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 17 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.

Born in the US to immigrant parents, Morénike Giwa Onaiwu’s advocacy journey began with middle and high school stints as a volunteer tutor; later, she served as an undergraduate working with refugee children in a housing project and as a mentor in public schools.

After graduating with a BA in International Relations, Morénike, spent several years in the non-profit sector working with a variety of disenfranchised groups, including women, at-risk teens, and refugee families.

In recent years, she has channeled the majority of her advocacy in volunteer community work.  Morenike currently chairs the Global Community Advisory Board for the NIH Division of AIDS (DAIDS) funded AIDS Clinical Trials Group (ACTG), which is the world’s oldest and largest international community HIV clinical trials program.  She also serves in various other capacities within DAIDS.

Morénike is a Houston Project-Wide Part D community advisory board member and has also previously chaired the Houston Ryan White Planning Council in addition to chairing its Operations and the Quality Assurance Committees and various Ryan White workgroups.  She is also a member of the advisory board of the AIDS Alliance for Women, Infants, Children, Youth, and Families.

Morénike formerly served on the CDC-funded elimination of Mother-to-Child HIV Transmission US Working Group and the Families and Schools Together Project.  She was one of the founding members of the Houston Area Partnership for Fetal Alcohol Spectrum Disorders (FASD).

She is the founder of the former Positive Playdates, a playdate group (now merged with a local nonprofit) that connected HIV affected families and refugee youth, and of the newly launched Advocacy Without Borders, an initiative to reduce disparities through education, community advocacy and self-empowerment.  Additionally, Morénike is currently involved in a variety of leadership efforts related to Ryan White HIV/AIDS Part D Program advocacy.

Morénike, is currently completing a graduate degree in Developmental Disabilities and will follow up with a doctoral program focusing on developing leadership skills within underrepresented groups such as disabled individuals and recent immigrants.

She is the proud mother of six beautiful biological and adoptive children; together they comprise a proud multicultural, multinational, neurodiverse, HIV affected family of color.  She blogs about her life at Who Needs Normalcy.

Sharon daVanport is the Founding Executive Director of Autism Women’s Network (AWN). As an autistic and disability rights activist, her public speaking engagements include topics on: violence against women and girls in vulnerable communities, health and wellness for women with disabilities, and how to effectively use privilege when amplifying the voices and work of disabled people who experience racial and gender inequality.

Sharon is committed to AWN’s mission to provide quality resources by developing inclusive and accessible opportunities for intersectional community. Honors include: ASAN’s Self-Advocate of the Year Award, LSS Award for advocacy focusing on autistic women and girls, and Autism Society of America’s Outstanding Literary Award for “What Every Autistic Girl Wishes her Parents Knew”.

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