There are lots of ways to support the work of ASAN!

Help Distribute our Resources

You can help by spreading the word about ASAN’s resources. This can be through posting on social media, referring our resources to people in your community who would benefit from them, or by using our resources in your advocacy work, such as in a state Developmental Disability Council or a meeting with your elected representatives.

Join Us

You can join us as a member and/or sign-up to get emails from us. We often send out local and national action alerts with instructions about how to get involved in specific actions; for example, calling/writing to your state Senators about an important bill.


If you’re interested in legislative/policy issues, you look at our Policy Toolkits and then start working on an issue in your state.

  • Click here to see a list of available resource guides from the Pacific Alliance on Disability Self Advocacy, including “Legislative Advocacy 101: Getting Your Voice Heard”

You can also submit personal testimony about how public policies have affected your life as an autistic person. These stories help our policy team advocate for policies that will positively impact the autistic community. You can share your experiences with our policy center at this form.

Organize a Fundraiser

The work we do wouldn’t be possible without our supporters. Almost anything can be a fundraiser – in the past, supporters have set up their own fundraising pages, donated proceeds from product sales, and even held a 72-hour-long Pokemon charity gaming marathon. Have an idea for a fundraiser, or need help getting set up? Take a look at our new Guide to Fundraising for ASAN, which includes information on different ways to fundraise as well as printable flyers and brochures you can use to share information while fundraising.

Autism Acceptance Month

April is Autism Acceptance Month! Too often, conversations about autism happen about us, without us. Organizations, conferences, and panels on autism often don’t include autistic voices. We are asking you to help solve this problem! One easy way you can help fix this is by taking our Pledge for Autistic Inclusion. The pledge tells event organizers that you won’t come to their events if they don’t include autistic people. That means event organizers will try harder to include autistic people! Make sure that autistic self-advocates get to be a part of every conversation about autism. Take our pledge today at AutismAcceptance.com

Day of Mourning

Every March 1, ASAN and the wider disability community hold vigils to mourn the lives of those we’ve lost and to bring awareness to the horrific trend of violence against our community. Here’s what you can do in your own community to help spread awareness of these tragedies – and help stop more from happening.

  1. Read and share our Anti-Filicide Toolkit.

This toolkit is intended to provide advocates and allies with concrete tools and resources to use in their own communities, including in response to local incidents. The toolkit includes information about how to understand and respond to filicide, frequently asked questions about filicide, and a guidebook for Day of Mourning vigil site coordinators.

  1. Sign up to be a Day of Mourning vigil site coordinator

For the last five years on March 1st, ASAN, ADAPT, AAPD, Not Dead Yet, the National Council on Independent Living, the Disability Rights Education & Defense Fund, and other disability rights organizations have come together to mourn the lives lost to filicide, bring awareness to these tragedies, and demand justice and equal protection under the law for all people with disabilities. Look for opportunities to sign up to be a a Day of Mourning vigil site coordinator on the ASAN website each January.

  1. Visit the Disability Day of Mourning memorial website

The Disability Day of Mourning memorial website can be found at disability-memorial.org. You can read about all of the currently documented victims of filicide and honor their memory. If you have new information, you can send links to news stories to info@autisticadvocacy.org.