- Large Print
- Propaganda
- Waite
- Japanese
- General
- Hayes, Chetwynd
- Sondheim
- Philosophy
- McKeone, Dixie
- Marriage
- General
- Jack & the Beanstalk
- Matthews, John
- ( M )
- General
- General
- Technology & Society
- Classics
- Interest
- DeLoach, Nora
- Jewelry
- Fiction
- Postcards
- Bedtime & Dreaming
- Chambers, Oswald
- Taylor, C.J.
- Business
- Verdi
- Europe
- Geronimo Stilton
- Some of our other sites:
- Books
- Clothing, Shoes and Accessories
- Baby Clothes and Accessories
- Cosmetics, Beauty Products and Fragrances
- Cellphones, Call Plans and Accessories
- Video Games
- DVDs
- Electronics, Gadgets and Computers
- Health and Personal Care
- Home and Garden
- Home DIY
- Jewelry
- Magazines and Newspapers
- Music Downloads
- Musical Instruments
- Office Equipment and Supplies
- Software and Games
- Sporting Goods
- Toys and Games
- Watches
- UK Books
- UK Video Games
- UK Home and Garden
- UK Electronics, Gadgets and Computers
- UK Baby Clothes and Accessories
- UK Software and Games
- UK Sporting Goods
- UK Toys and Games
Books : Health, Mind & Body : Disorders & Diseases : Genetic
-
Tried everything but still not feeling better?
If your depression keeps coming back or is even getting worse, then you may be suffering from bipolar II or “soft” bipolar disorder. Commonly misdiagnosed, these mood disorders are characterized by recurring bouts of depression along with anxiety, irritability, mood swings, sleep problems, or intrusive thoughts.
Why Am I Still Depressed? shows you how to identify if you have a nonmanic form of bipolar disorder and how to work with your doctor to safely and effectively treat it.
Author James R. Phelps, M.D., gives you the latest tools and knowledge so you can:
- Understand the Mood Spectrum, a powerful new tool for diagnosis
- Know all your treatment options, including mood-stabilizing medications and research-tested psychotherapies
- Examine the potential hazards of taking antidepressant medications
- Manage your condition with exercise and lifestyle changes
- Help family and friends with this condition understand their diagnosis and find treatment
-
Fight the impact of MS through fitness with specially designed exercises.
In the U.S. alone, approximately 400,000 people have multiple sclerosis (MS). MS is an autoimmune disease that affects the central nervous system. There are a variety of symptoms of MS and it affects people in different ways, but there is no cure.
Fitness can help strengthen debilitated bodies, and make living with the disease a little easier. Exercises for Multiple Sclerosis outlines a detailed exercise plan that can help MS sufferers overcome their symptoms, especially fatigue and mobility problems. The latest book in the popular Exercises for series, Exercises for Multiple Sclerosis provides a tested program for people living with MS, making it an essential reference for anyone who suffers from MS.
The exercises are clearly photographed in easy-to-follow sequences and contain complete descriptions. If you or someone you know suffers from MS, you need this book. Exercises for Multiple Sclerosis will help MS sufferers to achieve a healthier, happier, more productive life. 100 photos.
-
Hemochromatosis is one of modern medicine's greatest oversights. A disorder that few people are able to pronounce at first glance, it is an inherited disorder of iron metabolism, not a blood disease, that can be fatal if not detected in time. Commonly misdiagnosed as arthritis, diabetes, heart disease, impotence, depression, and liver disease, hereditary hemochromatosis is common in people of northern European descent and is most prominent among the Scots and the Irish. Undetected hemochromatosis frequently is fatal, and that is why it is emerging as one of the most important health issues of the new millennium. It's real, it's common, and it can kill you. The Iron Disorders Institute Guide to Hemochromatosis is a reference book for home use. It contains helpful charts, diet and nutrition information, treatment guidelines, a glossary of terms, and compelling personal stories of people living with this disorder. Written by the top researchers and experts in university and research hospitals from all over the United States, it is destined to become the definitive source for information about the disorder for millions of families world-wide.
-
At some point in our lives, many of us will face the crisis of an unexpected illness. For parents, the fear, anxiety and confusion resulting from a cancer diagnosis can be particularly devastating.
When A Parent Has Cancer is a book for families written from the heart of experience. A mother, physician, and cancer survivor, Dr Wendy Harpham offers clear, direct, and sympathetic advice for parents challenged with the task of raising normal, healthy children while they struggle with a potentially life–threatening disease.
Dr Harpham lays the groundwork of her book with specific plans for helping children through the upheaval of a parent's diagnosis and treatment, remission and recovery, and if necessary, confronting the possibility of death. She emphasises the importance of being honest with children about the gravity of the illness, while assuring them that their basic needs will always be met.
Included is Becky and the Worry Cup, an illustrated children's book that tells the story of a seven–year–old girl's experiences with her mother's cancer.
-
Many parents of children with Down syndrome would like to help their child improve nutrition and manage weight, but don't know where to begin. Now, this much-needed book looks at all aspects of nutrition and healthy living for children with Down syndrome, from birth through young adulthood. The author, a mother of a child with Down syndrome and a registered dietitian, encourages parents to start teaching healthy habits early but stresses that it's never too late to start, no matter what age. Based on years of personal and professional experience and supported by the latest medical research and insights from other parents and adults with Down syndrome, chapters cover:Breast and bottle feeding
Basic nutrition and physiology
Celiac disease
Diabetes
Alternative therapies
Food and school
Weight management
Fitness and exercise
Cooking and menu planning
Education activities
The appendices contain cookbook lists, information on calculating calorie needs, and more. Resource and reading lists round out this practical, comprehensive guide.
With this handbook, parents, dietitians, and therapists will understand the connection between Down syndrome, diet, and nutrition, and be in a better position to guide children toward a healthier future.
-
From the gene that causes people to age prematurely to the "bitter gene" that may spawn broccoli haters, this book explores a few of the more exotic locales on the human genome, highlighting some of the tragic and bizarre ways our bodies go wrong when genes fall prey to mutation and the curious ways in which genes have evolved for our survival.
Lisa Seachrist Chiu offers here a smorgasbord of stories about rare and not so rare genetic quirks--the gene that makes some people smell like a fish, the Black Urine Gene, the Werewolf Gene, the Calico Cat Gene. We read about the Dracula Gene, a mutation in zebra fish that causes blood cells to explode on contact with light, and suites of genes that also influence behavior and physical characteristics. The Tangier Island Gene, first discovered after physicians discovered a boy with orange tonsils (scientists now realize that the child's odd condition comes from an inability to process cholesterol). And Wilson's Disease, a gene defect that fails to clear copper from the body, which can trigger schizophrenia and other neurological symptoms, and can be fatal if left untreated. On the plus side, we read about the Myostatin gene, a mutation which allows muscles to become much larger than usual and enhances strength--indeed, the mutations have produced beefier cows and at least one stronger human. And there is also the much-envied Cheeseburger Gene, which allows a lucky few to eat virtually anything they want and remain razor thin.
While fascinating us with stories of genetic peculiarities, Chiu also manages to explain much cutting-edge research in modern genetics, resulting in a book that is both informative and entertaining. It is a must read for everyone who loves popular science or is curious about the human body.
-
Progress in genetic and reproductive technology now offers us the possibility of choosing what kinds of children we do and don't have. Should we welcome this power, or should we fear its implications? There is no ethical question more urgent than this: we may be at a turning-point in the history of humanity. The renowned moral philosopher and best-selling author Jonathan Glover shows us how we might try to answer this question, and other provoking and disturbing questions to which it leads.
Surely parents owe it to their children to give them the best life they can? Increasingly we are able to reduce the number of babies born with disabilities and disorders. But there is a powerful new challenge to conventional thinking about the desirability of doing so: this comes from the voices of those who have these conditions. They call into question the very definition of disability. How do we justify trying to avoid bringing people like them into being?
In 2002 a deaf couple used sperm donated by a friend with hereditary deafness to have a deaf baby: they took the view that deafness is not a disability, but a difference. Starting with the issues raised by this case, Jonathan Glover examines the emotive idea of "eugenics", and the ethics of attempting to enhance people, for non-medical reasons, by means of genetic choices. Should parents be free, not only to have children free from disabilities, but to choose, for instance, the colour of their eyes or hair? This is no longer a distant prospect, but an existing power which we cannot wish away. What impact will such interventions have, both on the individuals concerned and on society as a whole?
Should we try to make general improvements to the genetic make-up of human beings? Is there a central core of human nature with which we must not interfere?
This beautifully clear book is written for anyone who cares about the rights and wrongs of parents' choices for their children, anyone who is concerned about our human future. Glover handles these uncomfortable questions in a controversial but always humane and sympathetic manner.
-
-
The Encyclopedia of Genetic Disorders and Birth Defects (Facts on File Library of Health and Living)
Comprehensive reference to congenital disorders and birth defects. Contains more than 1,000 updated and revised entries listed in alphabetical format. Covers basic genetics to the latest screening and diagnostic techniques. For researchers and clinicians. Previous edition: c1991.
-
Reveals the psychic causes of illness and how to decode and resolve them
• Explains how we inherit illness from our ancestors via cellular memory and provides protocols for diagnosis and treatment
• Demonstrates how illness is an ally that enables individuals to restore balance to both their life and that of their family tree
Biogenealogy: Decoding the Psychic Roots of Illness offers protocols for diagnosis and treatment for conflicts that can span generations. While the idea that emotional stress lies at the origin of every illness is becoming more readily acceptable today, it also is possible to trace the root cause of an illness to our ancestors--their unresolved psychic distress can become part of the cellular memory inherited by their descendants. Until the issue has been settled successfully, it will continue to trigger illnesses in the generations that follow to offset the mind’s inability to resolve the problem. Illness is the body’s way of protecting those who experience severe emotional shock or excessive amounts of stress.
Illness is therefore an ally, rather than the adversary conventional medicine purports it to be. Understanding illness in this way directs us to look for the psychic conflict that underlies it in order to eliminate the disease, rather than merely dealing with its overt physical symptoms. For example, diabetes, which creates excess sugar in the bloodstream, can be triggered by the stress caused by feelings of powerlessness: To compensate for the sense of powerlessness, the body manufactures more sugar to fuel the muscles. To stop this excess sugar production, the psychic distress beneath it must be resolved or it will be passed on to the next generation. When we discover the solutions that create harmony in the body and in our life, the body will no longer have to manufacture illness to restore a sense of balance, and illness will no longer be part of the bequest we leave our descendants.
-
Down syndrome is a genetic condition which causes varying degrees of learning disability as well as other health problems. Nearly one baby in every 1000 born in the UK has the condition. Parents are often frightened and confused by the birth of a baby with Down syndrome, and they need reassurance as well as up-to-date information regarding the condition.
The new edition of this highly regarded book for parents of children with Down syndrome covers a number of important new developments in research and clinical practice that have occurred in the field in recent years. These include several newly recognised medical conditions that are known to occur more commonly in patients with Down syndrome, for example, glaucoma, gastrointestinal malformations, feeding difficulties, gastro-oesophageal reflux, coeliac disease, and diabetes. This expanded edition also includes new recommendations regarding routine health checks in line with those of the UK Down Syndrome Medical Interest Group (UKDSMIG). Additionally the book covers new prenatal screening methods which have been developed to identify Down syndrome during pregnancy.
-
Wexler tells two stories, the one of her family's emotional odyssey after her mother was diagnosed with Huntington's disease, and the relentless efforts to find the gene and a cure, and the news that she had a 50/50 chance of getting it also. This book comes from her unique position of being both reporter of how scientists sought a cure and someone who could be saved by it.
-
A medical memoir and poetic meditation on raising a child with a genetic disorder
Clare Dunsford is the mother of a twenty-one-yearold son with Fragile X syndrome, the most common inherited cause of mental retardation. Spelling Love with an X is the first literary memoir about living with Fragile X, which affects the lives of over a million people in the U.S., including those with the full mutation, their families, and treatment professionals.
When her son was first diagnosed, at age seven, Dunsford received the devastating news that she and three of her four siblings carry the Fragile X premutation and had therefore unknowingly passed on the full mutation to several of their children. An English professor by training, Dunsford draws on classic poetry to explore her new identity as a genetically "flawed" individual and reflect on her life with J.P., a colorful young man with great verbal dexterity and a lovably cheeky streak. "My instinct to find order and consolation in literature," she writes, "lends a distinct voice to the story of my family's DNA." Brimming with warmth and intelligence, Spelling Love with an X shares the disarming insights of a compassionate scholar on motherhood, literature, and genetic inheritance.
"Part poetry, part scientific inquiry, this wonderful memoir is, above all, the story of being complexly human in a world filled with fragility and strength, shadow and light. Clare Dunsford navigates the X that has mapped her own and her son's paths with humor, honesty, and clear-sighted intelligence—and in prose that sings."
—Elizabeth Graver, author of The Honey Thief and Awake
"Clare Dunsford does much more than inform us concerning a disorder we know too little about. Through a prose both lucid and beautiful, she is able to communicate the strangeness, even the poetry, of fragile X."
—Clara Claiborne Park, author of The Siege: A Family's Journey into the World of an Autistic Child and Exiting Nirvana: A Daughter's Life with Autism
"Spelling Love with an X is a beautifully written journey of a woman toward understanding—of herself, her son, and the twists of fate and DNA that bind them and all of us. Clare Dunsford's powerful and moving memoir is rich with humor, poetry and, most of all, love."
—Mitchell Zuckoff, author of Choosing Naia: A Family's Journey
-
Tests are a standard part of modern medicine. We willingly screen our blood, urine, vision, and hearing, and submit to a host of other exams with names so complicated that we can only refer to them by their initials: PET, ECG, CT, and MRI. Genetic tests of our risks for disease are the latest trend in medicine, touted as an approach to informed and targeted treatment. They offer hope for some, but also raise medical, ethical, and psychological concerns for many including when genetic information is worth having.
To Test or Not to Test arms readers with questions that should be considered before they pursue genetic screening, about the information genetic testic can provide, and general logistical questions about risk and timing of testing.
Do the benefits of having the genetic information outweigh the problems that testing can bring?
Determining the answers is no easy task. In this highly readable book, Doris Teichler Zallen provides a template that can guide individuals and families through the decision-making process and offers additional resources where they can gain more information. She shares interviews with genetic specialists, doctors, and researchers, as well as the personal stories of nearly 100 people who have faced genetic-testing decisions. Her examples focus on genetic testing for four types of illnesses: breast/ovarian cancer (different disorders but closely connected), colon cancer, late-onset Alzheimer s disease, and hereditary hemochromatosis. From the more common diseases to the rare hereditary conditions, we learn what genetic screening is all about and what it can tell us about our risks.
Given that we are now bombarded with ads in magazines and on television hawking the importance of pursuing genetic-testing, it is critical that we approach this tough issue with an arsenal of good information. To Test or Not to Test is an essential consumer tool-kit for the genetic decision-making process.
-
Cystic fibrosis afflicts approximately 30,000 Americans. The average age of survival has been steadily increasing, but not quickly enough: a child born with cystic fibrosis today can only expect to live 35 to 40 years.
In this valuable new addition to the Your Personal Health series, Dr. Wayne Kepron offers a comprehensive look at the disease that afflicts so many young people. Topics include:
- Symptoms of cystic fibrosis Making a diagnosis Complications of the disease Treatments (including lung transplants) Techniques and precautions in lung care Transition into adulthood Prospects for gene therapy End-of-life issues
Using diagrams, charts and case studies, Cystic Fibrosis is designed for patients, their families, and caregivers. It is both a quick reference guide and a tool for in-depth study.
-
It was no coincidence. Apron Strings is the painful but courageous story of Diane Tropea Greene and her family, a family that was decimated by cancer. Diane later learned that her cancer was caused by the BRCA2 gene mutation for breast cancer, which affected both the women and men in Diane s family including Diane. But knowledge is power, and the lesson of the Tropea family is important for anyone who suspects their family has too many cancer diagnoses to be coincidental.
-
The tragedy of cystic fibrosis has been touchingly recounted before, but this is the first book to portray the symbiotic relationship between twins who share this life-threatening disease through adulthood. Isabel Stenzel Byrnes and Anabel Stenzel tell of their struggle to pursue normal lives while grappling with the realization that they might die young. Their story reflects the physical and emotional challenges of a particularly aggressive form of CF and tells how the twins bicultural heritage Japanese and German influenced the way they coped. The Power of Two is an honest and gripping portrayal of day-to-day health care, the impact of chronic illness on marriage and family, and the importance of a support network to continuing survival. These two remarkable sisters have much to teach about the power of perseverance and about the ultimate power of hope.
-
This book has been created for patients who have decided to make education and research an integral part of the treatment process. Although it also gives information useful to doctors, caregivers and other health professionals, it tells patients where and how to look for information covering virtually all topics related to hemochromatosis (also Bronze Diabetes; Cirrhosis, congenital pigmentary; Familial Hemochromatosis; Hemochromatosis Syndrome; Hemosiderosis; Iron Overload Disease), from the essentials to the most advanced areas of research. The title of this book includes the word official. This reflects the fact that the sourcebook draws from public, academic, government, and peer-reviewed research. Selected readings from various agencies are reproduced to give you some of the latest official information available to date on hemochromatosis. Given patients' increasing sophistication in using the Internet, abundant references to reliable Internet-based resources are provided throughout this sourcebook. Where possible, guidance is provided on how to obtain free-of-charge, primary research results as well as more detailed information via the Internet. E-book and electronic versions of this sourcebook are fully interactive with each of the Internet sites mentioned (clicking on a hyperlink automatically opens your browser to the site indicated). Hard-copy users of this sourcebook can type cited Web addresses directly into their browsers to obtain access to the corresponding sites. In addition to extensive references accessible via the Internet, chapters include glossaries of technical or uncommon terms.
-
Mary Beth Busby and Megan Massey have something in common--they are both mothers of two sons with Fragile X syndrome (the most common form of inherited mental retardation and the most common cause of autism). When Mary Beth Busby's sons, Robert and Jack, were born in 1964 and 1965, Fragile X had not even been identified as a genetic abnormality. By the time Megan Massey's sons Jack and Jacob were born in 1989 and 1991, a few researchers had identified it, but few pediatricians knew it existed. Today it is known that Fragile X affects 1 in 4000 males and 1 in 6000 females of all races and ethnic groups. Mary Beth and Megan met when they both became active in the Fragile X Research Foundation (FRAXA). They wrote "Dear Megan" to offer hope and support to the millions of parents who care for and love their disabled children. Written in the form of intimate letters between the two authors--who are separated in age by a generation--the book reveals the personal side of parents struggling with the challenges of school systems and health systems, marriage, and life to care for their disabled sons. It also shows the joy and love they find through these special children and adults.
-
One of the most common genetic disorders in America is also one of the most frequently misdiagnosed. But anyone who has just learned they have hemochromatosis will have lots of questions: How did I get it? Can I pass it to my children? How can I avoid organ damage? The answers are in Living with Hemochromatosis by Dr. Gregory T. Everson and Hedy Weinberg.Over 30 million people in the United States carry the gene for hemochromatosis, and almost 2 million have developed the condition. Hemochromatosis, also known as "iron overload" or "bronze diabetes," causes the body to retain much more iron than it should. Because it is often not diagnosed until the patient is over 40 years old, the long-term iron buildup can damage not only cells and tissues, but also larger organs including the heart and liver.
But there is hope. Living with Hemochromatosis guides patients through the whole spectrum of this condition, from early to delayed diagnosis, and answers their questions. It contains valuable information about recognizing the signs and symptoms of hemochromatosisÐand why it is frequently misdiagnosed.
Living with Hemochromatosis also offers advice about genetic testing, and how to interpret the results. There is up-to-date information about treatment options, including phlebotomy, liver transplants, and new areas of research. The authors provide patients and their families with guidance on coping with the physical, emotional, and financial issues, as well as nutritional recommendations and much more. 25 b/w photos.