Every July, we come together for #AFMAwarenessMonth to amplify voices, share stories, and drive change for people living with acute flaccid myelitis. From people diagnosed and caregivers to researchers, policymakers, and advocates – every voice matters.
1 Minute
Share our social media posts, or create your own! Follow us on our platforms (Instagram, FB, X, LinkedIn, TikTok) and help share facts and resources about AFM. Easy peasy!
1 Hour
Meet others in the rare neuroimmune disorders community at our online community meetup on Friday, June 20! Anyone is welcome, no matter where you are located. Sign up here.
1 Day
Host a gathering or event for AFM Awareness Month. No event is too small! Whether you create a gathering for five people or fifty, you will make an impact. If you’re already hosting an event, sign up here, and we’ll add it event to our calendar.
