Navigating NMOSD in Canada
Calling Canadians impacted by NMOSD: you're invited for a live patient education webinar about how to navigate life with neuromyelitis optica spectrum disorder in Canada. Join us on Wednesday, November […]
Calling Canadians impacted by NMOSD: you're invited for a live patient education webinar about how to navigate life with neuromyelitis optica spectrum disorder in Canada. Join us on Wednesday, November […]
We're coming to Toronto! Are you an AE*, MG*, MOGAD* or NMOSD* patient, partner, care-partner, clinician, nurse, researcher and/or advocate in Canada? You're invited to our event on Saturday, November […]
We warmly invite you to join our upcoming Human Collective Project (HCP) meeting for the Indian rare neuroimmune community, taking place online via Zoom. Our special guest speaker, Dr. Garima Yadav, a respected physical therapist, will share valuable insights on maintaining physical wellbeing while living with rare neuroimmune conditions, followed by an engaging Question and […]
Εσείς ή κάποιος που αγαπάτε επηρεάζεστε από το MOGAD; Σας προσκαλούμε να συμμετάσχετε στο επερχόμενο πρόγραμμά μας αφιερωμένο στην MOGAD τη Δευτέρα 10 Νοεμβρίου στις 6 μ.μ. EET. Θα συμμετάσχουν […]
The Caregivers Human Collective Project (HCP) is a groundbreaking support group hosted by The Sumaira Foundation, created specifically for caregivers of individuals living with rare neuroimmune diseases like NMOSD and MOGAD. This first-of-its-kind session offers a safe, inclusive space for family members, partners, siblings, children, and loved ones to connect, share, and be heard. Led […]
Bent u of kent u iemand die getroffen is door MOGAD? U bent uitgenodigd voor een webinar over MOGAD en klinische studies op 18 november. We zullen worden vergezeld door […]
TSF Italia è lieta di invitare tutti i pazienti italiani affetti da encefalite autoimmune, miastenia grave, MOGAD e NMOSD, i loro caregiver e i medici interessati a queste patologie a […]
The Mental Health Monday meetings began as a way to address the various mental and emotional concerns that individuals experience when dealing with rare neuroimmune diseases. Patients, caregivers, and loved […]
TSF France, en partenariat avec le MIRCEM, présente le 3ème week-end Patients et Aidants de la NMOSD et de la MOGAD les 29 et 30 novembre à Lyon ! L'évènement, complétement gratuit, aura lieu au Mama Shelter de Lyon, rue Domer, les 29 et 30 novembre 2025. Nous sommes ravis d'être accompagnés par les experts […]
The Sumaira Foundation Canada is pleased to invite you to an important educational webinar on Thursday, December 11th at 7:30 PM EST. This session will explore the evolving treatment options for individuals living with AQP4+ NMOSD, seronegative NMOSD, and MOGAD in Canada. We will be joined by Dr. Alexandra Muccilli from the University of Toronto, […]
The Caregivers Human Collective Project (HCP) is a groundbreaking support group hosted by The Sumaira Foundation, created specifically for caregivers of individuals living with rare neuroimmune diseases like NMOSD and MOGAD. This first-of-its-kind session offers a safe, inclusive space for family members, partners, siblings, children, and loved ones to connect, share, and be heard. Led […]
Patients living with rare conditions in the US frequently face extra complexities when seeking access to specialized treatments, off-label therapies, or less common care pathways. Prior authorizations may take longer, documentation requirements may be more intensive, and appeals may present additional hurdles. Join us on December 16th at 7 PM EST for a special webinar […]
