legal recognition of alternative forms ofparentage.The first empirical study in Canada to address the legal dimensions ofplanned lesbian families, this book makes an important contribution tofamily law, queer studies, and law reform literature.

In the past few decades, gays and lesbians, along with theirfamilies, have become more visible members of Canadian society,enjoying increasing levels of legal recognition. In the area of legalparenthood, however, significant questions remain unanswered. InTransforming Law's Family, Fiona Kelly explores thecomplex issues encountered by planned lesbian families as they work todefine their parental rights, roles, and family structures within thetenets of family law.While Canadian courts recognize lesbian parenthood in somecircumstances, a number of issues that are largely unique to plannedlesbian families – such as the legal status of known spermdonors and non-biological mothers – persist. Drawing oninterviews with lesbian mothers, this groundbreaking book illuminatesthe changing definitions of family and suggests a model for law reformthat would enable the legal recognition of alternative forms ofparentage.The first empirical study in Canada to address the legal dimensions ofplanned lesbian families, this book makes an important contribution tofamily law, queer studies, and law reform literature.

Focusing on theoretical, policy and practice issues which are predicted to become fundamental priorities in the near future, the contributors to this important book examine how dementia care works around the globe. They explore the theory underpinning dementia care, the applications of this theory in the latest dementia care research and how this research is influencing and shaping practice. The contributors are leading practitioners, policy influencers and researchers who analyse case studies from the UK, the USA, Canada, Australia, India, France and Malta with the aim of encouraging a dialogue and exchange of interdisciplinary initiatives and ideas. Their insights into how policy and dementia strategies are developed, and the range of approaches that can be taken in dementia care practice, are a positive step towards ensuring that the needs of people with dementia around the world are met, both now and in the future. This book makes essential reading for practitioners, researchers, policy makers and students in the field of dementia care.

How are siblings who were conceived using the same sperm or egg donor making connections in the absence of legal support? What is it like to discover you are part of a 50+ donor sibling group? How are donor conceived adults using new technologies to connect with genetic family and explore their identity? This edited collection considers the donor linking experiences of donor conceived adults and children, recipient parents, and donors in a global context. It includes contributions from legal academics, social workers, sociologists, psychologists, and policy makers who work in the assisted conception field. As a result, it will be of particular interest to scholars of reproductive law, sociology, and digital media and reproductive technologies. It will also engage those following the debate around donor linking and the use of do-it-yourself technologies, including direct-to-consumer genetic testing and social media.

How are siblings who were conceived using the same sperm or egg donor making connections in the absence of legal support? What is it like to discover you are part of a 50+ donor sibling group? How are donor conceived adults using new technologies to connect with genetic family and explore their identity? This edited collection considers the donor linking experiences of donor conceived adults and children, recipient parents, and donors in a global context. It includes contributions from legal academics, social workers, sociologists, psychologists, and policy makers who work in the assisted conception field. As a result, it will be of particular interest to scholars of reproductive law, sociology, and digital media and reproductive technologies. It will also engage those following the debate around donor linking and the use of do-it-yourself technologies, including direct-to-consumer genetic testing and social media.

Since the end of the Second World War, increasing numbers of women have decided to become mothers without intending the biological father or a partner to participate in parenting. Many conceive via donor insemination or adopt; others become pregnant after a brief sexual relationship and decide to parent alone.Using a feminist socio-legal framework, Autonomous Motherhood? probes fundamental assumptions within the law about the nature of family and parenting. Drawing on a range of empirical evidence, including legislative history, case studies, and interviews with single mothers, the authors conclude that while women may now have the economic and social freedom to parent alone, they must still negotiate a socio-legal framework that suggests their choice goes against the interests of society, fatherhood, and children.

Since the end of the Second World War, increasing numbers of women have decided to become mothers without intending the biological father or a partner to participate in parenting. Many conceive via donor insemination or adopt; others become pregnant after a brief sexual relationship and decide to parent alone.Using a feminist socio-legal framework, Autonomous Motherhood? probes fundamental assumptions within the law about the nature of family and parenting. Drawing on a range of empirical evidence, including legislative history, case studies, and interviews with single mothers, the authors conclude that while women may now have the economic and social freedom to parent alone, they must still negotiate a socio-legal framework that suggests their choice goes against the interests of society, fatherhood, and children.

Since the end of the Second World War, increasing numbers of women have decided to become mothers without intending the biological father or a partner to participate in parenting. Many conceive via donor insemination or adopt; others become pregnant after a brief sexual relationship and decide to parent alone.Using a feminist socio-legal framework, Autonomous Motherhood? probes fundamental assumptions within the law about the nature of family and parenting. Drawing on a range of empirical evidence, including legislative history, case studies, and interviews with single mothers, the authors conclude that while women may now have the economic and social freedom to parent alone, they must still negotiate a socio-legal framework that suggests their choice goes against the interests of society, fatherhood, and children.

Human rights are a key issue for all healthcare and social care practitioners, and almost every aspect of dementia care has a human rights dimension. How can we balance the individual's right for dignity, autonomy and privacy against the backdrop of time constraints, duty of care and limited resources? Can a person with dementia be supported to participate in decision making? Is assistive technology always empowering? What must it feel like to be denied a dementia- specific service because of one's age? This practice guide addresses these along with other critical questions, helping you to better understand the diverse and often complex dimensions of dementia caregiving. It provides a new framework to enable you to apply a human rights approach to real life situations, placing the person with dementia at the centre stage and keeping their dignity, independence, sense of purpose and quality of life at the fore. The book builds on person-centred principles, uses case studies to demonstrate theory and provides new analytical tools to support all those committed to best practice in dementia care.

Human rights are a key issue for all healthcare and social care practitioners, and almost every aspect of dementia care has a human rights dimension. How can we balance the individual's right for dignity, autonomy and privacy against the backdrop of time constraints, duty of care and limited resources? Can a person with dementia be supported to participate in decision making? Is assistive technology always empowering? What must it feel like to be denied a dementia- specific service because of one's age? This practice guide addresses these along with other critical questions, helping you to better understand the diverse and often complex dimensions of dementia caregiving. It provides a new framework to enable you to apply a human rights approach to real life situations, placing the person with dementia at the centre stage and keeping their dignity, independence, sense of purpose and quality of life at the fore. The book builds on person-centred principles, uses case studies to demonstrate theory and provides new analytical tools to support all those committed to best practice in dementia care.