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Showing posts with label cherubs. Show all posts
Showing posts with label cherubs. Show all posts

Friday, April 13, 2012

CDH and CHERUBS on CNN iReport!

Please read, recommend and repost as well as comment to help us convince CNN to make this national news!

Senator Sessions Works With Charity To Help Save 1600 Babies Born Each Year With Mysterious Birth Defect

http://ireport.cnn.com/docs/DOC-775825



PRESS RELEASE: Sessions to Address “Parade of Cherubs” in Washington to Raise Awareness for Congenital Diaphragmatic Hernia (CDH)

FOR IMMEDIATE RELEASE

Media Contact:
Kelly Maicon
919.741.9784
kelly@anuevents.com

Sessions to Address “Parade of Cherubs” in Washington to Raise Awareness for Congenital Diaphragmatic Hernia (CDH)

WAKE FOREST, NC (April 9, 2012) – On Thursday, April 19, U.S. Sen. Jeff Sessions (R-AL) will meet with over 250 people participating in a “Parade of Cherubs” in Washington, DC, to raise awareness of a birth defect called congenital diaphragmatic hernia (CDH). Sen. Sessions’ two-year old grandson, Jim Beau, is a CDH survivor. In Jim Beau’s honor, the Senator’s family will take part in the event, and Sen. Sessions is requesting a Congressional Bill for the benefit of Congenital Diaphragmatic Hernia Research.

CDH is a birth defect of the diaphragm. It occurs when the diaphragm fails to form or to close totally and an opening allows abdominal organs into the chest cavity, inhibiting lung growth. CDH affects approximately one in every 2,500 babies, or about 1,600 babies in the United States each year. It is as common as cystic fibrosis and spina bifida. Roughly 50 percent of babies born with CDH do not survive. The cause is still unknown.

“CDH awareness and research is very important and especially to me because my grandson, Jim Beau, was born with CDH in 2009,” said Senator Sessions. “This is a life threatening birth defect that not many people have heard about. Only 50 percent of the babies survive and that number could and should be higher. Research and awareness are key and we are excited that CHERUBS chose to parade in DC this year.”

The parade has been organized through CHERUBS, a North-Carolina based grassroots nonprofit organization started by Dawn Williamson whose son, Shane, died in 1999 at the age of six from CDH complications. Children donned in wings will begin the three-mile walk at 10:00 a.m. at the Lincoln Memorial; they will travel past the Washington Monument and the White House, and conclude at the U.S. Capitol Building.

Massachusetts General's CDH Genetic Study Lab will have representatives walking in the parade. During their visit to Washington they will take blood samples from relatives of CDH victims for genetic research.

“We are thrilled to have so many survivors and families affected by CDH as well as the medical community come out to support the cause,” said Dawn Williamson, president and founder of CHERUBS. “Families from all corners of the country plan to participate in the parade, and we expect the number to grow as we get closer to the event.”

Several other cities across the U.S. are hosting a cherubs parade on the same day including, Chicago and Peoria, Ill.; Denver; Portland, Ore.; Seattle; and St. Louis. The St. Louis Fetal Treatment Institute, known for conducting in utero procedures on CDH babies, has been an integral part of organizing their local event. There will also be a national candle lighting in the U.K.

A virtual parade of Cherubs has been set up on Facebook and Twitter so people can show their support by uploading photos and videos from their smaller awareness/fundraiser events.

If you would like to help spread the word, or to learn more about CHERUBS and the upcoming parades, please visit www.cdhsupport.org.

###

Additional Events:

Washington DC Parade of CHERUBS takes place on April 19, 2012 starting at the Lincoln Memorial at 10:00.  It is being led by Dawn Williamson, President of CHERUBS and mother to Shane, a non-survivor and Melissa Larrison, Virginia State Representative and mother to Hanna Larrison, also a non-survivor.  http://cdhawareness.eventbrite.com

The Denver Parade of CHERUBS takes place on April 19, 2012, at Sand Creek Park starting at 3:30 pm. The event will start with the reading of the proclamation issued by Governor Hickenlooper and will follow with recognition of the health care professionals in Colorado who lend so much to the conduct and advancement of medical treatment for this congenital defect. A moment of silence will be observed in memory of those CHERUBS who have been lost to CDH. Finally, participants will take part in a three-stage balloon release in memory of our CHERUB Angels, in honor of our CHERUB Warriors, and in anticipation of those CHERUBS who will arrive soon. The event was organized by Nicolle Colvin the Colorado State Representative for CHERUBS, Victoria Grover, and Jennifer Rodi.  http://denverparadeofcherubs.eventbrite.com/

The Peoria Parade of Cherubs takes place on April 22, 2012 in Glen Oak Park beginning at 2:00 pm. The event was organized by Kristin Aigner and Sarah Polich. Kristin is an RN in the NICU and coordinates CDH Follow up Clinic at OSF St Francis Medical Center and is the sister of Christopher, who was born with CDH in 1973. Christopher grew his wings and flew to Heaven two months after he was born. Sarah 's daughter, Kalianna, was born with CDH and is now a happy, thriving 8 month old. The Parade route is around Glen Oak park, followed by a ceremony to honor Cherubs in Heaven, ending with the joy of being together, refreshments and kids playing in the park. 
http://peoria2012paradeofcherubs.eventbrite.com/

The Seattle Parade of CHERUBS takes place on April 19, 2012 and is being organized by CHERUBS Washington State Representative, Christina Stembler, whose Son, Hunter Stembler, was born with CDH. Christina invites Everyone that has been affected in any way by CDH, to take part in the parade. Meet on Pier 62/63 next to the Seattle Aquarium at 11:00 A.M. We will be walking to Waterfront Park and Releasing Balloons in Loving Memory of all CHERUBS lost and in celebration of CDH Warriors and the awareness that they share on a Daily basis.  http://seattleparadeofcherubs.eventbrite.com/

CHERUBS is working with Children's Memorial Hospital to put on the Chicago Parade of Cherubs. The Illinois Representative for CHERUBS, Neil Rubenstein, is organizinng the Chicago Parade. Starting at 11:00 a.m., participants will take part in a balloon launch at Oz Park to pay respect to all those Cherubs lost. Then they will be walk 1.2 miles by the hospital and the Ronald McDonald House (which so many CDH families frequent during their child's often long stay at the hospital). Close to 70 people (from three states) are expected to participate in this awareness event.  http://chicagoparadeofcherubs.eventbrite.com/

The St Louis Parade of CHERUBS takes place on April 19, 2012 and is a joint project of CHERUBS and the St. Louis Fetal Care Institute.  It will include a walk around the hospital grounds, a presentation, candle lighting and lighted balloon release.  http://stlouis2012paradeofcherubs.eventbrite.com/

Oregon & SW Washington members of CHERUBS will be holding Portland's "Parade of Cherubs" for the International CDH Awareness Daily Celebration in conjunction with several other cities in the USA & UK on Thursday, April 19th from 1:00 pm - 3:00 pm at Legacy Emanuel Hospital in Portland, OR. The local event is being coordinated by CHERUBS Oregon Co-Rep grandmother Shelly Moore & mother Alicia Gilbert to CDH angel Jayden Gilbert who died in March of 2010 after a 23 day fight against CDH & complications, and member Andrea Martin whose 12 year old daughter Sarah is a CDH survivor. http://portlandparadeofcherubs.eventbrite.com/

CHERUBS United Kingdom Representatives Clair Maher and Melanie Parsons are working with member Cara Stevenson to coordinate a national Light Up the Night Event with candles and lanterns. 
https://www.facebook.com/cdhsupport#!/events/248708328546723/

A Virtual Parade of Cherubs will include 100's of CDH families submitting stories, photos and video over social media.  More information can be found at https://www.facebook.com/CherubsVirtualParade

Congressional Bill - http://www.cdhbills.org

Saturday, March 10, 2012

CHERUBS In The Great Human Race on March 24




CHERUBS is thrilled to once again participate in the Great Human Race!!!!

Come join us and raise money and awareness for CDH!

REGISTER HERE - http://www.sportoften.com/events/eventDetails.cfm?pEventId=8026 

Make sure to list CHERUBS as your charity!


Facebook Event Page - https://www.facebook.com/events/310866708948911/





http://www.thevolunteercenter.org/tp42/page.asp?ID=143674

The Volunteer Center of Durham's 17th Annual GREAT HUMAN RACE is a 5k run and community walk that supports area nonprofits. This unique fundraising event supports 100+ nonprofits, schools and faith-based groups

provides an opportunity for any nonprofit agency to raise money for their own organization enables businesses and individuals to support the nonprofit of their choice has raised over $1.6 million since it's inception in 1996
broke fundraising records in 2011, raising $260,000 leading the way, Coalition to Unchain Dogs, raising over $34,000 for their organization expecting 1,000 runners and 2,000 walkers in 2012!


There are plenty of ways to get involved...run, walk, volunteer, donate or raise money for your favorite nonprofit.

The Great Human Race is excited to announce a NEW event venue and course Northgate Mall, in Durham, NC, is our new host. We will be able to expand our Nonprofit Marketplace and continue to offer the popular kids inflatable playground area, exciting local entertainment and refreshments. Parking is plentiful and Northgate Mall is easily accessible from all directions.

The new 5k course will wind through the historic Watts Hospital-Hillandale neighborhood. This gently rolling course will take runners and walkers through one of the loveliest and most active neighborhoods in Durham, a grand urban gesture.

Event Details:
Date: Saturday, March 24, 2012 (Rain or shine)
Location: Northgate Mall (near Sears Automotive) www.northgatemall.com
Day of Race Runner Registration: begins: 7:00am
Run starts: 8:30am
Walk starts: Immediately following runners 
REGISTER HERE - http://www.sportoften.com/events/eventDetails.cfm?pEventId=8026 

Make sure to list CHERUBS as your charity!

 

Monday, September 12, 2011

CHERUBS 2011 Holiday Vendor Show - November 13, 2011 in Wake Forest, NC

CHERUBS 2011 Holiday Vendor Show

November 13, 2011 ~  2:00 pm - 6:00 pm
Millroom At The Factory on South Main St.
Wake Forest, NC





CDH Christmas Vendor ShowOn November 13th at the Factory in Wake Forest, CHERUBS will hold our first annual Christmas Vendor Show!!!!    It will feature local vendors offering a variety of holiday gift items.    It will also include Angel Trees - artificial, pre-lit Christmas trees sponsored and decorated by local charities to be auctioned off for the those charities.  Special visit by Santa Clause, who will post for photos with children for a donation to CHERUBS.


FREE ADMISSION TO THE PUBLIC.



Our Vendors




CDH Christmas Vendor ShowLocal Charities
  • Download a Angel Tree Application Form
  • $100 per pre-lit, artifical tree
  • Each tree theme must be unique and pre-approved by CHERUBS
  • Silent auction bid starts at $100, all proceeds go to your charity
  • Tree must be fully decorated by 1:30 pm
  • Tree must be taken down and delivered to auction winner
     

Friday, October 1, 2010

2010 Masquerading Angels Ball



Come join us on the eve of Halloween for 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.

Our formal black and white masquerade ball encourages men to wear tuxedos and women to wear white.  Dust off your wedding dresses ladies, you are encouraged to wear it again or you can opt for a black dress or formal costume.

Event:  CHERUBS Masquerading Angels Ball

Date:  Saturday, October 30, 2010

Time:   6:00 - 7:00 cocktail hour, 7:00 - Midnight Ball

Location:   Hilton Durham near Duke University, 3800 Hillsborough Road, Durham, NC 22705

Beneficiary:  CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support. Money raised from this event will go to CHERUBS to fund services to further help families of children born with Congenital Diaphragmatic Hernia.  CHERUBS is a 501(c)III international children's charity.

Attire:  Our FORMAL black and white masquerade ball encourages men to wear tuxedos and women to wear white.  Dust off your wedding dresses ladies, you are encouraged to wear it again or you can opt for a black dress.   Ladies dresses must be floor length.  FORMAL period costumes are welcome, such as the one to the left.   Masks are required, some will be available for purchase at the event.   Not acceptible; typical Halloween costumes, short dresses, street clothes and scary masks.

Tickets:  $50.00.  Tickets include entry to event, casino, auction, ballroom.  It also includes entertainment, hors d'oeuvres, drinks, 2 raffle tickets, 1 bar ticket, 2 casino chips.   

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

Master of Ceremonies:  Bob the Blade from 96 Rocks

Special Guests:  Miss Raleigh, actress and model, Wendy Petty and Miss Durham County, Jacquetta Taborn

Live Band:  Bull City Syndicate / Mars Cafe

Casino:   Take a spin on the roulette wheel or try your hand at blackjack in our Casino Lounge.

Silent Auction:   Come browse our auction items donated by celebrities, local artists, local businesses and members of the charity.

Games:  Heads or Tails, Raffle, Poker, Guess the Angel Feathers and More.  Win amazing prizes!

Photographs:   Have your formal portrait taken, a reminder of a wonderful night.   Taken by Jim Shaw Photography.

More Information:   http://www.cherubsangelball.org


2010 Masquerading Angels Ball



Come join us on the eve of Halloween for 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.

Our formal black and white masquerade ball encourages men to wear tuxedos and women to wear white.  Dust off your wedding dresses ladies, you are encouraged to wear it again or you can opt for a black dress or formal costume.

Event:  CHERUBS Masquerading Angels Ball

Date:  Saturday, October 30, 2010

Time:   6:00 - 7:00 cocktail hour, 7:00 - Midnight Ball

Location:   Hilton Durham near Duke University, 3800 Hillsborough Road, Durham, NC 22705

Beneficiary:  CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support. Money raised from this event will go to CHERUBS to fund services to further help families of children born with Congenital Diaphragmatic Hernia.  CHERUBS is a 501(c)III international children's charity.

Attire:  Our FORMAL black and white masquerade ball encourages men to wear tuxedos and women to wear white.  Dust off your wedding dresses ladies, you are encouraged to wear it again or you can opt for a black dress.   Ladies dresses must be floor length.  FORMAL period costumes are welcome, such as the one to the left.   Masks are required, some will be available for purchase at the event.   Not acceptible; typical Halloween costumes, short dresses, street clothes and scary masks.

Tickets:  $50.00.  Tickets include entry to event, casino, auction, ballroom.  It also includes entertainment, hors d'oeuvres, drinks, 2 raffle tickets, 1 bar ticket, 2 casino chips.   

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

Master of Ceremonies:  Bob the Blade from 96 Rocks

Special Guests:  Miss Raleigh, actress and model, Wendy Petty and Miss Durham County, Jacquetta Taborn

Live Band:  Bull City Syndicate / Mars Cafe

Casino:   Take a spin on the roulette wheel or try your hand at blackjack in our Casino Lounge.

Silent Auction:   Come browse our auction items donated by celebrities, local artists, local businesses and members of the charity.

Games:  Heads or Tails, Raffle, Poker, Guess the Angel Feathers and More.  Win amazing prizes!

Photographs:   Have your formal portrait taken, a reminder of a wonderful night.   Taken by Jim Shaw Photography.

More Information:   http://www.cherubsangelball.org


Tuesday, June 15, 2010

2010 NC Zoo Trip on June 26th!


Date:  Saturday, June 26, 2010
Time:  9:30am - 3:30pm
Location:  Asheboro Zoo, Asheboro, NC


CHERUBS - http://www.cdhsupport.org/

NC CHERUBS Blog - http://cherubsnc.blogspot.com/

NC Zoo - http://www.nczoo.org/

Zoo Tickets - http://www.nczoo.org/visit/tickets.html


We will be there and hope to see you all there. This will be a great event! You can meet other NC CDH families, see the zoo, participate in the Save the Cherubs campaign and more!!!!

ALL members are welcome - expectant, survivors and grieving families!!! Si...blings, cousins, etc are welcome too! There is a lot of walking in the zoo so make sure to wear comfy shoes and bring strollers for the little ones.

If you can make it, please make sure to RSVP by checking "attending" on the event page. If you want to participate in Save the Cherubs, let me know so I can bring enough wings and make sure to have your paperwork with you and signed! :)

http://www.facebook.com/event.php?eid=113107268716137&ref=mf

We hope to see all of you there!!!! :)


Cheryl Sandoval
NC Survivors Parent Representative
910-551-7276
northcarolina@cherubs-cdh.org

Dawn Williamson
(temporary) NC Grieving Parent Representative
CHERUBS President & Founder
919-610-0129
dawn.williamson@cdhsupport.org

3 CDH Charities, 2 Contests!

It's a busy time on Facebook, there are now 3 CDH charities in 2 contests and all 3 need your help!   This is a quick, free way to help families affected by Congenital Diaphragmatic Hernia!

CHERUBS made it to Phase II in the APX Gives Back contest!!!!!


You can vote by going to http://www.facebook.com/apxalarm?ref=mf

Then click LIKE.
Next click the "Start nominating and voting".  
Click on the blue logo for Eastern charities
Scroll down and find CHERUBS and endorse us! EVERY DAY!  Repost too please! :)

On Friday, we were in 1st place but now in Phase II the votes have been reset so we need to get all the votes we can!!!   We have a chance to win $100,000!!!!  All winnings from this contest will go to CDH Research and CDH Support!!!!!!!! 



Almost 2 weeks ago we told everyone to get ready for the Chase contest to vote for Real Hope for CDH, now the contest has started and we have 2 members of ACDHO in the Chase Community Giving contest!!!!

 Dr. Kays watching over one of his cherubs

Real Hope for CDH in the Chase contest!

http://apps.facebook.com/chasecommunitygiving/charities/201505045-real-hope-for-cdh-foundation

Real Hope for CDH, affectionately known as "Kays Kids" is an ACDHO charity that helps fund the research of Dr. David Kays at the University of Florida in Gainesville / SHANDS.   Dr. Kays pioneered the "gentle ventilation" technique of ventilating CDH babies.  He is a wonderful doctor, a great man, a friend of CHERUBS for over 10 years and a saint to every family whose cherubs have been under his care.   All winnings from this contest will go directly to Congenital Diaphragmatic Hernia Research to learn how to better treat babies born with CDH.  To learn more about Real Hope for CDH, you can visit http://www.realhopeforcdh.com


The Olivia Raine Foundation (another ACDHO organization!) is also in the Chase Contest! 



Olivia Raine Richards

http://apps.facebook.com/chasecommunitygiving/charities/261968725-olivia-raine-foundation

The Olivia Raine Foundation is named in memory of cherub, Olivia Raine Richards.   Her family started this foundation in Michigan to help grieving parents pay for their childrens' funerals.   They are very low on funding right now and can use all the help they can get!   Please vote for them in the contest!  For more info or to make a donation, go to http://oliviaraine.org/


Thursday, April 8, 2010

New CDH Awareness Song and Video! "I'll Never Let You Go" by The Jammies

 This video includes many NC cherubs!

New CDH Awareness Song and Video!



"I'll Never Let You Go" by The Jammies

Available on iTunes soon. Proceeds donated to CHERUBS to help raise CDH Awareness


Featuring 736 children and adults born with Congenital Diaphragmatic Hernia, affectionately known as "cherubs". Members of CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support http://www.cdhsupport.org



Save the Cherubs CDH Awareness Campaign - http://www.savethecherubs.org

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. 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.

2010 Triangle March for Babies



Join CHERUBS as we represent the CDH community and help to raise awareness of birth defects in the Triangle March for Babies benefitting the March of Dimes.

http://www.marchforbabies.org/team/t1364045

Save the Cherubs Congenital Diaphragmatic Hernia Awareness Campaign

We have 6 North Carolina cherubs participating in this campaign!

Save the Cherubs
Congenital Diaphragmatic Hernia Awareness Campaign




Photo Taken By Mandy Sroka Photography - http://www.mandysrokaphotography.com/
Cherubs are everywhere.  They are your next door neighbor's new baby.   The little girl on the swingset at the park.   The teenager that sits behind your son in high school geometry class.   The person behind you in the grocery store line.    Their scars are hidden under clothes, their stories a bit sad and taboo to talk about - so the miracles are not seen with the naked eye and you have probably mistaken a cherub for a "normal" person many times.   But they are there; walkling miracles with invisible wings.   And missing babies that belong to the grieving parents who you don't see grieve;  your local bank teller, the man who held a door for you at the gas station, the old woman who drove the car in front of you at the stop light this morning.   Cherubs are everywhere.

Unless you have been affected personally by CDH, you probably have never heard of it.   The mission of "Save the Cherubs" is to make Congenital Diaphragmatic Hernia a phrase everyone knows how to say and everyone knows what it means.  By raising awareness, we hope to raise research funds to save these babies - Save the Cherubs.

Congenital Diaphragmatic Hernia occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth.   Babies born with CDH often endure long hospitalizations and other complications such as pulmonary hypertension, infections, feeding issues, asthma and temporary developmental delay.    Some babies develop worse complications and sadly, 50% of babies born with CDH do not survive.    The cause of CDH is not known.

Cherubs are people who were born with Congenital Diaphragmatic Hernia, a severe and often fatal birth defect that occurs as often as Cystic Fibrosis and Spina Bifida.  Every 10 minutes a baby is born with CDH - adding up to over half a million babies since 2000.   Yet, CDH is given very little media attention, virtually no research money and until CHERUBS came along in 1995 there was no information and no support for families of babies diagnosed with CDH.   We have no national telethons, no large corporate sponsorships.   We have been struggling for years to bring attention to CDH and now, we are going to do so on a national level.

For 15 years, cherubs have been the awareness symbol of Congenital Diaphragmatic Hernia (CDH).   Through this project, families around the world are working with CHERUBS, photographers and the media to raise CDH awareness in a unique and striking photo and marketing campaign, which we hope will take your breath away and make you want to learn more about CDH and how you can help save these children.

CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support  was founded in 1995 to give hope and information to families of children affected by Congenital Diaphragmatic Hernia (CDH).    We are a 501(c)III non-profit global CDH organization with members in 38 countries.    Run solely by volunteers and donations, CHERUBS strives to allow families to have free access to information materials, support services, awareness projects and to make a CDH connection with other families going through the same ordeal.  We are just a grassroots organization of families working hard to make a difference and trying to give Congenital Diaphragmatic Hernia Awareness wings to take flight.

CHERUBS is fighting hard to search for the cause, prevention and best treatments of CDH.   We invite you to help us to help these families and to help Save The Cherubs.


Congenital Diaphragmatic Hernia Awareness Ribbon

Media & Press Information for the "Save the Cherubs" Campaign




March 18, 2010 Press Release:

CONTACT:
Dawn Williamson *
awareness@cdhsupport.org
919.610.0129
http://www.savethecherubs.org




New 'Save The Cherubs' Campaign Brings Awareness To Little Known Deadly Birth Defect That Has Affected Over Half A Million Babies In The Past Decade


After struggling since 1995 to bring more awareness to Congenital Diaphragmatic Hernia, a birth defect that affects 1600 babies each year in the U.S., CHERUBS announces a national CDH Awareness Campaign.



Raleigh, NC - CHERUBS, a grassroots non-profit organization created and run by parents of children born with a severe birth defect, is leading the way in raising Congenital Diaphragmatic Hernia Awareness through a new campaign called "Save the Cherubs"

Founded in 1995 by Dawn Williamson, CHERUBS is the world’s first and largest Congenital Diaphragmatic Hernia (CDH) organization with over 3000 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 at Duke University Medical Center in Durham, North Carolina and endured many more hospitals both at Duke and at the University of North Carolina at Chapel Hill.  Immediately after Shane’s birth, Dawn searched for a support group, but there were none available.  After spending hundreds of hours in the hospital's medical library researching CDH and finding support only from parents she met at the hospital, Dawn felt a great need for a CDH support group.

“I wanted to create an organization to help those parents of children with CDH,” said Williamson. “I know exactly how it feels to be going through everything that they have to deal with and have no one to turn to, and I want them to know that CHERUBS is there for them every step of the way.”

CHERUBS serves the CDH community without charging parents or medical care providers for it’s services.  The amount of information and services that this group provides is staggering given that it receives no grant funding and has no paid employees. Fundraisers help to provide the services that CHERUBS offers, often on a shoe-string budget. Many charities are struggling during this economy and it is especially hard for smaller charities without marketing budgets to compete for media attention for awareness and for research funds.

CDH affects 1 in every 2500 babies, representing approximately 1600 babies in the United States each year and over 600,000 babies since the year 2000 - half of which do not survive. Some of the surviving babies, like Torrence’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, pulmonary hypertension or other long-term pulmonary problems.

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.  
“Once a child come homes, it is not uncommon for a parent of a child with CDH to have to explain the birth defect to their pediatrician or general practitioner.  When the medical community is not that aware of something as common as CDH, it makes it almost impossible to raise public awareness but we are determined to change that."

CHERUBS is indeed determined.   In addition to all of their other services and projects, they have taken on a national campaign to catch the attention of the public.   In their new "Save the Cherubs" campaign, the charity is working with photographers and families around the country to capture these children and the affects of CDH on camera.


"The mission of 'Save the Cherubs' is to make Congenital Diaphragmatic Hernia a phrase everyone knows how to say and everyone knows the meaning of.  Our campaign is a media blitz using photos of the kids dressed as cherubs (street clothes with wings) in photos doing real life things to emphasize that these kids are real… they exist, they could be on the playground playing with your kids. They could be the children of the people you shop beside or the baby your neighbor lost but no one knows because there is no awareness!"

The charity seems to have no shortage of photographers and models and hope that the media and marketing worlds will join in as well.   "We are raising money to try to pay for billboard advertisements, magazine ads and newspaper ads.  Our members are all joining it to contact marketing companies to see if they will donate space to help raise awareness.   Local newspapers, television stations and magazines through the country are also joining in and covering our campaign photo shoots.  This truly is a group effort of CDH families, photographers, the media, marketing companies and CHERUBS and we really believe that through this campaign we will have the opportunity to inform millions of people about CDH.   It is a momentous event because this is the biggest CDH Awareness project ever created."

"By raising awareness, we hope to raise research funds to save these babies - Save the Cherubs." 
said Williamson.  “There is still so much research that needs to be done and so many babies that need to be saved.”

"In 2010 this birth defect should not still exist, much less still have so many unanswered questions and so little research. We will keep fighting, keep researching and keep raising awareness until the cause and prevention of CDH is found. We work toward saving babies in the future and honoring those we have already lost.  
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 so that more babies are lost to this birth defect.  To have more research funds, we need more awareness."

We plan to work on several projects this year including an educational video on Congenital Diaphragmatic Hernia that will be free to families and hospitals. We also just published a CDH Baby Book are working on two Congressional Bills and are in the midst of planning many events, including our CHERUBS Angel Ball in Durham in August and our 2010 International CDH Conference in San Francisco in July.   We are always so busy at CHERUBS and try so hard to bring more attention to this birth defect and more services to families”.

If you would like to join in on this campaign or make a donation to help further their efforts, you can reach CHERUBS through the campaign web site at http://www.savethecherubs.org


###

About CHERUBS

CHERUBS is an international charity located in North Carolina founded in 1995. CHERUBS serves families of children and adults born with Congenital Diaphragmatic Hernia (CDH). CHERUBS has over 3000 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.

Representing CHERUBS and CDH Awareness at the 2010 Durham, NC "Great Human Race"

 

On Saturday, March 27th, CHERUBS members participated in the Triangle's Great Human Race.  It is an annual 5k walk / run for local Raleigh - Durham non-profit organizations.   

We had about 20 people represent CHERUBS and raise CDH awareness in honor or in memory of their cherubs! We even had an expectant mom who is 6 months pregnant join in!   Families representing CHERUBS included Gene and Becky Hobbs in memory of Andrew Hobbs, Craig and Dawn Williamson in memory of Shane Torrence, and Kendrah Kidd and Chris Ward in honor of their cherub who is due this summer.  

We had fun and we raised money for a good cause.  The final numbers aren't in yet but we raised over $1200 in our first year in the event!!!!  Not bad for walkers who literally finished LAST in the walk!  :)

It was so wonderful to meet new families and spend time with old friends.  Just walking and talking and knowing you're not going down the path alone can make such a huge difference to a CDH family! 

It was a very successful event.  One that we hope to participate in every year.   A huge thank you to the family and friends of Andrew Hobbs for all their hard work and for bringing CHERUBS into this wonderful event!


 



On the way back from the race, Dawn got a chance to meet another CDH mom, Julie Younce, mom of CDH survivor Aaron!

CHERUBS Members in North Carolina




CHERUBS Members in North Carolina as of January 1, 2010



Survivors:



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Non-Survivors:








Expectant families were not included.