Making library websites accessible : a practical guide for librarians-book

Nothing About Us Without Us

Autistics for Autistics Ontario (A4A) is Canada’s national autistic self-advocacy organization. We are an international affiliate of the Autistic Self Advocacy Network (ASAN). We are an autistic-led organization. We work in partnership with other disability groups to educate the public and transform Canada’s autism policies from a charity perspective to a RIGHTS perspective. Along with our Parent Alliance, we advocate for our federal, provincial and territorial governments to consult directly with autistic people when developing the policies that affect our lives.

To ensure that people with disabilities are treated as equals and that they are given the same decisions, choices, rights, responsibilities, and chances to speak up to empower themselves; opportunities to make new friends, and to learn from their mistakes.

Content about autism by autistic and neurodivergent people. A resource for autistic adults, parents of autistic children, educators, and physicians.

Support our work: https://democracynow.org/giveCivil rights leader Bishop William Barber joins us to discuss his calls for more awareness and justice for dis...

Imagining anti-ableist liberation beyond the rubrics of access and inclusion In the thirty years since the Americans with Disabilities Act was signed into law, the lives of disabled people have not improved nearly as much as activists and politicians had hoped. In Crip Negativity , J. Logan Smilges shows us what's gone wrong and what we can do to fix it. Leveling a strong critique of the category of disability and liberal disability politics, Smilges asks and imagines what horizons might exist for the liberation of those oppressed by ableism-beyond access and inclusion. Inspired by models of negativity in queer studies, Black studies, and crip theory, Smilges proposes that bad crip feelings might help all of us to care gently for one another, even as we demand more from the world than we currently believe to be possible. Forerunners: Ideas First is a thought-in-process series of breakthrough digital publications. Written between fresh ideas and finished books, Forerunners draws on scholarly work initiated in notable blogs, social media, conference plenaries, journal articles, and the synergy of academic exchange. This is gray literature publishing: where intense thinking, change, and speculation take place in scholarship.

Guest Post by Mari Cheney, Associate Director of Research and InstructionBoley Law Library, Lewis & Clark Law School I had the immense honor of attending this year’s annual meeting in Boston us…

"Neurodiversity in the Workplace presents a timely and needed perspective on the role and responsibility of employers, and those working to increase the effectiveness of workplace practices, to examine the many ways we preclude large segments of the population from employment and how we can create opportunities for building a truly inclusive work environment"--

"A bold new assessment of the multipronged attack on American rights, and how to push back, from experts at the Fletcher School at Tufts and the Carr Center at Harvard. In fifteen accessible chapters dealing with voting rights, freedom of speech, criminal justice, gun rights, LGBTQ+ rights, disability rights, religious freedom, privacy, immigration, and more, three renowned thought-leaders, including a former assistant secretary of state, John Shattuck, Sushma Raman, and Mathias Risse present a comprehensive account of the current state of rights in America-along with concrete recommendations to policy makers and citizens for reimagining them"--

"In The Future Is Disabled, Leah Laksmi Piepzna-Samarasinha asks some provocative questions: What if, in the near future, the majority of people will be disabled - and what if that's not a bad thing? And what if disability justice and disabled wisdom are crucial to creating a future in which it's possible to survive fascism, climate change, and pandemics and to bring about liberation? Building on the work of their game-changing book Care Work: Dreaming Disability Justice, Piepzna-Samarasinha writes about disability justice at the end of the world, documenting the many ways disabled people kept and are keeping each other - and the rest of the world - alive during Trump, fascism and the COVID-19 pandemic. Other subjects include crip interdependence, care and mutual aid in real life, disabled community building, and disabled art practice as survival and joy. Written over the course of two years of disabled isolation during the pandemic, this is a book of love letters to other disabled QTBIPOC (and those concerned about disability justice, the care crisis, and surviving the apocalypse); honour songs for kin who are gone; recipes for survival; questions and real talk about care, organizing, disabled families, and kin networks and communities; and wild brown disabled femme joy in the face of death. With passion and power, The Future Is Disabled remembers our dead and insists on our future." --