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Dancing in the Rain

"Life is not about waiting for the storm to pass...it's about learning to dance in the rain." - Vivian Greene

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Dancing in the Rain | jennychildress.blogspot.com Reviews
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&quot;Life is not about waiting for the storm to pass...it&#39;s about learning to dance in the rain.&quot; - Vivian Greene
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2 julia's story
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4 about trisomy 18
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8 trisomy 18 awareness
9 rare trisomy parents
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Dancing in the Rain | jennychildress.blogspot.com Reviews

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&quot;Life is not about waiting for the storm to pass...it&#39;s about learning to dance in the rain.&quot; - Vivian Greene

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Dancing in the Rain: March 2015

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Dancing in the Rain. A Trisomy 18 Journey. Life is not about waiting for the storm to pass. It's about learning to dance in the rain. - Vivian Greene. Wednesday, March 18, 2015. Trisomy 18 Awareness Day 2015: 18 Things You Should Know. March 18 is Trisomy 18 Awareness Day. In recognition of this day each year, I share a list I compiled of "18 things I think everyone should know about Trisomy 18". 1 Trisomy 18 is also known as Edwards Syndrome. 6 99% of families with a child living with trisomy 18 describ...

2

Dancing in the Rain: Julia's Story

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Dancing in the Rain. A Trisomy 18 Journey. Life is not about waiting for the storm to pass. It's about learning to dance in the rain. - Vivian Greene. I found out I was pregnant with our much anticipated third child in April 2010. At 21 weeks, we had a routine level 2 ultrasound to do an anatomy scan. At this appointment, I was told that the baby (a girl! She did very well with it and we continued to feed her as often as she would eat! That will always be one of the best days of my life. By plane to spen...

3

Dancing in the Rain: September 2013

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Dancing in the Rain. A Trisomy 18 Journey. Life is not about waiting for the storm to pass. It's about learning to dance in the rain. - Vivian Greene. Monday, September 30, 2013. I am thankful to have had her in my life for so long. I am thankful to have had a wonderful relationship with her and to have many wonderful memories as a child and as an adult. I am most thankful that she met all four of my children. Here she is with me as a baby and with each of my littles. I love and miss them both so much.

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Dancing in the Rain: June 2013

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Dancing in the Rain. A Trisomy 18 Journey. Life is not about waiting for the storm to pass. It's about learning to dance in the rain. - Vivian Greene. Sunday, June 30, 2013. For the fourth week of the Illuminate class, the journal assignment was to write about where we see ourselves one year from now. The photo assignment revolved around one word that holds significance for us right now. We were to photograph the letters of our one word found in nature, architecture, and design. For week two, click here.

5

Dancing in the Rain: Two Years Gone

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Dancing in the Rain. A Trisomy 18 Journey. Life is not about waiting for the storm to pass. It's about learning to dance in the rain. - Vivian Greene. Monday, December 16, 2013. Two years today since Julia drew her last breath. Since I have no words of my own today here is one of my favorite poems. This poem was read at Julia's memorial service. Love you, Julia. I stopped by today to read through your pictures and memories of sweet Julia. Smiling through tears. December 17, 2013 at 11:24 AM.

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One Day at a Time: Avery's Name Gallery

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One Day at a Time. The story of a mom trying to figure out life without her daughter.one day at a time. Avery's name written all around the world. Thank you to everyone who has taken the time to remember Avery in pictures. More are always welcome! By Me and the Hubby. In the Pennsylvania Snow. I found this on our trip home from Vegas in the Delta Sky Mall Magazine. From Avery's cousins-Tucker and Jack. From BLM Lisa in IL. From BLM Vanessa in CA. From BLM Angel in Ontario. From BLM Dani in Salt Lake City.

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One Day at a Time: Capture your grief 2012

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One Day at a Time. The story of a mom trying to figure out life without her daughter.one day at a time. Wednesday, November 5, 2014. Capture your grief 2012. Day 1: Sunrise- Titusville, Fl. I find these lyrics fitting to where I am currently and the topic for today, " We were born to be the ones,. To show the faithless what we've done. And there's a fire inside, It burns like the surface of the sun.". Day 2: Heart ❤️ I hold both of my beautiful daughters in my heart. At times I can be completely overcome...

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One Day at a Time: Unfamiliar Territory

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One Day at a Time. The story of a mom trying to figure out life without her daughter.one day at a time. Sunday, May 17, 2015. I've hit an odd place in my journey. Early on the tears flowed like waterfalls. Everything was dark, pitch black. There was no hope, there was no happiness, just a black hole of never ending pain. And I truly couldn't imagine a life that was any different. I mean, how could I? Lose her too. She keeps us busy, she makes us smile, she makes us cry, she makes our hearts fill with...

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One Day at a Time: 3 years

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One Day at a Time. The story of a mom trying to figure out life without her daughter.one day at a time. Friday, June 12, 2015. The clock just hit midnight and just like that, it's June 12th.again, I've been laying in bed for over an hour trying to will myself to sleep and stop my mind from wandering to no avail. My thoughts. I can't help but relive that night. Yet it's killing me that the memories are getting fuzzy. I remember the timeline. In bed around 10, up at midnight. Blogs that have helped me.

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One Day at a Time: Experiences

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One Day at a Time. The story of a mom trying to figure out life without her daughter.one day at a time. Thursday, January 29, 2015. Before I knew I was pregnant, I spent a long weekend in NYC visiting my former college roommate and one of my absolute best friends, Sarah. And while I didn't know it until a few days after I arrived home, Avery was with me for that trip. She was around 4 weeks at the time and got to experience all of NYC as a little gummy bear. She spent 9 months and 6 days knowing nothing ...

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MY LIFE WITH ZANE: July 2014

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MY LIFE WITH ZANE. Our son was diagnosed with Trisomy 18 five days after birth. We were told he probably would live for two months- no more. He has managed to defy the odds placed against him. Zane is now nine. 8220;Every day is a journey,. And the journey itself is home.”. 9829;♥♥. Enter your email address:. Zane in the News. East Valley Tribune Photo. Susan Oloier, Author. Our Life on the Road. So Crazy Broken-Hearted After All These Years. Love and a Leap of Faith. Susan Oloier, Author. One of the thi...

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MY LIFE WITH ZANE: February 2015

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MY LIFE WITH ZANE. Our son was diagnosed with Trisomy 18 five days after birth. We were told he probably would live for two months- no more. He has managed to defy the odds placed against him. Zane is now nine. 8220;Every day is a journey,. And the journey itself is home.”. 9829;♥♥. Enter your email address:. Zane in the News. East Valley Tribune Photo. Susan Oloier, Author. Our Life on the Road. So Crazy Broken-Hearted After All These Years. Love and a Leap of Faith. Susan Oloier, Author. As it stands r...

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MY LIFE WITH ZANE: March 2014

http://mylifewithzane.blogspot.com/2014_03_01_archive.html

MY LIFE WITH ZANE. Our son was diagnosed with Trisomy 18 five days after birth. We were told he probably would live for two months- no more. He has managed to defy the odds placed against him. Zane is now nine. 8220;Every day is a journey,. And the journey itself is home.”. 9829;♥♥. Enter your email address:. Zane in the News. East Valley Tribune Photo. Susan Oloier, Author. Our Life on the Road. So Crazy Broken-Hearted After All These Years. Love and a Leap of Faith. Susan Oloier, Author. Due to illness...

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