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Congratulations to Pres-elect Biden on a successful campaign. All Americans need to come together to support Pres-elect Biden. Our nation will only be successful if the new admin is. We must work together to enact bipartisan legislation & solve the problems our country faces 1/2— Francis Rooney (@RepRooney) November 8, 2020 337

COLLEGE STATION, Texas -- Two sororities at Texas A&M University are forced to quarantine after having been exposed to COVID-19.The university announced the activities and members of Kappa Kappa Gamma and Delta Delta Delta are experiencing exposure to the virus.Texas A&M has initiated chapter-wide quarantine and contact tracing for those who live in the sorority houses or elsewhere and were in contact.The chapters have been responsive and are responsibly following required steps to continue operations, according to the university.Students, faculty, or staff who receive a positive diagnosis or believe they have been exposed to a positive case must complete a form through the university's reporting portal.Gatherings have also been restricted to 10 or fewer people.Texas A&M kicked off the fall semester both online and in-person on August 19.This story was first reported by Sydney Isenberg at KXXV in Waco, Texas. 942

Considered the coronavirus holy grail, antibodies are believed to give us some level of immunity from the virus. They form after a person fights off COVID-19 and can be detected through a serological test, better known as an antibody test. "There are some really great companies building antibody tests, and there are some not so great, bad actors, building antibody tests. So you have to be really careful," says Jon Carder, co-founder and CEO of Vessel, a San Diego company created four years ago to provide in-home wellness tests. Early in the pandemic, the U.S. Food and Drug Administration allowed these tests to be sold and distributed without federal review, as long as the company notified the FDA it was offering a test, performed self-validation studies, and included a disclaimer on the test results. The FDA is now cracking down on the bad actors, creating a list of tests that should no longer be distributed. Only a handful of manufacturers have been granted FDA Emergency Use Authorization, meeting a certain threshold for accuracy.Carder says states and even countries have been fooled by the bad actors, purchasing inadequate tests. "We were talking to a city government, a big city, and were blown away when we got a response that they were thinking about buying antibody tests from a certain manufacture who had claimed they were FDA approved. And the state had sort of taken their word for it, and they weren't," said Carder. Vessel had been preparing to release its in-home wellness tracker, which tests for health markers like vitamins, minerals, toxins, and cortisol. When the pandemic hit, the company adapted its technology to be used in the fight against COVID-19. "We take existing antibody tests, the good ones, the ones that are accurate and that the FDA has approved for emergency use, and we enable those to be done safely and accurately at home," said Carder. They've created a kit with step-by-step instructions to do the blood test at home. The test card is then scanned through the Vessel app and provides results from a medical professional within a half-hour. The FDA has already approved in-home tests to diagnose active infections – but Carder says the sample must be sent to a lab, and the user must have symptoms or another qualification to get one. And he says they can be costly. "Ours could be one of the first, or the first, antibody test done at home, no lab needed," said Carder. Just this week, the FDA issued three warning letters to companies making false claims on their in-home antibody tests.Vessel has completed its usability studies and is now in clinical trials with the FDA. "Our job is to prove it can be done safely at home and to show that via clinical trials. The FDA really makes the call if they're going to enable antibody testing at home," said Carder. He says the test would be cost-effective, anywhere from -, or around with medical consultation. If approved by the FDA, Carder estimates millions of people could be tested within the first few months. "There's something really great about the peace-of-mind that comes from doing a test, and that may be one of the biggest benefits," said Carder. But while the FDA is only approving the most accurate tests, none are 100 percent accurate and could still lead to false positives. 3314

COPENHAGEN, Denmark (AP) — Volvo Cars says it is recalling nearly 2.1 million vehicles worldwide as a preventive measure after the company discovered that a steel wire connected to the front seat belts can be weakened.The front seat belts are anchored to the car via this steel cable which can be subject to wear and tear.There have been no reports of injuries or accidents linked to the fault. The Swedish carmaker says the recall has been declared to avoid future issues.The recall is the biggest ever for the brand. The affected models are Volvo S60, S60L, S60CC, V60, V60CC, XC60, V70, XC70, S80 och S80L manufactured between 2006 and 2019, The Associated Press has learned.No current models are included in the recall.Volvo Cars has been owned by China’s Zhejiang Geely Holding Group since 2010. 808

CLEVELAND — President Donald Trump has weighed in on the report that Cleveland's Major League Baseball club will soon drop its controversial team name "Indians" calling it the latest example of “cancel culture.”On Sunday, The New York Times reported the team is planning to drop the nickname it has used for more than a century and will become the latest franchise to abandon Native American imagery.Manager Terry Francona said in July that he believed the time had come for the team to change its name after more than 100 years.“I think it’s time to move forward,” Francona said. “It’s a very difficult subject. It’s also delicate.”The New York Times said the team could announce plans for a new nickname as soon as this week. 735