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Joe Biden is using a campaign stop in economically decimated Nevada to hammer President Donald Trump and Senate Republicans for not doing more to help Americans deal with the economic fallout of the coronavirus pandemic.WATCH RECAP:The Democratic presidential candidate told supporters Friday at a socially distanced drive-in rally outside Las Vegas that Trump “ignores you” and has “no urgency to deliver hard-working Americans ... what they need desperately.” He says Republican Senate leader Mitch McConnell wants to let state and local governments “go bankrupt.”During the event, Biden told his supporters that President Trump's personal conduct has been "reckless" since he was diagnosed with COVID-19 last week. Trump was released from Walter Reed Medical Center on Monday."His reckless personal conduct since his diagnosis, the destabilizing effect it’s having on our government is unconscionable. He didn't take the necessary precautions to protect himself or others. The longer Donald Trump is president, the more reckless he gets," Biden said.Biden blasted Trump for pulling out of congressional negotiations for another round of pandemic economic relief and reversing himself Friday. Biden noted it’s been months since House Democrats passed a .4 trillion package for businesses, individuals, and local and state governments dealing with cratering tax revenues and increased costs.Nevada has been hit especially hard in the pandemic economy as tourism to Las Vegas has fallen drastically. The state’s 13.2% unemployment rate in September was the nation’s highest.Earlier in the day, Biden spoke at the East Las Vegas Community Center where he told supporters that he can’t win without strong support from Hispanics.Biden is telling Latinos in Nevada that they can “determine the outcome” of the November election and help deliver a Democratic victory big enough to keep President Donald Trump from pushing “phony challenges” to the results.Latinos are on track to surpass Black voters as the single largest nonwhite share of the U.S. electorate. Biden told a masked, socially distanced crowd that voting in decisive numbers is “the thing that guarantees significant influence over what happens next” because politicians respond to those that “delivered the vote.”Biden drew parallels between his family lineage as Irish Catholic immigrants and much of the Latino community that he said is hurt by Trump’s hard-line immigration policies. Biden says “family and faith” link his experiences with the Hispanic community.Early voting starts in Nevada Oct. 17. Hillary Clinton won the state in 2016, but it remains a battleground. 2645

Join @SmithsonianNMAI online this #VeteransDay for the opening of the new National Native American Veterans Memorial. Learn more about the memorial and what it represents, and watch the completion ceremony and virtual tour: https://t.co/cZPSZPc0ix #NNAVM #NativeAmericanVeterans pic.twitter.com/wOBDLC2VaA— Smithsonian (@smithsonian) November 11, 2020 359

JUPITER, Fla. — Groundbreaking research out of the Scripps Research Institute in Jupiter, Florida found a genetic explanation for the pain processing and sensory issues some children living with autism face."To see the biology in the lab turn out that has parallels to what’s going on in these children takes it so far beyond just an academic endeavor," said Dr. Gavin Rumbaugh, a neuroscientist at Scripps. "You go home every day thinking, unbelievably, I may actually be making a difference in someone's life."One of those children who Rumbaugh hopes to help with his research is 10-year-old Beckett, who lives in Texas."We wanted to understand generally in the lab how genes like SYNGAP1 affect the way the brain functions and we thought what better way was then to look and see how this gene may directly affect sensory processing, and then further on ask the question, 'Does the change in sensory processing actually lead directly to learning, memory and behavioral impairment?' " he said.Beckett has a genetic mutation of SYNGAP1, which researchers have now found causes certain issues he faces, particularly, having an extremely high pain threshold while also experiencing heightened sensitivity to another kind of stimuli. Beckett and other children living with this genetic mutation also often have epilepsy."It's all about quality of life. Everybody deserves to live their best life and that's my mission," said Monica Weldon, Beckett's mom.Weldon said the research being done in Jupiter could change her son's life and the lives of hundreds of other children around the world with the same genetic abnormality and symptoms, some of whom whose families she's connected with online."That is the power I believe of a patient group that is motivated to find treatments for their loved ones," Weldon said. "Also, you've got scientists who are listening. They're willing to listen and they're willing to learn."The next step in Rumbaugh's research is to look at treating the symptoms from the genetic mutation. 2043

KANSAS CITY, Mo. — Doctors and nurses are celebrating the recovery of a 23-year-old man who spent months in the hospital with a severe COVID-19 infection.In early April, Shakell Avery began feeling some of the COVID-19 symptoms. He went to the emergency room, and within 48 hours, he was on a ventilator fighting for his life due to the virus.After spending months in the hospital, he recovered, thanks to a convalescent plasma donor from New York and medical staff from Menorah Medical Center and Research Medical Center.It's been a celebration ever since his family heard the news their loved one was coming home."You definitely feel the love," Avery said. "It's like they were waiting for a celebrity to come to town."In late June, Shakell's doctors and nurses also celebrated his recovery."As hard as these days have been for some of us on the front line, it's worth it," said Dr. Marjorie Wongs with Menorah Medical Center said. "It makes it worth it."It's a different story from just a few months ago when Avery first contracted the virus.He shared how he felt right before he went to the hospital."I played sports, I played football, and I've never felt body aches like that," Avery said.Ultimately, it was the shortness of breath that worried him and his family."I mean just taking real deep breaths, and I still couldn't get it, and I thought, 'something's wrong,'" Avery said.He spent more than two months at Menorah Medical Center."He had life-threatening COVID-19," Wongs said. "He had severe pneumonia and required a ventilator. He had respiratory failure.""I remember before I went in and then when I woke up at the hospital," Avery said. "I don't really remember much at Menorah."Nurses and staff put up a tent for the family to say hello through the window and draw pictures because they couldn't physically be inside with him at the time.Avery's family said it was such a blessing to see the healthcare staff doing what they could to see their loved one, especially since Avery was in the hospital for a total of 79 days."Initially, you hear two weeks, three weeks," Shakell's mother, Wiletta Avery said. "When he was put on a ventilator, that was the hardest thing for me."Wiletta Avery then heard what no mother wants to hear."On April 11th, 4:30 in the morning, I'll never forget. They call and they're explaining to us that there's nothing they can do for him. He was maxed out on ventilation," Avery's mother said. "At that point they allowed me to go up and see him. And you know, they're not letting people into these hospitals, so when they say, 'You can come up,' you pretty much know what that means as if this will be my last time seeing him."While seeing him, she asked him to do just one thing."I just asked him, I need you to fight for me," she said. "I need you to fight."Wongs said there was a push to get convalescent plasma for Avery, but it wasn't an easy process."We contacted local blood banks; no one had any plasma available. We started looking for donors ourselves," Wongs said. "We even were contemplating flying a donor to another state, to where they could do the collection because we didn't even have collection capabilities in Kansas City until much later."Avery's family members also went to social media, pleading someone who recovered from COVID-19 to help save Shakell's life.They eventually found a donor."We ended up getting a donor from New York City. They were able to ship that plasma to us from the community blood center," Wongs said.They transfused those antibodies into Avery's body."It's experimental. This is the first patient that I had given convalescent plasma to. It's been reported out for other infections, but you know, this was our first patient," Wongs said.And it worked."To see he improved with it was just amazing for us," Wongs said. "I think it is definitely going to be one of the bridging therapies until we get to a vaccine or some sort of a cure. It is definitely one of the first things I go to now in patients that have severe, life-threatening COVID. I know we are using it much more than we were now."Menorah Medical Center and Research Medical Center worked together to make the transfusion happen."We are part of a national clinical trial," Wongs said. "I think we'll have some data that comes out later this summer as to the efficacy of convalescent plasma, but those of us on the ground that are using it, we think the data is going to be promising."Avery was only in his early 20s when he contracted the virus."It's definitely something I don't want anybody to go through," he said. "I just felt real depressed, robbed... like somebody just snatched you out your livelihood."While Avery recovered from the virus, it hasn't been a full overnight recovery."You don't just come home and everything is right back to normal. I had to learn how to walk again, I had to learn how to stand up straight on my own, with no support. I'm still having to learn how to properly get up steps," Avery said. "I used to be active, moving, and now it's just like, everything that you learn that's new, that's second nature to you, you have to relearn. So it's difficult. The fight really ain't over until it's 100 percent over."Avery has a message for young adults his age."When you decide to step outside, no mask, no sanitizer, no care in the world, think about whose father you're taking away from that kid. Think about whose mother you're taking away, whose grandparent, whose daughter, whose son," he said.He said he hopes more people take this virus seriously."Don't think you're invincible, I used to think that," Avery said. "Take this as serious as you would anything else. Take this as serious as life, cause it's that serious."Avery says financially, it's been hard too, as bills didn't stop while he was in the hospital for months and now continues to work on physical therapy.His family has set up a GoFundMe page to help with financial assistance.This story was originally published by Rae Daniel on KSHB in Kansas City. 6012

LA JOLLA, Calif. (KGTV) — A La Jolla woman may have new evidence that the iconic sea wall at the Children's Pool is increasingly crumbling.Architectural historian Diane Kane spent time in 2017 and 2018 taking photos of different parts of the sea wall in an effort to earn it a historical designation. She recently went back to take more and found that the wall's walking path is increasingly disintegrated, and its railings even more rusted over. RELATED: Coastal Commission approves permit to protect seals during pupping season"I don't know if we had a particularly strong winter last year or if this is just at a point where it's had deferred maintenance for so long that it's really starting to go quickly," Kane said.Ellen Browning Scripps donated the wall in 1931, creating what's now known as the Children's Pool. Kane, a trustee of the La Jolla Community Planning Association, says a historic designation could help generate funds to preserve the sea wall. She spent two years writing a historic report, which she submitted to the National Register of Historic Places. RELATED: San Diego conservationists test high-tech approach to combat poachingThe agency returned her application earlier this year because the photos she took had people in them, a disqualifying factor. That's why she went back to the sea wall in recent weeks to take more photos, at which point she noticed the changes. A spokesman for the City of San Diego was not immediately available for comment. 1488