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Posted by: The Sumaira Foundation in News & Announcements
August 14, 2023 – The Sumaira Foundation (TSF) is pleased to welcome Leda Bresnov to our leadership team as International Ambassador Liaison. As of August 2023, the Foundation is proud […]
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On Saturday, July 22, 2023, we hosted TSF’s Southern California Patient Day for NMOSD & MOGAD at UCLA Meyer and Renee Luskin Conference Center in Los Angeles where we were […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
June 21, 2023 — The Sumaira Foundation is pleased to welcome Álvaro Cobo-Calvo, MD, PhD, of the Multiple Sclerosis Centre of Catalonia (CEMCAT) in Barcelona, Spain, to join TSF’s Medical Advisory […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On June 13, 2023, TSF’s India Ambassador, Clarinda Cerejo participated in a multi-stakeholder workshop on the national rare disease policy of India in Delhi, India. The workshop was organized by […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
June 14, 2023 — The Sumaira Foundation (TSF), a global patient advocacy organization focused on rare neuroimmune conditions, is delighted to announce Tim Walbert, chairman, president and chief executive officer […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
May 26, 2023 — The Sumaira Foundation is pleased to welcome Sara Salama, MD, PhD, of Alexandra University (Egypt) to join TSF’s Medical Advisory Board. Dr. Salama’s involvement makes her the […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
May 26, 2023 — The Sumaira Foundation is pleased to welcome Salman Aljarallah, MBBS, of King Saud University in Riyadh, KSA, to join TSF’s Medical Advisory Board. Dr. Salama’s involvement makes […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
For those of you who joined us last month for TSF’s 6th Annual Gala, we can’t thank you enough for making it a night to remember! Beyond fundraising for research, […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
“You have to grab life by the horns and enjoy every moment. Even if you’re not ill, you should do that!” April 7, 2023 — The Sumaira Foundation’s (TSF) first […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
这是一个有关中国NMO之家联合创始人小高从病痛中“站起来”，重新出发去寻找生命意义的故事。现在，他期待着NMO病友大会在中国举办，期待着与TSF共同用我们的努力照亮NMO和MOG患者的世界。他说他还会继续在NMO病友会的建设上走很远很远的路，直到医学领域发现治愈的光芒，直到病友们能摆脱疾病带来的痛苦，直到NMO和MOG病友们都能重新拾起对世界的热爱…
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