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Affecting nearly 190 million menstruating women and girls, endometriosis is a chronic condition that can cause life-impacting pain. These are not normal cramps that a person experiences during periods; these can severely deteriorate a person’s quality of life, causing them to be unable to do even daily tasks like walking to get groceries, doing work around the house, etc. This condition is caused when the uterine lining grows outside the uterus, which then causes severe pain in the pelvis and also causes reproductive issues like infertility. However, what causes endometriosis?
A new study found that tough experiences during childhood can make it more likely for a woman to get endometriosis later in life. Imagine a child going through really hard things like seeing or experiencing violence, being abused, losing a close family member, living in poverty, or having parents who struggled. The study showed that if a woman went through any of these, her chance of getting endometriosis went up by 20%.
Endometriosis is a fairly common condition, affecting about 1 out of every 10 women. Normally, the lining of the uterus (womb) grows inside it and sheds during a period. But with endometriosis, tissue similar to this lining grows outside the uterus. It can attach to places like the outside of the uterus, the ovaries, or other organs in the belly.
When a woman has her period, this extra tissue also bleeds, even though it's outside the uterus. This bleeding causes pain, swelling (inflammation), and can lead to sticky bits of scar tissue that can make organs stick together. Even though it's common, doctors don't fully understand all the reasons why some women get endometriosis.
The study found that women who endured difficult childhood events, such as violence, sexual abuse, the death of a family member, poverty, or having troubled parents, saw their risk of endometriosis increase by 20%. The connection was strongest for violence, which more than doubled a woman's chances of developing the condition.
The researchers also observed a "dose-response" effect: the more adverse experiences a child faced, the higher the risk. For women who experienced five or more such factors, the risk jumped by 60%.
For this study, researchers looked at the health records of over 1.3 million women in Sweden. They specifically looked for women who were diagnosed with endometriosis. Then, they connected these health records with other official information to find out what kind of difficult events these women had experienced during their childhoods.
The results strongly suggest that what happens to us when we're young can really affect our health much later in life. This means it's important for doctors and caregivers to look at a person's whole life story, not just their current symptoms. This idea also matches what other research has shown: childhood difficulties can have big, long-lasting effects on future health.
While the study clearly shows a strong connection, it doesn't mean that childhood trauma directly causes endometriosis. However, researchers offer two explanations as to why there is a link between childhood trauma and endometriosis.
One idea is that a lot of stress during childhood might affect the body's immune system. The immune system is like your body's defense team. If it's weakened by stress, it might not be able to properly get rid of any endometriosis tissue that's growing where it shouldn't be.
Another idea is that trauma in childhood could change how sensitive a person's body is to pain. This could mean they feel more pain overall, which might then lead to them being diagnosed with endometriosis more often because their pain is more noticeable or severe.
“The Boys” actress Erin Moriarty is using her platform to spotlight an often-overlooked autoimmune condition— Graves' disease. In an intimate Instagram post, Moriarty, 30, explained how she thought her symptoms were just stress and exhaustion but was properly diagnosed with Graves' disease last month—an autoimmune disease that impacts 1 in 100 Americans.
Erin Moriarty, posted on Instagram to announce she has been diagnosed with Graves' disease. At first, she had written off her symptoms as just "stress and fatigue." But after treatment began last month, she felt an incredible change in her health. "Within 24 hours of starting treatment, I started feeling the light turn back on — and it's just gotten brighter ever since," she posted. Encouraging her fans to listen to their own health, she added, "If your light is fading, even a little bit, go get checked."
This revelation doesn't just underscore the need to heed our bodies—it also yanks Graves' disease out of medical invisibility and into mainstream health conversation. Here's what you need to know about the condition, its symptoms, who it most affects, and how early diagnosis can be a life-saver.
Graves' disease is an autoimmune disease where the immune system mistakenly targets the thyroid gland, leading it to release excessive hormones beyond what the body requires. It results in hyperthyroidism—overactive metabolism—and impacts almost every organ in the body.
As stated by the National Institutes of Health, this hormonal excess can interrupt the normal energy balance of the body and lead to a wide range of symptoms that may go unseen or be attributed to contemporary stressors.
Moriarty's story is typical of numerous instances in which early symptoms of autoimmune malfunction are written off. "Autoimmune disease presents differently in everybody/every body," she wrote. In her case, it was a strange degree of fatigue and emotional burnout. "If I hadn't attributed it all to stress and fatigue, I would've caught this sooner."
Within 24 hours of starting treatment, Moriarty reported feeling "the light coming back on"—evidence of how rapidly Graves' disease can recover with the proper treatment when caught early.
Graves' disease has no one, obvious symptom. Rather, it's usually a disorienting mix of physical and emotional symptoms. Early signs are:
One of the more overt effects is Graves' ophthalmopathy—occasionally seen in a third of patients—which may result in:
It is rare that patients will develop Graves' dermopathy, a thickened and colored skin eruption, particularly on the shins.
Though precise causes are unknown, the Cleveland Clinic identifies a combination of environmental and genetic factors. A renegade immune system starts to make antibodies that hyperstimulate the thyroid gland. Heredity accounts for approximately 79% of the risk factor, but stress, infections, and hormonal changes may serve as the trigger.
Moriarty's experience is familiar to many young women who discount recurring symptoms until they have reached a crisis point. "Within 24 hours of starting treatment," she wrote, "I began to feel the light coming on."
Graves' disease is a relatively uncommon condition, but it strikes disproportionately against women, five times more likely to be diagnosed than men. Risk factors are:
Women in their 20s and 30s—such as Moriarty—are especially susceptible, making it even more important to be aware of it early on, says Yale Medicine.
In the U.S., treatment usually begins with medicines known as antithyroid medications, such as methimazole or propylthiouracil, which suppress the production of thyroid hormones. Most individuals start feeling better within a short time, but complete remission takes anywhere from 12 to 18 months.
When medications do not bring long-term relief from Graves' disease, more intensive measures may be needed. Radioiodine therapy is a common technique that destroys the excess thyroid tissue. When the condition is more severe or does not respond to other measures, a thyroidectomy might be necessary. Because both procedures can result in hypothyroidism, hormone replacement therapy is usually lifelong to sustain hormonal equilibrium. As in the case of Erin Moriarty, identifying symptoms early and taking prompt action can greatly enhance the quality of life and avert complications.
Untreated, Graves' disease can severely impact overall health and result in several complications. One of the more alarming risks is atrial fibrillation, a form of irregular heart rhythm that can worsen to heart failure or stroke. In extreme cases, the patient can suffer a thyroid storm — a sudden and life-threatening injection of thyroid hormones. The disease also leads to osteoporosis over time, making the patient more prone to fractures through weakened bones. Furthermore, there's also a higher risk of developing thyroid cancer. For pregnant women, the stakes are even greater: if left untreated, Graves' disease can result in severe consequences including miscarriage, preeclampsia, preterm labor, and low birth weight. These complications make early diagnosis and continued management critically important.
Celebrity disclosures like Moriarty’s bring invaluable attention to conditions that are often misunderstood or stigmatized. By sharing her journey, Moriarty not only shed light on Graves’ disease but also issued a crucial call to action,“Go get checked.”
If you’ve been experiencing persistent fatigue, rapid heartbeat, or unexplained weight loss, don’t ignore the signs. In Moriarty’s words: “If yours is dimming, even slightly, go get checked.”
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Memory loss can be seen as a normal sign of aging. As our age progresses, so does our ability to retain certain things. Dementia, however, is different than just forgetting things. It not only affects your memories, but it also changes your behavior patterns and thinking capabilities as well. It can change a person to their core, even the things that may be a huge part of their personality.
A charity is highlighting key dementia symptoms that are more than just "normal aging." A recent survey shows that a huge 85% of people in the UK put off getting help. Getting a diagnosis early means the person can get the best support and treatment they need as soon as possible.
Dementia has no cure; hence, the best way to ensure one's quality of life does not severely decline, one must get treatment quickly. While you may not be able to eradicate the disease, you can get its symptoms under control.
A survey by the Alzheimer's Society found that only a third of people tell their doctor about dementia symptoms within a month of noticing them. This includes noticing symptoms in themselves or a loved one. Only 15% sought help "immediately," meaning most people (75%) waited to get advice.
Many of the 1,100 people surveyed stayed quiet because they weren't sure if the symptoms were from dementia or just normal aging. About one in three people (33%) who noticed symptoms kept their worries to themselves for over a month. Another 11% hadn't even talked about their concerns despite seeing the first signs. This delay often leads to people waiting a long time for medical advice, with almost a quarter waiting more than six months to see a doctor.
Early signs of dementia, like trouble following conversations, difficulty concentrating, and memory lapses, are often mistaken for normal aging things like hearing loss or simply forgetting things. The survey also found that 16% of people actively "avoid" getting a diagnosis because they're scared of how it might affect their relationships. Plus, 44% worried about family or caregivers starting to "talk down" to them.
The survey pointed out seven possible early signs of dementia:
The former CEO of the Alzheimer's Society emphasized the need to be more open about dementia, saying we "can't continue to avoid the 'd' word."
The charity helps explain the difference between signs of Alzheimer's and dementia versus typical age-related changes. Signs of Alzheimer's and dementia often include:
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Mental workload refers to the amount of cognitive effort someone is using at any given moment. For jobs that require intense focus and decision-making, staying in an optimal zone of workload is key. Too little, and the person may get bored and lose concentration. Too much, and they may become overwhelmed, risking mistakes.
Traditional tools to measure mental workload, like questionnaires or wired EEG (electroencephalography) and EOG (electrooculography) devices, are often bulky or unreliable. Questionnaires are subjective and taken after tasks, and existing EEG/EOG systems don’t allow for freedom of movement or real-time alerts.
The e-tattoo is made of a stretchable, graphite-based conductive material and is stuck to the forehead with a conductive adhesive. It includes:
All components are coated with additional conductive materials for accurate signals. The electrodes send data wirelessly to a computer or device, enabling real-time monitoring.
The device is disposable and custom-made, while the circuit and battery are reusable. According to the researchers, the entire setup is expected to cost under $200.
To test the device, the team recruited six participants for a “working memory” task involving letter and location recognition. Each participant was shown a sequence of letters and asked to click a mouse if the letter or its position matched one shown previously. The difficulty level varied across four stages.
As tasks became harder, EEG readings showed increased brainwave activity linked to higher mental effort. The researchers then fed this data, along with task difficulty, into a machine-learning algorithm. After training, the algorithm successfully predicted a participant’s mental workload based on EEG and EOG data alone—better than random chance.
Dr. Nanshu Lu, one of the lead authors of the study published in the journal Device, said the ultimate goal is to enable the e-tattoo to decode signals and send real-time alerts to an app. That way, users can recognize when they are approaching cognitive overload and take steps to delegate tasks, rest, or refocus.
But Lu cautions that the solution is not simply switching to an easier task. “Optimal mental performance occurs when the workload is just right—not too high, not too low,” she explained.
As development continues, the e-tattoo may soon become a powerful tool to support mental well-being and precision in professions where lives depend on focus.
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