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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
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 NMO, Patient, Voices of NMO
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 […]
Read MorePosted by: 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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 22, 2024 — The Sumaira Foundation is delighted to announce a new partnership with the Caminemos Foundation, a Mexican non-profit patient advocacy organization working in the area of demyelinating […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 15, 2024 — The Sumaira Foundation is thrilled to announce Dr. Zhila Maghbooli, from the Multiple Sclerosis Research Center of Tehran University of Medical Sciences, Iran, as the first […]
Read MorePosted 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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Il 18 novembre 2023 TSF Italia ha ospitato la sua prima giornata internazionale dedicata ai pazienti in Italia, a Verona. Si sono uniti a noi 50 pazienti, operatori sanitari e […]
Read MorePosted 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 […]
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