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LIVING WITH ALPHA-1 ANTITRYPSIN MANGEL: THE COMPLETE GUIDE (2019 TPB) {J8}
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Standort: Oakville, Connecticut, USA
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eBay-Artikelnr.:267149781383
Artikelmerkmale
- Artikelzustand
- ISBN
- 9781578268092
Über dieses Produkt
Product Identifiers
Publisher
Hatherleigh Company, The Limited, T.H.E.
ISBN-10
1578268095
ISBN-13
9781578268092
eBay Product ID (ePID)
8038384406
Product Key Features
Number of Pages
96 Pages
Publication Name
Living with Alpha-1 Antitrypsin Deficiency (A1AD) : Complete Guide to Risk Factors, Symptoms and Treatment Options
Language
English
Subject
Reference, Pulmonary & Thoracic Medicine, Endocrinology & Metabolism, Genetics, Diseases / Respiratory, Diseases / Genetic
Publication Year
2019
Type
Textbook
Subject Area
Health & Fitness, Medical
Series
Living with Ser.
Format
Trade Paperback
Dimensions
Item Height
0.2 in
Item Weight
5.1 Oz
Item Length
9 in
Item Width
6 in
Additional Product Features
Intended Audience
Trade
LCCN
2019-286558
Reviews
"Samantha Bowick expertly blends clinical explanations of Alpha-1 Antitrypsin Deficiency with patient testimony, providing insight into the everyday challenges experienced by those who battle this rare condition. Living with Alpha-1 Antitrypsin Deficiency outlines the common misconceptions about this condition and the financial hardship it places on patients. Whether you're an Alpha-1 patient, a family member or friend, there is something for everyone within Bowick's work." -- Scott Bruun, Executive Director of the Chronic Disease Coalition
Illustrated
Yes
Synopsis
A knowledgeable handbook with a patient's perspective for those afflicted with the incurable disease known as Alpha-1 Antitrypsin deficiency (A1AD). Alpha-1 Antitrypsin deficiency (A1AD) is a rare genetic, incurable disease which causes the liver to not produce enough of a certain protein that protects and keeps the lungs functional. 100,000 people in the United States have A1AD and 19 million more are carriers for the disease. Since it's so rare, the information available about A1AD has been lacking especially for those suffering unknowingly with the disease. Living with Alpha-1 Antitrypsin Deficiency offers the most up-to-date and comprehensive information on this illness and includes first-hand experience from someone managing the disease. Living with Alpha-1 Antitrypsin Deficiency also includes expert advice from doctors and researchers tackling the disease, with tips on recognizing symptoms and getting the most effective help possible., Alpha-1 Antitrypsin deficiency is a rare genetic, incurable disease which a deficiency in a protein that keeps the lungs functional. It is thought that 25,000 people in the UK have the genetic condition, according to the British Lung Foundation. This book offers the most up-to-date and comprehensive information on this illness and includes first-hand experience from someone managing the disease. Living with Alpha-1 Antitrypsin Deficiency also includes expert advice from doctors and researchers tackling the disease, with tips on recognising symptoms and getting the most effective help possible., BEST BOOK AWARD 2019 FINALIST - HEALTH: GENERAL (AMERICAN BOOK FEST) A knowledgeable handbook with a patient's perspective for those afflicted with the incurable disease known as Alpha-1 Antitrypsin deficiency (A1AD). Alpha-1 Antitrypsin deficiency (A1AD) is a rare genetic, incurable disease which causes the liver to not produce enough of a certain protein that protects and keeps the lungs functional. 100,000 people in the United States have A1AD and 19 million more are carriers for the disease. Since it's so rare, the information available about A1AD has been lacking especially for those suffering unknowingly with the disease. Living with Alpha-1 Antitrypsin Deficiency offers the most up-to-date and comprehensive information on this illness and includes first-hand experience from someone managing the disease. Living with Alpha-1 Antitrypsin Deficiency also includes expert advice from doctors and researchers tackling the disease, with tips on recognizing symptoms and getting the most effective help possible., Learning to manage the symptoms of alpha-1 antitrypsin deficiency (A1AD) can seem overwhelming. But by taking everything one day at a time and making sure you're provided with the care and support you need, you can still live a life that is fulfilling and meaningful. Living with Alpha-1 Antitrypsin Deficiency includes: Easy-to-understand information on the latest surgical and non-surgical treatment options, Traditional and alternative medical options for abroad, full-body approach to wellness, Guidance on self-care techniques for patients, families and caregivers, Valuable medical and community resources for A1AD sufferers, While there is currently no cure for A1AD, patients can take action to reduce their symptoms and improve their overall well-being by practicing proper self-care and following a comprehensive wellness plan. Don't just live with A1AD-live well. Book jacket., A knowledgeable handbook for those afflicted with the incurable disease known as Alpha-1 Antitrypsin deficiency (A1AD).
LC Classification Number
RC632.A43B69 2019
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