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Posted by: The Sumaira Foundation in News & Announcements
You are invited to attend TSF’s old Hollywood-themed 5th NMO Awareness Gala Saturday, March 26, 2022 at 7 PM Mandarin Oriental, Boston We’ve set an ambitious goal to raise $250,000 […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Christy and I’ve been fighting this disease without knowing what I was up against since before 2008… I started calling this thing my “venom” because it reminded […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
December 1, 2021 — The Sumaira Foundation is proud to announce the grant recipients of TSF’s 2021 SPARK and Unicorn grants. Congratulations to our 5 recipients who each received $25,000 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
November 22, 2021 – The Sumaira Foundation is pleased to welcome Professor Romain Marignier as the 1st international NMO specialist to join TSF’s medical advisory board. Romain Marignier, MD Pr. […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
October 15, 2021 — The Sumaira Foundation for NMO is pleased to welcome Michael Devlin to its Board of Directors. Michael Devlin Michael has spent most of his career focused […]
Read MorePosted by: The Sumaira Foundation in NMO, Voices of NMO
Tiffany was a military brat with both of her parents serving in the Navy, so joining up herself seemed the obvious choice for her. She enlisted in 2006 and met […]
Read MorePosted 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
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 […]
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