I have lost all confidence in the medical system. The paperwork, policy, process, and politics had as much to do with Sarah running out of time and now this family's loss. I understand the need to validate and protect safety of the masses but this is not a totally "new" drug. It's been used for years with no ADEs. If I'm dying and request treatment, that should be my decision with no arguments. This is beginning to sound like a legislative issue that needs to happen. What happened to the Right to Try that was hacked a few months ago? There's a difference in "do no harm" and blocking someone's dying wishes to try.