babybeehelms blogspot.com

Baby Bees Journey

On February 2, 2012, our unborn baby girl Bee was diagnosed with a congenital diaphragmatic hernia CDH. This is going to be a journey.

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LINKS TO WEB SITE

One Day at a Time.

Friday, January 30, 2015. Has it really been nearly a year since I last posted? It really does feel like time speeds up when you have children. I am honestly in awe that we are fast approaching one year since he gave the g-tube the boot.

Bessom Blessings

Saturday, July 27, 2013. Tuesday, July 9, 2013. Faith is the gaze of a soul upon a saving God. Matthew, Bethany, Ryan Olivia and Knox.

Breathing for Baby Clay Our CDH Story

Wednesday, November 4, 2015. We now have a little 4 year old man with NO trach, a head full of beautiful hair, and all kinds of spunk. 160; Now we are officially DONE with the trach saga. 2 hours, 2 times a w.

Finley Anabelles Blog Our CDH journey

8220;This race is a labor of love for our family. We are entirely volunteer led and run.

Our little girl Esthers CDH story

Sunday, April 12, 2015. Sometimes we burn with a blazing fire and excitement that is uncontainable. Other times we are just going thru the motions. I miss my daughter Esther. I long to be with her and my Savior.

Search Our Hearts CDH Blog Directory

Submit or Remove a Blog. Welcome to Search Our Hearts. A directory of Congenital Diaphragmatic Hernia Community Blogs started and maintained by friends, family and organizations of CDH survivors and angels.

Our CDH fighter Little A Just another WordPress.com site

Our CDH fighter Little A. Happy New Year my love! January 2, 2014. This year has been such a roller coaster. We started the year off with we all being in the winter shut down. You were getting your monthly RSV shots, we all had to shower as soon as we return from work, shopping , school and sanitizers were everywhere. It was so hard but we survived. Though spring came late, we all rushed out the door as fast as we could. You are an independent soul, a fighter, you perseve.

Lilys CDH story

Our second baby girl, Lily, was diagnosed as having a left diaphragmatic hernia at 20 weeks gestation. This is the story of her journey. Thursday, October 4, 2012. Whatever the cause, it needs to be fixed soon. Lily will be having brain surgery on Tuesday or Wednesday to place a shunt. This shunt will go from the ventricles in her brain to her abdominal cavity. The extra fluid will drain into there and be absorbed and removed. Yesterday, Lily had her 6 month check-up.

Sunnis Story

At 21 weeks gestation, our baby girl Sunni was diagnosed with a Congenital Diaphragmatic Hernia. This is her story documented with all the ups and downs that she and her family will face together. Monday, April 7, 2014. Its been almost a YEAR! I think I have been putting this off for long enough. My last post was nearly a year ago. My, my, my; how things have changed- for the better HALLELUJAH! Next blog will be about how she is now. Saturday, May 18, 2013.

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Baby Bees Journey

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On February 2, 2012, our unborn baby girl Bee was diagnosed with a congenital diaphragmatic hernia CDH. This is going to be a journey.

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This web page babybeehelms.blogspot.com states the following, "On February 2, 2012, our unborn baby girl Bee was diagnosed with a congenital diaphragmatic hernia CDH." We saw that the webpage said " This is going to be a journey." It also said " Thursday, May 15, 2014. Bonnie had a rough week around Easter. Shes doing great now, and if you want the abbreviated version of this story which, thank you Jesus, has a happy ending, skip to the end. Otherwise, hang on tight for the play-by-play. She slept okay-ish through the night, but would cry and whimper occasionally."

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