This blog is dedicated to my sweet baby boy William, who was born on 9/20/2013 with a bilateral cleft lip and palate. I created this blog to capture the multi-year journey we are about to embark upon and to share our story with anyone who is interested. Hopefully, our story will help other families who are in the same situation, and will maybe even spread some awareness about this common birth defect.
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Danielle Zierer
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John●●●●burg , New Jersey, 07825
United States
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Danielle Zierer
206 M●●●●●treet
John●●●●burg , New Jersey, 07825
United States
View this contact
Danielle Zierer
206 M●●●●●treet
John●●●●burg , New Jersey, 07825
United States
View this contact
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The Sweetest Little Smile | cleftcutie.com Reviews
https://cleftcutie.com
This blog is dedicated to my sweet baby boy William, who was born on 9/20/2013 with a bilateral cleft lip and palate. I created this blog to capture the multi-year journey we are about to embark upon and to share our story with anyone who is interested. Hopefully, our story will help other families who are in the same situation, and will maybe even spread some awareness about this common birth defect.
cleftcutie.com
The Sweetest Little Smile: February 2015
http://www.cleftcutie.com/2015_02_01_archive.html
The Sweetest Little Smile. This blog is dedicated to my sweet baby boy William, who was born on 9/20/2013 with a bilateral cleft lip and palate. I created this blog to capture the multi-year journey we are about to embark upon and to share our story with anyone who is interested. Hopefully, our story will help other families who are in the same situation, and will maybe even spread some awareness about this common birth defect. Wednesday, February 4, 2015. Happy New Year, everyone! Where I am able to pro...
The Sweetest Little Smile: September 2014
http://www.cleftcutie.com/2014_09_01_archive.html
The Sweetest Little Smile. This blog is dedicated to my sweet baby boy William, who was born on 9/20/2013 with a bilateral cleft lip and palate. I created this blog to capture the multi-year journey we are about to embark upon and to share our story with anyone who is interested. Hopefully, our story will help other families who are in the same situation, and will maybe even spread some awareness about this common birth defect. Saturday, September 20, 2014. Which means. WE MADE IT! This year I had the he...
The Sweetest Little Smile: Preparing for Cleft Palate Surgery and Will's First Birthday!
http://www.cleftcutie.com/2014/06/cleft-palate-surgery-fundraising.html
The Sweetest Little Smile. This blog is dedicated to my sweet baby boy William, who was born on 9/20/2013 with a bilateral cleft lip and palate. I created this blog to capture the multi-year journey we are about to embark upon and to share our story with anyone who is interested. Hopefully, our story will help other families who are in the same situation, and will maybe even spread some awareness about this common birth defect. Wednesday, June 11, 2014. The first organization is Smile Train: support....
The Sweetest Little Smile: Happy "Smile-versary" Will: One year since cleft lip repair!!
http://www.cleftcutie.com/2015/02/wills-cleft-lip-repair-anniversary.html
The Sweetest Little Smile. This blog is dedicated to my sweet baby boy William, who was born on 9/20/2013 with a bilateral cleft lip and palate. I created this blog to capture the multi-year journey we are about to embark upon and to share our story with anyone who is interested. Hopefully, our story will help other families who are in the same situation, and will maybe even spread some awareness about this common birth defect. Wednesday, February 4, 2015. Happy New Year, everyone! Where I am able to pro...
The Sweetest Little Smile: March 2014
http://www.cleftcutie.com/2014_03_01_archive.html
The Sweetest Little Smile. This blog is dedicated to my sweet baby boy William, who was born on 9/20/2013 with a bilateral cleft lip and palate. I created this blog to capture the multi-year journey we are about to embark upon and to share our story with anyone who is interested. Hopefully, our story will help other families who are in the same situation, and will maybe even spread some awareness about this common birth defect. Friday, March 28, 2014. But let me tell you, that nose takes WORK!
TOTAL PAGES IN THIS WEBSITE
19
Our Journey: September 2013
http://www.cleft-notes.com/2013_09_01_archive.html
Every mothers worst nightmare is hearing the words."there is something wrong with your child". And it doesn't make the blow any less painful, when they are talking about your unborn child.a child who you have yet to meet. This nightmare is now our reality and this blog is going to document our journey. Monday, September 30, 2013. When Days Feel like Weeks. For those of you that don’t already know, we welcomed Isla Pearl Smith into the world at 11:38 am on Wednesday September 25. And her oxygen actually d...
Our Journey: July 2014
http://www.cleft-notes.com/2014_07_01_archive.html
Every mothers worst nightmare is hearing the words."there is something wrong with your child". And it doesn't make the blow any less painful, when they are talking about your unborn child.a child who you have yet to meet. This nightmare is now our reality and this blog is going to document our journey. Thursday, July 24, 2014. The hardest part about all this is going to be our recovery time. Our plastic surgeon has very strict post -op rules. 6 weeks of wearing arm restraints. 6 weeks of no solids. They ...
Our Journey: Looming Palate Repair
http://www.cleft-notes.com/2014/07/looming-palate-repair.html
Every mothers worst nightmare is hearing the words."there is something wrong with your child". And it doesn't make the blow any less painful, when they are talking about your unborn child.a child who you have yet to meet. This nightmare is now our reality and this blog is going to document our journey. Monday, July 21, 2014. I will keep everyone posted as time goes on.but just wanted to let everyone know to keep her in your prayers over the coming weeks. Subscribe to: Post Comments (Atom).
Our Journey: Cleftopedia
http://www.cleft-notes.com/2014/03/cleftopedia.html
Every mothers worst nightmare is hearing the words."there is something wrong with your child". And it doesn't make the blow any less painful, when they are talking about your unborn child.a child who you have yet to meet. This nightmare is now our reality and this blog is going to document our journey. Thursday, March 27, 2014. Wellit's been six weeks since Isla's cleft lip repair, so it's safe to say that we've made it to the other side! We now have our official palate surgery date.August 7th! Is it was...
Our Journey: January 2015
http://www.cleft-notes.com/2015_01_01_archive.html
Every mothers worst nightmare is hearing the words."there is something wrong with your child". And it doesn't make the blow any less painful, when they are talking about your unborn child.a child who you have yet to meet. This nightmare is now our reality and this blog is going to document our journey. Friday, January 16, 2015. Our First Cleft Team Meeting. Yesterday we had our first "cleft team meeting". For those of you who don't know what this is, once a year we meet with her team which consist of:.
Our Journey: February 2014
http://www.cleft-notes.com/2014_02_01_archive.html
Every mothers worst nightmare is hearing the words."there is something wrong with your child". And it doesn't make the blow any less painful, when they are talking about your unborn child.a child who you have yet to meet. This nightmare is now our reality and this blog is going to document our journey. Thursday, February 13, 2014. Making it through to the other side. Was Isla going to handle anesthesia ok? Was I going to like her knew smile? The next few hours were horrible for me. All I could think ...
Our Journey: October 2013
http://www.cleft-notes.com/2013_10_01_archive.html
Every mothers worst nightmare is hearing the words."there is something wrong with your child". And it doesn't make the blow any less painful, when they are talking about your unborn child.a child who you have yet to meet. This nightmare is now our reality and this blog is going to document our journey. Thursday, October 31, 2013. We're officially on the road to repair! The alternative is to let the nose do what it wants and then wait until she's 4 or 5 in order for her to have her first nose job. Isla is...
Birthdays: Danielle Zierer - Smile Train
http://support.smiletrain.org/goto/smilesforwill
Will's First Birthday Fund for Smiles. Goal: $1,250.00. Achieved: $1,411.00. We Love You So Much! Ema and Pop Pop. Joe and Erica Bratsch. Deanna and Brett Yetman. Tina, Jason, Justin and Jordan. Aunt Helen and Uncle Bob. Megan, Bryan, and Nolan Bailey. Mrs Kristi M Furkey. Aunt Pat and Uncle Joe. Uncle Jerry and Aunt Liz. Dana and Brian Hawley. Dave, Michele, Isabela and Rui. Rob, Shannon, Bobby and Brooke. Beverly Brian and Carter. Sara Tolba and Seleem. My Personal Web Log. Our Vision and Mission.
Our Journey: March 2014
http://www.cleft-notes.com/2014_03_01_archive.html
Every mothers worst nightmare is hearing the words."there is something wrong with your child". And it doesn't make the blow any less painful, when they are talking about your unborn child.a child who you have yet to meet. This nightmare is now our reality and this blog is going to document our journey. Thursday, March 27, 2014. Wellit's been six weeks since Isla's cleft lip repair, so it's safe to say that we've made it to the other side! We now have our official palate surgery date.August 7th! Is it was...
Our Journey: August 2014
http://www.cleft-notes.com/2014_08_01_archive.html
Every mothers worst nightmare is hearing the words."there is something wrong with your child". And it doesn't make the blow any less painful, when they are talking about your unborn child.a child who you have yet to meet. This nightmare is now our reality and this blog is going to document our journey. Monday, August 18, 2014. But how do you explain that to a 10 month old? 2 long hours go by and our pager finally goes off! For any moms having to bring your child into surgery.just know that the WORST ...
TOTAL LINKS TO THIS WEBSITE
22
cleftclub.org - Registered at Namecheap.com
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Cleft Club Radio - podcast for cleft lip & palate community
Cleft Club Radio - podcast for cleft lip and palate community. Tuesday, October 23, 2007. Where did I go? Listen to find out. And no I have not given up on podcasting! Be sure to visit SmilePodcastNetwork.com. Posted by Calvero at 10/23/2007 01:22:00 AM. Wednesday, November 23, 2005. Cleft Club Radio - Nov. 23, 2005 - Short show to say hello and more shows will be coming. Next one will be a full, regular show :). Posted by Calvero at 11/23/2005 04:27:00 PM. Thursday, August 04, 2005. August 4, 2005.
Cleft Coffee
One Cup at a Time. The Cleft is a globally impacting coffee distributor who embraces Christian values as we work within the marketplace. Our custom roasting, competitive pricing and global impact set apart not only The Cleft Coffee but the Cleft customers. When you purchase coffee from the Cleft, you’re getting more than an outstanding quality coffee at a great price you’re making a difference in the lives of uncountable children and families throughout the world.
About The Cleft Collective | Cleft CollectiveCleft Collective
The Cleft Collective is the world’s largest cleft lip and palate research programme. An initiative of the UK-based charity, the Healing Foundation. What has caused my child’s cleft? What are the best treatments for my child? Will my child be OK (both now and in the longer term)? The Healing Foundation Cleft and Craniofacial Clinical Research Centre. About this research and how you can get involved, please follow the links below. I have a cleft or my child has a cleft. The University of Manchester, the Un...
menschenkinder.eu - dr. oliver blume - anna schaal
Webdesign von AO DESIGN München -. Internet-Seiten Homepages, Internet-Agentur, Flash-Websites. Redaktionelle Betreuung: Anna Schaal. Menschenkinder.eu - dr. oliver blume. Flash plugin wird gesucht . . . Webdesign by ao design münchen.
The Sweetest Little Smile
The Sweetest Little Smile. This blog is dedicated to my sweet baby boy William, who was born on 9/20/2013 with a bilateral cleft lip and palate. I created this blog to capture the multi-year journey we are about to embark upon and to share our story with anyone who is interested. Hopefully, our story will help other families who are in the same situation, and will maybe even spread some awareness about this common birth defect. Wednesday, September 9, 2015. This is my calling and I am loving every minute...
Cleft Lip Injury Lawsuits
FIND OUT IF YOU QUALIFY TODAY. Cleft lips or palates can affect the visual appearance of ones face and can lead to feeding/eating and speech problems as well as ear infections. Many times, surgery is required to correct and treat the defect to ensure the future health of the affected child. Recent reports link the use of certain prescription drugs during pregnancy to birth defects including cleft lips and cleft palates. Drugs that may be linked to cleft lip and palates in children:. Or Topiramate, Paxil.
Clef Technology | Clef Technology | Solving Pipe leakages with technology
Clef Technology Clef Technology Solving Pipe leakages with technology. Clef Technology is a tech start up devising solutions to help solve pipeline leakages. Our technology is cloud based which means you can be warned of a potential pipe leakage before it happens. Pipe leakages, technology, pipe leaks solutions. Your best solution for Pipe Leakage. The most advanced technology to repair your pipe. Meet Clef Technology - the all new technology designed to solve pipe leakage. Each Clef Device operates inde...
Event Solutions
We provide event planning solutions for individuals and corporate organizations. Saturday, June 14, 2014. My Top 6 Tips On Choosing The Right Event Venue. As the name connotes event venue is basically where an event is being held. Event venue can be traditional locations like school field,private resident,event centers,hotels,museums,. Above is a typical example of an event in the desert. Regardless of where you want to have your event these are my 6 favorite tips a DIY event planner must have;. You crea...
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