One goal behind the Max video-streaming app rebrand has been to improve the app’s interface.

BEIJING Luckin Coffee said on Tuesday that it sold more than 5.42 million cups of the alcohol-infused latte

Halloween is nearly upon us, and if you're queer, you know what that means: It's our season. ICYMI, Halloween is practically an LGBTQ+ national holiday. A whole month (yes, here in this queer household we celebrate Halloween all October long), dedicated to the freaks and weirdos and being your most flamboyant and/or unhinged self? Queer AF. Which is why I have to ask — why are couples costumes so insufferably straight?

The “Mona Lisa” has given up a secret

Garth Brooks is looking forward to creating an inviting atmosphere at his new bar, and that apparently includes serving Bud Light.

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. Read More Four ‘red flag’ bowel cancer symptoms that can show two years before diagnosis Mother left ‘looking like Freddy Krueger’ reveals first skin cancer warning sign Woman ‘can barely move her hands’ after years of gel nails Charity boss speaks out over ‘traumatic’ encounter with royal aide Ukraine war’s heaviest fight rages in east - follow live

The hectic fashion season reaches its last stop in Paris on Monday, with the biggest intrigue being whether beloved brand Balmain can recover from the...

Mexican officials and the conservation group Sea Shepherd say experts will set out in two ships in a bid to locate the few remaining vaquita marina, the world's most endangered marine mammal

Yet another social media challenge has resulted in the tragic death of a young person, with the company behind by the viral ‘One Chip Challenge’ now confirming it is taking its product off US shelves. Harris Walobah, 14, told a school nurse last week that he had bad stomach ache after eating the chip given to him by a classmate – according to his mother Lois, who shared details of the incident with NBC10 Boston. In a description on its website, manufacturer Paqui states the chip – which comes in a coffin-shaped box – is seasoned with the Carolina Reaper and Naga Viper peppers, with the former holding the Guinness World Record for the hottest pepper at an average of 1.5 million Scoville heat units (SHU) and up to 2.2 million SHU. After going home, Harris reported feeling better, but his brother yelled at 4:30pm that his sibling had passed out, with Harris taken to a nearby hospital where he was pronounced dead. The family of the Massachusetts teenager claim he died from “complications” caused by the viral ‘One Chip Challenge’, though a post-mortem is yet to be carried out. A GoFundMe set up to help the family with funeral expenses stands at more than $34,000 at the time of writing. On the fundraiser, Harris’s cousin Tashia Roberts describes her relative as an “intelligent, quirky and incredibly talented young man” who “loved video games and playing basketball”. Now, Paqui have updated their page on this year’s challenge to stress: “The Paqui One Chip Challenge is intended for adults only, with clear and prominent labelling highlighting the chip is not intended for children or anyone sensitive to spicy foods or who has food allergies, is pregnant or has underlying health conditions.” They continued: “We have seen an increase in teens and other individuals not heeding these warnings. “As a result, while the product continues to adhere to food safety standards, out of an abundance of caution, we are actively working with our retailers to remove the product from shelves.” Meanwhile people who have already purchased the single-serve One Chip Challenge product can call a helpline for refunds. Sign up to 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.

Replicas of Rihanna’s jumpsuit during the Super Bowl just hit online stores – and sold out in less than 24 hours. Luxury fashion brand Loewe took to Instagram on 19 October to announce the launch of its red cargo jumpsuit. The product arrived months after Rhianna made headlines at this year’s Super Bowl halftime show, during which she announced her second pregnancy while wearing a red jumpsuit over her matching sheer bodysuit. The company went on to describe the inspiration behind the jumpsuit and some of its features, with reference to the singer’s performance in February. “A special edition release inspired by the iconic Super Bowl look worn by Rihanna is now available online and in selected stores,” the company wrote, alongside photos of Rihana’s show and of the brand’s jumpsuit. “The cargo jumpsuit and trousers feature a range of utility details drawing upon flight gear and the halftime show’s dynamic scenography.” On Loewe’s website, the jumpsuit is available in poppy red – which imitates the colour of Rihanna’s outfit – and black. The website specified that the outfit is “crafted in medium-weight cotton canvas” and weighed about 1.2 kg. Some of the other features of the look, which is being sold for $2,900, include an “elasticated belt”, “Elasticated ankle cuffs with zip detail,” and “sipped jet pockets at the front”. The outfit is also described as a “relaxed fit” with a straight-legged pants style. As of 20 October, the poppy red jumpsuit is already sold out in all sizes. However, the black version of the cargo look is still available, but only in select sizes. Although the red jumpsuit is sold out online, it has continued to be sold in some of Loewes stores, which are in Dubai, Madrid, and other locations. Back in February of this year, Rihanna first took the stage in an iconic all-red look and high ponytail at State Farm Stadium in Glendale, Arizona. The Super Bowl show also marked her official return to live performances, after a five-year hiatus. During the 12-minute performance, she performed a mash-up of some of her biggest hits, including “Only Girl (In the World)”, “We Found Love”, “Work”, and “Wild Thoughts”. While speaking at a press conference before the Super Bowl, the “Disturbia” singer described how her son RZA, who she shares with partner A$AP Rocky, ultimately encouraged her to perform at the event. “When you become a mom, there’s something that just happens where you feel like you could take on the world,” she said. “You can do anything, and the Super Bowl is one of the biggest stages in the world. So as scary as that was because I haven’t been on stage in seven years, there’s something exhilarating about the challenge of it all.” She added: “And it’s important for me to do this, this year it’s important for representation and it’s important for my son to see that.” In August, TMZ was the first to report that Rihanna and Rocky had welcomed their second child, with the outlet claiming that the baby arrived on 3 August in Los Angeles. Although the beauty mogul has yet to publicly comment on the arrival of her second child, she and her partner posed for some photos with the newborn, Riot Rose, in September. In the picture, taken and posted by Miles Diggs, Rocky was seen holding Riot, while RZA stood next to his mother, who was leaning against a car. The also photo marked the first public image of the family of four together. Read More I’m not surprised Victoria’s Secret has dropped its rebrand – I used to work there Why Travis Kelce relies on ‘instinct’ and ‘panic’ when getting dressed Victoria’s Secret ditches feminist makeover after sales slump I’m not surprised Victoria’s Secret has dropped its rebrand – I used to work there Why Travis Kelce relies on ‘instinct’ and ‘panic’ when getting dressed Victoria’s Secret ditches feminist makeover after sales slump

Picture yourself in the dentist's chair. Everything is going fine. Then the dentist asks whether

In Janet Planet, silence is everything. Playwright Annie Baker's directorial debut thrives in the stretches