One of the themes we've heard in the questions is, where would we like additional data? I think your question highlights an area where we would all benefit from additional data in terms of the particular needs of people from different communities.
What I can tell you anecdotally from what we hear from caregivers is that one of the challenges they may face in going into different health care settings is barriers to access based on language or based on a lack of understanding, if they're a newcomer, about how the system may work. We find that caregivers need information around system navigation. They need information around how to engage with different health care providers, and that may come with a different cultural context.
We hear from caregivers that culture really matters in terms of how they've taken on this caregiving role and how it's navigated within a family. Certainly, we hear that within certain cultures there is an automatic expectation that caregiving roles will be taken on by women, so women feel an additional burden of expectation within their caregiving role, but this isn't an area where we have clear demographic data in order to provide significant insights.