Nick’s Story: How I Turned Diagnosis into Advocacy: Navigating NMOSD, MS and LGBTQIA+ Representation
Posted by: The Sumaira Foundation in Multiple Sclerosis, Patient, Voices of NMO
On January 30, 2023, I was diagnosed with relapsing-remitting multiple sclerosis following the onset of nearly complete vision loss in my left eye. That day marked a profound turning point […]
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