Description

The most comprehensive guide available on hereditary cancers, from understanding risk, prevention, and genetic counseling and testing to treatment, quality of life, and more.

Up to 10 percent of cancers are caused by inherited mutations in specific genes. Finding out that you or your loved ones may be at increased risk of developing cancer because of a genetic mutation raises a lot of questions: Is cancer inevitable? Is there anything I should do differently in my life? Will my children also be at higher risk of cancer? Should I have preemptive treatments or surgery? This comprehensive guide provides answers to these questions and more.

Written by three passionate patient advocates, this book is a compilation of the trusted information and support provided for more than two decades by Facing Our Risk of Cancer Empowered (FORCE), the de facto voice of the hereditary cancer community. Combining the latest scientific research with national guidelines, expert advice, and compelling patient stories, the book offers previvors (those who have a mutation but have never been diagnosed), survivors, and their families the guidance they need to face the unique physical and emotional challenges of living in a high-risk body.

An ideal resource for genetic counselors, physicians, nurses, advocates, and others who support and care for the hereditary cancer community, Living with Hereditary Cancer Risk also provides coverage of

• signs of inherited cancer risk in a family;
• the value of genetic counseling and testing;
• mutations in BRCA, Lynch Syndrome, and other genes that elevate cancer risk;
• risk-reducing strategies;
• traditional treatments and newer personalized approaches, including immunotherapies and PARP inhibitors;
• nationally recommended guidelines for prevention, early detection, and treatment;
• insurance coverage and discrimination protections; and
• coping with sexual health, fertility, menopause, and other quality of life issues.

Living with Hereditary Cancer Risk: What You and Your Family Need to Know

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£41.50

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Hardback by Kathy Steligo , Sue Friedman

1 in stock

Short Description:

The most comprehensive guide available on hereditary cancers, from understanding risk, prevention, and genetic counseling and testing to treatment, quality... Read more

    Publisher: Johns Hopkins University Press
    Publication Date: 22/11/2022
    ISBN13: 9781421444253, 978-1421444253
    ISBN10: 1421444259

    Number of Pages: 496

    Non Fiction , Health & Wellbeing

    Description

    The most comprehensive guide available on hereditary cancers, from understanding risk, prevention, and genetic counseling and testing to treatment, quality of life, and more.

    Up to 10 percent of cancers are caused by inherited mutations in specific genes. Finding out that you or your loved ones may be at increased risk of developing cancer because of a genetic mutation raises a lot of questions: Is cancer inevitable? Is there anything I should do differently in my life? Will my children also be at higher risk of cancer? Should I have preemptive treatments or surgery? This comprehensive guide provides answers to these questions and more.

    Written by three passionate patient advocates, this book is a compilation of the trusted information and support provided for more than two decades by Facing Our Risk of Cancer Empowered (FORCE), the de facto voice of the hereditary cancer community. Combining the latest scientific research with national guidelines, expert advice, and compelling patient stories, the book offers previvors (those who have a mutation but have never been diagnosed), survivors, and their families the guidance they need to face the unique physical and emotional challenges of living in a high-risk body.

    An ideal resource for genetic counselors, physicians, nurses, advocates, and others who support and care for the hereditary cancer community, Living with Hereditary Cancer Risk also provides coverage of

    • signs of inherited cancer risk in a family;
    • the value of genetic counseling and testing;
    • mutations in BRCA, Lynch Syndrome, and other genes that elevate cancer risk;
    • risk-reducing strategies;
    • traditional treatments and newer personalized approaches, including immunotherapies and PARP inhibitors;
    • nationally recommended guidelines for prevention, early detection, and treatment;
    • insurance coverage and discrimination protections; and
    • coping with sexual health, fertility, menopause, and other quality of life issues.

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