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Patient
Posted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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 […]
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Posted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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 Multiple Sclerosis, Patient, Voices of TSF
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 MOGAD, Patient, Voices of TSF
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 NMOSD, Patient, Voices of TSF
With a vulnerable yet advocational heart, I would love to re-introduce myself to the NMO community! My name is Alyson Tignor (née Pugh) and I am so much more than […]
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Posted by: The Sumaira Foundation in NMOSD, Patient, Transverse Myelitis (TM), Voices of TSF
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 NMOSD, Patient, Voices of TSF
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 NMOSD, Patient, Professional, Voices of TSF
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 NMOSD, Patient, Voices of TSF
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 NMOSD, Patient, Voices of TSF
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, […]
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