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A group of bipartisan attorneys general from 51 states and territories on Friday wrote to Education Secretary Betsy DeVos urging the Department of Education automatically forgive the student loan debt of eligible veterans who became disabled through their military service."We write, as the Attorneys General of our jurisdictions, to urge the Department of Education to take prompt action to satisfy its statutory mandate to discharge the student loans of veterans who are permanently and totally disabled or otherwise unemployable," 546

SCURRY, Texas -- The world of opioid addiction, the path it takes people on and the destruction it causes, is a world foreign to some but all too familiar to others. “When I was 19, is when I was first introduced to opioids,” said Andrew Rogers. Rogers is one of an estimated 1.7 million people in the U.S. addicted to opioids. “I went from pain pills which were easily available to heroin. The pain pills have actually gotten harder and more expensive to get so it’s just cheaper and easier to get heroin,” added Rogers, “from there on it was on.” Before he got hooked on heroin, Rogers had a bright future ahead of him with a full-ride scholarship to college on a pre-med track. But instead he has spent the last nine years in some pretty dark places. “It has made me do things I never thought I would do,” said Rogers. “I’ve overdosed twice. I’ve had friends who have died from it. I’ve actually had to hold one of my friends while he was passing away.” Like so many addicts, Rogers has tried quitting. In total he has been to rehab and detoxed 18 times. At the end of September, he checked himself into treatment again at The Treehouse, a recovery center. “We take the approach of treating the whole person,” said Dr. Ted Bender who is CEO of The Treehouse. “Teaching them how to think more rationally, teaching them how to handle the stress and emotion regulation. Teaching them how to have fun again and enjoy life again and become part of a community.” For nearly a decade, Bender has been trying to help so many people like Andrew Rogers. “We’re losing about a football stadium of people every single year to this epidemic. You know what would make an immediate impact – significant federal funding,” said Bender. “Recovery in itself isn’t the hard part. The hard part is getting the help you need,” said Rogers. When asked what is motivating him this time around, to stay clean and win in this fight against his addiction, Rogers says it is his 4-year-old daughter and his family. 2010

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

A jury found a former South Florida police officer guilty on Thursday in the fatal shooting of a motorist whose vehicle had broken down.Nouman Raja was 164

A Department of Justice office sent its employees, including immigration judges, a daily news briefing that included a link to a blog featuring racial and anti-Semitic slurs, according to a letter sent by an immigration judges union.The department's Executive Office for Immigration Review sent an office-wide collection of "news" items on Monday -- which the agency says is compiled by a contractor -- that included the link from the white nationalist website VDare, the letter states.The incident was 514

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