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Posted 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, Transverse Myelitis (TM), Voices of TSF
I was diagnosed with Neuromyelitis Optica in June of 2012 after two hospitalizations totaling 5 months, during which I lost all my strength, ability to move and all feeling from […]
Read MorePosted by: The Sumaira Foundation in NMOSD, ON, Patient, Transverse Myelitis (TM), Voices of TSF
Meet Dionne, a vibrant 46-year old, former nurse, mother of 2 from New Orleans, Louisiana who has been living with NMO since 2009. Click below to watch Dionne share her […]
Read MorePosted by: The Sumaira Foundation in NMOSD, ON, Patient, Transverse Myelitis (TM), Voices of TSF
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, […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Transverse Myelitis (TM), Voices of TSF
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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 MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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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