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2023 Virtual Legislative Lobby Day

Posted by: The Sumaira Foundation in

Autoimmune Association

Join autoimmune patient advocates nationwide on March 29, 2023, for the National Coalition of Autoimmune Patient Groups’ first virtual Congressional Fly-in Day. Advocates will meet virtually with legislators and staff […]

TSF Partners with PAN Foundation

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 […]

Christy’s NMO Story – Being Heard Makes All the Difference

Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO

Christy Abercrombie

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 […]

Julie’s NMO Story – Transforming Curses Into Blessings

Posted 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 […]

EVENT RECAP | NMO Picnic in the Park

Posted by: The Sumaira Foundation in News & Announcements

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 […]

Industry Partners

Alexion

Genentech

Portal Instruments

Community Partners

Autoimmune Association

Brain Health Center of the Rockies

couch pennies foundation

emsp

global advocacy alliance

National Infusion Center Association

Siegel Rare Neroimmune Association

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