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Myleene Klass has said that if the government does not implement changes to the way woman are treated following miscarriages then it no longer “deserves power”. The former Hear’Say singer met with the Minister for Women’s Health, Maria Caulfield, on Monday (10 July) at the Tommy’s National Centre for Miscarriage Research in Birmingham. Klass, who had previously been outspoken about her four miscarriages, organised the visit at the pregnancy charity’s centre – located in Birmingham Women’s Hospital which also contains an early pregnancy unit – alongside Labour MP Olivia Blake. The 45-year-old presenter urged the government to make sure women receive medical intervention after every miscarriage, not just three, 24 hours specialist care and support for pregnancy and for data to be collected to understand the scale of the issue. According to the NHS website, if a woman has had three or more miscarriages in a row then further tests will be given to understand the cause. Klass told the PA news agency that a soon to be published pregnancy loss review, which looks at improving NHS gynaecology and maternity care, could provide a “massive” change if implemented. She said: “If the policy (does) include these changes, the face of women’s health care is going to change unrecognizably and it will be a wonderful time for our children and our children’s children to know that we made a movement happen that actually protected women’s health.” When asked how she would feel if there are no changes, Klass said: “A health secretary and a health department and a government that doesn’t look after the people, that is in a position and empowered to do so, doesn’t deserve to hold (onto) that power.” The mother to daughters Ava and Hero and son Apollo said she has been “very frustrated” after a “real David and Goliath” battle with the government. She said: “I do find that women’s health is so far down on the agenda and it’s so misogynistic as to why it really is, from the tablets we are given to take, all the way through to the treatment that we receive, or rather the lack of treatment that we receive. “I think it’s pretty evident that we were told to just put up and shut up and that is not the world that we live in anymore.” Klass added that care for women going through miscarriages is not addressed as it is “taboo” and “makes people uncomfortable”. She said: “It’s so cruel when you have experienced the process of it, I’ve never done so much paperwork. “A little baby that never existed and yet the paperwork is excessive and you’re asking a woman to sign away… what do they refer to it as? The products of pregnancy, even our paperwork is incorrect.” Klass also said that the difference between women receiving care in an early pregnancy unit are a “lottery” as in certain parts of the country the centres can be closed during certain hours and at the weekend. She added: “So this is something that is actually costing the economy more, because people are being sent to the wrong places and really desperately suffering with their PTSD.” Klass said that one treatment, a steroid hormone called progesterone, should be administered to more women at risk and GPs should receive more training about the drug. Klass said: “If there is still a heartbeat and you’re bleeding (and) you are given progesterone, you’ve got a chance, I know this better than anybody because that’s how I had my son. “Can you imagine if you do suffer a miscarriage you sometimes or very often have to wait for your GP to then sign you off to get the secondary scan? That means… you have to wait to have your baby removed.” Klass said she hopes things have “shifted” after Caulfield’s visit. In a statement, the minister said the work done by Tommy’s is “so important” as pregnancy loss can be “hugely devastating and traumatic” and thanked those at the centre for sharing their stories. Caulfield said: “I’ll keep working to ensure women and their families can access the best possible care following complications in pregnancy. “The independent review into pregnancy loss – the findings of which will be published shortly – will consider how we can improve care so women and families receive the support they need.” Read More It took until my thirties to realise I might not be white Woman exits plane after tirade about passenger who is ‘not real’: ‘I’m not about to be Final Destination-ed’ ‘We call them Picky Bits’: Nigella Lawson responds to viral ‘Girl Dinner’ trend Charity boss speaks out over ‘traumatic’ encounter with royal aide Ukraine war’s heaviest fight rages in east - follow live

Venice has confirmed the first dates for its 'experimental' entry fee for day-trippers. Overnight guests are exempt from the charge but will have to register for a QR code to prove their exemption.

MGM Resorts International said the recent computer hack that shut down many services at its casino hotels will

A grandmother who contracted sepsis which made her hallucinate, have “blotchy skin” and turn the “colour of stone” later found out that her four-year-old grandson had the condition and Strep A at the same time as her, with the pair being “lucky to be alive”. Lorna Conaghan, 63, a retired business control analyst from Gourock, Scotland, and her grandson, Alfie Crawford, four, had sepsis at the same time, and Lorna “just couldn’t believe it”. In September 2022, Lorna was due to have a shoulder replacement, but on the morning of the surgery, she “did not feel right” and felt “on edge and weak” – but put it down to nerves. Little did she know this was her first warning sign of sepsis. After informing the doctors, they soon realised that one of her organs was infected and she was admitted to the hospital’s high dependency unit. The following day, Lorna was diagnosed with sepsis as her skin began to look mottled, and doctors told her that she “would have been dead” if it was caught any later. After having antibiotics and a few more hospital visits, Lorna began to recover, but it has taken her 11 months to “go back to normal” and have regulated blood pressure. When Lorna was in hospital, her grandson Alfie, who was three at the time, had chicken pox and a cold, which developed into sepsis and Strep A. Lorna thinks that because Alfie’s mum knew about her symptoms of sepsis, it helped her realise something was wrong. Alfie’s lungs were “full of pus”, so he was put on a ventilator and was in an induced coma for over a week. He also had to “learn to walk again”, and slowly has been able to make a full recovery – with Lorna saying the family are “so lucky to still have him”. Lorna told PA Real Life: “Alfie got sick when I was in hospital, and when I found out I just couldn’t believe it. “I think me having sepsis made Alfie’s mum realise that he had more than just a cold and chicken pox. “We’re both so lucky to still be here and that Alfie is back to running around and having balls of energy.” On July 4 2022, Lorna broke her arm after slipping on her dog’s tennis ball and ended up needing a shoulder replacement. On the day of the surgery, September 30 2022, at Inverclyde Royal Hospital, Greenock, she began to “not feel right” but put it down to nerves. She said: “I told the doctors and they tested me for Covid, but I was negative, and after a few more tests they thought one of my organs might be infected. “They thought it was my heart to begin with, but they couldn’t figure out what organ it was. “The biochemist worked out which antibiotic would best kill the infection, so I was put on that straight away.” Lorna stayed in the hospital for nine days, with seven of them being on the high dependency unit. She said: “They thought it was my kidneys, so they were trying to get them functioning again. “With hindsight, it was terrifying, but I didn’t realise how serious it was at the time. “I was a strange colour, the colour of stone, and I was all blotchy. “Doctors said if they caught it much later, or if I wasn’t in hospital, I would have been dead.” Four weeks later, Lorna was admitted to the high dependency unit again after her GP noticed she had extremely low blood pressure and low heart rate. She said: “I was so confused – when family members would visit me, I’d ask them to leave because I was hallucinating and didn’t want them to see me like that. “I thought there was a castle outside the hospital – I thought I was seeing it outside my window, and I remember thinking that we’ll have to go there once I’m out of hospital.” Since then, it has taken Lorna 11 months to get “back to normal” and her blood pressure regulated. She said: “I’m still having problems with my liver, but now I’m just tired. It’s really taken it out of me. I can only take the dog so far, I’m just so tired all the time.” While Lorna was in hospital, Alfie’s mum informed her that he was feeling unwell. Stephanie did not want to worry Lorna when she was already sick, but it turned out that Alfie, who was three at the time, had also contracted sepsis. Lorna said: “He came home from nursery with chicken pox, and also had a bit of a cold. “Then it just got worse – he was having terrible pains in his back, and I think Stephanie had just listened to what I had said about my symptoms, and it made her realise subconsciously that he might be more unwell than he is coming across. “They called the paramedics, and that night he got a lot worse – when they arrived at A&E, she took him up to the desk and said, ‘We’re going to have a dead child if we don’t do something’.” Within half an hour, Alfie was admitted to intensive care at Glasgow Children’s Hospital and doctors soon realised his lungs were “full of pus” and that he had sepsis, which had turned into Strep A. So, Alfie was put on a ventilator and was in an induced coma for over a week. “Doctors made it clear to Alfie’s family that it was indeed life-threatening and that he was very lucky to be alive Lorna Conaghan Lorna said: “He had to learn to walk again – he was so weak after he woke up. “Doctors made it clear to Alfie’s family that it was indeed life-threatening and that he was very lucky to be alive. “His legs were so weak – he hadn’t eaten much while being poorly.” After having antibiotics and being in the induced coma, Alfie is now “running around”. Lorna said: “With me, I’ve had a good life, but it was so unfair to think that little Alfie could have died – he hasn’t had a life yet. “We’re just so lucky to still have him with us. “This whole experience has made me appreciate everything – when I take the dog for a walk I have a sit down on the bench and take in all the lovely scenery. “I have treated every day since Alfie and I got better as a bonus day in my life.” Read More Amy Dowden reveals ‘life-threatening’ sepsis diagnosis amid cancer treatment BBC Radio 2’s Tony Blackburn reveals he had sepsis and pneumonia in health update Martha Mills: Parents of girl who died after NHS mistakes call for new right to get second opinion Charity boss speaks out over ‘traumatic’ encounter with royal aide Ukraine war’s heaviest fight rages in east - follow live

Miller Lite's 'woke' ad from March has been unlisted from the internet and doesn’t appear on the beer brand’s social media pages

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Shirlie Kemp has revealed that a doctor told her to “get over” her endometriosis, despite it making her periods more painful than childbirth. In a new interview, the Pepsi & Shirlie singer, 61, has discussed her experiences with the medical condition, which made her periods so painful she was “bedridden” as a teenager. Endometriosis is a condition where cells similar to those in the uterus are found elsewhere in the body, leading to inflammation, pain and scar tissue. It affects approximately one in 10 women and people assigned female at birth in the UK. “I could have kissed the doctor who said, ‘You sound like you’ve got endometriosis,’” she told The Times. “From 16 I was bedridden when I had a period. I suffered horrendous pain.” Kemp – who is married to Spandau Ballet musician Martin Kemp – continued: “A male doctor said, ‘What a load of nonsense. She’ll get over it,’ and gave me tablets that made me vomit. I didn’t even know there was a private health system until I was in Wham!. “A private female doctor gave my symptoms a name. When I went into labour I thought, this is not as bad as a period.” When a person has endometriosis, the cells similar to those in the womb follow the menstrual cycle, building up and breaking down. However, the blood has no way to escape, with common symptoms including pelvic pain, painful periods, pain during or after sex, pain when urinating, painful bowel movements, fatigue and difficulty getting pregnant. Kemp says that she was told endometriosis could affect her fertility, saying: “My husband wasn’t ready to have a baby. He was a rock star. “When the doctor told me that endometriosis can affect your fertility, I said, ‘Martin, I’ve got to have a baby. I have a problem with my fertility.’” Kemp’s experience with doctors isn’t uncommon. In March, a study by charity Endometriosis UK found that three in four women and those assigned female at birth would not go to a doctor with potential endometriosis symptoms. Among those who are reluctant to see a doctor, 24 per cent said it was because they think painful periods are part of life, and 23 per cent didn’t think it was serious enough to bother a GP with. Read More Britney Spears shares first statement after ‘shock’ Sam Asghari divorce: ‘I couldn’t take the pain anymore’ Kid Rock spotted drinking Bud Light months after shooting up beer cases during transphobic rant From tofu chicken wings to chickpea bacon – how and why you should be making plant-based meat at home The 20 worst kinds of pain humans can experience Chrissy Teigen posts topless photo to remind fans to get mammograms Influencer Caleb Coffee hospitalised after falling off cliff in Hawaii

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