How Charlie Mouse Learned About Cystic Fibrosis
by
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I have learned that when you have 65 Roses, you need to take a lot of medicines, do treatments, therapies and eat a special diet just to stay healthy. There were times when Timmy really did not want to do any of it; he just wanted to play like everyone else. If Timmy did not do it all, he knew he would just feel sick, so it was best just to get them done.
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About the Book
Explaining to fellow peers about Cystic Fibrosis and how it effects your everyday life, can be very tricky. Especially if you are a young child learning yourself. New friendships are always exciting! Join Charlie Mouse and Timmy while they build a friendship and Charlie Mouse learns about Cystic Fibrosis.
About the Author
Shortly after the birth of our son, came the diagnoses of Cystic Fibrosis. Like many others I had no idea what Cystic Fibrosis was or what that meant for our son. The reality of it all was ………….and still is heart wrenching, for currently there is no cure for Cystic Fibrosis. Suddenly life as we knew it stopped and a new chapter began. This new life became a juggling act, of appointments, dietary needs, medications, treatments and therapies, along with a healthy splash of everyday life. I wrote this book as my way of helping raise awareness of Cystic Fibrosis. Not only for young children who have Cystic Fibrosis but also for their fellow peers. With knowledge comes understanding. Please join with me to help raise funding for Cystic Fibrosis. ALL profits from this book will be donated toward CF Research into finding a cure.