Two iconic Texas brands have come together to create a Dr Pepper Float ice cream.

This past July marked 35 years since a barefoot Bruce Willis yippi-ki-yayed his way into

Super Sale Alert: Products in this story may be marked down for Prime Big Deal Days. Shop our full coverage of the event here — or, dive directly into the deals here.

By Giuseppe Fonte ROME Italy's government will meet with supermarkets and small retailers' associations on Wednesday to address

Whether you’re an olfactory fanatic looking for your new signature scent or you’re just starting to dip your toes into the genderless scented pool, we all need a new scent every once in a while — especially for Pride month. But in a world full of colognes and perfumes with harsh gendered lines, it’s hard to figure out which are the truly unisex fragrances. And what exactly do we mean by that?

Hello, it’s been a scorching week, both literally and in markets. Here’s something to help you catch up

The Food and Drug Administration has approved a new type of drug to treat hot flashes caused by menopause

Many people with Huntington’s disease are being turned away from traditional mental health support, a charity has claimed as it called for more to be done to help people with the condition. Some mental health services have told patients that they do not have the specialist care needed, leading to the Huntington’s Disease Association calling for better help and support for people living with the disease. Huntington’s disease is a condition that stops parts of the brain working properly over time and can lead to problems with movement, cognition (perception, awareness, thinking, judgment) and mental health. Most people with the inherited condition will start to show symptoms between the ages of 30 and 50 and it gradually gets worse for around 10 to 25 years until the person dies. During all this time, my mental health was worsening. I’d seen my uncle commit suicide a few years before after his diagnosis and him not receiving the correct support and I was at a similar point Daniel Johnston There is no cure for Huntington’s disease or any way to stop it getting worse. A small new poll of 105 people with the condition, shared with the PA news agency, found that 85% had attempted to access community mental health services. But among this group, 56% claimed they had been denied access to care, the Huntington’s Disease Association said. Daniel Johnston, from Horam, East Sussex, said his local mental health service “didn’t know” where to refer him. The 41-year-old father of two said: “When I tested positive for Huntington’s, there was no specific pathway from that point for any mental health support. “I was confused, upset and angry about the diagnosis. I didn’t, and still don’t, fully understand my feelings of confusion and anger. “I wasn’t referred to a professional psychologist or anyone who knows how to support someone with a life-changing diagnosis such as Huntington’s. “During all this time, my mental health was worsening. I’d seen my uncle commit suicide a few years before after his diagnosis and him not receiving the correct support and I was at a similar point. “It was only when I explained to my consultant in our six-monthly appointment earlier this year the extent of my thoughts that he contacted the crisis team for me, and they began a course of daily calls for two weeks. “From this point onwards it’s been getting better, but I feel so sad for others who slip through the net so easily. “It’s as if people get afraid when you mention Huntington’s and there’s confusion around treating Huntington’s and treating mental health. “I’m not surprised by the amount of people being denied access to mental health support services due to having Huntington’s – I have been one of those people and it’s really scary.” The charity said hurdles often occur for patients after they have been referred by their GP for mental health support. Local mental health teams have told patients that Huntington’s “doesn’t fall under the remit of what they’re able to provide treatment for”. The charity has launched a new campaign, Mindful of Huntington’s, to raise awareness of the cognitive impairment symptoms of the disease, and has called for greater access to mental health support. Cath Stanley, chief executive of the Huntington’s Disease Association, said: “Many people think of Huntington’s as a disease which impacts movement, but that is only half the story, and the non-physical symptoms are often overlooked. “At the Huntington’s Disease Association, we find people will most commonly be referred to mental health services due to cognitive symptoms such as irritability and aggression. “Throughout May, we will be focusing on these cognitive symptoms and the life-changing impact they can have. “The stark findings we’re announcing can’t be ignored – people are asking for much-needed mental health support, being turned away, and their health is deteriorating further. It is disappointing but not surprising to see that there’s still a lot of misunderstanding around Huntington’s.” To find out more visit: www.hda.org.uk Read More Charity boss speaks out over ‘traumatic’ encounter with royal aide Ukraine war’s heaviest fight rages in east - follow live Scottish first minister Yousaf calls cost of coronation ‘uncomfortable’ King Charles and other royals return to work after coronation Prince Harry’s ghostwriter opens up about harassment after ‘Spare’

By Casey Hall SHANGHAI Chinese luxury liquor-maker Kweichow Moutai is again looking to diversify from its fiery baijiu

A good book packs power

Saying goodbye to your family and going off to college for the first time is an extremely daunting and intimidating experience — even more so if you’re the first person in your family to do so and are trying to navigate an academic system that wasn’t made with you in mind. For Latine students across the US, Hispanic-serving institutions (HSIs) might help bridge the cultural gap that emerges between Latine students entering higher education and institutions that have historically excluded non-white students.

Cristina Amaya has a very simple goal for Latinx in Gaming, the nonprofit she cofounded that aims to connect video game-loving Latines and help them thrive in the industry. “I don’t want us to exist five years from now because we won’t need to,” she said during Thursday’s Refinery29 Twitch stream. “The end goal is that we have everything we need … There are just so many resources within companies, within schools, networks that exist [that] it should be easy for Latines to enter the workforce and come into gaming the same way it might be with other folks.”