Millions of Americans with disabilities are being overlooked during the pandemic recovery, stuck at home without therapy or social programs, and struggling to book Covid-19 vaccinations.

In Connecticut, a switch March 1 to an age-based inoculation system angered advocates, who said the decision bumped special-needs residents. Disability-rights groups in Arizona are pushing for swifter access to shots, citing a higher Covid-19 death risk. Coast to coast, vaccination-booking websites that lack adaptive software are confounding people with vision problems.

“One year into the pandemic, we’re just getting around to wonder how to make vaccine sign-up universal and accessible,” Bryan Bashin, chief executive officer of San Francisco-based LightHouse for the Blind and Visually Impaired.

About 1 in 4 adult Americans, or 61 million people, have a disability that can affect mobility, cognitive function, hearing and sight, according to the U.S. Centers for Disease Control and Prevention. Thirty years after the Americans With Disabilities Act fundamentally changed how public and private entities must treat them, the pandemic is demonstrating once again how the disabled can be forgotten, advocates say.

In New Jersey, 29-year-old Evan Hookey of Princeton, who has autism, scored the first of two vaccine shots Feb. 21. His mother, Gina, said that after more than a year at home, he was so excited to be around people again that “you might have thought he was going to a birthday party.”

It’s not certain when Hookey will return to his job, stacking inventory at a Wawa convenience store, or his day program, where he exercises, socializes and does meal prep and art projects. Governor Phil Murphy’s administration is allowing some of the state’s 400 such programs to reopen with 50% capacity and other restrictions on March 29.

In Wilbraham, Massachusetts, Brad Kane and his wife have gone more than a year without home therapy for four children with autism, ages 7 to 13. Each had been getting two to four hours of attention a day, five days a week. When the pandemic hit, the sessions ended with no sign of when they’ll restart. Some of the children have regressed.

“It’s harder to get them to do the things they need to do, like speech and emotional development,” said Kane, an editor. “Even getting everyone to sleep at the same times is an uphill battle.”

In February, Kaiser Health News and WebAIM, a nonprofit group that works on internet accessibility from Utah State University, identified almost 100 government vaccination websites lacking screen-reading technology for people with difficulty seeing. The count may be far higher because even some sites with the software can link to others without, according to the National Federation of the Blind, a Baltimore group that advocates for more than 7 million Americans with a visual disability.

“I should have the same options that anyone else has,” said Chris Danielson, federation spokesman. “Booking a shot is frustrating for everybody, with most people trying several times. We’re not asking for special treatment—we just want the same barriers, not more.”

Some activists have set up Facebook pages to direct people with paralysis and other conditions to states where they qualify for early shots.

Legal Fights
In some places, advocates have gone to court in search of equal access.

The Idaho legislature on March 5 entered into a legal agreement to ensure that people with disabilities can testify before committees remotely. It resolved a federal lawsuit brought in January by five disability-rights groups that said in-person appearances put them at risk for the novel coronavirus.

A federal lawsuit by the Arc Maryland, claiming unequal access to Covid-19 vaccines, led several county governments in March to alter their websites to note that people with intellectual and development disabilities are eligible for the shots.

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