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	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Patient, Voices of NMO
            
			At age eight, when I first started chemotherapy for my autoimmune disease, the neurologist told my parents the maximum amount of time I could be on it was three years, […]
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	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Voices of NMO
            
			The year was 2007 and I had just returned to school from summer break, twelve years old and excited to start the 7th grade with new classmates and new opportunities. […]
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			The Sumaira Foundation
        in  News & Announcements
            
			On Saturday, July 22, 2023, we hosted TSF’s Southern California Patient Day for NMOSD & MOGAD at UCLA Meyer and Renee Luskin Conference Center in Los Angeles where we were […]
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	        Posted by:
        
			The Sumaira Foundation
        in  
            
			Partecipa al nostro prossimo Webinar dal titolo: NMOSD sieronegativa – giovedì 27 luglio alle 17.00 con la dr. Elia Sechi, neurologo presso l’Università degli Studi di Sassari. Chi parteciperà di […]
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	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			June 21, 2023 — The Sumaira Foundation is pleased to welcome Álvaro Cobo-Calvo, MD, PhD, of the Multiple Sclerosis Centre of Catalonia (CEMCAT) in Barcelona, Spain, to join TSF’s Medical Advisory […]
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	        Posted by:
        
			The Sumaira Foundation
        in  
            
			The Sumaira Foundation is pleased to invite you to TSF’s Southern California Patient Day, a special day dedicated to NMOSD & MOGAD patients, caregivers and clinicians. Join us for a […]
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	        Posted by:
        
			The Sumaira Foundation
        in  Caregiver, NMO, Professional, Voices of NMO
            
			I am a caregiver to my daughter, Nell, who was diagnosed with NMO at age 9. Prior to her diagnosis, she was an active, vibrant girl playing travel lacrosse, robustly […]
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	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			June 14, 2023 — The Sumaira Foundation (TSF), a global patient advocacy organization focused on rare neuroimmune conditions, is delighted to announce Tim Walbert, chairman, president and chief executive officer […]
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	        Posted by:
        
			The Sumaira Foundation
        in  
            
			The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
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	        Posted by:
        
			The Sumaira Foundation
        in  
            
			The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
            Read
                More