The Journey Continues

When Curtis Warfield was diagnosed with kidney disease, his life changed forever. After receiving a life-saving living donor transplant, he chose not to focus on fear but on purpose. In this episode, he shares his powerful path from peritoneal dialysis to becoming a kidney advocate, peer mentor, and voice for patient-centered care. Hear how Curtis is working to advance legislation, support other patients, and push for research that truly reflects the patient experience.

In this special episode, host Monica Fox is interviewed by her daughter, Olivia Fox. Together, they share the emotional journey of Monica’s life-saving kidney transplant, reflect on the impact of this experience, and discuss the passion it sparked to help others facing kidney disease. Hear a story of hope, gratitude, and the power of family. This episode is sponsored by Fresenius Kidney Care.

Glenda Roberts has lived with kidney disease for decades, navigating the challenges of dialysis and transplant while carving a path as a national advocate. In this episode, she shares her journey from patient to leader, how she ensures patients’ voices are heard in research and healthcare, and practical advice for anyone looking to make an impact. Hear why Every Voice Counts in shaping the future of kidney care.

Becoming a living kidney donor is one of the most selfless acts a person can take, but it’s also a deeply personal decision. What does it really take to become a living donor? We explore the journey of donation, from the tests and surgeries to the emotional support along the way. Hear how one choice can change lives, bust common myths, and how one decision can change two lives forever.

When her brother’s kidney failure became life-threatening, Monique Hoskins didn’t hesitate: she stepped up as a living kidney donor. In this episode of The Journey Continues, Monique shares her decision-making process, the challenges of surgery and recovery, and how this selfless act brought her family closer together. She also discusses her mission to advocate for living donation, raising awareness, and inspiring others to make a difference.

Mom Jen Strouse and her hero/son EJ have faced more health challenges in his 10 years than most families will face in a lifetime. Born with just one kidney that wasn't fully functioning, he eventually received a kidney transplant that unfortunately came with even more complications. Through it all, Jen has remained resilient and works hard to create some normalcy for her son. 

Follow EJ's journey on Facebook here. 

Diagnosed with juvenile insulin dependent diabetes at age four, Daja Weathers had no idea how her future would look. Although complications later in life led her to a kidney and pancreas transplant, advocating for organ donor awareness and transplantation has now become her mission. 

When Brooke Wozniak learned fellow volleyball mom Sue suffered from the same rare condition as her own mother, she offered Sue her kidney without hesitation. That spur-of-the-moment decision became a mission for Brooke – one she wanted to see all the way through.

Chicago Public Schools’ Deputy Chief Talent Officer Jerry Taylor’s college experience was turned upside down when he learned he was living with a rare kidney disease – one that would later claim the lives of his mother and beloved sister. Jerry’s years on dialysis, strong support system, and advocacy work help him inspire others who are facing similar struggles.

 Leah Howell, PhD is a not just a kidney recipient, she’s an advocate, kidney ambassador, and this year she’s a marathon runner.  She and her 21-year-old transplanted kidney Joey are training for the Chicago Marathon with Team Kidney to show the world just what transplant recipients are capable of.

Follow Leah’s journey on social media! You can find her on Facebook and Instagram