Which of the following is part of the dying person's bill of rights?

The first statement, "I have the right to have my questions answered honestly," is a fundamental aspect of the dying person's bill of rights. This principle underscores the importance of transparency and communication in end-of-life care. Individuals facing the end of life often have numerous questions regarding their condition, treatment options, and what to expect as they near death. Honest answers to these questions help them make informed decisions and provide a sense of control during a vulnerable time.

The other statements, while they may resonate with certain rights that individuals might feel they possess, do not encapsulate the essence of the core rights typically associated with the dying person's bill of rights. For example, the right to avoid all medications may conflict with the need for pain management or treatment during the dying process. Similarly, while having the right to refuse visitors can be an important consideration, it is not universally recognized as a key component of the bill of rights. Lastly, the right to choose caregivers is significant but may not be expressed as a standalone principle in this context, as caregivers are often assigned based on various factors that include availability and expertise.