Choose Your Language:
Chinese (Simplified) 
Chinese (Traditional) 
Danish 
Dutch 
English 
French 
German 
Italian 
Portuguese 
Spanish Posted by: The Sumaira Foundation in News & Announcements
WASHINGTON, May 26, 2022—The PAN Foundation and The Sumaira Foundation (TSF) today announced they are launching a new partnership to help people living with neuromyelitis optica spectrum disorder (NMOSD), providing […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Christy and I’ve been fighting this disease without knowing what I was up against since before 2008… I started calling this thing my “venom” because it reminded […]
Read MorePosted by: The Sumaira Foundation in NMO, ON, Patient, TM, Voices of NMO
Julie has had NMO for at least a dozen years. From before and since that time, she has been diagnosed with a number of other conditions. She has been […]
Read MorePosted by: The Sumaira Foundation in Events
Thank you to everyone who made our NMO picnic in the Park such a wonderful day! We loved kicking off autumn at the Parkman Bandstand in Boston Common, especially alongside our NMO superheroes, families, friends + and the […]
Read More
