Finding useful health information on the Internet can be difficult, but we’re here to help. This page gathers quality information from trusted sources. You can learn more about the disease, visit handpicked websites, and find resources to help you in your daily life. Need more information? Click the menu on the left to find more!
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Medical Disclaimer
The medical information on this site is provided as an information resource only, and is not to be used or relied on for any diagnostic or treatment purposes. This information is not intended to be patient education, does not create any patient-physician relationship, and should not be used as a substitute for professional diagnosis and treatment.
Devic Disease
Neuromyelitis Optica
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Overview
Description for this condition is not yet available.
Trusted Medical Sites
Mayo Clinic
A website that provides disease symptoms and treatment information.
Genetic & Rare Diseases Information Center (GARD)
GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.
Support Organizations
Support organizations can provide help and guidance in areas such as peer matching, education and training, and therapy and counseling.
Disease Resources
Resources can help guide your quest for factual and reliable information.
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Medical Professional Network
Search by name, country, state, and specialization to find the institutions and experts in rare neuroimmune disorders near you and connect your health care team to our medical experts to ensure you are getting the best care possible.
Rare Neuroimmune Disorders Symposium
Attend lectures by leading clinicians, participate in workshops, and get to know people from around the world who have these disorders. All symposium talks are recorded and are available in the Resource Library and on our YouTube page.
Ask the Expert Podcast
We have moderated podcasts on a wide variety of topics that affect people living with rare neuroimmune disorders.
Newsletters
Our Newsletters are delivered through email and, if you choose, through regular mail. Newsletters feature the latest information and inspiration about SRNA and our community, and highlight events, opportunities, and research updates.
Weekly Blog
We feature helpful blogs written by SRNA members, as well as clinical experts in rare neuroimmune disorders. The blogs cover a wide variety of topics that affect the lives of people with these disorders.