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Raising Diaphragmatic Hernia Children.

Hospital and Doctor Reviews. Sunday, January 4, 2015. Why is it 2015 and yet STILL many have not heard about the birth defect, congenital diaphragmatic hernia? 1 out of 2500 babies are born with it. It's not rare! My daughter was born with CDH in 2006. She is a survivor. This is LEFT congenital diaphragmatic hernia. The hole is the diaphragm is in the left side. This is RIGHT congenital diaphragmatic hernia. The hole in the diaphragm is in the right side. Terri L. Helmick. Saturday, May 3, 2014. My husba...

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Raising Diaphragmatic Hernia Children. | cdhkids.blogspot.com Reviews

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Hospital and Doctor Reviews. Sunday, January 4, 2015. Why is it 2015 and yet STILL many have not heard about the birth defect, congenital diaphragmatic hernia? 1 out of 2500 babies are born with it. It's not rare! My daughter was born with CDH in 2006. She is a survivor. This is LEFT congenital diaphragmatic hernia. The hole is the diaphragm is in the left side. This is RIGHT congenital diaphragmatic hernia. The hole in the diaphragm is in the right side. Terri L. Helmick. Saturday, May 3, 2014. My husba...

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Raising Diaphragmatic Hernia Children. | cdhkids.blogspot.com Reviews

https://cdhkids.blogspot.com

Hospital and Doctor Reviews. Sunday, January 4, 2015. Why is it 2015 and yet STILL many have not heard about the birth defect, congenital diaphragmatic hernia? 1 out of 2500 babies are born with it. It's not rare! My daughter was born with CDH in 2006. She is a survivor. This is LEFT congenital diaphragmatic hernia. The hole is the diaphragm is in the left side. This is RIGHT congenital diaphragmatic hernia. The hole in the diaphragm is in the right side. Terri L. Helmick. Saturday, May 3, 2014. My husba...

INTERNAL PAGES

cdhkids.blogspot.com

1

Raising Diaphragmatic Hernia Children.: Featured CDHer~ James

http://cdhkids.blogspot.com/2012/06/featured-cdher-james.html

Hospital and Doctor Reviews. Monday, June 4, 2012. He was breathing room air before long and after eight weeks was discharged and able to come home with us. He did not need any oxygen support or monitors or even a feeding tube for when he came home. All of this was new and terrifying for us because we had 2 healthy girls at home. James had feeding issues and massive reflux and needed a Nissen fundoplication when he was three. He has fought and worked very hard and I am so proud to be his mom! This site o...

2

Raising Diaphragmatic Hernia Children.: Featured CDHer~ Tracey

http://cdhkids.blogspot.com/2013/06/featured-cdher-tracey.html

Hospital and Doctor Reviews. Saturday, June 29, 2013. Tracy thank you for your amazing story. My daughter Sydney was born with RCDH years ago. She was in the NICCU 224 and she too has the liver in the middle of her abs. I am always worried for the future since the Docs. keep telling me that 5 years ago a baby with Syds. severity did not survive. You have given me hope that she will lead a normal life. June 29, 2013 at 6:44 PM. They did not sever your appendix during the CDH repair operation? Its nice to ...

3

Raising Diaphragmatic Hernia Children.: Featured CDHer~ Lillian

http://cdhkids.blogspot.com/2014/05/featured-cdher-lillian_3.html

Hospital and Doctor Reviews. Saturday, May 3, 2014. First things first. Lillian is, as my phrase goes, Beautifully Unique! I, too, was born with CDH. I am thirty years old, now! I was also undiagnosed at first, because the doctors- who were watching me- did not know what was ailing my failure-to-thrive little body. As resulted {Like with Lillian} my lung collapsed. As an adult survivor, I havent got any CDH-related health issues other than mild asthma which did not develop until I was 21. ;). This site o...

4

Raising Diaphragmatic Hernia Children.: "Living with Scars" project

http://cdhkids.blogspot.com/2014/02/living-with-scars-project.html

Hospital and Doctor Reviews. Tuesday, February 11, 2014. Living with Scars" project. Hello and Welcome to the Blog. Today we are celebrating our three year Birthday! It's so exciting to be able to connect with so many people on line through face book, our blog and through email. Will you join us today? Here is my daughter Ava. What do I think about when I see my daughter's CDH scars? I have a feeling of complete gratefulness that she is here with us today. I feel very blessed! A diaphragmatic hernia is a...

5

Raising Diaphragmatic Hernia Children.: Educate!

http://cdhkids.blogspot.com/2015/01/educate.html

Hospital and Doctor Reviews. Sunday, January 4, 2015. Why is it 2015 and yet STILL many have not heard about the birth defect, congenital diaphragmatic hernia? 1 out of 2500 babies are born with it. It's not rare! My daughter was born with CDH in 2006. She is a survivor. This is LEFT congenital diaphragmatic hernia. The hole is the diaphragm is in the left side. This is RIGHT congenital diaphragmatic hernia. The hole in the diaphragm is in the right side. Terri L. Helmick. Translate- Raising CDH Children.

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Skittle's Rainbow of Hope: 25 weeks.....

http://skittlesjourney.blogspot.com/2011/11/25-weeks.html

Skittle's Rainbow of Hope. Monday, November 14, 2011. And the countdown is on. 95 days left before induction. That is both exciting, and absolutely nerve wracking at the same time! Been a relatively quiet week, considering. Besides the m/w and neonatologist appointment. Hoping to get the referral process to Portland started ASAP! I am still battling hyperemesis. Stormy is a movin and groovin a lot now. Doesn't sleep as much as she use to. My pelvis is killing me, but what's new? I'm in for it now! To lig...

breathingforclay.blogspot.com

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...

breathingforclay.blogspot.com

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.

breathingforclay.blogspot.com

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 ...

breathingforclay.blogspot.com

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,...

breathingforclay.blogspot.com

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...

breathingforclay.blogspot.com

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.

babyallisonsstory.blogspot.com

Baby Allison: March 2011

http://babyallisonsstory.blogspot.com/2011_03_01_archive.html

Fluid levels look to have stabilized at the 26cm after the jump last week. No jump this week, we are still at 26 - Woo Hoo! Posted by Alexis and Steve. All other testing they did today was great. Allison is doing a great job growing and moving. Her heart rate is where it belongs and so is mine. No visible signs of preterm labor thus far. Posted by Alexis and Steve. Another good check up today! So, the only bad news we have is that the bills are now starting to file in. Yikes! Posted by Alexis and Steve.

searchourhearts.wordpress.com

Support Organizations | Search Our Hearts

https://searchourhearts.wordpress.com/support-organizations

Skip to primary content. Submit or Remove a Blog. Raising Diaphragmatic Hernia Children. CDH Study at Children’s Hospital Boston. One thought on “ Support Organizations. November 23, 2011 at 11:09 pm. I recommend you adding the DHREAMS ( http:/ www.cdhgenetics.com/. Research study for CDH and also the other study at Children’s Hospital of Boston ( http:/ www.childrenshospital.org/clinicalservices/Site1943/mainpageS1943P13.html. Leave a Reply Cancel reply. Enter your comment here. Blog at WordPress.com.

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cdhkids.blogspot.com

Raising Diaphragmatic Hernia Children.

Hospital and Doctor Reviews. Sunday, January 4, 2015. Why is it 2015 and yet STILL many have not heard about the birth defect, congenital diaphragmatic hernia? 1 out of 2500 babies are born with it. It's not rare! My daughter was born with CDH in 2006. She is a survivor. This is LEFT congenital diaphragmatic hernia. The hole is the diaphragm is in the left side. This is RIGHT congenital diaphragmatic hernia. The hole in the diaphragm is in the right side. Terri L. Helmick. Saturday, May 3, 2014. My husba...

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