National Multiple Sclerosis Society

“My queer identity cannot be dismissed, and my lived experience cannot be reduced to a single idea, perception … or box.”

Over 700 people gathered June 15-16 to learn from leading scientific and healthcare experts and to give voice to the unique needs of the Black MS community.

Tips to help manage spasms and stiffness.

New vaccine guidance for people living with MS plus the latest information and resources.

Meet Chidiebere Ibe, the medical student creating medical illustrations with Black skin to promote diversity and address bias.