The experience of other states suggests that this is not going to be a walk in the
park. There are a few bright spots nationally, but results are not encouraging. A
gols should not be to enroll all potentially eligible children: more realistic might be 60
percent of them in 3-5 years.
We will need to make extra effort with regard to trust issues (trusting the
government, especially around immigration). This will require additional materials and
media efforts, but it will mostly be achieved by face-to-face communication.
Community and migrant health centers (CHCs/MHCs) are central players and could serve as
the lead agency (agencies) for this proposal. However, they cant do the job alone.
Families who are already bringing their kids to the centers must be helped and must be
part of the strategy. But the families who are not bringing their kids to any
provider are most prone to waiting until an illness or injury is very acute before seeking
care, and they are probably also the hardest to reach. Many channels must be
used to reach them.
Schools will be central. The Federal government is pushing approaches coordinated with
application for school lunch programs; the State has specifically emphasized tie-ins with
school-based heath services, and school nurses are well-positioned to identify uninsured
kids.
The dollars most States offer to provide are not enough to do the outreach exclusively
(or even primarily) by hiring "outreach workers." For example, if we have a
budget of $400,000 with $250,000 in the first year, for a county with almost 100,000
potential eligibles, we could hire and supervise at most about 10 full time workers
(leaving no funding for evaluation, reporting etc.). If they were doing direct
outreach themselves (as opposed to recruiting and training "partners"), it is
doubtful they could penetrate much of the potential population.
We suggest that staffing be concentrated on skilled and energetic organizers
and trainers rather than directly hiring outreach workers. Other resources
can be leveraged such as VISTA/Americorps, and other funding should be sought to
supplement State funds for the first two to three years.
I would also hope the same CHIP coalition or a subgroup could sponsor such a proposal
to the State and other funders to show the benefits of good follow-through in
assuring access, quality care and improved health outcomes by making sure these families
develop good primary care relationships.
Project objectives should include numbers of families and children identified, numbers
of applications initiated, numbers of kids actually enrolled. A fairly sophisticated (yet
clear and simple) information system will be required to track these results to meet
reporting and QA requirements, consistent with sound confidentiality practice. For
example, how do we avoid double-counting families with uninsured kids if they show up at a
health fair, are identified by school health officials and also show up at a CHC?