SRNA | connect. care. cure. ™ Revenue
Non-profit Organizations • 
PO Box 826962, Philadelphia, United States • 11-20 Employees
SRNA | connect. care. cure. ™ revenue & valuation
| Annual revenue | $1,283,325 |
| Revenue per employee | $86,000 |
| Estimated valuation?This valuation is estimated based on industry average for the Non-profit Organizations industry and current estimated revenues | $4,200,000 |
| Total funding | No funding |
Key Contacts at SRNA | connect. care. cure. ™
Lydia Dubose
Associate Director Of Community And Volunteer Engagement
Chitra Krishnan
Executive Director
Company overview
| Headquarters | PO Box 826962, Philadelphia, Pennsylvania 19182-6962, US |
| Phone number | +120222023 |
| Website | |
| NAICS | 813 |
| Keywords | Acute Disseminated Encephalomyelitis, Acute Flaccid Myelitis, Neuromyelitis Optica Spectrum Disorder, Optic Neuritis, Transverse Myelitis, Mog Antibody Disease |
| Founded | 1994 |
| Employees | 11-20 |
| Socials |
SRNA | connect. care. cure. ™ Email Formats
SRNA | connect. care. cure. ™ uses 2 email formats. The most common is {first initial}{last name} (e.g., jdoe@myelitis.org), used 50% of the time.
| Format | Example | Percentage |
|---|---|---|
{first initial}{last name} | jdoe@myelitis.org | 100% |
About SRNA | connect. care. cure. ™
The Siegel Rare Neuroimmune Association (SRNA) is a not-for-profit international foundation dedicated to the support of children, adolescents, and adults with a spectrum of rare neuroimmune disorders including: Acute Disseminated Encephalomyelitis (ADEM), Acute Flaccid Myelitis (AFM), MOG Antibody Disease (MOGAD), Neuromyelitis Optica Spectrum Disorder (NMOSD), Optic Neuritis (ON) and Transverse Myelitis (TM). Founded in 1994 by family members and persons with these diagnoses, The TMA was incorporated on November 25, 1996 in the state of Washington and we became a 501(c)(3) organization on December 9, 1996. Membership of SRNA includes individuals with these rare disorders, their family members and caregivers, and the medical professionals who treat individuals with these disorders. SRNA currently has approximately 14,000 members from more than 80 different countries and has a large number of support groups across the United States and around the world. There are no membership fees. Our goal is to advance a comprehensive network dedicated to the care of our members through the development of professionals specializing in these rare disorders, centers of excellence focused on these disorders around the world, and our international community support system. Additionally, we are focused on strategic research priorities with our Board of Directors and Scientific Council to further the understanding of the causes of ADEM, AFM, MOGAD, NMOSD, ON, and TM, and to develop new acute and regenerative therapies.
Employees by Management Level
Total employees: 11-20
Seniority
Employees
Funding Data
SRNA | connect. care. cure. ™ has never raised funding before.
SRNA | connect. care. cure. ™ Tech Stack
Discover the technologies and tools that power SRNA | connect. care. cure. ™'s digital infrastructure, from frameworks to analytics platforms.
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Frequently asked questions
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