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Thread: CHERUBS North Carolina Get-Together

  1. #1

    CHERUBS North Carolina Get-Together

    North Carolina Get-Together
    May 17, 2009
    Pullen Park, Raleigh, NC

    CHERUBS informal get-together at Pullen Park for families affected by CDH.

    Pullen Park is a great place for kids to have fun as well with a train, carousel, playground and more.

    We’ll be reserving an area for parents to talk while the kids play (siblings welcome!). Meet other families, talk to survivors, give support and have FUN!

    We will also have a balloon release for the CDH Day of Prayer and Education (May 17) in honor and in memory of cherubs!

    ** For privacy, security and insurance purposes, you must be a member of CHERUBS to attend a CHERUBS event. Membership is free, you can sign up at http://www.cdhsupport.org/events

    ALL CHERUBS members are welcome to attend, no matter what state you live in!
    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
    Awesome Dawn! Wish that we could be there as Pullen Park is GREAT!! You will have a great day!

  3. #3
    Dawn I am putting this on my calander!
    cdh found at birth. 28 days NICU. Vent 7 days. Repair at 3 days. No ECMO. NG Tube 28 days http://i319.photobucket.com/albums/m...don/0004-1.jpg

  4. #4
    I am going to see what I can work out to make it.
    Donna Easley mother of Alexander born 9-28-06 with RCDH ECMO 9 days- ASD- chronic lung disease- pulmonary hypertension- tracheomalacia- reflux- nissen- g-tube- trach and home vent since 6/2007 overall a happy and rotten 2 year old and little brother to Walker (5) http://www.totsites.com/tot/alexeasley http://webpages.charter.net/jtejctn/cdhsmall.jpeg

  5. #5
    That would be great if you ladies can come! We'll have a small group (maybe 20 or so) but we'll have fun and we'll have an adult survivor there as well.
    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.

  6. #6
    I'm going to get the balloons donated and with all the kids at that park, we can get a lot of people involved and raise a ton of awareness!
    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.

  7. #7
    That sounds awesome!
    Donna Easley mother of Alexander born 9-28-06 with RCDH ECMO 9 days- ASD- chronic lung disease- pulmonary hypertension- tracheomalacia- reflux- nissen- g-tube- trach and home vent since 6/2007 overall a happy and rotten 2 year old and little brother to Walker (5) http://www.totsites.com/tot/alexeasley http://webpages.charter.net/jtejctn/cdhsmall.jpeg

  8. #8
    Senior Member
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    Awesome Dawn! I wish I could come! Can't wait to see pics!
    Corin New England State Rep [img]http://i171.photobucket.com/albums/u312/GabrielMommy1118/1-3.jpg[/img] [url]www.gabriel-nava.virtual-memorials.com[/url] Gabriels website [url]http://www.youtube.com/watch?v=N66S-vt5sI8[/url] Gabriels Video [url]http://corinscrazylife.blogspot.com/[/url] My Blog [url]http://newenglandcherubs.wordpress.com[/url] New England Blog

  9. #9
    AWESOME!!!!!!!
    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]

  10. #10
    ummm, kim will be there.

    Me, don't know because of health
    aunt nancy

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