The lower chamber of Mexico’s congress has once again turned to spectacle, giving hours of its time to a controversial character pressing the case for “non-human beings” he said were found in Peru

Pilots on the Air India plane that was stranded in Russia had received an indication of low oil

Some of the most used platforms for travel and online shopping said Tuesday they’re going to team up to battle fake reviews

Luci Baines Johnson was a somewhat impatient 18-year-old on Aug. 6, 1965, when she happened to be on what she called “daddy duty,” meaning “I was supposed to accompany him to important occasions.” The occasion that day was President Lyndon Johnson’s scheduled signing of the Voting Rights Act, which Congress had passed the day before. She assumed the ceremony would be in the East Room of the White House, where the Civil Rights Act had been signed the previous year. “And that would probably take an hour and then I could be on my way,” she recalled in a recent interview from the LBJ Presidential Library in Austin, Texas. Instead, her father met her and guided her to the South Portico, where the presidential motorcade was waiting. They were going to Congress. Knowing a trip to Capitol Hill would take more time than she anticipated, she asked why. “‘We are going to Congress because there are going to be some courageous men and women who may not be returning to Congress because of the stand they have taken on voting rights,’” she recalled her father telling her. ”‘And there are going to be some extraordinary men and women who will be able to come to the Congress because of this great day. That’s why we’re going to Congress.’” Johnson, who stood behind her father during the signings, knew the significance of the law and asked him afterward why he had presented the first signing pen to Senate Minority Leader Everett Dirksen, a Republican from Illinois, when so many civil rights champions were on hand. “Luci Baines, I did not have to say or do anything to convince one of those great civil rights leaders to be for that legislation,” she recalled him saying. “If Everett Dirksen hadn’t been willing to be so courageous to support it, too, and more importantly brought his people along ... we’d never have had a law.” Johnson said personal relationships and events in her father’s life influenced his thinking on civil rights and voting rights, as well as many of the social programs he helped establish. Some of that can be traced to his life before politics when he was a teacher in Cotulla, Texas, where most of his students were Mexican American. They were wonderful and eager, but often hungry and very poor, she said. “He thought he’d grown up poor so he would understand what their plight was like,” she said. “But he had never gone without a toothbrush. He had never gone without toothpaste. He had never gone without shoes. He had never known the kind of discrimination that they had known.” “He swore if he ever got in a position to change the trajectory of the lives of people of color” he would, she said. Johnson said she was saddened in 2013 when the Supreme Court released its ruling in Shelby County v. Holder, which essentially ended a provision of the Voting Rights Act mandating the way states were included on the list of those needing to get advance approval for voting-related changes. “I cried because I knew what was coming. I knew that there were parts of this country, including my home state, my father’s home state, that would take advantage of the fact that there would no longer be an opportunity to have the federal government ensure that everyone in the community had the right and equal access to the voting booth,” she said. “I have seen over a lifetime so much take place that has tried to close the doors on all those rights,” she said. “I’m 75 years old now, and my energies are less than they once were, but for all of my days I will do all I can to try to keep those doors open to people of color, people who are discriminated against because of their age, or their ethnicity or their physical handicaps.” With the Supreme Court due to rule on another major pillar of the Voting Rights Act, Johnson said she wants to keep fighting to try to maintain her father’s legacy and protect voting rights. “I don’t want to get to heaven one day, and I hope I do, and have to say to my father, it was gutted to death on my watch,” she said. ___ The Associated Press coverage of race and voting receives support from the Jonathan Logan Family Foundation. See more about AP’s democracy initiative here. The AP is solely responsible for all content.

Silvio Berlusconi cast a spell over Italy — and nearly led it to financial ruin

Incumbent George Weah will face Joseph Boakai, separated by around 7,000 votes in the first round.

Social media companies are once again under scrutiny, this time in France as the country’s president blames TikTok, Snapchat and other platforms for helping fuel widespread riots over the fatal police shooting of a 17-year-old driver

Shark patrols are ramping up off Long Island beaches after five people were bitten in two days by marine animals that are likely sharks, authorities say.

On a recent sunny afternoon, Joshua Radebe patted down asphalt into a neatly filled pothole on a busy

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?

The previous management team at Brazilian retailer Americanas SA carried out fraudulent accounting practices and hid them from

Rayan Bashir says she is struggling after being left in hotels for weeks since arriving from Sudan.