Yet that was the nickname given to Camp Jened, a summer camp for children, teens and adults with disabilities that operated in the Catskill Mountains of New York from 1951 to 1977. The camp is the subject of a documentary on the origins of the disability rights movement released earlier this year.
Before Americans began to see the falsehoods and dangers of such stereotypes, it was common to use terms like gimp, deformed, imbecile, freak, retarded and cripple to describe a person with a disability.
“Today that’s like the ‘N’ word, but that was what you were called in those days. You were seen as crippled and perceived not able to take care of yourself or accomplish things,” said retired Rep. Tony Coelho, who has lived with epilepsy since an accident at age 16.
“The young people getting out of their wheelchairs, not able to use their lower extremities, but still crawling up those marble steps … ” said Coelho with obvious emotion.
“All of a sudden it was visual: The Capitol steps are not inclusive for people in wheelchairs and for people with disabilities. I knew this was going to really change things. We passed the bill in the House by a big margin.”
Among those protesters were a number of former “Crip” campers. Most spent their summers there during the protests of the late 1960’s and early 1970’s, when the camp counselors, mostly college students, were heavily influenced by hippie counterculture.
Strict rules and the typical structure of camp life were discarded and “Crip Camp” became a place to experiment with drugs, sex, independence and grand ideas for change.
For young people who were used to the world seeing them as incapable and unworthy, the experience was transformative.
“Even when we were that young, we helped empower each other. It was allowing us to recognize that the status quo is not what it needed to be,” said former camper Judith “Judy” Heumann, who had polio as a child and uses a wheelchair.
Heumann is one of the starring characters in “Crip Camp: A Disability Revolution,” which captured acclaim at the Sundance Festival and was released in March on Netflix. The film was produced by Higher Ground Productions, the company founded by former President Barack Obama and former first lady Michelle Obama
Raw and powerful, shocking and inspiring, the documentary follows Heumann and other former campers as they become nationally visible activists during the 1970s and into the 1980s.
“Crip Camp is both a gripping look at the history of the disability rights movement and a timely call to action, urging us to explore our own duty to fight for the dignity of all people,” Obama said in a statement.
In 1977, she and more than 100 disabled activists — including several former Crip Camp alumni — staged a 28-day sit-in at a San Francisco federal building in a bid to influence regulations that were defining the rights of people with disabilities. The dramatic and successful event captured the attention of the nation and set the stage for the 1990 passage of the Americans with Disabilities Act.
“We demonstrated to the entire nation that disabled people could take control over our own lives and take leadership in the struggle for equality,” Heumann said.
The fight continues
“The anniversary is really great; it’s important,” Coelho said. “We’ve made a lot of progress, but we need to do more.”
During the coronavirus pandemic, those disparities have become pronounced, with many states choosing to triage people with disabilities, Coelho said, putting them last on lists for ventilators and other lifesaving measures.
“If you have a disability, they say you have less quality of life years than if you don’t have a disability,” he said. “Consequently, if there’s a ventilator, it should go to the person who has a better quality of life or life expectancy.
“We’re aggressively working to change it and we’ll get there. But can you believe they would actually do that in this day and age?” he said.
Another issue that has come to critical mass during the pandemic is a lack of web accessibility.
Why would being able to fully navigate a website be such a burning issue? Just think about how you pay bills, shop, find a doctor and make an appointment — and especially in the time of Covid-19 — order groceries and anything else.
Because the internet was still an infant at the time the ADA passed, the legislation doesn’t directly cover digital accessibility. But it needs to and now, advocates say.
“There have been lawsuits filed — in 2019 over 2,000 were filed and one of them got all the way to the Supreme Court and won,” Coelho said. “Now the issue is how do we get legislation as opposed to a court decision?”
Redesigning a website to fix accessibility issues can be a huge investment, so companies have sprung up that retrofit current designs. Fixes might include the ability to increase volume and font size, adjust contrast, caption pictures and streamline links, which disability advocates say often benefit the rest of us with fading hearing and eyesight as well.
“What people don’t realize is that an accommodation made for someone with a disability actually becomes a convenience for people without the disability,” Coelho said, pointing to an example in the physical world.
“Take curb cuts on streets in neighborhoods,” he said. “They help bicyclists cross the street as much as they assist those in wheelchairs.”
If companies — and the nation — could take an inclusive attitude and realize they are not just helping those with disabilities, but everyone, the battle for equal rights for people with disabilities would be won, advocates say.
Until then, people with disabilities will continue to speak out proudly, demanding their full rights as American citizens, just as those kids did so many years ago in “Crip Camp.”
“I thank God for my epilepsy because it’s made me a stronger, better person, but a lot of us in the community feel that way,” Coelho says. “We don’t feel like we’re handicapped. We feel like we got something that makes us better and stronger, and we’re going to be out there fighting.”