Last month, I had the privilege of participating in Conversations on Cannabis, an educational series presented by Florida A&M University’s Medical Marijuana Education and Research Initiative (MMERI). The topic was one that resonates deeply with me—medical marijuana and its potential to bring relief to those living with chronic illnesses like Multiple Sclerosis.
Living with MS has taught me a great deal about strength, resilience, and the complexity of the human body. It’s also taught me how frustrating the search for effective symptom management can be. While I don’t currently have a medical marijuana card, I understand firsthand the relentless nature of MS—fatigue, neuropathy, mobility challenges—and the long list of prescription medications we often rely on.
The conversation, which featured the insightful and compassionate Dr. Terel Newton, was both empowering and educational. It wasn’t just about the science of cannabis—it was about patient stories, lived experiences, and breaking through the stigma to consider all options for relief.
What made this experience even more meaningful was the chance to speak not only as a person living with MS, but as a community advocate through my nonprofit, On My Nerves. This organization was born from my desire to bridge the gap between patients and resources—to create a space where people living with MS feel seen, supported, and informed.
Being part of this discussion reminded me why I do this work. Advocacy isn’t just about raising our voices—it’s about connecting, educating, and inspiring change. It’s about turning our challenges into catalysts for community, empowerment, and hope.
I’m incredibly grateful to MMERI and FAMU for creating space for these important conversations. The more we talk, the more we learn—and the more we move forward, together.
If you’re interested in learning more, I invite you to:
Let’s keep the conversation going.
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