The web Directory of Information Materials for People Affected by Cancer is regularly updated and currently has details of over 1,900 booklets, leaflets, books and audiovisual materials for people affected by cancer. Most have been published in the last five years but we have included some older ones that are still useful.
Please enter a word or phrase into the search box to find relevant materials. If you want to search for a phrase, please use quotes, eg “Macmillan Cancer Support”, “Breast cancer”. If you have any questions about the web directory please contact Sue Hawkins firstname.lastname@example.org
Macmillan Cancer Support|Diabetes UK
This booklet is for anyone who has cancer and also has diabetes. You may also want to read it if you have been told your cancer treatment may increase your risk of developing diabetes. It explains how some tests and cancer treatments can affect your diabetes and make it difficult to control your blood sugar. It also has some tips to help you cope with the side effects of cancer treatment if you have diabetes.
Pancreatic Cancer UK
Easy read information using pictures and simple words to explain how symptoms like diet problems and pain are treated, and how you can get support.
World Cancer Research Fund
This simple guide to staying healthy includes tips and advice on small changes people can make to their diet and lifestyle to help reduce the risk of cancer, as well as heart disease, type 2 diabetes and stroke.
Sudden, severe ill health comes as a shock and presents several challenges, most notably, loss of confidence. Suddenly people are afraid to take exercise, have sex or even go to the shops. Their entire self-image takes a battering, and this roller-coaster of uncertainty often leads to anxiety and depression. This book looks at the learning curve involved in sudden and chronic illness, and explores key ways to build psychological resilience during this time of challenge. Whether it concerns cancer, heart disease, diabetes, or a mental health condition, it explores the common psychological issues that arise when someone’s usual health and routine are disrupted, and discusses the impact of illness on relationships and family. Drawing on CBT techniques, it offers practical self-help strategies to help deal with peoples changed expectations of themselves, and with the related lifestyle changes. (Publisher)
'How to be sick: A Buddhist-inspired guide for the chronically ill' and their caregiver is about living skilfully with the challenges of any chronic illness or condition. I wrote it for sufferers and for their caregivers (the latter includes people involved in hospice, chaplaincy, and elder care; for those interested in chronic illnesses and conditions (health professionals, family and friends); and for people interested in Buddhism (illness can function as a metaphor for suffering which, along with the cessation of suffering, is at the heart of the Buddha’s teaching). Chronic illnesses or conditions - such as arthritis, heart disease, and diabetes (three among dozens) - while not immediately life-threatening, are life-disrupting and stressful. The book is unique in that each chapter contains easy-to-learn tools and practices to help the chronically ill and their caregivers live skilfully, maintain equanimity, and even find joy despite the profound changes in their lives. A recurring theme in the book is that, although one’s body may be sick, one’s mind can be at peace. Some of the practices presented are traditionally Buddhist. Others I devised after becoming ill. Two are from the work of Byron Katie. Each practice is illustrated with examples from my own experience, so the book is also highly personal. The practices are intended to help with the following types of challenges: Suffering due to the relentlessness of physical symptoms; Blaming oneself for being sick; Cursory or dismissive treatment by doctors and medical professionals; The inability to visit with friends, participate in family gatherings, and take part in other social events; Feeling ignored by family or friends; Suffering due to uncertainty about the future; Coping with the disappointment of failed treatments; Caretaker burnout. At the end of the book is a handy reference guide, summarizing the specific tools and practices that can help with each of the above challenges. (Publisher)