Logan O’Hoppe and Randal Grichuk homered, Tyler Anderson earned his second win since the All-Star break and the Los Angeles Angels defeated the Cleveland Guardians 6-2

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Senator John Fetterman (D-PA) delivered an emotional speech about his disability to commemorate the 33rd anniversary of the Americans with Disabilities Act. Mr Fetterman spoke via video message in his signature Carhartt shirt at the American Association of People with Disabilities’ celebration of the landmark law that passed in 1990 with overwhelming bipartisan support. During his campaign for Senate last year, Mr Fetterman suffered a stroke which affected his auditory processing. As a result, he now uses speech-to-text technology. “The reality is that all Americans should be able to get access to the support that they need,” he said. “The Americans with Disabilities Act makes this possible.” In February, Mr Fetterman checked into Walter Reed Medical Center to undergo treatment for depression. He checked out at the end of March and has since returned to the United States Senate. “I want to thank your community for the work that you have done to make sure people with disabilities can run for and win office,” he said. Mr Fetterman appeared at the celebration with other elected officials including Sen Tammy Duckworth (D-IL); Steny Hoyer (D-MD), the former House majority whip; and Rep Debbie Dingell (D-MI). Transportation Secretary Pete Buttigieg also attended. “Now that I’m a senator, I’m going to continue to fight for disability rights in DC,” Mr Fetterman said. But many of the people at the event also highlighted the work that needed to be done to make places more accessible. Ms Duckworth, who lost both of her legs serving in the Iraq War, talked about how she took her two daughters to see the Barbie movie but could not go because the elevator did not work. “And so my two girls watched a movie with their nanny with me sitting outside for two and a half hours waiting for them to be done,” Ms Duckworth said, noting how nobody had informed her that the elevator was broken until after she bought a ticket. “It is 2023 folks we can and will and should do better.” She also pointed out how it is still legal to pay people with disabilities below the minimum wage and that medical equipment continues to get broken when people with disabilities travel by air. As a result, she said she is pushing for wheelchairs to be considered complex medical devices so they could not be destroyed. Similarly, Transportation Secretary Pete Buttigieg appeared over the video to discuss how the Transportation Department had begun preliminary work to stay in their wheelchairs as they fly. “And today we’re pleased to officially announce the rule that will increase the size of accessibility of airplane bathrooms to better accommodate access on board,” he said. The anniversary comes after many people who helped pass the ADA such as disability rights Judith Heumann and the late Sen Lowell Weicker, a Republican from Connecticut, and C Boyden Gray, an adviser to former president George HW Bush, passed away earlier this year. Ms Duckworth spoke about how eventually, plenty of people will need to use the accommodations that the ADA guarantees. “I hope one day you develop one because that will mean that you've lived a long life and maybe that you'll care about disabled access,” she said. Read More Back in hoodies and gym shorts, Fetterman tackles Senate life after depression treatment Hunter Biden’s plea deal appears at risk of falling apart. What happens next? Trump wants to see Biden impeached, and other Republicans are quick to pile on House UFO hearing probes claims of physics defying technology

Chicago White Sox All-Star Luis Robert Jr. plans to participate in baseball’s Home Run Derby in Seattle on Monday

'Oppenheimer's cinematic presentation is staggering as the reel stretches over 11 miles in length and weighs more than 600 pounds

A woman who was born with a rare inherited skin blistering disorder which caused her to get “bullied” and feel “like a freak” throughout her childhood and teenage years, as well as forcing her onto a soft food diet of “bananas and custard” for weeks at a time, now writes inclusive children’s books with a focus on disability to encourage “other children to grow up with confidence”. Vie Portland, a 52-year-old confidence coach, author and speaker from Winchester, was born with epidermolysis bullosa simplex generalised intermediate but was not formally diagnosed with the skin condition until she was 28. According to the NHS, epidermolysis bullosa (EB) is a rare inherited skin disorder that causes the skin to become very fragile, and any trauma or friction to the skin can cause painful blisters. Vie is yet to find a treatment that helps her condition, and her feet are regularly covered with huge internal blisters which feel like she has “stones under (her) skin.” Her condition even means that she cannot eat “anything acidic or too peppery” and often spends weeks eating “just bananas and custard”. She has also developed thoracic outlet syndrome, chronic bursitis, and often has spasms, because of walking with a limp to try to ease the pain. Now, Vie writes inclusive children’s books to raise awareness about living with a disability, because she grew up “afraid that there was no one else like (her)”, and hopes to write a book about someone with her condition next. Vie told PA Real Life: “So it feels like I’ve got stones under my skin all the time on my feet and it doesn’t matter how much you try to explain that to someone people just don’t get it. “Even things like if I meet friends for a drink in a lovely pub garden – I’ll be in agony because of walking on gravel and it takes so much energy out of me. “I can’t eat anything acidic or too peppery – sometimes I have to eat just bananas and custard for weeks.” Vie was born with the skin condition, saying: “I was born with no skin on my bottom and had some skin missing on my left foot. “The charity that works with people that have EB wasn’t around then – I spoke to someone recently from Debra, the charity, and they said if you looked at all the people on a double-decker bus, you’d expect to find at least one person with psoriasis. “But, you’d have to wait for over 700 buses before you met someone with EB.” As a child, Vie regularly had huge blisters all over her feet and the back of her heels. She explained: “I remember wearing jelly shoes one summer, and heat and friction are two of my triggers. “Throughout the day, blisters grew around the rubber shoes and I had to have the pair of shoes cut off my feet – it was excruciating.” When Vie was a teenager, she was very self-conscious of her condition, she explained: “I was in constant pain, and I struggled with all shoes and walking anywhere. “We’re always told not to pop blisters, but when you have EB they tell you to pop them because they get so big. “I didn’t know that at the time and it was just so painful. “People were noticing how I walk and I was embarrassed to show my feet – I didn’t have a normal childhood because of this. “Even something as simple as opening a bottle makes several layers of skin come off and cause me to have raw skin all over my hands, I was told this was weird by other people.” Doctors were baffled by Vie’s condition, over the years, she was told she had different types of eczema and even that she was allergic to her own sweat. But, at age 28, she was diagnosed with EB by a dermatologist in London. She said: “I just grew up believing that it was my fault and I was afraid that there was no one else like me.” “It all just made sense. “They even took pictures of my feet for a medical journal because it was so rare.” After getting her diagnosis, Vie began researching the charity DEBRA, which specialises in EB. She said: “I started finding out that there were people like me – it was amazing, growing up, I was bullied and felt like a freak.” Since then, Vie has sadly not been able to find a treatment that helps her condition. “There’s no cure for EB but things have moved on a lot over the past 20 years,” she said. “We have special types of dressings and creams which can help alleviate the pain.” On top of this, because Vie has been walking “unusually” for most of her life, she has developed thoracic outlet syndrome, chronic bursitis, and often has spasms. Vie said: “It can be frustrating at times because it just feels like no one will ever understand what it is like. “For most people, blisters are a bit painful, but it’s all right, but for me, it’s one of the worst pains in the world.” Now, Vie is focussing on raising awareness about living with a disability, and has recently written two inclusive children’s books called ‘Where Are We Going?’ and ‘Who Am I?’. She said: “I want other children to grow up with confidence and not to feel like a freak like me. “Children aren’t born with prejudice and I think it’s really important to teach them about all of our amazing cultures and worlds. “In my books, I don’t explicitly say the character is disabled until the discussion questions at the end – I want the character to be accepted and not defined by their disability. “I think people have more in common with each other than things that are different, and that’s a beautiful thing. “I’m hoping to write a book about someone with my condition – that’s my next plan.” Read More Charity boss speaks out over ‘traumatic’ encounter with royal aide Ukraine war’s heaviest fight rages in east - follow live Fraser Franks undergoing heart surgery – four years after ‘hidden’ condition cut short football career 4 viral TikTok make-up trends you’ll actually want to try Childhood Cancer Awareness Month: What are the warning signs that your child might have cancer?

Hurricane Hilary is expected to slam into Southern California on Sunday as a rare tropical storm, unleashing floods, fierce winds and heavy downpours as residents evacuate, parks and beaches close and first responders brace for water rescues.

Kaia Gerber has issued some guidance for her elder brother Presley Gerber about taking care of his skin in the sun. Presley, 24, and Kaia, 21, are the children of model Cindy Crawford and Rande Gerber, a businessman. Both siblings followed in their mother’s footsteps and have successful modelling careers, often sharing their work and off-duty looks on social media. On Saturday (19 August), Presley shared photos of himself on a sandy beach while topless. The images show him with a bandana draped around his shoulders. In the caption to the Instagram post, Presley wrote: “Sunscreen’s a myth”. In fact, sun protection provides an essential barrier to harmful UVA and UVB rays. According to the American Cancer Society, UVB rays are responsible for the majority of cases of skin cancer. In disagreement with her brother’s statement, Kaia left a public comment on the post to give him some alternative guidance. “Hi Presley! It’s me, your sister!” she began her message. “Remember me from childhood? We share the same parents [wacky face emoji] I actually wanted to share with you that sunscreen is not a myth!! It is real!! I actually use it myself!!” Fans and followers have jumped in on their exchange, with many leaving laughing emojis at the humorous tone of Kaia’s message. “Absolutely! Sharing is caring @presleygerber!” one fan remarked. “Sis has got your back! You've raised them well @cindycrawford!” Another simply wrote: “Love your brain Kaia!!” Earlier this year, Kaia shared her thoughts on the “nepo baby” debate, which highlights the privilege enjoyed by those in the entertainment and creative industries who have famous parents. Speaking to Elle in January, the model and actor acknowledged the ways that nepotism had helped her career. “I won’t deny the privilege that I have,” she said. “Even if it’s just the fact that I have a really great source of information and someone to give me great advice, that alone I feel very fortunate for.” She also shared a comment that Crawford made about her daughter’s busy modelling career. “My mom always joked, ‘If I could call and book a Chanel campaign, it would be for me and not you,’” Gerber added. “But I also have met amazing people through my mom whom I now get to work with.” Read More Stylist comes to bride-to-be’s rescue after hair is ‘destroyed’ just before wedding Geri Halliwell says she was ‘quite grumpy’ to Christian Horner in their early relationship Prince William criticised for including Charlotte in apology for missing Lionesses final James Blunt claims he changed his age on his Wikipedia page Shirlie Kemp says male doctor told her to ‘get over’ endometriosis Chrissy Teigen posts topless photo to remind fans to get mammograms

One of the hottest IPO markets this year is not in a country brimming with global tech giants, nor does it rank among the top 10 global economies by size.