CHERUBS- The Association of Congenital Diaphragmatic Hernia Research, Advocacy, and Support
CHERUBS Volunteers - On-Call Parents

 
 
We are so proud to have so many parents volunteer to be on-call! They are there to listen, lend a shoulder, and support other parents. If you need to talk, please do not hesitate to call one of these parents - they know exactly what you are going through and they want to listen. Please, only parents of children with CDH use these numbers. Our volunteers cannot give out medical advice or answer medical questions. If you need medical advice, please consult your child's doctor- if you have a question, please call CHERUBS' office at (252) 492-6003.
 
 
 

 
For Expectant Parents


Kate Crawford- (412) 414-7073
Kerrie Chamberlain - (541) 664-9016 
Tammy Spohr - (530) 273-2156



For Parents of Survivors


Elaine Moats- (406) 234-5038 
Tara Hall- (614) 275-0858
Ashley Jackson - (225) 271-04096
Andrea Ryan - (610) 927-9356
Daniel Hunter - older cherubs

For Grieving Parents

Corin Nava- (401) 524-9182
Freedom Green- (410) 363-7465
Kim Switzer (Canada) 
Danielle Kessner- (03) 5135 6999 (Australia)

 


 

 
CHERUBS- The Association of Congenital Diaphragmatic Hernia Research, Advocacy, and Support
DISCLAIMER:The information on all pages of this web site is for education only. It is not meant to be used in place of proper medical care and advice. CHERUBS does not encourage or discourage any medical treatments or procedures. Our purpose is to educate families and medical care providers so that they may make the best decisions for the patients' interests. You can not compare your child to other children born with CDH, they are all different. The opinions aired by members are not necessarily the views of all members, staff, or of CHERUBS.


 

 
Congenital Diaphragmatic Hernia Statistics

Click here to find out how many babies have been born with CDH since 2000.
Congenital Diaphragmatic Hernia

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CHERUBS is proud to a member of The Alliance of Congenital Diaphragmatic Hernia Organizations.

Alliance of Congenital Diaphragmatic Hernia Organizations

CDH Organizations from around the world, working together on one goal.  Helping families affected by Congenital Diaphragmatic Hernia.



We have had over 1 million visitors since November 14, 1997, with an average of 300,000 hits per month since 2007
This web site was last updated May 5, 2009
Our member section is updated 24 hours a day, 7 days a week.
   


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Copyrights of all graphics except photos and business logos (unless otherwise stated) are owned by CHERUBS & Sunset Web Design.
 
 

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