Thanks so much! I must admit that I find myself looking at the sweet photos and reading their Care Pages over and over, I was unaware that some of the children have became angels, some since the trees went up, until you all pointed that out to me. I now have the Carepages bookmarked to follow and check on.
Neuroblastoma is considered rare, only affect about 600 kids per year, and therefore only gets very little funding for Research from the government.
I also find myself being very stressed right now as I will call Monday to get the results of some of Tyler's scan. I can't seem to get into the Holiday spirit at all, I'm so worried. As some of you may already know, not a lot of kids survive this Cancer.

. The kids that do often suffer from long term side effects, the treatment is very toxic and potent. This is another reason why research is so important, they really need to find less toxic drugs and a cure to treat Neuroblastoma as well as other Cancers. Tyler is very blessed to only have hearing loss, bone pain, one kidney, low immune system and low blood counts, we were told he can still develop toxcity problems and organ failure late term. Several children have passed away during treatment do to organ failure and side effects from treatment.
Thanks so much to everyone