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Its 5:30 p.m. and most of the 20 and 30-year-old students in this class have just come here from a day at work. But now, they’re here to learn the basics of buying auto insurance.It’s part of a unique initiative called the 236

DUBLIN, Ireland – St. Patrick’s Day is normally associated with large crowds of green, but celebrations may be a bit muted this year due to the ongoing coronavirus outbreak. Cities are beginning to cancel their St. Paddy’s Day parades in response to the outbreak of COVID-19, the disease caused by the virus.The Ireland government announced Monday that it is canceling all of its parades, including the Dublin parade, the largest in the country. “Due to the unique nature and scale of the St Patrick’s Day festivities, in terms of size, the mass gathering of local and international travelers, and the continued progression of community transmission in some European countries, along with the emergence of a small number of cases of local transmission in Ireland, the Government has decided that St Patrick’s Day parades, including the Dublin parade, will not proceed,” 884

A family in Ohio says they're excited to add another family member."We’re anti-gender reveal normally,” said Love Gwaltney.Not this time — for this kid, they’re doing it big.The Akron family got a cake, a professional photographer and a box filled with balloons, but instead of something pink or blue popping out, their oldest child, Grey Schoolcraft, emerged."The gender reveal was kind of our way of telling family,” said Gwaltney.They revealed to the family their firstborn, who used to be their daughter, is now their son. Love says they got it wrong 17 years ago, so she and her son's stepdad Brandon Gwaltney threw a gender reveal party just for him."We’ve always been very open and very embracing with the kids and how they feel,” said Brandon.The rising senior says it wasn’t easy coming to terms with it all."It was a long, long, long, long process,” said Grey.At first, Grey says he wasn’t sure where he felt most comfortable."I originally said that I was non-binary, and then eventually it became that I was gender fluid and I jumped between a lot of different labels before I finally found something that kind of fit,” he said.After the photoshoot and social media post, Grey’s immediate and extended family have embraced him as well as thousands of strangers on the internet, but of course, there are the negative comments."If you’re going to claim that somebody dosen’t know who they are, then you need to stop assuming that somebody’s allowed to be straight then at 17 and it's just the heteronormative to assume everyone is straight until they say otherwise,” said Grey.Grey’s parents say they've gotten their fair share of concerns too."I don’t think it's as crazy and abnormal as people might think, when you actually get down to it and think about it feels mostly like stuff that we went through when we were trying to figure out who we want to be and what we want to grow up to be and identify as,” said Brandon.Each time they look back at this day and see Grey’s contagious smile, Love and Brandon say they don’t regret a thing."People always ask me, they’re like well what if Grey changes his mind?” said Love. “My response to that is I’d rather 100 percent support Grey in the label and the platform that he’s at and him change his mind then to not support him and realize down the road that this is his final destination and I have failed my child.” WEWS' Amanda VanAllen first reported this story. 2445

INDIANAPOLIS — The U.S. Food and Drug Administration on Monday granted emergency use authorization to Eli Lilly and Company's experimental COVID-19 antibody treatment bamlanivimab.According to a statement from the company, the drug is authorized for the treatment of mild to moderate COVID-19 in adults and pediatric patients 12 years and older with a positive COVID-19 test who are at high risk for progressing to severe COVID-19 and/or hospitalization. Lilly said in a statement the drug should be administered as soon as possible after a positive COVID-19 test and within 10 days of symptom onset. The authorization allows for the distribution and emergency use of bamlanivimab, which is administered via a single intravenous infusion."This emergency authorization allows us to make bamlanivimab available as a COVID-19 treatment for recently diagnosed, high-risk patients — adding a valuable tool for doctors fighting the now-increasing burden of this global pandemic," David A. Ricks, Lilly's chairman and CEO, said. "The rapid development and availability of bamlanivimab could not have been achieved without the relentless work of our Lilly team, collaboration across the industry and the urgent work being done by the government to ensure appropriate allocation to patients who need it the most."The emergency use authorization is based on data from BLAZE-1, a randomized, double-blind, placebo-controlled Phase 2 study in patients with recently diagnosed mild to moderate COVID-19 in the outpatient setting. Patients treated with the drug showed reduced viral load and rates of symptoms and hospitalization, Lilly said in the statement. Infusion reactions and other allergic hypersensitivity events have been reported, Lilly said. The emergency use authorization includes a warning for hypersensitivity including anaphylaxis and infusion-related reactions.Lilly said the drug is not authorized for use in patients who are hospitalized due to COVID-19 or who require oxygen therapy due to COVID-19 or who require an increase in baseline oxygen flow rate due to COVID-19 in those on chronic oxygen therapy due to underlying non-COVID-19 related comorbidity."The BLAZE-1 data show bamlanivimab, when given early in the disease course, may help patients clear the virus and reduce COVID-related hospitalizations, supporting our belief that neutralizing antibodies can be an important therapeutic option for patients fighting this virus," Daniel Skovronsky, M.D., Ph.D., Lilly's chief scientific officer and president of Lilly Research Laboratories, said. "We're proud of the speed with which we have been able to bring patients this therapy specifically designed to treat COVID-19. We thank those who have contributed to this medical advancement, particularly the clinical trial investigators and participants around the country." This article was written by Bob Blake for WRTV. 2906

A major warning from scientists around the world: Do not depend on antibodies for permanent immunity from COVID-19. This comes on the heels of several studies showing that antibodies only last in our bodies for about two to three months.“That’s normal,” said Dr. Michael Teng, a professor at the University of South Florida's College of Internal Medicine and a researcher.According to Dr. Teng, our immune system creates antibodies when a virus enters our bodies. Their main purpose is to stop the virus from getting into our cells. Having few or no antibodies isn’t necessarily a bad thing, and it doesn’t mean you’ll be reinfected with the virus right away.“Antibodies are supposed to go down after a while,” Dr. Teng said. “You’re not supposed to have high elevated levels of antibodies for weeks on end. It’s not normal.”Scientists were hoping the antibodies produced from COVID-19 would stick around as long as antibodies produced from other forms of coronavirus, like SARS. Now that studies have shown that they don’t, they say we should rely on treatment, and working to come up with a vaccine.There are several potential vaccines being tested right now, but don’t expect to get your hands on one any time soon.“The fastest vaccine that we ever made was the Mumps vaccine and that took four years,” said Dr. Teng. WFTS' JJ Burton first reported this story. 1386

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