The Affordable Care Act ACA provides new health insurance coverage opportunities and extends non-discrimination protections to millions of individuals, including people with HIV. Greater access to insurance coverage has the potential to improve continuous access to care and treatment for people with HIV which can positively impact individual health outcomes and reduced the risk of HIV transmission. As a follow-up, this report provides a second look at how the ACA is impacting people with HIV two years into these new coverage opportunities, based on focus groups conducted with HIV positive individuals from the same states in early , after the third round of open enrollment. Groups were conducted with HIV positive individuals who gained insurance coverage — through either the Marketplaces or Medicaid expansion- in California and New York and with those who remained uninsured, largely because they fell into the coverage gap, in Florida, Georgia, and Texas. Key findings include: While in , participants who gained insurance coverage were still in the early stages of figuring out how to use it, insured participants in this round of research reported using their coverage regularly to meet their HIV care and treatment needs. They reported that their health is easier to manage as a result of gaining coverage and appear better able to navigate using insurance than their counterparts. They have found relief and security in becoming covered. Still, despite some increased comfort with coverage, participants remain unsure of how to fully assess plan options and, as in , put a lot of trust in case managers to help make enrollment decisions. They continue to lack some basic insurance literacy but unique to this round of research, many participants across the sites knew that access to health care varied across the country. Those with insurance recognized its benefits but some worry about being able to maintain coverage. Those with private insurance worry about costs and those with Medicaid find recertification stressful. Only a few participants have made changes to their plans since first enrolling. One individual switched to a different metal level plan by choice and was unexpectedly met with higher costs and two others were moved into new coverage automatically. As was found in the groups, those who live in non-Medicaid expansion states and remain uninsured, largely because they fall into the coverage gap, feel that they can meet their HIV care and treatment needs through the Ryan White Program, which they say is lifesaving, but have many other health problems that are going unaddressed. When they learn that their state chose not to expand Medicaid, they are dismayed but not surprised. Almost all say if their state later expanded the program they would enroll, especially those who have past experience with Medicaid coverage. More than gaining insurance, most report that their finances are the biggest stress in their lives; they struggle to make ends meet and many face substantial medical debt. Just as in , many respondents report close relationships with their HIV providers. They say having a provider who is a specialist and who has a consistent role in their lives is important and in seeking out new coverage many prioritize being able to maintain these relationships. Choice in pharmacies was also important with respondents identifying a range of preferences regarding how they get their medications. The Ryan White Program continues to provide a crucial role in the lives of almost all the participants, especially the uninsured. Ryan White clients were enormously grateful for the program but like Medicaid enrollees, faced challenges around recertification time. Unlike in , those who have gained coverage tend to be less aware they are still connected to the program despite reporting using support services like case management that are funded by Ryan White.

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