Maximizing Enrollment for Kids: Results from a Diagnostic Assessment of Enrollment and Retention in Eight States
Maximizing Enrollment for Kids, a $15 million initiative of the Robert Wood Johnson Foundation (RWJF) launched in June 2008 and directed by the National Academy for State Health Policy (NASHP), aims to increase enrollment and retention of eligible children into Medicaid and CHIP programs and to establish and promote best practices among states.
In the first year of the Maximizing Enrollment for Kids program NASHP collaborated with Health Management Associates (HMA) to conduct a baseline assessment of each grantee states’ policies and processes for enrolling and retaining children in coverage. The findings of these assessments provide a foundation for the work of these states over the next three years to improve enrollment of eligible children. These reports summarize the information gathered from the assessments of all eight states (Alabama, Illinois, Louisiana, Massachusetts, New York, Utah, Virginia, Wisconsin), organized by themes of states’ work identified through that process, and presented as strengths, challenges and opportunities in each area.
| Synthesis | 1.3 MB |
| Eight States | 1.3 MB |
| Alabama | 1.2 MB |
| Illinois | 1.2 MB |
| Louisiana | 463.7 KB |
| Wisconsin | 473.1 KB |
| Massachusetts | 1.1 MB |
| New York | 496.2 KB |
| Utah | 1.2 MB |
| Virginia | 488.6 KB |

For individuals living with complex, often chronic conditions, and their families, palliative care can provide relief from symptoms, improve satisfaction and outcomes, and help address critical mental and spiritual needs during difficult times. Now more than ever, there is growing recognition of the importance of palliative care services for individuals with serious illness, such as advance care planning, pain and symptom management, care coordination, and team-based, multi-disciplinary support. These services can help patients and families cope with the symptoms and stressors of disease, better anticipate and avoid crises, and reduce unnecessary and/or unwanted care. While this model is grounded in evidence that demonstrates improved quality of life, better outcomes, and reduced cost for patients, only a fraction of individuals who could benefit from palliative care receive it. 























































































































































