Non-profit scale SRNA is a global, membership-driven nonprofit with 11-50 employees and revenue between 1M and 10M, suggesting capacity for larger program partnerships, sponsorships, and multi-year grant opportunities.

Patient-centered network With approximately 14,000 members across 80+ countries and extensive support groups, SRNA represents a broad, engaged community for awareness campaigns, clinical education programs, and patient-first product or service initiatives.

Research focus SRNA prioritizes strategic research on rare neuroimmune disorders and supports centers of excellence, presenting opportunities for research collaborations, clinical trial sponsorships, and data-sharing initiatives.

Digital engagement Active online presence, partnerships, and recent digital community initiatives (Discord server, podcasts, educational content) indicate receptiveness to tech-enabled programs, telehealth partnerships, and digital learning platforms.

Funding potential With revenue in the 1–10M range and partnerships history, SRNA is a viable candidate for grant funding, sponsorship deals, educational program funding, and collaborative campaigns with healthcare and pharma affiliates.