Raising awareness of the condition that took my only child at age 6 and a half - Congenital Diaphragmatic Hernia CDH takes the lives of 15,000 children every year and harms 15,000 more. Will you care? http://www.cdhsupport.org In memory of Shane Torrence (1/28/93 - 9/11/99)
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Shane's Street - Raising Congenital Diaphragmatic Hernia Awareness | cherubshane.blogspot.com Reviews
https://cherubshane.blogspot.com
Raising awareness of the condition that took my only child at age 6 and a half - Congenital Diaphragmatic Hernia CDH takes the lives of 15,000 children every year and harms 15,000 more. Will you care? http://www.cdhsupport.org In memory of Shane Torrence (1/28/93 - 9/11/99)
cherubshane.blogspot.com
Shane's Street - Raising Congenital Diaphragmatic Hernia Awareness: CHERUBS rang the Closing Bell on the New York Stock Exchange
http://cherubshane.blogspot.com/2014/09/cherubs-rang-closing-bell-on-new-york.html
In memory of Shane Torrence (1/28/93 - 9/11/99). A mom on a mission raising awareness of the condition that took my only child at age 6 and a half - Congenital Diaphragmatic Hernia CDH takes the lives of 15,000 children every year and harms 15,000 more. Http:/ www.cdhsupport.org. Friday, September 26, 2014. CHERUBS rang the Closing Bell on the New York Stock Exchange. This is where I was last month. View the video at https:/ www.nyse.com/bell/recent. Congenital diaphragmatic hernia awareness.
Shane's Street - Raising Congenital Diaphragmatic Hernia Awareness: September 2014
http://cherubshane.blogspot.com/2014_09_01_archive.html
In memory of Shane Torrence (1/28/93 - 9/11/99). A mom on a mission raising awareness of the condition that took my only child at age 6 and a half - Congenital Diaphragmatic Hernia CDH takes the lives of 15,000 children every year and harms 15,000 more. Http:/ www.cdhsupport.org. Friday, September 26, 2014. CHERUBS rang the Closing Bell on the New York Stock Exchange. This is where I was last month. View the video at https:/ www.nyse.com/bell/recent. Congenital diaphragmatic hernia awareness. This is the...
Shane's Street - Raising Congenital Diaphragmatic Hernia Awareness: January 2015
http://cherubshane.blogspot.com/2015_01_01_archive.html
In memory of Shane Torrence (1/28/93 - 9/11/99). A mom on a mission raising awareness of the condition that took my only child at age 6 and a half - Congenital Diaphragmatic Hernia CDH takes the lives of 15,000 children every year and harms 15,000 more. Http:/ www.cdhsupport.org. Wednesday, January 28, 2015. Happy 22nd Birthday, Shane. So much has happened. Since my last post in September. So many good things. Awards, events and now we are close to raising $1 Million for CDH. Subscribe to: Posts (Atom).
Shane's Street - Raising Congenital Diaphragmatic Hernia Awareness: Shane's Story - Chapter 15
http://cherubshane.blogspot.com/2014/04/shanes-story-chapter-15.html
In memory of Shane Torrence (1/28/93 - 9/11/99). A mom on a mission raising awareness of the condition that took my only child at age 6 and a half - Congenital Diaphragmatic Hernia CDH takes the lives of 15,000 children every year and harms 15,000 more. Http:/ www.cdhsupport.org. Friday, April 25, 2014. Shane's Story - Chapter 15. WARNING: This may be too hard to read for many but it's part of Shane's story). Hadn't I done everything right? This couldn't be happening. His headstone has pictures of Elmo, ...
Shane's Street - Raising Congenital Diaphragmatic Hernia Awareness: Happy 22nd Birthday, Shane
http://cherubshane.blogspot.com/2015/01/happy-22nd-birthday-shane.html
In memory of Shane Torrence (1/28/93 - 9/11/99). A mom on a mission raising awareness of the condition that took my only child at age 6 and a half - Congenital Diaphragmatic Hernia CDH takes the lives of 15,000 children every year and harms 15,000 more. Http:/ www.cdhsupport.org. Wednesday, January 28, 2015. Happy 22nd Birthday, Shane. So much has happened. Since my last post in September. So many good things. Awards, events and now we are close to raising $1 Million for CDH. This is me and Shane.
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Breathing for Baby Clay: Our CDH Story: Wake up, Clay belly!
http://breathingforclay.blogspot.com/2013/10/wake-up-clay-belly.html
Breathing for Baby Clay: Our CDH Story. Saturday, October 5, 2013. Wake up, Clay belly! Praying for poop.that's what we've been doing since surgery. He finally had a decent bowel movement tonight, nothing huge, but hey.it's a start! And it was without the help of a suppository so that's good he did it all on his own. Gettin lots of momma lovins.I think we're both tired of hospital living :/. October 5, 2013 at 8:29 PM. Thinking of you guys! October 7, 2013 at 8:54 AM. You are praying for poop? Im glad th...
Breathing for Baby Clay: Our CDH Story: September 2013
http://breathingforclay.blogspot.com/2013_09_01_archive.html
Breathing for Baby Clay: Our CDH Story. Friday, September 27, 2013. Of course, things never go as planned with Mr. Clayton Cash and this trip to the hospital has been no different. Lil turkey likes to keep us on our toes! Repair surgery #3 was scheduled for Thursday morning, instead we found ourselves in the ER with a fever and a cough. We've moved from the PICU to a regular room today and have been told they want to keep us here until surgery day, which sounds like may happen next Tuesday or Thursday.
Breathing for Baby Clay: Our CDH Story: October 2013
http://breathingforclay.blogspot.com/2013_10_01_archive.html
Breathing for Baby Clay: Our CDH Story. Thursday, October 10, 2013. At full feeds but feeling puny :(. Well the good news is, we are up to full feeds of 56ml/hr and he's doing great with that so far! His g-tube is still racked, and will have to be for another week or so, then we can work on condensing feeds into boluses. So, we will be here for another day or two until we get something figured out. Y'all say a prayer for my lil man. This never gets any easier :(. Saturday, October 5, 2013. He has perked ...
Breathing for Baby Clay: Our CDH Story: September 2012
http://breathingforclay.blogspot.com/2012_09_01_archive.html
Breathing for Baby Clay: Our CDH Story. Sunday, September 16, 2012. Back in the big city :/. Well we've had an eventful few days to say the least. In my last blog, I was excited that our doc discontinued some of Clays meds: diuril, sodium chloride, and potassium chloride. We had to have a BMP drawn this past Wednesday to make sure his electrolyte levels weren't missing the supplements. Can just I say how bad it SUCKS to watch your baby get poked with a needle every 6 hours? And this wasn't a little poke,...
Breathing for Baby Clay: Our CDH Story: January 2013
http://breathingforclay.blogspot.com/2013_01_01_archive.html
Breathing for Baby Clay: Our CDH Story. Thursday, January 24, 2013. Clay was scheduled to have the Nissen Fundoplication surgery this coming Tuesday, January 29th. I've been dreading it more and more everyday.both the actual procedure, but more so for the 7-10 day recovery in the PICU (or more, knowing how things usually go with Mr. Clay-bug). Thank y'all for keeping up with us.we appreciate the support more than you'll ever know! Here's a few pictures of the silly boy:. Him's bad to the bone. Raising Di...
Breathing for Baby Clay: Our CDH Story: Repair surgery hold-up...
http://breathingforclay.blogspot.com/2013/09/repair-surgery-hold-up.html
Breathing for Baby Clay: Our CDH Story. Friday, September 27, 2013. Of course, things never go as planned with Mr. Clayton Cash and this trip to the hospital has been no different. Lil turkey likes to keep us on our toes! Repair surgery #3 was scheduled for Thursday morning, instead we found ourselves in the ER with a fever and a cough. We've moved from the PICU to a regular room today and have been told they want to keep us here until surgery day, which sounds like may happen next Tuesday or Thursday.
nicholassparkscherubs.blogspot.com
Dear Nicholas Sparks: About This Blog
http://nicholassparkscherubs.blogspot.com/p/why-this-blog-was-created-in-high-hopes.html
A crazy quest to raise awareness for the 1000's of children fighting Congenital Diaphragmatic Hernia. This blog was created in high hopes that one crazy mom, along with other crazy parents and friends, can implore author Nicholas Sparks to write a book about a family dealing with Congenital Diaphragmatic Hernia (CDH). I'm Dawn Williamson, mom to Shane. Shane was born with CDH in 1993 and lost his battle in 1999. In 1995, I started a charity, CHERUBS. To be clear, we are only asking Mr. Sparks to meet...
Breathing for Baby Clay: Our CDH Story: At full feeds but feeling puny :(
http://breathingforclay.blogspot.com/2013/10/at-full-feeds-but-feeling-puny.html
Breathing for Baby Clay: Our CDH Story. Thursday, October 10, 2013. At full feeds but feeling puny :(. Well the good news is, we are up to full feeds of 56ml/hr and he's doing great with that so far! His g-tube is still racked, and will have to be for another week or so, then we can work on condensing feeds into boluses. So, we will be here for another day or two until we get something figured out. Y'all say a prayer for my lil man. This never gets any easier :(. October 10, 2013 at 10:56 AM. My Blessed ...
Breathing for Baby Clay: Our CDH Story: June 2013
http://breathingforclay.blogspot.com/2013_06_01_archive.html
Breathing for Baby Clay: Our CDH Story. Wednesday, June 26, 2013. Choosing faith instead of fear. Holy smokes, we made it a year.one year ago today, we were bringing Clay home to the hills for the very first time. Can you say proud? Cause that's what I am. I have kept my baby alive. And I'd even venture to say thriving. At home, with a ventilator, oxygen and a feeding tube. Yes, yes, yessssssssssssss, I'm proud. But as you all know, that wasn't in the plan. Still, bringing him home with a ventilator, oxy...
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Cherubs Foundation
CHERUBS FOUNDATION INTERNATIONAL – GHANA. The motto of cherubs foundation will appear here. Http:/ www.cherubsfoundation.org/wp-content/uploads/2016/07/image1.jpg. Http:/ www.cherubsfoundation.org/wp-content/uploads/2016/07/image2.jpg. Http:/ www.cherubsfoundation.org/wp-content/uploads/2016/07/image3.jpg. Http:/ www.cherubsfoundation.org/wp-content/uploads/2016/07/image4.jpg. Our Ongoing project block for the girls and the little children. POBox KS 4292 Kumasi. 233 208 172 511 / 233 264 442 882.
Cherub's Garden | The greatest WordPress.com site in all the land!
The greatest WordPress.com site in all the land! Sorry, but nothing matched your search criteria. Perhaps searching will help you find what you are looking for. Cherub’s Garden Comments. Cherub's Instagram Pictures. Follow Cherub's Garden on WordPress.com. Follow Cherub's Garden via Email. Enter your email address to follow Cherub's Garden and receive notifications of new posts by email. Join 1 other follower. Follow Cherub’s RSS feed here. Search Cherub’s Garden. Cherub’s sign in.
Cherub's Girls | An Ongoing Homeschool Portfolio
An Ongoing Homeschool Portfolio. Naomi Ayers Self Reflection Portfolio Review 2013/2014. Xandra Ayers Self Reflection Portfolio Review 2013/2014. July 27, 2014. We love games, no mater if they’re learning games or just for fun. Fun at the Lane Public Library. July 27, 2014. Xandra and Naomi love the library. It’s like a second home to them. We visit the library weekly, if not more for activities, reading clubs, story time, and of course to check out books! July 27, 2014. Friend time at Miami University.
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Shane's Street - Raising Congenital Diaphragmatic Hernia Awareness
Raising awareness of the condition that took my only child at age 6 and a half - Congenital Diaphragmatic Hernia CDH takes the lives of 15,000 children every year and harms 15,000 more. Will you care? Http:/ www.cdhsupport.org In memory of Shane Torrence (1/28/93 - 9/11/99). In memory of Shane Torrence (1/28/93 - 9/11/99). Http:/ www.cdhsupport.org. Sunday, January 28, 2018. Happy 25th Birthday, Shane. 25 years ago today. how can it be 25 years? I still feel 25 years old myself. Sunday, September 11, 2016.
Preschool & Daycare in Whitinsville MA & Grafton MA | Cherub's Haven
North St. Location. Millbury St. Location. Welcome to Cherub's Haven. Cherub's Haven provides quality childcare, preschool, and after school care to families residing in Whitinsville and the surrounding areas. Children learn daily life skills, manners, and early childhood education that will help them as they grow and further their education. If you're looking for a safe, friendly, and caring childcare center, contact us. North St. Location. Millbury St. Location. 2014 Internet Marketing and SEO by Next!
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Cherubs India Blog | Congenital Diaphragmatic Hernia Support Group in India
November 9, 2008 at 5:38 pm · Filed under Uncategorized. Welcome to Cherubs India. If you are here because you have recently heard of a diagnosis of CDH or Congenital Diaphragmatic Hernia from any doctor here in India, heres your chance to stop for a moment and take a big gulp of hope. It is a bad diagnosis and a terrible medical condition with many complications, but you can make the most of the chances if you are armed with the right information. The Congenital Diaphragmatic Hernia Blogs Webring.
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Best House Cleaners Melbourne | Cleaning Agency Melbourne
House Cleaners and Cleaning Service. Why trust Cherubs in the Home for your tailored house cleaning solutions? You've heard it all before. The difference is that we mean it! We are committed to your piece of mind, and delivering the best cleaning services for you! Choose from our Professional services from our House Cleaners in Melbourne below. And Call us on 03 92128000 to book now :. Regular & Weekly Cleaning. For an indicative quote, please complete the following information and send through: [contact...
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