Latest news with #DermNet
Daily Mirror
24-04-2025
- Health
- Daily Mirror
'I asked ChatGPT for a palm reading and dark prediction sent me running to doctor's'
A woman who asked the AI tool ChatGPT to give her a palm reading for fun was left horrified when it made a rather dark prediction that sent her running to the doctor's This woman's experience with ChatGPT sent her running to the doctor's. In today's world, many of us have used some form of AI chatbot or large language model (LLM) to find out the answers to some pressing questions we might have. You can use this artificial intelligence for everything from finding cleaning tips to brushing up on your world history, and it's fast becoming an alternative to inputting your request into a Google search. One thing these chatbots can do that a search engine can't, however, is simulate human-like conversations. You can ask an AI chatbot to read your horoscope, give you a motivational speech, or even tell you a joke. However, one woman was left horrified when she asked ChatGPT, one of the most popular AI chatbots, to give her a palm reading. She initially sent a picture of her hand to the chatbot for fun, thinking it would provide interesting insights into her emotional well-being, her relationships, and her thinking patterns - but it gave her one very dark prediction. Rin shared a video on TikTok in which she said instead of giving her the palm reading she asked for, ChatGPT's response honed in on the small mole she has on her palm underneath her index finger. The chatbot recommended she get the mole "checked" by a professional because it could be "acral lentiginous melanoma", a rare type of skin cancer that develops on the palms of hands, soles of feet, or under the nails. She said: "Look at that mole. That popped up in 2020 after I had my son. I've never considered it to be anything dangerous; I was just like, 'Oh, that's weird, a new mole. A hand mole. That's uncommon'." Acral lentiginous melanoma (ALM) is a rare subtype of melanoma that is slow-growing and can take months to years to become invasive. It is the least common subtype of melanoma diagnosed overall, with DermNet stating it accounts for just 2-3% of melanoma diagnoses. While anyone can get ALM, it is more common in people with dark skin. In fact, despite it being an uncommon type of melanoma in the wider population, it is the most common type in people with darker skin tones. As it grows, ALM often becomes darker and wider. In the comments of her video, Rin stated hers has "gotten lighter" over time rather than darker, so the mole may not be a sign of anything severe. However, commenters still urged her to get it checked out by a doctor, as it's always better to be safe. Symptoms of melanoma There are different types of melanoma, but the first sign is often a new mole or a change in the appearance of an existing mole. Moles caused by melanoma can sometimes be itchy or painful, and can also bleed, change shape, or change colour. According to NHS Inform, there is a handy "ABCDE" checklist you can use to tell the difference between a normal mole and a melanoma. Look out for the following: Asymmetrical – melanomas have 2 very different halves and are an irregular shape Border – melanomas have a notched or ragged border Colours – melanomas will be a mix of 2 or more colours Diameter – melanomas are larger than 6mm (1/4 inch) in diameter. Enlargement or elevation – a mole that changes size over time is more likely to be a melanoma When to see a GP The NHS states you should see a GP if you have a mole that has changed size, shape or colour or if your mole is itchy, painful, bleeding, or crusty. You should also see a GP if you have an unusual mark on your skin that has not gone away after a few weeks. These are not an immediate indicator of melanoma, but spotting the signs early and getting yourself checked out could make it easier to treat if it is something serious. Moles only need treating if they're a sign of melanoma. If your GP thinks your mole is melanoma, you'll be referred to a specialist in hospital, where the main treatment is often to remove the mole.
Miami Herald
09-04-2025
- Health
- Miami Herald
TikToker Hannah Campbell loses 10-month-old daughter to rare skin disorder
A TikTok influencer is urging her followers to fight for a cure after losing her 10-month-old daughter to a terminal illness. On April 8, Hannah Campbell — who gave birth to Elliana Rose in May 2024 — shared a TikTok video in memory of her daughter, who died the night before. 'Our sweet girl Elliana Rose lost her battle last night. She passed peacefully, wrapped in love,' Campbell wrote in the video's caption. 'I don't know what to do with myself today. I'm heartbroken, and I'm angry.' Elliana Rose was diagnosed with a rare and highly severe condition called Junctional Epidermolysis Bullosa (JEB) at 2 weeks old. Campbell has documented her daughter's battle on TikTok since September to help raise awareness for the disease. 'No child should have to endure what she did. EB stole her from us. Let's fight for a cure so no other family has to feel this. Thank you for loving her with us,' Campbell added in the caption. According to DermNet, epidermolysis bullosa (EB) is 'a group of inherited diseases that are characterised by blistering lesions on the skin and mucous membranes.' The painful blisters can appear anywhere on the body and form from the slightest touch. It affects both the external and internal well-being of the individual. 'An estimated 1 in 50,000 people in the United States' have EB, according to Cleveland Clinic. While there is currently no cure for the disease, some patients can see their condition improve with age. In a March TikTok video explaining her daughter's condition, Campbell wrote that the disease 'causes daily pain, wounds and lifelong challenges.' She noted that her daughter requires 'constant wound care, special medical supplies and adaptive equipment to keep her comfortable and safe,' per E! News. 'There is no cure, but there is hope,' Campbell added. 'Every child with EB deserves a future without pain. Spreading awareness leads to research, treatments and one day a cure.' Campbell's latest update came just a few days after posting a video explaining that her daughter 'hasn't opened her beautiful eyes in 24 hours.' In the caption, Campbell added that Elliana was 'still with us, but her body is tired.' 'She hasn't opened her eyes, eaten, and can hardly cry. We're holding her close and loving her through every breath,' she wrote. In addition to using her TikTok to spread awareness to her more than 700,000 followers, Campbell founded Elliana's Hope for Healing — a fundraiser that hopes to find a cure for EB by 2030. On its official website, Campbell wrote that it was 'unlikely Elliana will live beyond her first year.' 'This fundraiser is being organized with the aim of providing support to Elliana and other babies facing similar health conditions,' Campbell wrote on the website. Campbell created the fundraiser with EB Research Partnership (EBRP), which was co-founded in 2010 by Jill and Eddie Vedder — the frontman for Pearl Jam — after their friend's son was diagnosed with EB. According to EBRP, Elliana was one of more than 400 million children and adults battling EB. 'Over the last decade, EBRP has made remarkable strides, including helping to accelerate the first two EB treatments FDA approved in 2023,' the nonprofit wrote on its website.
Yahoo
21-02-2025
- Health
- Yahoo
Noticing This Sign On Your Knuckles Can Reveal High Cholesterol
According to the British Heart Foundation, 'There are around 7.6 million people living with heart and circulatory diseases in the UK.' They estimate that roughly half of us will go on to develop heart conditions in our lifetimes. Unfortunately, some of the red flag signs of high blood pressure and increased LDL cholesterol can be hard to spot. They usually have no symptoms at all. Sometimes, however, signs of a genetic risk factor called familial hypercholesterolaemia can be visible on the body. Familial hypercholesterolaemia (FH), which affects about one in every 250 people, is a genetic condition that can make people up to 13 times more likely than those without FH to develop coronary heart disease. Many people with FH do not know they have it, even though early treatment has been shown to give those with the predisposition as long a life as those without it. However there are three 'classic signs' of the condition which appear on peoples' eyes and hands, the British Heart Foundation says. Though it doesn't always come with symptoms, FH is associated with three telltale signs. The first is small bumps around your eyes ― especially if they're yellowish and near the inner corner of your eye. This is called Xanthelasmas. Secondly, those with FH might notice a thin, white rim around the iris (coloured part) of their eye. This is called a corneal arcus, and is more likely to be a sign of FH if the person who has it is younger. Another sign, called tendon xanthomata, leads to swelling in areas like your knuckles, the back of your ankle, and the Achilles tendon. It can take the form of lumps and bumps in the area, and like both other signs, is due to cholesterol deposits. DermNet says they are usually 'slowly enlarging' and can be 'smooth, firm to palpation, and mobile'. You can get your cholesterol tested by your GP if you're concerned. If they think you have FH, they might refer you to a specialist who may give you genetic tests. Speak to your doctor as soon as possible if you think you might have FH; the earlier the treatment, the better the management can be. Symptoms aren't the only way you might be able to spot FH. According to the British Heart Foundation, you should also speak to a doctor 'If a close relative has had a heart attack at a young age (before 55 in a man and before 65 in a woman)'. Treatment often involves statins and lifestyle changes. So THAT's What Those Tiny Itchy Bumps On Your Fingers Are Noticing These Bumps Around Your Eyes Could Reveal Heart Issues Here's What Are Considered Normal Cholesterol Levels, By Age
