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			The Sumaira Foundation
        in  NMO, Patient, TM, Voices of NMO
            
			My biggest fear in life was that I would have some incurable sickness or disease. Not heights, nor spiders, nor public speaking. It was getting sick. Both of my parents […]
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	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Patient, Voices of NMO
            
			Today this is where I am – right here and right now. God has a plan, yesterday is gone and tomorrow may never be – It’s up to me as […]
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	        Posted by:
        
			The Sumaira Foundation
        in  NMO, ON, Patient, TM, Voices of NMO
            
			My name is Kellin. I am a 28-year-old South African NMO patient and this is my story… Late in 2015, my father suddenly passed away. It was a shock to […]
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	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Patient, Voices of NMO
            
			Freshman year of college is a time to form your sense of identity, but when I started school, I thought that forming this ‘new’ me meant dying my hair blue, […]
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	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			August 18, 2020 – The Sumaira Foundation is  pleased to present NMOSD/MOG-AD Support Groups & Pages Our team hopes that this document will serve as a valuable resource to our […]
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	        Posted by:
        
			The Sumaira Foundation
        in  MOG, NMO, Professional, TM, Voices of NMO
            
			Maureen is a nurse. She worked in neurocritical care at Johns Hopkins Hospital for many years before she had ever heard of NMO. But in 2007, shortly after Dr. Benjamin […]
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	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			July 29, 2020 – The Sumaira Foundation for NMO is pleased to welcome Stacey Clardy, MD, PhD to its medical advisory board. Stacey Clardy, MD, PhD Dr. Clardy is Associate […]
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	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			Although we would prefer to get together in person, we look forward to coming together virtually in October to commemorate six years of TSF. Please join us on Saturday, October 24 […]
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	        Posted by:
        
			The Sumaira Foundation
        in  NMO, ON, Patient, TM, Voices of NMO
            
			My name is Mitchel Navarro. I’m 34 years old, a wife, and a proud momma to two beautiful children – a girl and a boy. I have a bachelors degree […]
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	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			July 13, 2020 — The Sumaira Foundation for NMO (TSF) and the National Infusion Center Association (NICA) are pleased to announce their partnership as of July 2020. The Sumaira Foundation for […]
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