Choose Your Language:
Posted by: The Sumaira Foundation in News & Announcements
August 10, 2022 – The Sumaira Foundation is pleased to welcome Dr. Sara Mariotto, neurologist at Azienda Ospedaliera Universitaria Integrata Verona (AOUI Verona), as the first member from Italy America to join […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On July 28, 2022, TSF was joined by 100 friends of the Foundation to celebrate 8 years of illuminating the darkness of NMOSD and MOGAD at The Envoy Hotel’s Lookout […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
BOSTON, MA, August 4, 2022 – The Sumaira Foundation (TSF), a nonprofit organization focused on the rare neuroimmune diseases of NMOSD and MOGAD, is pleased to announce that it is […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Every day we wake up, we surely never expect our day to end with everything turned upside down – and our life changed forever. But it is exactly what happened […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
FUNDING OPPORTUNITY ANNOUNCEMENT In 2022, The Sumaira Foundation is awarding research grants (maximum award up to $25,000) to nonprofit organizations, researchers, and/or institutions engaged in research into prevention, treatments, and a cure(s) for neuromyelitis optica […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
While I was pregnant, I began having blurred vision. I went to see ophthalmologists, opticians, and general practitioners, but they kept saying nothing was wrong. I was sent to see […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
You’re invited to attend an exclusive summer event to Celebrate 8 Years of TSF Thursday, July 28 @ at 6:30 PM The Envoy Hotel Lookout Rooftop & Bar (70 Sleeper […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Hi, my name is Noelani. I am 30 years old, was born and raised in Hawaii but currently reside in Nevada! Looking back, there were signs throughout my childhood of […]
Read MorePosted 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, Voices of NMO
It started innocuously. In 2008 we moved to Ottawa with my employer for my career in pest control. On a gray, cloudy but humid day, I was out removing a […]
Read More
