Search results

HI Can anyone provide some comparisons between going to XCell in Germany and getting your own stem cells from hip bone and injected by lumbar puncture to treat CP vs using umbilical cord stem cells via catheter? I know Steenblock says UCSCT are better for CP, plus avoids damaging fragile little...

Anyone had any experience/results using this supplement in helping CP?

Hi there, just starting this thread on behalf of my new friend Donna in Ausy. She is hoping to go to Duke University to have her daughter who has CP, treated with her sibling's cord blood which she has stored. They are currently checking to see if it is a match. The question is: Do Duke...

Hi all We are coming! And here's the article to prove it! Thought this might encourage some of the Southern Hemisphere readers to get involved, and get talking about this therapy. We need to make a noise so that we can get some of the action happening down here! Sorry, it's a bit fiddly...

My name is Janine and my daughter has severe CP, microcephaly and epilepsy. We live in New Zealand so are MILES away from where everything is happening but are dying to get over there and get some treatment and have the application etc underway. The big frustrating part will be fundraising to...