Listening to the Body: A Journey of Diagnosis, Research, and Recovery with Tracy Phillips

Real change starts when every voice is heard.

In this episode of Voices of Inclusive Research, Renarda Jones welcomes Tracy Phillips, a dedicated advocate for inclusion in clinical trials. Tracy shares her deep insights into the critical role genuine representation plays in transforming clinical research and ensuring no community is left behind. She emphasizes the importance of intentional outreach, offering thoughtful strategies to bridge the gaps in underrepresented communities and make clinical research more equitable and impactful.

This conversation is packed with actionable insights, offering a practical roadmap for researchers, healthcare professionals, and advocates who are committed to making a difference. Tracy’s perspective on amplifying every voice in clinical research reminds listeners that true inclusivity is not just an ideal but a necessity for driving meaningful change and delivering better healthcare outcomes for all.

If you’re looking to be inspired and equipped with ideas to break down barriers in clinical research, this episode is a must-listen. Tracy and Renarda challenge the status quo and call for bold, innovative steps to ensure everyone’s voice is heard and valued in the research landscape. Listen now to join the conversation, spark meaningful change, and help shape a more inclusive and equitable future in clinical research. This episode isn’t just about learning—it’s about being part of a movement that transforms how research connects with the world.

Must-Hear Insights and Key Moments

• The Power of Support Networks: Tracy Phillips emphasizes the importance of a reliable support network during critical health challenges. His journey revealed the true nature of his relationships, showing who genuinely stood by him in tough times.
• The Importance of Advocacy and Research: Tracy’s story highlights the need for patients to be their own advocates by conducting thorough research and asking questions. He stresses that understanding treatment options, side effects, and clinical trial opportunities is crucial for informed decision-making.
• Stress and Healing: Tracy underscores the detrimental impact of stress on health, particularly for individuals managing conditions like multiple myeloma. He advocates for setting boundaries with stressful individuals and environments to create a healing space.
• Challenges in Clinical Trial Access: Tracy shares his frustration with being disqualified from clinical trials after starting medication. He stresses the need for better education for newly diagnosed patients about trial eligibility and timing.
• Gratitude and Perspective: Despite his diagnosis, Tracy maintains a sense of gratitude and humor, finding silver linings in his experience, such as deeper connections with loved ones and an appreciation for life.
• The Role of Healthcare Providers: Tracy's journey reveals the gaps in communication between healthcare teams and patients, particularly in providing clear, actionable guidance. He calls for more collaboration between healthcare providers and clinical researchers to inform patients about trials early in their diagnosis.

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