babyjacobrondeau blogspot.com

One Day at a Time

A blog about our journey with our son diagnosed with a Congenital Diaphragmatic Hernia CDH

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LINKS TO WEB SITE

Our Cleft journey and so much more.

Well well well, here we go again. The guilt of not documenting for the kids has won over. Hoping to be able to use this as a place to keep memories, funny stories and to share my thousands of pictures that I take. The boys loved the sunshine, water and most importantly, the fishing. What visit is complete with out a visit to Slide Waters.

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.

Lucys Light

Friday, June 29, 2012. I know that Lucy is with God and that is the best place she could be. We appreciate your continued prayers as we try to live lives that will allow us to be with Lucy again someday in Heaven. Saturday, April 14, 2012. Tuesday, March 27, 2012. Your minds in Christ Jesus.

tyce.gina.drew.will

Our neighbors gave us some tickets to a game and we brought the boys. It was a gorgeous day and so beautiful at the stadium. Drew was in heaven and Will was happy to have cotton candy! Tyce and I had a lot of fun enjoying the game, our boys, and the sunshine. Our tall guy in yellow. Drew played in the Puyallup Rec league this winter. He loved every minute of it.

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One Day at a Time

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A blog about our journey with our son diagnosed with a Congenital Diaphragmatic Hernia CDH

CONTENT

This web page babyjacobrondeau.blogspot.com states the following, "A place of opportunity to show love and care for the Rondeau Family as they face the unknown journey of delivering and caring for their son, Jacob, who has a Congenital Diaphragmatic Hernia." We saw that the webpage said " Words from Our Friend, a Mommy of a CDH Survivor." It also said " Lets Start at the Very Beginning. Welcome To Holland-Sept 18, 2011. They arent sure what to expect in the future daysweeks, but their perinatologist says they are in the best of hands. Both UW Hospital and Seattle Childrens are renowned for ."

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Agora somos quatro!!

O Blog começou quando morávamos em Blumenau, e podíamos assim compartilhar com amigos e familiares um pouquinho da emoção de construir uma família linda e abençoada! Já se passaram mais de 3 anos, e hoje este é um lugarzinho aconchegante em que publicamos os momentos mais especiais do nossos tesourinhos! Terça-feira, 30 de junho de 2015. Agora sim, família completa! E no dia 30 de junho de 2015 nossa princesinha resolveu nascer! Gabi, estamos muito felizes com a sua chegada! Links para esta postagem.