Organization for Latino Health Advocacy
Leading public policy development and public health research to improve health outcomes in underserved communities.
Leading public policy development and public health research to improve health outcomes in underserved communities.
Patient advocacy focused on increased access to affordable, culturally competent healthcare services for medically underserved communities, including oral and mental health services.
Implement public policy initiatives to address the disproportionate rates of chronic diseases, such as obesity, diabetes, and cardiovascular disease, within medically underserved and rural communities.
Establish evidence-based interventions to address the upstream drivers of Latino health disparities in low-resourced communities, including food insecurity, violence prevention, and environmental health.
Ensure women are included in clinical research, drug development, and the design of public health interventions.
Support public policy to improve the health and well-being of all immigrants, including access to trauma-informed care and preventive health services for those with limited English proficiency.
The Organization for Latino Health Advocacy (OLHA) is a national advocacy organization focused on empowering underserved communities in the U.S. to achieve optimal health and well-being.
Our vision is to see a future where all members of the Latino community have equitable access to the resources, knowledge, and support they need to live healthy, fulfilling lives.
Jeanette is a prominent health policy advocate with over 20 years of experience dedicated to improving health outcomes for underserved communities in the U.S. Before establishing OLHA, Jeanette founded the Latina Health Collab, a consulting firm aimed at engaging diverse stakeholders in patient advocacy. Jeanette has held leadership roles in several national nonprofits, including the Biotechnology Innovation Organization (BIO), UnidosUS (formerly the National Council of La Raza), the National Consumers League, and the American Academy of Family Physicians.
Jeanette began her career in the legislative office of the National Cancer Institute at the National Institutes of Health, culminating in over a decade of public service in the U.S. Department of Health and Human Services. She serves on the board of directors for the Society for Hispanic Rare Diseases and Mom Congress. Jeanette holds a Bachelor's in political science from California State University, Los Angeles, and a Master's in public policy from American University in Washington, D.C.
Sabrina is a results-driven leader and passionate advocate for equitable healthcare. As Vice President of Multicultural Initiatives and Engagement at McUlksy Health Force, she works with her team to amplify underrepresented voices and drive meaningful change in health access and outcomes. With over 20 years of experience in business devel
Sabrina is a results-driven leader and passionate advocate for equitable healthcare. As Vice President of Multicultural Initiatives and Engagement at McUlksy Health Force, she works with her team to amplify underrepresented voices and drive meaningful change in health access and outcomes. With over 20 years of experience in business development, media and communications, Sabrina brings a unique ability to bridge the worlds of advocacy and industry. Her career includes leadership roles at NBC Universal, Telemundo, and Univision, making her an expert at engaging U.S. Hispanic and minority communities using culturally relevant strategies. Fluent in English and Spanish, she brings a bilingual, bicultural lens to all her work. Sabrina holds a Bachelor‘s degree in biology and chemistry from St. Joseph's College in Indiana. Prior to attending college in Indiana, Sabrina pursued medical studies in Argentina which ignited her passion for advocacy and making a difference in people’s lives through health-focused work.
Estela is a passionate advocate for health equity, leading impactful initiatives that blend healthcare, community engagement, and patient empowerment. As president and co-founder of Looms for Lupus and Mata Advocacy and Support (MAS), Estela drives awareness for lupus, fibromyalgia, mental health, and community wellness. With over 30 year
Estela is a passionate advocate for health equity, leading impactful initiatives that blend healthcare, community engagement, and patient empowerment. As president and co-founder of Looms for Lupus and Mata Advocacy and Support (MAS), Estela drives awareness for lupus, fibromyalgia, mental health, and community wellness. With over 30 years of healthcare experience and personal insights as both a patient and caregiver, she fosters meaningful connections across diverse communities, bridging industry and patient advocacy voices. Her influence spans local to global platforms, collaborating with organizations like the U.S. Department of Health and Human Services, U.S. Food and Drug Administration, National Institutes of Health: All of Us Research program, and Scripps Research Digital Trials Center. Estela also serves as Chair of the California Chronic Care Coalition Board, the City of Baldwin Park Stakeholder Oversight Committee, and Congresswoman Grace Napolitano’s Mental Health Consortium.
Dr. Bruna is an associate professor of medical anthropology at Western Washington University, where he is also a founding faculty member of the Institute for Critical Disability Studies and an affiliate faculty member of the Center for Cross-Cultural Research. Dr. Bruna brings more than two decades of experience with interdisciplinary an
Dr. Bruna is an associate professor of medical anthropology at Western Washington University, where he is also a founding faculty member of the Institute for Critical Disability Studies and an affiliate faculty member of the Center for Cross-Cultural Research. Dr. Bruna brings more than two decades of experience with interdisciplinary and cross-methodological health disparity research, including work addressing chronic disease prevention, disability studies, and research with rural populations. He served as a senior advisor to the Director of the Agency for Healthcare Research and Quality (AHRQ) under the Biden- Harris Administration. His previous research has been funded by the Robert Wood Johnson Foundation Center for Health Policy, the Andrew W. Mellon Foundation, and the Smithsonian Institution, among others. Dr. Bruna holds a B.A. and M.A. from the University of Chicago and an M.A. and Ph.D. in anthropology from the University of New Mexico, where he researched chronic disease prevention on the U.S.-Mexico border.
Michele is the Founding Director of Culture IQ, a full-service market research and strategic communications firm dedicated to amplifying the voices of multicultural consumers and voters and delivering actionable insights to companies, policymakers, candidates, and campaigns. She is a skilled researcher in both English and Spanish, with ex
Michele is the Founding Director of Culture IQ, a full-service market research and strategic communications firm dedicated to amplifying the voices of multicultural consumers and voters and delivering actionable insights to companies, policymakers, candidates, and campaigns. She is a skilled researcher in both English and Spanish, with expertise in issue advocacy, message development and consumer engagement. Michele brings a unique perspective to the research world from her background in the media and entertainment industry, where she gained recognition as an Emmy-award winning producer. Prior to founding Culture IQ, Michele led consumer insights, marketing and promotions efforts for top Spanish-language networks Telemundo and Univision. She is passionate about empowering underrepresented communities and ensuring their voices are heard. Michele holds a Bachelor's degree in Spanish from Scripps College and a Master's from the American Graduate School of International Management (Thunderbird).
Sinsi Hernández-Cancio, JD, is a national health and health care equity policy and advocacy thought leader with 25 years of experience advancing equal opportunity for women and families of color, and almost 20 years advocating for increased health care access and improved quality of care for underserved communities. Prior to joining the
Sinsi Hernández-Cancio, JD, is a national health and health care equity policy and advocacy thought leader with 25 years of experience advancing equal opportunity for women and families of color, and almost 20 years advocating for increased health care access and improved quality of care for underserved communities. Prior to joining the National Partnership’s staff, she was the founding director of Families USA’s Center on Health Equity Action for System Transformation. Sinsi has served on numerous advisory committees for organizations, including the National Academy of Medicine, the National Committee for Quality Assurance, the Patient Centered Outcomes Research Institute, the Robert Wood Johnson Foundation, the National Center for Complex Health and Social Needs, and the American Association of Pediatrics. She has published extensively and made numerous appearances in both local and national media, including English and Spanish television, radio, and print outlets. She earned an A.B. from Princeton University’s Woodrow Wilson School of Public and International Affairs and a J.D. from New York University School of Law.
Pam is a lifelong patient advocate dedicated to breaking down barriers to care and improving care coordination. With a strong focus on mental and emotional well-being, she champions support services and education for both patients and healthcare professionals. Pam collaborates closely with industry leaders, patient advocates, clinicians,
Pam is a lifelong patient advocate dedicated to breaking down barriers to care and improving care coordination. With a strong focus on mental and emotional well-being, she champions support services and education for both patients and healthcare professionals. Pam collaborates closely with industry leaders, patient advocates, clinicians, policymakers, and researchers to shorten the diagnostic odyssey, accelerate clinical research, and enhance healthcare accessibility. Her expertise spans executive leadership roles in rare disease advocacy at Global Genes and healthcare communications organizations, as well as key positions in biotech and pharmaceutical companies across medical affairs, marketing, and patient advocacy. She also serves on the board of directors for several patient advocacy organizations, including the Patient Empowerment Network, the Organization for Latino Health Advocacy, Uplifting Athletes, and Raregivers. Pam holds a Bachelor's degree in neuroscience from Colgate University and a Master’s degree in public health from Columbia University.
Pedro is a public health leader and equity advocate with over 15 years of experience advancing health access and outcomes for underserved communities. His career spans public service, nonprofit leadership, and national initiatives focused on closing health disparities across systems and populations. Pedro currently serves as Director of
Pedro is a public health leader and equity advocate with over 15 years of experience advancing health access and outcomes for underserved communities. His career spans public service, nonprofit leadership, and national initiatives focused on closing health disparities across systems and populations. Pedro currently serves as Director of Health at UnidosUS, where he leads efforts to strengthen vaccine equity, improve health access, and support community-based solutions to public health challenges. He has held leadership and technical roles across local, state, and federal levels, contributing to major initiatives addressing maternal and child health, injury and violence prevention, overdose and suicide prevention, and public health preparedness. Pedro began his career in local and state health departments and has advised on several federally funded programs. A trained epidemiologist, he integrates data, policy, and community collaboration to drive sustainable impact. He holds a Bachelor’s in public health sciences from the University of California, Irvine, and a Master’s in public health from Loma Linda University.
The Organization for Latino Health Advocacy is a 501(c)(3) nonprofit organization (Federal tax ID number 86-0212873). All gifts to the Organization for Latino Health Advocacy are considered tax-deductible to the extent permitted by law.
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