Board of Directors
The Pulmonary Fibrosis Foundation (PFF) is proud to have a committed board of directors to help guide the activities that support our important mission. Please feel free to contact the Foundation with questions.
Members of the board are actively involved in the PFF’s activities and participate in fundraising, promoting awareness, and advocating for the pulmonary fibrosis community.
The Foundation seeks qualified candidates to join its board of directors. The PFF’s directors lay the groundwork for the Foundation’s strategic vision and contribute significantly to resource development. A central focus of the board of the directors is fundraising.
Dr. Pan is a physician-scientist executive with experience in clinical practice, managed care, physician group management, healthcare quality improvement, healthcare information technology, chronic care management, enterprise sales and marketing and more. Dr. Pan wants to transform the way in which healthcare products and services are delivered and reimbursed to improve patient outcomes. He is Co-Founder and Chief Medical Officer for Salusive, Inc. in Emeryville, Calif. There, Dr. Pan is responsible for managing clinical operations and formulating corporate strategy as well as working with the business development team. Previously, Dr. Pan was Medical Director and Health Economist for Genentech, a member of the Roche Group.
Pat Rosa is a retired executive with Wells Fargo & Company. Pat has 30+ years of experience in the Risk Management, Information Security and Information Technology fields. She performed key roles contributing to governance and oversight responsibilities. Pat is an active member of the PFF’s Development Committee since 2017, and took over Chairperson responsibilities in 2023. Pat is also a member of the Nominating and Governance Committee and co-developed an enhanced onboarding process for new Directors that are elected to the PFF’s Board of Directors.
Pat’s personal experience with idiopathic pulmonary fibrosis (IPF) was as a caregiver for her late husband, Tony Rosa, who passed away from the disease in October 2007. Pat has made it her personal mission to support the cause in finding a cure by participating in the PFF Walks and supporting the Broadway Belts annual fundraiser.
Pat has a B.A. in Psychology and Education from College of Mount Saint Vincent in Riverdale, N.Y. She has a Master’s in Education in Reading, Language and Literacy from University of North Carolina at Charlotte (UNCC). Pat is a hospice volunteer with the non-profit organization, VIA Health Partners, since 2009. Pat is an avid reader and yoga practitioner. She lives in Charlotte, NC and has one daughter, Stephanie, a rescued Golden doodle, Josie, and a rescued black cat, Luna.
Laurie Chandler is a retired principal of Vigilant Capital, LLC, bringing more than 30 years of expertise in financial management and wealth planning services. She began her involvement with the Pulmonary Fibrosis Foundation (PFF) in 2016 as a member of the Development Committee. Currently, Laurie chairs the Finance Committee and serves as Treasurer of the Foundation.
Laurie’s commitment to the PFF is deeply personal. She was diagnosed with interstitial lung disease (ILD) caused by Short Telomeres Syndrome, a genetic condition that went undiagnosed for over seven years despite extensive efforts to identify the cause. This experience has fueled her mission to accelerate time to diagnosis and support the search for a cure. Laurie actively advances this cause through participation in PFF Walks, speaking at the PFF Summit, and supporting the annual Broadway Belts fundraising event. In recognition of her dedication, she received the PFF’s Ralph Howard Legacy Award in 2021.
Laurie holds an MBA from Southern New Hampshire University, is a retired Certified Financial Planner™, and is a graduate of the Cannon Financial Institute for Trust, Estate, and Financial Planning. In addition to her work with the PFF, Laurie serves on the Brigham and Women’s Hospital Lung Center Advisory Board. Her previous leadership roles include serving as a trustee of Southern New Hampshire University, a board member of the Northern New England Financial Planning Association, and chair of the Estate Planning Council of New Hampshire. Laurie and her husband, Clarke, divide their time between New Castle, NH, and Port St. Lucie, FL.
Wheaton, IL
Martin Attwell’s family has been deeply affected by pulmonary fibrosis as both his father and father-in-law passed away from the disease. Martin became involved with the Pulmonary Fibrosis Foundation in 2014 and currently serves on the Finance Committee. He was a key member of the Strategic Planning Committee that developed the PFF 2020 Strategic Plan. His family has been strong supporters of the PFF Walk since its inception and he has been a frequent attendee at the PFF Summit, Annual Volunteer Meeting, and Broadway Belts for PFF!.
Martin has worked in the Energy and Health Insurance sectors for more than 30 years. He began his career as a Software Engineer in London. He had a long career with BP and Amoco in various roles in Finance, IT and Organizational Change in the UK and the US where he led many large-scale process improvement and organizational change projects. Most recently, he was Director of Organizational Effectiveness at Health Care Service Corporation.
He holds an MBA from the University of Chicago, Law Degree from the University of London, and a Bachelor of Science in Mathematics from Imperial College, London. He is certified as both a Project Management and Change Management professional. He currently lives in the Chicago area with his wife, Colleen. In his spare time, he enjoys traveling, collecting antique maps, and supporting his favorite “football” team Chelsea FC.
Grant Ballantyne is a senior manager in BerryDunn’s not-for-profit practice group, where he specializes in providing attestation services to a wide variety of not-for-profit organizations. With almost 20 years of experience, he has been assisting his clients by performing audits and reviews, providing advisory services, as well as performing audits in accordance with the Federal Uniform Guidance requirements.
Grant earned his Bachelor of Science degree at the University of New Hampshire and became a certified public accountant in 2013. Grant has services on the Finance Committee for PFF since 2024 and quickly became interested in serving in a larger capacity. In addition to his role with PFF, Grant also serves as the Treasurer of the Board of Students Run Chicago.
Grant resides in Chicago with his wife and their two dogs. Grant and his wife spend their free time exploring the many food options of Chicago, and are both avid distance runners, exploring the streets and sights of Chicago.
Harold R. Collard, MD, MS, is the vice chancellor for Research at UCSF. In this role, Collard oversees and stewards UCSF’s research mission.
Collard is professor of Medicine and Health Policy in the Division of Pulmonary, Critical Care, Allergy and Sleep, Department of Medicine, School of Medicine. A board-certified pulmonologist, he joined UCSF’s faculty in 2005 and served for 12 years as director of the Interstitial Lung Disease Program. Collard is an internationally recognized leader in the care and research of patients with interstitial lung disease. He has over 200 peer-reviewed research publications and was awarded the 2019 Gold Medal in Interstitial Lung Disease from the European Respiratory Society for his research leadership in the field. Collard also received the 2020 American Thoracic Society Clinical Problems Assembly Mentorship Award in recognition of his central role in developing the next generation of interstitial lung disease research leaders.
Deeply committed to advancing UCSF’s research mission, Collard previously served as associate vice chancellor of Clinical Research and director of UCSF’s Clinical and Translational Science Institute. In this role, he helped to position the University as a leader in the NIH’s national consortium of clinical research institutions and developed programs to support the needs of its clinical trialists and biospecimen-based researchers. During this time, Collard also helped lead the UCSF research community through the early phases of the SARS CoV-2 pandemic, advocating strongly for their needs.
Collard believes the next decade will be a critical period for UCSF’s research community and views the vice chancellor for Research as a crucial champion and steward of the University’s research mission. His priorities for UCSF include ensuring, enabling, and positioning its research community for success across the spectrum of disciplines and departments; making UCSF a partner of choice for clinical trials; ensuring curiosity-driven science remains a foundational component of research activities; and growing relationships with community partners and policymakers to prioritize and promote health research. Collard also is strongly committed to UCSF PRIDE Values and building a community of trust and opportunity for all.
Collard received his AB cum laude in Biochemical Sciences and Molecular Biology from Harvard College, and his MD from Duke University. He completed internship, residency, and chief residency in Internal Medicine at UCSF and completed a fellowship in Pulmonary and Critical Care Medicine at the University of Colorado. As part of his research training, Collard earned a Certificate in Clinical Science from the University of Colorado and an MS in Health Law and Policy from the UC Hastings College of the Law and UCSF.
New York City, NY
Terence Hales is a corporate real estate executive based in New York City. He has over 20 years of industry experience and has worked for a number of global Fortune 100 companies including Time Warner, Bear Stearns, Lehman Brothers, CBS Corporation, and Pfizer Inc. In his previous roles he was responsible for real estate strategy, transaction management, and cost efficiency. Terence is currently the Director of Global Real Estate for Zoetis Inc., the former Pfizer Animal Health Division. Mr. Hales is the founder of the NYC Run-Walk-Hike for Pulmonary Fibrosis, which has raised more than $400,000 toward PF research and patient services. Mr. Hales’s father was diagnosed with PF and subsequently underwent a successful double-lung transplant in 2007, surviving for 13 years post-transplant. Mr. Hales was previously a board member of the Coalition for Pulmonary Fibrosis, where his work included lobbying members of congress to support research funding for pulmonary fibrosis. Mr. Hales has a Bachelor of Science in Finance and a Masters of Business Administration from Fordham University.
New York City, NY
Julie Halston is an actress with a long list of theatrical and television credits. She began her career co-starring in the comedy plays of Charles Busch in the 1980s, and was a founding member of his theatre company, Theatre-in-Limbo. In 1992 she wrote and performed a series of one-woman shows, Julie Halston’s Lifetime of Comedy, which eventually earned her a CBS network development deal for a sitcom pilot. In the late 1990s and 2000s she appeared in a steady stream of Broadway and Off-Broadway shows including The Man Who Came to Dinner (2000), Hairspray (2002), Gypsy (2003), Anything Goes (2012), and Tootsie (2019). She has received the Richard Seff Award for her portrayal of Gay Wellington in You Can’t Take It With You (2014). She also has numerous film and TV credits. She earned her BA in Theatre Arts from Hofstra University.
Julie’s husband Ralph Howard, celebrated and veteran radio news anchor, was diagnosed with PF in 2008. He received a life-extending lung transplant 2010, but ultimately lost his battle in August of 2018. Julie is the host of the largest PFF fundraiser Broadway Belts for PFF!, which has raised over $2M since its debut in 2011. Julie recently launched a new half-hour comedy talk show, Virtual Halston, during the COVID-19 2020 pandemic, and has used the show in part to encourage support of the PFF.
Evanston, IL
Jeff Harris is a partner in the Chicago office of Smith, Gambrell & Russell, LLP, which is headquartered in Atlanta. His business litigation practice of over 40 years includes matters relating to construction, commercial real estate, corporate and partnership disputes, professional liability and fiduciary duties.
Mr. Harris joined the Board of the Pulmonary Fibrosis Foundation in 2018. He previously served as the President of the Mary D. Harris Memorial Foundation, as the Chair of the Board of Gift of Hope Organ & Tissue Donor Network, as the Chair of the Board of the Coalition for Pulmonary Fibrosis, and as the former Vice-President of LAH Oil, Inc. In 2005, he received the Frank Cabral Humanitarian Award from the Coalition for Pulmonary Fibrosis in recognition of his contributions to furthering education, patient support and research regarding the disease.
Mr. Harris received his undergraduate degree from Miami University in Oxford, Ohio and his Juris Doctorate from Washington & Lee University in Lexington, Virginia.
Menlo Park, CA
Susan Jacobs is a research nurse manager in the Division of Pulmonary, Allergy and Critical Care Medicine as well as a nurse coordinator in the Interstitial Lung Disease Program, both for Stanford Medical Center; she has been with Stanford since 1998. Her primary area of interest is improving symptom management for patients with chronic lung disease.
From 1996 to 1998 she served as project manager for an NIH grant studying Dyspnea with UCSF, and from 1991 to 1996 she was manager and clinical coordinator for the Pulmonary Rehabilitation Program at Seton Medical Center. From 1988 to 1991 she was a pulmonary nurse specialist and study coordinator for Veterans Hospital Medical Center. She served as an educational coordinator in the Cardiothoracic Surgical ICU at Stanford Medical Center (1982-1986) after receiving her MS in Pulmonary Nursing in 1982 from UCSF; prior to this she was a critical care nurse at Providence Hospital (1975-1976) and Sequoia Hospital (1976-1982). She received her BS in Nursing in 1975 from California State University at Chico.
Susan is lead author on the first national patient survey of almost 2000 supplemental oxygen users in the US. She is also lead author on the recently published ATS clinical practice guideline on Home Oxygen Therapy for Adults with Chronic Lung Disease and has chaired the ATS Oxygen Special Interest Group since 2018. Susan collaborates with policy makers and advocacy groups to address care gaps for patients using supplemental oxygen. She received the National LAM Foundation Leader award in 2014, Outstanding Clinician Award from the California Thoracic Society in 2016, and the ATS PAR Award of Excellence in 2020. She is a Fellow of the American Academy of Nursing (2019). Susan serves on the PFF Medical Advisory Board, has served as faculty for the PFF Summit since its inception in 2011, and has been an active member of the Summit Program Organizing Committee since 2016.
Heather Kagel lives in northern New York and has been engaged with the Pulmonary Fibrosis Foundation since 2015. A retired attorney and Privacy Compliance Professional, Heather is a PFF Ambassador Emeritus and started a Dallas walk called Ready. Set. Breathe. That walk has since become the PFF Dallas Walk and continues to raise substantial funds for the PFF.
Heather was diagnosed with IPF with a TERC mutation in 2013. In 2016, she was diagnosed with, and beat, oral squamous cell carcinoma (OSCC), representing another complication arising from her genetic mutation. Thankfully, and with much gratitude to her donor, in October 2019, Heather received a double lung transplant at UT Southwestern in Dallas, Texas.
Heather is also on the Board of Directors of Team Telomere, whose focus is on patients with telomere biology disorders (TBDs). Heather is passionate about raising awareness of, research for, and supporting those with pulmonary fibrosis and TBDs. Through awareness campaigns, fundraising activities, and speaking with patients, medical providers, and pharmaceutical companies, Heather continues to work to better the lives of, and treatments for, those with these life-threatening diseases.
Heather lives with her husband Rick and their dog Huckleberry. She loves cheering on her children Mitchell (26) and Samantha (24) as they live active and healthy lives.
Wethersfield, Connecticut
PJ Kamani is the CEO of ABC Language Services, a language services provider based in Connecticut. Prior to starting this venture in 2001, PJ was involved in other B-to-B service enterprises in partnership with a Canadian company. Earlier in his career, he managed the Francophone Africa loan portfolio for Equator Bank, a subsidiary of HSBC Bank.
With a family long afflicted by idiopathic pulmonary fibrosis, PJ has lost two siblings and a parent to the disease. He, himself, has recently been diagnosed with the disease.
With a long history of volunteerism, PJ has been a member of the PFF Finance Committee since October 2019 and joined the Board in March 2021. Prior to this, he served on the Finance Committee of the National Marrow Donor Program (NMDP – BeTheMatch) for 8 years (chairing the Committee for two) and on the Board of Directors of the NMDP for 8 years.
PJ received his Bachelor’s Degree from the Haile Selassie I University in Ethiopia and his MBA from the Harvard Business School.
Making Connecticut his home with his wife Sonia, PJ is an avid NE Patriots fan and enjoys traveling and books.
Devi Kumar-Nambiar is an experienced in-house attorney with a wide breadth of legal and business experience. She is Vice President and Deputy General Counsel of CPS Energy in San Antonio. Ms. Kumar-Nambiar is respected and trusted by peers and leaders to provide reasonable and solution-oriented counsel while building strong team relationships. Her husband, Dr. Anoop Nambiar, is the Founding Director of the Center for Interstitial Lung Disease at the University of Texas, San Antonio. Ms. Kumar-Nambiar secured a partnership with the San Antonio Legal Services Association to assist the San Antonio Pulmonary Fibrosis Support Group with help on a variety of documents and directives related to their care.
William T. Schmidt was named President & CEO of the Pulmonary Fibrosis Foundation (PFF) in August 2017 and retired in 2022. As President & CEO, Mr. Schmidt was responsible for the overall management and direction of the Foundation. Prior to joining PFF, for 12 years he was CEO of the Foundation Fighting Blindness, the largest non-governmental source of funding for retinal degenerative disease research in the world.
Mr. Schmidt has extensive experience as a senior executive for a number of high-profile and respected health research advocacy organizations, including the Juvenile Diabetes Research Foundation International (JDRF). As Vice President of Public Affairs at JDRF, he directed the government relations, communications, media relations and foundation relations departments.
An honors graduate of Amherst College, Mr. Schmidt also received his J.D. from the DePaul University College of Law and completed the Kellogg Graduate School of Management’s Executive Development Program.
Members Emeriti
Retiring members of the PFF Board of Directors who have made exceptional contributions to the Foundation are honored with the status "Member Emeritus."
- Daniel M. Rose, MD, Chairman Emeritus
- Colleen Attwell
- Joseph Borus, Esq.
- Thomas E. Hales
- Mike Henderson, Chairman Emeritus
- Dave Steffy
- Stephen A. Wald, PhD