checkingbackwithzac blogspot.com

Checking Back with Zac

Welcome to Checking Back with Zac. If you are reading this, chances are you already know a lot about this special little boy. If you don39;t, I would like to tell you a little about him. Zachary James Moller was born May 1st, 2010 with a condition called Giant Congenital Melanocytic Nevus. This very rare condition affects only 1 in 500,000 so I guess you could say he39;s one in a half-million.

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LINKS TO WEB SITE

Everybody Loves Austin

Tuesday, March 13, 2018. I have been remiss in not posting on this blog in a few years and have had people ask what has been going on with Austin. If you would like to learn more about Nevus Outreach or support available for parents of children with NCM please see the sidebar. Wednesday, April 2, 2014. Thank you so much for reading! Sunday, September 23, 2012. We are so thankful fo.

The Wonderful World of Vance

to just walk around and see what we could see.

Jules-n-Jud Luke Andrew

Friday, December 27, 2013. Here is our Christmas 2013 in pictures. Can you tell from the pictures who does NOT like to have their picture taken? We enjoyed going to Breakfast with Santa at Crosspoint. Andrew does NOT like Santa! Luke LOVES him though! BUT Andrew liked getting a sucker from Santa! We made reindeer food. This picture just cracks me up! Tays is looking good though.

Sarcastic Stilettos

Tuesday, October 30, 2012. So, I have to say I was pretty excited when Influenster. Asked me to be a reviewer of their beauty box - the VoxBox. I got it the other day and it was like opening a present! So, ya wanna know what I got? I know you do! There were some great items, including some full size items. Read on for my reviews of some of the products! So, the first up is the Slatkin and Co. Next, I tried the Goody spin pins.

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Checking Back with Zac

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Welcome to Checking Back with Zac. If you are reading this, chances are you already know a lot about this special little boy. If you don39;t, I would like to tell you a little about him. Zachary James Moller was born May 1st, 2010 with a condition called Giant Congenital Melanocytic Nevus. This very rare condition affects only 1 in 500,000 so I guess you could say he39;s one in a half-million.

CONTENT

This web page checkingbackwithzac.blogspot.com states the following, "Sunday, October 18, 2015." We saw that the webpage said " Wine, Tom Selleck, and Expansion." It also said " Please pray for my little guys health. He has the most amazing spirit and joyful heart. Please pray that God gives us the strength we need to keep the pace, stay the course, and appreciate our own journey. Sunday, March 22, 2015. Even today, he is fully aware that his bubbles need to come out. This has been a VERY vocal round of expansion. Gone are the days of simple distractions like a light-up toy or even the i."

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