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Posted by: The Sumaira Foundation in News & Announcements
Dr. Grace Gombolay, Sumaira Ahmed, Nell Choi, Alanna Yee, Nakeshia Nickerson and Tara Zier. On Saturday, July 20, 2024, the American Academy of Neurology (AAN) marked a historic milestone with […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On July 18, 2024, we were grateful and honored to celebrate 10 years of The Sumaira Foundation in Atlanta alongside physicians, community members, patients, supporters, and our TSF team. Our […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
14 de agosto de 2024 – A Fundação Sumaira (TSF) tem a honra de anunciar uma nova parceria com a Associação Brasileira de Neuromielite Óptica (ABNMO) que busca avançar na […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Much has changed in my world since my initial story had been published on TSF’s website in 2020. (scroll below to read the original piece) One of the more notable […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On Saturday, June 15, 2024, we hosted our Cleveland Patient Day for NMOSD & MOGAD in collaboration with Dr. Amy Kunchok, Dr. Mary Rensel and Dr. Justin Abbatemarco at Cleveland […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Je m’appelle Nelly, j’ai 44 ans et je vis dans un joli village dans l’Oise et j’ai la MOGAD. Sans le savoir cette maladie m’avait déjà fait un petit clin […]
Read MorePosted by: The Sumaira Foundation in Caregiver, MOG, Voices of NMO
Ciao a tutti, mi presento, sono la mamma di Auri. Mi piace presentarmi così, perché questa è la sua storia, la storia di una bambina bella e forte che nel […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On Saturday, March 9, 2024, we hosted our New England Patient Day for NMOSD & MOGAD in Boston in collaboration with Dr. Michael Levy and Dr. Marcelo Matiello of Massachusetts […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
With a vulnerable yet advocational heart, I would love to re-introduce myself to the NMO community! My name is Alyson Tignor (née Pugh) and I am so much more than […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, TM, Voices of NMO
It all began in early 2020 when Kayla noticed a tingling sensation in her right leg. She didn’t think too much about it and figured it would go away. Thinking […]
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