Love Island’s Olivia Bowen Pregnancy Update: Shares How She Grappled With News Of Vanishing Twin Syndrome

Updated Aug 6, 2025 | 11:27 AM IST

SummaryThought to be rare, we all have heard of situations where a twin pregnancy ends up as a single birth of a healthy baby, despite previous inclinations. Olivia Bowen shares her experience with the vanishing twin syndrome.
Love Island’s Olivia Bowen Pregnancy Update – Shares How She Grappled With News Of Vanishing Twin Syndrome

(Credit-Olivia Bowen/Instgaram)

Vanishing Twin Syndrome: The former Love Island contestant Olivia Bowen has recently shared a pregnancy update, following her post about her struggles to grapple with the reality that she will no longer be having twins, but just one healthy young baby.

Within a few weeks of her sharing her twin pregnancy with her fans, she followed up with another post where she broke the devastating news of finding only one baby in the womb.

In the caption she said, “The crazy sickness, the biggest surprise of our lives finding out we were having twins, imagining our lives with two new babies, then the complete heartache of dealing with vanishing twin syndrome & losing one of our babies”.

However, as devastating as the news may be, it is important to note that this is a more common occurrence than people realize. The National Institute of Health, US, statistics show that half of the pregnancies with three gestational sacs go through it and 36% of twin pregnancies also experience this. But what exactly is Vanishing Twin Syndrome?

Also Read: Walking Dead Actress Kelley Mack Dies At 33 After Battling Glioma

What Is Vanishing Twin Syndrome?

According to the American Pregnancy Association vanishing twin syndrome was first recognized in 1945. It's what happens when one of two or more babies in a pregnancy dies in the womb. The other twin, the placenta, or the mother's body then absorbs the dead baby's tissue. This makes it look like one of the babies has "vanished."

Thanks to early ultrasounds, doctors can now spot this more often. It's believed that vanishing twin syndrome happens in about 21-30% of pregnancies with more than one baby.

(Credit-American Pregnancy Association)

Causes and Signs of Vanishing Twin Syndrome

Most of the time, doctors don't know exactly why vanishing twin syndrome happens. However, they've found that the baby who is lost often had chromosomal problems, while the surviving twin is usually healthy. It seems these problems are there from the very beginning of the pregnancy. Another possible cause is that the umbilical cord didn't attach correctly. The signs of a possible vanishing twin syndrome usually happen early in the first trimester. They can include:

  • Bleeding
  • Cramping in the uterus
  • Pain in the pelvis
  • Research shows that this syndrome is more common in women over the age of 30.

How Does The Vanishing Twin Syndrome Affect The Mother And Baby?

If a twin is lost in the first three months of pregnancy, the surviving baby and the mother are usually fine. The living twin's chances of being healthy are very good.

If a twin is lost in the second or third trimester, there can be more risks for the surviving baby, including a higher chance of developing cerebral palsy. In these cases, the dead twin's body can get flattened by the pressure of the growing, healthy twin. At birth, doctors might find this flattened twin, which they call fetus compressus or fetus papyraceous.

How Do You Diagnoses Vanishing Twin Syndrome?

In the past, doctors could only figure out if a twin had died by looking at the placenta after the baby was born. Now, an early ultrasound can show twins in the first trimester. A later ultrasound might then show that one of the babies is no longer there. For example, a woman might see two heartbeats at 7 weeks but only one at her next visit.

If a twin is lost in the first trimester, no special medical care is usually needed for the mother or the surviving baby. However, if the death happens in the second or third trimester, the pregnancy may be treated as high-risk.

If you are pregnant and experience bleeding, cramping, or pelvic pain, you should see a doctor. An ultrasound will help them determine if a fetus is still viable before considering any procedures.

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Ozempic Launches In India At Rs 2,200 For Starter Dose: All You Need To Know

Updated Dec 13, 2025 | 04:24 PM IST

SummaryNovo Nordisk has launched its popular diabetes drug Ozempic in India, with the weekly 0.25 mg starter dose priced at ₹2,200. Approved for adults with type 2 diabetes, the injectable works alongside diet and exercise to help control blood sugar and support weight management.
ozempic price in india 2200

Credits: Canva

Danish drugmaker Novo Nordisk has officially introduced its widely known diabetes medication Ozempic in India, pricing the starter dose of 0.25 mg at ₹2,200 per week. According to a Reuters report, the injectable medicine will be available in three strengths in the country: 0.25 mg, 0.5 mg and 1 mg.

Ozempic is a once-weekly injectable prescribed for people living with type 2 diabetes.

Ozempic Price In India

The weekly injection received approval from the US Food and Drug Administration in 2017 for treating type 2 diabetes. Since then, it has grown into a global blockbuster and is also commonly prescribed off-label for weight loss because of its appetite-suppressing effects.

The lowest strength will cost ₹2,200 per week. Prices for the higher doses have also been announced, as per the Reuters report.

Here are the details:

  • 1 mg dose: ₹11,175/month
  • 0.5 mg dose: ₹10,170/month
  • 0.25 mg dose: ₹8,800/month

All you need To know About Ozempic

India’s drug regulator, the Central Drugs Standard Control Organisation (CDSCO), approved Ozempic, also known as semaglutide, in October this year for adults with type 2 diabetes.

As per the US FDA, Ozempic is prescribed along with diet and exercise to improve blood sugar control in adults with type 2 diabetes mellitus. It is also indicated to reduce the risk of major cardiovascular events in adults with type 2 diabetes who already have heart disease.

As per NDTV Profit, currently, Wegovy is priced at Rs 2,712 per week for the 0.25 mg dose, while the 0.5 mg dose costs Rs 3,462 weekly. The 1 mg dose is also priced at Rs 3,462 per week, and the 1.7 mg dose is available at Rs 4,100 per week. Mounjaro (tirzepatide), a combination therapy of GLP-1 receptor agonist and GIP that helps improve blood sugar control in adults with type 2 diabetes when paired with a healthy diet and regular exercise, is priced at Rs 13,500 per month for the 2.5 mg dose.

How Does Ozempic Help In Weight Loss?

Ozempic mimics the action of a naturally occurring hormone called GLP-1. Here’s how it supports weight loss, as outlined in an earlier HT report.

  • It boosts insulin release when blood sugar levels increase.
  • It slows down the emptying of food from the stomach, helping people feel full for longer after meals.
  • At higher doses, it can also curb appetite, which may aid weight management efforts.

Possible Side-Effects Of Ozempic

As previously reported by Mayo Clinic, some potential side-effects of Ozempic include:

  • An increased risk of inflammation of the pancreas.
  • Possible gallbladder-related problems.
  • According to the FDA, the most commonly reported side effects, seen in at least 5 per cent of patients taking Ozempic, include nausea, vomiting, diarrhoea, abdominal pain and constipation.

This article is intended for informational purposes only and should not be taken as a replacement for professional medical advice.

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Delhi Air Quality Hits ‘Severe,’ GRAP-3 Curbs Kick In: Full List Of Restrictions Explained

Updated Dec 13, 2025 | 02:45 PM IST

SummaryDelhi’s GRAP rules have been tightened, with stricter anti-pollution measures now kicking in earlier as air quality worsens. Here’s what has changed and how the revised stages affect offices, work-from-home rules, and other measures,
Delhi Air Quality Hits ‘Severe,’ GRAP-3 Curbs Kick In

Credits: Canva

Anti-pollution measures under GRAP-3 came into force in Delhi on Saturday as air quality slipped into the “severe” bracket. By noon, the national capital reported an Air Quality Index of 405, according to figures released by the Central Pollution Control Board (CPCB). Earlier in the day, Delhi’s AQI hovered close to 390 during the morning hours.

Delhi Air Quality Hits ‘Severe'

Each winter, Delhi and the surrounding NCR (National Capital Region) bring in curbs under the Graded Response Action Plan, which divides air quality into four levels: Stage 1 (Poor, AQI 201–300), Stage 2 (Very Poor, AQI 301–400), Stage 3 (Severe, AQI 401–450) and Stage 4 (Severe Plus, AQI above 450).

Under GRAP-3, non-essential construction and demolition activities have been halted, along with stone crushing and mining operations. The measures also include restrictions on older diesel goods vehicles within Delhi. Schools up to Class 5 are required to move to a hybrid learning model, while offices across Delhi-NCR may function with only 50 per cent staff strength, as per Press Information Bureau.

Hazardous AQI levels have become a recurring feature across several parts of Delhi during the winter months. Quoting environmental experts, an IANS report linked the sharp decline in air quality to a mix of stagnant wind conditions, vehicle emissions, industrial pollution and seasonal factors such as crop residue burning in neighbouring states.

What Changed in GRAP?

The biggest shift under the updated GRAP framework is that stricter steps will now come into force earlier, instead of waiting for air quality to deteriorate further.

As per Press Information Bureau, under the revised system, measures that were earlier reserved for Stage 4 will now apply at Stage 3 itself. This means that once the AQI reaches the 301–400 range, public, municipal and private offices will function with only 50 percent staff. Central government offices will also move to work-from-home at this stage, rather than waiting for the AQI to cross 450.

In the same way, actions that earlier fell under Stage 3 have now been pushed to Stage 2. As a result, staggered timings for government offices will begin as soon as the AQI enters the 201–300 category.

Stage 2 measures have also been advanced to Stage 1. This brings uninterrupted power supply arrangements into effect earlier, at an AQI level of 101–200, to reduce the need for diesel generator use and limit additional emissions.

Delhi AQI: GRAP Stage 3 Restrictions Announced

In response to the worsening situation, the Delhi government confirmed that the Commission for Air Quality Management (CAQM) has activated all measures under Stage III of GRAP, which falls under the “Severe” air quality category with AQI levels between 401 and 450, across the entire NCR.

These Stage 3 curbs will apply in addition to the existing Stage I and Stage II measures. Authorities, including NCR Pollution Control Boards, have been instructed to step up enforcement to prevent further deterioration of air quality across the region.

  • Ban on the transportation of construction materials such as sand and cement, particularly on non-paved roads
  • Complete suspension of demolition and construction work unless unavoidable, including earthwork, piling and trenching
  • Advisory for private firms to permit work-from-home or hybrid arrangements to reduce traffic-related pollution
  • Restrictions on inter-state diesel buses entering or operating within Delhi
  • Prohibition on BS-3 petrol and BS-4 diesel four-wheelers in Delhi and nearby NCR districts
  • Shutdown of stone crushers, mining operations and hot-mix plants that do not run on clean fuel
  • Ban on the use of diesel generator sets, except for emergency and essential services

GRAP III Imposed in Delhi-NCR: What’s Allowed

Even as Stage III of the Graded Response Action Plan comes into force, certain essential activities and services will continue to operate to minimise disruption to daily life.

  • Essential infrastructure and public service projects permitted include:
  • Metro, railway, airport, highway, defence, healthcare and sanitation-related projects
  • Construction work linked to critical infrastructure, provided strict dust control and proper waste management norms are followed
  • Vehicles used by persons with disabilities
  • Recommended measures under GRAP III include:
  • Greater use of public transport to reduce private vehicle emissions
  • Hybrid or online classes for students up to Grade 5 to limit outdoor exposure and traffic movement

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US FDA Approves First At-Home Device To Treat Depression – Here’s What You Need To Know

Updated Dec 13, 2025 | 02:08 PM IST

SummaryThe US Food and Drug Administration has approved the first at-home brain stimulation device for treating depression, detailing how the Flow Neuroscience headset works, the science behind its approval, who it is meant for, and why experts see it as a major shift in how depression care could be delivered outside clinics.
FDA Approves First At-Home Brain Stimulation Device for Depression

The U.S. Food and Drug Administration has cleared an at-home brain stimulation headset developed by Flow Neuroscience to help treat depression, giving patients another option beyond standard antidepressant drugs, which many people struggle to stay on because of long-term side effects, the company announced on Thursday.

Rates of depression in the U.S. have climbed sharply, rising by about 60% over the past ten years and now affecting more than 20 million adults, according to data from the Centers for Disease Control and Prevention.

FDA Approves First At-Home Brain Stimulation Device For Treatment of Depression

The US Food and Drug Administration (FDA) has approved a home-use brain stimulation device designed to treat major depressive disorder in adults. The device, known as FL-100 and made by Flow Neuroscience, is the first at-home treatment of its kind to receive approval in the United States.

The FDA’s decision was supported by results from the Empower phase 2 clinical trial, which found that 58% of participants reached remission after 10 weeks of treatment. Flow Neuroscience also reported that among users worldwide, 77% noticed an improvement in symptoms within three weeks. To date, more than 55,000 patients have used the device in regions including Europe, the UK, Switzerland, and Hong Kong.

Brain Stimulation Device For Depression: How Will The Headset Work?

The prescription device, called FL-100, uses transcranial direct current stimulation to send a mild electrical current to the brain’s prefrontal cortex, an area involved in mood control and stress response. According to Flow, this part of the brain is often less active in people living with depression, a condition that affects over 20 million adults across the U.S.

Flow noted that roughly one in three people with depression does not respond adequately to antidepressant medications, and many others discontinue them because of unwanted side effects.

“Flow’s FDA approval marks a turning point in depression care, representing the first real move away from medication-only treatment toward technology-based therapies with fewer side effects,” said Flow CEO Erin Lee in a statement.

During the study, participants wore the headset for 30 minutes per session while resting, beginning with five sessions a week for the first three weeks, then reducing to three sessions per week for the rest of the trial. The program also included live remote monitoring through video calls.

Researchers observed benefits in patients who were already taking antidepressants for treatment-resistant depression or receiving psychotherapy, as well as in those who were not using medication at all.

“Among people using Flow in real-world settings, 77% report feeling better in as little as three weeks,” said Kultar Garcha, M.D., chief medical officer at Flow. “A treatment that was once limited to clinics can now be used at home, offering a practical way to widen access to effective depression care.”

Flow said it plans to launch the headset commercially in the U.S. in the second quarter of next year and intends to explore its potential use for conditions such as traumatic brain injury, addiction, and sleep disorders.

“We want Flow to become part of the standard pathway for treating depression,” Lee said. “Our focus is clear: to help as many people as possible reach remission and regain their quality of life.”

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