Please Read, Kindly Asking for Everyone's Help for Donations! Update 1st Page


More for his tree :)

all the very best Tyler and family, take care,

Gaspode

My code: 15915
 
After viewing the stories of the neuroblastoma children and their families, I am really committed to trying to encourage those I know to support this research. Here goes a repeat donation to lunchforlife.org
Giving Code is 15956

Good Luck Tyler. Sandie
 
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. :sad1:. 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 :grouphug:
 
sweetpeakaris said:
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. :sad1:. 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 :grouphug:

Hope you get good results tomorrow!!
We have a family friend who was diagnosed with this cancer when she was 1. She is doing okay now, but i remember for awhile it was not sure what would happen. I shared this site with the family
 
I love the picture of Tyler! What a smile, he must light up the room when he walks in.
To those of you that have donated I say thank you. To those of you that haven't, please do. I know I sound like a broken record, but $5.00 is such a small amount. Read some of the stories. It is astounding what these children must endure.
 
Thanks, We managed to get the Tree up so I was able to sneak a more recent pic of Tyler before he headed off to Boys Scouts, I noticed after I took it, his face was a little dirty with juice, lol!
 


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