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Posted by: The Sumaira Foundation in News & Announcements
The Sumaira Foundation for NMO (TSF) is proud to announce the launch of the TSF Ambassador Program by introducing the inaugural ambassador, Phil Tucker. Phil is an NMO warrior from […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
On Monday morning, Pam had a headache. For a woman who never got headaches, this was notable. In addition, when she turned her eyes right and left, she experienced eye […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Nothing can fell Marie. No matter the punches that NMO throws, Marie just gets up again and keeps on going. A strong young woman who has learned to live with […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Jamie was diagnosed with Non-Hodgkins Lymphoma at the age of 35. Her condition was such that she didn’t need treatment, just monitoring. She was even healthy enough to have a […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On October 11, 2018, The Sumaira Foundation for NMO (TSF) announced its partnership with the Transverse Myelitis Association (TMA). Both organizations specialize in raising awareness for rare neuro-immune disorders while […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
My entire life, I was always a healthy and energetic person… I have played tons of sports and never went to the doctor unless it was for a sports physical. […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Sumaira’s NMO Story From the Transverse Myelitis Association blog, In Their Own Words (October 4, 2018) My name is Sumaira and I am the founder and executive director of The Sumaira Foundation […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
We are proud to announce the launch of TSF Spark Grants! Frequently Asked Questions Who is eligible for the grant award? Clinical, translational and basic researchers with experience in […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Here is my story of how I was diagnosed with Neuromyelitis Optica and just how scary it can be knowing that something is wrong but not being able to find […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
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