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Thread: Lets get CDH on the Oprah Show.

  1. #1

    Lets get CDH on the Oprah Show.

    I've already emailed the Oprah Show about Bryston and CDH.

    I think if more of us send in our stories then maybe they will do a show on it.

    If you are interested heres the link to submit your story.

    http://www.oprah.com/email/reach/email_showideas.jhtml

  2. #2
    I will email them!! I hope that they will do a show on CDH and help get the word out there!!
    Mommy to Haylee 01/26/2004 and My cherub Asher 07/04/2007- LCDH discovered at 18 weeks- medical termination at 24 weeks. Hypoplastic left lung and right jaw- pulmonary hypertension- Secundum type ASD- left liver lobe- stomach- appendix- and small bowel herniated www.freewebs.com/babyasher Ashers webpage http://www.youtube.com/watch?v=dxS8F4dkHjE Ashers video montage

  3. #3
    Great Idea!! That would definitely get CDH out there!

    Kim Richards
    Mom to Olivia 8/30/02-9/19/02 LCDH

  4. #4
    Awesome idea, Tammy!
    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
    Senior Member
    Join Date
    May 2007
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    Great Idea Tammy! I just emailed them!
    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

  6. #6
    I just e-mailed them again too. I'm going to make it a point to e-mail once a week. If at least 25 of us e-mail every week, then the odds will be higher that they will read one of our e-mails.
    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
    I wrote my letter to the Oprah show tonight! I hope other mom's will send in their stories. lets spread the word about CHERUBS and CDH!!!
    Kristin Morrow- mother of Landen James 9/18/07 (LCDH- diagnosed at 19 weeks in utero- CDH repair at 4 days old- chest tube due to secondary pneumothorax for 6 days- HFOV for 8 days- inhaled nitric oxide for 6 days- high flow nasal cannula oxygen for 14 days; battled drug withdrawl & an oral aversion- NICU stay 28 days) http://i102.photobucket.com/albums/m.../cdhribbon.jpg

  8. #8
    Great idea! I will send in my story too! i actually used to send it in way back when but havent in a while!
    Just a quick question for you guys who already did..did you sent in the "short " version of your childs story? or more lengthy? i have trouble shortening mine up..but i dont want them to just by pass it since its too long! thanks!!

    gg
    Georgia - WA Rep www.wacherubs.blogspot.com www.gebowfamily.blogspot.com Mom to Ariana LCDH 3/26/04* & Darren 2/23/06 *diagnosed 20wk- pyloric stenosis- extra digit- imperferated anus- Vent- Oscillating Vent- Cpap- ND & GJ tube fed- Oxygen- central line- scoliosis- small for her age- Mostly happy & bossy 4 1/2 year old!

  9. #9
    I had to shorten my story from the one I wrote for the Today show. Oprah only allows 2000 characters...which isn't much at all. I found it so hard to try and fit everything in without leaving anything out, but I guess if they are interested then we can just tell our whole stories on the show. hope that helps
    Kristin Morrow- mother of Landen James 9/18/07 (LCDH- diagnosed at 19 weeks in utero- CDH repair at 4 days old- chest tube due to secondary pneumothorax for 6 days- HFOV for 8 days- inhaled nitric oxide for 6 days- high flow nasal cannula oxygen for 14 days; battled drug withdrawl & an oral aversion- NICU stay 28 days) http://i102.photobucket.com/albums/m.../cdhribbon.jpg

  10. #10
    Guest
    I as well emailed Oprah. I think that is a great idea

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