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to CHERUBS- The Association of Congenital Diaphragmatic Hernia Research,
Advocacy, and Support |
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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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Everytime you search on-line, please use Goodsearch.com
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Sarah Elizabeth Rehm
11/22/98 - 11/24/98
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Congenital Diaphragmatic Hernia Research, Advocacy, and Support
Welcome
to our new 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!
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 2300 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.
For
more information on CHERUBS and CDH, please feel free to browse
our
site by using the navigation bar at the top of our web site.
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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Easter 2008, 8 years old
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Congenital Diaphragmatic Hernia Research, Advocacy, and Support
We
have a lot going on at CHERUBS; our new web site, new volunteers, a
charity
ball & golf tournament being planned, lots of new items in our
e-store
including maternity wear, local get-togethers and a grieving parents
get-together,
our newsletter is out, we have a new Angels for Cherubs program, and
much,
much more!
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Our
Awareness Activities:
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Our On-Line
Services:
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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.
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 June 7, 2008
Our
member section is updated 24 hours a day, 7 days a week.

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