惠水算命准的人(和田算命哪里准) (今日更新中)

LAKELAND, Fla. — While a 10-year-old boy is still recovering after a dangerous fall from a zip line at the Urban Air Adventure Park in September, his mother is warning others. Kimberly Barnes filed a lawsuit against against the company that owns the Lakeland, Florida, facility, UATP Management, on Monday. She says employees were negligent and didn’t fasten her son into the harness on the "Sky Ride" properly. Her legal team also alleges a design flaw with the harness. In a press conference on Tuesday, Barnes and her attorney Steven Capriati, with Morgan and Morgan, addressed the media. The mother recalled when she got the frantic phone call on Sept. 1. “He had fallen, there was a very high fall,” Barnes said. The lawsuit says her son fell more than 20 feet. Video from inside the facility shows the 10-year-old falling into a hard concrete floor. He was airlifted and suffered serious injuries, including several broken ribs, a collapsed lung and head injuries.Two months later, Barnes says her son is still struggling to go to school and fighting for normalcy. “He is doing the best he can he wants to have his normal life back and have his normal routine, but it’s a day by day process for him,” she said.In a 911 call obtained Tuesday, two employees called for help saying the boy had fallen off the zip line and needed an ambulance.Although awake and lucid, the boy can be heard in the background of the call screaming in pain. He's heard complaining of back, foot and head pain.“He is in danger and do not splint any injuries. Reassure him help is on the way,” the dispatcher says. In the lawsuit, Barnes is asking for at least ,000 in compensation to pay for medical expenses and any other ongoing issues her son may deal with.In a statement Urban Air said: 1787

It’s a boot camp workout at Vital Strength and Fitness in Denver, and as the sweat starts pouring, the athletes are looking for an edge. “The quicker you can recover, the more you can train,” says gym owner Vinnie Lopez. “The more you can train, the more you get better.” To help with his post-workout recovery, Lopez, a former MMA fighter, turns to intravenous therapy. “It makes you feel superhuman,” Lopez says of IV therapy. “Which is why it’s not allowed in mixed martial arts anymore, because it brings you back better than you felt before.” Banned by some sports but now coveted by many businesses, these bags of saline and vitamins are being marketed to give your body a boost. Now, more people are paying big bucks to have these medical potions pumped into their bodies. “Honestly, it’s a game changer,” former NFL cheerleader Erica Beard says of using IVs. “You can notice a difference in your energy level.”Beard, a mother of two, gets an IV drip once a month at Denver Hydrate. She says these vitamin cocktails help fight fatigue and improve her health.“It helps with muscle recovery and staying hydrated,” she says. “It’s not easy drinking enough water as we need to.”From Nashville to Las Vegas, IV therapy bars are popping up across the country, targeting everyone form weekend warriors to those nursing a hangover. It costs anywhere from to 0 a session. But does it really work, or is this just a pumped-up placebo effect? “It really helps,” says ER nurse Gianna Nardi, who administers IV drips on the side. “You're going to absorb 100 percent of the vitamins.”Many other medical professionals, however, say IVs aren't worth the cost. They say many symptoms people are trying to cure aren't caused by dehydration and that most people can just drink the fluids they need.However, Beard disagrees with the claims. “I think it’s funny that they think its placebo,” she says. They can hate on it until they try it.” 1946

INDIANAPOLIS, Ind. — For years, Joy Thornton has been a pastor in one of Indianapolis' toughest neighborhoods. He has regularly told young black men to stay out of trouble. That's a task he thought was possible until 229

India has successfully launched a mission to soft land a rover on the moon, in a landmark moment for a nation trying to become a space superpower.The country's latest lunar mission, Chandrayaan-2, which means "moon vehicle" in Sanskrit, took off from the Satish Dhawan Space Center at Sriharikota in Andhra Pradesh state at 2:43 p.m., Monday local time (5:13 am ET).The launch was originally scheduled for July 15, but was abruptly called off just 56 minutes before lift-off due to a "technical snag." India is now on the way to becoming the fourth country -- in addition to United States, China and the former Soviet Union -- to make a soft-landing on the lunar surface.The Chandrayaan-2, which weighs 3.8 tons and carries 13 payloads, has three elements -- lunar orbiter, lander and rover, all developed by the Indian Space Research Organization (ISRO).It will travel for two months, before positioning itself in a circular orbit 62 miles (100km) above the moon's surface. From there, the lander -- named Vikram after the pioneer of the Indian space program Vikram Sarabhai -- will separate from the main vessel and gently land on the moon's surface near its South Pole.A robotic rover named Pragyan (meaning "wisdom") will then deploy and spend one lunar day, or 14 Earth days, collecting mineral and chemical samples from the moon's surface for remote scientific analysis.Over the next year, the orbiter will map the lunar surface and study the outer atmosphere of the moon.Kailasavadivoo Sivan, ISRO chairman, said in June that the last 15 minutes of the landing "are going to be the most terrifying moments for us."As well as coinciding with the 50th anniversary of the Apollo moon landing, the launch comes as other space agencies revisit the idea of sending humans to the moon and beyond -- NASA has touted a bold plan to return American astronauts to the moon by 2024.India's space ambitionsThis mission is significant for India -- the country wants to become a major space player and put Indian astronauts in space by 2022."India wants to show, especially since Prime Minister (Narendra) Modi came into office, that India is a major power, and that India has to be treated as a major Indo-Pacific power," said Rajeswari Pillai Rajagopalan, head of the nuclear and space policy initiative at the Observer Research Foundation.Chandrayaan-1, India's maiden lunar mission, discovered water molecules on the surface of the moon. As part of that mission, an impact probe crashed into the moon's south polar region in a controlled landing.India's attempted soft-landing is a far greater technical challenge than the controlled crash of Chandrayaan-1.The two Chandrayaan missions are a precursor to Chandrayaan-3, which is scheduled to make a return mission to the moon in 2023-2024.In 2014, India became the first Asian nation to reach the Red Planet, when it put the Mangalyaan probe into orbit around Mars. The Mars Orbiter Mission famously cost million -- less than the 0 million than Hollywood spent making space thriller "Gravity."In 2017, India 3072

It’s hard to regard Ellie as a menace.When Greg Manteufel is frustrated or feeling down, she sits by him. At night, she sleeps under his covers. At dinner, she’s there next to him, knowing he’ll throw something her way. She belies the stereotype of the vicious pit bull.“We love her like she’s our daughter,” he said of the dog.And yet, Ellie may be the reason Manteufel nearly died.Gravely ill, he lost parts of his arms and legs, as well as the skin of his nose and part of his upper lip. The cause was capnocytophaga (cap-noh-seye-TOE’-fah-gah), a germ from Ellie’s mouth or from another dog he encountered.Capnocytophaga is commonly found in the saliva of cats and dogs and almost never leads to people getting sick, unless the person has a compromised immune system. But Manteufel was perfectly healthy. In fact, he doesn’t think he’d ever used his health insurance before he fell ill.The case is extremely rare and doctors at his hospital, Froedtert & the Medical College of Wisconsin, had no explanation for why he got so sick. But over the last 10 years there have been at least five other healthy people who have had severe reactions to the germ. A team of researchers connected with Harvard Medical School has developed a theory on why — a gene change in all the victims.And their finding means doctors can’t rule out the capnocytophaga bacteria could strike Manteufel and other victims again.___Greg Manteufel thought he was getting the flu in June of 2018. He had a fever, vomiting and diarrhea. But when he started getting confused, his family took him to the hospital.Doctors did blood cultures and found capnocytophaga, which caused sepsis, a severe blood infection that led to his blood pressure dropping and many of his organs shutting down.“Do what you have to,” he told the doctors.He had so much to live for — foremost, his wife of 16 years, Dawn, and 26-year-old son, Mike. He was just starting to get really good at his day job, painting houses. He cherished his Harley Davidson Electric Glide. He was in the middle of fixing up his ’66 El Camino. And of course there was Ellie, the pup.And so he persisted, through more than 20 surgeries, including amputations of his left and right arms just below the elbow, and legs through the middle of the knee.His wife and son stayed optimistic, because he was.“Greg said he didn’t come this far to lay down and let this beat him,” Dawn Manteufel said.He was out of the in-patient rehab unit in about two weeks, learning to move from his wheelchair to the bed, toilet and car. The usual stay is three to four weeks, said Dr. David Del Toro, medical director for the inpatient rehab unit at Froedtert.Manteufel made similar quick advances using his arm prosthetics and leg prosthetics.“He does not seem like any other patient I’ve met before,” Del Toro said. “He’s just, you know, full speed ahead.”Meanwhile, researchers at Brigham and Women’s Hospital in Boston, connected to Harvard Medical School, as well as Dana-Farber Cancer Institute and Beth Israel Deaconess Medical Center had been investigating cases like his.The team has done genetic testing on five otherwise healthy people who suffered capnocytophaga infections to see if they could find anything in common. They discovered all had a gene connected to the immune system that was working differently — a genetic variant.“It was a really thrilling moment,” said Elizabeth Fieg, a genetic counselor at Brigham and Women’s Hospital. “The stakes are so high with these cases and the patients have gone through so much.”They believe it makes those people more susceptible to developing severe medical problems from capnocytophaga. But they are also trying to determine if there are other risk factors.Of the five in the study, three survived with amputations and two did not. Fieg hopes their research can determine why some did not survive.She also hopes if their theory is confirmed, it will help diagnose cases faster, and perhaps save lives and limbs.That’s why Greg Manteufel jumped at the chance to take part when he was approached in August.Researchers need to gather more evidence, but hope to publish their study in the next year to 18 months.___Manteufel’s life now includes frequent occupational therapy appointments to perfect his use of arm prosthetics — the kind with metal moveable hooks at the end. He’s using a fork regularly and he’s now working on picking up the TV remote, opening doorknobs, cutting vegetables and doing the dishes.He’s using shortened leg prosthetics, called stubbies, to get his body conditioned to eventually use to full-sized ones. Those are expected to arrive any day.Plastic surgeons plan another surgery to perfect his nose. They’ve already moved skin from his forehead there. It looks oversized now, but it will eventually fit in with the rest of his face.He plans to get his car revamped so he can drive with prosthetics. He wants to get a special pole so he can go fishing again. He is even considering going back to work painting.He’s also become less quiet and a lot more outgoing. “Now everybody I see wants to hear something or talk to me. I tell them a 15-minute story about what happened. They probably want me to leave, you know,” he said, chuckling.Ellie’s often by his side.“She loves kids. She loves puppies. Other dogs,” Manteufel said.As harmless as she seems, she may have capnocytophaga germ.The results of Manteufel’s genetic tests are expected in three to four months. Fieg said people with the gene variant are at increased risk for recurrent capnocytophaga or other infections in the future.While Manteufel doesn’t like the sound of that, he said Ellie’s accidentally scratched him since he’s been home and even licked his mouth. He’s been fine.And even if he does have the gene variant, he said, it changes nothing.“We didn’t even bother testing her,” said Manteufel. “We weren’t going to get rid of her if it was her that caused it anyway.”“We just love her to death.” 5972

来源：资阳报