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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!


Neuromyelitis optica spectrum disorder

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Type of Disease: Rare Condition or Disease

Trusted Medical Sites

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.
Displaying 1-5 of 26 results.
FSHD Basics
Added On: Jul 15, 2019
Category: General
Language(s): English
A brief overview of the disease.
Our Hope Ambassadors
Added On: Jun 20, 2019
Category: General
They are a community of heroes for a common cause – to advance diagnosis, treatment, research, and awareness of rare neuroimmune disorders, and to share their stories with others.
Smart Patients Online Community
Added On: Jun 20, 2019
Category: General
Join an online community of patients and caregivers. Be connected directly to other members via the Smart Patients Online Health Community.
Annual Quality of Life Family Camp
Added On: Jun 20, 2019
Category: General
The TMA is proud to offer a camp. The camp helps children with these disorders and their family members experience the joys of summer camp and develop relationships and connect with others who experience the same symptoms and conditions.
Global Support Group Network
Added On: Jun 20, 2019
Category: General
Join a support group near you and benefit from the insights and experiences of people whose lives have been affected by a rare neuro-immune disorder. Learn their stories and share yours.