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.
Are you an NMOSD*, MOGAD*, AE*, MG* or SPS* patient, caregiver, clinician, nurse, researcher and/or advocate in the Chicagoland area? You're invited to our event on Saturday, July 26th at Rush University Medical Center's Searle Center. We are proud to collaborate on this event with the Chicago MS Alliance. Join us for a day of […]
The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 pandemic in 2020, when most NMOSD/MOGAD felt particularly isolated and vulnerable to the coronavirus as immunosuppressed/immunocompromised members of society. The isolation many of us experienced […]
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, recognition of outstanding achievements in the field and networking with a community dedicated to pushing the boundaries of science and technology. During this time, we […]
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 opportunity to learn about the latest research advancements directly impacting your ongoing care and treatment options. The programme will include engaging roundtable discussions led by […]
