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Thread: Google Doodle for CDH

  1. #1

    Google Doodle for CDH

    (Letter from Dawn)

    Alrighty folks, we have a mission to accomplish!!!! Can we all e-mail Google and get them to do a Doodle for April 19th???



    My e-mail to proposals@google.com (write your own. Keep it simple!).... .

    Dear Google,


    April 19th in the International Celebration of Congenital Diaphragmatic Hernia Awareness Daily. CDH is a severe birth defect that strikes 1 in every 2500 babies = a baby every 10 minutes in the world. 50% of babies born with CDH do not survive. The cause is unknown.

    Never heard of CDH? Most haven't, though it's as common as Spina Bifida and Cystic Fibrosis with over 700,000 babies affected since 2000. Here at CHERUBS we've struggled to raise awareness for 17 years. Without awareness there are no research funds.

    http://www.cdhsupport.org/

    A CDH Doodle would raise awareness on an astronomical level for these babies and get them the attention and help they so desperately need. What better reason to doodle and who can resist cute little cherubs (the symbol for CDH) or the ribbon with the baby colors and clouds on a pretty spring day in April?

    Please consider this proposal.

    On behalf of over 3800 families of babies born with CDH,

    --
    Dawn M. Torrence Williamson
    President & Founder
    mom to Shane (1/28/93-9/11/99), born with CDH

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

    http://www.cdhsupport.org/
    Phone - 919-610-0129
    Fax - 815-425-9155
    Mailing Address - 3650 Rogers Rd #290, Wake Forest, NC 27587, USA
    Office: 1725 S. Main St, Suite 202, Wake Forest, NC 27587
    Attached Images Attached Images
    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
    That is an awesome idea! I'll have to write my letter this weekend!
    Mommy to a Miracle: Ericka Elizabeth (3.18.2009)-LCDH diagnosed in utero at 29 weeks- Venitlator- Nitric Oxide- Repair surgery at 13 days- Venous Venous ECMO at 16 days- Venous Arterial ECMO at 21 days- came off ECMO at 36 days- off oxygen support at 84 days- G-tube surgery at 78 days- home at 100 days..FINALLY! I'm so proud of her and all the progress we have made! All meds and g-tube DC'd on May 5th- 2010. She's still a skinny minny but she's healthy and happy! She's amazing!
    ERICKA'S JOURNEY: http://www.onetruemedia.com/shared?p...39&skin_id=801 www.myspace.com/tracy_leigh

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