#130: Living with MS Abroad: Robert Joyce on Research, Resilience and a New Life in Spain
In this interview, Robert Joyce talks about living with MS abroad. He shares his move from Ireland to Spain, differences in healthcare, and how climate affects his health. We also explore his blog A 30 Minute Life and why patient involvement makes research stronger.
#120: From MS to Advocacy. How One Young Scientist Is Changing the Conversation with Luigi Azzarone
Luigi Azzarone received his MS diagnosis at just 17 years old — an experience that not only reshaped his daily life but also sparked his journey into MS advocacy and scientific research. In this podcast episode, he shares how the question “What’s happening in my body?” led to a deep interest in neuroimmunology. Today, Luigi […]
#105: The Sumaira Foundation & NMO: How One Woman’s Journey is Changing Lives Worldwide
Neuromyelitis Optica Spectrum Disorder (NMOSD) is a rare autoimmune disease that can feel isolating and overwhelming. But for Sumaira Ahmed, her diagnosis became the spark that ignited a global movement. In this episode, we dive into her personal journey with NMO, the challenges she faced, and the resilience that led her to create The Sumaira […]
#090: Empowering the black MS community – advocacy, awareness, and support with Natalie Diana Busari
Natalie focuses primarily on advocacy, awareness and support in her work to empower women and girls from the black MS community.
