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LAKE POWELL, Utah — A baby from St. George has set the record for the youngest child to water-ski, his family says.Casey and Mindi Humpherys posted a photo and a video of 6-month-old Rich skiing at Lake Powell on Instagram earlier this week, captioned "I went water skiing for my 6 month birthday. Apparently that’s a big deal… #worldrecord" on an account dedicated to photos of the boy growing up and going on outdoor adventures. His parents, on their own individual Instagram accounts, specified that Rich was six months and four days old at the time — beating the youngest-known record by six days. The previous record was set by Auburn Absher in 2016 at six months and 10 days old, according to reports from BuzzFeed and ABC News. No official records are available for the youngest child to water-ski."Take one look at this kid and tell me he isn’t having the time of his life! Such a little stud!" his dad added. This story originally reported by Spencer Burt on fox13now.com. 1028

DENVER — The Broncos' game against the New England Patriots has been postponed to Monday over concerns about positive COVID-19 cases among the Patriots, sources confirmed to Scripps station KMGH on Thursday.A decision needed to be made Thursday, as the timing of the game would impact practices and other scheduling into the weekend.Patriots quarterback Cam Newton tested positive before the team's game against the Kansas City Chiefs, a matchup that was moved to Monday. Following the Patriots-Chiefs game, New England cornerback Stephon Gilmore also tested positive. No Broncos players have tested positive for COVID-19.The Broncos-Patriots postponement comes as the league is also working to contain an outbreak of cases among the Tennessee Titans, whose Week 4 game against the Steelers was postponed after several positive cases. This article was written by Troy Renck for KMGH. 903

Here's a look at all the local mall hours around San Diego to make sure your holiday shopping goes smoothly.Fashion Valley Mall (7007 Friars Rd.) 160

TAMPA, Fla. — The Tampa Bay area is known for its crystal clear beaches and white sand.Many people see the saltwater as a place to relax and kick back, but Dr. Serene Al-Momen sees it as a vast area of opportunity to stop the spread of the coronavirus.Specifically with what lies under the surface."The jellyfish is the component of the sensor that basically makes the cell emit light when a pathogen from the air is connected to it or binds to it," Dr. Al-Momen said.Dr. Al-Momen is the CEO of the company Senseware. She said the jellyfish is helping her team identify the coronavirus in the air.Her team works to find what's in the air behind the scenes. They do it with a sensor box not much bigger than an Amazon Echo at home.The sensor can detect pathogens in the air like Ecoli, SARS and anthrax.In March, they shifted gears in what type of pathogen they wanted to find."We took what we had and we kind of improved on it to really meet the challenges of today with COVID," Dr. Al-Momen said.The sensor can count particles down to the smallest micron that the common eye would never catch.To detect the coronavirus, they made adjustments."For COVID, we have the SARS code 2 antibody in that cell. So, what happens is when we get the sample of the air and the sensor gets the sample of the air there is a pathogen that binds into the cell and connects to it it will emit light," Dr. Al-Momen said.To help identify pathogens scientists use a luminescent component from a jellyfish; something that is nothing new when working to identify viruses and diseases."This particular methodology was created in the early 2000s by the MIT Lincoln Labs to specifically identify anthrax threats when anthrax was an issue," Dr. Al-Momen said.The jellyfish's protein helps light up a cell when a pathogen from the air is connected to or binds to it.The team then uses sophisticated algorithms that measure the intensity of the light that can determine whether it's positive or negative.The sensors cost tens of thousands of dollars and are geared towards larger corporations such as hospitals and senior care facilities.Senseware is currently in the Beta testing phase and they hope to offer the machine commercially by November.For more information about Senseware, visit their website. This story originally reported by Vanessa Araiza on abcactionnews.com. 2372

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