My Experience with Chronic Illness

Hi everyone, and welcome to this quick episode. I wanted to take a moment to introduce myself and share some of my journey with chronic illness. I live with rheumatoid arthritis and hypermobile Ehlers-Danlos Syndrome, two conditions that have touched almost every part of my life. For me, illness hasn’t just been about navigating symptoms, treatments, or doctors’ offices. It’s been about confronting the larger systems of ableism and sexism that shape how people are seen, treated, and valued.

Living in a body that doesn’t always cooperate has forced me to redefine what makes me worthy: not productivity, not being “easy” or “convenient,” but the inherent value I hold as a person. That hasn’t been an easy lesson. It’s been a process of learning through frustration, sadness, resilience, and the slow unlearning of the belief that my worth is tied to how well I can perform for others.

By sharing my story, I aim to contribute to the ongoing development of this platform, fostering open and honest conversations about illness, identity, and care. This podcast is about making space for the messy truths of living with chronic conditions, and also about the power we find in telling our stories and building community.

Take care of your spoons!
If you're interested in being interviewed for this podcast or want to let me know your thoughts on this episode, email me at dickersonmm@g.cofc.edu and follow @thesickgazepod on instagram!