
cleft-notes.com
Our JourneyHere's our journey from the beginning once we found out that our daugther would be born with a cleft lip/palate
http://www.cleft-notes.com/
Here's our journey from the beginning once we found out that our daugther would be born with a cleft lip/palate
http://www.cleft-notes.com/
TODAY'S RATING
>1,000,000
Date Range
HIGHEST TRAFFIC ON
Wednesday
LOAD TIME
0.4 seconds
16x16
32x32
dara lewenthal
28291●●●●●e way
mur●●●eta , California, 92563
United States
View this contact
dara lewenthal
28291●●●●●e way
mur●●●eta , California, 92563
United States
View this contact
dara lewenthal
28291●●●●●e way
mur●●●eta , California, 92563
United States
View this contact
11
YEARS
10
MONTHS
25
DAYS
GODADDY.COM, LLC
WHOIS : whois.godaddy.com
REFERRED : http://registrar.godaddy.com
PAGES IN
THIS WEBSITE
19
SSL
EXTERNAL LINKS
20
SITE IP
216.239.32.21
LOAD TIME
0.408 sec
SCORE
6.2
Our Journey | cleft-notes.com Reviews
https://cleft-notes.com
Here's our journey from the beginning once we found out that our daugther would be born with a cleft lip/palate
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...
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: 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: December 2013
http://www.cleft-notes.com/2013_12_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. Sunday, December 29, 2013. Stage two of the NAM. Finally we are working on her nose. I'm not too sure she's as happy about it as I am.even though she looks pretty happy here. Subscribe to: Posts (Atom).
Our Journey: The NAM is back!!
http://www.cleft-notes.com/2014/02/the-nam-is-back.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, February 7, 2014. The NAM is back! But as we were driving down to San Diego I got a call from the hospital. They've moved up her surgery date again! Now it's on Tuesday the 11th! The NAM is back!
TOTAL PAGES IN THIS WEBSITE
19
The Sweetest Little Smile: On the Other Side of Cleft Palate Surgery!
http://www.cleftcutie.com/2014/09/cleft-palate-surgery.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, September 17, 2014. On the Other Side of Cleft Palate Surgery!
The Sweetest Little Smile: Dear William
http://www.cleftcutie.com/2014/09/dear-william-first-birthday.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: Living Tape Free
http://www.cleftcutie.com/2014/04/no-NAM-no-stents-tape-free.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, April 30, 2014. I'm just in awe. Speechless really. It's unbelieva...
The Sweetest Little Smile: April 2014
http://www.cleftcutie.com/2014_04_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, April 30, 2014. I'm just in awe. Speechless really. It's unbelieva...
The Sweetest Little Smile: The Countdown to Cleft Palate Repair Begins!
http://www.cleftcutie.com/2014/08/cleftpalaterepairsurgery.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. Tuesday, August 12, 2014. The Countdown to Cleft Palate Repair Begins! And do...
The Sweetest Little Smile: March 2015
http://www.cleftcutie.com/2015_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. Wednesday, March 11, 2015. It's since become quite a debate in the cleft comm...
The Sweetest Little Smile: October 2013
http://www.cleftcutie.com/2013_10_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. Tuesday, October 29, 2013. Cleft schmeft (no, really! And here is Will at 1 m...
The Sweetest Little Smile: February 2014
http://www.cleftcutie.com/2014_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. Saturday, February 22, 2014. On the Flip Side of Cleft Lip Repair.
The Sweetest Little Smile: June 2014
http://www.cleftcutie.com/2014_06_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, June 11, 2014. The first organization is Smile Train: support....
The Sweetest Little Smile: August 2014
http://www.cleftcutie.com/2014_08_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. Tuesday, August 12, 2014. The Countdown to Cleft Palate Repair Begins! And do...
TOTAL LINKS TO THIS WEBSITE
20
Cleft-Kinder-Hilfe/Professor Hermann Sailer Stiftung
Cleft-Kinder-Hilfe/Professor Hermann Sailer Stiftung.
Hilfe für Kinder mit Lippen-Kiefer-Gaumenspalte (Spaltkinder) | Cleft-Kinder-Hilfe Professor Hermann Sailer Stiftung |
Hilfe für Kinder mit Lippen-Kiefer-Gaumenspalte (Spaltkinder) Cleft-Kinder-Hilfe Professor Hermann Sailer Stiftung. Hilfe für Kinder mit Lippen-Kiefer-Gaumenspalte (Spaltkinder). Kostenlose Operationen und Nachbehandlungen (z. T. jahrelang). Information und Aufklärung der Landbevölkerung durch sogenannte Cleft-Camps. Verpflegung und Transport der Cleft-Patienten und deren Angehörigen. Aus- und Weiterbildung indischer Ärzte nach internationalen Behandlungsrichtlinien. Weiterlesen über Jahresbericht 2016.
Sie sehen hier eine soeben freigeschaltete Homepage
Price Request - BuyDomains
Url=' escape(document.location.href) , 'Chat367233609785093432', 'toolbar=0,scrollbars=0,location=0,statusbar=0,menubar=0,resizable=0,width=640,height=500');return false;". Need a price instantly? Just give us a call. Toll Free in the U.S. We can give you the price over the phone, help you with the purchase process, and answer any questions. Get a price in less than 24 hours. Fill out the form below. One of our domain experts will have a price to you within 24 business hours. United States of America.
Cleft Lips
Thursday, March 18, 2010. New Arm Restraints are now up on my website. I am so excited:. Saturday, October 31, 2009. Http:/ kidswithcleftsutah.blogspot.com. Tuesday, September 15, 2009. Baby Grace Has Arrived. Wednesday, September 9, 2009. I just got these bracelets in for Craniofacial Acceptance Month! Now to track down everyone I can to wear them! Tuesday, September 1, 2009. September is Craniofacial Month! Labels: craniofacial month september. Saturday, August 29, 2009. An Option for Babies Hands.
Our Journey
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:.
A Cleft of Diamonds - Home
A Cleft of Diamonds. Hello and welcome to the official webpage for. A Cleft of Diamonds. Another superb novel from Welsh/Australian author Tony Matthews. For those of you who have read some of Tony's other books, not just his novels but also his popular histories, you'll know that. A Cleft of Diamonds. Will keep you riveted right through to the end. A Cleft of Diamonds. Has been described as: '. a story to captivate the heart and set the blood racing.'. It is envisaged that Tony will write at least two h...
FENTES LABIO-MAXILLO-PALATINES …………………………. CLEFT LIP & PALATE …………………………. LIPPEN-KIEFER-GAUMENSPALTE
FENTES LABIO-MAXILLO-PALATINES …………………………. CLEFT LIP and PALATE …………………………. LIPPEN-KIEFER-GAUMENSPALTEN. How will I be able to feed my baby? What the orthodontist can do. Middle ear otitis, hearing status and grommets. Français) congrès & conférences. Multi-disciplinary Cleft Lip and Palate team of Lausanne, CHUV. Facial clefts (lip, lip and alveolus, with or without cleft of the palate) are also referred to as CLP. These are among the most common congenital anomalies in human. But the primary goal is to...
FENTES LABIO-MAXILLO-PALATINES …………………………. CLEFT LIP & PALATE …………………………. LIPPEN-KIEFER-GAUMENSPALTE
FENTES LABIO-MAXILLO-PALATINES …………………………. CLEFT LIP and PALATE …………………………. LIPPEN-KIEFER-GAUMENSPALTEN. Aller au contenu principal. PRISE EN CHARGE GLOBALE. L’équipe FLMP du CHUV, Lausanne. Le Sourire aux Lèvres. Comment pourrai-je alimenter mon bébé? La plaque de tétée. Prise en charge orthodontique. Les possibilités de l’orthodontie. Otite moyenne, audition, drains trans-tympaniques. Congrès & conférences. PRISE EN CHARGE GLOBALE. L’équipe pluri-disciplinaire FLMP. Et résume son fonctionnement en traç...
Account Suspended
This Account has been suspended. Your web hosting account has been Suspended. To find out the reason and have your account re-enabled please phone or SMS: ( 61) 0421 400 969.
Home - Cleft Lip and Palate
CLEFT LIP and PALATE: From the "inside out". Welcome to my website! This website serves as an opportunity for persons interested in learning more about life from someone with a cleft lip and cleft palate. It is my goal to provide you with my unique perspective as a speech therapist who grew up with a cleft lip and palate.