Patient Advisory Council
The Patient Advisory Council will provide essential patient perspectives to shape the Center's strategy, methods, and priorities, while also supporting broader patient engagement efforts.
Desiree Collins-Bradley
Patient Partner Innovation Community
Desiree Collins-Bradley
Patient Partner Innovation Community
Desiree Collins-Bradley is a resident of Houston, Texas. Her passion is patient and family engagement in healthcare and ensuring that patient’s voices are always represented at all levels of shared decision-making.
She is a mother of three wonderful children. Her daughter was born with a genetic disorder Jarcho Levin Syndrome. It is extremely rare and often carries a very high mortality rate and grim prognosis. Her medical journey has inspired her to become an advocate not only for her daughter but in the medical community. She believes in the pillars of family-centered care, and it is her passion to spread the importance and awareness of them. She has become involved in several committees at the hospital, including the Newborn Center Family Advisory Committee, of which she was the Co-chair and one of the founding members. She is also a Family Leader Faculty for the Vermont Oxford Network, which focuses on NICU improvement projects globally. She is also the Project Coordinator for Project DOCC Houston, a nonprofit organization focusing on the importance of partnerships between physicians and families of those taking care of a chronically ill or disabled family member. She currently manages a very interactive patient network PPIC, Patient Partner Innovation Community of over 3,000 members across the country. Her goal is to inspire other patients and caregivers to become activated in their healthcare communities. She is a strong advocate for patient populations at most social risk. She has worked on several SDOH, Social Determinants of Health initiatives with the National Quality Forum. Through their partnership, she has participated in panel discussions at congressional briefings in Washington, DC. She is passionate about health equity and has been able to exercise that passion through membership as a strategic advisor for AMA’s Rise to Health Coalition.
Olivia Dieni, MPH
Cystic Fibrosis Foundation
Olivia Dieni, MPH
Cystic Fibrosis Foundation
Olivia Dieni is the Manager of Healthcare Access at the Cystic Fibrosis Foundation, where she has served for six years. In her role, Olivia amplifies the voice of the CF community within the U.S. healthcare system, advocating for equitable and affordable access to care. She oversees the Foundation’s policy and advocacy research portfolio focused on cost and access, including data collection and analysis related to drug coverage, care center access, and systemic barriers such as cost and administrative burden. Olivia also leads the Foundation’s payer engagement strategy and collaborates closely with the policy team to address access challenges, ensuring that all individuals with CF can receive high-quality care. She holds a Bachelor of Science from Cornell University and a Master of Public Health from the Johns Hopkins Bloomberg School of Public Health.
Maryjan Fiala
University of Nebraska Medical Center
Maryjan Fiala
University of Nebraska Medical Center
Maryjan Fiala is an entrepreneurial-minded educator with more than fifteen years of experience working with diverse adult learners. She has been teaching undergraduate business courses for community colleges for more than ten years, most recently within her state’s correctional system. To complement graduate degrees in adult, occupational, and continuing education and organizational management, Maryjan is pursuing a PhD in adult learning and leadership. Her research interests focus on the construction of knowledge among patients/families and healthcare professionals, reflecting her dedication to advancing patient and family engagement across health systems. Maryjan’s commitment to patient and family advocacy was inspired by her youngest son's complex medical journey. After an extremely premature birth and nearly 19 months inpatient, he transitioned to home, still requiring ventilator support and around-the-clock care. Building from her lived experience, Maryjan strives to elevate patient and family perspectives locally, regionally, and nationally.
Darcel Jackson
Children's National Hospital
Darcel Jackson
Children's National Hospital
Darcel Jackson is dedicated to promoting inclusive and equitable care for all. With 18 years of experience in transforming the healthcare system and family caregiving, Darcel currently serves as the Manager of Patient and Family Centered Care at Children’s National Hospital. In this role, she collaborates closely with patients and families to ensure their voices are central to the organization’s mission and values. Darcel leads efforts to design, implement, and evaluate programs that enhance family-centered care by actively involving patients and families as co-designers and co-facilitators on various committees and projects.
Her journey with her late daughter, Anniyah, who had complex medical needs, continues to fuel her commitment to transparency and health equity along with a passion for championing a healthcare system that prioritizes patient and family collaboration.
Jessica Johnson, MPH
National Eczema Association
Jessica Johnson, MPH
National Eczema Association
Jessica K. Johnson is the Sr. Director of Community Research & Engagement at the National Eczema Association (NEA). In this role, she leads the strategic development, growth, and implementation of NEA’s research and real-world data initiatives, as well as the organization’s community engagement portfolio. This work includes oversight of NEA’s Ambassador Program, which connects more than 600 patients and caregivers across the United States with opportunities to share their lived experiences with researchers, biopharmaceutical companies, legislators, policymakers, and other key stakeholders.
Prior to joining NEA, Jessica served as a senior researcher in the Center for Community Health at Northwestern University Feinberg School of Medicine, where she led and contributed to the design, implementation, and dissemination of a diverse, patient-centered research portfolio engaging patients and stakeholders nationwide. Jessica holds a Master of Public Health from SUNY Upstate Medical University and Syracuse University and brings over 13 years of experience in the science and practice of community-based participatory research (CBPR) and patient-centered outcomes research (PCOR).
Natalie Mamerow
Coalition of Skin Diseases
Natalie Mamerow
Coalition of Skin Diseases
As the Executive Director of the Coalition of Skin Diseases (CSD), Natalie Mamerow advocates on behalf of the 84 million Americans living with a skin condition. Her passion for this work is deeply personal. Natalie was diagnosed with alopecia areata in high school, and over time her condition progressed to alopecia universalis, leading to the loss of every hair on her body.
Navigating high school, college, early adulthood, and her professional life with visible hair loss brought challenges - including anxiety, shame, and eventually the decision to shave her remaining hair before losing it entirely. Today, she alternates between wearing wigs in professional settings and embracing her bald head during the activities she loves, from barre to kayaking to running around with her two small daughters. Having access to high-quality wigs restored her confidence, and she remains acutely aware that most people with alopecia cannot rely on insurance coverage for this medical need.
For more than a decade, Natalie has been an active advocate through the National Alopecia Areata Foundation’s Legislative Liaison program and previously served as the Capital Area Support Group Leader. At the CSD, she continues her commitment to ensuring that those with alopecia - and all individuals with skin diseases - feel supported, seen, and empowered through community and policy advocacy.
Stephanie Marshall
The Assistance Fund
Stephanie Marshall
The Assistance Fund
Stephanie Marshall is the Director of Patient Advocacy for The Assistance Fund (TAF), an independent charitable patient assistance organization that provides financial assistance to patients living with life-threatening, chronic, and rare diseases.
With more than 25 years policy, advocacy, and communications experience in the public, private, and non-profit sectors, Stephanie has devoted her entire career to improving health and quality of life for individuals, families, and communities. At TAF, she collaborates with patient advocacy organizations to ensure TAF’s programs and services meet the needs of patients and caregivers.
Yadira Montoya, MSPH
National Alliance for Caregiving
Alex Sheehan, DrPH(c), MPA, MPP, MSc, MBA
Tulane University
Alex Sheehan, DrPH(c), MPA, MPP, MSc, MBA
Tulane University
Alex has spent more than 10 years working at the crossroads of reentry systems and lived experience with serious mental illness. He works as a Behavioral Health Program Manager managing a portfolio of programs, initiatives and contracts that improve access to mental and behavioral health care treatment and recovery supports. Additionally, Alex is also the Co-Founder of the Doctoral and Postdoc Health Equity and Policy Scholars Support Network, a community of Doctoral-level Scholars focused on advancing health equity through lived experience and innovative policy development.
Alex is currently a third-year Doctor of Public Health (DrPH) student at Tulane University Celia Scott Weatherhead School of Public Health and Tropical Medicine and a Fellow in the Robert Wood Johnson Foundation Health Policy Research Scholars program at Johns Hopkins Bloomberg School of Public Health. His research focuses on lived experience with mental illness and substance use to improve state and federal mental and behavioral healthcare policies, helping reduce disparities and create better outcomes for people seeking care.
Alex has brought his lived experience leadership perspective to mental health and patient advocacy work at local, state, national, and global levels. He has been honored to have worked with organizations such as Valley Cities Behavioral Health Care, King County, WA, all levels of NAMI (local, state, and national), Camden Coalition, American Public Health Association, Foundations for the National Institutes of Health, and Global Mental Health Peer Network. He believes that meaningful policy change happens when it is rooted in equity, dignity, and guided by individuals with lived or living experience.
Maanya Tarnal
University of Michigan
Maanya Tarnal
University of Michigan
Maanya Tarnal is a junior at the University of Michigan, pursuing a degree in Public Health and Psychology. With a strong interest in health equity, she is passionate about improving patient engagement and advocacy within the healthcare system. Her goal, in her professional career, is to address systemic disparities, enhance the quality of care and ensure individuals - especially those in underserved communities - have access to affordable, reliable and patient-centered services.
Diagnosed with epilepsy at the age of 16, Maanya initially struggled to navigate life with her condition. This personal experience shaped her understanding of the challenges patients face. Three years after her diagnosis, she began volunteering at the Epilepsy Foundation of Michigan, where she found her passion: public health.
Professionally, Maanya has dedicated herself to advancing patient-centered initiatives. In 2023, she interned with the Epilepsy Foundation of Michigan, leading the creation, distribution and analysis of the 2023 Michigan Epilepsy Needs-Based Assessment, ensuring the patient voice was central to understanding community needs. This past summer, she expanded her work nationally as an intern with the Epilepsy Foundation of America, assisting the Multicultural Outreach and Health Equity department. There, she developed a comprehensive plan for a pilot seizure training program, identifying practical ways to implement it on college campuses to better engage and support students living with epilepsy.
Adam Thompson
Independent Consultant
Adam Thompson
Independent Consultant
Adam Thompson is an independent consultant supporting health systems, communities, and patients to improve health outcomes. He holds a bachelor’s degree in Theology from Georgetown University and will graduate in December of 2022 with his Masters in Public Health from the Jefferson College of Population Health where he was named the 2022 Public Health Student of the Year. He is currently the Co-Chair of the Primary Care and Chronic Disease Standing Committee for the National Quality Forum where he also serves on the Board of Directors. He is 2010 recipient of the Leadership in Quality Award from CQII and the HIV/AIDS Bureau. He co-developed several national trainings for Ryan White communities including the Training of Consumers on Quality, the Building Leaders of Color, and ELEVATE & ESCALATE programs. Mr. Thompson is the former Regional Partner Director for the South Jersey AIDS Education and Training Center and brings over 17 years of experience in health care improvement and patient engagement.
Danny van Leeuwen, Opa, RN, MPH
Health Hats
Danny van Leeuwen, Opa, RN, MPH
Health Hats
Danny van Leeuwen, Opa, RN, MPH, is a 2-legged, cisgender, old, white man of privilege known as Health Hats with Multiple Sclerosis, committed to health equity and learning and sharing what works for best health. He serves people who help others by leveraging his privilege and experience as a person with disabilities, nurse, care partner, informaticist, and quality management leader to open seats at the table of healthcare governance, design, operations, and research for under-represented and under-served communities. Danny is especially interested in building capacity for successful community-research partnerships. Danny is a podcaster, vlogger (https://linktr.ee/healthhats), and technical and subject matter expert for measure and app development, pain management, and AI use in health decision-making. Danny is on the Board of Governors of the Patient-Centered Research Institute (PCORI). He hosts mastermind groups for solo entrepreneurs, podcasters, not-for-profit board members, and those advancing patient industry partnerships. Danny plays baritone saxophone in a Latin Band and Dixieland Band in his spare time.
Joseph Washington, PharmD, MS, MPH
Independent Consulltant
Joseph Washington, PharmD, MS, MPH
Independent Consulltant
Joseph Washington, PharmD, MS, MPH is a Manager in Market Access Commercialization at Cencora (formerly AmerisourceBergen). In this role, he supports several mid to large biopharmaceutical companies to drive formulary access for their assets. His responsibilities include leading scientific direction and tactical development of projects in diverse disease areas.
Dr. Washington started his career at Cencora with a Health Outcomes and Market Access fellowship. Prior to joining Cencora, Dr. Washington served in both policy and public health roles. In the 117th Congress he led the distribution strategy for COVID-19 vaccines across Florida District 9. And he worked at the Centers for Disease Control and Prevention in the Division of Diabetes Translation.
Dr. Washington received his Doctor of Pharmacy in conjunction with his Master of Public Health degree from the University of Florida. During that time, he served as the National President of the Student National Pharmaceutical Association and was honored with the Townes R. Leigh Award for leadership. He also completed a Master of Science degree in Pharmaceutical Outcomes and Policy, with a concentration in applied pharmacoeconomics, from the University of Florida.
Tiffany Westrich-Robertson
AiArthritis
Tiffany Westrich-Robertson
AiArthritis
Tiffany Westrich-Robertson is the CEO and original founder of AiArthritis (the International Foundation for Autoimmune & Autoinflammatory Arthritis) and a person living with axial spondyloarthritis. She also leads the Ensuring Access through Collaborative Health (EACH) and associated Patient Inclusion Council (PIC), a national, two-part, disease agnostic coalition advocating for drug affordability policies that benefit patients.
In 2015, she authored the Ethics of Step Therapy paper, concluding preferred drug recommendations are biased towards patients who meet general patient population standards. For the remaining ‘atypical’ patients, the onus for choosing therapies should default on the doctor, who is ethically obligated to treat the unique characteristics of the patient. These findings have influenced her work to advocate in favor of fair access to treatments that are considerate of individual needs, and cognizant that personalized and precision medicine is on the horizon. Since then, Tiffany has been laser focused on Precision Medicine, Value Assessments, and data that drives policy decisions.
Tiffany is a former college educator - winning “Favorite Teacher” twice in 10 years, a trained focus group moderator, and an expert in Research Advocacy (data to drive public policy). She serves on many advisory panels, including IVI Patient Council and is the Patient Co-Chair for the ICER Patient Council.
Marc Yale
International Pemphigus Pemphigoid Foundation
Marc Yale
International Pemphigus Pemphigoid Foundation
Marc Yale was diagnosed in 2007 with Cicatricial Pemphigoid, a rare autoimmune blistering skin disease. Like others with a rare disease, he experienced delays in diagnosis and difficulty finding a knowledgeable physician. Eventually, Marc lost the vision in his left eye from the disease. This inspired him to help others with the disease. In 2008, he joined the International Pemphigus and Pemphigoid Foundation (IPPF) as a Peer Health Coach. He worked with people to improve their quality of life and encouraged them to become self-advocates. In 2009, he helped develop the Pemphigus and Pemphigoid Comprehensive Disease Profile giving experts insight into the patient perspective. In 2016, Marc became the Executive Director of the IPPF until .2020 after he experienced a disease relapse. He moved into the role of Advocacy & Research Coordinator for the IPPF so that he could focus on research and advocacy for all of those affected by pemphigus and pemphigoid and now serves as the IPPF Research & Policy Advisor.
He has served as a member of the American Academy of Dermatology Drug Transparency Task Force, committee advisor for Rare Disease Legislative Advocates, and as a panel expert for Rare Disease International’s World Health Organization (WHO) Collaborative Global Network for Rare Diseases Panel of Experts to ensure a lasting impact on the lives of people living with a rare disease around the globe. In 2022, Marc helped establish the World Skin Health Coalition, A multi-stakeholder group of like-minded organizations focused on putting medical dermatology on the global health agenda. He currently sits on the Executive Board of Directors for The International Alliance for Dermatological Patient Organizations (GlobalSkin) as their President, on the Rare Disease Advisory Council of the Patient Centered Outcomes Research Institute (PCORI) and is a member of the Rare Project Advisory Board of the Center for Innovation and Value Research. Marc is a patient expert and Fellow of the European Patients Academy on Therapeutic Innovation (EUPATI).
He resides in Ventura, California with his wife, Beth of 35 years.