Innovation in Our DNA: Family, Genetics & the Changing Story of Multiple Myeloma
Innovation in multiple myeloma isn’t only found in research and new tools — it also lives in our families and shared experiences. During Myeloma Awareness Month, Nia Bailey, President of the Byrd Cancer Education & Advocacy Foundation, shares her family’s multigenerational cancer journey and how that experience led to advocacy, awareness, and community education that are reshaping how multiple myeloma is recognized and navigated across generations.
Valarie introduces the agenda of the event and our featured speaker Dr. Nia Imani Bailey, DPA, M.A.Ed., RT(T)
Dr. Bailey talks about genetics and multiple myeloma
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Valarie Traynham
Valarie embarked on her myeloma journey back in 2015, and ever since she's been on a mission. As a resilient myeloma thriver, her passion lies in not just navigating her own path but also in illuminating the journey for others. With a steadfast commitment to understanding the intricacies of the disease, she champions education, shedding light on health inequities that often lurk in the shadows. Driven by a profound belief in fairness, Valarie tirelessly advocates for equitable access to top-tier healthcare, clinical trials, and tailored treatments. Her journey as a beacon of knowledge and support began when she assumed the role of a support group leader. Today, she continues to extend her hand as a myeloma coach, mentor angel, and the guiding force behind the Black Myeloma Health Community. Valarie's voice echoes far and wide as she fearlessly confronts the disparities faced by myeloma patients. Through collaborative efforts with healthcare providers, she strives to forge pathways to solutions, ensuring that every individual receives the care they deserve. Join Valarie on her journey of empowerment and advocacy as she lights the way toward a brighter, more equitable future in myeloma care.