Scams and financial fraud are constantly evolving, and knowing what to look for can help you protect yourself and your loved ones. In the final session of our three-part Financial […]
¿Usted o un ser querido vive con NMOSD? Lo invitamos a acompañarnos en un webinar especial titulado **"Comprendiendo el anticuerpo AQP4 en NMOSD"**, con la Dra. Pilar Perachino, de Argentina. […]
Join TSF and IPMSSG on October 20, 2026, on the 22nd floor of the SickKids Patient Support Centre for an exclusive evening connecting global leaders in neuroimmunology. Enjoy an inspiring […]
Are you a clinician, researcher, fellow, resident or trainee interested in NMOSD, MOGAD and related neuroimmunological disorders? Join us for an evening of discussion, mentorship and networking with leading experts […]
Steroids can be an important part of treatment for many rare neuroimmune conditions, but what happens when they’re used over a longer period of time? Join Dr. Amy Kunchok for […]
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 […]
The Caregivers Human Collective Project (HCP) is a groundbreaking support group hosted by The Sumaira Foundation, created specifically for caregivers of individuals living with rare neuroimmune diseases like NMOSD and […]
À tous les patients et aidants touchés par des maladies auto-immunes et auto-inflammatoires rares en France et en Belgique ! Vous ou l'un de vos proches est touché par : […]
We're coming to Los Angeles! TSF is inviting patients and caregivers impacted by rare neuroinflammatory & related disorders from California & the west coast! Are you or your loved one impacted […]
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 […]
The Caregivers Human Collective Project (HCP) is a groundbreaking support group hosted by The Sumaira Foundation, created specifically for caregivers of individuals living with rare neuroimmune diseases like NMOSD and […]
