United Kingdom Support Group
Virtual Event
Come connect with others and discuss what it’s like living with a rare neuroimmune disorder. Ask questions, share your stories, or just listen – everyone is welcome.
Over the past couple of weeks and months, we have all grown increasingly aware of the significant impact COVID-19/coronavirus is having on people and organizations across the country and the world. While SRNA highly values community-led events and the relationship-building nature of our in-person programming —such as awareness events and support group meetings— we value the health and well-being of our community members more. With that in mind, our team is currently revising and re-assessing our upcoming in-person offerings to take protective measures that prioritize collective community health.
SRNA is monitoring and following guidance from the World Health Organization, the Centers for Disease Control & Prevention, local Public Health Officials, our specialized centers, medical experts and partners. We have decided to not host in-person support group meetings and gatherings for the next 4 weeks when we will re-assess the situation. Below, you will find specific updates on upcoming programming and events within the next 4 weeks.
We look forward to opportunities to continue connecting with you and welcome any questions, comments, or concerns you may have in the meantime.
The SRNA Team
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Online Support Group Meeting
Virtual Event
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Siblings Support Group Meeting
Zoom
Virtual Event
This is an opportunity to connect with other siblings of people diagnosed with rare neuroimmune disorders. Share your experiences and receive support from those who understand.
Young Adults Group
Virtual Event
Join us for an online social hour hosted by Aidan M. for those in their 20's and 30's with ADEM, AFM, MOGAD, NMOSD, ON, or TM! Connect with others and […]
Siblings Support Group Meeting
Zoom
Virtual Event
This is an opportunity to connect with other siblings of people diagnosed with rare neuroimmune disorders. Share your experiences and receive support from those who understand.
Siblings Support Group Meeting
Zoom
Virtual Event
This is an opportunity to connect with other siblings of people diagnosed with rare neuroimmune disorders. Share your experiences and receive support from those who understand.
Questions about COVID-19?
As the spread of COVID-19 continues across the world, it’s important our community knows and understands the risks associated with this virus in the setting of a rare neuroimmune disorder. We are hoping to create an FAQ document to answer your questions. Please share your questions with us and help us shape this document!
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