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 pandemic in 2020, when most NMOSD/MOGAD felt particularly isolated and vulnerable to the coronavirus as immunosuppressed/immunocompromised members of society. The isolation many of us experienced […]
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. Ce programme sera animé par le Pr Jérôme de Seze (Université de Strasbourg - France) et le Dr Sophie Elands (Hôpital Érasme - Hôpital Universitaire […]
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. This program will feature Dr. Saif Huda (The Walton Centre - UK), Dr. Silvia Messina (Nuffield Department of Clinical Neurosciences - UK) and Dr. Katharina […]
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 الممارسات لتحسين جودة الحياة، واستراتيجيات علاجية للتعامل مع الأمراض المصاحبة. سيحظى الحضور أيضًا بفرصة لطرح الأسئلة والنقاش مع الخبراء في هذا المجال
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 pandemic in 2020, when most NMOSD/MOGAD felt particularly isolated and vulnerable to the coronavirus as immunosuppressed/immunocompromised members of society. The isolation many of us experienced […]
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, recognition of outstanding achievements in the field and networking with a community dedicated to pushing the boundaries of science and technology. During this time, we […]
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 opportunity to learn about the latest research advancements directly impacting your ongoing care and treatment options. The programme will include engaging roundtable discussions led by […]
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, TSF Ambassador of MA and NMOSD patient who says, "As many of you know, almost 3 years ago, in May of 2022, I was diagnoses […]
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 to our event on Saturday, October 18th at the UW Medicine Neurosciences Institute. Join us for a day of education, community, and fun to: Meet […]
