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Lawrence County, Indiana, prosecutors filed criminal charges Thursday against a Mitchell Community Schools nurse for stealing students' medication and ingesting it herself.Carol Sanders is charged with felony official misconduct, felony neglect of a dependent and five counts of misdemeanor theft.Police arrested Sanders Thursday and she was booked into the Lawrence County Jail.A staff member at Burris Elementary launched an investigation earlier this month after medication belonging to students went missing.Sanders admitted to stealing amphetamines, Ritalin, Zyrtec and other medications from students at Burris Elementary and Hatfield Elementary.The school nurse also admitted to replacing some of the students’ medications with baby aspirin.Sanders said she stole the medications between February 25 and March 7 of 2019, court records show.“Carol stated she stole the medication because she is an addict,” read the probable cause affidavit. “Carol admitted to needing help with her addiction.”Carol Sanders also admitted that this is not the first time she’s been terminated from a nursing job for stealing and ingesting medication.Sanders said she omitted that information to the school district during the hiring process.Superintendent Dr. Mike Wilcox said the district performed an expanded criminal history check and no prior history was reported.Wilcox provided the following statement. “The Mitchell Community School Family is deeply concerned about this event. This, or any other, issue that forces us to question the safety of any Mitchell student immediately becomes our top priority. Our outstanding school administrators and school resource officer responded firmly, fairly, and in a timely manner. The parents of our students effected by this event, who were contacted immediately and have shown remarkable support. Mrs. Sanders is no longer employed by Mitchell Community Schools. She has submitted her letter of resignation, The Mitchell team of students, families, community members, and educators will continue to analyze current practices and collaborate on best solutions in regard to all Mitchell students."Sanders is scheduled for an initial hearing in Lawrence County on March 25. No attorney is listed for her. 2251

It's official...New York Mayor Bill de Blasio is running for President of the United States. Here's his announcement video... pic.twitter.com/A9gDtfLzGo— Yashar Ali ?? (@yashar) May 16, 2019 202

It's fitting that the orange-hued, googly-eyed mascot once written off as nightmare fuel made a 7-year-old fan's dream come true.Gritty, the idiosyncratic mascot of the National Hockey League's Philadelphia Flyers, made a rare off-ice appearance Tuesday to surprise Caiden O'Rourke, a double amputee with two rare conditions, after he was fitted with a custom prosthetic leg adorned with Gritty's unblinking face.Caiden, who's a few days shy of 8, was born with ectrodactyly, a bone deformity that means he's missing some bones and digits on his hands and feet, and amniotic band syndrome, which resulted in the amputation of his lower right leg in the womb, Shriners Hospital for Children in Philadelphia said in a statement.As a young and growing double amputee, he's regularly fitted for new prosthetics, the hospital said. And as a true Philadelphian, he prefers them peppered with the logos of his favorite local teams.When the Flyers' resident monster caught wind of Caiden's request for his new left leg -- orange, of course, covered in miniature Grittys -- he waddled on in to Caiden's hospital room, flanked by two Flyers cheerleaders.Mouth agape, Caiden hugged his hero, who gave him a custom jersey. He showed Gritty the above-knee prosthetic on his right leg, covered in the Flyers' logo.Gritty, it seemed, was wowed -- though his googly eyes made it hard to tell for sure.Prosthetics haven't slowed Caiden for a second. He's a hockey and baseball player who keeps up with his two older brothers.He still goes to daily therapy to gain full use of his right hand, which was reconstructed with two new digits in a 2014 foot-to-hand transplant, the hospital said.Gritty, a furry monster who's mute save for some squeaky hands, was 1752

Justice Ruth Bader Ginsburg revealed Tuesday that she traveled with retired Justice John Paul Stevens "in the last week of his life" to Lisbon, Portugal, for a conference where the two justices attended meetings, visited museums, vineyards and castles."Perhaps he knew at age 99, distant travel was a risk," Ginsburg said during Stevens' funeral at Arlington National Cemetery, "but he wanted to experience fully the joys of being alive, and he did just that almost to the end."Ginsburg, 86, said that as the "next eldest in attendance" she had the opportunity to ride with him on long drives and his mind "remained vibrant" and he spoke not only of court cases but footnotes in various opinions."His conversation was engaging, his memory amazing," she said. As they were leaving the US ambassador's residence during their last evening in Lisbon, Ginsburg told Stevens, "My dream is to remain on the court as long as you did."His immediate response, she said, was "Stay longer!"Justice Sonia Sotomayor also accompanied her colleagues on the trip which was hosted by New York University. The event was from July 8-12.Stevens died in Florida on the evening of July 16, according to a press release from the court, after suffering a stroke on July 15. The release did not say where Stevens was when he fell ill.Ginsburg talked about his approach to the law and his willingness to continue "learning on the job." She also mentioned that on the 30th anniversary of his appointment to the court, President Gerald Ford wrote a letter praising his nominee.A day after laying in repose at the Supreme Court, Stevens -- a World War II veteran -- was buried in a private ceremony. According to a court spokeswoman, there was a Navy casket team, a firing team and a bugler.Stevens served in the United States Navy from 1942 to 1945 and was awarded the Bronze Star for his service on a codebreaking team.The private service -- closed to the press -- was also attended by Stevens' former clerks. On Monday, 70 of them lined the stairs of the Supreme Court as the casket was carried to the Great Hall for a day of mourning. The clerks took turns standing vigil as visitors, including President Donald Trump, stopped by to pay their respects.At Tuesday's private funeral, David Barron, who served as a clerk during the 1995-96 term and is now a judge on the 1st US Circuit Court of Appeals, called his former boss "unassuming" but "supremely competent.""He believed fiercely in independence, in not going along with the crowd, in stating your own views no matter how distinctive, and in the capacity of the country to handle disagreement, even strong disagreement, and to learn from it, if respectfully offered and respectfully received," Barron said.Another eulogy was delivered by Stevens' granddaughter, Hannah Mullen, who said that he was the "great Justice, the great man" but that he was also "the greatest grandpa in the world.""He was the kind of grandpa who taught us how to catch lightning bugs," she said, adding that he used his anti-trust skills to try to "trounce" his grandson John in Monopoly.She spoke about his career, his big dissents and the opinions he wrote that no other justice joined."I hope like him, we remain graceful in victory and undaunted in defeat -- brave enough to dissent and, if no one will join us, brave enough to dissent alone," she said. 3374

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