Cystic Fibrosis: The Ultimate Teen Guide

Przednia okładka
Scarecrow Press, 2006 - 259
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.
 

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Spis treści

Medical Disclaimer
Acknowledgments
Introduction
Cystic Fibrosis The Facts
A Genetic Disorder
A Diagnosis
A Daily Challenge
Good Days and Bad Days
Other Compilations
A Second Chance The Lung Transplant
In the End
Just over the Horizon
Afterword
The Fabulous List of CF Resources
Glossary
Prawa autorskie

Living and Laughing

Kluczowe wyrazy i wyrażenia

Informacje o autorze (2006)

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.

Informacje bibliograficzne