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Raising A Child With HLHS...

Raising A Child With HLHS. HELPFUL PLACES TO GO. HLHSkids.com - Parent Resources. HLHSKIDS.COM A Website for Parents and Families. Friday, April 4, 2014. It's hard to believe that nearly 2 years have gone by since my last post here. My sincerest apologies. We've been enjoying life, which is something I couldn't have even imagined being able to do at this time 4 years ago. The truth is, Rosemary has defied the odds and is living as full of a life as any other child her age. How to move forward. As heart p...

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Raising A Child With HLHS... | hlhskids.blogspot.com Reviews
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Raising A Child With HLHS. HELPFUL PLACES TO GO. HLHSkids.com - Parent Resources. HLHSKIDS.COM A Website for Parents and Families. Friday, April 4, 2014. It's hard to believe that nearly 2 years have gone by since my last post here. My sincerest apologies. We've been enjoying life, which is something I couldn't have even imagined being able to do at this time 4 years ago. The truth is, Rosemary has defied the odds and is living as full of a life as any other child her age. How to move forward. As heart p...
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Raising A Child With HLHS... | hlhskids.blogspot.com Reviews

https://hlhskids.blogspot.com

Raising A Child With HLHS. HELPFUL PLACES TO GO. HLHSkids.com - Parent Resources. HLHSKIDS.COM A Website for Parents and Families. Friday, April 4, 2014. It's hard to believe that nearly 2 years have gone by since my last post here. My sincerest apologies. We've been enjoying life, which is something I couldn't have even imagined being able to do at this time 4 years ago. The truth is, Rosemary has defied the odds and is living as full of a life as any other child her age. How to move forward. As heart p...

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hlhskids.blogspot.com hlhskids.blogspot.com
1

Raising A Child With HLHS...: Overdue Update...

http://www.hlhskids.blogspot.com/2014/04/overdue-update.html

Raising A Child With HLHS. HELPFUL PLACES TO GO. HLHSkids.com - Parent Resources. HLHSKIDS.COM A Website for Parents and Families. Friday, April 4, 2014. It's hard to believe that nearly 2 years have gone by since my last post here. My sincerest apologies. We've been enjoying life, which is something I couldn't have even imagined being able to do at this time 4 years ago. The truth is, Rosemary has defied the odds and is living as full of a life as any other child her age. How to move forward. As heart p...

2

Raising A Child With HLHS...: May 2010

http://www.hlhskids.blogspot.com/2010_05_01_archive.html

Raising A Child With HLHS. HELPFUL PLACES TO GO. HLHSkids.com - Parent Resources. HLHSKIDS.COM A Website for Parents and Families. Monday, May 10, 2010. Being home has provided Rosemary with the absolute best medicine, freedom. She is running and playing and acting like a toddler again. Life has definitely been good to us. We've been given a new opportunity at life with Rosie and we have so many people to thank for that. To the staff at Children's National Medical Center in DC, where do I begin? I love l...

3

Raising A Child With HLHS...: Beautiful Purpose

http://www.hlhskids.blogspot.com/2010/03/beautiful-purpose.html

Raising A Child With HLHS. HELPFUL PLACES TO GO. HLHSkids.com - Parent Resources. HLHSKIDS.COM A Website for Parents and Families. Saturday, March 13, 2010. This week has changed my life forever, it's the tip of my new iceberg. As I sit here in the CICU thinking about all that had to be processed from Monday until now, I understand a little more what my life's purpose is and I am eternally grateful. Labels: HLHS Hemi Fontan Jonas hope open heart surgery. Josh, Sandy, Jaclyn, and Kinsey. HLHSkids.com ...

4

Raising A Child With HLHS...: July 2012

http://www.hlhskids.blogspot.com/2012_07_01_archive.html

Raising A Child With HLHS. HELPFUL PLACES TO GO. HLHSkids.com - Parent Resources. HLHSKIDS.COM A Website for Parents and Families. Sunday, July 15, 2012. Links to this post. Subscribe to: Posts (Atom). Subscribe To My Blog. HLHSkids.com - A Website For Parents and Families of Children With HLHS. Promote Your Page Too. What topics would you like to hear about? This little turkey is a living miracle. And SUPER she is. Looking like a paratrooper, really carrying her own. View my complete profile.

5

Raising A Child With HLHS...: Pockets of Joy

http://www.hlhskids.blogspot.com/2012/07/pockets-of-joy.html

Raising A Child With HLHS. HELPFUL PLACES TO GO. HLHSkids.com - Parent Resources. HLHSKIDS.COM A Website for Parents and Families. Sunday, July 15, 2012. You lived in Homer City, PA. I live in New Florence, PA. How nice to meet you! Our 3rd baby, Faith Ann, was born (unknowingly to us) with HLHS. She lived 9 days and went into shock. Shes a walking testomony that God is alive and well. Doctors said, shes too far gone, she wont make it thru the night. She is now 2 1/2 and going strong! Subscribe To My Blog.

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Caelen Gorman: October 2014

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

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Sunday, October 19, 2014. But come on, has anyone ever seen Caelen get stage fright? But overall, it was an absolutely amazing experience, and I can't thank Brian, Tyler and their team enough for giving us that gift. Plus.they totally rocked it! How lucky is Caelen that his first concert was FGL? Mine was Paul Anka, thanks mom. Captain Ma...

caelengorman.blogspot.com caelengorman.blogspot.com

Caelen Gorman: November 2013

http://caelengorman.blogspot.com/2013_11_01_archive.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Thursday, November 28, 2013. Happy Thanksgiving and Happy Chanukah friends. We have so much to be thankful for this year. I'm grateful for our first Thanksgiving in Florida with family and friends. Caelen is adapting well and the weather is certainly helping his lungs. And sorry to our friends up north, but being able to wear flip...Caele...

caelengorman.blogspot.com caelengorman.blogspot.com

Caelen Gorman: December 2013

http://caelengorman.blogspot.com/2013_12_01_archive.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Tuesday, December 24, 2013. Merry Christmas Eve to all of our friends. We just had a wonderful family dinner with our friends the Cohens again, and it was more reflective this time for me. Merry Christmas to all, and to all of our prayer angels, we wish you a good night. And a Happy Anniversary in Heaven to Grandma Doris and Grandpa Joe.

caelengorman.blogspot.com caelengorman.blogspot.com

Caelen Gorman: Heart Walk tomorrow - please donate

http://caelengorman.blogspot.com/2014/09/heart-walk-tomorrow-please-donate.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, September 26, 2014. Heart Walk tomorrow - please donate. Tomorrow we walk for the American Heart Association, Caelen and all of our heart warrior friends. We are $875 short of our goal, sooo close! I'm putting out a last minute request to try and reach our goal. Thank you all,. Subscribe to: Post Comments (Atom).

caelengorman.blogspot.com caelengorman.blogspot.com

Caelen Gorman: March 2015

http://caelengorman.blogspot.com/2015_03_01_archive.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, March 27, 2015. I know I haven't updated since FL GA Line concert, but those of you on FB have watched Caelen's updates, so I'm only partly behind. Speaking of, if you haven't already seen, I created a FB page just for Caelen it's called Super Caelen, check it out:. Https:/ www.facebook.com/SuperCaelen. There are even more excitin...

caelengorman.blogspot.com caelengorman.blogspot.com

Caelen Gorman: May 2014

http://caelengorman.blogspot.com/2014_05_01_archive.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Thursday, May 29, 2014. I am really excited to share that Caelen and I have moved into our new house! Like, over the moon excited! Now, every single toy of his is now on display and out of boxes. Caelen gets his own room where he has a desk for school, his art on the walls, and his insane Disney Cars collection all in one place. So now it...

caelengorman.blogspot.com caelengorman.blogspot.com

Caelen Gorman: Celebrating 5 with a cover story

http://caelengorman.blogspot.com/2014/08/celebrating-5-with-cover-story.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, August 22, 2014. Celebrating 5 with a cover story. There is so much good going on right now that I have to try and contain my excitement in this blog. I will try and minimize additional exclamation points, but it's going to be hard.cause I'm so excited! First off, Caelen is doing really well! Now, on the the good stuff! Twice as m...

caelengorman.blogspot.com caelengorman.blogspot.com

Caelen Gorman: 2014 Heart Walk

http://caelengorman.blogspot.com/2014/09/2014-heart-walk.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Thursday, September 18, 2014. Our goal is to raise $10,000 this year between Troy and Caelen, and we are so close! Out of all the teams walking, we are in the top 4 with only 9 days to go, thanks to all of the wonderful friends that have donated! Http:/ palmbeachheartwalk.kintera.org/faf/donorReg/donorPledge.asp? Love, Katye and Caelen.

caelengorman.blogspot.com caelengorman.blogspot.com

Caelen Gorman: March 2014

http://caelengorman.blogspot.com/2014_03_01_archive.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, March 28, 2014. This one's for you Weston. I returned last night from Weston's memorial and celebration of life in Philly. It's hard to sum up all of the 24 hrs of my short trip, but if there is one word I could use, it would be Love. All of our lives will go on, and we should make the most that we can with the time we're given.

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Raising A Child With HLHS...

Raising A Child With HLHS. HELPFUL PLACES TO GO. HLHSkids.com - Parent Resources. HLHSKIDS.COM A Website for Parents and Families. Friday, April 4, 2014. It's hard to believe that nearly 2 years have gone by since my last post here. My sincerest apologies. We've been enjoying life, which is something I couldn't have even imagined being able to do at this time 4 years ago. The truth is, Rosemary has defied the odds and is living as full of a life as any other child her age. How to move forward. As heart p...

hlhskids.com hlhskids.com

HLHSkids.coma place of Hopefor parents & families

Welcome. I have opened the doors to this site to provide you with an outlet of information and personal insight into raising a child with Hypoplastic Left Heart Syndrome. HLHS) and other CHDs. I feel that it is important to be able to relate to this kind of experience, on your time. Put a smile on your child’s face, be their source for positive energy. Love and happiness are contagious. You cannot fear what you love, nor love what you fear. You have today, don’t worry about tomorrow. Find...

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