Here is Bug's attempt to crawl, where there's a will there will be a way, right!?!
A blog to the world who might see a fraction of the joys and challenges of raising a miracle baby! Carter was born with Congenital Hydrocephalus & Macrocephaly in November 2007. He was also diagnosed with Cortical Vision Impairment and Hearing Impairment. Doctors said there was little hope for a full life...well we'd like to show the world what a full life looks like! We have triumphed over many obstacles, yet have many more to face. This is our story.
Showing posts with label Hydrocephalus. Show all posts
Showing posts with label Hydrocephalus. Show all posts
Saturday, November 15, 2008
Saturday, November 1, 2008
Tuesday, October 21, 2008
Monday, September 22, 2008
WALK
TEAM CARTER

Drum roll please...we raised $1,688.00 for research for the Hydrocephalus Association! We came in 2nd place for the most money raised and 1st place for the most people who came out and walked! I'd like to give an extra special thank you to those who have donated, those who went out and raised funds for us, and those who came out and walked with us. Your support will be forever remembered and your love is forever planted. You have made a difference in these children's lives and the outcome of their futures, thank you so much!

Thank you Bill, Anita, Melissa, Michelle & Steven (A couple of rest breaks, and a questionable lead)
Thank you Dave, Tonya & Garrett (1.4 miles, no big deal right?!?)
Thank you Mark & Pat (hurt foot and still smiling)
Thank you Jen & Jensen (Glad you found us!)
I just want to send out a special THANK YOU to all of you who donated who couldn't come out and walk. Thank you so much for all of the donations you gave and funds you raised, we feel so blessed from the support you have shown to our family.
All Teams

Wednesday, September 10, 2008
10 DAYS
I just wanted to Thank everyone who have donated so far, we really feel love and support from all of our family and friends, we've collected $825 which is so great! Well there's only 10 more days of fundraising until our walk and we'd love more donations, so go out and bug all you know. We've got pledge forms if you need them, just let us know. So our walk is a week from Saturday at Sugarhouse park (just off I-80 and 1300 East) from 8:30am-1:00pm. They say there is fun stuff for the kids and a lot of them will be on trikes and scooters and bikes. So it will be a morning of family fun (I guess, we've just heard, we've never been). Again, thank you so much for working as hard as you have to help our family and so many more who are effected by hydrocephalus.
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