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Our little yellow man

Sunday, January 1, 2012. Yet another fun thing at Primary Children's hospital. Actual size Spider-Man statue. Not to be confused with Phil Spiderman. Tuesday, July 14, 2009. So, sorry it's taken so long to update. Charlie only had to stay at PCMC for 3 days. Came home with another PICC and just got that out last week. Since then, fever-free and loving the summer weather. Here's a few hospital pics and fun home pics. Late night ice cream treats:). HmmmMaybe a doctor some day? Playing footsie with Hailey.

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Our little yellow man | chucknick.blogspot.com Reviews
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Sunday, January 1, 2012. Yet another fun thing at Primary Children's hospital. Actual size Spider-Man statue. Not to be confused with Phil Spiderman. Tuesday, July 14, 2009. So, sorry it's taken so long to update. Charlie only had to stay at PCMC for 3 days. Came home with another PICC and just got that out last week. Since then, fever-free and loving the summer weather. Here's a few hospital pics and fun home pics. Late night ice cream treats:). HmmmMaybe a doctor some day? Playing footsie with Hailey.
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Our little yellow man | chucknick.blogspot.com Reviews

https://chucknick.blogspot.com

Sunday, January 1, 2012. Yet another fun thing at Primary Children's hospital. Actual size Spider-Man statue. Not to be confused with Phil Spiderman. Tuesday, July 14, 2009. So, sorry it's taken so long to update. Charlie only had to stay at PCMC for 3 days. Came home with another PICC and just got that out last week. Since then, fever-free and loving the summer weather. Here's a few hospital pics and fun home pics. Late night ice cream treats:). HmmmMaybe a doctor some day? Playing footsie with Hailey.

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1

Our little yellow man: Year 2011 Overview

http://chucknick.blogspot.com/2012/09/year-2011-overview.html

Sunday, January 1, 2012. Yet another fun thing at Primary Children's hospital. Actual size Spider-Man statue. Not to be confused with Phil Spiderman. Subscribe to: Post Comments (Atom). Http:/ nqcampbellfamily.blogspot.com. Fall Break Day 3. The gift of life.4 years ago. An ode to Bob Marley- every little thing- turned out alright! Livin for Livi Quilt Cause. The hazards of an overly large lunch. View my complete profile. Simple template. Template images by gaffera.

2

Our little yellow man: April 2008

http://chucknick.blogspot.com/2008_04_01_archive.html

Thursday, April 17, 2008. Sorry its been so long. Well, Charlie is doing FANTASTIC! We are soooooo happy! His last appointment with Dr. Book was last month and went wonderful. There is a chance that he may never even need a transplant. Wouldn't that be awesome? Also, his labs looked much better. Liver enzymes were about the same, ALT 51 and AST 94, and vitamin D level was normal at 37. And the most shocking was his ggt level, which had been as high as 2600, is now at 80! Here is a few latest pics.

3

Our little yellow man: October 2007

http://chucknick.blogspot.com/2007_10_01_archive.html

Monday, October 22, 2007. We just got back from Charlie's appointment with his GI doctor, Dr. Book. She said that the surgery is definitly working and that we should be thrilled with the results! Well, we are thrilled and feeling so very blessed to be among the top 30%! Which means goodbye to his PICC line. Nick and I will be so happy to get some more sleep, but Charlie may not be so happy as he has grown quite accustomed and attached to the line:). All in all, a great week! Tuesday, October 16, 2007.

4

Our little yellow man: May 2009

http://chucknick.blogspot.com/2009_05_01_archive.html

Thursday, May 7, 2009. For the time being we're keeping him on both meds for a bit. Subscribe to: Posts (Atom). Http:/ nqcampbellfamily.blogspot.com. Fall Break Day 3. The gift of life.4 years ago. An ode to Bob Marley- every little thing- turned out alright! Livin for Livi Quilt Cause. The hazards of an overly large lunch. View my complete profile. Simple template. Template images by gaffera.

5

Our little yellow man: November 2007

http://chucknick.blogspot.com/2007_11_01_archive.html

Tuesday, November 27, 2007. Charlie was able to come home on Sunday. Yea! It's so nice to be out of the hospital. I think Charlie was starting to think that it was his second home:). Saturday, November 24, 2007. Well, I lied. I found out today that he is actually coming home tomorrow. Probably. It will depend on how his blood cultures look from today. Also, he is scheduled for a heart echo on Monday to make sure the bacteria is not in his heart. I'll update more later. Friday, November 23, 2007. Other ho...

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Lydia's Liver Story: August 2011

http://lydiasliverstory.blogspot.com/2011_08_01_archive.html

Monday, August 15, 2011. Links to this post. Subscribe to: Posts (Atom). Spenc and Lydia enjoying some brocolli (at least the taste of it for Lydia since she just sucks out the flavor and spits it out). Lydia's liver friends and other blogs we follow. I took Lyds to get her regularly scheduled labs tw.

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Ember's Story: July 2010

http://emberriley.blogspot.com/2010_07_01_archive.html

Sunday, July 25, 2010. Ember didn't care, she was determined to hold her. She settled for touching her and saying "Awww Baby" a lot. I hate to leave this update on a sad note, so here's a cute thought. Ember's hair is now just long enough to put into pigtails! It is the most adorable thing I have seen yet! I will try to post pics soon. Jeannie, Jane, Angel, Mommy, etc. Subscribe to: Posts (Atom). To follow up on the first part of our journey, please go to www.caringbridge.com/visit/emberzstory. A blog fo...

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Lydia's Liver Story: February 2010

http://lydiasliverstory.blogspot.com/2010_02_01_archive.html

Saturday, February 27, 2010. Dallin is my sweet, sweet boy. Links to this post. Tuesday, February 23, 2010. Well if you can tell by the title we have had trouble. Janene went down for here MRI for being the doner. She took Lydia up to her moms and when Lydia woke up from her nap there was blood on the carpet. Long story short Janene stayed at PMCH and Maureen, my mother-in-law, took Lydia down to meet her. Links to this post. Wednesday, February 17, 2010. Links to this post. Friday, February 12, 2010.

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Lydia's Liver Story: Make-A-Wish

http://lydiasliverstory.blogspot.com/2012/01/make-wish.html

Saturday, January 14, 2012. To learn more about this amazing place and see pictures of the fun places there.). We finished out the day with riding lots of fun rides and seeing the sights at Universal Studios. January 29, 2012 at 9:57 PM. Great job of recapping the trip- so glad the whole family got to enjoy the adventure! February 1, 2012 at 9:15 PM. What an exciting vacation that was for your family! I am amazed at all the Make a Wish Foundation can do! What a sweetheart she is! June 20, 2012 at 10:46 PM.

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Lydia's Liver Story: April 2010

http://lydiasliverstory.blogspot.com/2010_04_01_archive.html

Friday, April 30, 2010. I posted some new pictures and vidoes of Lydia smiling, laughing, and wiggling on the transplant link on the right side of the blog. Or, you can just click here on Transplant. Links to this post. Wednesday, April 28, 2010. New PIC Line and Drain Tube. They have sucked out about a pop can of fluid. Hopefully that will help her lung have room to breath. She has had major withdrawals. A lot today to make up for that. I hope she sleeps. Through the night with how much sleep. Her centr...

lydiasliverstory.blogspot.com lydiasliverstory.blogspot.com

Lydia's Liver Story: March 2011

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

Wednesday, March 30, 2011. Picc gone and Chemo done! Lydia had a ct scan on Thurs. and a full blood lab work up to determine if her PTLD was gone. She showed no traces of it so she is officially done with Chemo. Yeah! Links to this post. Thursday, March 10, 2011. Lydia had her last chemo treatment on Thursday, Feb. 24th. Yipee! Links to this post. Subscribe to: Posts (Atom). Spenc and Lydia enjoying some brocolli (at least the taste of it for Lydia since she just sucks out the flavor and spits it out).

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Campbell Clan: December 2009

http://nqcampbellfamily.blogspot.com/2009_12_01_archive.html

Wednesday, December 2, 2009. Holy crap it's been a while since the last post! Sorry Here's whats been going on since May. Charlie has taken a liking to Natalie:) Hailey fell (again) and scratched up her face. Then Kayla followed suit jumping down a flight of stairs into the corner of the front door. Grandpa Campbell sewed her up. She was comforted only by the ER nurses putting a bandage on her doll's forehead too. We got a new bed for Nat! Kayla loves her new lil' sis. Ring around the rosie with Grandma.

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Campbell Clan: May 2009

http://nqcampbellfamily.blogspot.com/2009_05_01_archive.html

Thursday, May 7, 2009. Just wanted to drop a line and tell everyone about our new little baby girl, Natalie Ann. She's 3 weeks old today and is such a wonderful baby. We have (obviously) been super busy with 4 kids under 3 1/2, so sorry it's taken us so long to update the blogs. Here's a few pics of Natalie and all the kids reactions to her :). Kayla has been so happy to finally meet her lil' sis. Hailey has been happy to have Natalie around, but still prefers her walking and talking siblings:).

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Our little yellow man

Sunday, January 1, 2012. Yet another fun thing at Primary Children's hospital. Actual size Spider-Man statue. Not to be confused with Phil Spiderman. Tuesday, July 14, 2009. So, sorry it's taken so long to update. Charlie only had to stay at PCMC for 3 days. Came home with another PICC and just got that out last week. Since then, fever-free and loving the summer weather. Here's a few hospital pics and fun home pics. Late night ice cream treats:). HmmmMaybe a doctor some day? Playing footsie with Hailey.

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