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Editorial Reviews. About the Author. With a strong background in health care, patient education Reclaiming Your Life After Diagnosis: The Cancer Support Community Handbook - Kindle edition by Kim Thiboldeaux, Mitch Golant, Mehmet Oz. Download it once and read it on your Kindle device, PC, phones or tablets.
Table of contents

In all, regular practice of these techniques offers a good chance of quality-of-life improvement for chronic pain sufferers. Learning that a parent has cancer can be a frightening experience for a child. This book encourages parents to be open and straightforward with their children about the diagnoses. It also helps children work through their anxieties and the changes that come with family illness. Drawing on extensive, evidence-based research and practice, this practical resource addresses the multi-faith needs of sick and dying children and young people in hospitals and the wider community.

Covering Islam, Christianity, Hinduism, Sikhism, Judaism and Buddhism, it provides the key information needed to help multi-disciplinary healthcare staff offer the best, culturally-appropriate care to sick children and their families.

Reclaiming Your Life After Diagnosis : The Cancer Support Community Handbook -

The book discusses daily, palliative, end of life and bereavement care in a range of settings, including hospitals, hospices, schools and home. The information provided covers those aspects of the religions discussed that are essential for healthcare staff to understand, including modesty and hygiene, taboos, food and prohibited products, age-related issues, sacred objects, visitors, and the expectations of the family.

It includes important information on the issues of disability and mental health in each faith as well as addressing the significance within different faith traditions of the transitions from childhood to adolescence to adulthood. A comprehensive resource, this book will be of immeasurable value to multi-disciplinary healthcare professionals including doctors, nurses, bereavement support and palliative care workers, carers, counsellors, chaplains and arts therapists.

This is a book for you. Not one you read, but one you create. Every page is a page to tell your story — who you are, where you came from and what you're thinking.

Reward Yourself

It can help you work through questions about your illness and understand your thoughts, feelings and experiences. For parents and caregivers, a comprehensive guide is available online that includes additional information on child development, grief and facilitating difficult conversations and open communication for terminally ill children and their families.

  • The Desert Sheikhs Innocent Queen: King of the Desert, Captive Bride / Hired: The Sheikhs Secretary Mistress (Mills & Boon M&B) (The Desert Kings, Book 2)!
  • Something called the Nocebo effect may be the culprit.
  • Les enjeux du cinéma espagnol : De la guerre à la postmodernité (Horizons Espagne) (French Edition).
  • Cryptic Crosswords: How a compiler thinks!
  • Cóctel de emociones/Conducta inapropiada (Pasión) (Spanish Edition).

Currently one million American teenagers live with a parent who is fighting cancer. My Parent Has Cancer and It Really Sucks is the first book written especially for teens to help during this tough time. Author Maya Silver was 15 when her mom was diagnosed with breast cancer. In a highly designed, engaging style, this book gives practical guidance that includes:. That no matter how rough things get, they will get through this difficult time. Nana, What's Cancer? Tessa is a year-old girl who wants to understand the confusing world of cancer and then to be able to explain it to other children.

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This bright and sympathetic book explains cancer and chemo to young children, with honesty, whimsy, and heart. An honest, and hopeful account of the year that Abigail and Adrienne's mother underwent treatment for breast cancer. Our Mom Is Getting Better. This very personal book is about family healing after a parent's treatment for cancer. Written and illustrated by three children whose mother is a cancer survivor.

Pain Is Really Strange. Answering questions such as 'how can I change my pain experience? Studies show that understanding how pain is created and maintained by the nervous system can significantly lessen the pain you experience. The narrator in this original, gently humorous book explains pain in an easy-to-understand, engaging graphic format and reveals how to change the mind's habits to transform pain.

In Paint Your Hair Blue , Sue Matthews takes you through the tale of heroic courage and devastating blows that characterized her daughter Taylor's odyssey through the world of pediatric cancer. This book serves in equal portions as an inspiring tale of the power of love and determination, and a cautionary tale of the need for parents and all caregivers to be their own advocates.

It will empower you, no matter what your circumstance, to take control of your own destiny. This book offers a new sense of empowerment for the intimate partners of people living with serious health problems. Most children cope much better with painful experiences if they are given honest information and preparation rather than protection from the pain. Compassionate, honest, and insightful, this easy-to-read guide will be useful for families and professionals. Living with a chronic illness can have a significant psychological impact on a child and his or her family, and it is essential that this aspect of their care is not overlooked.

Promoting Psychological Well-Being in Children with Acute and Chronic Illness provides a comprehensive guide to promoting the psychological well-being of children with chronic illnesses and medical conditions, covering support within health, social services and education. It discusses issues such as the impact of diagnosis and the experiences of children and their families in managing their medical condition and treatment.

Strategies to support children and help them to cope with medical conditions are demonstrated, including cognitive behavioural and systemic approaches, and techniques such as relaxation and motivational interviewing. Case examples from clinical practice are given to illustrate the application of psychological ideas and frameworks to a variety of medical conditions and psychological difficulties.

The book also includes a comprehensive resources section of where to look for further information. When someone you love receives a terminal diagnosis, the whole family is suddenly faced with a prolonged crisis. While medical advances have given us the gift of extending life, meaning that a loved one could survive months or even years before dying, it has also changed the way we grieve.

  • Parenting is Childs Play: The Teenage Years: The Teenage Years;
  • Easy Street?
  • Tag: Cancer Support.
  • Matthews Children (Mills & Boon Cherish) (Three Good Men, Book 2);
  • A King Ruled in the East.

A Story about Cancer with a Happy Ending. I think about everything I'll miss if they tell me I'm going to die A teenage girl heads towards the hospital waiting room where the doctors are going to tell her how much time she's got to live.

Psychological care for people affected by cancer

As she walks, she thinks about her journey up to this point This is a story about cancer with a happy ending. It's about life, love, and especially, hope. Taking Cancer to School. This is the story of Max, a kid living with cancer. When read aloud, other children can start to identify why a peer with cancer may be treated differently and begin to empathize with the peer. In addition, children with cancer or children who have conditions that set them apart as being different begin to feel accepted and safe.

Book includes a Kid Quiz to reinforce new information and Ten Tips for Teachers to provide additional facts and ideas for teacher use. Death is a part of life. We used to understand this, and in the past, loved ones generally died at home with family around them. But in just a few generations, death has become a medical event, and we have lost the ability to make this last part of life more personal and meaningful.

Today people want to regain control over health-care decisions for themselves and their loved ones.

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Noted palliative-care educator and researcher Kathy Kortes-Miller shows readers how to identify and reframe limiting beliefs about dying with humor and compassion. With robust resource lists, Kortes-Miller addresses:. Far from morbid, these conversations are full of meaning and life — and the relief that comes from knowing what your loved ones want, and what you want for yourself.

Parents with cancer often need help talking with children about the illness. The Unexpected Journey of Caring is a practical guide to finding personal meaning in the 21st century care experience. Readers are invited to actively reclaim and remake how they think of themselves, their care situation, and their capacities to provide care for their loved one and themselves.

Personal transformation is usually an experience we actively seek out, not one that hunts us down. Becoming a caregiver is one transformation that comes at us, requiring us to rethink everything we once knew. They must not only care for a loved one, but also access hidden community resources, collaborate with medical professionals, craft new narratives consistent with the changing nature of their care role, coordinate care with family, seek information and peer support using a variety of digital platforms, and negotiate social support — all while attempting to manage conflicts between work, life, and relationship roles.

The moments that mark us in the transition from loved one to caregiver matter because if we don't make sense of how we are being transformed, we risk undervaluing our care experiences, denying our evolving beliefs, and feeling underappreciated, burned out, and overwhelmed. Informed by original caregiver research and proven advocacy strategies, this book speaks to caregiving as it unfolds, in all of its confusion, chaos, and messiness. There are no promises to help caregivers return to a life they knew before caregiving. This book greets caregivers wherever they are in their journey.

Grieving the death of a loved one is difficult at any age, but it can be particularly difficult during college and young adulthood. From developing a sense of identity to living away from family and adjusting to life on and off campus, college students and young adults face a unique set of issues.

These issues often make it difficult for young adults to talk about their loss, leading to a sense of isolation, different-ness and a pressure to pretend that everything is OK. The narratives included in this book are honest, engaging and heartfelt, and they help other students and young people know that they are not alone and that there are others who 'get' what they are going through.

The narratives are usefully divided by themes, such as isolation, forced maturity and life transition challenges, and include commentary by the authors on grief responses and coping strategies. Each section also ends with helpful questions for reflection. There is nothing good about cancer. It is frightening, disrupts lives, and affects nearly all members of our society.