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Beauty and the Beast may be a fairy tale, but for one woman its moral rings true in real life.
When Alix Miller goes to New Hampshire to paint a portrait of Leland Crompton, she is following family tradition- Miller artists have always painted the Crompton aristocrats. But the reclusive Leland is hideously disfigured by a rare genetic disease, and Alix is uncomfortable rendering him on canvas. She begins the task anyway, and through her...
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"A leading geneticist explores what promises to be one of the most transformative advances in health and medicine in history. Almost every week, another exciting headline appears about new advances in the field of genetics. Genetic testing is experiencing the exponential growth once seen with the Internet, and the plummeting cost of DNA sequencing makes it increasingly accessible for individuals and families. Dr. Steven M. Lipkin suggests that today's...
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"Kate’s life in Baton Rouge, full of friends and family, gymnastics and Girl Scouts, is just plain great. But then, at the age of twelve, she suddenly develops a mysterious shoulder pain that won’t go away . . . and that will change her life forever. It turns out that Kate has one of the rarest genetic disorders in the world, Fibrodysplasia Ossificans Progressiva. FOP causes bone to form in places in the body where it shouldn’t, and there’s...
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"Vanessa lives life on her own terms -- one day at a time, every day to its fullest. She can't afford to think about whether she has the same fatal genetic condition as her older sister. After all, she has way too much to do, traveling the globe and showing millions of YouTube followers the joy in seizing every moment. But lately, life has been anything but pure joy, and travel has come to an abrupt halt. After her younger step-sister drops off an...
7) True to you
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After a devastating heartbreak three years ago, genealogist and historical village owner Nora Bradford has decided that burying her nose in her work and her books is far safer than romance in the here and now. Unlike Nora, former Navy SEAL and Medal of Honor recipient John Lawson is a modern-day man, usually 100 percent focused on the present. But when he's diagnosed with an inherited condition, he's forced to dig into the secrets of his past and...
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"In this novel in blank verse, twelve-year-old Cass struggles to cope with her father's recurring cancers that have dominated her whole life, with the knowledge that he is likely to die soon because the latest recurrence is worse--and with the possibilitythat she may have inherited the genetic disease, Li-Fraumeni Syndrome, that causes the cancers" Provided by publisher.
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On paper, Coach Rob Mendez sounds like any other football coach on any other field across America: passionate, authoritative, knowledgeable. But he’s unlike any other coach you know--in fact, he’s probably unlike any other person you know.
Born with an extraordinarily rare condition called tetra-Amelia syndrome, Rob has no arms or legs. He moves with the assistance of a custom-made, motorized wheelchair that he operates with his back and shoulders.
Many...
Description
Clare has been in love with Henry her entire life. She believes they are destined to be together, even though she never knows when they will be separated: Henry is a time traveler, cursed with a rare genetic anomaly that causes him to live his life on a shifting timeline, skipping back and forth through his lifespan with no control. Despite the fact that Henry's travels force them apart with no warning, Clare desperately tries to build a life with...
12) Saving the Tasmanian devil: how science is helping the world's largest marsupial carnivore survive
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"In this addition to the critically acclaimed Scientist in the Field series, Dorothy Patent follows the scientists trying to put a stop to a gruesome disease before it's too late. Tasmanian devils are dying at an alarming rate from a type of tumor that appears to be contagious. What scientists are learning while researching the Tasmanian devil has potential to affect all animals, and even humans, as they learn more about how to prevent and hopefully...
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"Praised by RJ Palacio as "wondrous"--this moving memoir follows a teenage boy with TC syndrome and his exceptional family from diagnosis at birth to now. "This touching memoir is a must-read for anyone who wants to know more about the real world experiences of a child with craniofacial differences and his extraordinary family. It's also more than that. It's a story about the love between a mother and a son, a child and his family, and the breadth...
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"The author's daughter was born with a very rare genetic syndrome and faced a daunting prognosis: she would be a fraction of normal size, have innumerable physical and mental difficulties and likely a shortened lifespan. Now, at age eight she is attendingstandard public school classes. This is the story of her family's journey" -- Provided by publisher.
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