FROM OUR BUDDY WILLS SITE - WE ARE HONORED TO KNOW YOU LACEY FAMILY ,AND WE TAKE OUR HATS OFF TO YOU FOR ALL YOU ARE DOING FOR OUR CHILDREN, YOU ARE INSPIRATIONS. WE ARE SO TOUCHED YOU INCLUDED DEQLANS STORY AND I WAS SO MOVED TO SEE EACH FACE, EACH STORY, A PART OF THESE AMAZING CHILDREN DISPLAYED FOR THE WORLD TO SEE AND LEARN FROM AND REALISE THE COURAGE , HEARTACHE, MIRACLES AND NEED FOR A CURE RIGHT IN FRONT OF OUR EYES.
Here is a slide show from Vicki from Saturday night that she posted on Friends of Will.Each of the tables in the hall honored a child still fighting NB, in NED status, or sadly who have lost their battle. Many of these children may be familiar to you as you may have visited links to their sites from Will's page in the past. There were balloons with a picture of each child on them, then their table had a few photos of that child, a few of their favorite items, and a brief synopsis of their history. It was very moving to me as I walked around the hall and would catch a glimpse of the smiling face of Lucas, or Max, or Katie as I was greeting friends and strangers alike all in united effort to help save kids lives.
THE EVENT RAISE OVER 40 000 US DOLLARS TO GO TOWARDS FINDING THE CURE FOR NEUROBLASTOMA! PLEASE, PLEASE CONTINUE DOING EVERYTHING YOU CAN TO HELP US FIND THAT CURE - WRITE TO OPRAH, SUPPORT FUNDRAISERS, PRAY, SEND IDEAS, HELP US RAISE THE FUNDS SO THAT THESE AMAZING DOCTORS CAN BE LEAD TO THE CURE FOR OUR KIDS.