The future of kidney health is ours to define.

Ada DeBold’s love for her son, Bobby, led the founding of the National Kidney Foundation. In 1950, Bobby was diagnosed with “nephrotic syndrome,” a fatal disease at the time. To save him, Ada established the National Nephrosis Foundation, bringing together doctors and families to fund research. Assisted by her husband Harry, Ada tirelessly networked and raised funds. Her relentless efforts enabled Bobby to participate in a groundbreaking drug trial, although it came too late to save him. Ada's initiative evolved into NKF, which continues her legacy.

Social media saved Daniel.

Daniel Kushnick had a 30+ year career in film/video production, then helped low-income people in NY State save on their energy bills.
He was diagnosed with polycystic kidney disease (PKD), progressing to stage five CKD. While Daniel was undergoing dialysis training, a kidney donor stepped forward, thanks to a social media campaign. He volunteers for NKF’s PEERs mentoring program and on an environmental committee. Dan seeks to help other patients and expand awareness about kidney disease.

Ewo Harrell is Vice Chair of NKF CO & NM Board of Advisors, a 2X kidney recipient, and health champion. Ewo was on dialysis for six months before receiving a kidney from her sister. Sadly, the kidney failed after 10 years, but her husband donated his kidney in a paired exchange and they are both doing great today. Ewo supports NKF through advocacy, volunteering, fundraising, and committee service. “I truly found my calling as an NKF advocate—helping to raise awareness while sharing my story with others.”

Jake Cheafsky has demonstrated unwavering support for NKF Serving the Carolinas for 10 years. This year marks the 10th anniversary of the third-party golf tournament he organizes in honor of his late daughter, Celia Jane. Jake and his wife, CJ, have raised over $100,000 for NKF through the Celia Jane Memorial Golf Tournament. He has also played a key role in funding and launching the Carolinas Pediatric Program. Now, as a newly appointed Board member, Jake continues to find innovative ways to support NKF’s mission.

Amy Hewitt, Executive Director for NKF Serving The West, celebrated her third work anniversary in March 2022 by becoming a living kidney donor for Wilson Du, aka the "Renal Warrior." She is dedicated to expanding NKF’s reach to better serve the growing kidney community.

Previously, Amy led Finance/HR for a restaurant company in Southern California. She discovered her passion for healthcare advocacy after meeting the founder of the Scleroderma Research Foundation. Inspired, Amy served as their Executive Director for 10 years.

Dr. Sumeska Thavarajah works tirelessly for NKF at local and national levels, intimately involved in day-to-day activities, always advocating for patients. Dr. Su led our Medical Advisory Board, spearheading many of their projects, continuing as advisor. From committees, to training students, to managing research grants, she does it all. She is a wealth of knowledge, from NKF history to kidney disease treatments for her patients. Dr. Su is not just a hero to constituents and staff, but also to her patients, their families, and colleagues.

Coyle Bauer's family first learned that something was amiss with his kidneys before he was born. Before Coyle's first birthday, his parents were told that he needed a transplant and to go on the wait list. In less than a year, Coyle's parents got the call that a kidney was available. Since Coyle's transplant, he and his family have been active in NKF, selflessly and tirelessly sharing their story, taking every opportunity to advocate for organ transplantation and promote kidney health awareness.

A dedicated nephrology social worker and patient advocate, Beth Witten, MSW, ACSW, LSCSW, has spent four decades improving lives of patients, care partners, and social workers. As former Chair of both the National Council and a local Chapter of Council of Nephrology Social Workers (CNSW), she expanded resources and education. With NKF and Medical Education Institute, she empowered patients with knowledge of treatment, finances, and quality of life. NKF’s Culpepper Exum Scholarship, made possible by Beth’s family, helps kidney patients pursue the dream of higher education.

When John Finelli’s wife, Susan, received a diagnosis of chronic kidney disease (CKD), he quickly transformed into caregiver mode. He researched how to control CKD, monitors her salt intake, exercises with her, and ensures that she gets plenty of rest. John accompanies Susan to all doctor appointments, monitors her GFR, and advocates for patient care. Together, John and Susan make a great NKF Voices for Kidney Health® advocacy team.

Jennifer Cramer Miller is the “poster child” of volunteering for NKF Serving Minnesota. She is a 4x kidney transplant recipient, after receiving a diagnosis of focal segmental glomerulosclerosis (FSGS). She's a self-proclaimed "incurable optimist." Jennifer is NKF MN’s Board Chair, serving for five years, an NKF PEERs mentor, advocate, and professional and patient educational speaker. She is often NKF MN Kidney Walks’ top fundraiser, engaging her entire network at NKF Golf, Galas, and Walks. She is also a generous personal contributor to NKF’s mission.

Jen Anderson’s tenacity and passion helped protect living kidney donors in Minnesota. She donated a kidney to a family member at 19, and is an NKF volunteer of three decades. Jen joined Minnesota’s NKF Board, quickly becoming Chair. She was absolutely crucial in passing Minnesota’s Living Donor Protection Act, forming alliances, and making connections with lawmakers. A longtime NKF Golf supporter, Jen re-started MN’s program, turning the event around financially. Jen is a connector, bringing companies and individuals "into the fold" of NKF’s family.

History Maker: NKF President (1968-1970), Dr. George Schreiner, was treating kidneys even before it was called “nephrology.” His work is responsible for many things we take for granted: advancing dialysis from experimental to routine treatment, saving millions; through advocacy, replacing “life or death” committees with Medicare coverage so all can get dialysis; helping pass the Uniform Anatomical Gift Act; and countless research contributions. Beloved by patients and colleagues, Dr. Schreiner was founding member of ASN and ISN, and Chief of Nephrology at Georgetown University Hospital.

For more than 25 years, Dr. Yolanda Thompson-Martin has been a tireless advocate for kidney health, serving as an Adult Family Nurse Practitioner and nephrology leader. A longtime member of NKF Serving Kansas and Western Missouri’s Medical Advisory Board, she helped develop the Renal Roundtable, a nationally recognized professional education program. She led patient empowerment programs, worked on policy initiatives, and mentored nephrology professionals. Dr. Thompson-Martin is deeply involved with NKF Spring Clinical Meetings and CKDintercept. Her passion, expertise, and leadership continue to transform kidney care.

Barbara Weis Malone is a dedicated nurse practitioner, educator, and advocate. She was instrumental in establishing the Advanced Practitioner (AP) track at NKF’s Clinical Meetings and the founding of the Council of Advanced Practitioners (CAP), one of the first organizations to unite nurse practitioners and physician assistants. Barbara’s impact extends through her clinical work at the University of Colorado Hospital, mentorship of future practitioners, and tireless volunteering at NKF walks, community events, and KEEP screenings. Her passion and leadership continue to elevate kidney care.

Shaul G. Massry, MD, was a trailblazer and leader in nephrology and at NKF. Dr. Massry served at tNKF Southern California Affiliate and National level as VP and Chair of the National Advisory Committee, increasing NKF’s research, leading to $200+ million investment. A strong organ donation advocate, he even obtained support from Pope John Paul II. As NKF President and Annual Meeting Chair, he expanded professional membership and education. He also led development of the first KDOQI bone guidelines. He was a true visionary and pioneer.

In 2008, college student Stacey Warr felt terrible: exhaustion, pain, and splitting headaches. For 11 years as her health declined, she sought opinions from primary care physicians and family practices. Finally, in 2019, a diagnosis: Stage 5 kidney disease. At 33, Stacey was on the transplant wait list. In 2023, she joined NKF as an Advocate to educate PCPs about warning signs and causes of CKD. She realized the power of her voice and speaks at numerous programs and events in the Washington, DC, area.

Mike Stevenson is a kidney transplant recipient who has been involved with NKF for more than 17 years. He has served on the NKF National Board and Finance Committee. Locally, he has been instrumental leadership transitions, supports all local events through funding connections and continuing engagement, and has gotten his whole family engaged with their local NKF. Mike Stevenson continues to lead the Columbus Board of advisors, sits on both Gala and Walk committees, and works closely with local staff to implement funding opportunities.

Jummy Olabanji, Anchor/Reporter for NBC4 Washington, and NKF Board Member, reached out to us because polycystic kidney disease runs in her family. She co-hosts Kidney Balls and Congressional Awards, announced the Wizards Organ Donation Awareness Tournament, kicked off Kidney Walk season, and hosted a Fireside Chat with actress Debbie Allen. For Kidney Month, Jummy and meteorologist Doug Kammerer wear kidney pins and share kidney disease information on air. Jummy received the National Capital Area Arthur P. Pasquarella Leadership in Action Award in 2023.

Lauren Drew is the Senior Director of Congressional Relations at NKF National and a living donor. She is uncomfortable with the idea of “hero,” but encourages everyone to consider living donation. “I would do it again in a heartbeat if that were possible!”

Kelli Strother became involved with NKF when her father was on dialysis. Inspired by living donors she met through NKF events, she became a paired-exchange living donor for her dad. She credits NKF for providing the education, resources, and support her family needed to navigate the donation process. Now, as Board Chair for NKF Colorado & New Mexico, she advocates for kidney patients, helps pass life-changing legislation, and mentors others. In 2024, she received The Arthur P. Pasquerella Leadership in Action Award for her dedication.

James M. Crawford, MD, PhD, is a Professor and Chair Emeritus of the Department of Pathology and Laboratory Medicine at Northwell Health and the Donald and Barbara Zucker School of Medicine at Hofstra/Northwell.

Dr. Crawford works with NKF on CKDintercept®, an initiative to improve kidney disease testing, recognition, and management in primary care, and to build a clinical and business case for health system leaders to improve testing and early diagnosis of CKD.

As parents of children who suffered from “nephrosis,” Virginia Clune and her husband Patrick felt it was important to bring awareness of the disease and build a support network for other parents and children. In 1966, the Clunes created the local Chapter of NKF in Kansas City. Since then, the Clunes with family and friends have been strong advocates for kidney health, with Virginia at the helm. Even in her 90s, she continues to be NKF’s champion. Her family’s generosity has a profound impact on the community.

Dr. Ahmed Awad has been a dedicated nephrologist, researcher, and advocate for kidney health for three-plus decades. A leader in kidney disease prevention and research, he helped establish Kansas City as a hub for kidney disease trials. As former NKF Board Chair and Early Intervention Program Chair, he played a key role in KDOQI approved early detection guidelines. He contributed to CKDintercept, NKF’s initiative to improve early diagnosis and slow progression. Appointed to Missouri’s CKD Task Force, Dr. Awad’s work shapes kidney care nationwide.

Ines Prada, Board Member for NKF Kentucky, has made significant contributions through her unwavering support. Polycystic kidney disease (PKD) runs in the Prada family, so the Mission is very personal. Her company has contributed financially to and supported NKF Golf. Ines is NKF KY Gala co-Chair, ensuring the event's success. Ines promotes family involvement and community engagement in these events, amplifying their impact. Her outstanding commitment earned her Volunteer of the Year in 2017. Her dedication strengthens the Mission and supports vital initiatives.

Ellie Kelepouris, MD, NKF PA Board member, is a key member of the local kidney community. A nephrologist for Penn Medicine and Professor of Clinical Medicine for Perelman School of Medicine at UPenn, Dr. Kelepouris has Chaired the NKF PA Medical Advisory Board for many years. She is dedicated to professional education of new nephrologists, as well as enhancing understanding in the professional community of new treatments and technologies. Most importantly, Dr. Kelepouris always advocates for and focuses her education on patients.

Joel Bolstein has dedicated more than 10 years of service to NKF Serving Eastern Pennsylvania and New Jersey, not only serving on the local Board of Advisors, but also as the NKF Philadelphia Golf Classic Event Chair. As Golf Chair, Joel has raised over 1 million dollars during his years of service. Joel has been instrumental to the success of Philadelphia Golf and his local NKF feels lucky to have him. He is a dedicated and engaged community partner.

Velma Scantlebury-White, MD, the first Black female transplant surgeon in the US, has performed 2000 kidney transplants over her 40-year career. Born in Barbados, emigrating to Brooklyn, her older sister’s death sparked her passion for medicine. Overcoming educational and career barriers, she graduated from Columbia, was a surgical intern/resident at Harlem Hospital, a research fellow, surgery instructor, and associate professor at University of Pittsburgh Medical Center. She is Associate Director of Kidney Transplant, Christiana Care Hospital, and a big supporter of NKF’s THE BIG ASK: THE BIG GIVE®.

As CEO of the National Kidney Foundation and a kidney transplant recipient, Kevin Longino has dedicated his leadership to advocacy, patient support, and advancing kidney research. Under his tenure, NKF has expanded transplant programs, strengthened public policy efforts, and launched key initiatives like the Innovation Fund and Transplants For All. A tireless advocate, Kevin has worked to improve early detection, increase transplant access, promote health equity and save lives. His leadership ensures that millions affected by kidney disease receive the care, resources, and support they need.

Dr. Cynthia Delgado is a nephrologist and health equity advocate dedicated to advancing kidney care for all. She co-chaired the NKF-ASN Task Force that developed a race-free approach to estimating kidney function, improving equity in diagnosis and treatment. As Associate Chief of Nephrology at the San Francisco VA and a professor at UCSF, her research focuses on CKD, frailty, and health outcomes. Recognized for her impact, Dr. Delgado was named to the TIME100 Health list and received NKF’s Garabed Eknoyan Award in 2023.

Samira Farouk, MD, MSCR, FNKF, FASN, FAST, FACP, is a transplant nephrologist, Associate Professor, and Program Director, at Mount Sinai. She is an innovator in medical education technologies, receiving multiple awards.

Dr. Farouk completed internship/residency and was Chief Fellow at Icahn School of Medicine, where she is a Master Educator.

Dr. Farouk founded NephSIM a nephrology education app. She supported #NephMadness, NKF’s education initiative. She is President of the New York Society of Nephrology, and a board member of NKF’s American Journal of Kidney Diseases.

Dr. Neil R. Powe is a distinguished professor of medicine at the University of California, San Francisco, and serves as the chief of medicine at the Priscilla Chan and Mark Zuckerberg San Francisco General Hospital. His research focuses on kidney disease epidemiology and health disparities. As co-chair of the NKF-ASN Task Force on Reassessing the Inclusion of Race in Diagnosing Kidney Diseases, Dr. Powe has been instrumental in developing race-free approaches to kidney function estimation. In recognition of his efforts to address racial bias in medical algorithms, he was named to TIME's 2024 list of the 100 most influential people in health.

Arthur P. Pasquarella, CRE is a kidney donor and has been a driving force behind NKF’s growth and impact, serving as a leader, advocate, and fundraiser for over 15 years. As Chair of NKF’s National Board of Directors, he championed strategic investments in advocacy, communications, and programs—strengthening NKF’s ability to serve patients, families, and professionals. Art was also a significant seed funder of the Innovation Fund, helping to accelerate breakthroughs in kidney care. His leadership continues to inspire and expand NKF’s reach, ensuring lasting change for the kidney community.

Sylvia E. Rosas, MD, MSCE, Immediate Past President NKF, is a nephrologist and epidemiologist at Joslin Diabetes Center, Boston. She is Director of the Latino Kidney Clinic and Associate Professor at Harvard Medical School and nephrologist at Beth Israel Deaconess. She received the NKF NE 2017 Physician of the Year and National Hispanic Medical Association Fellow of the Year Awards. She is an NKF volunteer, including NKF Spring Clinical Meetings committee, Young Investigator Forum judge, and member of the Scientific Advisory Board and NKF NE.

Ken Couls is a dedicated NKF Board member and volunteer. He is the NKF Golf Classic Chair (four years in a row), brings in Golf teams and sponsorships, serves as Finance Chairman on the NKF OH Board, sits on the National Audit Committee, volunteers with Your Kidneys and Youth kidney health education program, and supports Drive for Dialysis program. Ken facilitates exceptional grant funding and brings in revenue keeping NKF OH going. Ken is a model Board Member, aiding the Mission any way he can.

Jim Adams’ passion for Mission work at NKF is apparent in all he does. He serves on the NKF Golf Classic Committee, is incoming Board of Advisors Chair, creates videos for social media, speaks about his kidney disease journey at events/programs, and opens doors for local and national NKF teams. Alongside generous financial support, Jim’s volunteerism knows no bounds, and you can often find him at Drive for Dialysis, stuffing bags for patients or assembling Golfer gift bags with his incredible team at Revolution Trucking.

At 9, Mary Baliker was diagnosed with kidney disease. At 17, she received her first transplant. 30+ years later, her service and career have included innumerable international, national, and state patient-centered initiatives. Mary is NKF’s Kidney Advocacy and Public Policy Committee Chair, a PEERs Mentor, and on workgroups for Patient Network Data Use and Publication, Transplant Advisory, and NKF Spring Clinical Meetings 2025 Patient Advisory Committees. In Wisconsin, she is an outspoken kidney advocate, on the NKFW Health Advisory Committee, and a past Board member.

Andrew S. Levey, MD, revolutionized how kidney function is estimated, using a simple blood test, by developing the original eGFR equation, which calculates how well kidneys remove wastes. He chaired the NKF KDOQI Chronic Kidney Disease (CKD) Guideline work group, which defined and classified the stages of CKD for the first time and transformed kidney care worldwide. Dr. Levey worked with the NKF and FDA to develop and validate new surrogate end points that made clinical trials for CKD feasible, leading to many new treatments.

Nathan W. Levin, MD, did pioneering work in evidence-based guidelines for people with kidney disease, as the Co-Chair of the Dialysis Outcomes Quality Initiative, and founding Co-Chair of both the NKF Kidney Disease Outcomes Quality Initiative (KDOQI), and the global guideline initiative Kidney Disease: Improving Global Outcomes (KDIGO). KDOQI Guidelines have improved the quality of care for kidney patients in the US and worldwide. Founder of the Renal Research Institute, Dr. Levin’s distinguished work includes: public health projects in Ghana, Uganda, Senegal; and numerous clinical and faculty positions.

Lisa Baxter inherited polycystic kidney disease (PKD) from her father. She has 11 relatives on dialysis. Lisa received a deceased donor kidney that she and her late husband, Mitch, called “Hannah,” for the daughter they did not get to have. Lisa has “Hannah” for six years and doing well.
 
Lisa is a social worker of 25 years, health campaign manager, author, advocate, volunteer, CEO, The Lisa Baxter Show host, and an NKF supporter. Regarding her kidney, “I thank God…it has been more than a blessing.”

Garabed Eknoyan, MD, Co-Chair of the original NKF Dialysis Outcomes Quality Initiative (DOQI), was on the team that changed kidney disease treatment in the US and around the world. Now known as KDOQI, the resulting guidelines continue to improve outcomes and quality of life of CKD patients. Today, The Garabed Eknoyan Award recognizes professionals who have made a significant impact on patient’s lives. Dr. Eknoyan, a highly regarded researcher, educator, and clinician, is a Professor at the Baylor College of Medicine in Houston.

A living donor to her neighbor’s son, Jackson, Beth Burbridge has shown immense selflessness. She has been an influential speaker at NKF Galas, Walks, THE BIG ASK: THE BIG GIVE® events, and the NKF KY Patient Summit. Awarded Volunteer of the Year at the 2021 Gift of Life Gala, Beth serves on the Kentucky NKF Board, is a Kidney Advocacy Committee member, and helped pass living donor PTO ordinances in Louisville and Lexington. She was key in bringing three companies into the Circle of Excellence.

Adam Teterus became a living kidney donor for his good friend and creative partner, Octavius A. Newman. Adam refers to the transplant as one of his most important collaborations. He was emcee of NKF’s 2024 Philadelphia Kidney Walk, as well as one of the Mission speakers. He is Director of Community for Indy Hall, a coworking community, and moonlights as a cabaret emcee. Adam believes neighborhoods are the most important resources in life, and attributes all his successes, including his transplant, to his community.

Frita M. Fisher, MD, is a triple board-certified nephrologist in Atlanta, and Board member of NKF Serving AL, GA & MS. She was honored with NKF’s 2018 Community Activist Award, founder of her own practice, and Medical Director of a non-profit dialysis unit (DCI). Dr. Frita loves taking care of patients and giving medical advice. She is an expert medical commentator, presenting for NKF. Dr. Frita’s mission is to share her medical knowledge in an easy-to-understand manner so people can live their happiest, healthiest lives.

Mónica gave her husband Gerardo the most precious gift imaginable: the opportunity for a new life.
For years Gerardo had self-medicated his gout condition due to lack of health insurance, which eventually led to kidney failure. When no one in her family was willing to donate a kidney, Monica bravely stepped forward. The surgery that saved his life was performed on the most appropriate day: Valentine's Day 2024.
Today Mónica and Gerardo are fierce defenders of organ donation.

Reg Chapman, News Anchor at WCCO, is an exceptional supporter and advocate for NKF Serving MN. Through his platform, Reg has helped raise awareness and shine a light on the vital work of NKF MN in serving the community. Reg generously promotes the Twin Cities Kidney Walk and is a fantastic emcee every year. He has also interviewed MN Board Member Jennifer Cramer Miller on WCCO in support of all her efforts for NKF.

Jason Koenig has demonstrated an unwavering commitment to the mission of NKF. His passion, hard work, and dedication make him a true hero, transforming lives and making a difference in the community. Jason lost his mother, Pat, to kidney disease when he was just 19 years old. He continues to honor his mother by making lives better and having a smile for everyone. Jason serves on the NKF Board, is the Chair of the Orange Gala, and is very giving of his time and resources.

Pat Klickna, an exceptional volunteer and NKF champion, dedicats her time, talent and story to further the Mission and vision of NKF. She volunteers for all local events and engages her entire family in supporting NKF. Pat has spoken about her transplantation journey and never hesitates to support NKF’s team. She has been a top Walk fundraiser, and has volunteered in the Local office and at events. Pat is a true inspiration and tries to connect with and support other people dealing with kidney disease.

Dr. Brown's passion for the patient experience shines through all he does for NKF Serving Maryland and Delaware. He is a wonderful Medical Advisory Board leader, reaching out to colleagues, patients, and families, stewarding nephrology fellows, and speaking at conferences. Asked what he enjoys most, Dr. Brown says, "… the thing that makes the NKF work so gratifying is that it has the most potential to help higher numbers of people at once, as opposed to seeing one patient at a time…”

Gene Blakenship epitomizes support to the kidney community in Oklahoma City, as well as to the entire State of Oklahoma. His continuous efforts are changing the landscape for Native American communities, and his passion, as a kidney transplant recipient, is fueled by an innate desire to see all people live healthy lives. In addition, his preventative approach resonates well with our NKF Mission. NKF Serving Texas and Oklahoma is proud of this Hero.

Miriam Godwin is a kidney donor and Vice President of Health Policy and Clinical Outcomes at the National Kidney Foundation. She previously led transformative initiatives at CMS, including the ESRD Treatment Choices Model, and supported groundbreaking programs like Kidney Care Choices. With a strong foundation in health policy, clinical trials, and drug development, Miriam has dedicated her career to advancing kidney care and increasing access to transplants. She holds a master’s degree in public policy from George Washington University.

Wendy Funk Schrag began her career as a dialysis social worker in 1990 and quickly became a champion for kidney patients and professionals alike. Her leadership in the Council of Nephrology Social Workers, where she served as Program Chair and President, helped advance support services and education. As Vice President for State Government Affairs at Fresenius Medical Care, Wendy drives legislative and advocacy initiatives across 27 states. She was the first social worker to receive the AAKP Medal of Excellence, recognizing her innovative approach and lasting impact.

Tamra and Jamie Johnson are devoted parents of their child suffering from kidney failure. Jamie selflessly donated a kidney to their daughter in a remarkable act of love. Inspired by their journey, the Johnsons became passionate advocates for kidney health. They are a leading fundraising team for Kansas City Kidney Walk, raising generous support. Their unwavering commitment is evident in their countless hours organizing and ensuring the event’s success. Jamie and Tamra chair the Walk Committee, where they inspire others with their enthusiasm and determination.

Laurie Hines is a dedicated leader and kidney health champion in Missouri. A living donor and former Director of the Missouri Kidney Program, Laurie was first to support and contribute to two pilot projects—the ShowMe CKDintercept and Changing Lives Through Transplant initiatives. Her leadership and advocacy for kidney patients has led to robust stakeholder engagement across MO. Laurie has been integral to the successful Mid-Missouri Kidney Walk and serves on the St. Louis NKF Board of Advisors. Laurie’s innovative ideas have strengthened NKF MO.

Perisco Wofford, MD, NKF Board member, is a nephrologist in Memphis, affiliated with multiple local hospitals, in practice for 20+ years. He is celebrated for his volunteer work as a doctor, assisting underserved communities, and supporting uninsured patients. "...I find it a moral obligation as a physician. We are here to help people no matter their insurance status." Whether an NKF panelist discussing CKD prevention, or encouraging young African American students to pursue nephrology, or fundraising, Dr. Wofford is the epitome of a dedicated professional and friend.

Donna Whittle is a true champion for hope, whose journey with CKD is deeply personal. In 1985, her boy was born with polycystic kidney disease (PKD) and never left the hospital. This led her to nursing to learn about her son’s condition and support others. Starting in the ER, she became a dialysis nurse. Her mother and grandson are dialysis patients. Her family, patients, and kidney community mean everything to her. She is a Mid-Missouri Kidney Walk Committee member and Walker. Her kindness and dedication inspire everyone.

Anthony Tuggle's commitment to the NKF has been unwavering. He was 2024 Atlanta Walk Chair, a former Board member of NKF Serving AL, GA & MS, Immediate Past National Board Chair, and current National Board member. A deceased donor kidney transplant recipient, Anthony plays a pivotal role in shaping the direction of our organization. As Atlanta’s Walk Chair (2018-2020), Anthony led the event to raise over $500,000, with his AT&T partnership generating an additional $200,000. He is currently chairing NKF’s National Development Committee.

Willie Kendrick, transplant recipient, brought a boots-on-the-ground NKF presence to the Wichita area. His determination provided local patients with a community of support. His leadership led to new relationships, substantial fundraising, and increased awareness. He personally took time to mentor and connect local patients with the information and resources they needed. KS Kidney Walk has an 11-year history because of his commitment. Willie lost his battle with kidney disease in 2024. His legacy lives on in his family, friends, colleagues, the community, and hundreds of patients.

Michelle L. Graham, MD, MME, FAAFP, channeled her early experiences with chronic illness into a life of service. She is the NKF of Wisconsin Board’s Governance Chair, and on their Health Advisory and Advancement Committees. She champions needs of patients, health professionals, and the kidney community. Michelle is President-Elect of the Wisconsin Medical Society’s Board and UnitedHealthcare Medicare & Retirement Chief Medical Officer for the Pacific Northwest, WA, OR, HI, & AK. She was in Marquis Who’s Who in America for 2024, and a Wisconsin Titan 100.

Andrea Weisman healing from a car crash, found a passion for organ donation, leading her to become an altruistic kidney donor. Andrea built campaigns to find living donors, created cheer kits for pediatric dialysis patients, and uses her platform as USOA Mrs. Waukesha County to build awareness. She serves on the Board and multiple committees of NKF of Wisconsin.
“I truly believe that I found my life’s calling at NKF Wisconsin. My personal mission is to educate and advocate for those waiting on their lifesaving gift.”

Mike Crowley was a frustrated parent—his two-year-old son was diagnosed with type 1 diabetes, and he wanted to help. He started volunteering and raising money for research, which grew into a career. He became CEO of NKF of Wisconsin, which has experienced new growth in educational events, awareness, and community partnerships. In January 2025, Crowley became an altruistic kidney donor. He looks forward to getting back to work and sharing his living donation journey. Mike is active in local government and with Breakthrough T1D.

Casey Grossman is a dedicated volunteer for the Long Island Kidney Walk, and a proponent of organ donation. Her grandfather died at 56 from kidney failure resulting from interstitial nephritis. It was passed on to her mom and uncle. Casey donated a kidney to her mother, and she feels so much joy that her mom has a full life, but IN continues to affect her family—her niece now entering kidney failure. Casey advocates, raises funds, and does it all with a wonderful perspective and attitude.

AnnMarie Link is a hero and leader. At 4 years old, AnnMarie’s son received the lifesaving gift of a kidney transplant. At that time, she committed to serve the kidney community and those affected by kidney disease. Twenty years later, AnnMarie continues to live her promise. As Chairperson of the Upstate and Western NY Board for nearly a decade, and recipient of the Outstanding Volunteer of the Year Award, she embodies joy, compassion, resilience, leadership, and unwavering dedication to our kidney community and the Mission.

David Knop has been an NKF Serving Texas Board member since 2017 and is currently Chair. He has won numerous awards, including the Arthur P. Pasquarella Award for service. He has volunteered at Camp Reynal (kidney camp for kids), Kidney Walk, NKF Golf and Gala events, and even donned the “Billy the Kidney” costume to entertain kids at Camp Reynal. David has served as Captain of TEAM DNA at TX’s annual Kidney Walks, raising more than $400,000.

Dr. Bradley A. Warady, MD, NKF Board Member, continues his career’s work: advocating for children with kidney disease. During three decades with NKF, he initiated a collaboration between NKF, American Academy of Pediatrics, and American Society of Pediatric Nephrology on patient and family education, and co-Chaired the first NKF workshop on CKD in Children—including patients and parents.
“There remains a great deal to be accomplished in…awareness, prevention and treatment.”
His summer camp for children with kidney disease, Camp ChiMer, has been operating nearly 40 years.

Olivia Dawli, a tremendous advocate, has shared her story at Long Island and NYC Kidney Walks, and will receive a Volunteer Award at the Connecticut Night of Hope Gala. Diagnosed with kidney failure, upon graduating college, her goals were on hold as she began dialysis. She feels lucky living her future because a person selflessly gave his kidney. Olivia’s now a registered nurse. She advocates for everyone with kidney disease, dialysis, transplantation, and those not with us—Most of all so people don't have to feel alone.

Jimmy O'Conor has been involved with the NKF his whole life. He was diagnosed with kidney disease at the age of 5 and received his first of three transplants from his mother, whom honors through his NKF work. Jimmy, owner of Woody's Dewey Beach restaurant, “home of the world-famous crabcake,” is a top Walker and Advocate. He did tremendous work getting a Delaware Living Donor Protection Act passed. Jimmy's wife is also a kidney donor, through paired exchange. They remain passionate about patients and awareness.

Laura Newsome is a 3X kidney recipient and a true Kidney Hero. With infectious energy, she champions the Southern California Kidney Walk, inspiring everyone she meets. Her passionate outreach to raise awareness and funds for kidney health touches lives in her community and beyond. Each year, we’re honored to have her officially kick off the Walk and cut the ribbon, setting an inspiring tone for our participants. Laura’s remarkable journey and dedication remind us all of the power of hope, resilience, and community.

Susan Finelli received a diagnosis of a tumor inside her right kidney in October 2018, resulting in a radical nephrectomy (kidney removal), after which she was diagnosed with Stage 3 CKD. Not being familiar with CKD or how to control it, Susan searched the Web, found and reached out to NKF where she found a wealth of information on how to control and live with the disease. Susan quickly became an NKF volunteer and, with her husband, actively advocates for patients, living donors, and caregivers.

Yue-Harn Ng, MD, MPH, Clinical Professor of Medicine and Director of the Transplant Fellowship Program in the Division of Nephrology at the University of Washington, champions equity in kidney care. A dedicated transplant nephrologist and clinical leader, she is committed to improving outcomes for all kidney patients. Dr. Ng lends her expertise to NKF by serving on numerous committees, educating and empowering medical professionals, patients, and care partners alike. Her tireless efforts and commitment to advancing kidney care make her a true Kidney Hero.

For years Gerardo Jimbo had self-medicated his gout condition due to lack of health insurance, which eventually led to kidney failure. After the diagnosis, he endured three years of home dialysis. When no one in his family was willing to donate a kidney, his wife Monica bravely stepped forward. After numerous tests, doctors determined that she was a matching donor. The surgery that saved Gerardo's life was performed on the most appropriate day: Valentine's Day 2024. Today Mónica and Gerardo are strong advocates of organ donation.

Kerri Ogrudek donated her kidney to her husband Bobby’s sister when he was not a match. This also inspired her to run the NYC Half Marathon for NKF—only ten months after the procedure. Bobby set up a fundraising page and ran several endurance races for NKF, including the TCS NYC Marathon, a 50 Mile Ultra Marathon, and VA’s 100 Mile Ultra Marathon, and spoke at the Long Island Kidney Walk. These extraordinary efforts have resulted in amazing fundraising for NKF.

Holly Mattix-Kramer, MD, MPH, is a leader, advances clinical knowledge and research, and engages in faculty mentorship as Past National NKF Board President, and current NKF and NKF of Illinois Board member. Her multi-level engagement includes serving on the NKF Scientific Advisory Board and NKF KDOQI leadership, advocacy for passing the 2019 Illinois Living Donor Protection Act, continued service as medical consultant for KidneyMobile, and financial support. She was 2024 Honoree of the NKFI Board Member Award and is passionate about our Mission.

Dan Emerson is the Director of Digital Marketing at the NKF National office. Starting in 2018, he has worked to engage with the kidney community and provide them with resources and information to support them on their health journey. In June of 2024, Dan donated his kidney to an anonymous recipient through a non-directed donation. He lives in Upstate New York with his husband and son.

Dr. Francis L. Delmonico is a renowned transplant surgeon and professor whose career spans more than 35 years at Harvard Medical School and Massachusetts General Hospital. A former NKF Board member and recipient of the David M. Hume Lifetime Achievement Award, he has shaped transplantation policies internationally. His leadership with the World Health Organization, The Transplantation Society, and the Declaration of Istanbul Custodian Group helped establish ethical standards for organ donation. His vision and advocacy continue to advance kidney care, offering hope and improved outcomes to patients around the world.

Dr. Paul Palevsky has dedicated his career to transforming kidney care through clinical excellence, research, and leadership. A past President of the National Kidney Foundation and a renowned nephrologist, Dr. Palevsky has played a pivotal role in advancing evidence-based treatment guidelines and shaping NKF’s clinical initiatives. His groundbreaking research, particularly in acute kidney injury and critical care nephrology, has improved outcomes for countless patients. Through his mentorship and advocacy, Dr. Palevsky continues to inspire the next generation of healthcare professionals and ensure that kidney patients receive the highest quality care.