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Q&A: Importance of Raising Awareness of NMOSD
Les Experts Santé: La Fondation Sumaira, focus sur la NMO & la MOGAD
Identifying Reasons, Barriers to Low Employment Rates in NMOSD: Farrah Mateen, MD, PhD
Malattie rare, è triestina l’ambasciatrice italiana della fondazione americana The Sumaira
NMOSD – A Rare Autoimmune Disease Personal Story – Leda Bresnov
Why awareness is the key to managing NMOSD
The Sumaira Foundation (TSF) annonce la création et le lancement de TSF France, apportant un soutien supplémentaire indispensable à la communauté française touchée par la NMO et la MOGAD
An appeal for a more inclusive, representative, and accessible National Rare Disease Policy
What is NMOSD? A rare disease, commonly misdiagnosed as MS.
The Patient Perspective on Neuromyelitis Optica Spectrum Disorder: Sumaira Ahmed
Female Disruptors: Sumaira Ahmed of The Sumaira Foundation On the Three Things You Need To Shake Up Your Industry
The Sumaira Foundation Announces Acquisition of the Connor B. Judge Foundation
In S1E6, DrugViu interviews Sumaira Ahmed about her diagnosis with NMOSD and vision for the future of The Sumaira Foundation.
Rare Incurable Condition leaves Ellesmore Port Mum with Sudden Sight Loss
NMOSD Your Way Podcast hosted by NMOSD Patient Ambassador, Lelainia
Horizon Therapeutics plc Launches #RARE is Representation Program to Elevate Global Rare Disease Equity
Make It Count: A Visit With Prominent NMO Advocate Sumaira Ahmed
Denver Teen, Family Helps Others Around the World With Rare Disease
Woman Making Science Meaningful
Discussing the Importance of Diversity, Equity, Inclusion, and Allyship in the Global Rare Disease Community
Podcast featuring Sumaira Ahmed
#RAREis Video – Meet Sumaira Ahmed
Medicare Drug-Pricing Debate Pits Savings Against Innovation
Somerville Resident Sumaira Ahmed Wins WEGO Award for her Work in Healthcare
Portal Instruments Partners with The Sumaira Foundation for NMO
WeWork Is Helping Women Founders Get Back to the Office
From Reel Life to Real Life: In Conversation with Sumaira Ahmed
How She Used her Diagnosis of NMO to Create Her Successful Organization
OPINION: Voting and Supporting the Biopharmaceutical Industry
Creating Community in Rare Disease
How to Prepare for Your First Infusion
Patient insights: Neuromyelitis Optica
30 Nonprofit Founders Who Will Impact the World in 2020
‘Illuminating the Darkness’ Around a Rare Disease
Listening & Learning from the Rare Disease Patient
Listening to the Rare Disease Patient Can Improve Outcomes
The Sumaira Foundation 4th Annual NMO Awareness Gala
NMO Awareness Gala
Rare Disease Day 2019: Neuromyelitis Optica
Warming Hearts on a Winter Day
The TMA Announces its Partnership with The Sumaira Foundation
3rd NMO Gala
NMO Awareness Gala
Meet Sumaira Ahmed of The Sumaira Foundation for NMO in Brookline
A Spark in the Dark: An Interview with Sumaira Ahmed
Urban and Elegant Wedding Ideas ft. Sumaira Ahmed
First-ever Boston Event to Form Network for NMO Patients
The Sumaira Foundation’s 2nd Annual NMO Awareness Gala
What is NMO?
Top 10 South Asian American Beauty Pageant to Know
Miss Bangladesh USA Seeks to Raise Awareness of a Rare Disease
Local Woman Launches Nonprofit for Autoimmune Disease
