Sure - I hope this helps people have a more accurate impression of what it is like to be a GBM patient and have to fight the people who are supposed to be helping you. Without the tumor tissue, the treatment is impossible, and we had to fight every step of the way to keep it and get it stored properly, as the hospital refused to help us. We were only able to do this as a result of hearing about immune therapies from a friend - all word of mouth - not through a recommendation from a doctor.
It is a wonder that they have gotten as many patients enrolled as they have.