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This Canadian brand's under-eye masks are Jessica Alba's go-to — and they actually softened my crow's feet

This Canadian brand's under-eye masks are Jessica Alba's go-to — and they actually softened my crow's feet

Yahoo29-05-2025
Like many people, I struggle with tired, puffy eyes when I wake up in the morning, regardless of how long I've slept. Also, my habit of late-night scrolling through social media for recipes and DIY projects I'll probably never do doesn't help the situation. But I'm also a busy mom of two young kids, and keeping up with their activities can be exhausting. And chances are I won't be escaping the dark circles anytime soon.
I have a drawer full of eye masks I can turn to whenever I need a quick pick-me-up, but the results aren't consistent, and most do little to relieve my under-eye bags. I felt a twinge of hope when I discovered the bestselling Grace & Stella Eye Masks, advertised as an "energy drink for your eyes." The best part? The brand is Canadian!
These sea moss and hyaluronic acid-infused eye masks help give your eyes the refresh they need.
These 'super hydrating' masks have thousands of five-star reviews and are a favourite of Jessica Alba — and they're 30 per cent off right now. But did they deliver? Read below and find out if I found these vegan eye masks to be "magic" or just meh.
These under-eye masks contain moisturizing ingredients such as hyaluronic acid, sea moss, amino acids and glycerin, all working together to help keep your eyes hydrated and smooth. Just moments after applying, the ingredients get to work, and within 20 minutes, you will have refreshed and rejuvenated under-eyes.
The cooling and anti-inflammatory hydrogel masks work quickly to reduce puffiness and brighten the delicate under-eye area.
In addition to the gold, the masks are also offered in pink and blue. Looking for a mask that helps with wrinkles and is energizing? Go for the gold. More concerned about hydrating and soothing? Blue is for you. All about boosting collagen? Think pink.
The vegan, dermatologist-tested patches are also paraben- and sulphate-free.
Sleep deprived? No one will ever know: After staying up late to work on a project (i.e. binge-watching "The Bear") and only getting three hours of sleep, I had to rush to an audition across town. I put these on while I was enjoying my morning coffee, and 30 minutes later, all evidence of my sleepless night was erased. Mind you, I was still exhausted, but luckily, on camera, no one could tell.
They're virtually fragrance-free: There's nothing more unsettling than a face or eye mask with a very strong scent. These are practically fragrance-free, and that's fine with me!
They soften fine lines: I don't have a ton of lines on my face (thank you, retinol), but the ones I do have are mostly around my eyes. If I get less than six hours of sleep, which is usually the case, those fine lines really pop. I put these on, and my crow's feet visibly soften. Mind you, they don't disappear, but they don't stick out, which works for me.
Great packaging: The individual packages are super convenient to throw in your bag for on-the-go use. Also, I never waste the remaining solution the masks are submerged in. The way it's packaged, I can easily remove the formula from the pouch and apply it directly to my face for all-over hydration.
Sensitive skin? You might want to avoid: The first time I used these under-eye masks, I did feel a little bit of discomfort and experienced some redness; however, it was less and less after each application. My friend, on the other hand, has really sensitive skin and she could only keep them on for 10 minutes.
These babies like to move: The masks have a tendency to slide out of position, which can be annoying if you like to wear them while doing other things, like me.
They tear easily: Be careful removing the patches from the packaging as they are delicate and tear easily.
⭐️ 4.2/5 stars
💬 33,000 ratings
🏆 "Super hydrating"
These "super hydrating" masks were a huge hit with a 44-year-old who puts them on during their morning commute to work.
Another reviewer called them "magic," reducing "99 per cent of the puffiness" and leaving their skin looking "fresh and healthy."
They're a "good break" for "tired eyes," wrote a third shopper, who did mention the masks "slide down" sometimes.
Another reviewer raved that these "must-have" masks are the "real deal." After using them, their under eyes were "more hydrated" and immediately "less puffy."
However, one user with sensitive skin found the masks "irritating" and was disappointed they made their skin "burn," removing them after only a minute.As a sleep-deprived mom who relishes her late nights, these Grace & Stella Eye Masks and I are in it for the long haul. I have never used a mask that so visibly improves the appearance of my eyes, reducing the puffiness and fine lines after just one use. It's not a panacea, and the dark circles start to creep back in as the day goes on, but for a few hours, my 47-year-old eyes look more youthful and awake. And being 30 per cent off right now, they're down to just $28. Keep in mind it may take a bit of time for more sensitive skin to adjust to the hydrogel formula, but if you can stick it out, I promise it will be so worth it.
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Justin Timberlake reveals ‘relentlessly debilitating' Lyme disease symptoms — Do you live in Ontario's high risk areas?
Justin Timberlake reveals ‘relentlessly debilitating' Lyme disease symptoms — Do you live in Ontario's high risk areas?

Hamilton Spectator

timean hour ago

  • Hamilton Spectator

Justin Timberlake reveals ‘relentlessly debilitating' Lyme disease symptoms — Do you live in Ontario's high risk areas?

Justin Timberlake has Lyme disease. The famous pop star confirmed his battle with 'relentlessly debilitating' Lyme disease symptoms in an Instagram post Thursday . 'When I first got the diagnosis I was shocked for sure,' he wrote. 'But, at least I could understand why I would be onstage and in a massive amount of nerve pain or, just feeling crazy fatigue or sickness.' Timberlake faced criticism for recent performances in Europe over what fans described as low-energy shows. It appears Lyme disease may be to blame. 'I was faced with a personal decision. Stop touring? Or, keep going and figure it out,' Timberlake wrote on Instagram. 'I decided the joy that performing brings me far outweighs the fleeting stress my body was feeling. I'm so glad I kept going.' Timberlake just completed his 'Forget Tomorrow World Tour' in Istanbul, Turkey on Tuesday. The tour started in Vancouver last April. A post shared by Justin Timberlake (@justintimberlake) Notable Canadian celebrities who have shared their diagnosis with Lyme disease include Avril Lavigne, Justin Bieber and Shania Twain. The blacklegged tick is known to transmit four tick-borne diseases — anaplasmosis, babesiosis, Lyme disease and Powassan virus — that are listed as Diseases of Public Health Significance by Public Health Ontario (PHO). Lyme disease occurs in stages. Symptoms can vary from person to person after being bitten by an infected blacklegged tick or western blacklegged tick. Signs and symptoms of each stage can overlap. 'In some people, Lyme disease may present in a later stage without a history of prior signs or symptoms,' the Public Health Agency of Canada (PHAC) explains. Early signs and symptoms of Lyme disease can manifest as: The erythema migrans rash is the most commonly reported sign of Lyme disease. PHAC explains it's an expanding skin rash that usually starts at the site of the tick bite slowly expanding over several days. The rash can be circular or oval-shaped, looking like a target or bull's eye. It can go unnoticed if it's on dark skin or a part of the body that's hard to see. PHAC says some people might not develop a rash at all. The bull's-eye shape of this rash is a clear sign of Lyme disease. Later symptoms of Lyme disease can appear days to months after an infected tick bite and might manifest as: In very rare cases, death can occur due to the complications involving an infection of the heart. Lyme disease is a growing concern in Canada particularly in southern Ontario, which is considered one of a few hot spots for ticks. Tick populations continue to climb in Ontario, as well as other parts of Canada. This year is expected to follow the trend . The Public Health Agency of Canada has a tool where you can type in your postal code and it will tell you if you're located in a risk area for Lyme disease. Some risk areas include spots in Windsor, Whitby, Waterloo, Uxbridge, The Blue Mountains, Tay Valley, St. Catharines, Smiths Falls, Scugog, Richmond Hill, Rideau Lakes, Renfrew, Prince Edward County, Port Hope, Perth, Peel, Ottawa, Oshawa, Orillia, Oakville, Niagara Falls, Newmarket, Mississauga, Milton, Markham, Hamilton, Clarington, Caledon, Burlington, Brampton, Kawartha Lakes, Barrie, Ajax and more. Map of five areas known for risk to tick exposure in Canada. The number of human reported Lyme disease cases in Canada in 2024 was 5,239, according to preliminary data from the PHAC. That's a jump from the 4,785 cases reported in 2023 and 2,525 in 2022. For a matter of perspective, only 144 cases were reported in 2009. Out of the 4,785 cases in 2023, 1,865 were reported in Ontario, according to Public Health Ontario data. 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UCSF doctor leads fight to restore wildfire health research grants cut by Trump order
UCSF doctor leads fight to restore wildfire health research grants cut by Trump order

San Francisco Chronicle​

time2 hours ago

  • San Francisco Chronicle​

UCSF doctor leads fight to restore wildfire health research grants cut by Trump order

SACRAMENTO — As smoke from Canadian wildfires drifted across North America and western U.S. states girded for their annual fire siege, Neeta Thakur was well into her search for ways to offset the damage of such fumes to people's health, especially among minority and low-income communities. For more than a decade, the UC San Francisco researcher relied on federal grants without incident. But Thakur, a doctor and a scientist, suddenly found herself leading the charge for public health science against President Donald Trump's political ideology. Thakur, 45, a pulmonologist who also is medical director of the Zuckerberg San Francisco General Hospital Chest Clinic, is the lead plaintiff among six UC researchers who in June won a class-action preliminary injunction against the efforts of several federal agencies to carry out Trump's executive orders seeking to eliminate research grants deemed to focus on areas of diversity, equity and inclusion. The administration has filed a notice of appeal, and the outcome, whether or not she and her colleagues prevail, could influence both the future of academic research and the health of those she's spent her life trying to help. 'When this moment hit us, where science was really under attack and lives are at stake, it doesn't surprise me that she stepped up,' said Margot Kushel, who directs the UCSF Action Research Center for Health Equity and has known Thakur for more than a decade through their work at the center and San Francisco General, the public county hospital. 'We don't think our work should be political, to be honest,' Kushel said. 'Saving people's lives and making sure people don't die doesn't seem to me that it should be a partisan issue.' Thakur said that after the abrupt funding cuts, she and the other researchers 'felt pretty powerless and found that the class-action lawsuit was a way for us to join together and sort of take a stance.' The suit was filed independently by the researchers and allowed them to show the harm inflicted not just on their own work 'but more broadly on public health and public health research,' she said. Thakur's study, which received more than $1.3 million in funding from the Environmental Protection Agency and was set to run through November, explores the impact of increased wildfire smoke on low-income communities and communities of color, populations that already experience heightened pollution and other environmental health disparities. The goal is to find ways to help residents limit their smoke exposure, Thakur said, adding that the results could help people no matter their circumstances. Preliminary findings show that smoke can trigger breathing emergencies among children days after exposure, knowledge that could lead to better treatment, and that smoke intensity may peak during just a few hours when protection is most needed, indicating the need for more precise and timely safety messaging. Thakur said her studies on health equity and health disparities saw growing federal support during the COVID pandemic and a national focus on racism spurred by the murder of George Floyd. The EPA had solicited the grant in 2021 for her and her team to research how climate change affects underserved communities. Trump, in one of several executive orders blocking federal funding for DEI programs, said they 'use dangerous, demeaning, and immoral race- and sex-based preferences' that he said have 'prioritized how people were born instead of what they were capable of doing.' EPA Administrator Lee Zeldin said in March that, in cooperation with the Department of Government Efficiency, the administration had canceled more than 400 grants topping $2 billion 'to rein in wasteful federal spending.' The order by U.S. District Judge Rita Lin in San Francisco temporarily blocking the grant terminations covered the EPA, as well as grants by the National Endowment for the Humanities and the National Science Foundation. Lin's ruling was not a nationwide injunction of the sort restricted by the U.S. Supreme Court in a June decision. The Trump administration agencies affected by the order have reinstated the UC grants as the lawsuit proceeds. The government filed a motion for a temporary stay on the order pending the outcome of its appeal, but a decision had not been issued as of publication. The EPA declined to comment on the judge's order blocking the attempted cancellation of the research funding, citing the ongoing litigation, and attorneys representing the government did not respond to requests for comment. Thakur defends the need for research that spotlights disadvantaged communities. Her interest in health equity stems from childhood experiences. The daughter of immigrants from India, with a physician and an engineer as parents, she grew up relatively well-off in a mixed-income neighborhood in Phoenix. While she prospered, however, she had friends who couldn't afford college or became pregnant as teenagers. 'I see my research being directed towards trying to understand how where you live and what you experience impacts your health,' Thakur said. When the grants were suspended in April, the researchers were unable to finish identifying ways to help protect communities from wildfire smoke. Thakur had to dismiss a student intern and dip into discretionary funds to pay her postdoctoral fellow. At least three research papers that could have directly affected public health were in danger of going unpublished without the funding, she said. The government reinstated her team's grants about three weeks after the judge's order, and Thakur is in the process of picking up the pieces. She's hopeful that researchers can publish two of the three studies they were working on. Thakur said she is now cautiously optimistic after experiencing 'a roller coaster of emotions.' Putting together a project and conducting the research takes years, she said, so 'to have all of that end suddenly, it brought me a range of emotions one thinks about when folks are experiencing grief. There's denial, anger.' But the Trump administration's actions have already sapped morale in the field. 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Early Warning Signs For MS Discovered—Appear 15 Years Before Main Symptoms
Early Warning Signs For MS Discovered—Appear 15 Years Before Main Symptoms

Newsweek

time5 hours ago

  • Newsweek

Early Warning Signs For MS Discovered—Appear 15 Years Before Main Symptoms

Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. Warning signs for multiple sclerosis (MS) could emerge more than a decade before the first classical symptoms occur—offering hope for earlier detection and better patient outcomes. This is the finding of researchers from the University of British Columbia (UBC), who have analyzed the health records of more than 12,000 people in the Canadian province and challenged assumptions about when the disease really begins. They discovered those living with MS—a chronic condition affecting the brain and spinal cord—began using healthcare services at elevated rates 15 years before their first 'typical' MS symptoms appeared. While MS affects people differently, symptoms often include feeling extremely tired, problems with your eyes or vision, numbness or a tingling feeling in different parts of the body, feeling off balance, muscle cramps and concentration/memory problems. "MS can be difficult to recognize as many of the earliest signs—like fatigue, headache, pain and mental health concerns—can be quite general and easily mistaken for other conditions," said paper author and UBC neurology professor Helen Tremlett in a statement. "Our findings dramatically shift the timeline for when these early warning signs are thought to begin, potentially opening the door to opportunities for earlier detection and intervention." Female doctor is taking the blood pressure of a young adult female patient during a medical consultation. Female doctor is taking the blood pressure of a young adult female patient during a medical consultation. Antonio_Diaz/Getty Images The study offers a clear picture to date of how patients engage with a range of healthcare providers in the years leading up to a MS diagnosis as they search for answers to "ill-defined" medical challenges. Diagnosis for the condition typically requires imaging (MRI) signals and a specific clinical presentation. The study tracked physician visits in the 25 years leading up to the onset of a patient's MS symptoms, as determined by a neurologist through detailed medical history and clinical assessments. Most previous studies have only examined trends in the five to 10 years leading up to a patient's first "demyelinating event" (the loss or damage of the myelin sheath, a protective covering surrounding nerve fibers in the brain and spinal cord) such as vision problems. Bruce Bebo, Executive Vice President of Research for the National Multiple Sclerosis Society, told Newsweek, "This is an impressive study by a world-class research team offering important new insights into the earliest manifestations of MS. "The ability to identify people at high risk for MS could trigger enhanced monitoring and subsequent identification of people in the earliest stage of disease. Treatment of MS at this earliest stage would likely result in significantly improved outcomes." The researchers revealed that, compared to the general population, people with MS had a steady build-up of healthcare engagement over 15 years with different types of doctor visits increasing at particular points. Some 15 years before symptom onset, patient visits to general practice physicians increased, as did visits to any physician for symptoms like fatigue, pain, dizziness and mental health conditions. At 12 years before, visits to a psychiatrist increased. Three to five years before diagnosis, emergency medicine and radiology visits increased. And one year before, physician visits across multiple specialties peaked, including neurology, emergency medicine and radiology. "These patterns suggest that MS has a long and complex prodromal phase—where something is happening beneath the surface but hasn't yet declared itself as MS," said paper author and UBC postdoctoral fellow Marta Ruiz-Algueró in a statement. "We're only now starting to understand what these early warning signs are, with mental health-related issues appearing to be among the earliest indicators." The study follows previous work by Tremlett and her team to characterize the early stages of MS, known as the 'prodromal phase', where subtle signs or other symptoms occur before the onset of more typical symptoms. These periods are well established in other neurological disorders like Parkinson's disease, where mood changes, sleep disturbances and constipation often arise years before the more familiar motor symptoms like tremors and stiffness. While the researchers point out the vast majority of people who experience general symptoms like fatigue and headaches won't go on to develop MS, they say recognizing and characterising the MS prodrome could one day help accelerate diagnosis and improve outcomes for patients. "By identifying these earlier red flags, we may eventually be able to intervene sooner—whether that's through monitoring, support or preventive strategies," said Dr. Tremlett. "It opens new avenues for research into early biomarkers, lifestyle factors and other potential triggers that may be at play during this previously overlooked phase of the disease." Could we use these early signs to reduce risk of MS developing? Bebo said: "It is likely that the central nervous system is already affected at this early stage of the disease, making true prevention unlikely. However, initiating treatment with a disease-modifying therapy at this point could halt disease progression." However, he added, "Many consider the onset of MS begins when autoreactive immune cells gain access to the central nervous system and start causing damage. "If we can identify the very earliest changes in the immune system prior to entry into the central nervous system and prevent these cells from getting access to the brain and spinal cord, it might be possible to prevent MS." Do you have a tip on a health story that Newsweek should be covering? Do you have a question about MS? Let us know via health@ Reference Ruiz-Algueró, M., Zhu, F., Chertcoff, A., Zhao, Y., Marrie, R. A., & Tremlett, H. (2025). Health Care Use Before Multiple Sclerosis Symptom Onset. JAMA Network Open, 8(8).

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