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Thread: CHERUBS and the American Pediatric Surgical Association

  1. #1

    CHERUBS and the American Pediatric Surgical Association

    This week in Puerto Rico, 3 CHERUBS Board Members represented our organization and CDH families at the APSA convention.

    We were able to talk to 100's of pediatric surgeons and start projects with several of them. We have an amazing project going on with the CDH Study Group, a group of about 90 CDH centers. We talked with doctors from every CDH center; we talked with many of the best CDH researchers in the world. We supplied data for families, ribbons for doctors (that were even worn during research speaches). Several surgeons even came up to us and thanked us for being there and for all we do for CDH families.... that touched our hearts so much to know they think we're doing a great service for their patients!!! We won't name all the doctors we talked to and we won't reveal our projects right now but we do want to thank the following for their invaluable information; Kevin and Pam Lally, Michael Harrison, David Kays, Priscilla Chui, Charles Stolar, Duncan Phillips, Bradley Rodgers and the doctors at UCSF, Boston Children's, Duke, CHOP, Cinncinnati Children's Hospital, the Canadian Pediatric Surgical Association and ACDHO.

    The conference went incredibly, amazingly well. We learned A TON about so many different things and now have all the absolute latest research on CDH. We talked with many surgeons on ways to help families, create more CDH awareness and research together. It was an extremely exciting and productive meeting.

    We even went snorkeling with a few of the surgeons and shared flights with some as well. Every opportunity educated us more and more about CDH and what all CDH research centers (including CHERUBS) has to offer.

    On Saturday we also met in person with Pam Lally of the CDH Study Group and looked over each of our databases (confidentially of course) and spent a few hours discussing our research and findings for both organizations. We have big, big, BIG plans and are so incredibly proud and honored to working with the CDH Study Group and all 90 CDH Research Centers. It is CHERUBS objective to work with ALL CDH research centers and to accomplish as much as possible in the realm of CDH Research.

    It took us 14 years to get here - but we did it. To do this research and have it make a difference. This is our 3rd attendance at an APSA conference - CHERUBS was the very first non-profit ever admitted into this event in 1995. In 2009, most of the surgeons knew exactly who CHERUBS is and what we stand for! We have come a long, long way since then!! We truly could not have had a more positive or productive conference or been made to feel more comfortable and welcomed and like part of the group.

    I have to say thank you to Barb and Bren…. they both did an amazing, amazing job and I am so, so proud of them and so grateful to them. Our Board Members paid for our travel expenses out of our own personal pockets and conference costs were paid for by grants. Not a single penny from donations went to help send CHERUBS to this conference but 1000's of CDH families will benefit from all the amazing things are happening!

    It's been an absolutely incredible week for CHERUBS and for all CDH families around the world!

    Stay tuned for more details, more research news and more research data!











    Mom of Shane (1/28/93-9/11/99) LCDH x6 and multiple complications and birth defects.

    Founder and President of CDH International.

    Executive Director of:

    CDH International USA
    CDH International UK
    CDH International Canada
    CDH International Switzerland
    CDH International Netherlands
    CDH International Singapore
    CDH International Hong Kong

    Messages may be answered by CDHi Team.

  2. #2
    Wow! That's amazing!
    Mom to Brooke-3/22/04- Braden-3/13/08-RCDH diagnosed at birth- treated at CHOP- CDH repair at 1 day old- home on day 12- Orchiopexy for undescended testicle (4/13/09)- Myringotomy with tubes bilateral (ear tube surgery-7/6/10)
    North Carolina State Co-Rep http://i291.photobucket.com/albums/l...bon-braden.jpg Braden's video http://www.onetruemedia.com/shared?p...edium=text_url

  3. #3
    Sounds like you 3 had a wonderful time and what wonderful work you are doing to further CDH research and awareness and helping all CDH families!!! I am so happy the trip was productive and I hope you have a lot to share with us all.
    Tracy - mom to Ian, LCDH diagnosed at birth, 4/3/04. Ian was born at 36 weeks, spent 53 1/2 days in NICU, 7 days on ECMO, surgery was on day 5, 29 days on a vent, 23 days was an oscillating vent, 546 days on oxygen. Inguinal right and left hernias and undescended left testicle surgeries were done on day 48. Currently has heart related medical issues and exercise induced asthma, but is one happy, happy boy!! Also mom to Cole - 13, Shane - 9, and Toby - 4. CHERUBS Parent Advisory Board Member and Co-Chair, Volunteer Co-Coordinator, and Wyoming State Representative.
    email: tmeats@cherubs-cdh.org

  4. #4
    Thank you ladies. I'll be posting summaries of the CDH research later today or tonight. There is so much exciting CDH research going on!!!!! Our database and the CDH Study Group database working together is the first research of it's kind and will hopefully open up all sorts of research information! Several hospitals are starting / updating their CDH research. 1 hospital is on the absolute verge of finding a genetic link to CDH. We have new stats for CDH, confirmation that the CDH survival rate is STILL just 50% (despite a lot of research articles and CDH sites stating otherwise). We know now how many CDH babies are seen per each of the 90 hospitals in the CDH Study Group. So many, many babies aren't making it to the CDH centers. We have a TON of work to do!!!

    I know I don't post much on the boards here lately... I hope you all understand why now... because I'm knee deep in all of this. We've been working hard on this, planning, researching... for the past 6 months. We had such a HARD time keeping all this secret from everyone!!! LOL And yet, there is so much more that we still can't tell... yet!
    Mom of Shane (1/28/93-9/11/99) LCDH x6 and multiple complications and birth defects.

    Founder and President of CDH International.

    Executive Director of:

    CDH International USA
    CDH International UK
    CDH International Canada
    CDH International Switzerland
    CDH International Netherlands
    CDH International Singapore
    CDH International Hong Kong

    Messages may be answered by CDHi Team.

  5. #5
    Very exciting Dawn! Thank you for all your hard work!
    Nicolle Colvin Mommy to Kasey James 11.16.08-12.19.08 Colorado Representative colorado.cherubs@gmail.com http://cherubscolorado.blogspot.com/

  6. #6
    Fantastic news...look forward to hearing the rest.
    Elaine- mom to Kristin 22- LCDH- nissen- ASD- oxygen till 2 1/2- g-tube till 4 1/2- bowel obstruction at 14 yrs old- only one lung. Also mom to Brittany 18- no CDH just 2 mths premie.

  7. #7
    Go DAWN!!!!!!! You are an amazing woman. Thanks or all your hard work!!!!!!!!!! ((((((((((((((((hugs)))))))))))))))))))
    Lots of Love- Carrie Mom to Colton Michael- RCDH-Surgery at 5 days for a repair and at 6 months to add a patch.

  8. #8
    Exciting news Dawn!!!
    Dawn, Barb and Bren thankyou so much for all your hardwork.
    Angela - mum to Max (LCDH 30/4/05 - 21/5/05) Also mum to Joseph 9- Christopher 7 and Dominic 2.

  9. #9
    WONDERFUL!!!
    Stephanie (Shelby's Mom LCDH 7-10-06)- ECMO 7 days- 2 DH repairs- hital hernia repair- Cliff Lip repair- Nissen and Mickey button. Shelby is eating and drinking by mouth now!!! THIS IS FANTASTIC!!!!! Mom to Lexi 8- Morgan 6 and Taylor 5. Blessed to have our little butterfly and our beautiful girls. [url]www.youtube.com/cdhsupport[/url] - Shelby's Journey [img]http://i258.photobucket.com/albums/hh257/gracebutterfly/CDHAwarenessRibbonShelbysmall.jpg[/img]

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