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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 group of Columbus-area middle-school students may have served food tainted with bodily fluids to teachers judging a year-end home economics class project, 169

(CNN) — The rancher and philanthropist best known for playing the original "Marlboro Man" has died after a life spent not smoking.Robert "Bob" Norris died in the care of Pikes Peak Hospice in Colorado Springs, Colorado, on Nov. 3, according to a 258

A family from Connecticut got quite the surprise when their 10-year-old son was called for jury duty.Fifth grade student Nick Dondero received the letter in the mail summoning him to show up.While the family found it a bit comical, they’re wondering how it even happened in the first place.Nick’s mom laughed about it and tucked it away.“Two, three weeks later, I’m going through to pay bills and I’m like ‘oh my gosh, I never sent this back,” she said.Each year, more than 550,000 people in Connecticut are selected for jury duty.The Connecticut Judicial Branch gets a list of names from four places: The Dept. of Motor Vehicles, the Dept. of Labor, Registrar of Voters, and the Dept. of Revenue Services.The list of names the Judicial Branch gets from Revenue Services does not include the date of birth. That is where Nick’s name came from and why he was summoned.“I was wondering what if I don’t go, I wanted to know if that was going to be a problem,” Nick said.It wasn’t a problem.The Judicial Branch said the Dondero family did the right thing. They checked a box on the summons letter saying he was underage and sent it back.Now, 10-year-old Nick is in the clear and does not have to report for jury duty. 1225

A 25-year-old mother was arrested in Mississippi after two of her three kids drowned when her locked vehicle rolled into a creek on Saturday. Leland police say they were called to check out the scene around 5:45 p.m. on March 9 after someone reported a Nissan Pathfinder floating in Deer Creek with kids trapped inside. The Leland Fire Chief and others had already found the vehicle and tried to break the windows to get the children out. They were only able to safely rescue one of the kids, 2-year-old Raelynn Johnson. Police say a dive team located the vehicle, which had drifted further downstream, about two hours later. The bodies of 4-year-old Steve Smith and 1-year-old Rasheed Johnson Jr. were located in the car. The mother, Jenea Monique Payne, reportedly told police she left the kids in the car while she went into a Stop-N-Shop store. She walked out to find the vehicle had rolled into the water. Payne was booked into jail on Monday and charged with two counts of manslaughter and one count of child neglect. Police say she was then released on her own Recognizance Bond by the county court. 1119