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Thread: Congenital Diaphragmatic Hernia Awareness

  1. #1

    Congenital Diaphragmatic Hernia Awareness

    We have LOTS of different CDH awareness campaigns going on within the CHERUBS Awareness Committee. If anyone is doing projects on their own, please let us know so we can help! It's always better to have more voices working together rather than just 1 or a few. Whether it's making graphics, videos, blogs, etc., you can post them to the CHERUBS Facebook Page directly and we can share that way or email us at awareness@cherubs-cdh.org. Make sure to make the posts public so everyone can see them not just your Facebook friends. We can not post things on the page unless you give permission to us first.
    Thanks everyone for raising Congenital Diaphragmatic Hernia!
    Felecia Marie Woodruff- CHERUBS Volunteer
    Pennsylvania State Representative, Awareness Committee Leader, Parent Advisory Board Member

    Daughter, Hayden, DOB October 8th, 2009. CHERUB SURVIVOR son, Bryson, DOB July 30th, 2012 born at The Children's Hospital of Philadelphia.
    21 Days ECMO, 6 Days Oscillator Ventilator, Day 32 CDH Surgery, Day 35 Got to hold him for the 1st time, 25 Days Conventional Ventilator plus 21 Days while on ECMO, 4 Days CPAP, 17 Days Nasal Cannulas, Day 90 Came Home from the NICU
    Bryson's Facebook page: www.facebook.com/brysonsbattleprayerpage
    My Facebook page: https://www.facebook.com/felecia.woodruff
    Email: fwoodruff@cherubs-cdh.org | awareness@cherubs-cdh.org

  2. #2
    The Awareness Committee is AMAZING!!! Thank you all for all that you do for all of our children!

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