I appreciate that these questionnaires are laid out in a brief and organized way. I think definitely helpful for newer clinicians/ newer to EPI and or working with families. I think I really appreciate that the questions about psychosis just goes out and asks families” Are there any other forms of treatment that you wish your relative was receiving?” Often I feel like families can be scared to speak up/don’t want to come across as “Demanding” as the video earlier in this section explained. One of the roles that I am curious to explore more is that of advocacy within the system- encouraging families (when appropriate) to push for more, and providing the safe space to talk about how advocating as a family member is not a bad thing.