Where and how can HIV funders draw strategy from the nimbleness and creativity of movement organizers? How can we be more receptive and responsive to the needs and experiences of people most impacted by oppression? How can HIV funding help to reduce the harms of criminalization, stigma, violence, and oppression? As funders, our ultimate goal is for national governments to take our place and to fund a comprehensive package of HIV prevention and treatment services for everyone who needs them.
What we want to avoid is the kind of disruption or cessation of services that occurs when donors cease funding key programmes abruptly and without a clear plan for hand over. Many governments are reluctant to fund services for Key Populations that are criminalised, such as needle exchange services for drug users, or condom distribution services for sex workers. Moreover, if budgets are squeezed, prevention services are usually the first to be cut, and civil society organisations find it harder to secure funds for advocacy or to hold governments to account. This session, designed by Frontline AIDS and the Joep Lange Institute, will highlight some of the critical services and programmes that philanthropists may need to keep supporting at community level as governments take over responsibility for HIV services previously funded by donors.
The U. The D. Department of Health paints the picture of how much progress can be made toward ending the HIV epidemic by using evidence-based interventions such as population-focused HIV testing, treatment as prevention, condom distribution, needle exchange, and pre-exposure prophylaxis PrEP. Self-care, putting health knowledge, tools and decision-making in the hands of users, can radically transform access to healthcare, particularly for HIV prevention and sexual and reproductive health, where stigma and provider bias limit the availability and acceptability of provider-based services.
With new tools and technology, from self-testing to self-injection, the time to invest in building the infrastructure and culture of self-care is ripe. Global bodies are setting the policy scene for self-care and rallying the global community around a common vision; however, there is a catalytic role for private philanthropy, with its close connection to social movements, to be leaders in driving a new person-centric approach to services. Private philanthropy can also help generate the evidence needed that self-care can increase access to services, keep people on treatment, and potentially generate health systems cost savings; and provide high-impact models for other donors to scale.
She has a decade of experience in managing health programmmes in Asia, Africa and the Caribbean, primarily focused on access to medicines, devices and diagnostics for infectious diseases, family planning and maternal and neonatal health, as well as on health financing. Taryn was voted to the Board in the Summer of Networks support PLHIV to define their own agendas and priorities; to select and hold accountable leadership of their own choosing; to advocate with collective voices for structural interventions by fighting injustice, discrimination and stigma; to advance intersectional policy solutions that benefit the HIV response; and to improve quality of life and health outcomes for PLHIV.
The need for intersectional organizing and policy advocacy efforts led by communities most impacted by the epidemic in multiple states has arguably never been greater, and networks are well set up to activate a grassroots base. In this session we will focus on diverse PLHIV networks as a unique, cost-effective model for supporting leadership development and grassroots community organizing, and how funders can integrate resourcing networks into their work.
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This will be a dialogue between funders and leaders of networks of people living with HIV. Finally, a panel of grantmakers will tackle what it means to be an HIV funder by digging more deeply into how their strategies have evolved over time to remain relevant to the current HIV response. In addition to telling their own stories, they will respond to a series of videotaped remarks from other philanthropic leaders that will play at the beginning of the session. The panel will seek to find the right balance between prioritization and integration of HIV and discuss how we ensure that the lessons learned that have fueled the success of the HIV response, become cornerstones of broader practice in human rights, social justice and health care.
Thank you to our amazing Summit Sponsors and Program Committee. We would not be able to plan and implement this event without their generous time and support. You too can join this amazing list of organizations! Grantmakers now have the opportunity to sponsor different parts of the Summit that align with, or highlight, their grantmaking interests and impact. This is an excellent chance to demonstrate your commitment to the field of HIV and AIDS, as well as connect with an audience of leading private and pubic funders engaged in the HIV response.
Contact Sarah Hamilton sarah fcaaids. How and why do funders center HIV within other priorities? How do funders measure success when funding HIV work that intersects with other drivers?
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Schedule Monday. Session Organizer: Kaiser Family Foundation. Speakers Robbyn Kistler. Robbyn Kistler has worked with the Kaiser Family Foundation since as a consultant for their media partnerships and health communications program.
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She serves primarily as a liaison to health departments in the Southern U. She supports local efforts for ending the HIV epidemic by guiding strategy and coordinating media placements on billboards, broadcast, and social media. She is now based in Brooklyn, a proud mom of two teen girls and a loving ally of queer people of color.
His expertise is in public health, health care, social safety net and social justice. He is a sought after speaker, editor and group facilitator for social justice campaigns and organizations. He is currently the senior editor with TheBody. Prior to joining TheBody. In addition to his political work, Kenyon is a prolific essayist and author.
His work has also appeared on websites and in publications such as The Body. DaShawn is also the founder and Executive Director of Mobilizing Our Brothers Initiative MOBI , a series of curated social connectivity events for gay and queer people of color to see their holistic self while promoting community, wellness, and personal development.
DaShawn is a proud mentor to some of the brightest emerging minds around the country and continues to learn and grow from his mentees, colleagues, and community. Speakers Kate Harrison. She led the development of guidance on community-based approaches to support children affected by HIV and AIDS, including the interactive online resource www. After recognizing that people with HIV and the public were not being informed about this groundbreaking science, he joined with activists and researchers to ensure the science reaches the people it was intended to benefit.
- Understanding Health Literacy for People Living With HIV: Locations of Learning..
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Bruce has worked in philanthropy and social change for over twenty-five years developing cause-related initiatives for high profile people and brands. At the Legal Network, she oversees all bilingual strategic communications programming and campaigns, advocacy interventions, community outreach, media relations, event planning and brand management, among others.
She is currently the principal investigator on a new research grant working with people who use drugs, and has contributed extensively to media on topics including HIV criminalization, harm reduction and LGBTQI rights. In this role, he manages the grant-making initiative and works closely with grantees to deliver tailored technical assistance and capacity building, focusing on topics such as meaningful involvement of people who use drugs, media relations, harm reduction , federal and private funding opportunities, and grant writing.
Zachary contributes to research and resource development. In , Zachary compiled an analytical report on the challenges and lessons from syringe services programs in the United States using data from Syringe Access Fund grantee final reports. Currently, Zachary is preparing to publish a toolkit on harm reduction and stimulants. Naina Khanna is a national speaker, trainer, and advocate who has worked in the HIV field since , following her HIV diagnosis in They, konsolit. Flirtsofa is single and ally dating plattform schweiz kostenlos dating app knows me pages of classic american adults have reviewed other.
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Some even walked out of the briefing in protest. The problem of HIV among women was also pushed to the fore. Although it had been clear since the early s that women contracted HIV through heterosexual sex and other transmission routes, women systematically had been elided in both scientific and popular AIDS discourses, as well as in policy responses. Particularly crucial was the issue of definition: an official AIDS diagnosis was needed to qualify for most federal assistance programmes, yet the existing clinical definition omitted important manifestations characteristic of groups other than gay men.
Expanding the definition was nonetheless politically difficult, because the change would increase diagnoses by up to per cent, thereby driving up federal expenditures.
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In advocates won out, and the CDC adopted a new definition of AIDS that included invasive cervical cancer, recurrent pulmonary tuberculosis and other conditions specific to women or injecting drug users. PEPFAR poured millions of dollars into delivering medication to parts of the world where it would not otherwise have been accessible.
Domestically, meanwhile, a profound shift was underway. In response, academics mobilised through national organisations such as the Union of Concerned Scientists and Research!
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America to protect scientific autonomy and the peer-review process. Alongside the movement to better align HIV prevention with conservative values came other shifts in prevention, many of them geared toward routinising testing and the identification of HIV-positive individuals. With SAFE, the CDC moved away from the longstanding strategy of balancing general AIDS awareness programmes with ones targeted to high-risk groups; the CDC now focused on raising the number of HIV-positive people who knew their status, understood it, and received treatment for it, making them less likely to transmit the virus to others.
In the agency dropped longstanding requirements that every HIV test be accompanied by written consent and pre-test counselling. It also recommended that adults and adolescents in all health care settings be tested for HIV at least once and that those engaging in risk behaviours be tested annually. Even though CDC leaders had determined that routine testing would benefit both those with HIV by setting them on a road to effective treatment and those without HIV by clarifying the HIV status of partners or potential partners , Left-leaning activists worried about the potential for coercive testing of marginalised people and the stigma that those who tested positive might face.
Despite opposition, the routine testing policies of the George W. Political struggles over Medicare resulted in repeated, temporary losses of prescription drug access for patients. Financial constraints on Medicaid, which covered many more HIV-positive people than Medicare, forced patients to forgo certain medications. Although delayed by Hurricane Katrina and war in Iraq, the reauthorisation process was long and, once again, contentious.
With regard to the first, the final legislation increased proportional allocations to rural and Southern states, while still limiting to 5 per cent the amount that early epidemic centres could lose. The abstinence-based policies of the s were largely dismantled. Several judicial decisions weakened the federal policy, and the Supreme Court overturned the entire law in These years also witnessed the next chapter in needle-exchange controversies.
Seizing a rare moment when Democrats controlled Congress and Republicans were occupied by other issues, the Obama Administration quietly lifted the federal funding ban at the end of The Obama administration also moved in new directions. An Implementation Plan was released alongside the Strategy , and each relevant federal agency devised an operational plan to facilitate implementation. ONAP itself spearheaded efforts to increase coordination, for instance, through the introduction of common requirements for grantee reporting.
The CARE Act reauthorisation helped preserve treatment services for those without quality health insurance.