Tag: the sumaira foundation
Posted by:
The Sumaira Foundation
in NMO, Patient.e, 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 Nouvelles et annonces
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
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 […]
Read
More
Posted by:
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 […]
Read
More
Posted by:
The Sumaira Foundation
in MOG, Proche-aidant.e, 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 […]
Read
More
Posted by:
The Sumaira Foundation
in NMO, Patient.e, 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 […]
Read
More
Posted by:
The Sumaira Foundation
in NMO, Patient.e, 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 […]
Read
More
Posted by:
The Sumaira Foundation
in NMO, Patient.e, 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 […]
Read
More
Posted by:
The Sumaira Foundation
in NMO, ON, Patient.e, 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 […]
Read
More
Posted by:
The Sumaira Foundation
in NMO, Patient.e, 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, […]
Read
More