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A day after they were given hope that a new facility would treat their 14-year-old son, a Monroe County, Michigan, family says they're again scrambling to find a new hospital to take himBobby Reyes was declared brain dead after suffering an asthma attack in late September. Doctors at CS Mott Children's Hospital told the family it was time to say goodbye. However, they went to court to get more time to find a new facility to take him. On Wednesday the family said a doctor at Allegiant Health Care of Phoenix had agreed to accept him for treatment.However, the family's attorney now says the doctor did not have the approval of administrators of Allegiant and they have disagreed with his decision. Beause of this, the transfer will not be taking place and the family posted an emotional video to Facebook saying the plug would be pulled on Friday. 863

A judge stands accused of having sex and alcohol in the courthouse, coercing staff, taking revenge that affected cases, and more.An anonymous person filed the complaint about Judge Dawn Gentry, a family court judge in Kenton County, to the Kentucky Judicial Conduct Commission on Nov. 18. The accusations include:Having sex with two staff members in the courthouse.Drinking alcohol in the courthouse.Coercing staff to help her with her campaign.Retaliating against those who did not support her. Holding pretrial conferences in child abuse cases without all attorneys presentFalsifying time sheets.Gentry could lose her seat if found guilty of serious ethics violations."They're very serious charges,” said attorney Richard Goldberg, who has experience with these types of cases.READ 798

This week people across the country are enjoying time with family and celebrating the day the Native Americans and pilgrims sat down for a meal together. But the history of Thanksgiving, and the relationship between the two groups, is not that simple.“There was a lot of cultural misunderstanding, and there was some just flat out theft, and murder, and those things happened too,” said Tressa Brown with the Kentucky Heritage Council.Brown says what's taught in schools often romanticizes the first Thanksgiving and fails to acknowledge the wrongdoings against American Indians.“The stories that we perpetuate tend to make at least the dominant culture feel good, not so much for the other cultures. This is not a day of Thanksgiving for native people,” said Brown.She says Native Americans traditionally give thanks every day, rather than one set day each year. A part of Brown’s work includes traveling to schools to educate students and teachers about appropriate ways to teach and celebrate the holiday.“I think it's really important that kids be taught respect for those cultures, respect for what is sacred among other people. And not to denigrate it by dressing up and, you know, hitting your hand over your mouth to make noise and speaking in broken English,” said Brown. Brown says many don't realize that Native Americans are modernized, and they live just like everyone else.“The American Indian cultures, multiple, are vibrant, alive, thriving,” said Brown. Right here in Kentucky there is a rich Native American history. So Brown says this Thanksgiving take time to read up on the culture, and put a stop to hurtful stereotypes.“Respect is due, respect for that history, and those people is due,” said Brown.She says there are groups in America who are making an effort to acknowledge the history of Native Americans and trying to make amends.Brown tells LEX 18 the Indigenous Peoples Day movement is one example of that. 1949

A bill that would prohibit abortions after tests indicate that a fetus may have Down syndrome overwhelmingly cleared the Arkansas state Senate and is now under consideration in the state House.The 209

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

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