Team Carter raised $2,334 for this year's walk! We are also so excited about Dr Walker's announcement that the government just awarded a grant of $1 Million to the Research efforts for Dr McCallister and Dr Walker's new research center here in Salt Lake, what an accomplishment. Dr Walker spoke at our walk about the wonderful research they've come out with and how this money will help them fund their findings for different ways of TREATING and PREVENTING Hydro. What angel's the researchers are, they work for next to nothing with very little funding. They are definitely doing great work for hydro families all over the world. Check out some of our exciting pics from the walk:
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.
Sunday, September 27, 2009
Friday, September 11, 2009
Saturday, September 5, 2009
TEAM CARTER!
Join our 3rd Annual Hydrocephalus Walk in Salt Lake City. You are invited to come out and walk with TEAM CARTER on Saturday, September 26, 2009 at 9:30 am at Sugarhouse Park. Last year we came in Second place for the most funds raised and First place for the most walkers who came out to support. You can view our page and register to walk at:
TEAM CARTER'S WEB PAGE
This website is where you would register to walk, make sure you order your free t-shirt when you register.
We have done several fund raisers for this walk and other hydro events so if you'd like to donate that would be great but we know we've tapped a lot of resources lately. Last year we did have several of our friends and family go around to their friends, families and co-workers and collect donations, that would also be great again this year.
Its our family goal to raise awareness about this condition that Carter lives with every day and we are determined to make a difference for him and others who live with this debilitating condition. We hope to see a cure in his lifetime and you can help us reach that goal with our fundraisers throughout the year.
Our web address for the walk page is: http://www.gifttool.com/athon/OurTeamPage?ID=1488&AID=794&TID=4635
Please e-mail us if you need more information or need help registering at hydroinutah@gmail.com
TEAM CARTER'S WEB PAGE
This website is where you would register to walk, make sure you order your free t-shirt when you register.
We have done several fund raisers for this walk and other hydro events so if you'd like to donate that would be great but we know we've tapped a lot of resources lately. Last year we did have several of our friends and family go around to their friends, families and co-workers and collect donations, that would also be great again this year.
Its our family goal to raise awareness about this condition that Carter lives with every day and we are determined to make a difference for him and others who live with this debilitating condition. We hope to see a cure in his lifetime and you can help us reach that goal with our fundraisers throughout the year.
Our web address for the walk page is: http://www.gifttool.com/athon/OurTeamPage?ID=1488&AID=794&TID=4635
Please e-mail us if you need more information or need help registering at hydroinutah@gmail.com
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