Sunday, October 10, 2010

CDH HOPE Totebag Project Baby Shower - October 16th in Wilkesboro, NC

Calling all NC family and friends.... the Younce family is hosting a CHERUBS Baby Shower to collect items for our CDH HOPE Totebags - Giving hope to families of babies diagnosed with CDH !!!! There will be games and lots of party fun! Just like a regular baby shower but for a great cause! 


Saturday, October 16 · 2:00pm - 5:00pm

LocationThe Ruby Pardue Blackburn Adult Health Care Center
1915 West Park Drive Suite 200
North Wilkesboro, NC
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Wish List
Disposable Cameras
Baby Blankets (any material but wool)
Button up newborn or preemie shirts
Small or preemie pacifiers
Travel packs of tissue
Plaster Handprint and Footprint Kits
Baby Booties
Baby Hats
Small bottles of lotion
Small bottles of hand sanitizer
Small picture frames ( for the baby's hospital bed)
Baby's first haircut holders
Gas Cards
Restaurant gift cards (national chains please)

CHERUBS H.O.P.E. (Helping Other Parents Expecting) Totebag Program assists families expecting babies born with Congenital Diaphragmatic Hernia by providing them with much needed free information and support items through a community project in which all CDH families can participate and honor their children while helping new families affected by Congenital Diaphragmatic Hernia.

Over 100 new and expectant CDH parents join CHERUBS each year. This project was created for them, to help them through the first few weeks and months in dealing with Congenital Diaphragmatic Hernia.

CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support. CHERUBS is the original CDH non-profit organization founded in 1995 to help families and medical care providers of children born with CDH.

What is CDH?

Congenital Diaphragmatic Hernia (CDH) is a devastating birth defect that affects 1 in every 2500 babies. CDH occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth. The cause is not known.

50% of babies diagnosed with CDH do not survive. Of those that do survive, sometimes long hospitalizations and other issues occur. It is incredibly important for CDH families to have accurate information of all the treatments for Congenital Diaphragmatic Hernia so that parents can make informed decisions for the babies' care. Items included are a CDH Awareness Ribbon totebag, personal care items for baby and information for the parents and family. Our CDH Baby Book is over 200 pages of valuable CDH information and advice.
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