Stories of Cherubs Vol. II

"Stories of Cherubs Vol. II" coming out in time for the holidays! To submit your child's story you must be a member of CHERUBS & give publishing permission on your membership form. Then just e-mail your story and photo to membership@cherubs-cdh.org with your cherub's name and date(s) in the subject line. Submission deadline is October 15th!

You can still purchase "Stories of Cherubs" on our cafepress store at: http://www.cafepress.com/cherubs.91971767



Over 500 pages and 300 stories and photos of children born with Congenital Diaphragmatic Hernia. Families tell tales of what life is like to have a child with CDH and to sometimes lose those children. Heartfelt and honest, these stories are a wonderful tribute to cherubs and their families. This book is must have for family members and friends who struggle to understand CDH as well as wonderful guidebook for new and expectant CDH parents.

Shane's Video

This is a video of my son's life.

Shane Torrence (1/28/93-9/11/99), Left-Sided Congenital Diaphragmatic Hernia

For CDH Families -Need Stories for CHERUBS newsletter & book

Hi Everyone,

We're ready to start on our next newsletter and we need more stories of families who have dealt with Congenital Diaphragmatic Hernia (survivors and those cherubs in heaven). Stories (and photos) will posted on our web site, in our Silver Lining newsletter and in the next edition of our book "Stories of Cherubs" due out this winter.

If you would like to include your cherub's story please e-mail it to membership@cherubs-cdh.org.

You can read over 300 stories of families who have been affected by CDH on our web site at http://www.cdhsupport.org/members/index.php?c=44

Dawn

CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support
http://www.cdhsupport.org