The Parker Reese Foundation

New Hope For Congenital Diaphragmatic Hernia

Need Pictures.

Posted by Jessica Singletary on June 15, 2008

****** UPDATE ******

Cristin brought up a great question about before and afters.  If your child is a survivor of CDH please send two pictures.  A NICU pic and a current pic. 

Thanks, Cristin!

 

We are wanting to put pictures of CDH babies through out the house and are asking each of you to send us either a 4×6 or a 5×7 picture of your choice of your child.  It will give the house so much meaning and will show other families just what this house is all about. 

When Ashley and I were given this opporunity we were blown away by Rob and JoAnna’s (homeowners) generosity and we wanted to do it not just for Parker but for every child who has been and will be born with congenital diaphragmatic hernia.  I want every person who walks in this house to feel what each of us feel every single day of our lives.  I want them to know all of our children. 

Please start digging out  the pictures and mail them to us at:

The Parker Reese Foundation

Post Office Box 2199

Elizabethtown, NC 28337

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One Response to “Need Pictures.”

  1. Cristin said

    Maybe a weird question but… Would you rather a baby picture, you know, in the hospital, tubes, wires etc…Or a ‘grown up’ picture… Or how about before and after??

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