yes, rick, i woud like to subscribe to the cc foundation newsletter, have much support from family, close friends an d business assoc that would like to supoort the foundation also – please contact me –
Welcome. We are happy for you to have found us although, we are sorry for the circumstances leading you to this site.
Your question is one that has been addressed by others in the past. In order to receive more responses, I believe it to be best to repeat your post in the
Cindy…. has your duaghter been diagnosed with CC per pathologhy report? If so from all of my research it is very rare for a young 3 yera old. PLease introduce your self in our introduction section and also post under experiences what is currently going on if you like . I’m sure many members of this site will respond with what knowledge they have concerning your daughter.
My 3 year old daughter has just been diagnosed at childrens hospital in los angeles–she had been having tummy aches-took her for an ultrasound–they saw spots –mri–biopsy
any thoughts-ideas how rare is this in a 3 year old