Description
The day-to-day dealings of life as a cystic fibrosis patient are described through a series of flashbacks to a time when the author was an 18-year-old volunteer at cystic fibrosis overnight camp. From diagnosis to death, this book leaves no aspect of CF untold as it includes a description of the illness; a comprehensive discussion of who gets the disease and why; an explanation of the procedures involved in diagnosing the disease; coverage of the arduous daily therapies involved in maintaining the life of a person with cystic fibrosis; and, now that people who have CF are living longer because of available therapies, the new challenges of dealing with CF-related diabetes as well as making decisions regarding lung transplants are all covered.
Title Metadata
Author: |
Apel, Melanie Ann |
Publisher: |
Scarecrow Press |
Language: |
English |
Copyright: |
2006 |
Number of Pages: |
280 |
Dewey: |
618.923 |
Dewey Range: |
600s |
Binding Type: |
Hardcover |
Interest Age: |
15 |