Failure!

So, a few things have come to light recently. I have been in contact with the pten research Foundation in London and they are only funding trials of Rapamycin in the USA. Why would this be? If anyone could email tom@ptenresearch.org to ask him why ld really appreciate it. If you do please copy me in so I have a record levymelanie@hotmail.com . Please keep sharing and getting people to sign this. We have to bring the standard of care for UK patients in line with our friends in the USA. I can't do this alone though. People power is the key! Xx