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Ava~ Hope for Congenital Diaphragmatic Hernia.

Tuesday, February 20, 2018. Scoliosis Back Check up. They want no metal on your body so we came prepared. She wore a bra that had no metal and a plain shirt with stretch leggings. (We caught the lady at the desk off guard.she said you will have to change out of your jeans. Ava says THESE are NOT Jeans they are leggings! Oh the Joys of what comes out of this child's mouth get me every time! Ava says "I guess it is doing something! We certainly can feel your love, support and prayers. God is good! Ava had ...

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Ava~ Hope for Congenital Diaphragmatic Hernia. | avaslifewithcdh.blogspot.com Reviews

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Tuesday, February 20, 2018. Scoliosis Back Check up. They want no metal on your body so we came prepared. She wore a bra that had no metal and a plain shirt with stretch leggings. (We caught the lady at the desk off guard.she said you will have to change out of your jeans. Ava says THESE are NOT Jeans they are leggings! Oh the Joys of what comes out of this child's mouth get me every time! Ava says I guess it is doing something! We certainly can feel your love, support and prayers. God is good! Ava had ...

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Ava~ Hope for Congenital Diaphragmatic Hernia. | avaslifewithcdh.blogspot.com Reviews

https://avaslifewithcdh.blogspot.com

Tuesday, February 20, 2018. Scoliosis Back Check up. They want no metal on your body so we came prepared. She wore a bra that had no metal and a plain shirt with stretch leggings. (We caught the lady at the desk off guard.she said you will have to change out of your jeans. Ava says THESE are NOT Jeans they are leggings! Oh the Joys of what comes out of this child's mouth get me every time! Ava says "I guess it is doing something! We certainly can feel your love, support and prayers. God is good! Ava had ...

INTERNAL PAGES

avaslifewithcdh.blogspot.com

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Ava~ Hope for Congenital Diaphragmatic Hernia.: Ava's Story

http://avaslifewithcdh.blogspot.com/p/avas-story.html

Ava's Beginning and Our Fight to Keep our Daughter. Every once in a while we are handed things in our life that seem impossible. We question God, we question ourselves. “Why? It doesn’t look like anything.” “Well, she said pulling him up onto her lap, Why don’t you look at it from up here.” Wow grandma it is pretty! 8221; Sometimes only God sees the finished product. We are only seeing the underneath, the mess. For the next few days I was literally a wreck. I couldn’t eat. I couldn’t ...I had grown up kn...

2

Ava~ Hope for Congenital Diaphragmatic Hernia.: A Change of Heart

http://avaslifewithcdh.blogspot.com/2014/11/a-change-of-heart.html

Friday, November 21, 2014. A Change of Heart. Then on Wednesday her heart rate dropped to 44. I went over to her and checked her pulse myself. I got 38 beats a minute and they were very shallow. I grew concerned. I woke her and the heart rate got better. I then let her go back to sleep but it continued to get lower and lower. The nurse asked if she wanted to remove all the stickers herself. Of course she did! There are 5 leads and the monitor itself is attached to her jeans. November 22, 2014 at 12:20 AM.

3

Ava~ Hope for Congenital Diaphragmatic Hernia.: Hope

http://avaslifewithcdh.blogspot.com/p/hope.html

Hope for Expectant Parents. YES the road is hard and sometimes very long. I encourage you to stay strong and have Faith. On the days that you feel beat down remember that God is with you. If God brings you to it, He can bring you through it! I've started a page on facebook called "Raising Healthy Congenital Diaphragmatic Hernia Children". We'd love to have you join the conversation. You will find SO much Hope there. See you soon! Terri Helmick (Ava's Mommy). Subscribe to: Posts (Atom). Want to Know More?

4

Ava~ Hope for Congenital Diaphragmatic Hernia.: July 2014

http://avaslifewithcdh.blogspot.com/2014_07_01_archive.html

Tuesday, July 22, 2014. Gastroenterology Visit and Summer fun! Hello Ava friends and followers. It’s been awhile since I last posted. And you know I always say no news is good news! Ava’s been having a great Summer. We went to visit family in St. Louis a few weeks ago to celebrate the 4th of July. We always have such a wonderful time. We are blessed to have such an amazing, supportive and loving family! As you can see Ava had the most fun of all! Yesterday I took her to her GI doctor. Ava still strug...

5

Ava~ Hope for Congenital Diaphragmatic Hernia.: What is CDH?

http://avaslifewithcdh.blogspot.com/p/what-is-cdh.html

What is Congenital Diaphragmatic Hernia? A diaphragmatic hernia is a birth defect in which there is an abnormal opening in the diaphragm, the muscle that helps you breathe. The opening allows part of the organs from the belly (stomach, spleen, liver, and intestines) to go up into the chest cavity near the lungs. Also forcing the heart to move. Congenital diaphragmatic hernia is seen in 1 out of every 2,500 live births. Subscribe to: Posts (Atom). Ava's visitors since October 2008. Want to Know More?

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thekeenafamilyblog.blogspot.com

Maddy's blog: home sweet home

http://thekeenafamilyblog.blogspot.com/2009/11/home-sweet-home.html

This blog is to help keep everyone up to date in the world of Madeline! Oh man. It's good to be home. Cant wait for pictures! November 28, 2009 at 9:55 AM. Subscribe to: Post Comments (Atom). Visits from my friends. View my complete profile. Kansas City, Kansas City here I come! Liquor and baby food? Rash, rash, go away. Ava Hope for Congenital Diaphragmatic Hernia! Pain in her Side.

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Maddy's blog: no internet...

http://thekeenafamilyblog.blogspot.com/2010/01/no-internet.html

This blog is to help keep everyone up to date in the world of Madeline! So, onto Maddy.we had her 9 month check-up today and she's doing great, physically and developmentally. She is still very advanced for her age in the gross and fine motor department, as well as the social aspects too. She is starting to test Jason and I lately though, purposely trying to get things (i.e. the cat! But, that's about it, I gotta get to work! I promise I will come in early one day and upload some new pics!

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Maddy's blog: September 2009

http://thekeenafamilyblog.blogspot.com/2009_09_01_archive.html

This blog is to help keep everyone up to date in the world of Madeline! So, today was a big day for Miss Maddy! She had solid food for the first time! We mixed some oatmeal cereal with some breastmilk and a little bit of pears. She didn't really know what to think at first, but then she was grabbing the spoon and trying to feed herself! It was cute and I got pictures! She didn't eat much, but from what I read, she was only supposed to eat about a tablespoon, so that is what I gave her. *WARNING! Oh, anot...

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Blog spot - IMOGENDYSON.CO.UK: May 2012

http://immiedee.blogspot.com/2012_05_01_archive.html

Blog spot - IMOGENDYSON.CO.UK. Wednesday, 23 May 2012. 65279;. Just the 3 of us. Links to this post. Thursday, 10 May 2012. Imogen's 7th birthday and party pics. Elena came as a surprise to Frankie and Benny's. It was Grandma's birthday too. Links to this post. Subscribe to: Posts (Atom). FEEDJIT Live Traffic Feed. A story about Imogen who was born with a Congenital Diaphragmatic hernia, and survived against all odds. View my complete profile. 65279;Just the 3 of us.

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Blog spot - IMOGENDYSON.CO.UK: April 2011

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Blog spot - IMOGENDYSON.CO.UK. Monday, 4 April 2011. Imogen's birthday tree flowers early. Links to this post. Subscribe to: Posts (Atom). FEEDJIT Live Traffic Feed. A story about Imogen who was born with a Congenital Diaphragmatic hernia, and survived against all odds. View my complete profile. Imogens birthday tree flowers early. Awesome Inc. template. Powered by Blogger.

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Mommy's Life with Zachery & Allie: July 2009

http://zacheryandallie.blogspot.com/2009_07_01_archive.html

Mommys Life with Zachery and Allie. Saturday, July 4, 2009. Happy 4th Of July. Hope eveyone has a safe and Happy 4th.Not much new with the kids, I don't remember if I posted about Allie also loosing a tooth, yep they are both one tooth less.she actually kocked hers out with he tooth brush.anyways I'm stressed about today, oh so many people will be at my house.Paul's wonderful idea! Subscribe to: Posts (Atom). At home 15days after diaphragmatic hernia repair. Singin The "Beach Song". Ice Cream face :).

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Maddy's blog: July 2009

http://thekeenafamilyblog.blogspot.com/2009_07_01_archive.html

This blog is to help keep everyone up to date in the world of Madeline! We have started trying different things to relieve the pain, and so far she likes the mesh feeders. We put an ice cube in there and she goes to town! She isn't a big fan of the teething rings if they are cold, but doesn't mind them if they are warm! Lil Miss is also trying to crawl. She moves about right now like a little inchworm. It's quite humorous! Head goes down, hips come up, knees go to the chest, and PUSH forward! I have no i...

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Ava's Lifeline Jamaica NY

Jamaica, NY 11434. Enjoy life more with various tips on healthy living from Ava’s Lifeline,. A service based in Jamaica, New York. Become versed on treating your illnesses by feeding your body with the right food, minerals, and vitamins. Place your trust in us and dedicate yourself to experiencing life with more energy, better hair and skin, and less medications. Provide your information in the form below to receive Health Tips, News and Updates! With more than 20 years of experience. Jamaica, New York.

avaslifewithcdh.blogspot.com

Ava~ Hope for Congenital Diaphragmatic Hernia.

Tuesday, February 20, 2018. Scoliosis Back Check up. They want no metal on your body so we came prepared. She wore a bra that had no metal and a plain shirt with stretch leggings. (We caught the lady at the desk off guard.she said you will have to change out of your jeans. Ava says THESE are NOT Jeans they are leggings! Oh the Joys of what comes out of this child's mouth get me every time! Ava says "I guess it is doing something! We certainly can feel your love, support and prayers. God is good! Ava had ...

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