My book I wrote is eligible for our 4-for-3 promotion on amazon.com

I

Iamqueenofeverything

New member
My name is Rebekah Phillips. I wrote a book called A Breath With God : My Battle with Cystic Fibrosis. I was diagnosed at age three months. I am now 34 years old and a teacher. I graduated from college with a degree in education.
Here are some highlights of the book:
• This is the book of my life and daily struggles with CF. In addition, I offer hope to those who are battling CF and any other disease.
• One section deals with TIPS FOR HOSPITAL VISITS on pages 96-97. Information will help those who visit patients in the hospital.
• One section deals with TIPS FOR HOSPITAL STAYS on pages 94-95. Information will help those who are hospitalized.
... • Information is provided about the Cystic Fibrosis Foundation and other organizations on pages 98-100.
• Additional information about the CF Foundation is on page 109.
I believe that this book will give others a realistic view of Cystic Fibrosis and how it affects the daily life of those with this disease. This book will increase awareness of CF and the great advances through research and treatments which have increased the life-span of those affected.

Here is the link:http://www.amazon.com/Breath-God-Ba...=sr_1_1?s=books&ie=UTF8&qid=1355354109&sr=1-1
 
R

rmotion

New member
Iamqueenofeverything said:
My name is Rebekah Phillips. I wrote a book called A Breath With God : My Battle with Cystic Fibrosis. I was diagnosed at age three months. I am now 34 years old and a teacher. I graduated from college with a degree in education.
Here are some highlights of the book:
• This is the book of my life and daily struggles with CF. In addition, I offer hope to those who are battling CF and any other disease.
• One section deals with TIPS FOR HOSPITAL VISITS on pages 96-97. Information will help those who visit patients in the hospital.
• One section deals with TIPS FOR HOSPITAL STAYS on pages 94-95. Information will help those who are hospitalized.
... • Information is provided about the Cystic Fibrosis Foundation and other organizations on pages 98-100.
• Additional information about the CF Foundation is on page 109.
I believe that this book will give others a realistic view of Cystic Fibrosis and how it affects the daily life of those with this disease. This book will increase awareness of CF and the great advances through research and treatments which have increased the life-span of those affected.

Here is the link:http://www.amazon.com/Breath-God-Ba...=sr_1_1?s=books&ie=UTF8&qid=1355354109&sr=1-1
Click to expand...

You need a 3rd party or a non profit to help you promote it. A press release not from you etc.
Looks good, good luck with it.
 
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