The Bloodline with Blood Cancer United Podcast

What happens when a resilience expert becomes the caregiver? When a loved one is diagnosed with blood cancer, you’re suddenly balancing fear, advocacy, and everyday life all at once. In this episode, we sit down with Karen Reivich, PhD, a resilience expert, caregiver, and wife of a lymphoma survivor. Karen opens up about the reality of supporting her husband through treatment and a clinical trial, sharing invaluable lessons on managing uncertainty, accepting help, and caring for yourself while

Brice Davis After being diagnosed with multiple myeloma at age 31, Brice Davis faced challenges that extended far beyond treatment alone. Join us as he talks about balancing fatherhood, navigating mental health struggles, rebuilding after setbacks, and adjusting to life with a chronic blood cancer. Brice reflects on the importance of community, resilience, and focusing on what matters most while creating a fulfilling life after diagnosis. DOWNLOAD TRANSCRIPT CLICK HERE to participate in our ep

AJ Kitt In this episode, four-time Olympic downhill skier AJ Kitt shares his diagnosis of chronic myeloid leukemia (CML) and how revolutionary medical advances transformed an unsettling diagnosis into a manageable part of his everyday life. AJ opens up about the initial shock of the news, the emotional toll it took on his young family, and how finding CML pioneer, Dr. Brian Druker, restored his confidence amid deep uncertainty. The conversation dives into his treatment with tyrosine kinase inh

Laura DeKraker Lang-Ree When a child is diagnosed with cancer, parents are suddenly expected to manage medications, appointments, treatment decisions, family life, and overwhelming emotions, often all at once. In this episode, we speak with Laura DeKraker Lang-Ree, pediatric cancer parent, advocate, and author of The Cancer Parent’s Handbook, about the practical guidance she wishes every family received from day one. Laura shares powerful insights from her family’s journey after her three-year

Jay Yang, MD You cannot have progress without research. In our latest episode, Dr. Jay Yang of the Karmanos Cancer Institute in Detroit, MI, breaks down the essentials of MDS care, from risk-based treatment plans to managing fatigue and exploring promising new therapies. Tune in to find out why the future of MDS treatment is brighter than ever. DOWNLOAD TRANSCRIPT CLICK HERE to participate in our episode survey. Mentioned on this episode: Myelodysplastic syndromes (MDS) MDS patient videos A

Kim and Josh Woda Two college students. Two lymphoma diagnoses. One unexpected love story. In this episode, we speak with Kim and Josh Woda, who were both diagnosed with Hodgkin lymphoma while attending college. They share how they navigated school during treatment, coped with relapse and stem cell transplant, found support in the cancer community, and unexpectedly found each other. Their story is a powerful reminder that connection, understanding, and hope can appear when you least expect it.