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Posted by: 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 […]
Read MorePosted by: 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 […]
Read MorePosted by: 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 […]
Read MorePosted by: 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, […]
Read MorePosted by: The Sumaira Foundation in NMO, ON, Patient, Voices of NMO
Life before NMO – I was an active mom, worked as a home health nurse case manager and an avid marathon/half marathon runner… Before work, I would wake up at […]
Read MorePosted by: 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”, […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
🐕 🐶 SALUTE TO SERVICE DOGS Submit high-resolution photos of your furry helpers for consideration to be featured in our 2020 Dogs Of NMO calendar Email photos of your service dogs […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMO, ON, Voices of NMO
My name is Veronica and this is my NMO story. I am not a patient but a mother/caregiver of an NMO patient. I have always been in a way, made […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Back in 2013 and 2014, I completed two 100km walks to raise money for Oxfam – something I am so proud to have done! BUT in 2016, when I tried […]
Read MorePosted by: 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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