National Network for Equitable Library Service

Some bugs have super-power like abilities. And then there's Burt the beetle. He's not strong and he can't run fast. He doesn't even bite. He's more of a hugger, really. But Burt wants more. He wants a SUPERPOWER. There's just one tiny problem: what kind of special abilities do June beetles have?

For as long as Saanvi can remember, she has been friends with her elderly neighbor Helen. They play cards and garden together and, especially, care for the wild birds that visit Helen's yard. When Helen dies suddenly, a "For Sale" sign goes up, and movers arrive, emptying the house of its furniture and stripping the yard of its birdfeeders. The sparrows and hummingbirds disappear. Soon a bulldozer tears down Helen's house. All winter, Saanvi walks numbly past the property as developers begin to build condos.

A moving and honest graphic memoir about the unexpected cancer journey of a young, queer, mixed-race woman. At the age of twenty-five, Kimiko Tobimatsu was a young, queer, mixed-race woman with no history of health problems whose world was turned upside down when she was diagnosed with breast cancer. In an instant, she became immersed in a new and complicated life of endless appointments, evaluations, and treatments, and difficult conversations with her partner and parents. Kimiko knew that this wasn't what being twenty-five was supposed to be like ...

In this intimate and moving graphic memoir, Teresa Wong writes and illustrates the story of her struggle with postpartum depression in the form of a letter to her daughter Scarlet. Equal parts heartbreaking and funny, Dear Scarlet perfectly captures the quiet desperation of those suffering from PPD and the profound feelings of inadequacy and loss. As Teresa grapples with her fears and anxieties and grasps at potential remedies, coping mechanisms, and her mother's Chinese elixirs, we come to understand one woman's battle against the cruel dynamics of postpartum depression.

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.

Agnes, Murderess is a graphic novel about the bloody folk legend of Agnes McVee, a roadhouse owner, madam, and serial killer in the Cariboo region of British Columbia during the gold rush.

A new and expanded version of Gord Hill's seminal illustrated history of Indigenous struggles in the Americas. When it was first published in 2010, The 500 Years of Resistance Comic Book was heralded as a groundbreaking illustrated history of Indigenous activism and resistance in the Americas over the previous 500 years, from contact to present day. Eleven years later, author and artist Gord Hill has revised and expanded the book, which is now available in colour for the first time.

The shocking images of neo-Nazis parading in Charlottesville, North Carolina in the summer of 2017 linger in the mind, but so do those of the passionate protestors who risked their lives to do the right thing. In this stirring graphic non-fiction book by the acclaimed author of The 500 Years of Resistance Comic Book, Gord Hill looks at the history of fascism over the last 100 years, and the concurrent antifa movements that work fastidiously to topple it.

In 1976, Ben Martini was diagnosed with schizophrenia. A decade later, his brother Oliver was told he had the same disease. For the past thirty years the Martini family has struggled to comprehend and cope with devastating illness, frustrated by a health care system lacking in resources and empathy, the imperfect science of medication, and the strain of mental illness on familial relationships.