Credits: Health and me
'Diagnostic Anomaly' is a Health And Me Series, where we dive deep into some of the rarest of rare diseases. Here, we trace such diseases and what causes them. We also try to bring case studies around the same.
Just the idea of bleeding for more than a few days each month is exhausting but imagine bleeding every day—for almost three years.
That's not a metaphor, that's the real-life experience of a young woman who's endured more than 1,000 consecutive days with continuous menstrual bleeding. No respite. No break. Only doctors, tests, hormone therapy, and bewilderment. Initially, it was apparently a textbook case of polycystic ovary syndrome (PCOS). But when the standard treatments didn't work and the bleeding continued to refuse to cease, her case became a medical enigma. It wasn't until almost day 950—and a hint from a TikTok follower—that she came across a potential solution: a rare anatomical anomaly called a bicornuate uterus, or what many refer to as a "heart-shaped uterus."
Poppy's nightmare started quietly, with stubborn spotting and profuse bleeding. At first, doctors thought she might have polycystic ovary syndrome (PCOS), a typical hormonal disorder that can impact menstruation. But this diagnosis wouldn't account for the intensity or longevity of her bleeding. She went through cycles of medications, ultrasounds, intrauterine devices (IUDs), and round-after-round of doctor visits—but nothing stopped the bleeding.
"My iron levels are rock bottom. I have headaches all the time, nausea, muscle and bone pain," she posted in one of her TikTok videos. Even after going through multiple rounds of testing and treatment, no doctor was able to find a specific reason for her persisting symptoms.
It wasn't until day 950 of her 1,000-day ordeal that a forgotten clue resurfaced—and it was in the first ultrasound she'd ever had. Courtesy of the crowd-sourced information provided by her social media friends, Poppy learned she could have a bicornuate uterus, or a "heart-shaped uterus."
This uncommon congenital condition, seen in fewer than 0.5% of women, results in the uterus forming two separate cavities rather than one. This developmental defect may significantly affect menstrual bleeding and fertility.
Bicornuate uterus is a condition that happens during fetal development where the two Mullerian ducts do not join to form one uterine cavity. Two horn-like parts develop instead, which is heart-shaped. Most often, it never gets noticed until something goes wrong, particularly during pregnancy or menstruation.
Although the condition is not necessarily dangerous, it has the potential to cause serious symptoms such as heavy or extended menstrual bleeding, pelvic pain, and painful sex. In severe instances, it can raise the risk of miscarriage, preterm labor, and other complications during pregnancy.
Why Was It Missed?
Medical staff usually miss a bicornuate uterus unless actively searching for uterine anomalies. And unless it is extremely serious or a patient is pregnant, years may pass before detection.
In Poppy's situation, the anomaly was detected on her initial scan but never marked as a possible problem by any of her physicians—a breakdown in communication that cost her almost three years of physical and emotional pain.
Having determined the probable reason for her ongoing bleeding, Poppy now is being subjected to additional tests, such as a detailed hormonal panel. Her IUD will be removed, and she will have a dilation and curettage (D&C) procedure done to remove abnormal tissue accumulation in her uterine lining.
The best hope is corrective surgery—a procedure known as metroplasty—that seeks to reshape the uterus into one cavity. Though controversial and only for specific situations, metroplasty has relieved many women of their symptoms and greatly enhanced their reproductive records.
For Poppy, living without daily bleeding seems unreal. She described the possibility of relief in one word: "heaven."
Can You Get Pregnant with a Bicornuate Uterus?
Yes, but the path is not sure to be smooth. Although a bicornuate uterus never in itself prevents conception, it does complicate the pregnancy process. Since the uterus will not have enough room to grow, risks like miscarriage, premature birth, and low birth weight are greater.
Physicians usually advise greater prenatal surveillance to monitor fetal growth and uterine development. Sometimes in advance, cesarean section births may be scheduled because of irregular baby positioning.
The condition is characterized by the healthcare provider as being "partial" or "complete" based on the depth of the indentation in the uterus. A partial bicornuate uterus has a shallow indentation, whereas a complete one displays a deep, heart-shaped division.
Not every woman with a bicornuate uterus needs surgery. For most, the condition is not a big deal and doesn't impact life much. But for women like Poppy—suffering tremendously without relief—surgical repair can be transformative.
Metroplasty, most commonly performed through minimally invasive laparoscopic intervention, is the excision of the dividing tissue to form a more traditional uterine form. Post-operative treatment typically involves waiting after the surgery before trying to conceive because there is a danger of uterine rupture.
What sets Poppy's case apart is the fact that she has utilized TikTok as a forum not only to rant about her frustrations but also to teach. Her candor about a very private and mostly forbidden health concern has inspired thousands of women to challenge their own diagnoses and stand up for themselves in medical environments.
Poppy's case is a powerful reminder of the value of perseverance, self-advocacy, and the strength of online communities. As she inches toward a possible solution, her saga continues to encourage women to raise their voices, ask questions, and demand answers.
Because sometimes, the clue to solving a medical mystery isn’t hidden—it’s just been ignored.
If you’ve been experiencing prolonged menstrual symptoms or unexplained pelvic pain, consult a gynecologist and ask whether a uterine anomaly like a bicornuate uterus could be involved. Early diagnosis can change the course of your health.
(Credit-Canva)
In the United States, someone dies from heart disease every 34 seconds, and nearly half of the population has some form of cardiovascular disease (CVD).
What makes these statistics scary is the number of people who experience mental health issues, which is one out of four adults.
A new report from Emory University shows a clear and strong link between mental health conditions and heart disease. The report found that having certain mental health disorders can increase your risk of developing heart disease by a significant amount—anywhere from 50% to 100%. For people who already have a heart condition, these disorders can make things much worse, raising their risk of poor outcomes by 60% to 170%.
The report, led by Dr. Viola Vaccarino and published in The Lancet Regional Health-Europe, highlights the strong link between mental health conditions and an increased risk of developing heart disease. Specifically, it found that certain mental health disorders can increase the risk of developing heart disease by 50% to 100%. For individuals who already have a heart condition, these disorders can worsen outcomes by 60% to 170%.
The report associated the following mental health conditions with these increased risks for developing CVD:
Major depression: 72% increased risk
PTSD: 57% increased risk
Bipolar disorder: 61% increased risk
Panic disorder: 50% increased risk
Phobic anxiety: 70% increased risk
Schizophrenia: nearly 100% increased risk
The study also found a two-way connection. Not only do mental health issues raise the risk for heart disease, but over 40% of people with heart disease also have a mental health condition. For example, a person with heart disease who also has major depression is more than twice as likely to die from their heart condition.
How Is Our Mental And Heart Health Connected?
The report explains how this link works inside the body. It shows that conditions like depression, schizophrenia, and PTSD can cause the body's natural stress response systems to act abnormally. These systems, called the autonomic nervous system and the hypothalamic-pituitary adrenal axis, control important body functions like heart rate and how we handle stress.
When these systems don't work correctly, they can cause long-term problems that harm the heart. This includes things like ongoing inflammation, issues with metabolism, and high blood pressure. All of these issues can raise the risk of developing heart disease over time.
What Are Some Mental Health Barriers That Affect Care?
For people with mental health conditions, getting the right medical care for their physical and mental health can be very difficult. The report points to several key problems.
Social and economic barriers
It can be tough for people with mental health conditions to afford or even get to doctors' appointments.
Communication issues
Sometimes, people may not understand health information or have trouble explaining their symptoms, which can make it harder to get the right diagnosis and treatment.
Stigma
There is still a lot of shame around mental health, which can stop people from seeking help. Doctors may also have their own biases. The report also notes that people with mental health conditions are often left out of clinical trials, so we don't have as much research on them.
Fragmented care
The way our healthcare system is set up often treats the mind and body as separate. This makes it hard to address all of a person's health needs at once.
Credits: Canva
If menopause had a social media profile, its relationship status with women’s health would be… “complicated”. Sure, the hot flashes and mood swings grab most of the headlines, but lurking quietly in the background is another issue: bone loss. Oestrogen is important when it comes to keeping bones strong. Once its levels dip during menopause, women become much more prone to osteoporosis.”
Bone is a living tissue that constantly rebuilds and repairs itself. Oestrogen is what keeps this construction site running smoothly. “When oestrogen drops, the balance between bone building and bone breakdown collapses,” explains Dr. Pramila Kalra, Consultant, Department of Endocrinology, Ramaiah Memorial Hospital. This leads to bones that weaken faster than they can repair.
And it’s not just an invisible problem on a scan. Weakened bones translate into fractures from the most minor of falls. Hips, spines, and wrists are the usual casualties. “To put it into perspective, women over 50 face a 15% lifetime risk of hip fracture, and recovering from one can seriously affect independence,” says Dr. Kalra.
“HRT replaces the hormones your body no longer produces enough of after menopause, and this can significantly slow down bone loss,” says Dr. Kalra. Not only does it help bones maintain their density, but in some cases, it can even nudge bone strength upwards.
HRT isn’t a one-size-fits-all pill. It comes in forms that suit different lifestyles: tablets, patches, gels, and even sprays. For women with a uterus, progesterone usually joins the prescription party to protect the uterine lining. And along with stronger bones, many women also notice relief from hot flashes, night sweats, and that infamous menopause brain fog.
Before you rush to the pharmacy, there are questions worth asking. “HRT works best for women who have severe menopausal symptoms or are at a high risk of osteoporosis,” says Dr. Kalra. Women who experience early menopause, particularly before age 45, are often strong candidates for HRT because their bones face years of oestrogen shortfall.
Safety concerns around HRT have caused plenty of headlines in the past. But newer research has changed the conversation. “When HRT is started within 10 years of menopause and before age 60, the benefits outweigh the risks for most women,” explains Dr. Kalra.
Still, the risks are not zero. There may be a slight increase in the chance of blood clots or breast cancer depending on personal health, the type of HRT, and how long it’s used. “That’s why an individualised discussion with your doctor is crucial. It’s about weighing your personal benefits against possible risks,” she stresses.
Dr. Kalra recommends thinking beyond medication. A diet rich in calcium and vitamin D, regular exercise—particularly weight-bearing workouts—and avoiding smoking and excessive alcohol are all essential. “HRT is most effective as part of a holistic bone health plan,” she says.
There’s no “universal prescription” for menopause management. “The decision to start HRT must be highly individualised,” advises Dr. Kalra. Your doctor will consider your family history, existing health conditions, and results from a bone density scan. Together, you can discuss the type, dose, and duration of therapy that best fits your needs.
The conversation should cover not just symptoms but also your future risks. “It’s not about erasing menopause—it’s about empowering women to make informed choices so they can stay active and independent for years to come,” says Dr. Kalra.
Menopause may be inevitable, but brittle bones don’t have to be. With the right support, including HRT where appropriate, women can safeguard their bone health and dramatically reduce their risk of fractures. “Think of it as investing in your future mobility and independence,” Dr. Kalra concludes.
Credits: Canva
Autism is often painted as a childhood condition, usually spotted in the school playground when social quirks or communication differences raise eyebrows. But what happens when those children grow up without anyone connecting the dots? According to new research from King’s College London, the answer is unsettling: most autistic adults over 40 are still flying under the diagnostic radar.
The review, published in the Annual Review of Developmental Psychology, estimates that a staggering 89 per cent of people over 40 with autism remain undiagnosed. To put that into perspective, while around 23 per cent of autistic children under 19 are missed, nearly 96 per cent of those over 60 have never been recognised as autistic. That’s not just a gap; that’s a canyon.
When the researchers broke it down by age and gender, the numbers looked even more lopsided. Among men aged 40 to 59, more than 91 per cent had never been diagnosed. For women in the same age group, the figure was almost 80 per cent. By the time people reached their sixties, both men and women crossed into the 96 to 97 per cent range of being undiagnosed.
Compare that with the 20 to 39 age group, where roughly half remained undiagnosed, and the generational divide becomes clear. Today’s younger adults are far more likely to be spotted, assessed and supported. Older adults, meanwhile, have often been left to muddle through without a name for their lifelong differences.
Gavin Stewart, lead author of the study, explains that a lack of diagnosis means many autistic adults were never offered the right support, leaving them more vulnerable to age-related problems. These range from social isolation to poor physical and mental health.
The review found that autistic people in middle age and beyond have higher rates of almost every health condition compared to non-autistic peers, like heart disease, neurological issues, autoimmune disorders, gastrointestinal problems, anxiety and depression. Add age-related conditions like osteoporosis, arthritis and Parkinson’s disease, and the picture gets even more complicated.
Even more concerning, autistic older adults were six times more likely to report suicidal thoughts or self-harm and four times more likely to develop early-onset dementia.
The study highlighted another layer of challenge: healthcare itself. Many older autistic adults face obstacles in accessing medical support due to communication differences, sensory sensitivities or simply not knowing how to navigate the system. Combine that with a shortage of healthcare professionals trained in recognising autism in adults, and it’s no wonder so many cases slip through the cracks.
Professor Francesca Happé, co-author of the review, stresses that this is a global public health issue. “Understanding the needs of autistic people as they age is a pressing global public health concern. As autistic people age, the nature of the challenges they face changes. We must adopt a lifespan approach that funds long-term research, integrates tailored healthcare, and expands social supports so that ageing autistic people can live happy and healthy lives,” she says. In other words, autism doesn’t disappear after childhood, so neither should support.
The findings also suggest that research into autism may have been skewed for years. If most older adults remain undiagnosed, then studies have largely overlooked them. That means our current understanding of how autistic people age is incomplete at best. No wonder policies and services have not caught up.
Employment struggles, strained relationships and social isolation were all noted as common experiences for older autistic adults. Without the framework of a diagnosis, many never knew why they felt out of step with the world, and their difficulties were often chalked up to personality flaws or “just how they are”.
If you’re wondering whether getting a diagnosis later in life makes a difference, the answer is yes. Recognition can bring clarity, opening doors to support systems, healthcare adaptations and even financial benefits. It can also reshape how family, friends and colleagues understand a person’s behaviour and needs.
The NHS encourages adults who suspect they might be autistic to speak to their GP and ask about a referral for an assessment. Specialists can help by gathering life history, speaking with people who know you well and observing how you interact with others.
The review ends with a clear message: it’s time to stop treating autism as a childhood-only issue. For too long, older autistic adults have been invisible, their experiences untold and their needs unmet. With diagnosis rates still alarmingly low, researchers are urging more studies, better services and a cultural shift that embraces autism across the lifespan.
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