The Humals. Humanoid Aliens. They dominated the spiral arm millennia ago then vanished without trace. Man had found traces of their presence, reverse-engineered their technology and speculated endlessly about their demise. But no one really knew what had happened. No one knew why they had disappeared or why so few traces of them remained. For James Hamilton the Humals were not something he concerned himself about. Not, that is, until a billionaire philanthropist seeks him out with a proposition he can't ignore. It started out as the offer of a lifetime. A way to finally end all his financial concerns and to do something good for humanity into the bargain. But as Hamilton was well aware, if something sounds too good to be true then it usually means trouble. Suspicious, Hamilton fears the worst and plans accordingly but even he is unprepared for the events that will follow. With precious few allies and more questions than answers, Hamilton must desperately try to piece together the clues in order to understand what is going on before it is too late. For what starts out as a journey for the betterment of mankind may well sow the seeds of its destruction.

Nilda Carlson has been trying to save enough money to go to America for months, so when a letter from Einar and Gerd Strand arrives, offering to pay her ticket, she jumps at the chance. Her younger brother Ivar accompanies her, and they can't wait to join their brother Rune and his family in the northern forests of Minnesota. Signe and Rune Carlson are thrilled to welcome Nilda and Ivar to America, but life on the farm remains a struggle. Though Gerd has softened and grown to love the Carlson family, Einar is still harsh and unforgiving, obsessed solely with felling as many trees as possible. Rune is trying to build a new home for his wife and children, but Einar refuses to help and forbids anyone from the nearby community from stepping foot on his land. What dark secret must lie in his past to have caused him to isolate himself--and anyone living under his roof--in this way? When a tragedy lays the truth bare, the Carlsons and Strands will have to come together like never before and become a true family.

The book depicts how medical-legal partnerships and legal aid can transform the lives of families in need. The text focuses on the plight of a small girl suffering with asthma because of a landlord's neglect of an apartment contaminated with mold. Torn between being evicted and the heath of their daughter, the family is connected to a legal representative by the doctor who cares for the child.

Nilda Carlson has been trying to save enough money to go to America for months, so when a letter from Einar and Gerd Strand arrives, offering to pay her ticket, she jumps at the chance. Her younger brother Ivar accompanies her, and they can't wait to join their brother Rune and his family in the northern forests of Minnesota. Signe and Rune Carlson are thrilled to welcome Nilda and Ivar to America, but life on the farm remains a struggle. Though Gerd has softened and grown to love the Carlson family, Einar is still harsh and unforgiving, obsessed solely with felling as many trees as possible. Rune is trying to build a new home for his wife and children, but Einar refuses to help and forbids anyone from the nearby community from stepping foot on his land. What dark secret must lie in his past to have caused him to isolate himself--and anyone living under his roof--in this way? When a tragedy lays the truth bare, the Carlsons and Strands will have to come together like never before and become a true family.

Eib shares amazing, true stories of those who have been through cancer and discovers that when God and cancer meet, hope is never far away. This book is packed with a daily dose of encouragement.

#1 NEW YORK TIMES BESTSELLER • PULITZER PRIZE FINALIST • This inspiring, exquisitely observed memoir finds hope and beauty in the face of insurmountable odds as an idealistic young neurosurgeon attempts to answer the question What makes a life worth living? NAMED ONE OF PASTE’S BEST MEMOIRS OF THE DECADE • NAMED ONE OF THE BEST BOOKS OF THE YEAR BY The New York Times Book Review • People • NPR • The Washington Post • Slate • Harper’s Bazaar • Time Out New York • Publishers Weekly • BookPage Finalist for the PEN Center USA Literary Award in Creative Nonfiction and the Books for a Better Life Award in Inspirational Memoir At the age of thirty-six, on the verge of completing a decade’s worth of training as a neurosurgeon, Paul Kalanithi was diagnosed with stage IV lung cancer. One day he was a doctor treating the dying, and the next he was a patient struggling to live. And just like that, the future he and his wife had imagined evaporated. When Breath Becomes Air chronicles Kalanithi’s transformation from a naïve medical student “possessed,” as he wrote, “by the question of what, given that all organisms die, makes a virtuous and meaningful life” into a neurosurgeon at Stanford working in the brain, the most critical place for human identity, and finally into a patient and new father confronting his own mortality. What makes life worth living in the face of death? What do you do when the future, no longer a ladder toward your goals in life, flattens out into a perpetual present? What does it mean to have a child, to nurture a new life as another fades away? These are some of the questions Kalanithi wrestles with in this profoundly moving, exquisitely observed memoir. Paul Kalanithi died in March 2015, while working on this book, yet his words live on as a guide and a gift to us all. “I began to realize that coming face to face with my own mortality, in a sense, had changed nothing and everything,” he wrote. “Seven words from Samuel Beckett began to repeat in my head: ‘I can’t go on. I’ll go on.’” When Breath Becomes Air is an unforgettable, life-affirming reflection on the challenge of facing death and on the relationship between doctor and patient, from a brilliant writer who became both.

The compelling story of a woman's lifelong battle with Cystic Fibrosis and her astonishing resilience despite a double lung transplant and a senseless murder.Anna Maynard was diagnosed with Cystic Fibrosis when she was six months old, at a time when average life expectancy for children afflicted with the genetic disorder was only fourteen years. Throughout her tumultuous childhood, Anna found for a life of normalcy and despite the death of her older sister, France-who succumbed to the same disease-Anna pursued her dream to live a long, productive life with courage, determination and hope.