What happens when one autoimmune or neuroimmune condition isn’t the whole story? For some patients, receiving multiple diagnoses can bring even more questions and uncertainty. Join Dr. Lilyana Amezcua from […]
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 […]
Turning Miles into Medical Progress - Join us on September 13th for TSF's 2nd 5K to raise money for research! Last year's inaugural 5K helped fund a groundbreaking AI-powered diagnostic […]
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 Michigan! Are you or your loved one impacted by: CIDP*, MG*, MOGAD*, or NMOSD*? You're invited to our event on Saturday, September 19th. Join us for a […]
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 […]
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 […]
¡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 […]
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 […]
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 […]
¿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. […]
