Showing posts with label contest. Show all posts
Showing posts with label contest. Show all posts

Sunday, December 1, 2013

$10,000 CDH Research Grant Contest



VOTING HAS BEGUN! Vote once a day, every day until December 30th for your favorite CDH organization to win $10,000!

https://www.facebook.com/cdhsupport/app_303561899745219


23 CDH Research Centers from around the world in the running to win a $10,000 Research Grant to the center with the most votes on December 30th.   


Who are you voting for?

  • Baylor College of Medicine CDH Genetic Lab (genetic research)
  • Boston Children's Hospital CDH Clinic (repair material research)
  • Cincinnati Children's Hospital and Medical Center (surgical repair)
  • DHREAMS Research Study (Congenital Diaphragmatic Hernia) Lab (genetic research)
  • Mass General CDH Genetic Research Study (genetic research)
  • OSF St. Francis Medical Center (CDH Clinic)
  • Shands at the University of Florida CDH Clinic (gentle ventilation research)
  • St. Louis Fetal Care Institute (fetal research)
  • Texas Children's Hospital (fetal research)
  • The Center for Fetal Diagnosis and Treatment at CHOP (fetal research)
  • UCSF Fetal Treatment Center (fetal research)
  • International CDH Study Group (long term CDH care)
  • Sydney Children’s Hospital (Australia)
  • Universitätsklinikum Mannheim gGmbH (Germany)
  • Université Paris Descartes (France)
  • Ospedali Pediatrico Bambino Gesu (Italy)
  • University Hospital Gasthuisberg (Belgium)
  • The Hospital for Sick Children (Canada)
  • National Center of Child Health and Development (Japan)
  • Sophia Children’s Hospital (Netherlands)
  • Liverpool University (United Kingdom)
  • University of Oxford (United Kingdom)
  • Scottish Congenital Diaphragmatic Hernia Clinical Network (Scotland)

Monday, September 9, 2013

Upcoming Congenital Diaphragmatic Hernia Events

$30,000 CDH Research Fund Drive

Learn how easy it is for you and your family to fundraise in honor or memory of your cherub by selling raffle tickets and/or creating a Firstgiving page.   Read more...  
Read more »
Upcoming Events:

Now:

September:
October:
November:
December:
2014:

Tuesday, December 4, 2012

CHERUBS sponsors $10,000 Facebook Contest to Benefit CDH Research




Something very exciting is going on at CHERUBS and we want YOU to be a part of it! Thanks to all of you wonderful members and fans for buying and selling raffle tickets we are ready to award a $10,000 CONGENITAL DIAPHRAGMATIC HERNIA RESEARCH GRANT!!!! 

We could choose a hospital ourselves but we thought it would be more fun, and raise more awareness, to get your help! So the hospital with the most votes by December 30th will win $10,000 for CDH Research!!!!!!!!!!!!

Vote at https://www.facebook.com/questions/10151158907097006

In the running are the following CDH labs and clinics:


  • Congenital Diaphragmatic Hernia (CDH) Genetic Research Study
  • DHREAMS Research Study (Congenital Diaphragmatic Hernia) Lab 
  • St. Louis Fetal Care Institute 
  • Baylor College of Medicine CDH Genetic Lab 
  • The Center for Fetal Diagnosis and Treatment at CHOP 
  • UCSF Fetal Treatment Center 
  • Shands at the University of Florida CDH Clinic 
  • Boston Children's Hospital CDH Clinic 

 These facilities were chosen based on research history and long-term research so that the most families can be helped.

The prize money was raised by members and friends of CHERUBS through a 50/50 raffle fundraiser over the summer and early fall.   9003 tickets were told to raise $9003.00.  The addition $997.00 comes from CHERUBS CDH Research Fund.

Vote at https://www.facebook.com/questions/10151158907097006

Congenital Diaphragmatic Hernia

Congenital Diaphragmatic Hernia CDH occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth.   CDH occurs in 1 of every 2500 births; somewhere in the world, a baby is born with CDH every 10 minutes. 50% of babies diagnosed with CDH do not survive.  The cause is not known.  Over a half million babies have been born with CDH since 2000. 

CDH is as common as Spina Bifida and Cystic Fibrosis but there is very little awareness and even less research.  1600 babies are born with CDH every year in the United States.  Globally, a baby is born with CDH every 10 minutes.

CHERUBS is working hard to raise more CDH Awareness, and in turn, more CDH Research, while we continue to support families affected by this devastating birth defect.


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

CHERUBS LogoCHERUBS is a Guidestar Partner In Trust CharityCHERUBS is the world's first, oldest, and largest CDH non-profit organization.  We are truly a grassroots organization - CDH families creating something out of nothing when there was no other CDH group, information and services in 1995.  CHERUBS was created to make sure that no family endures Congenital Diaphragmatic Hernia without support or accurate information.  Our Board of Directors includes CDH parents, grandparents, survivors, nurses, doctors and the world's top CDH researchers. CHERUBS is run solely by volunteers and donations.  At CHERUBS, every CDH family has an opportunity to honor or remember our children while doing good to help others and work together as a CDH community. No other charity in the world has such a respected, educated or experienced group of leaders who care so much about the CDH community.

CHERUBS was not created by one family or for one family.   It was not created in honor or in memory of one child.   It is, and has always been, a group effort to help all families affected by Congenital Diaphragmatic Hernia.   It is built upon the experiences of CDH families, collaborations with CDH researchers and a strong desire to raise CDH awareness through projects and events created in honor and in memory of cherubs.   CHERUBS was named for all the babies lost to Congenital Diaphragmatic Hernia.

We are proud to serve over 4100 families in 54 countries and all 50 states affected by CDH since our creation.   Through our dozens of free ground-breaking services and the friendships made within our member community, CHERUBS has positively affected the lives of 1000's of CDH families and inspired many new CDH charities and project who have followed in our footsteps. We will continue to lead until Congenital Diaphragmatic Hernia is no more. We are devoted to finding the cause, prevention and best treatments for CDH.

Learn more about us through the links to the left.




Top Rated Charity of 2012 by Great Non-Profits



Top Rated Charity of 2012 by Great Non-Profits


Monday, October 4, 2010

Vote Reminder, Vote for CDH Pepsi Refresh Video and more!



As you all know, it's imperative to get on the leaderboard within the first 10 days of the contest.  so let's work extra hard the next few day to do that! 

Also, the rankings are wonky for the first week each month from the charities that roll over in the contest (like ours) so don't get discouraged by our placing right now - it will go up!

Remember, you can vote 3 ways each day!


Through Pepsi Refresh - http://www.voteforcdh.org   - vote for all 5 at once and vote also for some other great charities that are supporting us!  PLEASE SHARE THIS LINK.

Vote through Facebook - http://apps.facebook.com/pepsirefresh  Make sure to "share" each project on your FB acct to get others to vote as well.

By text - 

$250k CDH RESEARCH - text message 102542 send to 73774 (pepsi)
$50k Awareness - text 102365 to 73774
$25k Hospital Kits - text 101211 to 73774
$25k Financial Assistance - text 101202 to 73774
$25k Care Packages - text 102123 to 73774

Vote and comment daily and win a chance to the Masquerading Angels Ball!   And earn casino chips for the event!  http://www.cherubsangelball.org

Don't forget to get your photos and videos in ASAP for the Vote for CDH in Pepsi Refresh video!  Please send them by TODAY to membership@cdhsupport.org

Please forward this message.  Post the link and voting info to your wall.  Ask family and friends to vote.   It takes just 2 minutes and these babies really need these grants.   Just by voting, we can help 1000's of babies and families affected by Congenital Diaphragmatic Hernia!

Thank you all!!!

--
Dawn M. Torrence Williamson
President & Founder

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

Volunteer run 501(c)III non-profit organization serving over 3000 CDH families in 38 countries.  Searching for the cause, prevention and best treatments of CDH since 1995.

http://www.cdhsupport.org
http://www.cdhresearch.org
http://cdhsupport.blogspot.com
http://www.cdhconference.org

Phone - 919-610-0129
Fax - 815-425-9155
Mailing Address - 3650 Rogers Rd #290, Wake Forest, NC 27587, USA

Saturday, October 2, 2010

Press Release: Congenital Diaphragmatic Hernia Charity Recruits Voters to Win $375,000 to Help Critically Ill Babies And Their Families

Press Release:  Congenital Diaphragmatic Hernia Charity Recruits Voters to Win $375,000 to Help Critically Ill Babies And Their Families


Local Nonprofit Organization In National Pepsi Refresh Contest In The Running For $375,000 To Help Raise Awareness and Research Funds for Devastating Birth Defect

10-01-2010

Raleigh, NC - CHERUBS, a non-profit organization founded to help families of children born with Congenital Diaphragmatic Hernia (CDH) has climbed an uphill battle for 15 years to raise awareness and research fund and to continue to finance support services.  Now, they battle alongside other charities to fight for funding in the Pepsi Refresh contest.

On the first of each month, for 6 months, up to a dozen volunteers stayed awake until midnight when Pepsi Refresh opened the application process for new projects.  Feverishly clicking their computer keys to be one of the 1000 application accepted in the 2 minutes the system was open each month before the application limit was reached.  Finally, in July two applications made it through and they were in the August contest;  $25,000 to provide financial assistance for families hospital travel expenses and $25,000 to provide easy-to-understand information for hospitals.  For CHERUBS, the contest now began.

Coming off the all-summer long APX Gives Back contest, in which they they won 2nd place nationally for a prize of $30,000, CHERUBS members and voters were tired but diligently went back to work to try to win a Pepsi grant.   "Never did we expect to be in 2 huge contest back-to-back, nor have this incredible opportunity to try to win funds of this size.  But here we are and we are so excited for the chance to be able to fund so many greatly needed projects” said CHERUBS President, Dawn Williamson.

The contest grew even bigger for CHERUBS when 3 more projects made it into the September contest;  $250,000 for research funds, $50,000 for an awareness campaign and $25,000 for care packages for families.  With their previous 2 projects making the top 100 and rolling over to another month's voting, CHERUBS now has 5 projects in Pepsi Refresh.contest, an unheardof accomplishment.  "5 projects are a lot, but we didn't plan this and this is 5 opportunities, not 5 sure wins.  We have a lot of work to do to win even 1 of these project grants" says Williamson.  "These projects are laid out, every cent won has plans attached to it to help babies and families affected by Congenital Diaphragmatic Hernia.  All 5 of these projects could help 1000's. 30,000 babies are born with CDH every year and 15,000 of those babies don't survive.  There are 100's of thousands of CDH families who need help.  This is the largest grant possibility for these families that has been ever available.  We are excited about this opportunity to do so much good!"

CHERUBS members are excited too. The charity's web site shows photos of children holding up signs and asking for votes, while wearing wings and holding cans of Pepsi.  Facebook is littered with adorable profile photographs of more children asking for votes.  There are videos, bumper stickers, flyers, banners, signs in yards, school projects and 1000's of posts on-line to raise awareness and votes.  "The excitement is contagious.  Our members are so happy to be able to do something to help other CDH families.  CDH makes you feel so helpless, we don't often get opportunties like this to really make a difference by doing something as simple as voting.  And to be able to use our own children's photos and stories to raise awareness on such a huge level is thrilling for so many of us!" says Williamson.

CHERUBS not only raising awareness and voting for cash for their cause but an added bonus is networking with other causes. “We are so excited to be in this contest and to be in the company of so many other wonderful charities and projects! We have learned so much about other causes and became friends with many. No matter who wins this contest each month, we will all come out as winners. This has been a wonderful platform to raise awareness for all of our causes”.

Founded in 1995 by Mrs. Williamson and based here in the Triangle, CHERUBS is the world’s first and largest CDH organization with over 3400 members in 38 different countries and all 50 states. Dawn is the mother of Shane Torrence (1/28/93-9/11/99), born with left-sided CDH and multiple birth defects. Shane spent his first 10 months in the pediatric intensive care unit of Duke University and had many other hospitalizations and surgeries at the University of North Carolina at Chapel Hill.

“I miss my son every single day; CDH took him from me and robbed him of any type of normalcy during his short life,” said Williamson. “No mother’s arms should ever ache for a child she can no longer hold.”

Williamson made it her life’s mission to help other families affected by Congenital Diaphragmatic Hernia. If there is any doubt of faithfulness to this mission you need only to read the glowing reviews families around the world have posted all over the internet about how CHERUBS has helped them through their darkest days, see all the services listed on their web sites or count the over 12,000 fans they have on Facebook.

Congenital Diaphragmatic Hernia occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth. It affects 1 in every 2500 babies, representing approximately 1600 babies in the United States each year, half of which do not survive. Some of the other half, like Williamson’s son, who only lived until the age of 6, end up suffering through life with lasting health problems such as feeding aversions, gastrointestinal problems, asthma, allergies, scoliosis, or long-term pulmonary problems.

In the U.S., there are annually more victims from CDH than tornados, hurricanes and lightening strikes combined. There are more children born each year with CDH than there are children born with Cystic Fibrosis or Spina Bifida, and although there is no known cure or typical treatment, there is still a significant lack of research and awareness in the public and medical communities about CDH. According to a Congressional Bill the charity is hoping to get passed for CDH Research, the estimated total annual economic impact of Congenital Diaphragmatic Hernia in the United States is in excess of $800,000,000 while annual grants allocated by the National Institutes of Health for CDH at several research facilities is currently estimated at less than $5,000,000. Through this contest and other efforts, CHERUBS hopes to raise more awareness and funds for research and family support. “These babies are dying by the thousands and there is no known cause. The survival rate is only 50%. This just cannot be acceptable” says Williamson.

“This contest has not only allowed us to dramatically raise awareness about Congenital Diaphragmatic Hernia but it has offered us the opportunity to raise more money for our charity than we ever have before. $375,000 can do so many things for the CDH community and we are so grateful to Pepsi Refresh and to everyone who is voting for us.” For a small charity powered by volunteers, donations and fundraisers and run in a spare room of Williamson’s home to save funds, $375,000 could indeed go a long way. “We have over 3300 members and all of our services are free to CDH families. We run a very large web site with forums for families to gain information and support 24 hours a day, an annual international Congenital Diaphragmatic Hernia conference, the world’s largest CDH research database, we send care packages to new and expectant parents and so many, many other services on less than $35,000 a year. Our budget averages about $10 of assistance per family, which is ridiculous but we somehow pull it off. Winning this contest could do so much for our ability to help more CDH families!” says Williamson.

Families affected by CDH agree. “I vote because my sweet baby Mallory has opened our eyes to a terribled condition that we knew nothing about at the time. And from the statistics we have learned about CDH it saddens me that this illness is so unknown. CHERUBS has been my crutch from day one of diagnosis. I cannot imagine going through all of this without the support and information I have gotten from the organization and its members. Mallory was born on Jan. 4th of 2010, and still going strong in the hospital, and CHERUBS has been there for us every step of the way. God bless you all, and thank you from the bottom of my heart” says mom Sara Jimel Givent.

“I am voting in memory of our sweet Joshua who was born on March 26, 2010 and was with us 16 days. We love him and miss him terribly. If CHERUBS can win the $100,000, maybe another family won't have to go through this” wrote dad Jeff Campbell.

“Voting for my son Brandon who was diagnosed with CDH two days before his delivery in 2004. The only information we could find that even gave us hope was "CHERUBS". His outlook was not good but he is strong and healthy today because of UNC Children’s Hospital and Brandon’s drive to survive. Thanks CHERUBS for all the hard work and dedication that you provide for families struggling with this horrible birth defect. You gave us hope when we had none and during the long stay in the hospital. This continued even when we were dealing with many of the issues after we finally got him home” writes Fayetteville resident Cheryl Sandoval.

The fight to help these families is also obviously apparent in the members of CHERUBS. “When I was lost and all alone I turned to the internet hoping to find someone who cared...I found CHERUBS and a WHOLE BUNCH of FABULOUS someones who KNEW how I felt without me having to explain...CHERUBS has been my lifeline through our journey with CDH. There is always someone there with a comforting word when you need it, or someone who listen to you rant and vent when need be. It's a WONDERFUL group of people who I am proud to call my CDH family. I'm so sorry we've all met due to CDH, but if we all stick together, there's no telling what we can do to help rid the world of this terrible birth defect” says Canadian mom Shana Kelly.

CHERUBS welcomes the community’s support and votes in this contest. If you would like to help this organization you can vote through their web site at http://www.voteforcdh.org or through Facebook or text.

Proceeds from the contest will benefit CHERUBS Research, Awareness and Support Funds, and Williamson is hoping that the contest will bring out many supporters and media to help gain recognition for both CDH and the organization’s efforts.

CHERUBS will also gladly accept any donations to help further their work. Tax-deductible donations can be made on-line at http://www.cdhdonations.org or mailed to CHERUBS, 3650 Rogers Rd #290, Wake Forest, NC 27587.

To help raise more awareness and money for the organization, as well as funds to continue research and outreach, CHERUBS will be hosting a key fundraising event this fall. The CHERUBS 2010 Masquerading Angels Ball will be a formal event held on October 30th at the Durham Hilton near Duke with celebrity guests, a live band, casino and an auction. More information on this event is available at http://www.cherubsangelball.org

“There is still so much research that needs to be done. In 2010 this birth defect should not still exist, much less still have so many unanswered questions and so little research,” said Williamson. “CHERUBS wants to be able to help as many families as possible, because we understand the hurt and confusion that comes along with having a child with CDH. We want to spare other families from the devastating effects of CDH and we will keep fighting, keep researching and keep raising awareness until the cause and prevention of CDH is found.”


About CHERUBS

CHERUBS is a 501(c)3 organization located in North Carolina. CHERUBS serves families of children and adults born with Congenital Diaphragmatic Hernia (CDH). As of June 2010, CHERUBS has over 3400 members in all 50 states and 38 countries. Board Members include the founding father of in-utero surgery, genetic counselors, epidemiologists, pediatric surgeons and parents of children born with CDH. CHERUBS is a volunteer-run organization and a United States Internal Revenue Service recognized 501(c)3 Non-Profit Organization.

http://www.voteforcdh.org
http://www.cdhsupport.org
http://www.cherubsangelball.org


 





























 

Wednesday, September 15, 2010

CHERUBS & APX Press Conference


photo by Michael Cunningham of APX Alarm


On Monday, September 13th, CHERUBS and APX Alarm held a press conference.   CHERUBS was presented with a $30,000 check by APX Gives Back.   Dawn's speech and these photos say it all...

photo by Michael Cunningham of APX Alarm


11 years ago today I was saying good-bye to my son at a funeral home. Instead of picking out colleges, I got to choose his headstone.  Instead of dressing him up for the prom, I got to choose the clothes he was buried in.  That is something that no parent should ever have to do.  I will never see him grow up, fall in love, get married, have a career or become a dad.  That is something no child should be robbed of.  But Congenital Diaphragmatic Hernia did that.  It took his life and it takes the lives of over 30,000 babies every year. 

Congenital Diaphragmatic Hernia (CDH) occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth.  50% of babies born with CDH do not survive, the other 50% that do make it often endure long hospitalizations and many major surgeries. 

Congenital Diaphragmatic Hernia is not a rare birth defect.  It is as common as Spina Bifida and Cystic Fibrosis.  Annually in the United States, more people are victims to CDH than lightening strikes, tornados, hurricanes, earthquakes and floods combined.  Every 10 minutes a baby is born with CDH, every 20 minutes a family is devastated as they say good-bye to their cherubs.  In the past 10 years, over 600,000 babies have been born worldwide with CDH.  It has taken the lives of over a quarter million babies since 2000.  Yet there is little research and even less awareness.

CHERUBS was founded in 1995, right here in the Triangle. We've spent the past 15 years trying to raise awareness of Congenital Diaphragmatic Hernia.  We have screamed, begged and pleaded with the world to pay attention to these babies.  We've built sites, blogs, we've invested years in sharing our stories and photos of our children.  Without awareness, there are no research funds.  It's heartbreaking for us families to watch these babies die and struggle to survive and to feel like the world doesn't care about these children.  Raising CDH Awareness has been a large, hard uphill climb for us.

Until APX Gives Back.  APX gave us a platform to raise awareness on a level we've never been able to before.  We reached 1000's through Facebook, flyers, e-mails and APX's blog and Facebook pages.  Our members, CDH families, did such an incredible job raising votes and awareness.  We collected over 25,000 votes.  We begged, pleaded, drove our family and friends nuts to vote but along the way, a funny thing happened.... people became aware of Congenital Diaphragmatic Hernia.  Strangers from other charities became friends and learned about CDH and voted for us.  Strangers on the street saw a flyer and voted for us.  1000's of people who had never heard of Congenital Diaphragmatic Hernia learned about the contest and voted for us.  We have met so many amazing people and our childrens' stories touched their hearts and they learned about CDH.  

APX did this.  Through their generousity in the APX Gives Back program, they helped us to not only raise awareness but gave us the opportunity to win $30,000.  2 amazing, amazing gifts.  CHERUBS is run strictly by volunteers.  We have no office.  No grant funding.  No sponsors.  We provide services to over 3200 families in 38 countries on a shoestring budget made up of donations, lots of sweat and tears and prayer.  Our annual donations average $30,000.  APX has DOUBLED our annual budget for this year. 

This means that we can now afford to get our research database up because we can hire a programmer to do the work I don't know how to do.  We can get a toll-free number so families can call us without incuring a phone bill.  We can send out newsletters again, update our member forums and supply more care packages to new and expectant families to give them hope at a time of a devastating diagnosis.  APX Gives Back made that all come true.

How do we thank APX for all of this?  There are no words.  But there is gratitude now where there was worry on how we would fund services.  There is pride on the faces of every CHERUBS family in what we worked so hard for all summer and accomplished.  And there is hope for the services and projects we can now offer them.   I know words do not suffice but on behalf of the 1000's of families that you have touched, thank you.







Thank you so much to the amazing people at APX Alarm;  to the employees who donated money to make this contest possible, to Anne Marie who feels like part of our CHERUBS family now, to Tom who was our guardian angel and go to guy during the contest, to Josh for doing such a great job leading such a great group of people and to Todd, for starting it all.   May God bless you all as much as you have blessed our cherubs and our charity.

And thank you to all of our amazing, amazing members who worked so hard all summer long to make this dream come true!!!!!   We have made our children proud!  :)