National Network for Equitable Library Service

A witty, winning, and revelatory personal narrative of the author's transition from sightedness to blindness and his quest to learn all he can about blindness as a distinct and rich culture all its own. We meet Andrew Leland as he's suspended in the strange liminal state of the soon-to-be blind: He's midway through his life with retinitis pigmentosa, a condition that ushers those who live with it from complete sightedness to complete blindness over a period of years, even decades.

Time to Think goes behind the headlines to reveal the truth about the NHS’s flagship gender service for children. The Gender Identity Development Service (GIDS), based at the Tavistock and Portman Trust in North London, was set up initially to provide - for the most part - talking therapies to young people who were questioning their gender identity. But in the last decade GIDS has referred more than a thousand children, some as young as nine years old, for medication to block their puberty.

When we need help, we count on doctors to put us back together. But what happens when doctors fall apart? Jillian Horton, a general internist, has no idea what to expect during her five-day retreat at Chapin Mill, a Zen centre in upstate New York. She just knows she desperately needs a break. At first she is deeply uncomfortable with the spartan accommodations, silent meals and scheduled bonding sessions.

An examination of the AIDS crisis critiques the federal government for its inaction, health authorities for their greed, and scientists for their desire for prestige in the face of the AIDS pandemic, in a twentieth anniversary edition of the acclaimed exposé.

To remedy means to heal, to cure, to set right, to make reparations. The Remedy invites writers and readers to imagine what we need to create healthy, resilient, and thriving LGBTQ communities. This anthology is a diverse collection of real-life stories from queer and trans people on their own health-care experiences and challenges, from gay men living with HIV who remember the systemic resistance to their health-care needs, to a lesbian couple dealing with the experience of cancer, to young trans people who struggle to find health-care providers who treat them with dignity and respect.

Everyone can live a happier life, especially those with chronic illnesses. Brian Orend's smart and accessible guide for people with illness, injury, or other challenges provides both a satisfying look into happiness as well as practical steps for living a measurably happier life. When Brian Orend began having debilitating seizures that his doctors couldn't explain, he began a quest to learn how he could be happier, even despite his challenging circumstances.

This book is about mental illness, family caregivers, Alzheimer's and dementia, and the health care system. It continues the story of the Martini family and their experiences with mental illness (which was earlier chronicled in the book Bitter Medicine: A Graphic Memoir of Mental Illness). In The Unravelling, Olivier Martini has lived with his mother, Catherine, since his diagnosis with schizophrenia thirty-six years ago.

What do you do when your outspoken, passionate, and quick-witted mother starts fading into a forgetful, fearful woman? In this powerful graphic memoir, Sarah Leavitt reveals how Alzheimer's disease transformed her mother Midge - and her family - forever. In spare black and white drawings and clear, candid prose, Sarah shares her family's journey through a harrowing range of emotions - shock, denial, hope, anger, frustration - all the while learning to cope, and managing to find moments of happiness.

Most people think Alzheimer's disease is the same as memory loss or hope that if they ignore it hard enough, it will go away. That was certainly Marion Agnew's hope when her mother -- a Queen's and Harvard/Radcliffe-educated mathematician, nuclear weapons researcher, award-winning professor and researcher, as well as a mother of five -- began drifting away from her. This moving memoir looks at grief and family, at love and music. It is a coming-to-terms reflection on the endurance of love and family.

Rain on a Distant Roof takes readers inside the frightening but fascinating world of Lyme disease in Canada. This is the story of one woman's struggle to understand the disease that’s destroying her body and mind. Armed with a confusing diagnosis, a baffling array of symptoms, and a body that’s filled with diabolical bacteria, she sets out to unravel the mysteries of her malady.