Anyone Who Needs Help Seeing Has 2 Million Pairs of Eyes Available With This App

When Rory Hoffman needs to read the labels on his cassette tapes, he opens up an app. Marian Helling Wildgruber finds the spices in her kitchen cabinet by pulling out her phone. Tabitha Jackson grabs her phone before she goes grocery shopping.
Hoffman, Wildgruber and Jackson all are blind or visually impaired. So tasks like reading labels, selecting the right herbs and navigating stores can prove challenging.
That’s where Be My Eyes comes in. It’s a mobile app that connects people who are blind or visually impaired with volunteers who have normal vision. By tapping their camera’s video function, volunteers can guide people with vision impairments in a variety of daily tasks.
The app launched in 2015, and within 11 days, it had 100,000 volunteers. Now, four years later, two million volunteers have joined Be My Eyes. It’s part of a movement coined microvolunteering, whereby small tasks performed by many people can add up to real impact  on a large scale. For Be My Eyes volunteers, there’s no commitment to a certain number of calls. It’s just a chance to help someone out when they need it.
There is an estimated 1.3 billion people with some form of visual impairment worldwide. People who are visually impaired might have family or neighbors they can rely on, but on-demand support 24/7 is unlikely. Sometimes an extra set of eyes is helpful.
Hoffman uses Be My Eyes a few times a week. He typically relies on a neighbor to help him with tasks that require normal vision, but it’s nice to know there’s immediate help at hand, he says.
“I don’t have to wait for anyone to come, I can just take care of it immediately.”
Hoffman, who is a musician, recently wanted to replace the strings on his guitar. But it was impossible for him to feel the slight differences between each string. So Hoffman pulled out his phone and using the phone’s voice recognition feature, made a call on Be My Eyes.
There, a volunteer popped up and read the guitar string labels. In just a few minutes, Hoffman had the right strings for his guitar.
“There are some times when having somebody with a pair of eyes just makes things helpful,” he says. “And to be able to just connect to somebody who’s available to help, that’s really a great idea.”
The app was founded by Hans Jørgen Wiberg, a Danish furniture designer. Widberg, who is visually impaired, was talking with a few of his blind friends when they said they all relied on FaceTime to connect with family and friends for assistance.
Widberg realized this idea could work with volunteers. He brought his idea to a startup weekend in Denmark in 2012, where he met Thelle Kristensen. Together they formed a team. It took two and a half years to develop and bring the app to the market.
“The fire in our belly was to make a worldwide network of volunteers to help out, and it’s been great to see the reaction with ten times as many sighted as blind people,” says Kristensen, the co-founder and CEO of Be My Eyes.
Lauren Traut was deep in conversation when her phone rang, and she received a notification from Be My Eyes that someone needed assistance.
“I told my friend, ‘Hold on. Pause. I got to take this call.’”
On the line was a woman who needed help reading a letter. It was from a church thanking her for a donation she recently made in honor of her husband and daughter who had recently passed.
Traut said the appreciation in the woman’s words had a lasting impact.
“Granted that task probably wasn’t life-changing for her,” Traut says, “But it’s simple things like that that maybe fully sighted people take for granted.”
Traut says the sheer magnitude of volunteers on the app is incredible. But this also means a single volunteer won’t get too many calls.
Traut downloaded the app in June 2017. Since then, she says she’s only received six or seven calls.
But for Wildgruber, it’s reassuring to know she won’t be bothering anyone.
“You know the volunteers are answering the phone if they want to,” she says. “And knowing that if you call a few times a day, you’re not bothering anyone.”
“Sometimes it’s a quick fix, other times it’s a longer conversation of what’s life like where you are,” says Christian Erfurt, the chief executive of Be My Eyes. “That reminds us that we’re not that different, and the gap between ‘us and them’ is minimized.”
More: The GovTech Apps Changing the Way We Live

Editor’s note: An earlier version of the headline incorrectly stated there were 100,000 volunteers on the app. The correct number is 2 million.

Curious About What to Say to a Person with a Disability? Here Are 5 Things to Say And 5 Things Not to Say

How do you feel when you spot a person with a disability? If you’re like most, you probably feel a complex rush of emotions. Out of compassion, you want to understand the person’s life and what it’s like to live without sight, hearing or full mobility. But out of ignorance or even fear, you rarely broach the awkward silence. To open the conversation with the 56.7 million Americans living with a disability, pull up a chair, look the person in the eye and read on to find out what the experts recommend saying and what’s better left unspoken.

What to Say

1. “Hey, did you see that movie?”

Some people avoid engaging in conversation with a person with a disability because they worry there’s just too many pitfalls. What if I accidentally ask a blind person if they see what I mean? What if I ask someone hard of hearing if they heard the latest news? While people who use one of these colloquialisms likely kick themselves as soon as the words leave their mouth, the person with a disability might not even notice. “Typically, an individual who is comfortable with his or her own disability is not offended by such phrases. I often say them myself, as it is just part of our vernacular,” says Anthony Stephens, director of advocacy and governmental affairs for the American Council of the Blind. Of course, there are exceptions, such as someone who has recently lost her sight or hearing might be sensitive. But above all, people with disabilities want to be treated like anyone else. Relax when you’re speaking, and generally don’t worry about this metaphorical language.

2. “Can I ask you what medical condition you have?”

A person’s disability is caused by a medical condition. That’s a reality most won’t shy away from and one that can guide your interaction. (Upon seeing someone in a wheelchair, many people wrongly assume that the person is totally incapacitated, and they start speaking slower or louder — despite a lack of evidence that the person’s hard of hearing or has cognitive disabilities.) After you’ve spoken about the medical condition, don’t ask for more information about daily challenges. Why? Not only could it seem like you’re prying, but also because many in the community believe that disabilities stem from society’s inability to adapt, rather than from any physical limitation. “It’s not that I can’t open the door,” says Ian Watlington, an advocacy specialist at the National Disability Rights Network who has cerebral palsy, “it’s that the door is too heavy.” Don’t press further, unless you know the person well or he volunteers information, or otherwise you’ll reduce his life to “a set of symptoms,” Watlington adds.

3. “Would it be helpful if I carried this over for you?”

Grabbing a blind person’s arm may throw them off balance. Lifting someone’s wheelchair by the handles could tip them onto the floor. It may be hard to resist when it looks like a person with a disability is struggling, but jumping into someone’s personal space is a big no-no. They already developed a different — but no less effective — way of navigating the world. Always ask if your help is needed first, and don’t take offense if someone declines it. “We know when to ask for help. Just wait for us to speak up,” suggests Tiffiny Carlson, a Minnesota blogger whose spinal cord was injured in a driving accident as a teen. “How would you like it if someone barrel-rolled themselves into your personal space? You wouldn’t. The same goes for us.”

4. “Our building is accessible to all.”

At its most fundamental level, having a disability can make it physically challenging to get around. The Americans with Disabilities Act (ADA), a massive civil rights bill passed in 1990, prohibits discrimination against those with disabilities in employment, access to public services, telecommunications and housing and other accommodations. The bill was the culmination of a decades-long campaign, which sought to show that people with disabilities could live independently as part of a community. “Like the African-Americans who sat in at segregated lunch counters and refused to move to the back of the bus, people with disabilities sat in federal buildings, obstructed the movement of inaccessible buses, and marched through the streets to protest injustice,” Arlene Mayerson, directing attorney of the Disability Rights Education & Defense Fund, writes in a history of the movement. ADA compliance is now widespread, but it’s always reassuring for a person with disabilities to feel welcomed (keep ramps unobstructed, trash bins out of aisles and display boards away from entrances), rather than being seen as a burden.

5. “You’re hired!”

While the ADA is responsible for revamped layouts of many workspaces, it hasn’t been nearly as effective at adding diversity to employment rosters. According to the 2010 Census, only 41 percent of working-age Americans with disabilities were employed, compared with 79 percent with no disability. Thanks to today’s technology, people with disabilities are usually able to work as effectively, if not more so, than any other applicant. Take Jerry Berrier, a blind person who was once ashamed that he couldn’t proofread his own memos at work and felt he wasn’t an asset. Once speech-to-text technology came online around 1985, his productivity soared. “People tend to expect very little of someone with disabilities. They just can’t imagine themselves being able to do what I’ve done, because they think of what would happen if they went blind right now. I’ve had 60 years of experience and a chance to get a lot of practice,” Berrier, who works at Perkins School for the Blind, says. “But I would like for people to be willing to [let me] do things if I feel like I can do them.” By offering employment opportunities, everyone benefits.

What (Definitely) Not to Say

1. “I’ll pray for you to be healed.”

Pity is one of the most offensive responses to a person’s disability. It’s an ineluctable reality for those who have them, and a significant number report they wouldn’t reverse their condition, even if they had the chance. While prayers may come from a genuine place, most people who are disabled would probably prefer if you send your good intentions to your congressman to fight for independent living facilities, safeguards for health coverage and enforcement of the ADA’s ban on employment discrimination.

Many people with disabilities also consider it equally patronizing to heap praise on their “inspirational” life. For those of us growing up in the Oprah generation, we don’t see the harm in a compliment. But as someone with a disability, Carlson explains, “We are just trying to live our lives like everyone else. Your comment will have the negative effect, reminding us how different people still think we are.”

2. “We’ve got two wheelchairs coming through.”

No one wants their personhood reduced to their equipment. Along with that, there’s plenty of other outdated, dehumanizing language to avoid: cripple, retard, victim, dumb or mute, insane, deformed, lame, invalid. Handicapped, in vogue for two decades after the 1970s, is also out of fashion as people came to prefer “disabilities,” a term that connoted a medical reality but didn’t imply a perpetual disadvantage in society, journalist Jack A. Nelson writes in “The Disabled, the Media, and the Information Age.” Some new terms like “differently abled” or “physically challenged” are also viewed as over-the-top, so hypersensitive as to be insensitive. “If you sprain your ankle, you’re physically challenged. That’s not the same as being culturally and physically defined as disabled,” says Watlington.
What’s considered best is to recognize a person’s humanity first, then their disability. Say a “person with epilepsy,” for example, rather than an “epileptic.” “To say that someone is ‘disabled’ implies that she or he is broken or flawed,” says Stephens. Using person-first language “attributes it more as a modifier and not an inherent part of their being,” Stephens adds. Of course, if you’re unsure which term a person prefers, asking will always get you the right answer.

3. “Were you born with that affliction?”

Besides often mistaking a disability for the whole person, people generally associate disabilities with suffering and pain. They can’t imagine a disabled person being happy and see her as a victim. “I have had perfect strangers come up to me and instead of greeting me or saying hello, they say, ‘What’s wrong? What happened?’” Tim Vaughn, marketing director for Eastman Kodak, tells DiversityInc. Like the rest of us, people with disabilities are looking for fulfillment in their lives — despite the extra hurdles they need to overcome. That’s not to say they don’t miss abilities, even ones they never had. “Anytime I hear someone talking about what’s outside the window, I lament that I can’t see,” Berrier says. But he finds other ways to bring himself joy like studying bird sounds, a beauty that surrounds all of us but that is ignored by most.

4. “You wouldn’t be able to handle children.”

One of the biggest upcoming battles disability advocates see on the horizon is protecting family life. Questions linger about whether a person with disabilities would be fit to take care of a child or might even pass on a hereditary condition to their child. But behind this argument lurks the assumption that people with disabilities are incapable, an argument used to justify the government’s sterilization of 60,000 Americans with disabilities by 1960. Just because someone may have physical challenges, however, does not mean she’d be a bad parent. “Any time we start making assumptions about what people can and cannot do, we’re getting into scary territory,” Watlington says.

5. “But how do you go to the bathroom?”

While it might be okay to inquire about someone’s medical condition, asking a stranger about the intimate details of their lives risks turning him or her into a sideshow curiosity. There is obviously a need to educate people about accessibility issues, but there’s also a limit to what needs to be discussed. You wouldn’t question anyone else about her restroom habits, and there’s no reason to think that a person’s disability makes it acceptable to ask.
MORE: Ever Wondered What to Say to a Homeless Person? Here Are 5 Things to Say and 5 Things Not to Say

This Non-Profit Thinks Autistic Kids Should Be Able to Enjoy The Same Things As Other Kids

It can be difficult for families with autistic children to enjoy public outings. Strangers sometimes find their behavior distracting or disruptive. But the Theater Development Fund wanted to help these families enjoy live theater, so the nonprofit organized four Broadway productions a year for people who need a little more understanding and a little less stimulation. In November the organization invited families to a special production of “Spider-Man: Turn Off the Dark,” where ushers handed out squeeze balls to help autistic kids relax. The producers turned the volume down by twenty percent and eliminated strobe lights because autistic people can be sensitive to loud noises and bright lights. In the lobby, experienced volunteers staffed break rooms and quiet areas where theater patrons could take a break whenever the stimulation became too intense in the packed house. The idea of making theater accessible to all people is taking hold off Broadway too—for example, the Lone Tree Arts Center near Denver recently staged a “sensory-friendly” performance of its holiday show. These programs join sensory-friendly movie screenings and restaurant nights in helping families struggling with Autism to enjoy themselves outside their homes.