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			The Sumaira Foundation
        in  NMO, Voices of NMO
            
			Nicole was a first-grade teacher and chorus director in a Title 1, low-income school district, where she was a beloved, appreciated, and award-winning professional…    In May of 2017, Nicole thought […]
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			The Sumaira Foundation
        in  NMO, Voices of NMO
            
			My name is Ryan. Three years ago, I was living the dream. I was happily married to my best friend, and we have three beautiful and perfectly healthy children.  We […]
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			The Sumaira Foundation
        in  News & Announcements
            
			January 8, 2021 — Since 2019, our small but mighty and growing community has seen three FDA-approved therapies. At TSF, we’re huge advocates for shared-decision making between patients and their […]
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			The Sumaira Foundation
        in  MOG, Voices of NMO
            
			It was the Friday before Halloween in 2018. Anthy was on her way home from work when she called her husband to see if she needed to pick up anything […]
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	        Posted by:
        
			The Sumaira Foundation
        in  Caregiver, MOG, Voices of NMO
            
			When your daughter suddenly goes blind in one eyes, you feel helpless. When the doctors don’t know what it is or why it happens, you feel frustrated. When this happens […]
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	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			November 25, 2020 — The Sumaira Foundation for NMO is pleased to present “Understanding the Canadian NMOSD Journey”, a 6-part live webinar series featuring Canadian patients, caregivers, clinicians, researchers, and […]
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	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Patient, TM, Voices of NMO
            
			On the evening of Sunday, 17th January 2010, my mother was putting up a fight with my brothers and I to go to bed while we were chasing each other […]
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	        Posted by:
        
			The Sumaira Foundation
        in  NMO, ON, Patient, Voices of NMO
            
			My name is AnneMarie and my journey with NMO began in 2002 when I was just 16 years old… One April morning, I woke up with a stabbing pain in […]
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	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			November 9, 2020 – We are proud to announce the grant recipients of TSF’s 2020 research grants. Congratulations to our recipients who received $25,000 to initiate their projects! Diagnostics in […]
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	        Posted by:
        
			The Sumaira Foundation
        in  NMO, ON, Patient, Voices of NMO
            
			My name is Jaime. I live in the small town of Exeter, Pennsylvania. I am a wife and a mother to a beautiful and healthy 15 year-old daughter. And I […]
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