Hi there everyone! Kaci's Mom told me about this forum. We are currently fundraising to go to the same clinic Kaci went to. We are in New Zealand (waaaaay down here beside Australia), so we're a bit far away from any action. Had originally thought we'd go to China, but feel a bit safer knowing the cells used with SRI/Ramirez are sourced and tested in the States.
Our daughter is 20 mths old and has spastic quad CP with secondary Microcephaly, Epilepsy and severe developmental delay and low vision. However, she is doing much better than predicted, is breastfed, eats 'soft lumpy' food, drinks some thickened liquids, walks if supported under her arms and enjoys water, music and knocking things over. We are about to start up a website and charity trust to fund Daryl's trip and also to help other families fund alternative therapies for CP (sort of like adamsusserfoundation.org).
