Better Together: State Strategies for Medicaid-Ryan White HIV/AIDS Program Coordination
Successful coordination between Medicaid and Ryan White HIV/AIDS programs is one key to improving care and services for persons living with HIV/AIDS. As more people living with HIV/AIDS gain health insurance coverage, effective coordination between programs remains critical. During this webinar, state officials will discuss promising practices for coordination in the areas of inter-agency communication, program eligibility, access to care, benefits, and prescription drugs. This webinar is supported through a cooperative agreement with the Health Resources and Services Administration.
Speakers:
- Kathy Witgert, Program Director, NASHP
- Dr. Karen Mark, Chief, Office of AIDS, Center for Infectious Diseases,Department of Public Health, California
- Dr. David Collier, Associate Medical Director, Bureau of TennCare, Tennessee
- H. Dawn Fukuda, Director, Office of HIV/AIDS, Bureau of Infectious Disease, Department of Public Health, Massachusetts
- Barbara Lantz, Manager, Quality and Care Management, Washington State Health Care Authority
| Click for the Webinar Slides | 489.7 KB |
| Click for the Associated Publication | 149.92 KB |

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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. 























































































































































