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The Sumaira Foundation
in News & Announcements
September 29, 2023 — The Sumaira Foundation is pleased to welcome Professor Orhan Aktas of Universitätsklinikum Düsseldorf in Germany to join TSF’s international Medical Advisory Board. Pr. Aktas joins TSF as […]
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The Sumaira Foundation
in NMO, Patient, Voices of NMO
May 15, 2021 – a date I’ll never forget, but I didn’t know then that it would change my life in such a drastic way… I woke up feeling nauseous, […]
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The Sumaira Foundation
in News & Announcements
On Friday, September 8, 2023, we were honored to celebrate 9 years of The Sumaira Foundation alongside many of the leading neuroimmunologists and researchers who were in Boston for the […]
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The Sumaira Foundation
in NMO, Patient, Voices of NMO
I am Preethi, residing in Coimbatore, famously known as the Manchester of South India. This narrative is a chronicle of my journey, one that reflects my triumph over adversities and […]
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The Sumaira Foundation
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The Human Collective Project (HCP) is TSF’s support group meetings offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
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The Sumaira Foundation
in NMO, Patient, Voices of NMO
My name is Kailee. I am a mom, wife, daughter, teacher, dance instructor, and I have neuromyelitis optica spectrum disorder (NMOSD). I was diagnosed at 25 years old, in May […]
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The Sumaira Foundation
in News & Announcements
September 5, 2023 — The Sumaira Foundation is pleased to welcome Professor Lekha Pandit of Nitte University in Mangalore, India, to join TSF’s international Medical Advisory Board. Pr. Pandit joins TSF […]
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Posted by:
The Sumaira Foundation
in
The Human Collective Project (HCP) is TSF’s support group meetings offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
Read
More
Posted by:
The Sumaira Foundation
in News & Announcements
August 14, 2023 – The Sumaira Foundation (TSF) is pleased to welcome Leda Bresnov to our leadership team as International Ambassador Liaison. As of August 2023, the Foundation is proud […]
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The Sumaira Foundation
in NMO, Patient, Voices of NMO
At age eight, when I first started chemotherapy for my autoimmune disease, the neurologist told my parents the maximum amount of time I could be on it was three years, […]
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