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 A. Knight is President of the American Association of Kidney Patients' Board of Directors. He is a former hemodialysis patient who received a kidney transplant approximately eleven years ago. He is former Vice President of the American Association of Kidney Patients (AAKP) and former Chair of the Public Policy Committee and a member of the Board of Directors of the Mid Atlantic Renal Coalition (MARC). He was recently appointed to the Steering Committee of the Kidney Precision Medicine Project (KPMP) housed at the National Institutes of Health (NIH) National Diabetes and Digestive and Kidney Diseases (NIDDK).

    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 was served as a liaison to the Congressional Black Caucus for his Member of Congress and 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. READ MORE

  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.

    SECRETARY, former AAKP Vice Presdident

    Mr. Abel is a kidney transplant patient from Morgantown, West Virginia. Mr. Abel is a self-employed Property Manager for Abel Enterprises, LLC. He currently owns and manages residential and commercial properties, including one large dialysis facility and a facility housing a large CKD clinic, both in rural West Virginia.

    In 2005-2007, he was integrally involved in the conducting some of the 25 free kidney disease screening events that helped more than 1,800 West Virginians, many of which were in conjunction with the NKF of the Alleghenies’ Kidney Early Evaluation Program. He assisted in the garnering of political support of state government for showcasing the screening programs and World Kidney Day recognition at the state Capitol. Mr. Abel has been a member of AAKP since 2010.

  4. 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.

    Lisa is a kidney transplant patient from Conway, AR and is a financial and marketing professional and Mortgage Loan Officer on the Bancorp South corporate team. Her skills include financial planning, marketing and development. Lisa is an Ambassador for the Arkansas Regional Organ Recovery Agency (ARORA) and active with awareness efforts for AAKP, the PKD Foundation and the Alport Syndrome Foundation. Lisa is the former Vice President of the Conway AK Health and Rehabilitation Board, former Director of Programs and Development for the American Association of Fundraising Professionals (AFP), the former Director of Development for an Arkansas non-profit aiding those with intellectual and developmental disabilities, and a Member of the School Board and Marketing Committee for St. Joseph School. She is the past president and a member of the Conway Rotary Club, a member of the Conway Noon Chamber of Commerce, and a member of the FCLI Faulkner County Leadership. She has served previous appointments on AAKP’s Board of Directors since 2013 and is the Co-Chair of the AAKP Program and Development Committee.
  3. patrick-gee-sr-cropped

    Patrick Gee is a former Peritoneal and Hemodialysis patient and current kidney transplant recipient since April 2017. Patrick retired from the Virginia Department of Corrections as a Major/Chief of Security. Patrick has a Bachelor’s and Master’s in Criminal Justice, with an emphasis in Public Administration from the University of Richmond, in Richmond, VA. He also has a Doctorate of Philosophy in Justice, Law and Criminology from a American University, Washington, DC. Patrick is the Founder & CEO of iAdvocate, Inc., non-profit Faith-based Health & Wellness organization. He is also a Licensed Minister at Mountain Movers Ministry in Richmond, VA.

    Patrick currently serves in the following capacities:

    • Quality Insights ESRD Network 5 Patient Advisory Committee Chair.
    • Founder & CEHD, iAdvocate, Inc., non-profit, Faith-based Health & Wellness organization.
    • Quality Insight ESRD Network 5 Medical Review B.O.D.
    • Patient Voice Ambassador for ASN’s Kidney 360 magazine.
    • Patient Family Centered-Care Partners (PFCCpartners) Advisory Board.
    • American Association of Kidney Patients (AAKP) B.O.D.
    • Chronic Disease Coalition Southeast Region Co-Chair.
    • Center for Dialysis Innovation (CDI) Patient Advisory Board.
    • Kidney Health Initiative (KHI) Patient Family Partnership Council.
    • American Society of Nephrology (ASN) Diabetic Kidney Disease-Collaborative Task Force.
    • Word Health Organization (WHO) Guideline Development Group (GDG) Clinical Practice Guideline on Corticosteroid and COVID-19.
    • APOLLO APOL1 Long-term Kidney Transplantation Outcomes Consortium’s Community Advisory Council.
    • Same Day Access Measurement for Primary Care and Mental Health Technical Expert Panel through the Veterans Administration.
    • BMJ Rapid Recommendation on STGLT2 Inhibitors Research Patient Representative.
    • PCORI Comparative Effectiveness of Home-Based Strategies to Control Blood Pressure in Patients with High Cardiovascular Risk During the COVID-19 Pandemic Workgroup.
    • PFA (Patient Family Advisors) Network member
    • PFCCpartners Diversity, Equity, and Inclusion Workgroup member
    • American Kidney Fund (AKF) Ambassador & Certified Kidney Coach
    • National Kidney Foundation (NKF) KAC member
    • Donate Life DC Ambassador
    • National Patient Family Engagement (NPFE)- Learning Action Network (LAN) Legacy SME member
    • Cardio Vascular Clinical Trialists (CVCT) Forum Faculty member.
    Mr. Hess is a home hemodialysis patient from Edmond, OK. He is a graduate of the University of Central Oklahoma with a major in Biology and a minor in English. Mr. Hess authored the book “Kidney Failure Won’t Stop Me”, published in July 2012. He is a former member of the ESRD Network 13 Patient Advisory Committee & the Medical Review Board. Mr. Hess has been a member of AAKP since 2010.

    Douglas S. Johnson, MD, Director and Vice Chairman of the Board for Dialysis Clinic, Inc., began serving on the Board of Trustees in 1995. Dr. Johnson is a board certified internist. He received his medical training at Vanderbilt University, graduating in 2006, and completed his internal medicine training at University of Tennessee/Baptist Hospital in June 2009. Since returning to DCI in 2009, he has helped to implement initiatives to ensure financial stability of the company while also helping to develop tools to ensure excellent patient outcomes and improve patient care. One of Dr. Johnson’s most recent projects has been the development of the DCI chronic kidney disease initiative into the more formal Reach Kidney Care program. Reach Kidney Care addresses the needs of individuals with chronic kidney disease, giving them access to one-on-one counseling with a care manager and nutrition counseling with a dietitian. The Reach Kidney Care team seeks to understand individuals’ health goals and provides education about kidney disease and treatment options to allow people to live their best life while minimizing the impact of kidney disease. By working with individuals to evaluate all treatment options and encourage pre-emptive transplant when appropriate, the Reach Kidney Care team hopes to delay or prevent kidney failure. REACH care managers also provide coordination and follow up for high risk patients receiving dialysis treatment. Reach Kidney Care currently provides care to more than 3,000 patients in twenty-one locations in eight states. Improving care of chronic kidney disease and increasing transplantation is a large part of Dr. Johnson’s plan to improve the future of care for individuals with kidney disease. To demonstrate methods for improving care, Dr. Johnson led DCI’s involvement in the Centers for Medicare and Medicaid (CMS) End Stage Renal Disease Seamless Care Organization (ESCO) project. Under Dr. Johnson’s leadership, DCI participated in the project with six ESCO projects, three of which lasted the full duration of the CMS demonstration project. In January, 2020, DCI submitted applications to transition these three ESCOs into Comprehensive Kidney Care Coordinated (CKCC) Model organizations. DCI also assisted thirty-nine nephrology practices in their submission of Kidney Care First (KCF) applications. Dr. Johnson also serves at DCI Donor Services, Inc. In addition, he sees patients in his internal medicine practice twice a week.

  6. JENNIFER JONESUSMC (ret.), AAKP National Ambassador

    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, American Kidney Fund Advocacy Network, and AKF Health Coach, and Veterans Transplantation Association.


    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.

    In 2008 David was living in Austin, TX when he was diagnosed with focal segmental glomerulosclerosis (FSGS). In 2011 David received his kidney transplant through the Pair Exchange Donation Program from University Transplant Center in San Antonio where he currently resides for 7 years.
    Born and raised in Brownsville, TX, 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 Texas border regions from Brownsville to El Paso, including Corpus Christi and San Angelo. David has volunteered for National Kidney Foundation, Texas Kidney Foundation, Texas Organ Sharing Alliance, and University Health System. As a member of the Advocacy Committee, he has lobbied for the National Kidney Foundation at our Nation’s Capital in Washington, D.C. and the Texas State Legislature on behalf of the Texas Kidney Foundation. Professionally, David is a former Patient Navigator at the University Transplant Center. He also served in serval leadership positions in local, state and national political campaigns. David likes to read history and biographies, golf and the San Antonio Spurs basketball team.
    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.

    Suzanne Ruff has been a freelance writer for the Charlotte Observer and author of the non-fiction award-winning book The Reluctant Donor. She has been published in Chicken Soup for the Soul books and various magazines.. She is a living kidney donor and serves on the executive Board of Directors at AAKP, the Living Donor Council of the National Kidney Foundation and volunteers for the PKD Foundation.

    For the past five years, she has served as a Co-Investigator on the PCORI Project: Putting Patients at the Center of Kidney Care Transitions (PrepareNow).

    Passionate about kidneys, Suzanne speaks, writes and volunteers about all aspects of kidney disease, organ donation and the gift of another day.


    Ms. Schaffer is currently the Executive Director for the Health Services Advisory Group, Inc. (HSAG). Her responsibilities include leading the ESRD NCC Federal contract under the Centers for Medicare and Medicaid Services (CMS). Ms. Schaffer oversees all deliverables, tasks, projects and personnel to meet goals and contract requirements within budget. She works to merge formal Quality Improvement processes and Data Analysis within Human Centered Design tools for an innovative approach across task lanes and serves as main point of contact for the contracting agency to develop relationships that inform tasks to anticipate and exceed expectations. Ms. Schaffer previously served as Associate Executive from July 2018-December 2019, whereas she took the position of Executive Director in December 2019.

    Ms. Schaffer is a registered dietitian (RD), received her Masters of Arts (MA) in Nutrition Education from Immaculata University and holds a Masters of Business Administrative (MBA), Strategy, Healthcare from Temple University.

    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).