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Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Much has changed in my world since my initial story had been published on TSF’s website in 2020. (scroll below to read the original piece) One of the more notable […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Hola ¿Tienes 2 minutos? Déjame contarte parte de mi historia. Esta comienza con el recuerdo de mi abuelo, él solía decir que todos tenemos una misión en la vida. Para […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On Saturday, June 15, 2024, we hosted our Cleveland Patient Day for NMOSD & MOGAD in collaboration with Dr. Amy Kunchok, Dr. Mary Rensel and Dr. Justin Abbatemarco at Cleveland […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
June 26, 2024 — At The Sumaira Foundation, we believe that pride and support for the LGBTQIA+ community extend beyond the confines of a single month. While Pride Month is […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
It all began in June 2020, the peak of when COVID-19 had finally hit Texas… Allow me to backtrack before I began with my symptoms for a bit: I have […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
New Partnership Extends Critical Financial Assistance and Supportive Services, Enhancing Care and Treatment Accessibility for Those Battling Neuromyelitis Optica Spectrum Disorder June 4, 2024 — The Sumaira Foundation (TSF) is […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
On January 30, 2023, I was diagnosed with relapsing-remitting multiple sclerosis following the onset of nearly complete vision loss in my left eye. That day marked a profound turning point […]
Read MorePosted by: 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 […]
Read MorePosted by: 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 […]
Read MorePosted by: 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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