Steroids can be an important part of treatment for many rare neuroimmune conditions, but what happens when they’re used over a longer period of time? Join Dr. Amy Kunchok for a patient-friendly discussion about the potential long-term side effects of steroids, what to watch for, and how patients can work with their healthcare team to […]
The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
Gemeinsam stärker: Ein Tag voller Wissen, Austausch und Begegnung für Menschen mit Morbus Basedow und endokriner Orbitopathie Im Rahmen der TED Awareness Week: Wir bringen Betroffene, Angehörige sowie Expertinnen und […]
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 […]
À tous les patients et aidants touchés par des maladies auto-immunes et auto-inflammatoires rares en France et en Belgique ! Vous ou l'un de vos proches est touché par : […]
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 […]
The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
We're coming to Los Angeles! TSF is inviting patients and caregivers impacted by rare neuroinflammatory & related disorders from California & the west coast! Are you or your loved one impacted […]
The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
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 […]
