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The Sumaira Foundation
in News & Announcements
December 5, 2019 – The Sumaira Foundation for NMO is pleased to welcome Joshua Katz, MD to its medical advisory board. Joshua Katz, MD Dr. Joshua Katz is the Co-Director […]
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The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
I have a rare, chronic neurological disease that affects my central nervous system. It’s caused me to become temporarily half-blind and feel throbbing pain everywhere… I was diagnosed with Neuromyelitis […]
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The Sumaira Foundation
in News & Announcements
November 13, 2019 – The Sumaira Foundation for NMO (TSF) and The MOG Project announced their partnership on November 13, 2019 in their shared mission to raise awareness for myelin […]
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The Sumaira Foundation
in News & Announcements
The NMO Clinic and Research Laboratory at Massachusetts General Hospital November 7, 2019 – Three board members of The Sumaira Foundation for NMO, Dr. Michael Levy, Dr. Marcelo Matiello, and […]
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The Sumaira Foundation
in NMO, Patient, Voices of NMO
Imagine this: You’re driving on a highway, and suddenly, your hands stop working completely. You can’t grip the wheel. Imagine the terror and the confusion… And then imagine, that, thank […]
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The Sumaira Foundation
in News & Announcements
October 30, 2019 – The Sumaira Foundation for NMO is pleased to welcome Bart Chwalisz, MD to its medical advisory board. Bart Chwalisz, MD Dr. Chwalisz grew up in Poznan, […]
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The Sumaira Foundation
in News & Announcements
On behalf of Harvard Medical School, Dr. Michael Levy and Dr. Marcelo Matiello, neurologists at Massachusetts General Hospital and course directors, hosted the inaugural continuing medical education program, “Autoimmune Neurology”, […]
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The Sumaira Foundation
in NMO, Patient, Voices of NMO
My name is Sherry. My experience with my disease is a little different and backwards… I was taking care of my father who had MS for many years and experienced […]
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The Sumaira Foundation
in News & Announcements
August 23, 2019 – The Sumaira Foundation for NMO (TSF) and Connor B. Judge Foundation (CBJF) are proud to present Demystifying NMO, a podcast series aimed at simplifying scientific jargon associated […]
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The Sumaira Foundation
in MOG, Patient, Voices of NMO
Now that I have been diagnosed with Myelin Oligodendrocyte Glycoprotein Antibody-Associated disease, or MOG-Ab disease, I have met others who are afflicted and have listened to their stories. They all […]
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