Liam's first time on River Rampage - he got drenched but loved every minute of it! Doesn't he look so small!
We wanted to do one last fun summer trip for the boys before school starts this Thursday. We took a day trip to Dollywood. We got there a little after the park opened and it was not very crowded at all. We walked on almost every ride and if we had to wait it wasn't longer than a few minutes. Last time we were there in May Adley was just shy of being able to ride all the big rides. We learned about a place where they will measure you and give you an armband that has the appropriate color that corresponds with your height category. This way you are measured once and simply just have to show your armband to get on the ride. Adley was thrilled that he was tall enough this time to ride any ride in the park. Eli and Liam also got moved up to the next category. Thank goodness for Eli because this kid has been dying to ride more rides. He and Adley are not afr
Man do I love this little boy! He is full of squeals, smiles, slobbers, hugs, crumbs and dirt. He is at such a fun age. Liam says a lot through the faces he makes because he is quite stubborn and shy and still not wanting to talk much. He says a hand full of words, shakes his head yes and no and is starting to make different sounds. He is making progress so I am not too worried anymore. And if you haven't heard or noticed....no more pacifier....Yay! Liam is growing up so fast but is still my most snugly baby. He loves to rock in the chair before nap and bed and when he gets up in the morning he often times runs to my room to crawl in bed with me for more snuggles. I just love it! Up next, to turn his crib into a toddler bed....then all signs of 'babyness' will be gone, ah so sad! Liam learned how to climb anything recently, kind of scary! This was a search for his paci back in March. The boy would do anything for that darn pacifier, but surprisingly it was prett
This week is EB awareness week! EB stand for Epidermolysis Bullosa. It is a rare, genetic skin disease that involves the connective tissues of your skin. The slightest friction to the skin can cause severe blistering. The EB kids are referred to as 'Butterfly children' because their skin is so fragile. To learn more go to http://www.debra.org/ . I came across this disease through a blog about little Jonah. You can follow Jonah by clicking on his picture to the right. I have since come across several EB kids that I follow on a regular basis. EB is a horrible, painful disease. This week I will be running in a 5K race in support of EB. A few of my friends from work and myself made shirts that have the kids we follow on the back. Unfortunately shortly after the shirt was made little sweet Bella passed away. She was at the University of Minnesota for a clinical trial for an EB bone marrow transplant. I think she was patient #12. So far this is the only hope these kids have. I miss B
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