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Patient
Posted by:
The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
Meet Megan, a 16 year old NMO patient who and YouTube sensation (@PerfectlyKnitBeauty) who has been coping with her chronic illness through the use of makeup. We laud her courage, […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, TM, Voices of NMO
She thought she had a bad sunburn… Lillian had gone camping with her daughter and her Girl Scout troop in September of 2015. When she returned home, her shoulders and […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
I was diagnosed with NMO on March 10, 2015… An MRI that was done while I was receiving inpatient care for sudden paralysis of my lower limbs showed a spinal […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
With respect to the patient’s desire to remain anonymous, we will refer to him as Matt. It started along with a very bad cold in late 2011. Eye pain and […]
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Posted by:
The Sumaira Foundation
in MOG, Patient, Voices of NMO
On a warm February evening at the University of Miami, I sat in my Music Business lecture and wondered from where this strange soreness had come. There was a lingering […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
Something Wasn’t Right I was the perfect example of the shiny student off to bigger and better things from the small country town where I grew up. I had a […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
February 1st, 2011 – I began having vision problems in my left eye and a few days later, it got drastically worse. I went to the Mass Eye and Ear Infirmary’s […]
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Posted 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 […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
My life changed eleven years ago when I was diagnosed with NMO. To this day, I still have moments where I reflect back on my story and feel every ounce […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
Since she already had been diagnosed with lupus, Raynaud syndrome, and Sjogren’s syndrome, Adria didn’t think much about the tingling in her hands that started in February of 2016. Besides, […]
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