Health Care Protocols and Standards for Treatment of Children in Foster Care: Overview of Issues
Much has been written concerning how health care needs of children in foster care have increased substantially over time and how it has become increasingly problematic for the child welfare system to address those needs. The literature seems to be in agreement that the problems encountered in the provision of adequate health care to this population are compounded by several other aspects of the system and its operation: changing placements of children that make continuity of care and continuity of the medical record difficult; child welfare agency’s necessary focus on the immediate (v. ongoing) health needs of any particular child (within the context of a growing caseload and greater needs); and lack of awareness of foster care specific issues on the part of Medicaid agencies.
| 1997.Mar_.health.care_.protocols.standards.treatment.children.foster.pdf | 446.8 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. 























































































































































