Human Collective Project | Africa
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 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 […]
Avez-vous été touché(e) ou l'un de vos proches par MOGAD ? Rejoignez-nous le mardi 2 septembre pour en savoir plus sur MOGAD et l'importance de la participation des patients aux essais cliniques. […]
Have you or someone close to you been affected by MOGAD? Join us on Thursday, September 4th to learn about MOGAD and the importance of patient participation in clinical trials. […]
سيناقش هذا الويبينار أحدث الطرق والرؤى حول إدارة الأعراض الأساسية والاعتلالات المصاحبة لاضطراب الطيف العصبي البصري .(NMOSD) سيركز المختصون المشاركون على التحديات التي يواجهها المرضى في التعامل مع المرض، وأفضل […]
HCP is a great way to meet others in similar circumstances in this rare community; it is a safe space to laugh, cry, vent, share wins, etc. This program is driven and led by TSF Patient and Caregiver Ambassadors worldwide.
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 […]
If you're attending ECTRIMS in Barcelona, we invite you to attend TSF's Research Update & Award Ceremony at Casa Llotja de Mar. Join us for an evening with research updates, […]
Join us on September 26, 2025 for ECTRIMS Patient Community Day – an exclusive, free event designed for individuals living with MOGAD, MS, NMOSD and related neurological conditions. Patient Community Day is an […]
Join us on Sunday September 28th in Weston, Massachusetts to run, walk, socialize, and raise funds. (Registration/attendance comes with a free t-shirt). This event is being organized by Terry Clark, […]
HCP is a great way to meet others in similar circumstances in this rare community; it is a safe space to laugh, cry, vent, share wins, etc. This program is driven and led by TSF Patient and Caregiver Ambassadors worldwide.
We're coming to Seattle! Are you an AE*, CNS Vasculitis, MOGAD*, neurosarcoidosis, NMOSD* or SPS* patient, partner, care-partner, clinician, nurse, researcher and/or advocate from the Pacific Northwest region? You're invited […]
