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The Sumaira Foundation
in MOG, Patient, Voices of NMO
Je m’appelle Nelly, j’ai 44 ans et je vis dans un joli village dans l’Oise et j’ai la MOGAD. Sans le savoir cette maladie m’avait déjà fait un petit clin […]
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The Sumaira Foundation
in Caregiver, MOG, Voices of NMO
Ciao a tutti, mi presento, sono la mamma di Auri. Mi piace presentarmi così, perché questa è la sua storia, la storia di una bambina bella e forte che nel […]
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The Sumaira Foundation
in News & Announcements
On Saturday, March 9, 2024, we hosted our New England Patient Day for NMOSD & MOGAD in Boston in collaboration with Dr. Michael Levy and Dr. Marcelo Matiello of Massachusetts […]
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The Sumaira Foundation
in NMO, Patient, TM, Voices of NMO
It all began in early 2020 when Kayla noticed a tingling sensation in her right leg. She didn’t think too much about it and figured it would go away. Thinking […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
Hello. Hola. My name is Marie and I am proud to be the Welcome Manager for The Sumaira Foundation. I was diagnosed with NMO in 2007 when I was only […]
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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 […]
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Posted 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 […]
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Posted 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 […]
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Posted 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. […]
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Posted 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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