What it’s really like to have Epilepsy, and what you can do to help
Kate Lambert is a drama teacher working with young people, many of whom have special needs. Her daughter Lille was diagnosed with epilepsy at the…
Kate Lambert is a drama teacher working with young people, many of whom have special needs. Her daughter Lille was diagnosed with epilepsy at the…
Last month, JKP Commissioning Editor Steve Jones and I packed our bags, books and banners and headed to the beautiful main campus of Queen’s University…
“We hope that the readers will be able to read this book and reconsider their own work, no matter where they work. Although globalisation is often thought of as damaging to local culture, the spread of information gives us all ways to learn from each other. Considering the benefits of meditation, holistic health and collectivist values as they apply to art therapy provides an angle that is not reflected in other literature. Instead of looking for a new series of techniques or interventions, we hope that readers will discover fundamentally new ways of conceptualising both their work and how they work.”
“Disputes inevitably test mediators’ skills to the limit. They are also a powerful reminder of what I refer to in some detail in the book: namely that they should never be applied outside of a framework of appropriate professional values, attitudes and cultural sensitivity and awareness. Skills, strategies and professionals practice can never be value-free.”
“This is the first time that dementia is a political priority, creating drivers for focusing on all aspects of dementia, from the anti-dementia drugs, to an increased knowledge about potential risk factors and preventions strategies as well as innovative ways to provide high quality support and care.”
A personal perspective from Tony Whatling, mediation consultant and trainer, and author of Mediation Skills and Strategies: A Practical Guide. Kabul revisited The flight from…
“[This] is not a book about disease but about finding solutions according to different ways of gaining back one’s physical, emotional and psychological energy balance. For many, it is also a path towards empowerment and finding a new meaning in daily activities.”
“I think that service users can give a perspective which can be lost without their inclusion. Service users can help to cut through some of the professional ‘jargon’ which excludes people, even other professionals sometimes. Professionals are often under considerable pressures to meet targets or stay within budgets, and even with the best will in the world they can start to lose sight of why they came into the profession in the first place. Service users can help to keep that perspective and keep values sharp.”
“The news that a parent has a terminal illness generally presents the family with a huge crisis. Everything about family life is catapulted into a maelstrom, routines change and nothing appears to be predictable anymore. If children are not included in conversations about their parent’s illness and possible imminent death they are going to witness all the changes without having any ‘concrete’ knowledge to use as a marker. They will be aware of the changes and know that something is very different but will not be able to form a consistent narrative. As a result they are in danger of piecing together the information they have gleaned and making erroneous conclusions.”
“Much of the decision-making for these very young children was of high quality, showed evidence of extreme care and was based on hard evidence. However the study also raised a number of concerns…the findings revealed a number of gaps in social worker knowledge and understanding, especially in areas of attachment theory and child development [and] there was evidence that delayed decision-making had detrimental consequences for the outcomes of these children – practitioners need to be fully aware of these consequences and the importance of taking swift action when babies are suffering significant harm…”