Kate talks with psychologist, Dr. Amy Sullivan and Elizabeth, who has been living with MS, about the emotional burden that people may experience when diagnosed with MS, as well as during various stages of the condition.

Kate talks with registered dietitian-nutritionist, Mona Bostick and physical therapist, Dr. Gretchen Hawley about eating well, moving well, and living well with MS.

Kate is joined by neurologist and MS specialist, Dr. Mitzi Joi Williams, and Dawn Morgan, a person living with MS and an influential voice in the community. They will discuss diversity, equity, and inclusion in the MS community in the second of two episodes.

Kate is joined by neurologist and MS specialist, Dr. Mitzi Joi Williams, and Dawn Morgan, a person living with MS and an influential voice in the community. They will discuss diversity, equity, and inclusion in the MS community in the first of two episodes.

Skeery and Dr. Barry Singer discuss changes in MS symptoms—which can be both cognitive and physical—and why you should talk with your health care practitioner about them.

Skeery and Dr. Maria Houtchens discuss evolving treatment approaches and considerations for relapsing MS—including receiving a COVID-19 vaccine.

Skeery speaks with Tim Coetzee of the NMSS, as well as innovators Maayan Ziv and David Hojah, about emerging technologies and designs that could help improve mobility and accessibility for those living with MS and other neurological conditions.

Kate, MS patient advocate, is joined by Diana and Kristen to discuss their individual journeys of being diagnosed with, and living with, MS.

Kate Milliken, patient advocate, takes an in-depth look at the role of MRI in MS with Dr. Robert Zivadinov MD, PhD, and Professor of Neurology at the University at Buffalo

Skeery talks telemedicine and virtual health care visits with Dr. Aaron Boster alongside his patient, Scott.