Choose Your Language:
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 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 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 […]
Read MorePosted by: 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, […]
Read MorePosted by: 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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
June 21, 2023 — The Sumaira Foundation is pleased to welcome Álvaro Cobo-Calvo, MD, PhD, of the Multiple Sclerosis Centre of Catalonia (CEMCAT) in Barcelona, Spain, to join TSF’s Medical Advisory […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMO, Professional, Voices of NMO
I am a caregiver to my daughter, Nell, who was diagnosed with NMO at age 9. Prior to her diagnosis, she was an active, vibrant girl playing travel lacrosse, robustly […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
On Monday, I woke up with a slight ache on the left side of my lower back which felt numb, like a bruise but without the pain. This numb spot […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Bonjour à tous, je m’appelle Fatiha. J’habite à Étalleville en Normandie. Je suis tombée malade le 20 février 2016. Date anniversaire de la mort de mon père. Double peine pour […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 3, 2023 — The Sumaira Foundation is pleased to welcome Fabienne Brilot, PhD, of the University of Sydney (Australia) to join TSF’s medical advisory board. Fabienne Brilot, PhD Professor […]
Read More
