What COVID-19 Is Teaching Us About the Future of Disability Rights

By Nicole LeBlanc: For Entire Post, Go Here…

This year the disability community celebrated the 30th anniversary of the Americans With Disabilities Act, which was signed into law in July 1990 by President George H.W. Bush. Upon signing this historic piece of bipartisan legislation, he is quoted as saying, “Let the shameful walls of exclusion finally come tumbling down.” This is by far one of my favorite quotes on the successes disability rights activists and their allies have had in the fight for true inclusion in all aspects of community life.

Many of the dreams and goals of the ADA are at the heart of creating a system of care that is truly person-centered. While the ADA has made advancements in things like physical accessibility and community integration, two areas where we as a society continue to fall short are integrated employment for adults with developmental disabilities and access to high-quality healthcare that meets our needs in a person-centered way. Several studies show people with disabilities are a Medically Underserved Population. We often have higher costs and worse health outcomes than the general population. Being declared an MUP by the CDC or Congress could allow for more training of medical providers, higher rates of pay for doctors providing care to us, and more focus on prevention and the social determinants of health.

It is my hope that in the next 30 years, we strive to eliminate health disparities and barriers to employment in the push for a world of true inclusion for all people with disabilities. I dream of a world of no ableism, racism, negative attitudes and stigma. Given that we are in the thick of a massive coronavirus pandemic, it only intensifies the urgent need to make this happen at all levels of government. This pandemic is giving the non-disabled world an idea of what it’s like to be disabled.

The disability community is the world’s largest minority group and we have so much further to go in achieving equality and equity for all. We need to shift the disability benefits system and change attitudes among providers, family members and employers on the benefits of hiring people with disabilities. To support higher rates of employment for people with disabilities we need to eliminate work disincentives in the Social Security benefits system and expand access to supported employment for those without access to home and community-based services. Only after we have done these and many other things will we see a societal shift in attitudes about disability.

I hope this nightmarish pandemic will ignite an intense focus on addressing health disparities and attitudinal barriers faced by people with disabilities so we can be valued for who we are and be given equal access to care and support across all settings.

I believe it is especially important to use this downtime and crisis to dream of a new and better normal — one that is accessible, accommodating and respects the intersectionality of all social justice movements. As Audre Lorde once said, “There is no such thing as a single-issue struggle, because we do not live single-issue lives.” We are all impacted by all social justice movements. Climate justice, economic justice, migrant justice, civil rights, women’s, workers’ and disability rights are all interconnected with one another. In times like these, the disability community must join forces with non-disability groups and give space for people of color especially to step up and lead the way in achieving the dream of a fully inclusive diverse world where everyone is respected for who they are. A world where no one is discriminated against due to race, gender, disability and so forth in all aspects of society.

I hope the COVID-19 pandemic will provide a catalyst to create a world that is more inclusive and accessible for all people with disabilities. Some of the ways to make this happen could include:

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