Who We Are
The National Autism Network (the Network) is a new, independent, community-led organization that brings together Autistic people, families, subject matter experts, and community partners to inform the federal government on how to carry out Canada’s Autism Strategy.


What We Do
The Network actively engages with Autistic people and their families to help shape community priorities and drive action to bring Canada’s Autism Strategy to life.
Our Values
Centers Lived and Living experiences: Creates space for Autistic people, families, caregivers, researchers, and community partners across the country to share their knowledge and shape decision-making
Supports Lifespan Needs: Promotes inclusive policies and supports from early childhood through adulthood and into older age
Champions Authentic Community Leadership: Ensures Autistic leadership across Canada plays an active and central role in the conversations that guide policy.
Prioritizes Inclusive Engagement: Champions equity and equal representation by ensuring that the perspectives of Indigenous Peoples (First Nations, Métis, Inuit, and Urban Indigenous), rural and remote communities, people with co-occurring conditions, non-speaking Autistic people, and racialized and historically marginalized groups are included and valued
Strengthens Cross-Sector Collaboration: Encourages on-going collaboration to build coordinated, sustainable solutions rooted in authentic experiences
Drives Systemic Change: Influences national priorities and policies by centering on real community input to shape decision-making
Our Job
Advises Government: Informs the National Autism Secretariat at the Public Health Agency of Canada (PHAC) on how best to implement Canada’s Autism Strategy
Connects Communities: Links organizations, service providers, governments, and community partners to promote an inclusive and coordinated approach to Canada’s Autism Strategy.
Meet The Team

Dr. Karen Bopp
Interim Chief Executive Officer
Read bioKaren has dedicated over 30 years to supporting and working in partnership with Autistic and Neurodivergent people and their families. She holds an M.Sc. in Speech-Language Pathology and a PhD in Special Education from the University of British Columbia (UBC), where she also completed a postdoctoral fellowship in Medicine and Education. Her career spans frontline clinical work, policy leadership, and advocacy. Karen began her career as a Speech-Language Pathologist supporting children on the spectrum and their families. In her role with the B.C government, she led the development of autism policy, cross-ministry initiatives, and improvements to services and systems. At UBC, she created professional development programs for primary care providers, dental professionals, employers, and early childcare workers to enhance accessibility and inclusion. Most recently, she worked with the B.C.’s Representative for Children and Youth, where she engaged with self-advocates, families, and community organizations to inform government policy and drive systemic change. Karen is honoured to serve as Interim CEO of Canada’s National Autism Network.

Max MacKellar
Project Operations Manager
Read bioMax brings over a decade of experience in project management, operations, and strategic planning across nonprofit, startup, and impact-driven sectors. With a strong foundation in building inclusive systems and leading cross-functional teams, Max specializes in creating collaborative, sustainable, and impact-driven operations that strengthen mission-based organizations. He previously founded a virtual movement platform focused on serving the 2SLGBTQIA+ community as well as those experiencing chronic illness and chronic pain.
As Project Operations Manager, Max leads the development of internal systems and structures that enable the Network’s mission. Drawing on both professional expertise and lived experience, he is deeply committed to equity, accessibility, and community-led change. Max is currently completing his studies in Masters of Business Administration at the University of British Columbia (UBC). His work focuses on building sustainable operations that will support the Network’s long-term growth while honouring the lived and living experiences of autistic people and their families.

Jen McCaffrey
Communications Coordinator
Read bioJen brings a decade of experience in digital communications, graphic design, and web development. She has worked with a range of community-focused organizations and businesses to help translate complex ideas into clear, approachable content that reflects the needs and values of the people it serves.
As Communications Coordinator for Canada’s National Autism Network, Jen leads the development and implementation of inclusive, bilingual communications strategies. She brings lived and living experience, and her personal journey navigating support gaps deeply informs her commitment to clear, non-stigmatizing, and community-centered messaging. She is dedicated to listening, learning, and ensuring that the Network’s communications reflect the real-life experiences of Autistic people and their families.

Elaina Moss
Committee & Council Engagement Coordinator
Read bioElaina Moss (They/Them) is a hard-of-hearing Autistic program and community development professional based in British Columbia. They have spent over a decade designing and leading mental health initiatives that centre lived and living experience, including peer support programs, community and workplace training programs, and a recovery college. They bring expertise in co-design, adult-education and psychoeducation, stakeholder engagement, and project management.
Elaina is passionate about building inclusive and collaborative spaces where Autistic perspectives meaningfully shape programs and systems, with particular interest in supporting Autistic people navigating chronic illness, concurrent disorders, intersecting identities, and those assigned female at birth who were late-diagnosed or late-identified, including women, non-binary, and agender individuals. Before moving into mental health and systems level work, they spent four years supporting preschool-aged non-speaking autistic children as a classroom support and music therapy assistant.
Outside of work, Elaina enjoys exploring their special interests in musical theatre, vocal technique, marine biology and narrative focused RPGS. They share their home with their spouse and two affectionate feline companions.

Olivia Tefft
Senior Research & Policy Analyst
Read bioAs an autistic woman diagnosed in early adulthood, Olivia Tefft believes strongly in the importance of integrating lived experience and empirical data to develop effective policies and programs. In her current role as Senior Research and Policy Analyst, she supports the National Autism Network’s mission through evidence-informed research, policy analysis, and reporting.
Olivia brings 8 years of experience in research, project coordination, and stakeholder engagement across the health sector. Previously, Olivia worked as a Policy Analyst at the Public Health Agency of Canada, where she conducted qualitative and quantitative analysis to inform public health data initiatives. During this time, she served on the Steering Committee for the Infinity Network for Neurodivergent Public Servants, where she helped to establish a first-of-its-kind network that now represents over 3,000 members across the federal public service. More recently, she worked at the Public Health Association of British Columbia, where she led a province-wide initiative to develop a community action plan to advance BC’s Population and Public Health Framework.
She holds a Master of Arts in Health and Exercise Psychology from the University of Manitoba, where her thesis used knowledge translation frameworks to examine how different understandings of chronic pain influence assessment and treatment approaches.
Based on Vancouver Island, Olivia enjoys exploring and learning about the local environment, playing video games, swimming, reading fantasy and sci-fi novels, weightlifting, listening to music, and spending quality time with her partner and three cats.

Jennifer Branston
Administrative Associate
Read bioJennifer Branston is a passionate advocate for Autism and accessibility, dedicated to promoting equity and challenging systemic ableism across British Columbia. Her commitment to inclusive communities is reflected in her previous service on the North Shore Disability Advisory Committee, as well as board roles with Autism Community Training (ACT) and Autism B.C.
Jennifer is a frequent speaker on neurodivergence, neuro affirmative practice and ableism, sharing her insights at institutions such as the University of British Columbia (UBC) and Simon Fraser University (SFU). As the past chair of the North Vancouver Parent Advisory Council (NVPAC), she led both its Diversity, Equity and Inclusion and Disability Advisory Committees for over seven years, offering valuable perspectives as both an Autistic adult and Autistic parent.
She also serves as a UBC Health Mentor and was honoured with the 2024 George Matthew Award for Excellence in Parent Leadership from the BC Confederation of Parent Advisory Councils (BCCPAC).
Through her leadership, advocacy, and public engagement, Jennifer works to foster inclusive practices and deepen understanding of Autism within educational and healthcare systems, as well as the broader community.

Rebekah Kintzinger
Accessibility Advisor
Read bioRebekah Kintzinger is a Canadian Autistic advocate, writer, and accessibility advisor based in Kelowna, BC. Diagnosed in 2012, Rebekah has spent over 7 years working to advance accessibility, equity, and inclusion for Autistic and disabled people across Canada, and internationally. Her work spans health, education, and policy, centering Autistic perspectives in publications, conferences, and government submissions.
She has been published in Autistics Aloud and the Canadian Journal of Autism Equity, spoken at national and international events, and been quoted in Senate discussions and news media.
Rebekah currently helps shape neuro-affirming communication practices and accessible content. She also mentors other Autistic people and collaborates on projects that center lived experience and systems change.
Creative and community-minded, Rebekah brings compassion and curiosity to everything from policy to parenting. She lives with her neurodivergent family, loves drawing and writing, and is known for re-enacting Monty Python skits with her kids.

Dr. Mackenzie Salt
Knowledge Broker
Read bioDr. Mackenzie Salt is an Autistic autism researcher and a research associate with the McMaster University Autism Research Team and the National Centre for Autism Collaboration. He is also a part-time assistant professor in the Department of Psychiatry and Behavioural Neurosciences at McMaster University. He holds a PhD in Cognitive Science of Language from McMaster University and he is a Health System Impact Fellowship program alumnus. He has a background in qualitative research and research engagement. He has worked with Autistic people for over 15 years and he is currently working on several projects, all involving gathering information from and learning from the experiences of Autistic adults and using the findings to inform policy change. He is also currently the Editor-in-Chief of the all-Autistic editorial board of the Canadian Journal of Autism Equity.
Meet The Board

Maddy Dever
Board Chair
Read bioI’m an Autistic advocate, writer, speaker, and parent of four Autistic young adults (ages 17–26). I live in the small rural town of Smiths Falls, just outside Ottawa, and bring both lived experience and governance knowledge to the table.
Over the past decade, I’ve worked across Canada to shift the conversation about autism and disability toward strengths, acceptance, and inclusion.
I advocate at all levels of government and with organizations across the country to ensure Autistics and their families are not only heard but meaningfully involved in shaping the policies and programs that impact us.
I’ve served the past four years as Co-Vice Chair of the Autism Alliance of Canada and am currently the Interim Chair of the Board of Directors for the National Autism Network. I’ve also been involved in research, education, and health care initiatives that prioritize co-design and lived experience leadership.
I am continuing to serve on the National Autism Network’s Board of Directors to support our mission of helping Autistics thrive by guiding governance with transparency, compassion, and the belief that real inclusion starts when we lead together.

Dani Marshall
Board Vice-Chair
Read bioMy name is Dani, and I live with my family in Gatineau, Quebec, where I’m a proud mother to two daughters. I am an Innu woman and a member of the Pekuakamiulnuatsh First Nation (Mashteuiatsh). My lived experiences deeply inform my work, and I am committed to ensuring Indigenous voices are heard and valued at every table I sit at.
I work as a Project Management Advisor with Indigenous Services Canada, focusing on child and family services reform and data modernization. I hold a Project Management Professional certification and am passionate about leading initiatives that support and empower communities.
As a neurodivergent person with lived experience of ADHD and autism, I bring a unique and intersectional perspective to both my professional and volunteer roles. I believe that representation matters—and that Indigenous and neurodiverse voices must be central in shaping the policies and communities that affect us.
Outside of my public service career, I volunteer with Girl Guides of Canada and actively organize within the Infinity Network, a community for neurodiverse public servants.
I am excited and honoured to be elected Board of Directors of the National Autism Network. I am looking forward to contribute my skills in governance, project management, and community building. Most importantly, I want to help strengthen a national voice that centres the perspectives, rights, and dignity of autistic and Indigenous people in Canada.

Amanda Hutchison
Read bioHello/Bonjour, my name is Amanda Hutchison and I’m a settler on Qayqayt First Nation land, colonially known as New Westminster, BC. With a professional background in provincial and federal public service, I exercise my creative spirit as a writer who breaks down cultural and societal trends to become more accessible.
To combat the time I spend online, I beach glass hunt, as it combines exercise, proximity to nature and pattern recognition, lighting up my neurodiverse brain. I self-diagnosed on the ASD in 2003 when a friend shared her clinical diagnosis with me, where I related to every single word on the document.
Today, I live openly as an Autistic adult which is due to disability support organizations such as AutismBC, The Canadian Centre for Rehabilitation and Work, and Neil Squire. My desire to be on the Board of Directors of the National Autism Network stems not only from my lived experience as an unsupported Autistic youth, but to speak for Autistic adults like myself who cannot maintain sustainable work and live on or below the poverty line.
I promise to advocate for enhancing and expanding investment in employment programs so many more Autistic people living in Canada are successfully employed.

Corey Walker
Read bioI live in Dawson Creek in Northern BC with my autistic wife. I am an autistic motivational speaker who equips and empowers autistic individuals and other neurodivergent people, as well as their families, to live full lives by sharing some of the strategies I’ve used to overcome many of the challenges in my life.
I believe that everybody has a right to a full and enriching life. I also share how their uniqueness can be used as a strength.
I was diagnosed as autistic while in my early 20s and have experienced both success and discrimination because of my diagnosis.
I have been involved with the Autism Alliance since 2019, joining their board in 2020 and have worked for various autism organizations between 2012 and 2022. During that period, I authored a toolkit on autistic employment (reflecting 172 autistic voices) and pushed for full inclusion of the autism community in society.
I joined the National Autism Network board because I feel we need voices from both smaller and larger centres to ensure Canada’s national autism strategy reflects the needs of the entire autism community. I will be a tireless advocate for all of those in the autism community, regardless of their location or background.

Debra Brin
Read bioI live in a rural Saskatchewan community and spend my time reading, writing and gardening. I discovered that I’m Autistic after retirement from a wide range of occupations that I could never figure out why they were not a good fit.
I was also the single parent of an Autistic son who lived to age 36. He was born in 1974 and also lived undiagnosed as we were both “skilled maskers”. There was awareness (and self-awareness) of our difference from others but not of our struggles.
I believe that I can help bring to the board the voice of the late- or non-diagnosed Autistics who never have the chance to make informed choices about their life’s path, their related medical issues, how to access support or even how to find other Autistics.
Many of us with sensory issues do eventually find each other in small towns, once we get a pension, where life is slower and quieter, and where we might afford housing.
Many of us end up unhoused at any stage in life. As well as perspective, I have skills and insights gleaned from my participation and leadership in social justice groups that could be valuable in the struggle to improve our opportunities and outcomes in life as Autistic people.
The National Autism Network gives me hope that we can make positive changes, even in light of the flood of misinformation coming into our country right now.

Evan Rubin
Read bioEvan Rubin, from Richmond, BC, is a passionate people connector, advocate, and strategic thinker with over 25 years of leadership experience across nonprofit and for-profit sectors. Known for his people-centered and creative approach, he has built strong relationships with grassroots organizations, national networks, government partners, and business leaders to advance inclusion and community collaboration.
Evan’s professional experience spans multiple sectors, including work as a Business Analyst and QA Project Manager for a multinational B2B retail procurement platform, establishing and managing the West Coast operations of a national recruitment agency, and most recently, a community-facing inclusion engagement role with an autism organization. There, he led initiatives focused on meaningful inclusion, community engagement, and lifespan support while strengthening partnerships and amplifying the voices of Autistic people and families in shaping inclusive practices.
In both professional and volunteer roles, Evan has built meaningful corporate and community partnerships and helped organizations grow through strategic planning, new program development, and new business initiatives. His collaborative approach has helped secure significant funding for nonprofits by creating new fundraising opportunities and corporate partnerships, cultivating donor and community engagement, and crafting and supporting successful grant applications.
As the proud dad of an Autistic son, Evan brings more than 20 years of lived and living experience. His family’s journey has given him deep insight into the barriers faced by Autistic people and families such as screening and diagnosis, economic inclusion, and access to services and resources. This fuels his drive to build a more inclusive Canada for Autistic individuals like his son and for families like his own.
Evan believes Autistic people and families must be meaningfully included in shaping priorities and action. His goal on the National Autism Network Board is to help drive real, lasting change, ensuring that policy, programming, and funding are informed by community wisdom, accountability, and sustained follow-through.

Lisa Lintott
Read bioMy name is Lisa, and I’m from Calgary, Alberta. I hold a Master of Public Health and work as a Research and Evaluation Specialist for a non-profit organization.
I’m passionate about learning and appropriately using data to create meaningful change. Outside work, I enjoy reading extensively and spending quality time outdoors with my family.
Recently, at age 53, I was diagnosed as Autistic and ADHDer, which has provided both clarity and new challenges. These diagnoses have initiated my journey toward a deeper understanding of myself and my needs, while also prompting questions about my identity and the support I require.
I am now receiving services from a local autism organization and starting to engage with the wider community. I joined the National Autism Network’s Board of Directors to share my lived experience, research skills, and neurodivergent perspective.
I aim to help develop inclusive policies and practices. This also presents an opportunity to learn from others, enhancing my life and bolstering my advocacy efforts. I value the importance of representation and collaboration and am excited about contributing to a world where everyone is heard, supported, and celebrated.

Lydia Clarke Rehman
Read bioMy name is Lydia Clarke Rehman, and I’m from Toronto, ON.
I hold a Bachelor of Science in Anthropology, a Bachelor of Laws, and a Master of Public Health in Indigenous Health, as well as a Postgraduate Certificate in Autism and Behavioural Science.
I have over five years of professional experience working in health research and supporting student success within higher education. I’m a lifelong-learner and I enjoy writing, reading, painting, travelling, community engagement, crafting jewelry, and fishing in my spare time!
I am autistic, and my experiences navigating systems that have often been inherently ableist have deeply shaped my passion for advocacy. These challenges have given me a critical perspective on accessibility and the need for meaningful inclusion of autistic and neurodivergent voices.
I am committed to building a Canada where the lived experiences of autistic individuals and their families shape policies, systems, and communities.
I bring my education, policy expertise, leadership, and lived experience to advocate for inclusion, equity, and opportunity across education, policy, and community life.
Serving on the Board of the National Autism Network will allow me to use these experiences to strengthen representation and create meaningful opportunities for autistic people nationwide.

Mathieu Giroux
Read bioI am an autistic person and considered unfit for employment. In addition, I live with multiple mental health diagnoses: anxiety, depression, self-harm, post-traumatic stress disorder, and suicidal episodes.
Despite this, I am very involved in the autism community in Quebec. For over 10 years, I have been a co-researcher in autism. I have co-authored several studies on various topics related to the inclusion of autistic people and developed a theoretical model on social camouflaging.
For the past five years, my focus has been on research projects that promote self-determination and stigma-free care for autistic people. I am also active at the provincial level as a member of the management committee of the Réseau National d’Expertise en TSA (RNETSA) and of the Réseau pour transformer les soins en autisme (RTSA-TACC).
My lived experience, combining strengths and challenges, along with the intersectionality of being part of the LGBTQ+ community and living with economic precarity offers me a valuable perspective on the diverse issues within the autistic community.
My interest in serving on the Board of Directors of the National Autism Network is rooted in the proverb: “Alone, I may go faster, but together we go further.” So, let’s go further, together!

Robin Carrey
Read bioMy name is Robin Carrey. I’m an AuDHD educator in Whitehorse, Yukon. I’m an avid reader, a diver-into-rabbit-holes, a dog-mom, and learning geek.
During my career as an educator, my teaching passions have been Theatre, Social Studies (via a social justice lens), English, and supporting my neurodivergent students.
Currently I work at our Department of Education as a Project Manager, my efforts split between our RISE (Reimagining Inclusive and Special Education) and Student Support Services divisions.
I grew up at a time when ADHD/Autism were not considered disorders that were found among little girls. It took decades to get an ADHD diagnosis, and my Autism remains self-diagnosed. My health care team all agree that I’m autistic, but no one is interested in taking on the cost of helping me get diagnosed (which is particularly difficult for a grown woman in the North).
I want to help create a Canada where the stigma against all NDs, including Autism, is dispelled, where we’re recognized interacting with, perceiving and processing the world differently, rather than being flawed. I want my students to live in a world where their ways of being in the world are accepted, valued and accurately understood.

Tom Jackman
Read bioTom is an advocate for acceptance of people on the autism spectrum.
He has been invited to speak and do presentations at many national conferences, including the Geneva Centre for Autism conference in Toronto, the pre-eminent international conference on autism.
Tom is featured in the film Autism Grows Up, a Kelly Brothers/Ability Hub production, which takes a look at the employment challenges of young adults living on the spectrum. He is also featured in the book “Autism: The Gift That Needs to Be Opened”; a resource aimed at improving the lives of parents, educators, and of those on the autism spectrum.
In 2013, Tom received a Queen’s Diamond Jubilee Medal to recognize his volunteer work with the Autism Society of Newfoundland and Labrador.
In 2023, Tom received the second annual Jim and Ginette Munson Autism Leadership Award from the Autism Alliance of Canada, in recognition of his demonstrated leadership and commitment to autism awareness and acceptance.
Tom was part of a team of Autistic adults and family members that assembled a Mental Health Literacy Guide for adults on the spectrum.
The Autism Mental Literacy Project (AM-Help) is available online, and is a project of York University, the Public Health Agency of Canada, and the Center for Addiction and Mental Health. This project also produced six animated YouTube videos about understanding autistic mental health and wellbeing, and the supports that are available.
Tom is a leader/ambassador for neurodiversity at Motormind Garage. Motormind Garage is a new innovative and inclusive Motorsports oriented program that brings together people from neurodiversity, plus many other brain related backgrounds such as concussions and dyslexia.
Motormind believes in the Power of Motorsports. Our activities revolve around Motorsports, from engine therapy to car builds. This unique and inclusive program for those into racing, race simulators, karting, and track racing allows individuals to be involved with automotive technology and motorsports, while developing transferable skills, which can lead to employment and future lifelong opportunities.
Tom recently completed a lengthy board term at Autism Canada, and has previously served on the board of the Autism Society of Newfoundland and Labrador.
Tom is on the Autism Action Council in Newfoundland and Labrador which implements the provincial Autism Action Plan. The plan is an initiative by the provincial government to improve autism services through a more integrated, “whole government” approach. The plan focuses on expanding and enhancing support for individuals with autism, and their families.
Tom is a community ambassador at Disability Without Poverty. From our board of directors to provincial coordinators, from our talented staff to visionary leadership, and from our board of directors to our community partners, disability without poverty is united with a shared purpose to foster prosperity, harness collective power, ignite passion, and ensure full participation for every person with a disability across Canada.
Tom is a member of the Autistic Advisory Team at (ACT) – Autism Community Training.
Tom lives in St. John’s Newfoundland and Labrador.
If you want to connect with Tom Jackman, you can contact him via email: tagjackman@gmail.com

Ying Wu, PhD
Read bioCalgary, Alberta
I am a PhD-trained scientist with over 30 years of experience in brain research at universities in China, the United States, and Canada.
Alongside my scientific career, I have been deeply involved in community initiatives focused on autism spectrum disorder (ASD) and family support. For more than a decade, I have supported local Chinese immigrant families raising children with ASD.
Since 2022, I have served as a member of the Provincial Parent Advisory Committee – Family Support for Children with Disabilities (FSCD). Since 2023, I have also served as a peer mentor and family advisor with Family-to-Family Connections at Alberta Children’s Hospital, and as a board member at Janus Academy, a private school dedicated to students with ASD.
As the proud mother of an autistic youth, I have developed a profound appreciation for the unique strengths and potential of every autistic individual. My lived experience has strengthened my belief that, with the right supports and inclusive environments, autistic individuals can thrive and make meaningful contributions to their communities.
In 2024, I co-founded Spectrum Promising Association (SPA), a nonprofit organization dedicated to advancing understanding, inclusion, and opportunities for autistic individuals.
Through a strength-based approach, SPA strives to create inclusive environments where individuals with ASD can flourish and be valued for their unique contributions.
I am eager to contribute my scientific expertise, community experience, and personal journey—while learning from others across Canada. By working together, sharing diverse perspectives, and building on our collective strengths, I believe we can create better outcomes for autistic individuals and their families.
