gabrielathan.blogspot.com
Gabriel Athan KostaridisI was born with a right-sided Congenital Diaphragmatic Hernia. This blog follows my journey from birth, to surgery and my recovery.
http://gabrielathan.blogspot.com/
I was born with a right-sided Congenital Diaphragmatic Hernia. This blog follows my journey from birth, to surgery and my recovery.
http://gabrielathan.blogspot.com/
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Gabriel Athan Kostaridis | gabrielathan.blogspot.com Reviews
https://gabrielathan.blogspot.com
I was born with a right-sided Congenital Diaphragmatic Hernia. This blog follows my journey from birth, to surgery and my recovery.
gabrielathan.blogspot.com
Gabriel Athan Kostaridis: Surgery Scheduled for Tomorrow
http://gabrielathan.blogspot.com/2008/07/surgery-scheduled-for-tomorrow.html
I was born with a right-sided Congenital Diaphragmatic Hernia. This blog follows my journey from birth, to surgery and my recovery. Tuesday, July 8, 2008. Surgery Scheduled for Tomorrow. Gabriel is set to go in for surgery tomorrow, Wednesday July 9th at 1:00pm. Please keep him in your prayers and we will update with good results. Will keep you all in our prayers. Take care,. July 8, 2008 at 9:00 PM. Keeping you all in my thoughts and prayers,. July 12, 2008 at 4:27 PM. Subscribe to: Post Comments (Atom).
Gabriel Athan Kostaridis: May 2008
http://gabrielathan.blogspot.com/2008_05_01_archive.html
I was born with a right-sided Congenital Diaphragmatic Hernia. This blog follows my journey from birth, to surgery and my recovery. Thursday, May 15, 2008. Getting Bigger Day.by.Day. Friday, May 2, 2008. Gabriel is Home Again! Gabriel was released from the hospital yesterday (May 1st, 2008.) He is currently home and resting. He is still on continuous feeds with a three hour break during the day. Hopefully this little stay in the hospital was his last. We are all glad to have him home. New York City, NY.
Gabriel Athan Kostaridis: G-tube and Fundo Surgery
http://gabrielathan.blogspot.com/2008/07/g-tube-and-fundo-surgery.html
I was born with a right-sided Congenital Diaphragmatic Hernia. This blog follows my journey from birth, to surgery and my recovery. Wednesday, July 2, 2008. G-tube and Fundo Surgery. Gabriel had an appointment with his surgeon, Dr. Stolar. Yesterday as a followup to the GI appointment we had last week and we have all come to the conclusion that it will be in his best interest to have a G-Tube inserted. While he is in there Dr. Stolar. Believes that a Fundoplaction. Has slowed down. The NG.
Gabriel Athan Kostaridis: June 2008
http://gabrielathan.blogspot.com/2008_06_01_archive.html
I was born with a right-sided Congenital Diaphragmatic Hernia. This blog follows my journey from birth, to surgery and my recovery. Wednesday, June 25, 2008. An Update on Gabriel-Athan. We even got todrop in to the NICU and visit with some of the doctors and nurses in the NICU today. They are such wonderful people and it made them happy to see him progressing so well. Enjoy the pics that we took of Gabriel and Demetra the other day. Subscribe to: Posts (Atom). New York City, NY. View my complete profile.
Gabriel Athan Kostaridis
http://gabrielathan.blogspot.com/2008/07/gabriel-athan-had-his-surgery-wednesday.html
I was born with a right-sided Congenital Diaphragmatic Hernia. This blog follows my journey from birth, to surgery and my recovery. Tuesday, July 15, 2008. Had his surgery Wednesday morning at 11:00am at Columbia Presbyterian Children's Hospital. He had a G-tube inserted and they performed a Nissen. On him. Hopefully the Nissen. Will reduce the amount of Reflux coming up and give him some relief. Gabriel is scheduled to be released tomorrow afternoon. Praying for his homecoming tomorrow! New York City, NY.
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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...
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...
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.
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?
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...
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?
Ava~ Hope for Congenital Diaphragmatic Hernia.: Appointment Day
http://avaslifewithcdh.blogspot.com/2015/07/appointment-day.html
Friday, July 17, 2015. Hello Ava followers. I feel like it's been a long time since I've updated. Hope things are well with all of you. Ava slowly got over the virus she had. Oddly she had a cough for a good month. We are happy that it finally found the door out! Yesterday we had checkups with three different doctors at the University of Iowa Hospital and Clinics. On our way. She was so happy for Ava as are we! The next thing she did was a lung function test. She was very worried about it this time f...
kadenmorrowsjourney.blogspot.com
Kaden's Journey: March 2009
http://kadenmorrowsjourney.blogspot.com/2009_03_01_archive.html
Our beautiful baby boy, Kaden James Morrow, had c.d.h. and this blog is all about his journey to live and our journey accepting his death. Help Raise Awareness in Memory of Kaden! Thursday, March 26, 2009. Make video montages at www.OneTrueMedia.com. Subscribe to: Posts (Atom). My name is Jamie and my husbands is James. We have an amazing 4 year old daughter named Kayleigh and a Warrior Angel for a son named Kaden. We just welcomed our newest addition, Kolton, in April! View my complete profile. Mommy to...
kadenmorrowsjourney.blogspot.com
Kaden's Journey: So Far So Good
http://kadenmorrowsjourney.blogspot.com/2008/09/so-far-so-good.html
Our beautiful baby boy, Kaden James Morrow, had c.d.h. and this blog is all about his journey to live and our journey accepting his death. Help Raise Awareness in Memory of Kaden! Wednesday, September 10, 2008. So Far So Good. Kenny and Jennifer Miller. I'm praying hard for Kaden to stay strong! September 10, 2008 at 1:31 AM. Jamie and James,. Your little Kaden is amazing everyone once again. Thank you so much for the update. We will continue our prayer and lung function chants. View my complete profile.
kadenmorrowsjourney.blogspot.com
Kaden's Journey: Surgery day went ok
http://kadenmorrowsjourney.blogspot.com/2008/09/surgery-day-went-ok.html
Our beautiful baby boy, Kaden James Morrow, had c.d.h. and this blog is all about his journey to live and our journey accepting his death. Help Raise Awareness in Memory of Kaden! Friday, September 5, 2008. Surgery day went ok. He made it through surgery, my little warrior! Surgery went ok,. They lowered his ecmo flow down to 150 and it stayed that way until a. Couple of hours ago b/c we wanted to make sure that the blood flowed. Fast enough as to not clot (now at 200). He had a minute amount of. Infecte...
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Gabriel Athan Kostaridis
I was born with a right-sided Congenital Diaphragmatic Hernia. This blog follows my journey from birth, to surgery and my recovery. Monday, March 2, 2009. His strength, courage and determination should be an example to be followed by us all. May God bless him with many years of health and happiness. Friday, October 31, 2008. Gabriel, Demi and Mom make Crain's New York Business. Tuesday, September 30, 2008. I have some pics for everyone to see. Monday, July 28, 2008. Gabriel Home and Doing Well. And he is...
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