CHERUBS- The Association of Congenital Diaphragmatic Hernia Research, Advocacy, and Support
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CHERUBS Congenital Diaphragmatic Hernia Charity - Make A Tax Deductible Donation

 
CHERUBS subsists off of donations.  Though we are trying, we currently are not receiving any grant funding and all donations go to help us continue our work in research and offering services and information to families and medical-care providers of children born with Congenital Diaphragmatic Hernia.  We are run strictly by volunteers, no one gets paid for working for CHERUBS, so every penny of your donation will directly help families.  CHERUBS is an IRS recognized 501(c) Non-Profit Organization and all donations are tax-deductible. 

CHERUBS is extremely excited to announce 5 new funds to help the CDH community!

Click on the links below to make a donation directly into a specific fund:

CDH Family Support Fund – this fund covers all support services, including our web sites, newsletters, conferences, New Member Packets, get-togethers and other general operating costs.  CHERUBS does a lot for CDH families and the CDH community and we incur quite a few costs during so.  Just 1 newsletter mailing is now over $3000 for printing and posting with so many members.  Our conferences are also expensive.   Our monthly expenses are several hundred dollars for ink, postage, web site hosting fees, fax number, etc.  It takes a lot to fund an organization with almost 3000 members.  Remember, no one at CHERUBS gets paid and we have no office so every penny directly helps CDH families.  And all of our services are FREE so we do charge membership fees.  Only 2% of our members donate annually so we depend on public donations quite a bit. And the occasional grant as well.

CDH Research Fund – to pay for the $1000 a year cost of  research database hosting and to raise money for research organizations such as the International CDH Study Group – unless a request is made to go a specific hospital.  The CDH Study Group is a collective group of over 30 hospitals around the world specializing in CDH research.  We chose to support groups like this one because we know that every cent will go directly to research on Congenital Diaphragmatic Hernia and research will be brooder and more advanced when collaborating with dozens of hospitals and researchers together.  

CDH Family Assistance Fund – A majority of this fund will go to help families with travel expenses such as airline tickets and gas.  It will not go to lodging because CHERUBS highly recommends the free lodging available at Ronald McDonald Houses.  Families will submit confidential applications to assistance and a committee will consider each request.  Our goal is to make sure that all CDH families can afford to get to their cherub’s medical center and have a place to stay so that they can concentrate on their children instead of travel worries.   We hope to assist a family through this fund by this fall.  The remaining small percentage of this fund will go to Gabe’s Gifts, a new program that helps new and expectant families by supplying them with items needed.  This project will start this summer!

CDH Awareness Fund – this fund will help raise awareness of Congenital Diaphragmatic Hernia through balloon releases, giving away free CDH ribbon buttons and brochures and other items.  It will also cover advertising costs, billboards, video production and much more.

CDH Scholarship Fund – for CDH survivors and siblings. Families can raise money to give scholarships in honor / memory of their cherubs.   We hope to award our first scholarship in 2010.

This will all be funded through donations, grants and fundraisers.  Member and the general public will be able to donate directly to a particular fund of their choosing.  Donations not allocated to a specific fund will be deposited into the CDH Family Support Fund.  We are very excited about all 5 of these new funds!



To make a donation to CHERUBS, you can choose through 2 different methods:

.Donate with a credit card through our on-line store.
 
We take donations by most major credit cards through PayPal.com.  PayPal.com is the internet's most respected "send a check by e-mail" program.  By using our on-line store, you can donate using your credit card.  Please make sure to include the address of the family if you are making a donation in honor/memory of someone else.    If a fund is not specified, your donation will go to our CDH Family Support Fund.

In Honor / Memory of:
Mailing Address To Send Donation Acknowledgement To:  




   

.Send your check or money order through regular postal mail.

You can make your check or money order out to CHERUBS.  Please send United States currency only.

Don't forget to add your donation information.  Our mailing address is:

CHERUBS
3650 Rogers Rd. #270.
Wake Forest, NC 27587
USA


 
 

.Donation Information.
 

Please e-mail or include in your postal mail, the following information:

Your name(s) - How you want your name listed on your receipt and in the Thank-You Column of our newsletter.
Your mailing address - So that we can send you a receipt for your deduction on next year's taxes.
In Honor/Memory - Is this donation in honor or in memory of someone?  Please make sure to give us their name(s) .

If you would a Donation Acknowledgment sent to the family of the person the donation was made in honor/memory of, please also send us their mailing address.  The Donation Acknowledgment will only list your name(s), the name of the person(s) the donation was made in honor/memory of, and the date of the donation.  We never list the amount of the donation.
 
 


 

Thank you for supporting CHERUBS!

 

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.
   


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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