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
since I last posted. We have been so busy this month. Adley had his Christmas program at his preschool - they studied Italy and dressed so cute. They sang the song, "when the moon hits your eye like a big pizza pie, that's amore . . ." (not sure of the exact title). Adley has sung it several times since to many people. I think he might be musical when he gets older. We all recovered from our sickness and made the journey to Arizona to see my family. We spent 12 days there and had a wonderful time. Surprisingly it was warmer here at home while we were gone then it was in Arizona. We got to go to the Lego store, which the boys loved. We played at a really fun park, visited with friends, made a gingerbread house and sugar cookies, ate at our favorite places, went to the movies, enjoyed a visit from Santa at the house and tried to get in some rest. We had family pictures taken for the first time in 5 years since my brothers were gone on their missions. We finally g
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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