Our 5th daughter, Meagan, was diagnosed with severe Congenital Hydrocephalus at our 20 week ultrasound. Her story has propelled our family on a new journey. I hope to keep track of Meagan's story here to help other parents who may face a Hydrocephalus diagnosis for their child, and to celebrate Meagan's life.
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Meagan | pricelesslittlepearl.blogspot.com Reviews
https://pricelesslittlepearl.blogspot.com
Our 5th daughter, Meagan, was diagnosed with severe Congenital Hydrocephalus at our 20 week ultrasound. Her story has propelled our family on a new journey. I hope to keep track of Meagan's story here to help other parents who may face a Hydrocephalus diagnosis for their child, and to celebrate Meagan's life.
pricelesslittlepearl.blogspot.com
Meagan: March Updates Part 2 - Walking Together
http://pricelesslittlepearl.blogspot.com/2015/03/march-updates-part-2-walking-together.html
Our 5th daughter, Meagan, was diagnosed with severe Congenital Hydrocephalus at our 20 week ultrasound. Her story has propelled our family on a new journey. I hope to keep track of Meagan's story here to help other parents who may face a Hydrocephalus diagnosis for their child, and to celebrate Meagan's life. Courtesy: TIffany Kay Photography. Tuesday, March 31, 2015. March Updates Part 2 - Walking Together. We finally had some success with this on Monday afternoon! So, despite the quite disastrous start...
Meagan: Independence
http://pricelesslittlepearl.blogspot.com/2015/07/independence.html
Our 5th daughter, Meagan, was diagnosed with severe Congenital Hydrocephalus at our 20 week ultrasound. Her story has propelled our family on a new journey. I hope to keep track of Meagan's story here to help other parents who may face a Hydrocephalus diagnosis for their child, and to celebrate Meagan's life. Courtesy: TIffany Kay Photography. Thursday, July 9, 2015. Trying on Pop's hat. Riding on my brother's old horse from. When we lived in Germany. Reilly having some fun after her soft shoe round.
Meagan: March Updates Part 1 - Walking outside....
http://pricelesslittlepearl.blogspot.com/2015/03/walking-outside-part-1.html
Our 5th daughter, Meagan, was diagnosed with severe Congenital Hydrocephalus at our 20 week ultrasound. Her story has propelled our family on a new journey. I hope to keep track of Meagan's story here to help other parents who may face a Hydrocephalus diagnosis for their child, and to celebrate Meagan's life. Courtesy: TIffany Kay Photography. Monday, March 30, 2015. March Updates Part 1 - Walking outside. It was so joy filled and giggly. I then heard the other girls chime in with "thank you! I'm not rea...
Meagan: The First Hit
http://pricelesslittlepearl.blogspot.com/2011/06/first-hit.html
Our 5th daughter, Meagan, was diagnosed with severe Congenital Hydrocephalus at our 20 week ultrasound. Her story has propelled our family on a new journey. I hope to keep track of Meagan's story here to help other parents who may face a Hydrocephalus diagnosis for their child, and to celebrate Meagan's life. Courtesy: TIffany Kay Photography. Tuesday, June 7, 2011. We walked in the ultrasound room, got ready and we were off on the adventure of seeing our baby! My doctor went over the pictures with me - ...
Meagan: Let the Light Shine
http://pricelesslittlepearl.blogspot.com/2015/08/let-light-shine.html
Our 5th daughter, Meagan, was diagnosed with severe Congenital Hydrocephalus at our 20 week ultrasound. Her story has propelled our family on a new journey. I hope to keep track of Meagan's story here to help other parents who may face a Hydrocephalus diagnosis for their child, and to celebrate Meagan's life. Courtesy: TIffany Kay Photography. Wednesday, August 12, 2015. Let the Light Shine. The summer flew by quickly and there were lots of happenings! My girls and me with my former dance teacher. She si...
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youjustmightfindyougetwhatyouneed.blogspot.com
Anything Can Be: June 2015
http://youjustmightfindyougetwhatyouneed.blogspot.com/2015_06_01_archive.html
Friday, June 19, 2015. Another year goes by. Obviously I have been woefully neglecting Addie's blog. This is mostly a good news thing. We have been crazy busy and she's been doing well! She requested a domino cake! Lol She loves playing with dominoes. She saw Dr. George in early May for her one year follow up, and I had to snap our traditional picture with him. I think she likes him as much as her mom does! I am in my next to last semester of grad school! Subscribe to: Posts (Atom). Me, the mom, wife and...
thejourneyoftheharts.blogspot.com
The Journey of The Hart's: Happy Valentine's Day!
http://thejourneyoftheharts.blogspot.com/2013/02/happy-valentines-day.html
The Journey of The Hart's. The chaos of our daily lives. Jonathan, April, Quincey and Isabelle. Or Better Yet.My Lifes a CIRCUS without the Tent! Friday, February 15, 2013. Oh, the post that I need to write in order to catch this little blog up. But anyway, here is a current picture of the girls on Valentine's Day, it is a rare occurrence when I actually get a picture of both girls smiling without tears involved. This does NOT occur with anyone else either. View my complete profile. We Are THAT Family.
thejourneyoftheharts.blogspot.com
The Journey of The Hart's: Merry Christmas......
http://thejourneyoftheharts.blogspot.com/2012/12/merry-christmas.html
The Journey of The Hart's. The chaos of our daily lives. Jonathan, April, Quincey and Isabelle. Or Better Yet.My Lifes a CIRCUS without the Tent! Tuesday, December 18, 2012. I am a proud mother of two beautiful girls that I have been so very BLESSED with. I am a wife to a wonderful husband that puts up with my chaos on a normal baisis. I proudly serve God our creator for he is the one who has gotten me to this point and continues to show me daily that he is holding me in his arms. View my complete profile.
Our Hydrocephalus Miracle: May 2012
http://ourhydromiracle.blogspot.com/2012_05_01_archive.html
Capturing the journey of our life with a miracle! Sunday, May 27, 2012. It's that time again, water day. Which signals the end of the school year. I can't believe Carly has finished her first full. And her second end of year celebration at the pre-school. She has one year left at the Dysart Early Childhood Education Center before. Dun, dun, dun. We are so pleased with her development and the education she has received. We have goals for the next year and hope to meet them all. Subscribe to: Posts (Atom).
thejourneyoftheharts.blogspot.com
The Journey of The Hart's: August 2012
http://thejourneyoftheharts.blogspot.com/2012_08_01_archive.html
The Journey of The Hart's. The chaos of our daily lives. Jonathan, April, Quincey and Isabelle. Or Better Yet.My Lifes a CIRCUS without the Tent! Tuesday, August 28, 2012. Quincey's a Character Kid. When I got the note from school that stated Quincey was a "Character Kid" my first reaction was.Yeah, y'all aren't telling me nothing new! Quincey was named "Character Kid" for the month of August for School Pride. Subscribe to: Posts (Atom). View my complete profile. Quinceys a Character Kid. Just the 6 of us.
thejourneyoftheharts.blogspot.com
The Journey of The Hart's: May 2012
http://thejourneyoftheharts.blogspot.com/2012_05_01_archive.html
The Journey of The Hart's. The chaos of our daily lives. Jonathan, April, Quincey and Isabelle. Or Better Yet.My Lifes a CIRCUS without the Tent! Friday, May 18, 2012. Friday, May 11, 2012. Isabelle Got a Big Girl Haircut. Subscribe to: Posts (Atom). View my complete profile. Isabelle Got a Big Girl Haircut. The Far Side Of Complexity. We Are THAT Family. This, That, and the Mother Thing. Our Journey with Fetal Hydrocephalus. Live Life In Wonder. The Hard Road Forward. I have hydro, hydro doesn't have me.
thejourneyoftheharts.blogspot.com
The Journey of The Hart's: April 2012
http://thejourneyoftheharts.blogspot.com/2012_04_01_archive.html
The Journey of The Hart's. The chaos of our daily lives. Jonathan, April, Quincey and Isabelle. Or Better Yet.My Lifes a CIRCUS without the Tent! Monday, April 16, 2012. The concept of blogging…. I go to my blog everyday as if expecting a new post! No really I go to my blog so I can see if the blogs I follow have posted anything new. Hope no one is stalking my page like that…HAHA! I’m just going to jump in with what’s going on right now and then back track here and there when I get a chance. Yes, you rea...
Our Hydrocephalus Miracle: August 2011
http://ourhydromiracle.blogspot.com/2011_08_01_archive.html
Capturing the journey of our life with a miracle! Tuesday, August 9, 2011. Is there sand on me? Subscribe to: Posts (Atom). 11/19/07- 18.3 weeks. 1367mm and 13.12mm. 3/6/08- 33.6 weeks. 3211mm and 28.19mm. Head circumference before surgery. Agenesis of the Corpus Callosum. Partial Septum Pellucidum agenesis. Grade III kidney reflux. And Four years pass by in a BLINK! A life of epilepsy. Another year goes by. Countdown to Sesame Place. Musings of a Hydro Mom. View my complete profile.
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Priceless Life Moments
Welcome to Priceless life moments.This website will launch soon.
Priceless Life Of Mine
April 09, 2018. All about the eyes and what I'm using right now. March 19, 2018. Bodega Cantina Spring menu launch Leicester. March 18, 2018. Styling H&M lace, over 40 style. March 04, 2018. The Chanel inspired jacket, over 40 style. February 19, 2018. Experiencing the Hydrafacial at Hampton Clinic. February 16, 2018. Visiting Stratford Upon Avon Things to do. February 14, 2018. Why you need a silk pillowcase in your life. January 30, 2018. Tips to unwind, pamper and sleep better. January 18, 2018.
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Priceless
Honesty. And maybe a bit too much information. Friday, July 18, 2014. We live in Colorado. It's beautiful here. We have gorgeous mountains, wildlife, amazing weather and an abundance of memories just waiting to be made. I have always wanted to be that family. You know that family? The one that hikes the Rocky Mountains,eats quinoa and goes fishing? Alas, we hike maybe once a year, have been fishing only once and no matter how many recipes I try.we just don't like quinoa. It does not. So, I finally did it!
Blog de pricelesslikeyou - Une semi-new life - Skyrock.com
Mot de passe :. J'ai oublié mon mot de passe. J'attaque le boulot, je change d'étude, je change de département à moitier, je change de région a moitier. Voila en fait cela mérite bien un nouveau blog. La vie ne vaut d'être vécu qu'a fond. Mise à jour :. Alala, c'est la rentrée pour beaucoup. Abonne-toi à mon blog! Samedi . MATCH Niark Niark Niark. Que dire à part quej'ai trop trop trop trop trop trop trop . hate d'y être. Je m'éclate déjà trop aux entrainements alorsqu'es-ce que ca sera en match. N'oubli...
pricelesslittlepearl.blogspot.com
Meagan
Our 5th daughter, Meagan, was diagnosed with severe Congenital Hydrocephalus at our 20 week ultrasound. Her story has propelled our family on a new journey. I hope to keep track of Meagan's story here to help other parents who may face a Hydrocephalus diagnosis for their child, and to celebrate Meagan's life. Courtesy: TIffany Kay Photography. Wednesday, October 26, 2016. Reilly's answer was "which time? How many 11 1/2 year old's have to ask "which" hospital stay I'm speaking of? Probably none in Reilly...
pricelesslittlethings.blogspot.com
Priceless Little Things
Non è che voglia fare il maître à penser, ma alcune cose mi sono capitate. E io ve le racconto. Mercoledì 12 agosto 2009. Et voilà il mio primo gadget. Ultimi posts! Il post originale è stato pubblicato sul mio blog dedicato allo sviluppo e alla programmazione, Develop Little Things. Martedì 11 agosto 2009. In pioppo, manico. In acero e tastiera. Infine l'estetica vintage (le forme sinuose stile jazzmaster o jaguar, il battipenna madreperla, i controlli di tono essenziali) e il grande impatto sonoro di q...
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