MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 4: Afferent visual system damage after optic neuritis in MOG-IgG-seropositive versus AQP4-IgG-seropositive patients
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Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
It started innocuously. In 2008 we moved to Ottawa with my employer for my career in pest control. On a gray, cloudy but humid day, I was out removing a […]
Read MorePosted by: The Sumaira Foundation in MOGAD, Patient, Voices of TSF
It all began with a tremor. It was September 2018, and I was off on maternity leave after having my second daughter earlier that year. As nice as that should […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
My name is Christy and I’ve been fighting this disease without knowing what I was up against since before 2008… I started calling this thing my “venom” because it reminded […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMOSD, Voices of TSF
Jarrie grew up on a farm and declares himself a simple man. I think otherwise. I think Jarrie is a man for whom love is simply enough. Jarrie married his […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
My NMO journey started just a few weeks after having my first baby girl in August 2020. Being a first time mom, I had no idea what postpartum should look […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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 MorePosted by: The Sumaira Foundation in Caregiver, MOGAD, Voices of TSF
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 MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, ON, Patient, Voices of TSF
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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