The Trauma of Captivity seeks to shed new light on a forgotten aspect of what it meant to be a prisoner of war: their homecoming. With primary source archive content and interviews with family members of prisoners of war from the Second World War, as well as the diary entries of a prisoner of war from the First World War, this book asks the question: what happened to prisoners of war when they returned home? Sons and daughters of returned prisoners of war share their harrowing stories of having a POW for a parent. The Trauma of Captivity also features a lengthy interview with modern-day prisoner of war John Peters, the RAF fast jet pilot who was captured when his Tornado plane crashed in the desert during the Gulf War. The Trauma of Captivity focuses on what help and support was made available to returning prisoners of war and how they fought to rediscover their roles in society.

A History of Girl Guides and Girl Scouts: Brownies, Rainbows and WAGGGS charts the evolution of the Girl Guides and Girl Scouts from its early days as a movement started before WW1 right through to the modern day. With real life interviews with Girl Guides and Girl Scouts from their 90s down to young children, this book looks at what being a Girl Guide has meant through the ages up to the present day. With dramatic and often emotional stories of what it was like to be an evacuated Brownie in the Second World War, a disabled Girl Guide and with tales of girls' heroism throughout the two great wars, this book extols the Guiding and Scouting movement as one that has evolved with women and girls' rights and its hopes for the future.

Biomedical research is increasingly carried out in low- and middle-income countries. International consensus has largely been achieved around the importance of valid consent and protecting research participants from harm. But what are the responsibilities of researchers and funders to share the benefits of their research with research participants and their communities? After setting out the legal, ethical and conceptual frameworks for benefit sharing, this collection analyses seven historical cases to identify the ethical and policy challenges that arise in relation to benefit sharing. A series of recommendations address possible ways forward to achieve justice for research participants in low- and middle-income countries.

Biomedical research is increasingly carried out in low- and middle-income countries. International consensus has largely been achieved around the importance of valid consent and protecting research participants from harm. But what are the responsibilities of researchers and funders to share the benefits of their research with research participants and their communities? After setting out the legal, ethical and conceptual frameworks for benefit sharing, this collection analyses seven historical cases to identify the ethical and policy challenges that arise in relation to benefit sharing. A series of recommendations address possible ways forward to achieve justice for research participants in low- and middle-income countries.