
Cystic Fibrosis
The Ultimate Teen Guide
Melanie Ann Apel(Author)
Scarecrow Press
Published on 17. April 2006
Book
Hardback
280 pages
978-0-8108-4821-4 (ISBN)
Description
Cystic Fibrosis: The Ultimate Teen Guide leaves no aspect of this disease untold. Based on a series of interviews with young people with CF and their family members, the day-to-day dealings of life as a cystic fibrosis patient are described. Some of the topics covered include a description of the illness; a comprehensive discussion of who gets the disease and why; an explanation of the procedures involved in diagnosing CF; coverage of the arduous daily therapies involved in maintaining the life of a person with CF; and the challenges of dealing with CF-related diabetes.
These teens' stories reflect how they live their lives to the fullest, how they are not bitter about their situations, and how they look forward to new medications, more-effective therapies, and-one day soon-a cure. Also included are stories told by people, now in their 30s and 40s, having CF who are still alive and coping well with the disease, demonstrating that progress is being made and that they can hope to live beyond their teen years, something that wasn't likely 20 years ago. This book is the ideal guide for any reader who wants positive medical information about CF, offering an extensive glossary and listings of books, websites, and organizations about Cystic Fibrosis.
These teens' stories reflect how they live their lives to the fullest, how they are not bitter about their situations, and how they look forward to new medications, more-effective therapies, and-one day soon-a cure. Also included are stories told by people, now in their 30s and 40s, having CF who are still alive and coping well with the disease, demonstrating that progress is being made and that they can hope to live beyond their teen years, something that wasn't likely 20 years ago. This book is the ideal guide for any reader who wants positive medical information about CF, offering an extensive glossary and listings of books, websites, and organizations about Cystic Fibrosis.
Reviews / Votes
A solid introduction to the disease...A plethora of stories accompanies each chapter....Young adults with the disease will feel a part of a worldwide community after reading this book. There is optimism as well as sadness here, but most of all there is the resonance of CF sufferers' voices telling others, 'You are not alone.' * School Library Journal * ...this great resource gives extensive medical and technical information as well as profound insight in the disease's human impact....this entry offers excellent research information for patients, families, and students. Its additional pages, however, provide even greater depth. Gripping personal accounts will pull in readers, teenage and adult, who are not familiar with the disease. * VOYA *More details
Series
Language
English
Place of publication
Lanham, MD
United States
Target group
Interest Age: From 12 to 18 years
Dimensions
Height: 260 mm
Width: 183 mm
Thickness: 19 mm
Weight
719 gr
ISBN-13
978-0-8108-4821-4 (9780810848214)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Person
Melanie Ann Apel began writing about CF in 1995 and has since published more than 40 non-fiction books for children and young adults. She worked as a pediatric respiratory therapist at Children's Memorial Hospital in Chicago for six years.
Content
Part 1 Medical Disclaimer
Part 2 Acknowledgments
Part 3 Introduction
Chapter 4 1. Cystic Fibrosis: The Facts
Chapter 5 2. A Genetic Disorder
Chapter 6 3. A Diagnosis
Chapter 7 4. A Daily Challenge
Chapter 8 5. Good Days and Bad Days
Chapter 9 6. Living and Laughing
Chapter 10 7. Other Complications
Chapter 11 8. A Second Chance: The Lung Transplant
Chapter 12 9. In the End
Chapter 13 10. Just over the Horizon
Part 14 Afterword
Part 15 The Fabulous List of CF Resources
Part 16 Glossary
Part 17 Glossary of CF Meds
Part 18 Bibliography
Part 19 Index
Part 20 About the Author
Part 2 Acknowledgments
Part 3 Introduction
Chapter 4 1. Cystic Fibrosis: The Facts
Chapter 5 2. A Genetic Disorder
Chapter 6 3. A Diagnosis
Chapter 7 4. A Daily Challenge
Chapter 8 5. Good Days and Bad Days
Chapter 9 6. Living and Laughing
Chapter 10 7. Other Complications
Chapter 11 8. A Second Chance: The Lung Transplant
Chapter 12 9. In the End
Chapter 13 10. Just over the Horizon
Part 14 Afterword
Part 15 The Fabulous List of CF Resources
Part 16 Glossary
Part 17 Glossary of CF Meds
Part 18 Bibliography
Part 19 Index
Part 20 About the Author