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Ava's Awareness Videos

Sunday, August 29, 2010. Photo and video editing at www.OneTrueMedia.com. Ava has come quite the distance. Her start at life was sure a tough one but it didn't end there. She has been battling the effects of cdh her entire life. We are truly blessed to call her our daughter. This is yet another updated version of her Congenital Diaphragmatic Hernia Story. She is my inspiration and my joy! Thursday, September 3, 2009. Photo and video editing at www.OneTrueMedia.com. Thursday, January 22, 2009. This video ...

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Ava's Awareness Videos | cdhawarenessvideos.blogspot.com Reviews
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Sunday, August 29, 2010. Photo and video editing at www.OneTrueMedia.com. Ava has come quite the distance. Her start at life was sure a tough one but it didn't end there. She has been battling the effects of cdh her entire life. We are truly blessed to call her our daughter. This is yet another updated version of her Congenital Diaphragmatic Hernia Story. She is my inspiration and my joy! Thursday, September 3, 2009. Photo and video editing at www.OneTrueMedia.com. Thursday, January 22, 2009. This video ...
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Ava's Awareness Videos | cdhawarenessvideos.blogspot.com Reviews

https://cdhawarenessvideos.blogspot.com

Sunday, August 29, 2010. Photo and video editing at www.OneTrueMedia.com. Ava has come quite the distance. Her start at life was sure a tough one but it didn't end there. She has been battling the effects of cdh her entire life. We are truly blessed to call her our daughter. This is yet another updated version of her Congenital Diaphragmatic Hernia Story. She is my inspiration and my joy! Thursday, September 3, 2009. Photo and video editing at www.OneTrueMedia.com. Thursday, January 22, 2009. This video ...

INTERNAL PAGES

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1

Ava's Awareness Videos: November 2008

http://www.cdhawarenessvideos.blogspot.com/2008_11_01_archive.html

Monday, November 17, 2008. Ava's strength through reherniation. Make an on-line slideshow at www.OneTrueMedia.com. I just want to make parents of CDH children aware that there are many signs of reherniation If in doubt please go to your Emergency room. Things can get out of control fast. This video high lights the first signs and syptoms. Subscribe to: Posts (Atom). Avas strength through reherniation. View my complete profile. Ava's Awareness Videos. There was an error in this gadget. Ava 30 months old.

2

Ava's Awareness Videos: September 2008

http://www.cdhawarenessvideos.blogspot.com/2008_09_01_archive.html

Saturday, September 27, 2008. Make video montages at www.OneTrueMedia.com. This video was inspired by Liz and Shane. Their daughter Nayeli also has CDH, they put all her ultrasound pictures together, which made me think about all Ava's ultrasound pictures. I cried watching Nayeli's video knowing that she is still safely inside Liz and her journey will begin in a few short weeks. Liz and Shane you two are wonderful parents! They have become special friends to us! Saturday, September 6, 2008. I was blessed...

3

Ava's Awareness Videos: "Ava's Awareness Walk"

http://www.cdhawarenessvideos.blogspot.com/2008/07/avas-awareness-walk.html

Wednesday, July 23, 2008. Make video montages at www.OneTrueMedia.com. We held our first annual, "Ava's Awareness Walk" at our local hospital. It was awesome to see so many out supporting Congenital Diaphragmatic Hernia Awareness Day with us! We know how important it is to raise Awareness to this very life threatning birth defect that still takes 50% of all babies that are diagnosed with it. Thanks to all that donated. It was a perfect day to honor Ava and all her friends! Never give up Hope. The thin mu...

4

Ava's Awareness Videos: July 2008

http://www.cdhawarenessvideos.blogspot.com/2008_07_01_archive.html

Wednesday, July 23, 2008. Make video montages at www.OneTrueMedia.com. I created this video of all the CDH babies for a special reason. I felt they needed a voice. I captured the emotions of the parents by putting messages by each child. You can just feel the love and support for these Congenital Diaphragmatic Hernia children. Yes 50% of the babies are now in Heaven but every single one of them are loved more than you could ever imagine! Never give up Hope. Ava's fight to survive. My Name is Ava and I'm ...

5

Ava's Awareness Videos: "Happy 2nd Birthday, Ava!"

http://www.cdhawarenessvideos.blogspot.com/2008/09/happy-2nd-birthday-ava.html

Saturday, September 6, 2008. Happy 2nd Birthday, Ava! Make an on-line slideshow at www.OneTrueMedia.com. Subscribe to: Post Comments (Atom). Happy 2nd Birthday, Ava! View my complete profile. Ava's Awareness Videos. There was an error in this gadget. Celebrating Life with Ava! Loving this Little Girl. Ava Hope for Congenital Diaphragmatic Hernia. Ava 30 months old. Ava's life-threatning birth defect. They told us that 50% of these babies die no matter how much help they give them at birth. Ava was co...

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The World According to Lexis: August 2008

http://lexidoll.blogspot.com/2008_08_01_archive.html

The World According to Lexis. Friday, August 29, 2008. Lexis is home today sick. Pray for her she is pretty miserable. Brian had to work so I called my Mom to stay with the girls while I took her to the doctor. Poor girl. He prescribed some antibodics and told her to rest. Here is how she is looking right now. She loves Subway so we got that for her. She is finally getting her appetite back. Created by my Mom,. Wednesday, August 27, 2008. Created by my Mom,. Saturday, August 16, 2008. Created by my Mom,.

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The World According to Lexis: May 2011

http://lexidoll.blogspot.com/2011_05_01_archive.html

The World According to Lexis. Sunday, May 15, 2011. Lexis and Emeline Creations. Lexis and Emeline has started a new project. with a little help from me their Mother. "Lexis and Emeline Creations." We decided to make a little money on the side and create beautiful hand-made hair accessories. It is very fun and the girls are loving it. Their work can be found on facebook. We'd love it if you'd stop by "like" us and please share this with all of your friends. Here is a few of the pieces. Created by my Mom,.

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The World According to Lexis: April 2009

http://lexidoll.blogspot.com/2009_04_01_archive.html

The World According to Lexis. Sunday, April 19, 2009. We are at the University due to complication with Ava. I hate being away from the girls. They adjust very well. They are staying with Grandpa and grandma D today then will be going to Grandma Karen’s tonight. A recent picture of Lexis. I needed a model for my photography she wasn’t interested but I did get this shot. We did just go to the park Friday night and I got these shots. Created by my Mom,. Subscribe to: Posts (Atom). Rockstar" by Miley Cirus.

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The World According to Lexis: Super Hereo Lexis

http://lexidoll.blogspot.com/2009/05/super-hereo-lexis.html

The World According to Lexis. Saturday, May 9, 2009. I just have to show you what Lexis looked like yesterday. She came up from the basement wearing this. She just had to turn around to let us all see the cape! She is such a character. Created by my Mom,. Subscribe to: Post Comments (Atom). Who is the beautiful girl in the world? Glittery texts by bigoo.ws. Lexis dreams of being a dancer one day. Don't Stop the Music" by Rihana. Old Blue Jeans" by Miley Cirus. Rockstar" by Miley Cirus.

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The World According to Lexis: May 2009

http://lexidoll.blogspot.com/2009_05_01_archive.html

The World According to Lexis. Saturday, May 9, 2009. I just have to show you what Lexis looked like yesterday. She came up from the basement wearing this. She just had to turn around to let us all see the cape! She is such a character. Created by my Mom,. Subscribe to: Posts (Atom). Who is the beautiful girl in the world? Glittery texts by bigoo.ws. Lexis dreams of being a dancer one day. Don't Stop the Music" by Rihana. Old Blue Jeans" by Miley Cirus. Rockstar" by Miley Cirus. Let's Dance" by Miley Cirus.

lexidoll.blogspot.com lexidoll.blogspot.com

The World According to Lexis: Lexis and Emeline Creations

http://lexidoll.blogspot.com/2011/05/lexis-and-emeline-creations.html

The World According to Lexis. Sunday, May 15, 2011. Lexis and Emeline Creations. Lexis and Emeline has started a new project. with a little help from me their Mother. "Lexis and Emeline Creations." We decided to make a little money on the side and create beautiful hand-made hair accessories. It is very fun and the girls are loving it. Their work can be found on facebook. We'd love it if you'd stop by "like" us and please share this with all of your friends. Here is a few of the pieces. Created by my Mom,.

emmerose.blogspot.com emmerose.blogspot.com

Emeline's World.: Wired Shut

http://emmerose.blogspot.com/2012/04/wired-shut.html

Tuesday, April 10, 2012. I took Emeline to the appointment myself as I really thought they were going to send us home saying she just needed to heal on her own. Wow was I wrong. The surgeon looked at her CT scan from the night before. He also ordered an x-ray. Emeline and I were both shocked when he showed us the x-ray and told us she was going to need surgery. "Surgery. WHAT? I had no option. Here was Emeline in the room right before surgery. How do you give them to someone you only met for 5 minutes?

emmerose.blogspot.com emmerose.blogspot.com

Emeline's World.: Mommy's helper

http://emmerose.blogspot.com/2009/01/mommys-helper.html

Sunday, January 25, 2009. So Emeline is my ultimate helper. She gets all of Ava's medical supplies and knows exactly which drawer they are in at all times. She is very smart and "on the ball". She is ready at the drop of the hat to pick up and do the next thing. Ava loves her sisters but Emeline makes her laugh. It is so cute to see them bond. It brings so much joy to my heart to see them playing and having a great time. If only she knew! Now how cute are these two? Created by my Mommy,.

emmerose.blogspot.com emmerose.blogspot.com

Emeline's World.: March 2011

http://emmerose.blogspot.com/2011_03_01_archive.html

Sunday, March 27, 2011. Emeline loves her Guitar! Emeline started taking lessons about two months. She is doing great. She learns something new at each lesson. AND she practices regularly. She looks so cute with her new guitar fit just for her. She just got new strings put on it this week end. I believe she is going to go far with this guitar. Emeline we are SUPER proud of you! Created by my Mommy,. Subscribe to: Posts (Atom). There was an error in this gadget. I Kissed a Girl" by Katy Perry.

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Congenital Diaphragmatic Hernia Awareness

Congenital Diaphragmatic Hernia Awareness. March 31st is Congenital Diaphragmatic Hernia Awareness Day! Make an on-line slide show at www.OneTrueMedia.com. Wednesday, September 10, 2008. Make video montages at www.OneTrueMedia.com. Nayeli is still safely inside her Mommy. Wednesday, June 4, 2008. Samuel's CDH Awareness Video. Kosair Children's Hospital, Louisville Kentucky. Nicu stay was 2 months. Thursday, May 15, 2008. Make an on-line slide show at www.OneTrueMedia.com. February 24-February 25, 2008.

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(CDH) Awareness - Breath of Hope, Inc.Breath of Hope, Inc.

About Breath of Hope, Inc. Pregnancy & Congenital…. Expecting a CDH Baby? Bringing Home a CDH Baby. CDH – After Birth Diagnoses. Resources and Products for CDH Children. Support & Education. Congenital Diaphragmatic Hernia Summit. Kindness Project for CDH. March 31st Is Congenital Diaphragmatic…. Kambrie’s CDH Fund. Wes Ryan’s CDH Story. Mateo’s CDH Journey. Your Donation @ Work. Congenital Diapragmatic Hernia (CDH) Awareness. WHAT IS A CONGENITAL DIAPHRAGMATIC HERNIA? Every time you stand up for an idea...

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(CDH) Awareness - Breath of Hope, Inc.Breath of Hope, Inc.

About Breath of Hope, Inc. Pregnancy & Congenital…. Expecting a CDH Baby? Bringing Home a CDH Baby. CDH – After Birth Diagnoses. Resources and Products for CDH Children. Support & Education. Congenital Diaphragmatic Hernia Summit. Kindness Project for CDH. March 31st Is Congenital Diaphragmatic…. Kambrie’s CDH Fund. Wes Ryan’s CDH Story. Mateo’s CDH Journey. Your Donation @ Work. Congenital Diapragmatic Hernia (CDH) Awareness. WHAT IS A CONGENITAL DIAPHRAGMATIC HERNIA? Every time you stand up for an idea...

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CDH International - Shop or Make a Donation to fight CDH

CDH Awareness Day 2018. 5 / CDH Support - $5.00 USD. 5 / CDH Research - $5.00 USD. 5 / CDH Awareness - $5.00 USD. 5 / CDH Scholarship Fund - $5.00 USD. 10 / CDH Support - $10.00 USD. 10 / CDH Research - $10.00 USD. 10 / CDH Awareness - $10.00 USD. 10 / CDH Scholarship Fund - $10.00 USD. 20 / CDH Support - $20.00 USD. 20 / CDH Research - $20.00 USD. 20 / CDH Awareness - $20.00 USD. 20 / CDH Scholarship Fund - $20.00 USD. 50 / CDH Support - $50.00 USD. 50 / CDH Research - $50.00 USD. Full details →.

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Ava's Awareness Videos

Sunday, August 29, 2010. Photo and video editing at www.OneTrueMedia.com. Ava has come quite the distance. Her start at life was sure a tough one but it didn't end there. She has been battling the effects of cdh her entire life. We are truly blessed to call her our daughter. This is yet another updated version of her Congenital Diaphragmatic Hernia Story. She is my inspiration and my joy! Thursday, September 3, 2009. Photo and video editing at www.OneTrueMedia.com. Thursday, January 22, 2009. This video ...

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