Corina Becker is from Kingston, Ontario, Canada. As a child, she was diagnosed with Attention Deficit Disorder and Learning Disabilities, and then with Asperger Syndrome in her late teens. She graduated from high school as an Ontario Scholar in 2003 and was accepted into the English Honors program at Wilfrid Laurier University. While at school, she lives both in dorm and off-campus student housing, and fulfilled duties as Media Coordinator for an on-campus club. She graduated in Fall 2008 with a Bachelor’s of Art in English and is now taking Distance Education courses in the Library and Information Technician Program at Mohawk College.

In 2005 and 2006, Corina worked at Kerry’s Place Autism Services as part of the Community Education and Awareness Team, organizing the Spectrum Art Show. Now, she is the Autism Women’s Network Forum Moderator, and runs her own blog No Stereotypes Here as well as giving autism awareness presentations with Kerry’s Place. In between moderating, blogging and schoolwork, Corina writes two novels, one comic, writes and draws two webcomics (Lord of the Shepherd  and Amhelaki Misadventures), paints, knits, plays flute, tries to read/watch as much manga/anime as possible, and occasionally plays a little DnD.

Elesia Ashkenazy lives in Portland, Oregon. She is passionate about Disability Rights and self-advocacy, and seeks to promote widespread understanding of the needs and rights of autistic individuals, especially females. She is also a parent of a son on the spectrum.

Elesia is the Community Council Chair and Research Assistant for Academic Autistic Spectrum Partnership in Research and Education (AASPIRE). She is also a member of the Community Advisory Board for the Partnering with People with Developmental Disabilities to Address Violence Project via the University of Montana Rural Institute.

Elesia worked as the Chapter & Outreach Coordinator for Autistic Self Advocacy Network (ASAN) for several years and is also a former Board member. In addition, she has served as a member of the Screening Identification and Assessment Subcommittee for the Oregon Commission on Autism Spectrum Disorder.

Outside of her advocacy and public speaking work, Elesia aspires to be a published author of Young Adult fiction. She is also a classically trained ballet dancer who continues to take class several times a week and performs whenever the opportunity arises. Elesia is fluent in American Sign Language (ASL) and is also a cochlear implant recipient. Be sure to check out her blog, Aspitude.

I’m an Autistic woman who is working towards her doctoral degree in cultural anthropology. In general, my research is about communication practices that help us maintain our shared autistic identity, community, and culture. I live, work, and play in southern California.

I am Lori. I am from New York and currently live in Baltimore, MD (US) with Karen, my wife and partner of 18 years, and our 2 cats Nikkyo and Buster.

I learned that I was autistic in 2005 after a lifetime of misdiagnoses. Since then, I have gone from thinking there was no one else like me in the world to finding a huge community of people who have had nearly identical life experiences as me. I have also been on a mission to help autistic people find each other on the internet.

I am a freelance web developer and build and maintain websites for AWN, for my clients, and for other autistic and non-profit organizations. I feel very lucky to be a part of the Autism Women’s Network and hope that someday I will be able to do this type of work for the autism community full time.

Lydia X. Z. Brown (Autistic Hoya) is a genderqueer and transracially/transnationally adopted East Asian autistic activist, writer, and speaker whose work has largely focused on violence against multiply-marginalized disabled people, especially institutionalization, incarceration, and policing. They have worked to advance transformative change through organizing in the streets, writing legislation, conducting anti-ableism workshops, testifying at regulatory and policy hearings, and disrupting institutional complacency everywhere from the academy to state agencies and the nonprofit-industrial complex. At present, Lydia serves as Chairperson of the Massachusetts Developmental Disabilities Council, founding board member of the Alliance for Citizen-Directed Services, stakeholder representative to the Massachusetts One Care Implementation Council overseeing health care for Medicaid/Medicare dually-eligible individuals, and board member of the Autism Women’s Network. In collaboration with E. Ashkenazy and Morénike Giwa-Onaiwu, Lydia is the lead editor and visionary behind All the Weight of Our Dreams, the first-ever anthology of writings and artwork by autistic people of color, published by the Autism Women’s Network in June 2017.

Most recently, Lydia has designed and teaches a course on critical disability theory, public policy, and intersectional social movements as a Visiting Lecturer at Tufts University’s Experimental College, beginning in Fall 2016. Lydia is a past Holley Law Fellow at the National LGBTQ Task Force, where they focused on reproductive justice and disability rights policy issues, and past Patricia Morrissey Disability Policy Fellow at the Institute for Educational Leadership, where they focused on employment opportunities for people with significant disabilities. Lydia also worked for the Autistic Self Advocacy Network for several years as part of the national public policy team, where Lydia worked on various issues relating to criminal justice and disability, healthcare disparities and service delivery models, and research and employment disparities. Additionally, Lydia has interned for the ACLU National Disability Rights Program, the Sylvia Rivera Law Project, the Movement Advancement Project, and the Disability Law Center of Massachusetts.

Lydia has been honored by the White House, the Washington Peace Center, the National Council on Independent Living, and the Disability Policy Consortium of Massachusetts. In 2015, Pacific Standard named Lydia a Top 30 Thinker under 30, and Mic named Lydia to its inaugural list of 50 impactful leaders, cultural influencers, and breakthrough innovators. Their work has been featured in various places, including Religion, Disability, and Interpersonal Violence, Barriers & Belonging: Personal Narratives of Disability, The Asian American Literary Review, Feminist Perspectives on Orange is the New Black, Criptiques, Torture in Healthcare Settings, QDA: A Queer Disability Anthology, Films for the Feminist Classroom, Tikkun, Disability Intersections, Black Girl Dangerous, hardboiled magazine, POOR Magazine, The Washington Post; Sojourners, The Establishment, Al Jazeera America, NBC News Asian America, HerCampus, AfterEllen, and Vice Broadly. Lydia is now a Public Interest Law Scholar at Northeastern University School of Law, where they co-founded the Disability Justice Caucus.

My name is Mara Fritts and I was diagnosed with Aspergers Syndrome in 2008. I have been married for fourteen years to my husband who was also diagnosed with AS in 2008. We have four children, three of which are currently on the autism spectrum.

I am currently a Stay-At-Home-Mom (SAHM) and homeschooling all of my children. I’d like to someday return to college for my degree in Anthropology. However with homeschooling I think I would be much better suited with a teaching degree at this point.

Before I became a SAHM I worked in Customer Service for 15 years with various insurance companies where I was involved with providing service for agents and customers in Life Insurance and Annuities where I gained extensive experience in finance.

I have been on staff at four Science Fiction Conventions, and I am in charge of registration travel arrangements with my husband’s business, as well as having been in charge of the Hospitality Suite.

I enjoy a good challenge and also love working with people. Being diagnosed with Aspergers has taught me many things. One of them is to accept people for who they are and look for the “why” in all situations. It has helped me to help my children reach their potential and teach them how to get around what some consider a disability. In our home we recognize it as a different way of thinking.

Morénike Giwa Onaiwu is a disabled woman of color, educator, writer, public speaker, parent, and global advocate. A proactive, resourceful individual in a multicultural, neurodiverse, serodifferent family, Morénike, who is American-born to immigrant parents and whose undergraduate and graduate degrees are in International Relations and Education, is passionate about human rights, justice, and inclusion.

She is involved in various social justice activism endeavors including HIV-related advocacy, disability rights, learning via technology, research, and gender and racial equity. A prolific writer, Morénike has written for and/or been featured in numerous blogs, abstracts, magazines, books, and other platforms, often drawing from her personal experiences as a late-diagnosed Autistic adult woman, a person of color, an Autistic parent of Autistic and non-Autistic children, and a survivor of intimate partner violence. In addition to writing, she is one of the editors (along with Lydia X.Z. Brown and E. Ashkenazy) of a groundbreaking anthology on autism and race as well as a co-coordinator of the Fund for Community Reparations for Autistic People of Color’s Interdependence, Survival, and Empowerment.

Morénike has been an invited speaker in the White House, at the United Nations Headquarters, and a keynote speaker and/or presenter at numerous peer-reviewed advocacy, education, disability, and research conferences. She has been the recipient of numerous awards, including the “Advocating for Another: Health Activist of the Year” 2014 WEGO Health Award and the “Service to the Self-Advocacy Movement” 2015 Autistic Self Advocacy Network Award.

Her executive experience includes board membership of a number of national research, disability, advocacy, and family service organizations, chairperson of both a large HRSA-funded local planning body and an international NIH-funded community research network, and leadership roles within various entities in addition to her work with the Autistic Women and Nonbinary Network’s Board of Directors and Chairing its Committee on Autism and Ethnicity.

Currently balancing her roles as a faculty member at a state college and as a doctoral student in an educational leadership program, Morénike considers herself a “lifelong learner” who is constantly growing and changing, hopefully for the better! She considers her wonderful children (biological and adopted and all of whom have various disabilities) to be her greatest accomplishment.

She can be reached at: morenike@awnnetwork.org

Sharon daVanport is the Founding Executive Director of Autistic Women & Nonbinary Network (AWN Network) ~ formerly known as Autism Women’s Network.

Sharon’s speaking invitations include the United Nations Headquarters on World Autism Awareness Day (Empowering Autistic Women & Girls) and The White House, Obama Administration (advising on topics regarding disability and autism.) In her work as a Disability & Autistic Rights Activist, she has consulted as an expert panelist advising government agencies, including the GAO, and various policy forums. Sharon speaks at national and local conferences and hosts workshops on topics including: health and wellness for women with disabilities, violence against women and girls in vulnerable communities, and how to effectively use privilege when amplifying the voices and work of disabled people who experience racial and gender inequality.

Honors include: ASAN’s Self-Advocate of the Year Award for service to the self-advocacy movement, LSS Award for advocacy focusing on autistic women and girls, and Autism Society of America’s Outstanding Literary Award for editing, “What Every Autistic Girl Wishes her Parents Knew”.

In her spare time she enjoys traveling, research, reading, music, and spending time with family and close friends.