As a person with rare diseases I am for this bill. Having access to experimental treatments doesn’t mean they are unsafe. It means that they don’t yet meet the requirements for approval. That could be anything from lack of testing subjects to satisfy numbers (try getting a huge sample out of a disease with ten people. It won’t qualify in any way), to money issues, paperwork, or simple backlogs. Anyone against this that doesn’t suffer from a rare or chronic or terminal disease can’t possibly understand that for us, the risk is worth it because out lives are for sure going to end, or be complete suffering anyway, and any chance to help us have a quantity or quality of life is well worth it.