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Posted by: The Sumaira Foundation in News & Announcements
September 21, 2021 — The Sumaira Foundation for NMO is pleased to welcome Stephanie Hamzo to its board of directors. Stephanie Hamzo With a true passion for patients, and dedication […]
Read MorePosted by: The Sumaira Foundation in NMO, Voices of NMO
My name is Mary Lou Gallegos. I was born and raised in San Antonio, Texas. I am the co-owner/founder of SA Perks L.L.C Detox Juices and Tonics. I am […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
August 16, 2021 – The Sumaira Foundation for NMO is pleased to welcome Elena Grebenciucova, MD to its medical advisory board. Elena Grebenciucova, MD Dr. Elena Grebenciucova is a neuro-immunologist […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On July 21, 2021, we gathered in person to celebrate 7 years of illuminating the darkness of neuromyelitis optica in Boston. With your support, we were able to raise over […]
Read MorePosted by: The Sumaira Foundation in NMO, Uncategorized, Voices of NMO
My NMO journey started just a few weeks after having my first baby girl in August 2020. Being a first time mom, I had no idea what postpartum should look […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
June 15, 2021 — The Sumaira Foundation for NMO (TSF) and Brain Health Center of the Rockies are pleased to announce their partnership as of June 2021. Brain Health […]
Read MorePosted by: The Sumaira Foundation in NMO, Voices of NMO
My first NMO symptoms hit three years ago when I was 9; I’m 12 now. To be fully transparent, I don’t actually fully remember that time very clearly. In January […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMO, Voices of NMO
August 29, 2017 will forever be embedded in my mind because it was the day my 9 year old daughter, Bella, woke up sick. It was the day that would […]
Read MorePosted by: The Sumaira Foundation in NMO, Voices of NMO
I am no stranger to rare diseases. At 17, I was diagnosed with Toxoplasmosis. At 22, Phyllodes tumors. Chiari Malformation I at 26. It was not until 2017, when I […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
March 23, 2021 — The Sumaira Foundation for NMO (TSF) and Portal Instruments are pleased to announce their partnership as of March 2021. Portal Instruments and TSF share a joint […]
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