When your child is living with a neuroimmune disease, the questions can feel endless. What is happening in their body? What does a diagnosis mean for their future? And how can parents and caregivers feel more confident navigating care? Join Dr. Kristen Fisher of Texas Children’s for an approachable conversation about pediatric neuroimmune diseases. Together, […]
We're coming to Miami! Are you or your loved one impacted by: CIDP*, MG*, MOGAD*, or NMOSD*? You're invited to our event on Saturday, September 26th. 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 about symptom management, treatments and therapies, […]
¡Nos vemos en Miami! ¿Usted o un ser querido vive con CIDP*, MG*, MOGAD* o NMOSD*? Lo invitamos a acompañarnos en nuestro evento el sábado 26 de septiembre. Acompáñenos a disfrutar de un día de educación, comunidad y convivencia para: • Conocer a pacientes, aliados, cuidadores y profesionales de la salud de su comunidad. • […]
Juniors in Neuroimmunology: Meet the Expert – 2nd Edition Il corso, dedicato a giovani neurologi e assistenti in formazione, si propone di fornire una formazione aggiornata sulla diagnosi e sul trattamento delle principali patologie autoimmuni a carico del Sistema Nervoso Centrale e Periferico (incluse NMOSD/MOGAD, encefaliti autoimmuni, miastenia gravis, neuropatie autoimmuni, miositi, sindromi paraneoplastiche e […]
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 […]
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 MOGAD. This first-of-its-kind session offers a safe, inclusive space for family members, partners, siblings, children, and loved ones to connect, share, and be heard. Led […]
¿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. En esta sesión, la Dra. Perachino explicará qué es el anticuerpo AQP4, cuál es su papel en el NMOSD, cómo contribuye al diagnóstico de la […]
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 […]
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 […]
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 […]
