Terry Clark, TSF Ambassador for Massachusetts and NMOSD warrior, has once again secured a proclamation declaring March 2026 as #NMOSD Awareness Month.

In recognition of this effort, Governor Maura Healey met with Terry to learn more about #neuromyelitisoptica.

Throwback to when the @boston.gov was illuminated pink for TSF's #NMO Awareness Month 😍🩷

#NMOSD #neuromyelitisoptica #Boston

Remembering that time when the @empirestatebldng.bsky.social was lit pink & orange to illuminate #NMO Awareness Month with The Sumaira Foundation 🩷😍🧡

To learn more about #neuromyelitisoptica / #NMOSD, visit www.sumairafoundation.org

Add my voice too. I woke up one day 11 years ago and couldn't walk. Rare disease blah blah. Things are better, but I'd rather *not* possess a handicap parking pass, if you know what I mean. #neuromyelitisoptica #nmo

CD19 CAR T-Cell Therapy in Autoimmune Disease — A Case Series with Follow-up | NEJM Treatment for autoimmune diseases such as systemic lupus erythematosus (SLE), idiopathic inflammatory myositis, and systemic sclerosis often involves long-term immune suppression. Resetting aberran...

One of the biggest scientific breakthroughs of 2024. #CAR-T therapy for autoimmune disease. Imagine a world where patients can receive 1 treatment and be cured! Looking forward to trials in #multiplesclerosis, #neuromyelitisoptica and #anti-MOGassociateddisorder!

www.nejm.org/doi/full/10....

Case #24: Sumaira Podcast Episode · Symptomatic: A Medical Mystery Podcast · S3 E6 · 44m

Sumaira's 10-year journey living with #NMOSD is featured in @iheartradio.bsky.social's "Symptomatic: A Medical Mystery Podcast" newest episode - Case #24: Sumaira.

Check it out:
podcasts.apple.com/us/podcast/c...

#NeuroSky #neuromyelitisoptica

Neuromyelitis Optica Neuromyelitis optica, also called NMO, is a rare yet severe autoimmune inflammatory process affecting the central nervous system.

www.hopkinsmedicine.org/health/condi...

#NMO #NMOSD #NeuromyelitisOptica #NeuromyelitisOpticaSpectrumDisorder #DevicsDisease

Meet Whitney and Addison, TSF Ambassadors of Kentucky 🌺

Addison was diagnosed with #NMOSD / #neuromyelitisoptica in 2021 and joins the Foundation as the youngest Ambassador alongside her mother, Whitney, who is her primary caregiver.

Welcome Whitney and Addison!

#SystemicExertionalIntoleranceDisease, #SEID , #autoimmune, #cysticfibrosis, #dystonia, #parkinsons, #PCOS, #cf, #Raynauds, #Sjogrens, #neuromyelitisOptica, #NMOSD, #narcolepsy, #urticaria, #idiopathichypersomnia, #Psoriasis, #PsoriaticArthritis, #UCTD, #MCTD, #hypersomnia, #CVID, #CPP, #PID,

4/6

Hi #MedSky / #NeuroSky! 👋🏾 My name is Sumaira and I have been living with #NMOSD / #neuromyelitisoptica for 10 years. I started The Sumaira Foundation (TSF) 2 months after my DX & really excited to connect and collaborate with while learning from experts around the world on this platform! 🌏 🌎 🌍