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A bartender in Missouri got a massive tip when a customer left her a winning lottery ticket worth ,000.It would sound like an unusual item to receive as a tip, but winner and Bleacher's Bar staff member Taylor Russey 231

A Facebook post of a 7-year-old Tulsa boy praying for a Tulsa police officer is going viral.Trey Elliott's mother, Brittany Elliott, shared a post on her Facebook page on June 1 that showed Trey praying for a Tulsa Police Officer.The powerful image shows Trey on his knee with his tiny hand placed on the shoulder of the Tulsa police officer who can be seen bending down. Both with their eyes closed in prayer."Today Trey (7) asked to pray for officers in the Tulsa Police Department," Brittany 507

A feature that Facebook shut down in the wake of last year's Cambridge Analytica scandal came back to haunt it on Wednesday, when it emerged that hundreds of millions of Facebook users' phone numbers had been found in an unprotected online database.Millions of American Facebook users' phone numbers are believed to be among those found. Facebook said there is no evidence that any accounts were compromised. Even so, the latest discovery is a reminder that even new, stricter security policies can't necessarily address past data leaks or abuses.Until April 2018, people could enter another person's phone number to find him or her on Facebook. The company shut down the feature in the weeks after the Cambridge Analytica scandal broke because it found "malicious actors" had abused the feature to gather public information on Facebook users, a process known as scraping."Given the scale and sophistication of the activity we've seen, we believe most people on Facebook could have had their public profile scraped in this way," Mike Schroepfer, Facebook's chief technology officer, 1095

The most popular museums in Washington, D.C. are now closed until a deal can be reached to end the government shutdown. Tourist Staci Jones flew to D.C. from Texas to see the African American Museum, the Smithsonian's newest and most popular museum. “It is frustrating that the one thing I wanted to do, I’m not gonna be able to do before I leave,” Jones says. Adonai Mahoungou came to D.C. from Mississippi and also wanted to see the museum.“I was really disappointed because I was getting ready to go to museums, have some fun,” says Mahoungou. “And to see that because of a government shutdown, disappointing, because I was ready! I was excited! Dang.” In addition to all Smithsonian museums being closed, the National Zoo is also closed, including the zoo's popular giant panda web cam. Outside of D.C., the shutdown is forcing some national parks to close because of health and safety concerns. Understaffed parks cannot keep up with overflowing toilets and trash cans. “It was kind of smelling bad down there, and I don't know how it's affecting the park with human waste and everything,” says Yosemite National Park visitor Katie Kensok. As more people start to feel the pain from the shutdown, President Trump and new Congress now face more pressure to come up with a solution. “Being from Texas, I don't work for the government. I didn't think it would affect me that much, but now, I’m starting to see, yeah, it does affect people who don't work for the government in other ways,” says Jones. “I just wish they would come together.” 1557

A Denver family is trying to raise million in order to cure their son with a rare genetic disease. Doctors told Amber Freed that her 2-year-old son is one of 34 people in the world to have this rare neurological genetic disease. “The disease is so rare, it doesn’t even have a name,” Freed said. “It’s called SLC6A1, because that is the gene that it effects.” The disease causes Maxwell to have trouble moving and communicating, and soon it will only get worse. “The most debilitating part of the disease will begin between the ages of 3 and 4,” Freed said. “So, we are in a fight against time.”Maxwell has a twin sister named Riley. “I noticed early on that Maxwell wasn’t progressing as much as Riley,” Freed said. “I noticed he couldn’t use his hands. The doctors told me that every baby can use their hands. That’s when I realized there was something wrong with him.”After multiple visits to the doctor, Freed was able to find a genetic specialist to give Maxwell a diagnosis. “He looked at me and said, ‘Something is very wrong with your son. I don’t know if he’s going to live,’” Freed said. “My soul was just crushed. It was a sadness I didn’t even know existed on earth. You never think something like this could happen. I left my career, and I had no other choice but to create my own miracle and to find a treatment forward to help Maxwell and all those others like him.” Freed searched for scientists trying to create a cure, which she found at the University of Texas Southwestern Medical Center in Dallas. “We’re working with diseases where kids are born with a defective gene,” said Steven Gray, an associate professor at UTSW in pediatrics. “Our approach is to replace that gene to fix the condition at the level of their DNA. We’re taking the DNA that those patients are missing and packaging that into a virus and use that virus as a molecular delivery truck to carry those genes back in their body and fix their DNA.” “It’s a rare disease, no one has ever heard of it,” Freed said. “But one rare disease messed with the wrong mother.” Freed said she has raised million to help with research for the cure and will need an additional million, in order to let Maxwell and many others continue to enjoy life. “I want Maxwell to have every opportunity that children should have in this life,” Freed said. “When he is having a good day, I just try and soak him in as much as I can. We don’t take anything for granted in this house.” If you want to help donate for the cure, you can do so by visiting 2535