The Parker Reese Foundation

New Hope For Congenital Diaphragmatic Hernia

Letters For CDH.

Posted by Jessica Singletary on April 22, 2009

Check out this new blog started by Kellie Myers, Carter’s mom!  This girl totally rocks and her vision is amazing and very inspiring!  She’s looking for ideas to help get this thing off the ground.  Share your thoughts, comments, concerns, questions!  This is an opportunity for the CDH community to come together and make a difference in CDH awareness and research.  Too many babies are dying for us to sit back idle wishing we had done something.  Let’s put our minds together and make Letters for CDH a huge success!!!


2 Responses to “Letters For CDH.”

  1. Kellie said

    Thanks Jes! I don’t want to be MY project but OUR project. Something the entire CDH community can call theirs. Something that brings us all together in a fun project. It kinda makes me giggle to think of our recipient sitting at a desk covered in thousands of turquoise envelopes!!

  2. Sarah said

    I just found your website- what a great foundation! We are excited about the Letters for CDH & I hope it will bring this defect to light!

    Sarah (Mom to RCDH Noah, now 2 1/2)

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