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Posted by: The Sumaira Foundation in NMO, Patient, Professional, Voices of NMO
Three years ago, right in the middle of my medical internship, I was diagnosed with Seronegative NMOSD. I took a leave of absence, not knowing if I could go back […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
November 8, 2023 — The Sumaira Foundation is pleased to welcome Professor Jefferson Becker of the Pontifical Catholic University of Rio Grande do Sul (PUCRS) in Brazil to join TSF’s international […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
When you and God have different plans, stories like ours get created. My name is Sonali Tambatkar and I live in Mumbai, India. It all started in May 2012: I […]
Read MorePosted by: The Sumaira Foundation in
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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
November 1, 2023 — The Sumaira Foundation is pleased to welcome Prof. Kazuo Fujihara of Fukushima Medical University School of Medicine in Japan to join TSF’s international Medical Advisory Board. […]
Read MorePosted by: The Sumaira Foundation in
Posted by: The Sumaira Foundation in
Posted by: The Sumaira Foundation in
Posted by: The Sumaira Foundation in
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 […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMO, Voices of NMO
You never know what someone’s going through. I have always been told this and I believe it. Still, I never really thought about it until my mom was diagnosed with […]
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