武清区龙济泌尿医院在哪(天津市龙济官方) (今日更新中)

You never know what the tide might bring in. Guests at a resort on Fort Lauderdale beach witnessed an unusual object wash up on shore: a 20-foot cross. “I was getting calls from the front desk, from the tiki bar, from the guests,” describes Frank Talerico, owner of Ocean Manor Resort. The large cross washed up on the beach outside the resort a few weeks ago. “When I saw it, I got goosebumps,” Talerico says. “I couldn't believe it.” It took 10 men in all to pull the cross out of the water.Since then, many have come by to see it in person. It’s even been blessed by a priest. “When we were here the other night, there were people kneeled all around it praying,” describes one woman.The resort has turned it into Fort Lauderdale's latest tourist attraction, bringing in people from all over the country. There are still questions regarding the origin of the cross. “You can't help but wonder what kind of journey it’s been on,” says one tourist. 964

A Las Vegas woman who has been charged with murder in regards to an incident in which an elderly man was pushed off a public bus has been released on bail.Cadesha Bishop, 25, was released from jail on 0,000 bond on Wednesday. She's due back in court on May 23.Bishop was charged with murder earlier this week following the death of Serge Fournier. The 74 year old man died earlier this month after he was pushed off a public bus in Las Vegas on March 21.Fournier initially refused medical treatment but went to the hospital later that day. On May 3, police were notified that the man had died from his injuries. The coroner ruled his death was a result of the injuries he received from being pushed.Homicide detectives later determined that Fournier had died from injuries sustained after being pushed. 818

A day at the beach turned into a frightening rescue for one 8-year-old boy after the giant unicorn-shaped raft he was playing on suddenly drifted out to sea.Declan O'Connor found himself holding on for life as high winds swept him further into the Atlantic Ocean, the unicorn's head and horn serving as a stand-in sail.Luckily for the boy, a team of rescuers were quickly on scene and retrieved him. Local rescue chief Tony Young credited the boy's decision to stick with the unicorn —a wise move, or else he might've drowned."We've rescued dozens of these things over the years, but this was the first time there was actually a little kid attached to it," Young told CNN affiliate 694

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 3-year-old girl is dead and a 4-year-old is hospitalized after their flotation devices slipped off and they went underwater at a pool party in Florida, authorities said.Harmony Williams was playing in the water at a Tampa apartment complex when she drowned. Witnesses pulled her out and tried to give her CPR, but she was pronounced dead at a local hospital, the 377

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