Posted 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 […]
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Posted 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 […]
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Posted 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 […]
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Posted 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 […]
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Posted 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 […]
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Posted 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 […]
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Posted by:
The Sumaira Foundation
in
HCP is a great way to meet others in similar circumstances in this rare community; it is a safe space to laugh, cry, vent, share wins, etc. This program is driven and led by TSF Patient and Caregiver Ambassadors worldwide.
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Posted by:
The Sumaira Foundation
in
HCP is a great way to meet others in similar circumstances in this rare community; it is a safe space to laugh, cry, vent, share wins, etc. This program is driven and led by TSF Patient and Caregiver Ambassadors worldwide.
Read
More
Posted by:
The Sumaira Foundation
in
HCP is a great way to meet others in similar circumstances in this rare community; it is a safe space to laugh, cry, vent, share wins, etc. This program is driven and led by TSF Patient and Caregiver Ambassadors worldwide.
Read
More