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Congenital Diaphragmatic Hernia (CDH) is a birth defect that occurs when the diaphragm does not fully form, allowing organs to enter the chest cavity preventing lung growth. CDH strikes 1 in every 2500 babies - 1600 babies each year in the U.S. alone. 50% of these babies do not survive. The cause is not known. It is CHERUBS quest to help lead the way in CDH research to find the cause, prevention and best treatment for these babies. Click on the graphic above for more information.
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Please help us to continue our work here at CHERUBS to raise more CDH
awareness, fund CDH research and to support families affected by CDH.
Our
staff is strictly volunteer and all donations are tax-deductible.
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Congenital Diaphragmatic Hernia Research, Advocacy, and Support
CHERUBS-
The Association of Congenital Diaphragmatic Hernia Research, Awareness,
and Support.
The
world's first and largest organization for families and medical care
providers affected by CDH. Where Congenital Diaphragmatic
Hernia Awareness is raised every day of the year, research is more than
just an abstract word or a future goal and our main objective always
has been and will be providing information, awareness, research and
support. The CDH Support Group about ALL families and
for ALL families - putting families and the CDH community first since
1995.
Welcome
to our web site! We invite all CDH parents to join our
free membership to access our on-line services.
Current
members can log-in by following our temporary
log-in instructions. Log In Trouble? E-Mail Us. Not A
Member? Click
Here to Join for Free!
IN
THE NEWS :
Sign
Petition to Stop
Ownership of
Congenital Diaphragamatic Hernia Awareness Trademark!
CHERUBS
was founded in 1995 to support families of children born with Congenital
Diaphragmatic Hernia (CDH) and to research possible causes and
better
treatments for CDH. Currently, CHERUBS is the world's largest CDH
organization, with over 2800 members in
37
countries and all 50 states; including parents, grandparents, foster
parents,
pediatric surgeons, genetic counselors, pediatricians, nurses, ECMO
directors,
respiratory therapists, and epidemiologists. CDH is a devastating
birth defect, affecting 1 in every 2500 babies. CHERUBS is an IRS
approved 501(c)III non-profit organization located in North
Carolina.
Membership for parents is free and our organization is run solely by
volunteers
and funded through donations from members and the public. CHERUBS
has been offering support and information to families affected by CDH
since 1995, raising awareness since 1995 and conducting research
surveys since 1997. We have worked tirelessly to help the
CDH community and to lead the support and education of parents dealing
with Congenital Diaphragmatic Hernia. CHERUBS has advocated
for research of CDH by promoting awareness and searching for the cause,
prevention and best treatment of Congenital Diaphragmatic Hernia.
For more
information on
CHERUBS
and CDH, please feel free to browse our site by using the
navigation
bar at the top of every page.
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Member
Log In
Not
A Member?
CDH Parent or Medical Professional?
Click
Here to Join for Free!
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Everytime you search on-line, please use Goodsearch.com
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Johnathan Robert Martin
2/26/99 - 6/9/99
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Kyle Thomas Peter
b. 11/27/97
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