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Thread: Stories of Cherubs Vol. II

  1. #1

    Stories of Cherubs Vol. II

    It's been 2 years since Vol. I so let's get Vol. II out this year!!! Vol. I had over 300 stories, I think we can add 200 at least to Vol. II. If you story was not in Vol. I, it will be in this edition.

    To submit your cherub's story and photo, please e-mail them membership@cherubs-cdh.org with Cherub's Story in the subject line.

    Please submit them by typing directly onto the e-mail or with a MS Word document or text file attachment. Photos need to be in jpg, png or bmp format. If you would like to update your cherub's story, you can send that too - please just make sure to note if it's in Vol. I or your story will be in Vol. II.

    These books are not only for us, family and friends but we would really, really, really (seriously - really) like to get you all to donate copies to your cherub's PICU or NICU in honor / memory of your cherub so that new parents can read them as well during their hospital stays (and it won't hurt the doctors and nurses to read them 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.

  2. #2
    I want to change Cole's picture but i think the story is ok
    where/how do i send the photo so you'll know its for the book
    wanna make sure he gets in this one, i want to buy several to pass out.

  3. #3
    Just send it to the same address with the same subject line as above.

    Oh and everyone please also add the following:

    Your name
    Your cherub's name
    Your cherub's date(s)
    Your town

    Sometimes people send me stories and photos without names and I can't recognize everyone just by e-mail addresses.
    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.

  4. #4
    Senior Member
    Join Date
    May 2007
    Posts
    2,446
    Blog Entries
    50
    when do we need the stories in by?
    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

  5. #5
    October 15th
    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
    Senior Member
    Join Date
    May 2007
    Posts
    2,446
    Blog Entries
    50
    Good, I have time to make myself write out his story
    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

  7. #7
    Dawn,
    I'll get my story and photo of Grayton to you by then. I'm just having trouble looking at the photos of her and, because she wasn't diagnosed in utero, I don't have as many pictures as I'd like to. I just knew we were going to bring her home......I'll get to work on it, though.
    Grayton Karleigh Creekbaum diagnosed at birth on 5/09/08 with RCDH and she went to heaven on 6/22/08. She also had Pulmenary Hypertension- problems with blood clotting factors- and she went through 5 EMCO machines which got her the title of "Queen of the ECMO" by the head nurse - hence the boa and crown! bowel- liver- small intestines up with gortex repair had her repair while on ECMO on ECMO for 44 days (her entire life) Nitrate for 30- vent for 34 days- oscilator for 10 days Our Blog: www.thecreekbaums.blogspot.com

  8. #8
    Dawn can we still buy Vol I? I seen it at the ball and would LOVE a copy!!

    Barb

  9. #9
    Barb, yes, it's on Cafepress, we won't take it down

    Leigh, you have a few months, take your time with the photos, I know it's hard. It took me a year before I could look at Shane's photos so I totally understand.
    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.

  10. #10
    Dawn, I know I sent in Ashers story and picture as it was in a newsletter but do you want me to re-submit them?
    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

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