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Twitter rolled out a 280 character limit for most of its users Tuesday, and, predictably, lots of people are unhappy.That doubles the original 140 character limit that Twitter has maintained since it launched in 2006.Twitter began testing longer tweets in late September, and found that once the novelty of tweeting longer wore off, most people in the test group didn't use all of the available characters. According to the company, only 5% of tweets sent by people in the 280-character test group were longer than 140 characters, and just 2% were over 190 characters.Many users complained about the initial tests. Now that just about everyone's got 280 characters to work with, more people say they're frustrated or confused by the decision. Others are using new characters to make jokes. Other people were curious about how the new parameters will change the way people interact on the platform.The big question on everyone's mind is how President Donald Trump, an avid Twitter user, will use the expanded space. The president tweeted two messages Tuesday that went beyond the old 140 character limit.But another Trump doesn't appear to like the change. Donald Trump, Jr. tweeted a critique of the expanded character limit -- although he used 195 characters to do so.  1286

VENTURA, Calif. (AP) — A study shows California’s stay-at-home order in response to the coronavirus outbreak seems to have saved some wildlife, as decreased traffic resulted in fewer collisions with mountain lions, deer and other large animals. The Ventura County Star reports a study by the Road Ecology Center at the University of California, Davis found traffic declined by about 75% after the emergency order went into effect in March. The number of animals struck and killed by vehicles also fell, including a 58% decrease in fatal crashes involving mountain lions between the 10 weeks before and 10 weeks after the order. 635

UPDATE: At approximately 3:40 p.m. CT, Slack said everything should be working as expected.------------ORIGINAL: You are not alone, Slack is having "performance issues" Monday morning.As the coronavirus pandemic forced thousands of companies to embrace a remote work situation, many embraced messaging programs to keep teams connected, including Slack.Monday morning, Slack reported just after 11 a.m. ET they were aware of issues.“Some users may be experiencing slowness with Slack in the desktop, browser, and mobile at this time. The issue is impacting sending messages and troubles with API calls,” their troubleshooting website stated.Two hours later and updates from the Slack team indicate they are still looking into the issues. They said users were reporting a range of performance concerns.“Some users may be unable to connect to Slack, while others are still experiencing general performance issues,” they said.Slack reported an outage last Tuesday, around 9 a.m. ET and it was resolved about an hour later. No word if the outages are related. 1062

UNION COUNTY, Ind. -- A recently approved medical device is tiny, but mighty in the fight against opioid abuse. The NSS-2 Bridge, a battery-powered device similar to a hearing aid, was created by Indiana-based Innovative Health Solutions. It helps reduce symptoms associated with opioid withdrawal, such as nausea, diarrhea, stomach pain and anxiety. It is worn behind the ear for five days at a time, sending electrical pulses to the brain. It’s the first FDA-approved device for use in helping to reduce the symptoms of opioid withdrawal, which is key because most addicts return to drugs to alleviate the pain from those symptoms.Kaylin Fairchild, 26, is living proof that the device can help. Nearly three years ago, heroin held her hostage. She overdosed while her son was in the backseat and it took four shots of Narcan to bring her back. To make things worse, she found her mother dead of a drug overdose in 2015.Rock bottom hit when the state took custody of her son for several months.But a new program at the Union County Health Department stepped in with hope."I thought they were full of (it)," Fairchild said. "I thought it was a bunch of talk. What is this little device, how's it going to make me feel any better?"Kaylin now has custody of her son and attends group meetings with the help of the device.Tom Schulte, who took painkillers because of knee injuries, says The Bridge helped him get to a life where he's no longer dependent on pills. "I couldn't hold a job," Schulte said. "I couldn't function without them."He is now doing well and is focused on landscaping jobs. See how The Bridge works below:The Bridge is not sold over the counter, and must be prescribed by a doctor. The device comes with a price tag of 0, but it can be covered by health insurance. Union County, Indiana says they've helped more than 200 people with the device since its FDA approval last year.  1972

U.S. government officials are putting an early end to a study testing an Eli Lilly antibody drug for people hospitalized with COVID-19 because it doesn’t seem to be helping them.Independent monitors had paused enrollment in the study two weeks ago because of a possible safety issue. But on Monday, the National Institute of Allergy and Infectious Diseases, which sponsors the study, said a closer look did not verify a safety problem but found a low chance that the drug would prove helpful for hospitalized patients.It is a setback for one of the most promising treatment approaches for COVID-19. President Donald Trump received a similar experimental, two-antibody drug from Regeneron Pharmaceuticals Inc. on an emergency basis when he was sickened with the coronavirus earlier this month.In a statement Lilly notes that the government is continuing a separate study testing the antibody drug in mild to moderately ill patients, to try to prevent hospitalization and severe illness. The company also is continuing its own studies testing the drug, which is being developed with the Canadian company AbCellera.Antibodies are proteins the body makes when an infection occurs; they attach to a virus and help it be eliminated. The experimental drugs are concentrated versions of one or two specific antibodies that worked best against the coronavirus in lab and animal tests.Lilly and Regeneron have asked the U.S. Food and Drug Administration to grant emergency use authorization for their drugs for COVID-19 while late-stage studies continue. Lilly says its request is based on other results suggesting the drug helps patients who are not hospitalized, and that it will continue to seek the FDA’s permission for emergency use.___The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Department of Science Education. The AP is solely responsible for all content. 1928