“Is it ever enough… or are we always waiting for the next breakthrough, the next voice, the next reason to hope?”
We found ourselves in an unexpected place for this episode: talking about Multiple Sclerosis (MS) through the lens of the NFL Draft.
Of course, the #1 overall draft pick and Heisman Trophy winner Fernando Mendoza was making lots of headlines, but the stories went way beyond his leadership on the football field.
Mendoza also was gaining attention for championing efforts to raise awareness and funding for research to end MS, the disease which his mom, Elsa, has lived with since 2008.
So when a high-profile moment shines a spotlight on MS, whether it’s with the #1 NFL draft pick or a celebrity diagnosis, it raises a bigger question:
What do we actually want from that attention?
Visibility definitely opens the doors for MS advocacy and research, but it can also create comparisons that don’t reflect the reality of living with MS. As with everything in MS, there is more than one answer.
In this episode, we explore the complicated mix of MS awareness, expectations, frustration, and hope that comes with seeing Multiple Sclerosis represented in the public eye and across media. We talk about:
- The impact of celebrity MS stories on awareness and perception
- Why increased visibility doesn’t always lead to a cure for MS
- How different voices shape the narrative around chronic illness and disability
- Why “control what you can control” matters when living with MS
We also reflect on how far the MS community has come—from just a few disease-modifying therapies to more than two dozen today—and why, even with that progress, it still can feel like we’re waiting.
Here are the links that offer further insights into our conversation:
- Listen to the MeSsy podcast with Christina Applegate and Jamie-Lynn Sigler
- Learn more about our Walk MS team, Team MonsterS, and how you can support us
- Check out the powerful video from Max the Dollar Kid and consider making your $1 donation
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We’d love to hear from you
What do you expect when celebrities or public figures talk about MS? Share your thoughts in the comments or email us at acoupletakesonms@gmail.com.
Remember to rate, review, and subscribe to A Couple Takes on MS Podcast for two insightful perspectives on this one multifaceted disease