CHERUBS - The Association of Congenital Diaphragmatic Hernia Research Awareness and Support
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CHERUBS - The Association of Congenital
Diaphragmatic Hernia Research, Awareness and Support
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Non-profit organization raising global CDH awareness, supporting all babies & families affected by CDH and
promoting
research into the causes, prevention & best treatments of CDH since 1995.
CHERUBS - The Association of Congenital Diaphragmatic Hernia Research Awareness and Support
CHERUBS Homepage
What is Congenital Diaphragmatic Hernia?
CHERUBS CDH Charity
Congenital Diaphragmatic Hernia Research
Congenital Diaphragmatic Hernia Awareness
Congenital Diaphragmatic Hernia Support
Congenital Diaphragmatic Hernia & CHERUBS News
CDH Conference, Fundraisers, Get-Togethers and More
Shop for CDH Awareness Gear
Make a Tax-Deductible Donation to CHERUBS
April 19th is the International Day of Congenital Diaphragmatic Hernia Awareness
CDH Support Forums Goodshop & Goodsearch for CHERUBSCDH Awareness ShopJoin the Angel ClubCDH HOPE Totebag ProjectCongenital Diaphragmatic Hernia Research BillCongenital Diaphragmatic Hernia Awareness
Pregnant with a baby diagnosed with CDH?Raising a special needs child born with CDH?Grieving the loss of a child born with CDH?
CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support



CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support

Preparing For The Birth Of Your Cherub



  • Learn as much as you can.  Read, read, read! 
  • Read all suggestions but do not take medical advice from anyone but your doctor!
  • Talk to your baby and read to him/her, even though you’re still pregnant.
  • Keep a diary or start a blog.  CHERUBS offers free blogs on our site to members.
  • Prepare a nursery and have a baby shower, just as you would if the baby was healthy.
  • Take pictures of your expanding belly.
  • Talk about how you feel, cry, scream- do whatever you need to do to cope.
  • Visit the hospital's NICU/PICU so that you can prepare yourself for what you will see.
  • Make sure to plan delivery at a hospital with ECMO.
  • Pack a bag (we have a list here in our Parent Reference Guide of suggested items to pack).
  • Designate one family member or friend to keep everyone informed before and after the birth so that you’re not overwhelmed with visitors and phone calls.
  • Prepare other children for a long hospitalization for the baby and what will happen.
  • Ask your doctor about steroid treatments to help the baby’s lung growth.
  • Talk to your partner about what is going on and might happen.   You both need to be on the same page and to be a team for your baby.
  • Try to get as much rest as you can.


 


CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support

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Copyright © 1995-2011.  CHERUBS.  All rights reserved.  Graphics & text created by CHERUBS may be used freely but we ask for a link back to our site.
CHERUBS is an IRS recognized public 501(c)III non-profit organization founded in 1995.
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CHERUBS - The Association of Congenital Diaphragmatic Hernia Research Awareness and Support
Mailing Address:  3650  Rogers Rd. #290, Wake Forest, NC 27587, USA
Office:  S. Main St, Wake Forest, NC 27587, USA
Telephone:  919-610-0129    Fax:  815-425-9155    Login Help  /  General Info