thecreekbaums.blogspot.com
The Creekbaums: September 2009
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Thursday, September 24, 2009. Links to this post. Labels: I just woke up from my nap. Yesterday Gray had his first visit with his pediatrician. While he'd previously lost a 6 ounces from his 8lb 2 oz birth, I'm happy to report he's back up to 8 lbs. When we took him back to the room at the doctor's office and placed him in his diaper on the examination table while waiting on the doctor to come in, he wet the table like I've never seen! Travis and I just died laughing! Links to this post. And he slept so ...
thecreekbaums.blogspot.com
The Creekbaums: October 2009
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Thursday, October 8, 2009. Gray: 3 weeks old. For all the War Eagle friends and fans! Links to this post. Tuesday, October 6, 2009. Happy Fall, Y'all! Gray now weighs 8 lbs 8 oz and seems to grow and change every day. He rarely cries and is, overall, just a very peaceful baby. We are so blessed - for many reasons. Our photographer, Monica Carroll ( http:/ www.monicacarroll.com/. Came last week to photograph Gray (can't wait to see the pics! Thanks so much for all of your prayers and well wishes! The Park...
avaslifewithcdh.blogspot.com
Ava~ Hope for Congenital Diaphragmatic Hernia.: December 2014
http://avaslifewithcdh.blogspot.com/2014_12_01_archive.html
Thursday, December 18, 2014. I took a few quick pictures as she was getting her x rays. She is such a pro at this! I got her antibiotic (Cefdinir) and some lunch. She fell asleep shortly after eating. I'm hoping we aren't looking at pneumonia. She has such a bad and constant cough. She will be missing out on her Christmas party at school. I do the school's yearbook so I will have to go and take pictures. I'll pick up her treats so hopefully that will make her feel better. How cute is this? Ava's visitors...
avaslifewithcdh.blogspot.com
Ava~ Hope for Congenital Diaphragmatic Hernia.: Ava's Story
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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...
avaslifewithcdh.blogspot.com
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.
avaslifewithcdh.blogspot.com
Ava~ Hope for Congenital Diaphragmatic Hernia.: Hope
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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?
avaslifewithcdh.blogspot.com
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...
avaslifewithcdh.blogspot.com
Ava~ Hope for Congenital Diaphragmatic Hernia.: What is CDH?
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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?
wyattjameskoger.blogspot.com
Wyatt James Koger, A Fighter from Birth: Congenital Diaphragmatic Hernia Awareness Day 2012
http://wyattjameskoger.blogspot.com/2012/03/congenital-diaphragmatic-hernia.html
Wyatt James Koger, A Fighter from Birth. Here is the story of my amazing and patient recovery. Saturday, March 31, 2012. Congenital Diaphragmatic Hernia Awareness Day 2012. What have we been up to lately? He is a smart little boy full of wonder and enthusiasm. We are so proud of all his accomplishments. He is eating more solid food each day. My goal for Wyatt is to be totally independent from the feeding tube and oxygen. He has one more year before Kindergarten, so I think we can do it! My CDH Blog List.