MS-Patienten Beiträge

Luigi Azzarone received his MS diagnosis at just 17 years old — an experience that not only reshaped his daily

Neuromyelitis Optica Spectrum Disorder (NMOSD) is a rare autoimmune disease that can feel isolating and overwhelming. But for Sumaira Ahmed,

In this episode, I am joined by Roxy Murray, also known as the “Multiple Sclerosis Fashionista”. Roxy is a passionate

Natalie focuses primarily on advocacy, awareness and support in her work to empower women and girls from the black MS community.

Meet NMO patient Leda Bresnov, a strong and inspiring woman who is originally from Brazil and has been living in

Today I’m talking to Crys about her life with multiple sclerosis as a first generation Latina. Crys was diagnosed at

MS patient and adovcate Rachel Horne sponsors a prize for women in MS research and campaigns for more diversity in clinical trials.

Blake Arnet talks about his motivation for the Dunk MS fundraiser event that takes place each spring in Los Angeles.

I show you how to make the best of your life with MS from family to career to hobbies. Thanks to science and research, a lot is possible nowadays.

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