TSF Research Update & Award Ceremony
If you're attending ECTRIMS in Barcelona, we invite you to attend TSF's Research Update & Award Ceremony at Casa Llotja de Mar. Join us for an evening with research updates, […]
If you're attending ECTRIMS in Barcelona, we invite you to attend TSF's Research Update & Award Ceremony at Casa Llotja de Mar. Join us for an evening with research updates, […]
Join us on September 26, 2025 for ECTRIMS Patient Community Day – an exclusive, free event designed for individuals living with MOGAD, MS, NMOSD and related neurological conditions. Patient Community Day is an […]
Join us on Sunday September 28th in Weston, Massachusetts to run, walk, socialize, and raise funds. (Registration/attendance comes with a free t-shirt). This event is being organized by Terry Clark, […]
Descubre por que el Yoga es para todos y puede ayudarte. El yoga no es esa idea que se tiene de una disciplina física. El Yoga es mas que físico, […]
HCP is a great way to meet others in similar circumstances in this rare community; it is a safe space to laugh, cry, vent, share wins, etc. This program is driven and led by TSF Patient and Caregiver Ambassadors worldwide.
Czy Ciebie lub kogoś bliskiego dotknęła plaga MOGAD? Dołącz do nas 14 października o godzinie 18:00 czasu środkowoeuropejskiego, aby zapoznać się z eksperckim przeglądem MOGAD, obejmującym objawy, rokowania i leczenie, […]
Siete tutti invitati al webinar - Salute femminile e NMOSD/MOGAD: dialogo su gravidanza, allattamento e sessualità - esclusivo di TSF Italia dedicato alle donne che vivono con NMOSD o MOGAD! Data: 15 ottobre alle 19:00 CET Relatrice: Dott.ssa Sara Carta, esperta in Neuroimmunologia presso l'Università di Verona Temi: Gravidanza, Allattamento e Sessualità - aspetti […]
We're coming to Seattle! Are you an AE*, CNS Vasculitis, MOGAD*, neurosarcoidosis, NMOSD* or SPS* patient, partner, care-partner, clinician, nurse, researcher and/or advocate from the Pacific Northwest region? You're invited […]
The Human Collective Project (HCP) is a community initiative for people living with NMOSD, MOGAD and other rare neuroimmune diseases, to come together in a safe, confidential and encouraging space. […]
The Mental Health Monday meetings began as a way to address the various mental and emotional concerns that individuals experience when dealing with rare neuroimmune diseases. Patients, caregivers, and loved […]
Calling Canadians impacted by NMOSD: you're invited for a live patient education webinar about how to navigate life with neuromyelitis optica spectrum disorder in Canada. Join us on Wednesday, November 5th at 7 PM EST for a live presentation and discussion with Dr. Dalia Rotstein, neurologist at The University of Toronto and a globally-recognized expert […]
We're coming to Toronto! Are you an AE*, MG*, MOGAD* or NMOSD* patient, partner, care-partner, clinician, nurse, researcher and/or advocate in Canada? You're invited to our event on Saturday, November 8th. Join us for a day of education, community, and fun to: Meet local patients, partners, care-partners and clinicians Ask experts questions in real time […]
