Home » NMOSD » Page 23
			
                Tag: NMOSD
			
			
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			  June 15, 2021 — The Sumaira Foundation for NMO (TSF) and Brain Health Center of the Rockies are pleased to announce their partnership as of June 2021. Brain Health […]
            Read
                More
            
            
            
        
	
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Voices of NMO
            
			My first NMO symptoms hit three years ago when I was 9; I’m 12 now. To be fully transparent, I don’t actually fully remember that time very clearly. In January […]
            Read
                More
            
            
            
        
	
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  Caregiver, NMO, Voices of NMO
            
			August 29, 2017 will forever be embedded in my mind because it was the day my 9 year old daughter, Bella, woke up sick. It was the day that would […]
            Read
                More
            
            
            
        
	
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Voices of NMO
            
			I am no stranger to rare diseases. At 17, I was diagnosed with Toxoplasmosis. At 22, Phyllodes tumors. Chiari Malformation I at 26. It was not until 2017, when I […]
            Read
                More
            
            
            
        
	
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			March 23, 2021 — The Sumaira Foundation for NMO (TSF) and Portal Instruments are pleased to announce their partnership as of March 2021. Portal Instruments and TSF share a joint […]
            Read
                More
            
            
            
        
	
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Voices of NMO
            
			The first time NMO hit me was on the evening before Thanksgiving in 2010… I clearly remember it because  my wife and I were on holiday in the United States. […]
            Read
                More
            
            
            
        
	
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Patient, Voices of NMO
            
			The differential diagnosis: It is a skill we learn early in medical school and it is designed to guide the clinician on considering the possible underlying causes of a patient’s […]
            Read
                More
            
            
            
        
	
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			Let’s celebrate! March is NMO Awareness Month and we’re proud to share all of the ways you can get involved and help illuminate the darkness of neuromyelitis optica Join the Campaign […]
            Read
                More
            
            
            
        
	
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  NMO, Voices of NMO
            
			My name is Allison and I am a married, busy mom of three children (17, 12 & 12 years old). My NMO journey started approximately seven years ago, when I […]
            Read
                More
            
            
            
        
	
        
            
			
	        Posted by:
        
			The Sumaira Foundation
        in  News & Announcements
            
			February 16, 2021 – The Sumaira Foundation for NMO (TSF) is pleased to announce the Light the Way Forward Grant made possible by a research grant from Viela Bio.  Viela […]
            Read
                More