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Cleftopedia Cleftopedia Cleft Teams

Cleftopedia is an informative website built to help new parents of children diagnosed with cleft lip and/or cleft palate. Find the right cleft team for you

http://www.cleftopedia.com/

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Cleftopedia Cleftopedia Cleft Teams | cleftopedia.com Reviews
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Cleftopedia is an informative website built to help new parents of children diagnosed with cleft lip and/or cleft palate. Find the right cleft team for you
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1 parent tips
2 resources
3 special feeders
4 cleft bottles
5 sippy cups
6 cleft binkies
7 pre surgical techniques
8 nam taping tips
9 latham
10 taping
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parent tips,resources,special feeders,cleft bottles,sippy cups,cleft binkies,pre surgical techniques,nam taping tips,latham,taping,lip adhesion,no presurgical,cleft teams,scar creams,special feeder suggestions,add your team,about us,shop,blog,sponsor
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Cleftopedia Cleftopedia Cleft Teams | cleftopedia.com Reviews

https://cleftopedia.com

Cleftopedia is an informative website built to help new parents of children diagnosed with cleft lip and/or cleft palate. Find the right cleft team for you

INTERNAL PAGES

cleftopedia.com cleftopedia.com
1

Cleftopedia Cleft teams in Chile

http://www.cleftopedia.com/cleft-teams/chile

Cleft Lip & Palate. Nasoalveolar Molding Device (NAM). If you’re searching for a cleft team in Chile for your child, here is a list of hospitals, teams, surgeons and their specific techniques. This list has been compiled by other mommies, so if you don’t see your team here, we will be happy to add it for you. Santiago Chile Cleft Teams. Prior to lip repair. Lip Repair done at 3 months/palate repair done at 12 months. Restrictions and Requirements after repair include: Use of arm restraints. I know not ma...

2

Cleftopedia Sippy Cups for cleft palate

http://www.cleftopedia.com/special-feeders/sippy-cups

Cleft Lip & Palate. Nasoalveolar Molding Device (NAM). Sippy Cups for Cleft Affected Children. When it comes time to begin transitioning to a sippy cup, there are many choices out there and finding the right one can be overwhelming (we know… we’ve been there! All of these cups are available at most major retailers or on Amazon unless otherwise noted. The sippy cups highlighted in this section are great before palate repair or in the weeks immediately post op as no suction is required. MOM TIP: if you cut...

3

Cleftopedia Cleft teams in the United Kingdom

http://www.cleftopedia.com/cleft-teams/united-kingdom

Cleft Lip & Palate. Nasoalveolar Molding Device (NAM). United Kingdom Cleft Teams. If you’re searching for a cleft team in the United Kingdom for your child, here is a list of hospitals, teams, surgeons and their specific techniques. This list has been compiled by other mommies, so if you don’t see your team here, we will be happy to add it for you. Bristol, UK Cleft Teams. University of Bristol Dental Hospital. Technique prior to lip repair. Lip Repair done at 4-5 months/palate repair done at 9-11 months.

4

Cleftopedia cleft lip special feeders

http://www.cleftopedia.com/special-feeders

Cleft Lip & Palate. Nasoalveolar Molding Device (NAM). Some of the first questions that you may ask yourself are…. Will I be able to breastfeed? How will I be able to feed my baby? We are here to help narrow down that selection for you, so we have compiled a list of bottles. That have worked for other mommies in the past who have cleft affected babies. Find us on Facebook. United States of America. Help to keep this website alive! Enter your Infotext or Widgets here.

5

Cleftopedia Zofran and Cleft Palate Debate

http://www.cleftopedia.com/zofran-cleft

Cleft Lip & Palate. Nasoalveolar Molding Device (NAM). February 24, 2015. Or should I ask, why are we allowing ourselves to think they are portraying it in a negative way? I don’t have the statistical facts, but just from what I’ve seen throughout support groups, there are far more cleft moms who did NOT take Zofran while pregnant than those who have. But does that mean we should shun the moms who did? What if there is a link? Was it something I did? So next time you hear the word Zofran and cleft in the...

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TOTAL PAGES IN THIS WEBSITE

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LINKS TO THIS WEBSITE

cleftcutie.com cleftcutie.com

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!

cleft-notes.com cleft-notes.com

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...

cleftcutie.com cleftcutie.com

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...

hferg.blogspot.com hferg.blogspot.com

Ferg Blog: October 2014

http://hferg.blogspot.com/2014_10_01_archive.html

Friday, October 24, 2014. My Favorite Thing About Social Media. It was as if the skies had opened up and God was shining a light directly towards this group. Women from all over the world. Women who have babies with special needs. Women who have EPed for years. yea that's right. YEARS! Talk about a wealth of knowledge! I could get on this group page at any hour of the night and ask any question I needed. Within minutes someone would be answering. Beth if you are reading this, thanks again! If you are won...

cleft-notes.com cleft-notes.com

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 ...

cleft-notes.com cleft-notes.com

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).

cleftcutie.com cleftcutie.com

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...

cleftcutie.com cleftcutie.com

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...

cleft-notes.com cleft-notes.com

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...

cleft-notes.com cleft-notes.com

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:.

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Cleftopedia Cleftopedia Cleft Teams

Cleft Lip & Palate. Nasoalveolar Molding Device (NAM). You are your child’s advocate. Find out what other mommies thought of their cleft team so that you can choose the right one for your child. Feeding does not have to be difficult and you have options. Find out about different feeders that you can use for your cleft affected child. Sponsor a Cuddle Pack by visiting the Cuddles for Clefts sponsorship page and help bring a smile to a child recovering from surgery. Find us on Facebook.

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