Advances in the long-term treatment of neuromyelitis optica spectrum disorder
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Posted by: The Sumaira Foundation in Caregiver, NMO, Voices of NMO
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 NMO, Uncategorized, Voices of NMO
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 NMO, ON, Patient, Voices of NMO
It was December 2019. I struggled almost every day with tension headaches (eyes and nose). My primary care doctor suspected I had migraines and prescribed me with migraine medication. I […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
March 31, 2020 — The Sumaira Foundation for NMO is pleased to present the results of the NMO community’s outreach efforts to have March declared “NMO Awareness Month” across the […]
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