『Living with Lupus: Wendy Rodgers on Survival, Advocacy & Healthcare Bias』のカバーアート

Living with Lupus: Wendy Rodgers on Survival, Advocacy & Healthcare Bias

Living with Lupus: Wendy Rodgers on Survival, Advocacy & Healthcare Bias

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概要

In this deeply moving episode of At the Table with Greg & Elliott, Greg Mathis Jr. and Elliott Cooper sit down with Wendy Rodgers, M.Ed, MPH, Director of Care and Support Services at the Lupus Foundation of America, for a powerful conversation about survival, advocacy, and purpose.

Wendy shares her journey living with lupus — a disease that began showing signs in her teens but went undiagnosed for years. After being dismissed by doctors and navigating medical bias, her lupus progressed to kidney failure at just 27 years old, ultimately leading to dialysis and a life-saving kidney transplant. She speaks candidly about the physical toll of autoimmune disease, the emotional weight of not being believed, and the financial devastation that chronic illness can bring.

The conversation expands beyond medicine into healthcare disparities affecting Black women, the importance of self-advocacy, and why participation in clinical research is critical for equitable treatment outcomes. Wendy also discusses faith, boundaries, mental health, and how learning to say “no” became part of her healing process.

With honesty and wisdom, Wendy reminds us that while lupus is unpredictable and often invisible, strength, community, and education can change outcomes. Her story is not just about illness — it’s about resilience, purpose, and fighting to live fully.

For lupus resources and support, visit lupus.org.

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