DOUBLE YOUR GIFTAll donations will be matched
dollar-for-dollar up to $200,000
Celebrating 30 years of SRNA. Together.
Hosted by the Robbins Family & Valiant Air CommandA Dinner and Gala Fundraiser
Celebrating 30 years of SRNA
2025 SRNA Quality of Life
Family Camp
June 29 – July 3, 2025LEARN MORE ON HOW TO APPLY
ENROLL TODAYThe first-ever online micro-course for people with ADEM, AFM, MOGAD, NMOSD, ON, and TM.LEARN MORE

SRNA

The nonprofit advocating for individuals with rare neuroimmune disorders

ADEM | AFM | MOGAD | NMOSD | ON | TM

Help us provide hope and help to those living with ADEM, AFM, MOGAD, NMOSD, ON, and TM.

No matter how much you choose to give, 100% will directly fund SRNA’s education, research, and community support programs.

International supporters: Please donate using this form

Hojas Informativas disponibles en Español

MFA
Mielitis Flácida Aguda

EMAD
Encefalomielitis Aguda Diseminada

MOGAD
Enfermedad de Anticuerpo MOG

NMOSD
Trastorno del Espectro Neuromielitis Óptica

NO
Neuritis Óptica

MT
Mielitis Transversa

Our Hope Ambassadors

“Time is of the essence when it comes to rare neuroimmune disorders and the time to get awareness out is now. I know this because my 2 ½ year old son has Acute Flaccid Myelitis (AFM) which is a subtype of Transverse Myelitis.”

Read more about Elisa’s and Noah’s story. Elisa and Noah are one of SRNA’s Hope Ambassadors, a community of heroes for a common cause.

2024 Education Sponsors

All educational content and programs are solely developed by the SRNA staff, members of the scientific board and approved by Board of Directors.