'This isn’t a grisly book; it is sharp, angry, punchily philosophical and often funny. It basically invents a new type of lifestyle aspiration: deathstyle.' The Times 'Callender’s joyous, thought-provoking book is an account of how his own early encounters with bereavement led to him becoming a new kind of undertaker.' Daily Mail 'Part memoir, part rant against the traditional funeral business, part manifesto, part just musing on death and facing it with compassion and courage. It’s lovely and thoughtful and may make you rethink a few things.' The Guardian ‘This book is a great work of craft and beauty.’ Salena Godden ‘This compelling personal story of a pioneering punk undertaker is a moving revelation.’ Love Reading ‘Inspiring and unforgettable.’ John Higgs, author of William Blake vs the World Death has shown me...the unbreakable core of love and courage that lies at the heart of what it means to be human. Ru Callender wanted to become a pioneering undertaker in order to offer people a more honest experience than the stilted formality of traditional ‘Victorian’ funerals. Driven by raw emotion and the unresolved grief of losing his own parents, Ru brought an outsider, ‘DIY’ ethos to the business of death, combined with the kinship and inspiration he found in rave culture, social outlaws and political nonconformists. Ru has carried coffins across windswept beaches, sat in pubs with caskets on beer-stained tables, helped children fire flaming arrows into their father’s funeral pyre, turned modern occult rituals into performance art and, with the band members of the KLF, is building the People’s Pyramid of bony bricks in Liverpool – all in the name of creating truly authentic experiences that celebrate those who are no longer here and those who remain. Radical, poignant, unflinchingly real and laugh-aloud funny, What Remains? will change the way you think about life, death and the human experience.

If you or someone you love has been diagnosed with Parkinson's Disease you're probably wrestling with fear, despair, and countless questions about the future. It's brighter than you think. In Parkinson's Disease for Dummies, you'll discover how to keep a positive attitude and lead an active, productive life as this user-friendly, guide pilots you through the important steps toward taking charge of your condition. It helps you:* Make sure you have an accurate diagnosis* Assemble and work with your health care team* Inform others about your condition* Choose the most effective medications* Establish a diet and exercise regimen* Consider surgical options, alternative therapies, and clinical trials* Maintain healthy personal and professional relationships* Adjust your routine as your PD progresses This one-stop resource provides proven coping skills, first-hand advice, and practical tools, such as worksheets to assess care options, questions to ask doctors, and current listings of care providers.

’n Reenboog deur my trane is ’n bron van ryke troos en bemoediging vir enigeen wat treur oor die verlies van ’n geliefde en wat genesing soek vir hulle verskeurde harte. Dit bied 31 dagstukkies, gebede en inspirerende aanhalings wat God se vertroosting in onstuimige tyde met die leser deel, asook ’n lys van beloftes uit die Bybel vir spesifieke behoeftes in tye van nood.

Letter from JoyI discovered that I was 'gluten intolerant' a couple of years ago whilst I was writing 'Nosh Gluten-Free'. Friends had asked me to write a gluten-free book, but during the process, I realised that the stomach pains, which I had thought were due to medication I was taking, were significantly relieved when I cut out gluten from my diet. I was glad to find the cause of the problem, but knew that this would make life challenging! So I began my journey of gluten-free living with the book 'NOSH Gluten-Free' to help me and now I have added this latest book, 'NOSH Gluten-Free Baking'. I have to be frank and say that the 'Baking' book has been the hardest book I have ever written; I have never had to deal with so many failed attempts in all my years of cooking! For instance, bread depends on gluten for its elasticity and 'bounce'. I must have made about 50 different breads, all of which ended up in the bin, before coming up with the new ones in this book, and my quest still goes on to find more. During the process of writing this book, one of the highlights would definitely be the puff pastry recipe. When that pastry came out of the oven, with its distinct, crispy layers, I could have done a little jig in the kitchen, right there and then! When we find we are gluten intolerant, or 'coeliac', it can seem like a 'life sentence of no treats'. We go into a cafe for coffee and cake and often find there is nothing we can eat - all the 'yummy'-looking ones are full of gluten! My aim in this book has been to reverse the 'sentence'. I have tried to include recipes for the many things we might like to eat in the coffee shops, as well as the regular desserts and savoury pastries that seemed to be 'forbidden'. I hope that you enjoy cooking and eating many of these re-found treats.

Peter and Vicky are five year old twins. They ask their mother if they can have a baby brother or sister. Family talks take place and in time, their mother is pregnant. As she progresses through the pregnancy it is discovered that she will have a baby girl, but she will be disabled. She will have Down's Syndrome. Everyone helps out and baby is born. She is very healthy, beautiful and much admired. I found this story quite a challenge to write as my daughter, Mary Elizabeth, who is 49 years old, has Down's Syndrome and Asperger Syndrome. An unusual combination. When I read the story to her, I asked her if she was upset by it. a No,a she said, a I found it interesting.a It is very realistic, believable, but a tear jerker in places.

Music is central to our experience of the world around us. it is a primary source of the way we experience, understand and interpret the world in which we live. It is one of the core experiences that define us, unite us and enrich us. This book arose out of John's professional care experience and personal experience as a carer for his father who had dementia. As a musician he understood the power of music to enrich the quality of life. This practical, fun and interactive book is designed to help people to draw together those pieces of music that are most significant to them. These become a compilation that can travel with them on their dementia journey and can be used in therapeutic ways to reconnect to their memories and impact on current mood.

THE SUNDAY TIMES BESTSELLER 'Essential reading' SUNDAY TIMES MAGAZINE 'A book of hope' OBSERVER 'A marvellous tour of insights' THE TIMES 'A must-read . . . I couldn't recommend it higher' MICHAEL BALL What can a diseased brain tell us about being human, living our own lives better and helping those with dementia get the best from theirs? When Wendy Mitchell was diagnosed with young-onset dementia at the age of fifty-eight, her brain was overwhelmed with images of the last stages of the disease - those familiar tropes, shortcuts and cliches that we are fed by the media, or even our own health professionals. But her diagnosis far from represented the end of her life. Instead, it was the start of a very different one. Wise, practical and life affirming, What I Wish People Knew About Dementia combines anecdotes, research and Wendy Mitchell's own brilliant wit and wisdom to tell readers exactly what she wishes they knew about dementia.

In this shockingly raw but beautifully written book, Michael Handrick unpicks the toxic narratives and myths built up by society of what it means to be a man, gay and working class. Moving through time and memory, from a rural council estate surrounded by snowdrop-filled forests, to searching for his sense of self across London, Italy, America and beyond, he explores how his struggles with mental health and abuse were compounded by stigmas around class, masculinity and sexuality. At this point in history, despite having more equal rights and media representation than ever before, the gay community is suffering a mental health epidemic. In a 2018 survey, Stonewall found that half of respondents had experienced depression, while other research shows 49 per cent of gay men have suffered from domestic abuse and 26 per cent have experienced rape, physical violence or stalking by an intimate partner. As he embarks on a journey to understand the root causes of the toxicity in our society, Handrick finds that the beginnings of the abuse, trauma and mental health crises faced by gay men, and the silence that surrounds them, remain unresolved. Difference is born on the lips, but it is society that shapes those words and actions. The mental health issues gay men live with, the abuse they go through, the stigma, prejudice and discrimination they face do not exist in a vacuum. They are created and catalysed in our societies. Difference is Born on the Lips is a call to come together and create a new conversation, and confront the systemic inequalities that the queer community should never have had to live with.

At thirty-nine, movie critic Mary Pols knew she wanted to have a baby. But never--not in a million years--on her own. When she finds herself unexpec-tedly expecting, she plunges into the greatest adventure of her life. With humor, insight, and compelling honesty, Pols reveals what it means to compromise in the name of love and to find joy in an accidental life, suddenly brimming with purpose.

Dit stel ouers in staat om van vroeg af en te midde van 'n druk lewe alledaagse geleenthede om hulle te gebruik om hul kleingoed gemaklik in die wereld van wiskunde in te lei. En dit verg geen spesiale kennis of opleiding van ouers nie; net 'n positiewe instelling en 'n opskerping van hulle interaksie met hul kleingoed om hulle al spelenderwys vertroud te maak met wiskundebegrippe.

Have you ever wondered what it is like to be dying? Knowing that you are within sight of reaching your own mortality? Sitting in a body that is not even recognised by your brain? Cilla knew! PSP (Progressive Supranuclear Palsy) affects thousands, yet there is little known about it. Perhaps the similarities between this illness and others have masked the effects, and for some this may come far too late due to misdiagnosis. This insight into the unique illness of PSP has been painstakingly put together for the exact purposes of showing how an illness can affect one person's life. The devotion to 'open up' in this frank, 'no holds barred' biography is to allow you, the reader, to see how an ordinary life can change in such a short time. This honest approach should allow both the sufferer and their eventual carers to help come to terms with both their illness and their own transience. Maybe, by proving how similar we all are, there might be an eventual understanding, which hopefully will go well beyond just one person. With the help of others, it has been possible to recall some human elements. Although, in truth, it is the sufferers own underlying feelings and personal memories that make this book so special. In this instance, like many of us, Cilla remembered what it felt like to be invincible. To be able to run, skip, hop, jump, climb and generally be able to do almost anything. Through this book, Cilla thought that if her experiences were made public then she could, at least, help othersa | indirectly or otherwise. The latter stages of the book, sadly, reflect the concluding stages of lifea | so be prepared to get to know Cilla in both life and her eventual death.

In 2001 verander Erika Murray-Theron se lewe onherroeplik toe haar man, Tom, met parkinsonsiekte gediagnoseer word.

Erika begin haar vertelling eers in 2011, toe Tom in ’n meer gevorderde stadium van die siekte verkeer. Dit is die rou optekening van saamleef met ’n geliefde met parkinsons: die ervaring om die fisieke en intellektuele aftakeling van jou lewensmaat te aanskou, die fisieke eise wat met die versorging van so iemand gepaard gaan, en die emosionele inspanning wat dit kos om jouself te staal teen dramatiese en stadige verlies.