Kyle Bradish had eight strikeouts in six dominant innings, Jorge Mateo hit an inside-the-park home run and the Baltimore Orioles beat the last-place Oakland Athletics 12-1 to complete a three-game sweep

Kami Rita Sherpa had stood at the top of the world just days earlier, exultant at having summited Mount Everest for a record 28th time.

The Golden State Warriors are reportedly trading Jordan Poole to the Washington Wizards in exchange for veteran point guard Chris Paul.To say the Washington Wizards are dealing would be an understatement in the NBA world. In the past week, the Wizards have traded Bradley Beal to the Suns, Krista...

Chinese commodities imports remained buoyant in September as the economy showed some signs of recovery and traders pinned

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By Daina Beth Solomon MEXICO CITY (Reuters) -U.S. labor officials on Friday asked Mexico to investigate alleged worker rights abuses

Philadelphia Eagles QB Jalen Hurts used previous disrespect from a Tampa Bay Buccaneers coach to motivate himself prior to Monday night's victory.

The woman who broke the internet by launching into a flummoxing rant aboard an American Airlines (AA) flight is doing everything she possibly can to rebrand herself as a beacon of positivity. Tiffany Gomas was widely christened the “crazy plane lady” after footage of her meltdown – during which she uttered the now immortal words “that motherf**ker is not real” – went viral online. The 38-year-old marketing executive has since addressed her actions, admitting that they were “completely unacceptable”. However, she has also urged viewers to appreciate that “we all have our bad moments”. And on Sunday, a week after sharing her tearful apology, she posted some groomed-but-relaxed photos of herself on Instagram, accompanied by the caption: “One moment doesn’t define you; but it can define your purpose.” In the snaps, Gomas looks a far cry from the frazzled, scraped-bun-banshee on board that AA aircraft and, instead, shows off her long, flowing hair as she poses barefoot on her kitchen floor. Emphasising her ambitions to become a motivational mental health guru, she added the hashtags: “#selflove #empowerment #motivation #staytuned.” The “stay tuned” refers to a project she has been promoting ever since sharing her public apology. She Texas-based exec insists that she wants to use the “life-altering” experience of becoming an internet personality to “do a little bit of good in the world” and has hinted that she’d like to become an influencer. Gomas ended her video message last week with the message: “Join me on my journey of promoting positive mental health and standing up against cyberbullying,” alongside a link to a new eponymous website. So far, the only content on the site is that same video, and a message reading: “Stay tuned”. It's Tiffany Gomas www.youtube.com Numerous admirers have commented on her recent photos, insisting she can’t possibly be “the same lady from the plane”. However, the 38-year-old has held her hands up and explained that whilst it was, indeed, her, she should not be “judged” for a one-off slip-up. In an interview with the Daily Mail, she said that in the wake of the incident, her life had “blown up”. “It’s frightening,” she admitted: “Things go viral and everything changes. “No one knows anyone else’s story, and no one should judge. No one knows what it’s like.” In the notorious clip, Gomas stormed to the front of the plane and declared that she was getting off because “that motherf**ker back there is not real.” “You can sit on this plane and you can die with them or not. I’m not going to,” she yelled before being removed by members of the cabin crew. Gomas flew into a rage following an argument with a relative, whom she accused of stealing her AirPods, according to police records reviewed by The New York Post. Because of her behaviour, passengers were forced to disembark Flight 1009 from Dallas to Orlando, before eventually being allowed to re-board – causing a delay of at least 3 hours, the US news outlet reported. Gomas was issued a warrant for criminal trespass after police found her sitting outside the airport terminal waiting for an Uber, however, she was neither arrested nor charged. Now, she clearly just wants to move on with her life. Onwards and upwards, eh, Tiff. Sign up for our free Indy100 weekly newsletter Have your say in our news democracy. Click the upvote icon at the top of the page to help raise this article through the indy100 rankings.

By Steven Scheer JERUSALEM Moody's Investors Service said on Tuesday that passage of a new law in Israel

The Michigan Attorney General's office says a Michigan Republican accused of participating in a fake elector plot had his case dismissed Thursday after a cooperation agreement was reached

A 25-year-old who has been mostly bed bound by a painful condition that is causing her brain to slip down her spine is pleading for help to raise funds for lifesaving treatment in the US to stabilise her skeleton. Desperate to raise the £200,000 she needs, Emily Balfour, from London, said she will eventually face permanent disability and is at risk of paralysis if she does not receive PICL, a procedure that injects stem cells into the spine through the back of the mouth. An ice-skating accident at the age of 14 flagged the alarming conditions that cause Emily to now live with “relentless levels of pain”. She was diagnosed with Ehlers-Danlos syndromes (EDS), a collection of rare conditions affecting the connective tissues that make her joints unstable and prone to dislocation, as well as craniocervical instability (CCI), meaning the area where her skull and spine meet is dangerously unstable. Emily also has Chiari malformation, which means the lower part of her brain has herniated and is pushing down through the top of her spinal column. “My health is continuing to deteriorate but I still haven’t managed to raise enough money to get the treatment I need in America,” Emily said. “It would be lifesaving for me and, unless I get the treatment, my life is on pause and stagnated, I’ve become largely bed bound. “And this issue doesn’t just affect me, there are so many people with this condition who are struggling to get funds for treatment abroad. Money is the barrier for us being able to live our lives.” In 2011, Emily was first diagnosed with EDS after an ice-skating accident resulted in a trip to the doctors. I want to keep my sense of agency but it’s getting more and more difficult. Emily Balfour Once a sporty and active teen, Emily is now confined to her bed most days. Due to Chiari malformation, Emily’s brain is pushing down through the top of her spinal column and she said medical specialists have informed her that some of her brain is no longer in her skull. Emily once had dreams of working in film, but she is unable to complete her degree and is also not able to work while she struggles with her health. She said: “I’m not able to participate in life, I’m unable to work and I keep having to delay the completion of my degree. “I have limited vision, I can’t see out of my left eye and I have recently dealt with limb paralysis.” Earlier this year, Emily was rushed to hospital after her left arm became paralysed and swollen. She said: “It looked like a dead person’s arm, I feared I’d never regain mobility of it. “It turned out I was struggling with blood flow to the arm, and I’ve regained limited use of my arm, but I’m high risk of it happening again. “I’ve seen people with these conditions lose function of their arms completely and that obviously concerns me because I live by myself. “I want to keep my sense of agency but it’s getting more and more difficult.” Emily said her brainstem has been damaged to the point where her body is not functioning and she suffers daily from extreme fatigue, periods of paralysis, and loss of vision. It’s incredibly frustrating and I have to accept that I can’t live the life I thought I would. Emily Balfour As a result, Emily now finds herself largely bed bound, is regularly in and out of hospital and suffers from excruciating symptoms which threaten irreversible physical disability and potentially death. Innovative treatment in the US to stabilise her skeleton will be life-changing for Emily, but it comes at a cost. She hopes to raise £200,000 for multiple stem cell treatments, medical care and accommodation in Colorado, USA, where she will undergo a procedure known as PICL to repair and strengthen the ligaments that keep her skull stable. She said: “I’m in relentless levels of pain and, the more activity I do where I’m moving my neck, the worse the pain is. “If I don’t get treatment then it’s looking likely that eventually I will lose the use of one or both of my arms. “The longer it goes on, I’m losing more and more years of my life.” Before her diagnosis, Emily had dreams of working in film, having attended the BFI Film Academy as a teen. She also had plans to travel after finishing her English degree, which is currently on hold. Emily said: “It’s incredibly frustrating and I have to accept that I can’t live the life I thought I would. “I’m seeing other people my age having fun and building their careers but until I get the PICL procedure, I’m stuck. “There are other people who are also in my situation and it’s not an easy journey but I just hope that these treatments will be easier to access closer to home so we can get back to living.” I just want to be able to complete my degree and have a normal life and not be stuck in this living hell. Emily Balfour Emily hopes more research into EDS will result in more treatment options becoming available. For Emily, she says the procedure will be a lifeline and enable her to start living again. “Getting treatment will change everything,” she said. “I wanted to write and make films, but I am now more interested in medicine and want to get a psychotherapy qualification and work in that field. “I used to be so passionate about movies and reading, but because of my brain and vision issues, I’m restricted to audiobooks now. I can’t even do basic things like watching TV, that once brought me so much joy. “I just want to be able to complete my degree and have a normal life and not be stuck in this living hell.” To donate to Emily’s fundraiser, visit: www.gofundme.com/f/urgent-treatment-for-emily. 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Star striker Sam Kerr says she’ll be available for Australia’s must-win Women’s World Cup game against Olympic champion Canada after missing the team’s first two group games because of a calf muscle injury