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Baby Abby's Heart-Our Journey with HLHS

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Baby Abby's Heart-Our Journey with HLHS | babyabbysheart.blogspot.com Reviews

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Baby Abby's Heart-Our Journey with HLHS: Abby Turns 5 !!!!!

http://babyabbysheart.blogspot.com/2011/12/abby-turns-5.html

Baby Abby's Heart-Our Journey with HLHS. Wednesday, December 21, 2011. Abby turned 5 years old yesterday! It has been an incredible 5 years and we are truly amazed at how Abby has grown and flourished with her HLHS heart repair. Cheers to another great and healthy year and many many more to come. All the best to you and yours this holiday season. Be well and have fun. Abby's Lucky Dad,. Subscribe to: Post Comments (Atom). Enter your email address to receive updates on Abby's progress.

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Baby Abby's Heart-Our Journey with HLHS: Happy Heart Day - 3 Years since her last surgery

http://babyabbysheart.blogspot.com/2013/05/happy-heart-day-3-years-since-her-last.html

Baby Abby's Heart-Our Journey with HLHS. Saturday, May 25, 2013. Happy Heart Day - 3 Years since her last surgery. Just a quick note to mark 3 years since Abby's 3rd surgery, the fontan procedure. Hard to believe it has been 3 full years since Abby had her 3rd surgery. I am happy to report that Abby is doing excellent and having fun as a 6 1/2 year old kindergartener. I took her training wheels off her bike the other day and she is now having fun on 2 wheels! All the best from Abby's Grateful Dad-.

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Baby Abby's Heart-Our Journey with HLHS: Abby's Happy Heart Day!

http://babyabbysheart.blogspot.com/2011/05/abbys-happy-heart-day.html

Baby Abby's Heart-Our Journey with HLHS. Thursday, May 26, 2011. Abby's Happy Heart Day! Today marks one year since Abby's third surgery and the completion of her heart repair. A big day for all of us and just wanted to mark it here on the blog. Abby is currently out in the backyard enjoying her new found ability to "pump" on the swing. Thanks for all your thoughts and prayers over the years and for keeping. Abby's Lucky Dad- Bryan. Subscribe to: Post Comments (Atom). Q&A Hypoplastic Left Heart Syndrome.

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Our little Wright Family: Vacation!!!

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Our little Wright Family. The adventures of a little family, dealing with the effects of CHD. Continuing with our vacation post. Thursday night after dinner we walked down to the ocean. here are a couple of pictures of Carla, loving the ocean. Carla swam, met friends and had a fun time. And we had no reason to linger in the morning, so got an early-ish start Friday morning. Here are the pics from Friday and Saturday. A lighthouse that claims to be "the most photographed" lighthouse in the world. Carla an...

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Friday, December 25, 2009. Merry Christmas from our family to yours! 9829; Michele ♥. I know this was a hard Christmas for you and your family! You all continue to be in my thoughts and prayers! December 25, 2009 at 8:29 PM. That is a beautiful card. Merry Christmas to your family. December 25, 2009 at 11:23 PM. We pray for countinous peace for your family. Even after Christmas. December 26, 2009 at 1:49 PM. December 26, 2009 at 3:25 PM. December 26, 2009 at 9:03 PM. Such a Beautiful Christmas Card.

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Gracie's Blog: Last Halloween

http://thegledhillfamily.blogspot.com/2009/10/last-halloween.html

Sunday, October 25, 2009. I wanted to include a few pictures from last year. Three out of the four pictures I did not post last year. The first one I did, I couldn't resist reposting this one again. My little lamby with a shy smile. We miss you our little GG. The football player, doctor, fashionista and lamby. My sweet little girl. 9829; Michele ♥. October 25, 2009 at 4:28 PM. Michele. Gracie in the lamby costume is one of my favorites. I just adore that precious smile! Thinking of you all often. Just wa...

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Jacob's Journey: October 2014

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

Tuesday, October 28, 2014. Wow, I can't believe how long it has been since I have updated Jake's blog. I haven't written in over a year! I apologize for the lack of updates, so much has happened over the last year. One big and exciting event was Jacob's Make-a-Wish trip! The last time I blogged Jake had just come home from having his Fontan (Last open heart surgery). I am happy to report that heart wise he has been doing great! Getting his EKG, such a big boy now. 1st day of Pre-K. I am not denying he is...

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Jacob's Journey: August 2013

http://jacobsspecialheart.blogspot.com/2013_08_01_archive.html

Thursday, August 15, 2013. Home and LOVING IT! THANK YOU FOR ALL OF THE PRAYERS! As you can see, they worked. I am sorry I have not updated the blog since we have been home but we have been busy. Jake is doing AMAZING. He is pretty much back to normal. Happy, playing and pretty much pushing every limit and restriction he was sent home on lol. As soon as we got home I set up my command center. Anyone who knows me also knows that I do better when I am in control (I am a serious control freak). Diuril is no...

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Jacob's Journey: October 2012

http://jacobsspecialheart.blogspot.com/2012_10_01_archive.html

Tuesday, October 23, 2012. Hitting the Odds (again): The Factor Five Leiden Gene. When we left off I was talking about our trip to Cincinnati. Well we have actually been there again since then but I will get to that in a minute. To finish the blog post I started TWO months ago, the second day Jake had a ultrasound of his clot (Which he screamed through). Fast forward 3 weeks which also happened to be 3 weeks ago (told you I am behind on updating). Jacob has 1 Factor Five Leiden gene. My little man didn't...

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Jacob's Journey: Long overdue update...

http://jacobsspecialheart.blogspot.com/2014/10/long-overdue-update.html

Tuesday, October 28, 2014. Wow, I can't believe how long it has been since I have updated Jake's blog. I haven't written in over a year! I apologize for the lack of updates, so much has happened over the last year. One big and exciting event was Jacob's Make-a-Wish trip! The last time I blogged Jake had just come home from having his Fontan (Last open heart surgery). I am happy to report that heart wise he has been doing great! Getting his EKG, such a big boy now. 1st day of Pre-K. I am not denying he is...

jacobsspecialheart.blogspot.com jacobsspecialheart.blogspot.com

Jacob's Journey: July 2013

http://jacobsspecialheart.blogspot.com/2013_07_01_archive.html

Wednesday, July 31, 2013. She left and we went on with our day. Since they wake Jake up like that he starts out the day trusting no one. He tells anyone who steps foot in our room "Bye-Bye. See you later". He is afraid of everyone. It is pretty sad, but he is so sweet about it. Next the fellow came in. He told me the X-ray looked a lot worse (My heart sank). Think there is enough stuff in his bed lol? Lol Wait. WHAT? Within 10 minutes he started vomiting. FINALLY AN ANSWER TO HIS VOMITING. Jake ate like ...

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Jacob's Journey: New Year... New Updates!

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Saturday, January 17, 2015. New Year. New Updates! I hope everyone had a great holiday season. The boys had a wonderful Christmas and got spoiled by Santa. Their elf (Ralphie). Came back to stay with us again and Jake LOVE it. Jake really got into the holiday spirit this year. He especially loved all of the decorations. It was so cute seeing how excited he was over Christmas. So that is great news as well. Dr Stines (Jake's local cardio). And purple fingernails are all the rage now, haven't you heard?

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Hypoplastic Left Heart Babies: Doing well-

http://hlhsbabies.blogspot.com/2014/10/doing-well.html

To start from the beginning, Click Here, then click "Newer Post" at the bottom to keep reading. Norwood, Stage 1. Glenn, Stage 2. Fontan, Stage 3. Tuesday, October 7, 2014. I know how comforting it is for parents to see other parents going through the same trials, but in the same respect, it is comforting to see those who came out of those trials WELL and are doing great! I thought I would share a little about what Jack is up to, and how his condition affects him today. He so tough, brave and incredibly ...

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Baby Abby's Heart-Our Journey with HLHS

Baby Abby's Heart-Our Journey with HLHS. Saturday, May 25, 2013. Happy Heart Day - 3 Years since her last surgery. Just a quick note to mark 3 years since Abby's 3rd surgery, the fontan procedure. Hard to believe it has been 3 full years since Abby had her 3rd surgery. I am happy to report that Abby is doing excellent and having fun as a 6 1/2 year old kindergartener. I took her training wheels off her bike the other day and she is now having fun on 2 wheels! All the best from Abby's Grateful Dad-. Today...

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