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Michael's Tree

Our journey through life ~ trisomy 18 diagnosis, life after loss and rainbow baby/babies, infertility, advanced maternal age and the new normal - dealing with grief.

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Michael's Tree | babymichaelsjourney.blogspot.com Reviews
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Our journey through life ~ trisomy 18 diagnosis, life after loss and rainbow baby/babies, infertility, advanced maternal age and the new normal - dealing with grief.
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Michael's Tree | babymichaelsjourney.blogspot.com Reviews

https://babymichaelsjourney.blogspot.com

Our journey through life ~ trisomy 18 diagnosis, life after loss and rainbow baby/babies, infertility, advanced maternal age and the new normal - dealing with grief.

INTERNAL PAGES

babymichaelsjourney.blogspot.com babymichaelsjourney.blogspot.com
1

Michael's Tree: December 2013

http://babymichaelsjourney.blogspot.com/2013_12_01_archive.html

Our journey through life trisomy 18 diagnosis, life after loss and rainbow baby/babies, infertility, advanced maternal age and the new normal - dealing with grief. Sunday, December 29, 2013. On the night you were born. Watching Michael's lantern float away. Super Wyatt - Michael's little brother, our suprise rainbow "pot of gold". Amazing Destin Sunset - just for tour 4th Heavenly Birthday. I have met some amazing people along the way, some people that have also gone through this and quite a few that I d...

2

Michael's Tree: Our Rainbow...

http://babymichaelsjourney.blogspot.com/2011/03/our-rainbow.html

Our journey through life trisomy 18 diagnosis, life after loss and rainbow baby/babies, infertility, advanced maternal age and the new normal - dealing with grief. Saturday, March 12, 2011. Ok I am going to give this a whirl because that US tech was so nice I want to share with you. The umbilical cord is up by his head and he is kind of folded up like a taco, so some of it looks distorted, but he has his daddy's lips that is a for sure! Subscribe to: Post Comments (Atom). Our gift from God.

3

Michael's Tree: Our little man...

http://babymichaelsjourney.blogspot.com/2011/06/our-little-man.html

Our journey through life trisomy 18 diagnosis, life after loss and rainbow baby/babies, infertility, advanced maternal age and the new normal - dealing with grief. Thursday, June 2, 2011. With love, we welcome William Lee Ketchersid April 25th, 2011 at 6lbs, 14oz and 20 inches long. June 2, 2011 at 1:13 PM. He is just beautiful and stunning! Thank you so much for sharing, we have all been waiting a long time to hear this wonderful news. Sending love! June 3, 2011 at 3:01 PM. What a beautiful rainbow!

4

Michael's Tree: On the night you were born...

http://babymichaelsjourney.blogspot.com/2013/12/on-night-you-were-born.html

Our journey through life trisomy 18 diagnosis, life after loss and rainbow baby/babies, infertility, advanced maternal age and the new normal - dealing with grief. Sunday, December 29, 2013. On the night you were born. Watching Michael's lantern float away. Super Wyatt - Michael's little brother, our suprise rainbow "pot of gold". Amazing Destin Sunset - just for tour 4th Heavenly Birthday. I have met some amazing people along the way, some people that have also gone through this and quite a few that I d...

5

Michael's Tree: October 2010

http://babymichaelsjourney.blogspot.com/2010_10_01_archive.html

Our journey through life trisomy 18 diagnosis, life after loss and rainbow baby/babies, infertility, advanced maternal age and the new normal - dealing with grief. Wednesday, October 13, 2010. Tomorrow is another day. Ok perhaps I am harboring a little teensy resentment. Thanks Shannon for my picture from A Walk to Remember! Monday, October 11, 2010. Thank you Shannon for remembering Michael. October is national Pregnancy and Infant Loss Awareness Month. Friday, October 8, 2010. This is so to the point a...

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jen-ourlittleking.blogspot.com jen-ourlittleking.blogspot.com

Our Little King: February 2011

http://jen-ourlittleking.blogspot.com/2011_02_01_archive.html

Learning how to be a mom to a child I can hold and a child in heaven. My son, Ryan, was diagnosed with a fatal genetic disorder during pregnancy. This is the story of our time with him and our journey as we live without him in our arms. There is a sacredness in tears. They are not the mark of weakness, but of power. They speak more eloquently than ten thousand tongues. They are the messengers of overwhelming grief.and of unspeakable love.". Sunday, February 27, 2011. God loves you no matter what". I firs...

jen-ourlittleking.blogspot.com jen-ourlittleking.blogspot.com

Our Little King: February 2013

http://jen-ourlittleking.blogspot.com/2013_02_01_archive.html

Learning how to be a mom to a child I can hold and a child in heaven. My son, Ryan, was diagnosed with a fatal genetic disorder during pregnancy. This is the story of our time with him and our journey as we live without him in our arms. There is a sacredness in tears. They are not the mark of weakness, but of power. They speak more eloquently than ten thousand tongues. They are the messengers of overwhelming grief.and of unspeakable love.". Thursday, February 14, 2013. Links to this post. I am a wife, mo...

jen-ourlittleking.blogspot.com jen-ourlittleking.blogspot.com

Our Little King: November 2010

http://jen-ourlittleking.blogspot.com/2010_11_01_archive.html

Learning how to be a mom to a child I can hold and a child in heaven. My son, Ryan, was diagnosed with a fatal genetic disorder during pregnancy. This is the story of our time with him and our journey as we live without him in our arms. There is a sacredness in tears. They are not the mark of weakness, but of power. They speak more eloquently than ten thousand tongues. They are the messengers of overwhelming grief.and of unspeakable love.". Sunday, November 28, 2010. All of Me (bowensheart.com). I won't ...

jen-ourlittleking.blogspot.com jen-ourlittleking.blogspot.com

Our Little King: January 2011

http://jen-ourlittleking.blogspot.com/2011_01_01_archive.html

Learning how to be a mom to a child I can hold and a child in heaven. My son, Ryan, was diagnosed with a fatal genetic disorder during pregnancy. This is the story of our time with him and our journey as we live without him in our arms. There is a sacredness in tears. They are not the mark of weakness, but of power. They speak more eloquently than ten thousand tongues. They are the messengers of overwhelming grief.and of unspeakable love.". Wednesday, January 26, 2011. Links to this post. How is it, that...

jen-ourlittleking.blogspot.com jen-ourlittleking.blogspot.com

Our Little King: The Redeemer

http://jen-ourlittleking.blogspot.com/2011/06/redeemer.html

Learning how to be a mom to a child I can hold and a child in heaven. My son, Ryan, was diagnosed with a fatal genetic disorder during pregnancy. This is the story of our time with him and our journey as we live without him in our arms. There is a sacredness in tears. They are not the mark of weakness, but of power. They speak more eloquently than ten thousand tongues. They are the messengers of overwhelming grief.and of unspeakable love.". Wednesday, June 1, 2011. I may never get back again. Cause You c...

destinitely.blogspot.com destinitely.blogspot.com

"Little Things" along the Emerald Coast: James Wyatt Ketchersid ~ A little late, but here he is!

http://destinitely.blogspot.com/2012/12/james-wyatt-ketchersid-little-late-but.html

Little Things" along the Emerald Coast. We live in Destin, Florida a small coastal fishing village community. The sand is like powdered sugar, you literally sink into it and the water is Emerald Green. We try to experience everything we can around here. These are some of the "little things" worth not missing. Tuesday, December 18, 2012. James Wyatt Ketchersid A little late, but here he is! Thank you Jessica James. He was so tiny. Laying in a dough bowl wrapped in his big brother Michael's.

jen-ourlittleking.blogspot.com jen-ourlittleking.blogspot.com

Our Little King: D day

http://jen-ourlittleking.blogspot.com/2011/07/d-day.html

Learning how to be a mom to a child I can hold and a child in heaven. My son, Ryan, was diagnosed with a fatal genetic disorder during pregnancy. This is the story of our time with him and our journey as we live without him in our arms. There is a sacredness in tears. They are not the mark of weakness, but of power. They speak more eloquently than ten thousand tongues. They are the messengers of overwhelming grief.and of unspeakable love.". Friday, July 1, 2011. Where has a year gone? I don't think I was...

jen-ourlittleking.blogspot.com jen-ourlittleking.blogspot.com

Our Little King

http://jen-ourlittleking.blogspot.com/2011/09/as-day-of-ryans-birthday-gets-closer-i.html

Learning how to be a mom to a child I can hold and a child in heaven. My son, Ryan, was diagnosed with a fatal genetic disorder during pregnancy. This is the story of our time with him and our journey as we live without him in our arms. There is a sacredness in tears. They are not the mark of weakness, but of power. They speak more eloquently than ten thousand tongues. They are the messengers of overwhelming grief.and of unspeakable love.". Thursday, September 15, 2011. Just Because time has passed.

jen-ourlittleking.blogspot.com jen-ourlittleking.blogspot.com

Our Little King: September 2011

http://jen-ourlittleking.blogspot.com/2011_09_01_archive.html

Learning how to be a mom to a child I can hold and a child in heaven. My son, Ryan, was diagnosed with a fatal genetic disorder during pregnancy. This is the story of our time with him and our journey as we live without him in our arms. There is a sacredness in tears. They are not the mark of weakness, but of power. They speak more eloquently than ten thousand tongues. They are the messengers of overwhelming grief.and of unspeakable love.". Thursday, September 15, 2011. Just Because time has passed.

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Monday, May 14, 2012. Happy Birthday, Michael! Four years ago today the world welcomed Michael and became a better place because of him. Happy 4th Birthday, Michael! Saturday, May 5, 2012. Thank you to everyone who donated to the Congenital Heart Walk! Thanks to you Team Mick raised more than $6,300, coming in as the #2 fundraising team! The DC walk raised more than $75,000 for this vital research. Much love and appreciation. Friday, April 27, 2012. Every dollar helps and no amount is too small. Well, al...

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Michael's Tree

Our journey through life trisomy 18 diagnosis, life after loss and rainbow baby/babies, infertility, advanced maternal age and the new normal - dealing with grief. Sunday, December 29, 2013. On the night you were born. Watching Michael's lantern float away. Super Wyatt - Michael's little brother, our suprise rainbow "pot of gold". Amazing Destin Sunset - just for tour 4th Heavenly Birthday. I have met some amazing people along the way, some people that have also gone through this and quite a few that I d...

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