Andrea & James’ MOG Story – Love Conquers MOG
Posted by: The Sumaira Foundation in Caregiver, MOGAD, Patient, Voices of TSF
Published May 1, 2019
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Choose Your Language:
Posted by: The Sumaira Foundation in Caregiver, MOGAD, Patient, Voices of TSF
Published May 1, 2019
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Transverse Myelitis (TM), Voices of TSF
While 2018 came ringing in with optimism, I was back in school getting my business degree and making moves to start a daycare center for children with special needs. I […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
Before I begin, I would like to thank you and tell you how much I appreciate you taking the time to read about my journey with neuromyelitis optica. Prior to […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
According to all of his medical tests, Greg is negative for both multiple sclerosis (MS) and neuromyelitis optica (NMO). Like many people misdiagnosed due to similar symptoms, Greg was considered […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
Greetings Everyone, I’m Shiela Marie Sta. Maria Rutaquio, from Binangonan, Rizal 1940 Philippines, who have this rare and incurable autoimmune disease called NMOSD (NEUROMYELITIS OPTICA SPECTRUM DISORDER), a demyelinating disease […]
Read MorePosted by: The Sumaira Foundation in MOGAD, NMOSD, Professional, Voices of TSF
Like many physician-researchers in my field, I spend a lot of time thinking about NMO, both inside and outside of the clinic. The science of NMO is fascinating to me […]
Read MorePosted by: The Sumaira Foundation in NMOSD, ON, Patient, Voices of TSF
My NMO story started about 15 years ago. I was a sophomore in high school and was just released for summer break… The very next day, I started to feel […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
I was a 26 year old working in the Pentagon in the Navy Executive Dining Facility. I was Active Duty Navy for almost 8 years… On October 18, 2017, I […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
Hello! My name is Joyce and I am from Pittsburgh, Pennsylvania. My NMO symptoms started with loss of bladder control, stress inconvenience, irritable bowel with constipation, and sensation loss in […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
I’m Ilene, the youngest of seven children. I come from a family of school teachers and musicians. I love board games, musicals, plays, happy movies, skeet ball, Tower of Terror […]
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