Advances in the long-term treatment of neuromyelitis optica spectrum disorder
Posted by: The Sumaira Foundation in
Choose Your Language:
Posted by: The Sumaira Foundation in
Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
When you and God have different plans, stories like ours get created. My name is Sonali Tambatkar and I live in Mumbai, India. It all started in May 2012: I […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Kailee. I am a mom, wife, daughter, teacher, dance instructor, and I have neuromyelitis optica spectrum disorder (NMOSD). I was diagnosed at 25 years old, in May […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
While I was pregnant, I began having blurred vision. I went to see ophthalmologists, opticians, and general practitioners, but they kept saying nothing was wrong. I was sent to see […]
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, Patient, Voices of NMO
I have never been a person that likes to sit still; I don’t even like going to the movies. If it was up to me, I would run from location […]
Read More
