Board of Directors

AAKP is proud of our National Board of Directors. Please click on photo for biographical information.

    PRESIDENT, former AAKP Vice President

    Richard Knight received his MBA from the University of Virginia Darden School of Business and his B.A. from Hampton University. He is a results-oriented business strategist with diverse experience in public and private sectors in Finance, Accounting, Business Development, Healthcare, and Non-Profits. Entrepreneurial experience includes starting and running several ventures. Currently, he is a business strategist, providing patient engagement consulting for healthcare organizations and businesses developing tools designed to leverage patient input and preferences in their care plans and quality measures. He serves as an adjunct professor at Bowie State University (BSU). He is a founding member of BSU’s College of Business Advisory Council.

    Mr. Knight is a healthcare professional and a former hemodialysis patient. He received a kidney transplant approximately fourteen years ago. He is President of the American Association of Kidney Patients (AAKP), which is the oldest and largest, independent kidney patient organization in the United States.

    Mr. Knight has a background in public policy and Congressional operations based on both his professional experience on Capitol Hill, where he served in various roles including communications, policy, and Legislative Director as well his advocacy work as a kidney transplant patient. While working in the U.S. House of Representatives, Mr. Knight served as a liaison to the Congressional Black Caucus for his Member of Congress. He was involved in substantial work with the House Energy and Commerce and Small Business Committees. Mr. Knight’s knowledge of Executive Branch agency budget and procurement policies is based on direct experience as a Federal government contractor and as a ten-year co-chair of the Baltimore Washington Corridor Chamber of Commerce Annual Regional Government Procurement Fair.

    As a policy expert and a national kidney patient advocate, Mr. Knight was appointed to serve as a member of the National Diabetes and Digestive and Kidney Diseases (NIDDK) Advisory Council. He was appointed to the Scientific Registry of Transplant Recipients (SRTR) Visiting Committee. Mr. Knight is the CoChair of the NIDDK Strategic Plan Stakeholder Engagement Subgroup. He was also appointed to the Steering Committee for NIDDK’s Kidney Precision Medicine Project as well as the Clinical Trials Transformation Initiative (CTTI), which is a public-private partnership to develop and drive adoption of practices that will increase the quality and efficiency of clinical trials. He has served as a member of six Technical Expert Panels (TEPs) for the Centers for Medicare and Medicaid Assistance (CMS). He was a member of CMS TEPs focusing on Emergency Department Readmissions Hospital Readmissions, the Fistula First Breakthrough Initiative, and recently on the End Stage Renal Disease Dialysis Facility Compare Star Ratings for the Arbor Research Collaborative for Health and the University of Michigan Kidney Epidemiology and Cost Center. He serves on the National Kidney Disease Education Program’s (NKDEP) Health Information Technology (HIT) Working Group. He also serves on the Steering Committee for the Precision Medicine Coalition’s More Than a Number Committee. Mr. Knight also serves on numerous Advisory Councils for industry partners on matters such as increasing patients in clinical trials and increasing minority participation in clinical trials.

  2. EDWARD V. HICKEY III VICE PRESIDENT, former Secretary and Chair, AAKP Veterans Health Initiative, U.S.M.C.

    Mr. Hickey is an attorney with O'Melveny & Myers, an international, 800 lawyer firm with 15 offices in the world’s financial and political centers. He is a member of the Litigation Department and Director of the firm’s eDiscovery staff attorneys, a role in which he leads all O’Melveny staff attorney operations firmwide. He served as an Infantry officer in the U.S.M.C. as a Lieutenant with postings in Quantico and Camp Pendleton. His distinguished public service career includes posts on Capitol Hill as an Administrative Assistant, as a Special Assistant at the United States Department of Commerce and, following the terror attacks of September 11, 2001, as the Senior Advisor for Homeland Security for the Director of the Office of Personnel Management under President George W. Bush. At OPM, Mr. Hickey also served as liaison to Veteran Service Organizations nationwide, including the Vietnam Veterans of America, AMVETS, the Veterans of Foreign Wars and the American Legion. Mr. Hickey coordinated extensively with elected leaders and staff in the U.S. House and Senate as well as the White House to represent veteran stakeholder interests in the preservation of veteran’s legal rights during reforms to U.S. Civil Service laws. He is a recipient of a Silver Helmet Award from AMVETS.

    In addition to his role at O’Melveny & Myers, Mr. Hickey is actively involved with community service efforts in California through the Inner City Law Center of Los Angeles, which services veterans and their families in the Los Angeles, California area. He is also active in the Armed Forces Committee and Veterans Legal Service Project of the Los Angeles County Bar Association, which works to identify and address opportunities to assist veterans, active military personnel, and reservists with their legal needs.


    Suzanne Ruff is a living kidney donor, and her professional finance experience includes service as a tax consultant at GE Fleet Services, real estate manager, bank teller and legal administrative assistant. Outside of AAKP, Suzanne has been a volunteer for The PKD Foundation since its formation in 1982. She has served as Co-Chair of the Finance Committee of the Twin Cities PKD Chapter from 2006-2010.  Suzanne’s professional writing experience includes positions as a freelance writer for the MN Eden Prairie News and the Charlotte Observer and she is the author of the award-winning, non-fiction book, The Reluctant Donor that chronicles the past seventy years of polycystic kidney disease (PKD) within her family. Suzanne’s family has a strong legacy with the AAKP that dates back to the 1980s, when while living in Florida as a young adult, Suzanne used to type the newsletters and stuff envelopes for the AAKP (known at that time as the National Association of Patients on Hemodialysis and Transplantation (NAPHT)) of which her father served as a National Board of Director.

    Suzanne, herself, has been a member of the AAKP Board of Directors since 2013 and is currently a member of the Executive Committee (EC), having served on this committee since 2017. As a actively engaged member of the EC, Suzanne has been instrumental in implementing AAKP’s integrated National Strategy, developed and approved by the BOD in 2014, which ensures that all organizational activities, including major corporate sponsorships and small dollar direct mail and online fundraising programs, national stakeholder and education initiatives, and federal policy and Congressional engagements, and budget aligns with the Association’s mission and prioritized activities. During Suzanne’s tenure on the AAKP Board, she has served on various committees including the Nominations Committee, Programs/Development Committee and Strategic Communications Committee and she has worked closely with Board leadership and the Executive Director to refine the ongoing activities that fall under the Centers for Patient Engagement and Advocacy as well as the Center for Patient Education and Research. Suzanne has served as a key contact for companies supporting AAKP activities and as a kidney disease subject matter expert on the AAKP Speaker’s Bureau, at the national level since inception in 2019. Beyond executive leadership responsibilities, Suzanne regularly contributes her skills and expertise to the organization, authoring numerous articles for AAKP’s blog and aakpRENALIFE magazine (samples below).

    Suzanne has encouraged AAKP’s expansion into the research, and federally funded research arena, as a living donor/AAKP representative. She has served as a Co-Investigator on the PCORI Project: Putting Patients at the Center of Kidney Care Transitions (PREPARE NOW) from 2015-2020 and is one of the authors of the recently published Engaging Patients and Family Members to Design and Implement Patient-Centered Kidney Disease Research (Read Here). Suzanne has helped organize and moderate research and patient engagement sessions designed for AAKP national and international events, including the Inaugural Global Summit on Kidney Innovation (2019) and numerous AAKP National Patient Meetings.

    Passionate about kidney patients and their treatments, options, and finding a cure, everything she does in the world of kidney disease is to honor her family members who suffered and suffer from kidney disease. Suzanne’s most humbling ‘achievement’ was when she has been told, more than once, that someone decided to be a living donor after reading The Reluctant Donor or hearing her speak.

    Prior to joining AAKP, Suzanne served on the Executive Committee for the NKF Living Donor Council (2010) and the NKF Peer Group program, including the Living Donor Peer Work Group. She has also been published in NKF’s The Journal of Nephrology Social Work.

    Links to a sample of Suzanne’s writing on behalf of AAKP research and AAKP’s Veterans Health Initiative (VHI) is below.

  4. DALE ROGERSSecretary As an infant, Dale was adopted into a family with three other adopted children. When he was 12 years of age, Dale was diagnosed with Type 1 diabetes. Some years later, as a young adult, he was diagnosed with hypertension. While working in upper management of a national food chain, the hypertension continued to escalate. As a result of job-related stress and subsequent stress in everyday life, Dale’s kidneys began to fail. Within a few years it was necessary to begin dialysis. The work-up to receive a kidney/pancreas transplant stretched for a period of 11 months. Incredibly, Dale’s adopted sister was a match. She donated a kidney while an unidentified donor provided a pancreas. The pancreas lasted 18 months and the kidney, nine years and two months at which time Dale had to once again resume dialysis. After undergoing a grueling six years and eight months of dialysis and having suffered numerous life-threatening medical situations, Dale received a life sustaining kidney transplant from an unknown donor. The transplant was well-received giving Dale a new lease on life. This gift has created for him a new focus and personal commitment to help others avoid some of the health-related hardships he has miraculously survived.
  5. PAUL T. CONWAYChair of Policy and Global Affairs; Immediate Past President Mr. Conway is Chair of Policy and Global Affairs, and Immediate Past President, of the American Association of Kidney Patients (AAKP), the nation’s largest kidney patient organization. He also serves as the Co-Chair of the AAKP Annual Global Summit on Kidney Disease Innovations, a strategic partnership with The George Washington University School of Medicine and Health Sciences. He has managed kidney disease for forty-years, including nearly three years on home dialysis and, for the past twenty-three years, as a kidney transplant recipient. He is a policy and communications professional with several decades of experience in White House and Cabinet-wide policy implementation, management, and communications. His public service career includes posts under three U.S. presidents, three Virginia governors and in support of five presidential transitions as well as multiple recognitions, including the Department of Homeland Security Secretary’s Silver Medal for exceptionally meritorious service to DHS and America. As a national kidney policy advocate, he is a recipient of the American Society of Nephrology President’s Medal and the AAKP President’s Medal for his efforts before the U.S. Congress and The White House. Since the COVID-19 outbreak, he has worked closely with federal agencies on high-risk patient education and is a participant in the U.S. Department of Health and Human Services (HHS) Kidney-COVID Public-Private Workgroup. His current federal engagement includes roles as: Chair of the U.S. Food and Drug Administration’s Patient Engagement Advisory Committee (PEAC) for medical device development; External Expert Panel member for the National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases (NIH/NIDDK) Kidney Precision Medicine Project (KPMP); liaison to the Center for Disease Control (CDC) Health Infection Control Practices Advisory Committee (HICPAC); and reviewer for the Department of Defense’s Congressionally Directed Medical Research Program (DOD/CDMRP). He has served as the chair or co-chair of multiple dialysis-related Technical Evaluation Panels for the Centers for Medicare and Medicaid Services (CMS). Since 2017, he has served on successive Presidential Rank Review Boards to recommend top Senior Executive Service members of the U.S. Civil Service to the White House for consideration for presidential recognition. As a kidney advocate, Mr. Conway serves as: Patient Voice Editor for the Clinical Journal of the American Society of Nephrology (CJASN); member of the American Board of Internal Medicine’s (ABIM) Nephrology Specialty Board; member of the Board of Directors’ Kidney Health Initiative (KHI); patient advisory board member for the University of Washington’s Center for Dialysis Innovation (CDI); and has served as a project team member for the FDA/Duke University Clinical Trial Transformation Initiative (CTTI) His previous federal posts include: Acting Federal Coordinator and Chief of Staff for the post-Katrina Office of Gulf Coast Rebuilding at the Department of Homeland Security; Chief of Staff of the U.S. Department of Labor; Chief of Staff of the Office of Personnel Management; Special Assistant in the White House Office of National Drug Control Policy; and Confidential Assistant at the Department of Education. In Virginia, Conway has served as: Deputy Secretary of Health and Human Resources; member of the Secure Commonwealth Panel for homeland security; and a member of the Board of Health Professions for medical licensing.
    Published Articles:
    CJASN: Nephrology Nomenclature: How to Accelerate Patient Anxiety, Suppress Engagement, and Mire the Advance of Medical Innovation

    Editorial: Of Presidents, Policies, and Patients



    In 1982 after undergoing a renal biopsy, Kent was diagnosed with focal segmental glomerulosclerosis (FSGS), a disease that causes scarring in the glomerulus of the kidney. In 1987, after two days of dialysis via central line, he received a kidney transplant from his brother Kip. He has been on Sandimmune (150 mg daily) and (5 mg Prednisone daily) since the transplant.

    Kent is a veteran of the United States Army and a retired RN, with work experience in the Veterans Administration and the private sector for over 40 years. Kent is on the AAKP board of Directors and is an active advocate and ambassador. He is an NKF peer mentor and advocate, and is the leader of the NKF KAC region He is an active consumer Peer Reviewer for PCORI and DoD. He has written articles relating to preemptive renal transplant and immunosuppressive drug coverage. He has been an active member of Nephcure International an agency seeking a cure for FSGS.

    Kent and his wife Catherine celebrated their 50th wedding anniversary in 2019. Kent is co-founder of Kidney Solutions, a 501c that helps patients find a kidney donor without fees or charges. Kent is committed to assisting and aiding those who have kidney disease.


    Catherine has a Doctorate in Nursing Practice. She is a retired professor of nursing and master’s in business administration. Kidney disease has made a significant impact on her life for over five years. She is currently a CKD/non-dialysis patient in search of a donor. Her deep commitment for assisting fellow kidney disease patients began when she was invited to participate in the National Institutes of Health (NIH) Kidney Precision Medicine Project (KPMP). 

    Catherine is part of the Kidney Precision Medicine Project (KPMP) Patient Engagement and Return of Results committee. Through the semi-annual meetings and phone conferences she has gained further insight into patient experiences participating in dialysis, transplant, and waiting for a transplant. Her local volunteer contributions to the KPMP include membership on the Community Advisory Board committee, strategizing community outreach engagement, and education. She has also served on a hospital grant committee securing research funds to advance treatments in chronic diseases. Catherine believes that transition of care is vital to the stability of kidney disease patients following hospitalization into the community. As a Board of Director for Case Management Society of America, educating case managers on supporting patients transitioning out of hospitalization has become a priority for her.

    Catherine has a firm foundation as a kidney disease patient. Her nursing career and years of nursing education have introduced her to students from multiple cultural backgrounds: Ethiopia, Africa, Australia, India, and American Indian. 

    Along with leadership experience in her personal career, Catherine views herself as a patient advocacy leader and has participated in numerous Hill days, which she views are vital to moving patient-centered policies forward.  

    Catherine believes equity of healthcare is a current revelation necessary to improve diverse inclusion in all aspects of healthcare. Building relationships and developing trust is a requirement to ensure healthcare equity and clinical trial involvement among all patient communities.

    As a kidney disease patient, Catherine has maintained a sense of stability through diet, exercise, and being compliant to provider directions and medication use.  She views her position as a positive outlook for others to be motivated to live each day and maintain their health. 

  3. JENNIFER JONESUSMC (ret.), AAKP National Ambassador, Executive Committee Member

    Retired Marine Veteran Jennifer Jones’ kidney journey began while deployed to Afghanistan in 2011. In what felt like a blink of an eye she went from serving as a Combat Camera Videographer to being medically retired in 2013 due to being diagnosed with a rare autoimmune disease called Membranoproliferative Glomerulonephritis (MPGN) Type 1, Idiopathic. Jennifer admits that at first she was considered a “challenging patient” because at first, she couldn’t accept the situation that she was in. She realized when she began dialysis that she had to accept her current situation and focus on what was within her control, which is becoming her own advocate and taking charge of her health and well-being. Once approved for a kidney transplant Jennifer began an active pursuit for a living altruistic donor. On April 2, 2015, she received a kidney transplant and a new sister, a selfless person who did not know her but felt compelled to save her life after hearing her story. She is passionate about kidney disease advocacy, innovation, and education. Her wish for every kidney patient is to become their own advocate, be able to properly navigate their health care system, co-create a plan with their health care team which included the dialysis modality they are comfortable with, a goal towards transplantation (if possible), and positive coping strategies. Jennifer is also a member of the Quality Insights Renal Network 5 Patient Advisory Committee, Veterans Transplantation Association, The Scientific Registry of Transplant Recipients Task 5 Steering Committee, and Rare Disease Diversity Coalition. 

  4. JANICE LEA, MD, MSC, FASN, Executive Committee Member

    Dr. Janice P. Lea, MD, MSc, FASN is a Professor of Medicine at Emory University and is board-certified in Nephrology and Hypertension.  She earned her medical degree at the University of Texas Medical Branch at Galveston and completed her residency in Internal Medicine and a Nephrology fellowship at Emory University affiliated hospitals.  She also received a Masters of Science Degree in Clinical Research from Emory’s School of Public Health. Dr. Lea is currently a Professor of Medicine at Emory University and is the Clinical Director of Nephrology and the Chief Medical Director of Emory Dialysis which serves over 750 patients. Dr. Lea is also the Medical Director for Home Dialysis at Emory Healthcare which currently serves  130 home patients.   Dr. Lea’s research and clinical expertise are in Hypertension, Chronic Kidney Disease, Health Disparities, and Dialysis. She is a nationally-renowned expert in Hypertension - designated a “Clinical Specialist in Hypertension” by the American Society of Hypertension. Dr. Lea also is designated a Master Clinician by Emory’s School of Medicine and serves as the Director of Telenephrology at Emory since 2017. In addition, she serves on the Board of Directors for the American Association of Kidney Patients.  Dr. Lea has been named one of Atlanta’s Top Doctors for the past 10 years and is recognized nationally for her expertise in clinical research and patient care.


    My name is James Myers. I live in Hammond, Indiana. I graduated from Valparaiso University Law School and I have 2 MBA’s in Business and Healthcare Administration. Polycystic Kidney Disease runs in my family. I’ve lost 5 members of my family to PKD, Including my Father. I have PKD. I was fortunate. Because of my family’s history, I was diagnosed at the age of 25, and was able to put off dialysis until the age of 58. I was on dialysis for 4 years and was transplanted on April 27th, 2016. I named my new kidney Woody. Woodrow is a family name, so I did this to honor my father and my grandfather.

    I am a full-time kidney advocate. I am a member of the AAKP. I hold leadership positions with the AAKP as a Member of the Board of Directors, an Ambassador for the State of Indiana. I have won several professional awards and honors including the Inaugural National Social Media Education and Advocacy Award from the AAKP and Robert Felter Memorial Award. I have been fortunate to give multiple seminars for the AAKP on Social Media and Kidney Disease and have been a Breakout Session Leader concerning the use of Social Media to advocate/raise awareness for kidney disease as well as a presentation about Facebook and it’s use to advocate for my fellow kidney patients. I helped to initiate the Pediatric Kidney Patients initiative (Kidney Pals), and I am part of the initiative for Kidneys and Veterans. I am the Chairman, Strategic Communications Committee, and a Member, 2019 National Patient Meeting Committee (Awarded).

    I am an Advocate for the National Kidney Foundation. In 2019, I was named the Advocate of the Year. For the NKF, I am a Statewide Advocate for the State of Indiana, Member of the Kidney Advocacy Committee, Leader of the KAC Social Media Group and a Regional Leader of Region #5(MI, OH, IN, KY, TN). I was influential in bringing about the NKF’s Pediatric Kidney Patient Initiative. I am an Ambassador for the AAKP, the Polycystic Kidney Disease Foundation, the Dialysis Patient Citizens, the Renal Support Network, the National Kidney Foundation of Indiana, More Than Just Your Kidneys and Waitlist Zero.

    I am a frequent speaker at the NKFI Kidney Walks in Merrillville, Indiana and Indianapolis, Indiana. I am a frequent traveler and speaker for kidney patients, including stops in 2018 at Boston, Kansas City, Washington, D.C., St. Petersburg, San Francisco and Kidney Week in San Diego.

    My specialty as an Advocate is my ability to utilize social media to help my fellow kidney patients and to raise awareness of the plights of the kidney patient. I am an administrator for 72 kidney pages on Facebook, another 50+ Kidney Groups of various topics, 10 blog pages and 9 e-newspapers. I am a very experienced advocate both at home and on the hill with my Members of Congress.

    My advocate nickname is Uncle Jim. If you have a kidney question or issue you need help with, please do not hesitate to contact me at I thank the AAKP for all the opportunities they have given to me.

  6. DAVID RODRIGUEZ AAKP Field Ambassador, Executive Committee Member

    David Rodriguez lived in Austin, Texas, when he was diagnosed with focal segmental glomerulosclerosis (FSGS). Three years after his diagnosis, David received his kidney transplant through the Pair-Exchange Donation Program at University Health Transplant Institute in San Antonio, TX.

    Originally a native of Brownsville, Texas, David serves as a patient advocate and spokesperson for organ, tissue, and eye donation, leading awareness campaigns about the benefits of organ donation throughout the state of Texas.

    David is a Field Ambassador, Public Policy Committee Member, and Member of the Executive Committee for the American Association of Kidney Patients (AAKP). David is a former member of the National Kidney Foundation, Texas Kidney Foundation, Texas Organ Sharing Alliance (TOSA), and a volunteer for the University Health System. As a member of the Advocacy Committee for the National Kidney Foundation (NKF) and an Ambassador of the American Kidney Fund (AKF), he lobbied at our nation’s capitol in Washington, D.C. He also lobbied at the Texas State Legislature at the Texas capitol on behalf of the Texas Kidney Foundation.

    David has served with AAKP/Vertex ICF Patient Advisory Committee and the SRTR Review Patient and Family Affairs Subcommittee.

    David published a Patient Voice article in the Clinical Journal of the American Society of Nephrology titled “Kidney Disease Burden and Kidney Transplantation: A True Story.”

    In 2017, David established Kidney Solutions – A Network of Transplant Experience, a non-profit organization with the mission to help guide those with chronic kidney disease, dialysis patients, and assist families in finding living kidney donors through their registered kidney transplant hospitals.

    David received the 2017 NKF Rita Littlefield Patient Spirit Award, 2017 TOSA Joan Wish Award for the Central Region, 2018 Texas Kidney Foundation Volunteer Year Award, and 2020 AAKP Presidential Volunteer Service Award.

    David is a former Patient Navigator and Patient Relationship Specialist at University Health Transplant Institute, where he visited inpatients at the Hospital and dialysis patients at dialysis treatment centers throughout Texas. David uses effective marketing and community outreach programs designed for patients with chronic kidney disease.

    David also shares his time as a bilingual speaker for a national speaker program dedicated to raising awareness about transplant options.

    In his time off, David enjoys playing golf, traveling, watching sports, and reading history and biographies.


    Ms. Schaeffer currently serves as the Vice President of Strategic Operations at Healthmap Solutions, after serving several years as an Executive Director of the Center for Medicare and Medicaid Services’ kidney contracts. Her focus remains on shaping the kidney care landscape to better support kidney transplant and home dialysis treatment choices. Ms. Schaeffer began her kidney care career as a registered dietitian (RD) in acute and out-patient dialysis units and later managing out-patient dialysis facilities.  

    Ms. Schaeffer maintains her RD credentials, received her Master of Arts degree in Nutrition Education from Immaculata University, and a Master of Business Administration degree from Temple University.

  8. LANA SCHMIDT, MBA, Executive Committee Member
    Ms. Schmidt is a kidney transplant recipient from Liberty, Illinois. She is on the Board of Directors for AAKP - American Association of Kidney Patients, an AAKP Ambassador and member of the policy and strategic communications committees and a member of the National Kidney Foundation.

    As a National Kidney Patient Advocate, Lana has served in many capacities throughout the kidney community over the years. She has raised kidney awareness from the patients’ perspective by publishing several magazine and newspaper articles, doing TV and radio interviews and speaking at conferences and meetings on kidney disease issues. She also started the Kidney Patients Support Group in her area.

    After 13 years on dialysis Lana received a kidney transplant from the University of Illinois in Chicago using a specialized drug, eculizumab because of her high antibodies. She was the first at this center to receive this drug with a deceased donor. She is now 4 years post-transplant.

    She is passionate to raise kidney awareness throughout our nation and wants to bring positive change for kidney patients to improve the quality of care and services and help them to be more informed and knowledgeable about the disease so they can make the best decisions for their quality of life.

    Dr. Barry H. Smith received his undergraduate degree (BA) at Harvard University with the Class of 1965; his PhD in Molecular Biology from the Massachusetts Institute of Techno logy (MIT) in 1968; and his MD from Cornell University Medical College in 1972. Dr. Smith carried out his residency training at both New York Hospital and Massachusetts General Hospital and served as the Deputy Chief of Surgical Neurology at The National Institutes of Health in Bethesda, Maryland from 1983-1988..  While there, he was involved in patient care, as well as basic and clinical research and issues relating to chronic illness and its costs to the U.S. healthcare system.  He continued and further developed these latter interests, especially those related to population health and the prevention of chronic illnesses, including kidney disease, in his subsequent work at Memorial-Sloan Kettering Cancer Center and as the Director of the Dreyfus Health Foundation (DHF) in New York City. As Director of DHF, he has worked with his colleagues on the development and implementation of community-based primary health programs in more than thirty-two countries.

    Dr. Smith became associated with The Rogosin Institute in 1966, but became a full-time member of its staff in 1988 and its President/CEO in 2008. Convinced that chronic and end-stage renal disease presents a special opportunity to develop a better model for the management of chronic illness, and also committed to the prevention of kidney disease and its major risk factors in diabetes and hypertension, he worked to expand the efforts of the Institute beyond the best in clinical care and research for better treatments to include population health and community mobilization for better health, as well as the development of its new Center for Health Action and Policy.

    Although he left The Institute in 2020 to found the Dreyfus Health Policy and Research Center, together with Dialysis Clinic, Inc that treats more than 15,000 patients on dialysis in 250 clinics in 28 U.S. States, manages acute kidney injury in at least 147 hospitals, prevents kidney disease progression through its REACH program, and has three organ procurement organizations  (Tennessee, New Mexico and northern California) for kidney transplantation, he has an ever-stronger commitment to improving the health (with particular emphasis on obesity, diabetes, and hypertension, as well as chronic kidney disease) of the people of Central Brooklyn in New York City and elsewhere, including the Mississippi Delta. This involves important partnerships with governmental and non-governmental agencies, local hospitals, primary care practices, and employers, as well as the people themselves.  Mobilizing individuals and the community to take more action and responsibility for their own health, providing community education regarding risk factors, better nutrition, and life styles that can prevent disease; screening and early detection of kidney disease; and referral for earlier and improved management of chronic illness, including CKD, are all part of a sustainable wellness/better-health/better quality-of -life model that he hopes will take root and spread across America one day soon.     

    Dr. Smith is a member of the American Society of Nephrology, Renal Physicians Association, National Renal Administrators Association, Society of Critical Care Medicine, New York Academy of Medicine, Alpha Omega Alpha, Sigma Xi, American Medical Association, and the American Public Health Association, among others. He is the author of more than 140 scientific and clinical papers, Co-Editor of Elsevier's Encyclopedia of Neuroscience, and an Editor of Problem Solving for Better Health : A Global Perspective (Springer), as well as New Delta Rising: A Tribute to the People of the Mississippi Delta (Universities of Mississippi Press).