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Warning to antidepressant users as heat wave temperatures hit 100 degrees

Warning to antidepressant users as heat wave temperatures hit 100 degrees

New York Post4 days ago

Can't take the heat? Your medication might be to blame.
Doctors are warning that people taking certain antidepressants could be at risk of serious health problems as temperatures soar into the triple digits.
They're urging users to take extra precautions as the tri-state swelters — before it's too late.
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3 Dr. Zachary Rubin is warning antidepressant users to be extra careful in the heat.
TikTok/@rubin_allergy
'If you're taking certain antidepressants, you may be at risk for developing heat intolerance and dehydration,' Dr. Zachary Rubin, a pediatrician and immunologist, warned in a recent TikTok video.
Studies show about 1 in 8 American adults take antidepressants. Research suggests that two major types can interfere with how the body regulates temperature.
The first group, selective serotonin reuptake inhibitors (SSRIs), includes widely prescribed drugs like Prozac (fluoxetine), Zoloft (sertraline), Lexapro (escitalopram), Paxil (paroxetine) and Celexa (citalopram).
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The second group, tricyclic antidepressants (TCAs), includes older meds such as Elavil (amitriptyline), Anafranil (clomipramine) and Silenor (doxepin).
Studies show these medications can spike internal body temps to 106°F or higher — while also throwing a wrench in the body's natural cooling system.
'You may excessively sweat or you may not be able to sweat quite as much,' Rubin explained.
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3 Sweat helps protect the body from overheating.
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That's no small issue: Sweating is the body's primary defense against overheating. Without it, your chances of heatstroke, organ failure and even death increases substantially.
Research shows SSRIs and TCAs may also mess with the hypothalamus, a part of the brain that helps regulate body temperature, thirst and blood pressure.
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'When the hypothalamus cannot control body temperature, someone can overheat,' Dr. David Tzall, a licensed psychologist, told Medical News Today.
That increased heat sensitivity increases your chances of heat exhaustion, which has symptoms such as dizziness, nausea, muscle cramps, headaches and heavy sweating, according to the Cleveland Clinic.
Left unchecked, heat exhaustion can quickly escalate into heat stroke — the most dangerous form of heat-related illness.
At that stage, the body can begin to shut down, triggering seizures, hot dry skin or intense sweating, loss of consciousness and serious brain trouble, including confusion, erratic behavior and slurred speech.
In extreme cases, heat stroke can cause permanent disability or death.
'If you begin to feel a rapid heartbeat, start sweating excessively, develop nausea, dizziness or leg cramping, immediately seek air conditioning and if necessary, have someone call 911,' Dr. Robert Glatter, an emergency medicine physician, told Health.com.
Still, experts say SSRIs and TCAs are safe and effective — as long as patients know the risks and can spot the warning signs before things turn dangerous.
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3 SSRIs are the most popular form of antidepressants on the market.
nenetus – stock.adobe.com
Rubin recommends staying hydrated, avoiding direct sun and wearing loose, light-colored clothing when temperatures climb.
'If you are struggling at all, make sure that you seek out help,' he said.
The warnings come as a once-in-a-century scorcher grips the East Coast, with more than 150 million Americans currently living under 'extreme' heat alerts.
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Each summer, more than 500 New Yorkers die prematurely because of hot weather, a figure that has been climbing in recent years.
'This week's heat wave could be deadly and life threatening if you are not prepared,' Mayor Eric Adams warned in a recent public safety alert.

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34 Reviewer-Loved Products To Nail Your Beauty Routine
34 Reviewer-Loved Products To Nail Your Beauty Routine

Buzz Feed

time43 minutes ago

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34 Reviewer-Loved Products To Nail Your Beauty Routine

A lightweight gel cream from Nivea so shockingly effective, you might trick people into thinking you have a filter on your skin. No, really — it actually happened for one reviewer! This uses the miracle-working abilities of an ingredient called ~Q10~ to deliver plumper, firmer-looking, more moisturized skin. A cult-classic Clinique Almost Lipstick Tinted Lip Balm in Black Honey if you want to keep dry, chapped lips AWAY. This bb is lightweight, slightly glossy, and has a little dash of magic. I mean, I'm guessing it's magic — because the way this glosses you up and complements all different skin tones so beautifully is beyond anything ordinary. A moisturizing hair serum here to breathe some life back into your locks and rescue them from eternal dryness. This delightful blend is derived from seven incredible oils: argan, olive, coconut, apricot, marula, jojoba, and camellia. This reviewer says it gives you gloss without the grease, and that the scent alone makes them want to keep using it! Medicube's "Zero Pore" Pads that do their job so well, they turned this skeptical reviewer into a believer. They contain lactic acid, salicylic acid, and a dual-textured surface to help control excess sebum while exfoliating dead skin and refining pores, all while keeping you looking like a true ~glow-getter~. A pore-clearing cleansing oil because it uses the calming powers of heartleaf oil to soothe irritated skin and eliminate makeup residue, blackheads, and sebum while preventing pore congestion. It's also hypoallergenic and works wonders for sensitive, acne-prone skin. A reviewer-beloved teeth-whitening pen — you'll see the difference almost immediately, and it'll help you avoid having to go get it done by a pro. 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A TikTok-famous VieBeauti eyelash growth serum to help with upkeep when you can't make it to the esthetician for extensions. Apply to your lashes daily to help them become longer and stronger within just a few weeks! You'll be resisting the urge to flutter your lashes like a cartoon character every time your S.O. walks by in no time. A surprisingly effective instant foot peeling spray that'll make your footsies so baby-soft and pretty, they'll be a good uh... backup plan. (You know, in case your current career doesn't pan out. 👀) This not only helps gently remove dead skin, but also moisturizes dry and cracked heels, so you'll really get some refreshing bang for your buck. For an ~extra~ peeling effect, use an exfoliating mitt! A bottle of Elizavecca Hair Treatment some reviewers say is even BETTER than Olaplex, which is over three times the price! 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Nurse Suddenly Lost Her Sight While Treating Patients. Then Came an Unexpected Diagnosis (Exclusive)
Nurse Suddenly Lost Her Sight While Treating Patients. Then Came an Unexpected Diagnosis (Exclusive)

Yahoo

time5 hours ago

  • Yahoo

Nurse Suddenly Lost Her Sight While Treating Patients. Then Came an Unexpected Diagnosis (Exclusive)

While working in the ER, Breanna T. suddenly lost her vision and kept treating patients as her sight deteriorated She was told it wasn't emergent, but days later, a specialist diagnosed her with acute angle closure glaucoma Breanna's vision has returned, but her story, and viral TikTok, have sparked wider conversations about advocacy and medication side effectsOne moment, Breanna T. was helping patients during a routine emergency room shift, and the next, the world around her was a blur. The ER nurse had no warning before her vision disappeared in both eyes, kicking off a frightening medical mystery that would later go viral on TikTok. In the video, Breanna reenacts what unfolded in those first 48 hours with a pointed 'put a finger down' challenge, recounting how she finished her shift while barely able to see, and the journey that followed before she received a diagnosis. 'I looked up to see who was calling my name, and I couldn't see her at all,' Breanna tells PEOPLE, describing the moment everything changed. 'It was just very shocking to me, because literally 10 seconds before that, I was seeing just fine.' She had just stepped out of a patient's room to assist a fellow nurse when the sudden loss of sight occurred. As panic swelled beneath the surface, her clinical instincts kicked in. 'I cleaned my glasses, I took my blood pressure, I took my blood sugar … I was just trying to go through everything I could think of to fix it,' she says. 'I was also at work, still responsible for helping care for patients, so I was doing my best to keep my composure.' Rather than alerting her team right away, Breanna first tried to troubleshoot the situation herself. She didn't want to raise the alarm until she had ruled out the basics. 'I was like, 'Here's the situation … do you guys have any ideas? Because I've already done everything I can think of,' ' she recalls telling her coworkers and several doctors. 'So then we started spitballing, trying to figure out what else we could test.' She had been trained to recognize red flags for emergencies and was deeply concerned about the possibility of a stroke. But her symptoms weren't fitting into any box. 'Loss of vision is a pretty standard stroke symptom,' she explains. 'But because it was both eyes at the same time and I had no other symptoms, I tried to stay levelheaded.' Her coworkers asked all the right questions, but nothing beyond her vision seemed to be affected. 'People were asking, 'Do you have a headache? Are you nauseous?' But literally, it was just my vision change,' she says. 'So I was honestly at a loss, because this didn't look like the heart attacks, strokes or brain bleeds I've seen before.' After confirming there were no immediate life-threatening causes, the ER team told her to follow up outpatient. As a nurse, Breanna understood why, but as a patient, it felt unsettling. 'I tell patients this all the time, and being on the other side of it was eye-opening,' she says. 'It wasn't life-threatening, but it was still scary not knowing what was going to happen next.' After her shift, she tried to book an urgent appointment with her optometrist, but found herself stuck. She couldn't even get far enough into a conversation to explain why she needed care. 'They'd say, 'We don't have openings,' before I could tell them I was having an emergent vision change,' she says. 'I felt stuck between a rock and a hard place.' With emergency services having done all they could, and no specialist available, she was left waiting and hoping. Her boyfriend began calling providers on her behalf, trying to get her seen. 'It was just really frustrating,' she says. 'I felt like I was being stopped before I was even able to tell anybody why I needed an immediate visit.' In total, Breanna spent five days with severely compromised vision. On the first day, she received contacts that somewhat helped, but even those came with side effects. 'They weren't perfect, and they gave me more headaches than not being able to see,' she says. 'So I was only wearing them when I absolutely had to.' When she finally got an appointment with an optometrist, she decided to go alone. She had no idea just how serious the visit would become. 'He stayed really calm, but started asking questions that felt odd,' she says. 'Then he told me my eye scans didn't look normal. My pressures were way above average, and he could see swelling.' The diagnosis was acute angle closure glaucoma, a rare condition that can come on rapidly and without warning. The optometrist told her she needed to see a specialist immediately or head straight to a hospital with ophthalmology on call. 'It was 4:30 p.m. on a Friday,' Breanna says. 'I was scared I'd have to go back to the ER and start all over again.' Though her boyfriend and mom rushed to be with her, Breanna had faced the alarming news alone. And in that moment, her thoughts went straight to her son. 'I'm a mom. I have a toddler,' she says. 'All I could think was, 'Am I going to be able to see my son grow up?' ' The disease typically takes years to develop, but Breanna had deteriorated within hours. Doctors were optimistic her case would be reversible, but the wait was excruciating. 'I wasn't ready to stop my medication, but that's what ended up solving it,' she says. 'I stopped taking it that day, and by the time it was out of my system, my vision returned.' Her care team believes the antidepressant triggered the event, likely due to an underlying condition. And for Breanna, the timeline made sense. 'The half-life of the medication lined up with when my vision came back,' she says. 'They're almost 99% sure it was [that].' Breanna hadn't been familiar with her diagnosis before that day. Glaucoma wasn't something she had seen often in the ER, especially not in this form. 'The patients I've cared for had long-term glaucoma, with black spots or floaters — not blurry vision like I had,' she says. 'Even the symptoms didn't line up.' At one point, she was even questioned about exposure to rare diseases due to her line of work. Ebola, measles and Lyme disease were all floated. 'I said no, and I still stand by no,' she says. 'But contact tracing takes weeks, so it's still something we may have to revisit.' Still, because her symptoms cleared after stopping the medication, her team now leans heavily toward that explanation. And they found something else along the way. 'I have an enlarged optic nerve on my left side, which predisposes me to glaucoma,' she says. 'That may be why it happened to me and not someone else.' Breanna will now have yearly checkups to monitor her eye health. The goal is early detection should anything change in the future. 'It was an incidental finding, but a good one,' she says. 'Even though my symptoms have resolved, I'm still at risk for developing another type of glaucoma later on.' Returning to work felt emotional and empowering. It reminded her why she became a nurse in the first place. 'I was just grateful to still be able to do my job,' she says. 'I didn't want to lose my career, and I didn't want to lose my motherhood.' Never miss a story — sign up for to stay up-to-date on the best of what PEOPLE has to offer​​, from celebrity news to compelling human interest stories. As for advice for others, Breanna wants people navigating confusing health issues to keep advocating for themselves, even when the answers are slow. It only takes one person to listen. 'You're your biggest advocate,' Breanna says. 'You're the only one who can really explain what's going on in your body.' She also acknowledges how often women are dismissed in medical spaces. And though she works in healthcare, she felt it herself. 'Being a woman makes it harder as they're quicker to brush you off,' she says. 'You just have to keep fighting until you find someone who takes you seriously.' Looking back, she wishes more people understood the emotional toll of being caught between not fitting a diagnosis and not getting answers. Her case didn't follow a pattern, which left even doctors unsure where to start. 'If you don't meet the classic symptoms, people don't know where to begin,' she says. 'That doesn't mean you're not sick.' Her TikTok has sparked wide conversation but she never meant to scare anyone. She just wanted to tell the truth. 'I wasn't making that video to tell people to stop their meds,' she says. 'If you're afraid of side effects, that's okay … just talk to your doctor first.' Read the original article on People

4 Words That Changed My Life After Diagnosis
4 Words That Changed My Life After Diagnosis

Buzz Feed

time6 hours ago

  • Buzz Feed

4 Words That Changed My Life After Diagnosis

One particularly stressful day a few years ago, while driving to an important work event, I was seized with a severe bout of tics. This was not unusual for me. I'd been ticcing nearly all my life, and stress always exacerbated my tics. On this day, my snorts and jerks were so out of control that I rear-ended a car. That's when I finally visited a neurologist. I needed to know, literally, what made me tic. What he told me — 'You have Tourette syndrome' — came as a shock. It was also a relief. For as long as I can remember, I've had the characteristic vocal and motor tics associated with the condition. Secreting them away in my mental lockbox, burying them well out of sight of others, was how I dealt with them. A diagnosis brought clarity, and it meant that I could deal with my tics in a healthier way — or so I thought. I grew up in a small western New York town in the 1980s, those heady days of ozone-depleting hairspray, goofy mullets, and syrupy synth pop. In my rural community, very few people knew what Tourette was. I certainly didn't. When I was a teenager, a television program, possibly 60 Minutes, aired an episode on the subject that I watched with my mom. It featured a young man who shouted obscenities in some large American city. By that time I'd been ticcing for years — in fact, I'd already been hiding my tics for years. But I didn't recognize myself in this program, because never, not once, did I swear or shout in public. When I was in elementary school, a teacher once stopped class to tell me to quit making noises and 'doing that thing you're doing with your head.' She actually demonstrated 'that thing' in front of my classmates because I was apparently annoying her and disrupting her lesson. Every head turned my way, and I put mine down, humiliated. I could not tell her that I couldn't help myself. In birding, there's something called a 'spark bird' — the bird that, when you first see it in the wild, truly gets you hooked on birding. But this was my spark moment, when I realized my tics were not 'normal' and that I needed to hide them if I wanted to be normal. If my mom made any connection between that kid we saw on TV and me, she didn't mention it, and my parents didn't take me to a neurologist to have me checked out. Because of that TV program, I assumed, wrongly, that having Tourette meant shouting obscenities in public. I learned that this version of Tourette is called coprolalia and, according to the Centers for Disease Control and Prevention, it 'only affects about 1 in 10 people with Tourette.' It is not as common as popular media likes to portray it. For me, ticcing has always meant a near-constant urge to do things with my body. 'Urge' may not be the right word for these head jerks, blinks, snorts, grunts, throat clearings, tongue clicks, etc., but it's the best I've got. From the moment I wake up to the moment I fall asleep, my body seems to have a will of its own. In any given hour, I probably tic at least 100 times. During periods of great stress, like when I rear-ended that car, my tics are like a parasitic fungus that assumes total control over my body. Nobody wants to twitch or make weird noises in public — to be the person people crane their necks to see. What's wrong with this guy? you imagine them thinking. After getting called out by my teacher, I only wanted to blend in — to become invisible — because when you're in elementary school, you don't want to be seen as a freak. You want to be like everyone else. I couldn't stop ticcing, but I discovered that I could make it less obvious. To shield myself from shame and embarrassment, I developed an arsenal of tic-hiding strategies. Instead of jerking my head, I would put my hand underneath the table and waggle my fingers or ball my fists repeatedly. Instead of snorting or chuffing — obvious and strange sounds — I'd click my tongue softly, like an irregular metronome. These tricks satisfied my near-constant urge to tic and kept me mostly hidden from view. I wasn't bullied or teased in school, as kids and adults with tics often are, but I probably would have been if I hadn't learned how to control my tics. I've been using these tricks ever since. When I'm out in public today, I'm keenly aware of my internal pressure to tic, but I've become adept at suppressing it, bottling it up and capping it tight. At home, where I'm free to be myself, it's a very different story. My tics come and go. Six months ago, I began squirting air from my mouth the way someone might blow hair off their face; a few weeks later, I started hocking as though to spit a loogie. Like uninvited guests overstaying their welcome, both tics remain with me as I write these words. Sometimes a particular tic will go away only to return a year later, like an exasperating big brother who'd gone off to college and come home with a sly grin and a shaggy beard. There is no cure for Tourette — all you can do is try to manage your tics. There are treatments available, ranging from antihypertensives like guanfacine and clonidine to alternative options like the antipsychotic drugs risperidone and Abilify. But I'd honestly rather have tics than the potential side effects these drugs can cause. When I was first diagnosed, I tried guanfacine and I'd wake up in the middle of the night so parched that it was like I'd swallowed sand; my sleeplessness felt more like a punishment, especially since the drug didn't even control my tics, so I quit taking the pill. Since then, I've chosen no other treatments, though I recently learned of a promising option I will try called 'comprehensive behavioral intervention for tics,' or CBIT. This doesn't involve any drugs. Instead, it trains you to change your behaviors and tic less. Researchers estimate that between 350,000 and 450,000 Americans have Tourette syndrome, while roughly 1 million have other persistent tic disorders. There's said to be insufficient evidence to determine the number of adults with Tourette because many people simply outgrow their tics by late adolescence. According to the Tourette Association of America, the condition 'occurs in 1 in 160 (0.6%) school-aged children, although it is estimated that 50% are going undiagnosed ' (italics mine). A 2022 survey by the group suggested that 1 in 10 children with a tic disorder 'attempted suicide at least once during the past 12 months.' That's a scary number, and it speaks to how difficult it is for many people with tics to feel comfortable in their own bodies. I'm glad that kids (and their parents) who are diagnosed with Tourette today now have resources available to them — including a supportive community — to feel less stigmatized or ostracized by this awkward thing in their lives. I did not outgrow my tics. Because it's hard to admit publicly something I've always internalized and associated with shame, few people know this part of me. Even if you're not bullied or harassed, hurt and humiliation run deep; they form scars that are easily scraped off. How many other adults fly under the radar, as I do? Who, like me, never outgrew their tics but developed strategies for concealing them? Who didn't benefit from services that the Tourette Association of America offers, or the wealth of research being done today? Who struggled to form truly lasting friendships for fear of being exposed as someone with tics? Apart from the nuisance of having tics, I live what society would likely deem a 'good' and 'regular' life. I have a wife, a child, a great job, a house, and a creative life as a writer and translator. I have Tourette, but Tourette doesn't have me — though my wife would certainly disagree with this. When we got together 25 years ago, I suppressed my tics in front of her, but you can't hide something like this from someone you live with. I no longer try. Even on those nights when my ticcing body keeps her up, she's supportive. Since I've spent a lifetime hiding my tics, I've become successful at blending in, even when I'm meeting people for work or on stage in front of an audience, giving a reading or interviewing authors. But I've also experienced moments of deep loneliness. Retreating into yourself is a good way to not be publicly embarrassed, but you pay a price. Eventually, you end up feeling like a ghost in your own life — known to no one but yourself and a few carefully curated individuals whom you trust. I don't make friends easily. Later this year, I will publish my debut novel, The Book of Losman, after translating more than a dozen novels from Danish and writing countless unsold manuscripts over the past 30 years. It's about a literary translator, like me, with Tourette, but that's where the similarities end. It's a speculative fiction about a man named Losman who lives in Copenhagen, Denmark, and gets involved in an experimental drug study to relive childhood memories in the hope of finding a cure for his Tourette. Why not? The beauty of fiction is that you can imagine anything you want, provided the world you create is believable. In real life, I can't go back in time to reassure the little kid who got called out in elementary school, but I'm old enough to understand something he couldn't: 'Normal' is a highly subjective word, one laced with many assumptions. At nearly 50 years old, my tics (and the need to control them) are ingrained in the very fabric of my being. Even after publishing this essay, I will continue to hide my tics in public. Why? The stigma is a great burden. The line between dignity and humiliation is, in the end, a thin one — at least for me. I truly admire those in the younger generation, who can go on TikTok or YouTube and put themselves out there for the world to see. That's not for me. But by sharing my story here, what I can do is help normalize Tourette and other tic disorders. People like me, we're all around you. All that we ask for is what every human being deserves: to live a judgment-free life.

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