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54 couples married in Gaza mass wedding celebration

admin - Latest News - December 2, 2025
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Dec. 2, 2025, 5:04 PM ESTBy Dareh GregorianPresident Donald Trump on Tuesday ripped Rep. Ilhan Omar, D-Minn., as “garbage” and said Somalis should “go back to where they came from.”“I don’t want them in our country. I’ll be honest with you, OK. Somebody will say, ‘Oh, that’s not politically correct.’ I don’t care. I don’t want them in our country. Their country is no good for a reason. Their country stinks, and we don’t want them in our country,” Trump said during a Cabinet meeting at the White House.“I can say that about other countries, too,” he added, as Homeland Security Secretary Kristi Noem sat nearby. In a social media post Monday night, Noem said, “I am recommending a full travel ban on every damn country that’s been flooding our nation with killers, leeches, and entitlement junkies.” A source familiar with the plan said today that about 30 countries will be on that list.Trump, however, focused most of his ire on Somalia and Omar.“With Somalia, which is barely a country, you know, they have no, they have no anything. They just run around killing each other. There’s no structure,” he said before turning to Omar, a progressive Democrat and Somali American he’s mocked and targeted for years.“I always watch her,” Trump said, saying she “hates everybody. And I think she’s an incompetent person. She’s a real terrible person.”Omar has served in Congress since 2019.Rep. Ilhan Omar, D-Minn., in St. Paul.Stephen Maturen / Getty Images fileLater, Trump called her “garbage. Her friends are garbage. These aren’t people that work. These aren’t people that say, ‘Let’s go, come on, let’s make this place great.’ These are people that do nothing but complain.””You know, if they came from paradise, and they said, ‘This isn’t paradise,’ but when they come from hell and they complain and do nothing but bitch, we don’t want them in our country. Let them go back to where they came from and fix it,” he added.A representative for Omar did not immediately respond to a request for comment.Trump’s remarks come as a senior law enforcement official told NBC News that Immigration and Customs Enforcement is planning an operation in the Minneapolis-St. Paul area this week. The official said ICE officers are not specifically targeting the Somali community, but may be arresting some Somalis who are in violation of immigration laws.The planned operation was first reported by The New York Times.The president’s remarks on Somalia came at the end of the public portion of a more-than-two-hour Cabinet meeting when a reporter asked him if Minnesota Gov. Tim Walz should resign over fraud related to Covid relief funds in the state.The New York Times reported that 59 people have been convicted on criminal charges relating to the fraud schemes in recent years, and most are of East African descent. In all, the scams raked in over $1 billion in taxpayer money.Trump said, “Somalians ripped off that state for billions of dollars, billions, every year, billions of dollars, and they contribute nothing.”Walz, the 2024 Democratic vice presidential nominee, told NBC News’ “Meet the Press” on Sunday the fraudsters are going to jail, and “to demonize an entire community on the actions of a few, it’s lazy.”There are an estimated 80,000 Somalis in Minnesota, and Walz said Trump is “demonizing an entire group of people who came here, fleeing civil war, and created a vibrant community that makes Minnesota and this country better. But that’s Donald Trump: deflect, demonize, come up with no solutions. He’s not going to help fix anything on fraud.”In his remarks Tuesday, Trump called Walz “a grossly incompetent man. There’s something wrong with him.”Dareh GregorianDareh Gregorian is a politics reporter for NBC News.Maya Rosenberg and Julia Ainsley contributed.
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Savewith a NBCUniversal ProfileCreate your free profile or log in to save this articleOct. 15, 2025, 5:08 PM EDTBy Kaitlin SullivanTwo months after she was born, Eliana Nachem got a cough that wouldn’t go away. Three weeks later, she also started having runny stool, prompting a visit to her pediatrician. Eliana didn’t have allergies or a gastrointestinal condition; instead, tests pointed to a problem with her immune system. At 4 months old, Eliana received her diagnosis: severe combined immunodeficiency, or SCID. Babies born with the extremely rare disease do not develop the cells required for a functioning immune system. Every germ becomes a potentially fatal threat and to stay healthy, children with the condition must live in a completely sterile environment. Without treatment, kids usually do not live past their second birthday.“I expected the worst, then I immediately went into research mode,” Eliana’s father, Jeff Nachem, said. The Nachems also got to work turning their home into a germ-free fortress, rehoming their pets, never opening the windows and opening the doors to outside as sparingly as possible. Eliana was kept inside, and on the rare instance when visitors came by, the family had disposable gowns, gloves and masks for them to wear. (SCID is sometimes referred to as “bubble boy disease.”) Eliana also started on a temporary therapy that replaced a missing enzyme in her body, called adenosine deaminase (ADA).In the midst of the strict protocol, they learned about a clinical trial in Los Angeles — 2,600 miles from their home in Fredericksburg, Virginia — that could help their daughter live a normal life.Jeff, Caroline and Eliana Nachem with Dr. Donald Kohn before Eliana’s gene therapy for ADA-SCID.Courtesy Caroline NachemScientists have identified about 20 gene variants that cause SCID. Eliana’s form of the disease, ADA-SCID, is diagnosed in fewer than 10 children born in the U.S. each year. (Under 100 babies are diagnosed with any form of SCID in a given year.)In 2014, when she was just 10 months old, Eliana was one of 62 children enrolled in a clinical trial for a gene therapy for ADA-SCID. In a study published Wednesday in the New England Journal of Medicine, researchers followed up on the results of that Phase 2 clinical trial. The update reported that all 62 kids, who received the treatment from 2012 to 2019, are alive today. In 59 of them, including Eliana, the gene therapy completely restored immune function, without requiring any additional treatment — a success rate of 95%.“This is one of the most successful gene therapy trials for an ultra-rare genetic disease that we have,” said Dr. Talal Mousallem, an associate professor of pediatrics at the Duke University School of Medicine. He was not involved with the trial. Correcting stem cellsThe treatment begins with doctors harvesting stem cells from the patient’s own bone marrow. These stem cells are purified in a lab, and then modified using an inactivated form of the virus that causes HIV. Instead of carrying the human immunodeficiency virus, this version carries the ADA gene that people with ADA-SCID are missing, reinserting the gene into the stem cell DNA. Before the customized treatment is reinfused back into the patient, they must undergo chemotherapy to get rid of the body’s existing stem cells and make room for the new ones. Once back in the body, the cells — which no longer carry the virus, just the gene it left behind — get to work building an immune system over the next year.“It’s a one-time delivery vehicle that takes the gene into the DNA of the stem cell, so every time it divides to make other cells, those cells carry that ADA gene,” said Dr. Donald Kohn, a pediatric bone marrow transplant physician at UCLA’s Broad Stem Cell Research Center, who led the trial. A less risky optionGene therapy clinical trials are underway for four subtypes of SCID, but the standard of care is still a bone marrow transplant, which builds an immune system using stem cells from a donor. The treatment can be risky and side effects further down the line.It’s ideal for bone marrow transplants to occur between siblings — who share about half of the same DNA — but two siblings only have about a 25% chance of being a match. In most cases, the donor is not a sibling, which introduces the risk that the donor’s immune cells will attack the recipient’s body, a phenomenon called graft-versus-host disease.The risk of graft-versus-host means kids who receive functioning stem cells from another person have to be on immunosuppressant drugs following the transplant, which keep the foreign cells from attacking their immune system.“Which slows down the progress, because you are suppressing the immune system while also trying to build an immune system,” Kohn said. People also have to undergo much higher doses of chemotherapy before receiving a donor bone marrow transplant than they do before undergoing gene therapy. “There can be effects [later in life] from being treated with chemotherapy, including growth, endocrine or fertility effects,” said Dr. Whitney Reid, an attending physician in the division of allergy and immunology at Children’s Hospital of Philadelphia, who was not involved in the trial. With gene therapy, “you can give those patients much lower doses of chemotherapy and there is a much lower chance of rejection,” she said. Eliana “was able to go from living in isolation to being able to go to preschool and go swimming in a public pool and play on a playground, and do all the things that every other kid gets to do,” her father said. Courtesy Caroline Nachem Having another therapy for ADA-SCID is particularly important, Reid added. Changes in the ADA gene cause toxins to build up in clumps of white blood cells called lymphocytes. This can cause hearing loss and learning difficulties as kids get older. Unlike other types of SCID, “it doesn’t only affect the immune system,” Reid said. Mousallem, of Duke University, said he hopes the success of this trial will open the door to gene therapies for other rare diseases that often go untreated, as well as SCID caused by other gene variants. “The data is great for ADA-SCID, and it is our hope that one day this becomes the standard of care,” he said. Eliana turns 12 years old next week and loves going to dance classes.“It’s amazing that she was able to go from living in isolation to being able to go to preschool and go swimming in a public pool and play on a playground, and do all the things that every other kid gets to do,” her father said. Eliana still undergoes testing twice a year to make sure her immune system hasn’t weakened. So far, so good.“We think it’s a lifelong therapy,” Kohn said. “Some of these kids are now 15 years old and are living normal lives. We treated them when they were little babies and now they’re going to prom.”Kaitlin SullivanKaitlin Sullivan is a contributor for NBCNews.com who has worked with NBC News Investigations. She reports on health, science and the environment and is a graduate of the Craig Newmark Graduate School of Journalism at City University of New York.
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