Dawn from CHERUBS CDH Support Group

www.myspace.com/diaphragmatichernia

I supported Cherubs The Assoc Of Congen... by voting for them to win $25k with #chasegiving. Please fan, vote, and RT! http://bit.ly/3Jo9ucCumartesi - Twitter devamı

  • Dawn from CHERUBS CDH Support Group

  • 36 / Kadın
  • Wake Forest, North Carolina, US
  • Son Giriş: 21.10.2009

143281041|36|11110|http://c4.ac-images.myspacecdn.com/images01/124/m_554057c44fbe1c865b13ffe9062e1d97.png

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İlgi Alanları

  • Genel



    CDH Awareness MySpace Layouts

    Do you like the layout of this profile? Feel free to snag it for your own! Coding is below. Just choose a template and copy and edit your profile and paste it into your "About Me" section.




    Congenital Diaphragmatic Hernia Awareness Myspace Template


    Snag our Black & White Skater Template (above)





    Congenital Diaphragmatic Hernia Awareness Myspace Template


    Snag our Blue Skater Template(above)





    Congenital Diaphragmatic Hernia Awareness Myspace Template


    Snag our Pink Skater Template (above)





    Congenital Diaphragmatic Hernia Awareness Myspace Template


    Snag our Black & White CDH Awareness Logo Template (above)





    Congenital Diaphragmatic Hernia Awareness Myspace Template


    Snag our Blue Clouds & CDH Ribbon Awareness Template (above)





    Congenital Diaphragmatic Hernia Awareness Myspace Template


    Snag our Pink Clouds & CDH Awareness Ribbon (above)





    Congenital Diaphragmatic Hernia Awareness Myspace Template


    Snag our Black & White Wings CDH Awareness Template (above)





    Congenital Diaphragmatic Hernia Awareness Myspace Template


    Snag our Blue Wings CDH Awareness Template (above)





    Congenital Diaphragmatic Hernia Awareness Myspace Template


    Snag our Pink Wings CDH Awareness Template (above)





    Our personalized CDH Awareness Ribbon Graphic to share and post. If you would like one in honor / memory of your cherub, please let us know!

    Congenital Diaphragmatic Hernia Awareness Ribbon



    Coding is below if you already have one of the above ribbons. For a large ribbon copy and paste the following coding and change the name shane to your cherub's name:

    Code for the large size is:


    Code for the smaller size (shown above) is:


    Please post our CDH Awareness Graphics to help encourage Congenital Diaphragmatic Hernia Awareness and Research. CDH occurs just as often as Spina Bifida and Cystic Fibrosis, yet hardly anyone has heard of it and there is barely any research being done on this birth defect that affects over 2000 babies in the US each year and takes the lives of half of them. Let's help change that!

    Congenital Diaphragmatic Hernia Awareness


    Copy and insert the following code on your Myspace to post our ribbon onto your profile:




    Congenital Diaphragmatic Hernia Awareness


    Copy and insert the following code on your Myspace to post our CDH logo onto your profile:



    Please don't forget that we have over 100 cherub logo characters up for adoption! There is surely one that looks like your cherub! :)

    You are welcome to use them *anywhere*. As your avatar here, on your facebook or myspace account, on your web site or blog - to download them and use them for address labels, scrapbooking, anything!



    You can even name your cherub character too. Here's an example below under the dotted line. To use the character of your choice go to http://www.cdhsupport.org/web/adopt.php and find the cherub that you want to use. In the code below change the name adam to whatever name the cherub character is named on our site (all lower case - make sure to use the name of the character there, not the name you want it to have). To change the name of the cherub, edit the name Bobby in the coding below. You can also change "I adopted my cherub" to something like "I support CHERUBS in honor / memory of _______".




    Donate to CHERUBS




    Search & Shop On-Line while Donating To CHERUBS for Free! ..

    CHERUBS Fundraisers and Congenital Diaphragmatic Hernia Awareness Items
    CHERUBS Fundraisers
    free web stats
  • Filmler

    Video of my son, my guardian cherub, Shane Torrence



    Video created by Corin, mom to cherub Gabriel, created for YouTube and Goodsearch's video contest for CHERUBS... it tells you about CDH and shows you some of our cherubs....
  • Televizyon

    ..
  • Kitaplar

    ..
  • Kahramanlar

    Random videos of cherubs submitted by members:

    Our heroes...


    ..............

Detaylar

  • Durum: Evli
  • Burada olma nedeni: Elektronik yazışma, Arkadaşlar
  • Burcu: Akrep
  • Çocuklar: Anneyim-Babayım mutluyum!

Şirketler

  • CHERUBS

    • US
    • Volunteer President & Founder
    1995-2008

Ne Diyor

Hakkımda:

..
This MySpace account is for CHERUBS, a support group for families and medical care providers of children born with Congenital Diaphragmatic Hernia (CDH).





CHERUBS was founded in 1995 to support families of children born with Congenital Diaphragmatic Hernia (CDH) and to increase awareness, research possible causes and better treatments for CDH. It is for ALL CDH FAMILIES, not in memory or honor of 1 cherub. It was formed to bring the entire CDH Community together to support each other and take a stand against CDH.



Currently, CHERUBS has over 2700 members in 38 countries and all 50 states. CHERUBS is an IRS approved 501(c)III organization that runs on volunteers and donations.

CDH is a devastating birth defect, affecting 1 in every 2500 babies. It occurs when the diaphragm fails to fully form, allowing the abdominal organs to enter the chest cavity and prevent lung growth. CDH has a 50% survival rate. The cause is not known.

For more information on CHERUBS and CDH, please visit our web site at http://www.cdhsupport.org
.. .. .. ..


I support CDH Public Awareness at CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support

Take A Stand Against CDH
http://vids.myspace.com/index.cfm?fuseaction=vids....




Congenital Diaphragmatic Hernia Research



"I Own Congenital Diaphragmatic Hernia Awareness"
http://www.youtube.com/watch?v=U4Unz-z4um4

Starring over 300 CDH families in the fight against the trademark on "Congenital Diaphragmatic Hernia Awareness" filed by Breath of Hope, Incorporated. http://www.ipetitions.com/petition/cd... http://ttabvue.uspto.gov/ttabvue/v?pn... http://www.cdhsupport.org http://www.cdhresearch.org

Kimle tanışmak isterim:



CHERUBS is always here to help all families affected by Congenital Diaphragmatic Hernia.


Some Important CHERUBS Links:

CHERUBS New Web Site - http://www.cdhsupport.org

Register / Sign Up with CHERUBS - http://www.cdhsupport.org/members/profile.php?mode=register

CHERUBS Member Portal - http://cdhsupport.org/members/index.php

Public & Member Forums - http://cdhsupport.org/members/index.php

CHERUBS Silver Lining Newsletter - http://www.cdhsupport.org/newsletter

CDH Research Library - http://cdhsupport.org/members/links.php

CHERUBS Photo Albums - http://cdhsupport.org/members/album.php

CHERUBS Member Albums - http://cdhsupport.org/members/album_personal_index.php

CHERUBS Member Blogs - http://cdhsupport.org/members/weblogs.php

CHERUBS Volunteers - http://www.cdhsupport.org/volunteers

Downloadable Information About Congenital Diaphragmatic Hernia - http://cdhsupport.org/members/dload.php

CHERUBS Timeline - http://www.cdhsupport.org/about/timeline.php

Arkadaş Alanı (Üst 7)

Dawn from CHERUBS CDH Support Group, 771 kişiyle arkadaş.
  1. Barbara
  2. *JD*Jessica Dykema
  3. Sometimes Miracles HideHeidi Carlson
  4. Crista
  5. jack ryan gillham
  6. Amy
  7. TomTom Anderson

Yorumlar

25 / 245 yorum görüntüleniyor
  • 22 Eyl 2009 12:59


  • 7 Eyl 2009 15:20


    MyHotComments.com
    I am truly blessed with the gift of your friendship. I'm very sorry that I haven't been in touch like I should have lately. With all that has been going on with Winston I have not gotten too many chances to be online. The weeks have really gone by fast. I praise God so much that Winston is improving and is almost back to 100%. Now we’re going through an uncertain future with JJ as he remains in ICU at the animal hospital. (Details on my blog if you're interested). Hopefully everything will be fine and back to normal soon. Will you please keep our family in your prayers? Thank you for understanding and continuing to be my friend.

    Love and Blessings Always,

    Sharon & Family†


    Winston's Site
  • 7 Eyl 2009 15:20





    Your friendship and support are more than appreciated.

    Hugs, Sharon

    Sending Lots Of Bullie Kisses Your Way,
    Winston, Gracie & JJ
    http://www.wingrace.com

    If you will, please read my lastest blog & pray for Gracie.
    For Dog Lovers: http://www.wingrace.com/T-ShirtsForGracie.htm
  • 27 Haz 2009 01:45


  • 5 Haz 2009 19:09



    I'm truly honored to have you as a new friend. I look forward to getting to know you and to our friendship. Please stay in touch!

    Take Care & God Bless,
    Sharon†
    *Proud Army Wife & Military Supporter
    *Bulldog Mom To Winston, Gracie & JJ
    *"Carolina’s PI" and Animal & Child Protection Advocate
    *NC, SC & GA State Director of Ms. Christian US Pageants
    “Celebrating the beauty inside and out of virtuous women!”
    *NC & SC State Director For Association Of Christian Investigators
    *Owner/Founder of Bulldog Co Network


    MyHotComments.com


    thanks for being my friend
  • 23 May 2009 00:01

    Thank you so much for putting this support on MySpace. I'm not real good at navigating web pages so I would get lost a lot on Cherubs. I look forward to chatting and reading information. We lost our baby girl to CDH along with other birth defects as well. God bless and again......thank you!
  • 9 May 2009 23:00

    MyHotComments.com
    MyHotComments HAPPY MOTHERS DAY!!!
  • 11 May 2009 01:32

  • 6 May 2009 15:09

    http://www.jacksonville.com/sports/golf/2009-05-06/story/families_with_special-needs_children_join_a_fantasy_world_at_players This is an article done on Sammy, the PGA, and PEDS care. PEDS care is an organization that works with kids with life threatining illnesses. They mention CDH but got it a little wrong. I sent him an email hopefully they will rn a correction on it. They said he was born without a diaphram. Sammy did have on he just had a hole in it. They also said his organs are in his chest, lol. They were obviously moved back to there aprox locations. I told him I don't think you can live with your organs in your chest, in the email I sent him. =0)
  • 6 May 2009 13:21

    Follow Wendy on twitter! http://twitter.com/wendypetty and go to ask.com and get Wendy's customized skin homepage!
  • 14 Nis 2009 15:04

    Photobucket


    Have a Great Week Pictures, Images and Photos

    Love The Mount Family
  • 4 Nis 2009 16:10


  • 24 Mar 2009 18:38

    ♥ Thanks for checking out my music ♥
  • 23 Mar 2009 19:37

    You did a wonderful job on the video!!! Thank you!
  • 21 Mar 2009 03:05

  • 2 Mar 2009 13:29

    Have A Great Day
  • 22 Şub 2009 06:40

    to you and all those who have lost a child you must read Room of Marvel by james bryan smith-i just finished it and it has changed me and how i will look at the loss of Gabby-this life is but only a minute away from eternity-and there we get to live w/ her forever!! this book really puts in in perspective, based on very true real events in the authors life and his dealings w/ 3 very big losses in 3 years, his good friend, his daughter, and his mom.
  • 14 Şub 2009 06:51

    Hey Dawn. Last month sometime a 21 year old girl born with CDH contacted me! I just remember and wanted to share it. I was so excited to talk to her. She was wanting to know how far things had come in the research for CDH. She said when she was born the survival rate for CDH was 50% and was wondering if things were any better. Sadly, I had to tell her that the survival rate is about the same and they still don't have an answer to why children are born with it. Sad, huh? Were not much better than we were 21 years ago. Well, I can't say that completly. At that hospital Sammy was born at the drs there had a survival rate of 91% and Dr Kays specializes in saving babies born with it. He had discovered things about vents and things that helped kids survive. There is a website dedicated to him I don't remember the direct address but you can google kayskids. Well, I just wanted to share.
    Jennie
  • 7 Oca 2009 14:34

    Hi Dawn, Thank you for the add!! Hope you are doing well:)
  • 25 Ara 2008 16:13




    Free Graphics - MySpace/Xanga/Friendster


    In Loving Memory of Kayla Mae Michele Childress 8/10/99-10/17/99
  • 18 Ara 2008 17:54

    happy holidays Pictures, Images and Photos
  • 12 Ara 2008 13:48

    I would like wings that are very soft and feminine looking and in the middle reading from top to bottom it should say "Cry no more" and that would be the body of the angel and then a halo at the top...THANK YOU THANK YOU THANK YOU!!!! I LOVE U!!!! What ever size u make shouldn't be an issue because they can shrink it if necessary.
  • 11 Ara 2008 20:06

    Alright cousin, I am in desperate need of a drawing because I go to the tattoo artist next week! LOVE YOU!!!
  • 11 Ara 2008 15:50

    kakoi MERRY CHRISTMAS my three boys
    imikimi - Customize Your World


    MERRY CHRISTMAS FROM MY FAMILY TO YOURS