山西高级多功能急救训练模拟人（心肺复苏CPR、气管插管、除颤起搏四合一功能、嵌入式系统）(双鸭山腕关节镜检查模型) (今日更新中)

A high school production of the iconic 1979 movie "Alien" has burst onto the scene and even garnered Hollywood's attention.Drama club students at New Jersey's North Bergen High School went all out for "Alien: The Play," including an elaborate alien costume.Glitch CEO Anil Dash shared a photo of the get up on Twitter."Everybody is (rightfully!) very excited about the North Bergen High School kids' version of Alien, staged as a high school play, with all props made from recycled materials," he tweeted.The Ridley Scott-directed science-fiction horror film stars Sigourney Weaver and centers on the crew of a commercial space ship that is invaded by a deadly extraterrestrial.Justin Pierson, a senior who worked on the sound crew for the play, 758

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 lot of unloading, probably 100 cases of wine being unboxed and stored nearby. Owner says there’s a lot more inside, the floor fell on top of it. @WCPO pic.twitter.com/mClL4tUPVs— Ally Kraemer (@AllyKraemer) June 13, 2019 234

A Macomb County, Michigan, mom is furious.She says her special needs son was silenced and shamed by adults at a school Christmas concert in Clinton Township.Her anger and disappointment has been echoed by many on social media. The L’Anse Creuse Middle School concert was earlier this week and 14-year-old Dominic Schroeder was super excited. He plays the saxophone and has been practicing the performance in band class and at home too.Dominic is cognitively impaired. Because of his special needs, he often practices with a plastic digital saxophone with ear-buds. The device can help the instructors measure his progression. On concert day Dominic was ready to perform using his own shiny saxophone. But according to his family, Dominic was told by an administrator that he could not play his instrument with the band. He was instructed to use the plastic saxophone - with earphones.Dominic was upset and his loved ones were too. We’re told he and his family did not agree to this. They also say, with this device, Dominic’s the only one who can hear his music. It is silent to the rest of the world.The family believes this is discrimination and exclusion. And they want answers.L’Anse Creuse Public Schools issued the following statement about this story: 1270

A dad is credited with rescuing his daughter Sunday after she was allegedly grabbed by a woman at a south Phoenix park. Phoenix police report that on Sunday afternoon, 43-year-old Denise Charlene Antone grabbed a 7-year-old girl at a park and wouldn't let her go.Police say Antone appeared to be under the influence of alcohol at the time. She allegedly grabbed the girl and refused to let her go, until the girl's father intervened. He demanded Antone release his daughter, which she eventually did. Antone was arrested for aggravated assault. 557

来源：资阳报