Showing posts with label chapel hill. Show all posts
Showing posts with label chapel hill. Show all posts

Monday, March 5, 2012

2012 CHERUBS Masquerading Angels Ball - Save the Date!

2012 CHERUBS Masquerading Angels Ball



October 20, 2012
6:00 pm - Midnight
Hampton Inn & Suites in Brier Creek
Raleigh, NC





We have just begun planning our 2012 event.  Stay tuned for more information!!!!









Formal Charity Masquerade Ball


Masquerade BallCome join us or a magical night for a good cause.  Celebrity guests, enchanting decor, amazing music, a casino, silent auction and beautiful attire will make this a night to remember.

Money raised from this event will go to CHERUBS to fund services to further help families of babues born with Congenital Diaphragmatic Hernia.  CHERUBS is a 501(c)III international children's charity.

Attire:  Our FORMAL  masquerade ball encourages men to wear tuxedos and women to wear floor-length gowns.  FORMAL period costumes are welcome.  Formal evening gowns are welcome.  Formal masquerade masks are highly encouraged.   Not acceptible; typical Halloween costumes, short dresses, street clothes and scary masks.   This event is no longer black & white and all colors of attire are welcome.

Age Requirement:  You must be 21 years old or older to attend.   CHERUBS reserves the right to refuse ticket sales when necessary.





Formal Charity Masquerade Ball




Our Organization:
CHERUBS is a 501(c)III organization located in North Carolina.   CHERUBS serves families of children and adults born with Congenital Diaphragmatic Hernia (CDH).   As of April 2008, we have over 2250 members in all 50 states and 33 countries.  Our Board Members include the founding father of in-utero surgery, genetic counselors, epidemiologists, pediatric surgeons and parents of children born with CDH.  We are a volunteer-run organization and a United States Internal Revenue Service recognized 501(c)III Non-Profit Organization.

www.cdhsupport.org


What is CDH?
Congenital Diaphragmatic Hernia (CDH) occurs in approximately 1 in every 2,500 births (1,600 cases in the U.S. each year).  The cause of CDH is not yet known.  The diaphragm is formed in the first trimester of pregnancy and controls the lungs' ability to inhale and exhale.  CDH occurs when the diaphragm fails to form or to close totally and an opening allows abdominal organs into the chest cavity.  This inhibits lung growth.     The cause is not yet known.

Roughly 50% of babies born with CDH do not survive.   Of the 50% that do survive, most will endure long hospital stays, feeding issues, asthma and other problems.  A few of the survivors suffer from severe long-term medical issues.

CDH occurs as frequently as Spina Bifida and Cystic Fibrosis, yet there is very little research being done and virtually no media coverage.

Wednesday, November 10, 2010

CHERUBS and CDH on TV

A few weeks ago, CHERUBS was on television to talk about CDH and the Masquerading Angels Ball.  So much has been going that we forgot to post it on our blog, so here it is! 

http://triangle.news14.com/content/in_depth/631902/in-depth--dawn-williamson--cherubs

Friday, October 8, 2010

Lots of CDH News!

We have a lot going in the next few weeks.  Please make sure to not miss out on anything:




Vote for CDH in Pepsi Refresh

http://www.voteforcdh.org



Our Congenital Diaphragmatic Hernia project is now ranked #11 nationally in the $250,000 category.  We have moved up over 40 places in the past 10 days!  We must make it to the top 2 positions to win this grant... we need your help.



2010 Masquerading Angels Ball


http://www.cherubsangelball.org


October 30th at the Durham Hilton near Duke University.  Live band, casino, silent auction and much more.  Many members are flying in from all parts of the U.S.  We would love to see you there too!    Vote in Pespi and you win a trip to the Masquerading Angels Ball or earn free casino chips.  Details on the site.



2010 Masquerading Angel Ball Basket Donations


Many of you are donating themed baskets in honor / memory of your cherubs.... thank you!!!!  Please get those to us by October 15th!  CHERUBS, 3650 Rogers Rd #290, Wake Forest, NC 27587



2010 Raffle for Romantic Hot Air Balloon Ride for 2 with Champagne

http://cdhangelball.blogspot.com/2010/10/cherubs-raffle-romantic-hot-air-balloon.html



Tickets are just $5.00 each and you can redeem your prize in 1 of over 140 cities in the United States until October 30, 2011.  Tickets on sale on-line only until October 28, 2010.  Drawing will take place at our Masquerading Angels Ball.



Trick or Treat for CHERUBS


http://www.trickortreatforcdh.info/


Many of our cherubs cannot eat by mouth so instead of collecting candy you can collect change for a good cause and raise CDH Awareness!






Tastefully Simple Fundraiser


http://www.tastefullysimple.com/Default.aspx?TabID=40  (Consultant ID#   0025718)  
 A Tastefully Simple Coordinator is donating 20% of her profits from all of the Tastefully Simple sales book party to CHERUBS.  She is opening this to anybody who is interested in having a book party, even if they don't live in her state. Everything can be done on-line.


If you are interested, or know anyone who may be interested, please contact Stacey Stocker at simplystocker@yahoo.com.


Scenty Fundraiser

https://barbarawagner.scentsy.us/Home

  CDH mom and CHERUBS Volunteer Barbara Wagner has started another SCENTSY fundraiser for CHERUBS!! 

 


2011 CDH Cherubs Calendars

Our 2011 calendars will go on sale on December 1st.   If you would like to submit your cherub's photo, please e-mail to membership@cdhsupport.org and make sure to include his/her name and date(s).  ALL cherubs are welcome (non-survivors too).  Photo submission deadline is October 31st.




Save the Cherubs CDH Awareness Campaign


http://www.savethecherubs.org


We also will have a 2011 Save the Cherubs calendar.  We need photos for the holiday months.  Photo submission deadline is October 31st.

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!  :)

Monday, August 30, 2010

Charity nabs $30K prize

CHERUBS in the Raleigh News & Observer Newspaper again!

 


Charity nabs $30K prize

Grant doubles budget

- Staff Writer

They're pink-haired and sleep-deprived, but they pulled it off.

CHERUBS, a nonprofit organization run out of a Wake Forest mom's spare bedroom, nabbed a $30,000 grant from APX Alarm Co. on Monday, thanks to 35,000 online votes they campaigned hard - and creatively - to get.

The grant will double the operating budget for the all-volunteer organization, which aids families of children born with an often fatal birth defect called congenital diaphragmatic hernia.


  • CHERUBS, a local nonprofit that helps families of children born with an often fatal birth defect called congenital diaphragmatic hernia, is in the running for two $25,000 grants in the Pepsi Refresh contest. Vote online at refresheverything.com , or at voteforcdh.org .
Since voting opened online in June, the group worked to drum up awareness and votes. That's where the pink hair comes in.

Volunteer and CDH mom Julie Younce of Wilkes County promised to dye her hair pink if 50 people would commit to vote every day for a week.

Her son, her best friend and her daughter soon joined her.

"When you have six kids, people don't typically expect you to have pink hair, so I've gotten a lot of questions about it," Younce said. "Which helps raise awareness, so it works really well!"

The money will be officially awarded to CHERUBS in September, but founder Dawn Williamson already has every penny accounted for. A large portion will go toward research, including work on a database of CDH medical histories that the group has been compiling for 10 years. The rest will go toward supplies for families dealing with their child's long-term hospital stay.

CHERUBS was in the running for the national grant of $100,000, but lost by fewer than 3,000 votes to the Utah Prader-Willi Syndrome Association. It's not the top prize they were aiming for, but in this case, second best is more than good enough, Williamson said.

Their final vote tally was 35,243 votes, according to APX Alarm spokesman Stuart Dean. Williamson chalks much of that up to their hard work and creative campaigning.

CHERUBS even got help from celebrities such as actress Patsy Pease from daytime drama "Days of Our Lives" pitching in on Facebook and Twitter to encourage folks nationwide to vote for CHERUBS.

The organization is still vying for two $25,000 grants from the August Pepsi Refresh contest at refresh everything.com .

Williamson passed on the hair dye, but says she'll get a winged CHERUBS tattoo on her diaphragm if they win one of the Pepsi grants.


Monday, August 23, 2010

PRESS RELEASE: Local Nonprofit Organization Wins $30,000 In National APX Gives Back Contest To Help Raise Awareness and Research Funds for Devastating Birth Defect



Local Nonprofit Organization Wins $30,000 In National APX Gives Back Contest To Help Raise Awareness and Research Funds for Devastating Birth Defect

08-23-2010

Raleigh, NC - CHERUBS, a non-profit organization founded to help families of children born with Congenital Diaphragmatic Hernia (CDH) learned about a contest on Facebook through a member expecting a baby with CDH.

Alarm company, APX, based out of Provo, Utah is known to be very generous to the non-profit community. This contest was yet another way that this company gives back. 5 lucky charities won $30,000 and another charity walked away with a grand prize of $100,000.

CHERUBS was one of the lucky charities who won $30,000 but they were also the 2nd in the nation, losing out of the first place prize by less than 3000 votes.  They raised over 35,000 votes through Facebook during the summer and came in a very close second-place.

"It was a very close race all along and we tried our best but we just didn't have the resources and manpower to pull it off this year.   But we gave them a run for their money and we won $30,000 for our cause so we definitely came of this contest as very big winners!" says CHERUBS President and Founder, Dawn Williamson of Wake Forest, NC.

The race wasn't without it's fair share of drama and suspense.   "There were some technical issues with the application software that didn't allow our charity to post links like others charities but that just made us work harder!  We bounced back between 1st and 2nd place throughout the contest so it was very nerve-wracking to say the least.  We had celebrities posting and tweeting for votes for us.  Doctors and researchers in their labs voting for us.  Kids made "vote for CHERUBS" signs and their parents took photos that we used throughout the contest.   Even soap star Patsy Pease took a photo with her son, who was born with CDH, to raise more votes.  We did raffles, passed out flyers, voter recruiting contests and we even had members dye their hair pink and blue to get more votes.   I myself even promised the charity members that I would get a tattoo if we won 1st place so on the bright side, I'll be avoiding that now!" says Williamson, laughing but she has since decided to get that tattoo if CHERUBS wins in the Pepsi Refresh grant contest that they are also currently competing in.

The APX Gives Back contest was made possible through a software application on the popular social media site, Facebook. It began on May 3rd with Facebook users nominating their favorite charities in 5 regions. On June 14th, the top 15 charities from each region made it to Phase II, where the votes were reset and the real competition began. The charity with the most overall votes on August 21st to be awarded $100,000, while the other charities in the remaining regions with the most votes will receive $30,000 donations.  CHERUBS won first place in the Eastern Division.

“We are so excited that we had the opportunity to be in this contest and to be in the company of so many other wonderful charities! We have learned so much about other causes and became friends with many, including members from the Prader-Willi Syndrome Foundation (the 1st place winning charity).   We also made wonderful friends and collaborations with other charities Now I Can, Military Moms and Wives of Brazoria County, Handprints of Hope and Quest.  No matter who won in this contest, we all came out as winners. This has been a wonderful platform to raise awareness for all of our causes” said Williamson.

The charity will be presented with an award check on September 14th, when the president of APX will fly out from Utah to present the $30,000 to Mrs. Williamson and other charity board and members at a press conference here in the Triangle.

Founded in 1995 by Mrs. Williamson and based here in the Triangle, CHERUBS is the world’s first and largest CDH organization with over 3300 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. I lost the chance to watch him grow up and grow into a young man; learn to ride a bike or drive a car; go to college or get married or have children of his own,” said Williamson. “No mother’s arms should ever ache for a child she can no longer hold. Shane was an amazing little boy that was always happy despite the fact that he spent so much of his life in the hospital. CDH devastated our family.”

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 11,000 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 hundreds 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. This $30,000 prize doubled our annual budget and we are so grateful to APX and to everyone who voted 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, $30,000 will 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 will do so much for our ability to help more CDH families!” says Williamson.

Proceeds from the contest will benefit CHERUBS Research 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.  "We raised so much Congenital Diaphragmatic Hernia awareness in this contest!  We introduced CDH to tens of thousands of people and that is more awareness than CDH has ever had in history.  We are so proud of that!" says the beaming Mrs. Williamson

The fight for funds for CHERUBS isn't over yet, they have also have 2 projects currently in the Pepsi Refresh contest;   $25,000 for financial help to families facing hospitalizations with their children to cover travel costs and $25,000 for CDH materials for hospitals.   "Both of these projects desperately need funding and would make a world of difference for families affected by CDH".

CHERUBS welcomes the community’s support and votes. If you would like to help this organization you can vote and learn more about Congenital Diaphragmatic Hernia at http://www.voteforcdh.org

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 3300 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