babyjacobrondeau.blogspot.com
One Day at a TimeA blog about our journey with our son diagnosed with a Congenital Diaphragmatic Hernia (CDH)
http://babyjacobrondeau.blogspot.com/
A blog about our journey with our son diagnosed with a Congenital Diaphragmatic Hernia (CDH)
http://babyjacobrondeau.blogspot.com/
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One Day at a Time | babyjacobrondeau.blogspot.com Reviews
https://babyjacobrondeau.blogspot.com
A blog about our journey with our son diagnosed with a Congenital Diaphragmatic Hernia (CDH)
babyjacobrondeau.blogspot.com
One Day at a Time: January 2012
http://babyjacobrondeau.blogspot.com/2012_01_01_archive.html
One Day at a Time. 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. Words from Our Friend, a Mommy of a CDH Survivor. Let's Start at the Very Beginning. No posts. Show all posts. No posts. Show all posts. Subscribe to: Posts (Atom). Prayer for Our Sick Child. Throughout history there have been times when God's people, full of faith, have stepped out not knowing how...
One Day at a Time: The Rondeau's
http://babyjacobrondeau.blogspot.com/p/rondeaus.html
One Day at a Time. 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. Words from Our Friend, a Mommy of a CDH Survivor. Let's Start at the Very Beginning. Andy and Katy are proud parents of Landon, 5, and Hazel, 20 months. Andy is a full-time teacher and Katy supplements their income as a substitute teacher. Subscribe to: Posts (Atom). Prayer for Our Sick Child.
One Day at a Time: False Alarm
http://babyjacobrondeau.blogspot.com/2012/08/false-alarm.html
One Day at a Time. 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. Words from Our Friend, a Mommy of a CDH Survivor. Let's Start at the Very Beginning. Glad we know the outcome so we can get some sleep tonight with no worries! Labels: Congenital Diaphragmatic Hernia. Subscribe to: Post Comments (Atom). Prayer for Our Sick Child. St Gerard, who, like the Savior, lo...
One Day at a Time: Welcome To Holland-Sept 18, 2011
http://babyjacobrondeau.blogspot.com/2011/09/septeber-15-2011.html
One Day at a Time. 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. Words from Our Friend, a Mommy of a CDH Survivor. Let's Start at the Very Beginning. Welcome To Holland-Sept 18, 2011. They aren't sure what to expect in the future days/weeks, but their perinatologist says they are in the best of hands. Both UW Hospital and Seattle Children's are renowned for ...
One Day at a Time: Growing so fast!
http://babyjacobrondeau.blogspot.com/2012/07/growing-so-fast.html
One Day at a Time. 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. Words from Our Friend, a Mommy of a CDH Survivor. Let's Start at the Very Beginning. Jul 28, 2012 -So here we are months since our last blog posting. Boy, how things have and are quickly changing! We don't have to come back for 4 months? Done that, ever! Slowly we are reclaiming our house, and it i...
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lucyslightandhope.blogspot.com
Lucy's Light: Lucy's Heaven Day
http://lucyslightandhope.blogspot.com/2012/03/lucys-heaven-day.html
Our story of life with our little girl, Lucia, aka "Lucy", who was diagnosed at 20 weeks with Mosaic Trisomy 16, a congenital diaphragmatic hernia, tetralogy of fallot, and IUGR. Tuesday, March 27, 2012. Some verses came to mind this morning that I think I never truly understood until now. Here are a few:. Hope fill you with. As you trust in him, so that you may overflow with hope by. Oh, and He has filled us with joy and peace in this difficult time! Understanding, will guard your hearts. May rest on me.
tyce.gina.drew.will: January 2012
http://thenasinecfamily.blogspot.com/2012_01_01_archive.html
We had a week in January where school was cancelled for 4 days! Played in the snow. We did a lot of this. Made donuts at 10:00 one night. Worked on 2 puzzles. We celebrated Grammy's birthday! Look what Santa brought! Mommy and Daddy I got just what I wanted! Noni, Julia and Jacob. My brother, cousin, and I with my 96 year old Auntie. Getting ready to open presents. By 10:30 for brunch. We met the whole Nasinec. And I were very thankful this Christmas season to have the gifts of Jesus, health, family, fri...
tyce.gina.drew.will: Christmas Eve
http://thenasinecfamily.blogspot.com/2012/01/christmas-eve.html
We brought a bottle of wine that we bought in Rome, Italy in 2003 to be corked. It was fun to share it with everyone at dinner. We weren't sure how. It would taste, but it was really good! Us with our boys! Will took this picture of the whole table. Not bad buddy! Drew and Will with their grandparents. Adorable picture! We went to Daniel's Broiler for dinner on Christmas Eve. This is a Nasinec. This year we dined with Tyce's. Games and of course eat. Drew loves oysters on the half shell.
lucyslightandhope.blogspot.com
Lucy's Light: Mayflies in February and Junebugs in April
http://lucyslightandhope.blogspot.com/2012/03/mayflies-in-february-and-junebugs-in.html
Our story of life with our little girl, Lucia, aka "Lucy", who was diagnosed at 20 weeks with Mosaic Trisomy 16, a congenital diaphragmatic hernia, tetralogy of fallot, and IUGR. Tuesday, March 20, 2012. Mayflies in February and Junebugs in April. After that appointment I met a wonderful lady, Karen, who showed me around the NICU, labor and delivery, and walked me to my cardiologist appointment. It's so nice to have kind people working with you in a time like this. Here are a couple of verses for today:.
Our Cleft journey… and so much more.: Now what?
http://bugbeefamily.blogspot.com/2011/10/now-what.html
Our Cleft Lip Journey. It stresses me out a bit. We have reverted to getting naps in the swing and car seat and he is refusing to be put down in his crib. I don't mind dealing with all this but when I have to rely on someone else to do it for 12 hours, it worries me. I am hoping for some major changes in the next 5 days. Sunday was a replay of the night before. He slept off and on in his swing. Luckily, my mother-in-law was here and took over at 5 am so that I could catch a few hours of sleep. I am a gra...
Our Cleft journey… and so much more.: 05.08
http://bugbeefamily.blogspot.com/2008_05_01_archive.html
Our Cleft Lip Journey. This Memorial weekend we spent it with our great friends Jeff and Lauren in Lake Chelan. The weather couldn't have been better! Visiting the local fire department, go cart racing with daddy (Dan and I both agreed that the $7 was worth it to see that smile on his face) and put-put golfing (Uncle Tom would be proud! Tyler-isms of the weekend. Sounding very frusterated as he was trying to get to sleep with a stuffy nose, "Mommy, my nose not working! Mommy, why I can't fly". I guess he...
Our Cleft journey… and so much more.: 02.08
http://bugbeefamily.blogspot.com/2008_02_01_archive.html
Our Cleft Lip Journey. I yuv everyone 'cause it balentine's day, mommy". Tyler had his very first Valentine's Day party at school yesterday. He was so excited to tell me about it that he could barely get the words out (literally! Tylerisms of the day. Mommy, my feelings hurt.". Why are your feelings hurt Tyler? Pointing to his tummy) "Because there is poop stuck in them.". Mommy, I want my bones come out now.". Tyler and mom at the Zoo. What crazy kids we have! I have begun this web site to keep family a...
Our Cleft journey… and so much more.: Our Cleft Lip Journey
http://bugbeefamily.blogspot.com/p/grahams-cleft-journey.html
Our Cleft Lip Journey. Our Cleft Lip Journey. January 21st, 2011 Dan and I walked into Seattle Ultrasound anxious yet excited to find out what this little bean was going to be. Never did it cross my mind that baby #3 might have something wrong. Baby #3, afterall, was going to be my girl. I was a horrible mother. What did I do to have hurt my baby? Did I cause this? The coming weeks were full of doctor's appointments, ultrasounds, genetics appointment, and tears. Each day I woke up only to remember th...
Our Cleft journey… and so much more.: 04.08
http://bugbeefamily.blogspot.com/2008_04_01_archive.html
Our Cleft Lip Journey. Look what Tyler did at school! Okay, so this may not be a big deal to all of you but it is for me! I will leave out the part about where the nipples are! The things that we get excited about are pretty crazy huh? I just had to share this one. Here is what happens when you leave your kid with Auntie Lauren and Uncle Jeff too long. They turn into a democrat. Tyler now proudly marches around the house chanting "Go Bama! Tyler and Claire goofing off after swimming lessons.
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The Chronicles of Jack
The Chronicles of Jack. I'm DCMum. I'm a stay at home mom to Toodles, born in 2010, and Squish, born in 2013. Ilove to cook, garden, live green, and dote on my precious kiddos. Toodles has Sensory Processing Disorder (SPD) and Autism Spectrum Disorder (ASD). Both kids have food allergies. It's a bit of a circus here, but I love it! View my complete profile. The water lilies and lotus blossoms were gorgeous. I'm not exactly sure what this face is. Daddy probably said something "funny.". Posted by DC Mum.
Letters to Jaco
Dear Jaco, Yes, I made a blog. For you. With pictures. Love, Nanay. Sunday, April 20, 2014. Will you remember this boardwalk? Will you remember this whole trip? Your first boat ride was so much fun! We couldn't stop smiling and we were singing/shouting too. You couldn't wait to get home just so you could ride the boat again. I'm glad you liked it. :). Thursday, April 17, 2014. This is a time when you were fearless, and you enjoyed it. I hope you keep on trying new things (but be smart about them! It's on...
Baby Jacob – Blind Irish Baby with Anophthalmos – Please Donate Now
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Jacob Allen Victorino Zeigler Sudden Infant Death Syndrome
If you have time Please vote for Jacob's page. If you already voted, Thank you! Jacob's awards are displayed proudly on his awards page. Our baby Jacob Allen, is on the new. 2004 SIDS T-shirts 2nd row 14th baby from the left. Please check out all the little angels lost so soon. SIDS Families Cafe Press Store! Http:/ www.cafeshops.com/sidsfamilies. This Angels Among Us. Site is owned by. Jacob Allen Victorino Zeigler Sudden Infant Death Syndrome. Want to join the Angels Among Us Net Ring. Site is owned by.
Jacob and Leah
Sunday, August 12, 2012. It's been awhile since I posted! Okay MONTHS, and we have been soo busy that I just haven't even thought to update the blog so i'll start with summer and then go onto the rest of the yr. This summer has been super busy. Jacob and Leah took swimming lessons and Leah graduated to level 2 since she has now learned how to swim short distances and does very well! Jimmy also coached Jacob's tball team as you can see in the picture below! He was a great coach and the kids had a great ti...
One Day at a Time
One Day at a Time. 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. Words from Our Friend, a Mommy of a CDH Survivor. Let's Start at the Very Beginning. Welcome To Holland-Sept 18, 2011. They aren't sure what to expect in the future days/weeks, but their perinatologist says they are in the best of hands. Both UW Hospital and Seattle Children's are renowned for ...
It's a...Virtual Shower!
Thursday, July 24, 2008. Our gorgeous girl- Piper Lily Grace Jacobs- was born on July 8, 2008 at 12:54pm, weighing in at 4lbs. 6oz. She is darling, a champion eater, and is packing on the weight with a rapidity that makes us quite proud. Her birth story is quite a saga- and I do plan to share it with you all, but first must manage to pull out from the current state of exhaustion that has gripped our household. Friday, July 4, 2008. My name is Tara, and I am a Contest-aholic. Fingers crossed, y'all! Shame...
babyjacobsjourney.blogspot.com
Jacob's Journey
Jacob was born at 25 weeks gestation due to mom's placenta abruption and placenta previa, and was 3 1/2 months early. He is in the NICU and we hope to bring him home by Christmas. Follow his progress: Click on the link to subscribe to this blog and it will appear in your "My Yahoo" or Google news feed. Or sign up to become a Follower. Sunday, September 25, 2011. Jacob's First Year Video. Saturday, December 18, 2010. Ready to go home - Dec 17 - 6 lbs. Big Brother and Sister welcome Jacob Home. We have bee...
babyjacobsjourney.com
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