I've been e-mailing back and forth on it, she's got things covered on her side. I'm just trying to reach out to people that may not fall under their umbrella. This public hearing is going to be critical.

I'm just concerned that the turnout at the last hearing was more about MMC's not wanting to lose their "caregiver" status at the time and less actual caregivers and patients. I expect the public to be more involved, as well.

This does not look good.