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Thread: E-mail Awareness Campaign

  1. #1

    E-mail Awareness Campaign

    Anyone up for a "CDH E-mail Awareness Campaign" ??

    I recieve a lot of forwards and I keep getting an e-mail for an Autism Awareness. Now I have got it like 3 times. This last time I was like "Omigosh how many times am I going to get this thing . . ." Just as I was about to delete it, the light bulb in my brain turned on. If I can get that e-mail that many times, we should try it for CDH!!

    I am going to start working on a heart string tugging e-mail. It is not going to be packed of information, I do not want to overload people's minds. Just enough that they need to know about CDH, how there is no cause and we need to prevent this from happening, along with a link to CHERUBS and probably our ribbon. Can someone tell me how to add a link on a picture? So they can just click on the picture and it will bring them to CHERUBS?

    I am going to try to use some pictures, now if I have your permission, let me know. Do not be offended if I do not use them. I have ideas in my head, but I do not know if they can reach my fingers to actually work out.

    If you would like to be included in the initial e-mail I send out, let me know!!! PM, Email or post your address.

    What I am thinking is when I send the e-mail out, at the bottom, I will put In Memory of Shannon. When you recieve the e-mail, and you forward it, make sure to put In memory/In honor of and your cherub's name.

    I will leave this post up for about a week maybe two, so then people can read it. In that time, I will start working on a gorgeous e-mail!! I will let everyone know before I send the e-mail out. Send it to everyone in your e-mail address! Make sure to tell family and friends to do the same when they get it!! Can you even imagine world wide how many people could get this e-mail?? I know a lot of people LOVE to do those forwards!!!

    E-mail Awareness Campaign, here we come!!!
    Mommy to Shannon Elizabeth (01/16/07-01/19/07 LCDH and HLHS) Peanut Shelbe (miscarried 9/23/07 @ 8 weeks- due 4/10/08 ) Gracie Kathleen & Lily Anne (8/28/08 Blessings from their big sisters!) Shannon's Website! [url]www.shannonelizabeth.virtual-memorials.com[/url]

  2. #2
    yes yes yes ..... !!!!!!!!!!!!!!!!!
    I think it would be great, i'm not a forwarder of emails so if folks get one from me they'll certainly pay attention to it!
    my email
    will PM you my email

  3. #3
    Kate-that is an awesome idea. I love it. My email is donnaeasley80@yahoo.com and if you like you have my permission to use Alex's picture.
    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

  4. #4
    I love it!!!!! Include me too as well please!!
    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
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    Kate- you can use Gabes photos if you want

    My email is Chefrinny@gmail.com
    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
    you are also welcome to use cole's pic if you wish or any i have :0)

  7. #7
    Kate, count me in xx
    Sharon - mum to Liam - 30/04/03 RCDH- 2 CDH repairs- Vent: 22 days- oxygen: 315 days- ectopic right kidney- NG Tube: 3 years & 7 months Chelsea-Rose - 08/03/99 Co-Rep for Australia - sknott@cherubs-cdh.org http://i281.photobucket.com/albums/k...nLiamsmall.jpg

  8. #8
    Kate--you already know to please include us!!!
    Please use Shelby's pictures too!!
    I think this is a FANTASTIC IDEA!!!!!!!
    You let me know - if I can be of any help.
    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]

  9. #9
    That's a fabulous idea Kate, good on ya! You are welcome to use Lily's picture if you want. My email is
    boofstoney@hotmail.com
    Danielle - Lily's mum. Lily 31.07.07- Diagnosed at Birth - LCDH- Repair: 13 hours old- Ventilator: 5 days- NG tube: 7 days- Hospital: 16 days. Also mum to Ethan 21/06/05 http://i256.photobucket.com/albums/h...nLilysmall.jpg

  10. #10
    Kate count me in too! I am sure you already know my email and feel free to use Jacob's pic
    [url=http://counters.families.com][img]http://tac.families.com/cb/205944.png[/img][/url] [URL=http://img529.imageshack.us/my.php?image=cdhawarenessribbonjacobpf0.jpg][img]http://img529.imageshack.us/img529/1527/cdhawarenessribbonjacobpf0.th.jpg[/img][/URL] [url]http://jacob-ogilvie.memory-of.com/[/url]

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