Singer Jesy Nelson recently shared an emotional update regarding the complications she is experiencing in her pregnancy with twin babies. Former Little Mix singer Jesy, who is having twins with partner Zion Foster, announced that she has been diagnosed with pre-twin-to-twin transfusion syndrome (pre-TTTS). The condition, which is present in pregnancies involving twins with a shared placenta, has serious risks involved and needs intense medical supervision. As Nelson embarks on this difficult journey, her story enlightens us about a rare but dangerous condition many expectant parents may not know much about.
Twin-to-twin transfusion syndrome is a rare but dangerous condition that arises in monochorionic twin pregnancies, in which identical twins share a single placenta. The placenta supplies the developing babies with oxygen, nutrients, and blood flow, but in TTTS, there is an imbalance of blood vessels that interconnect the twins, and thus the vital resources are not evenly distributed. One twin, or the donor twin, shares excess blood with the other, referred to as the recipient twin. This leads to one baby becoming malnourished and possibly anemic, and the other in danger of heart problems due to too much blood.
Nelson described her diagnosis in a heartfelt Instagram video, explaining that she is currently in the pre-stage of TTTS and undergoing frequent monitoring. "I am being scanned twice a week, and each time, things have gotten a little worse," she shared, expressing her fears and hopes for the health of her babies.
If left untreated, TTTS can have devastating consequences. Medical research indicates that:
TTTS usually advances in stages, beginning with minimal changes in fluid levels and worsening as one twin continues to get an unequal share of blood. In extreme cases, fetal laser surgery, referred to as the Solomon technique, can be employed to divide the blood vessels and balance the twins.
Identical twins may develop differently, and their own unique form of placental sharing can have a dramatic effect on pregnancy risk. Jesy Nelson's twins are considered monochorionic diamniotic (mono/di), which means they share a placenta but have two amniotic sacs. This is the type of pregnancy in about 70% of identical twin pregnancies and carries an increased risk of complications like TTTS, umbilical cord entanglement, and growth restriction.
Conversely, dichorionic diamniotic (di/di) twins both have a separate placenta and amniotic sac, which greatly diminishes the threat of TTTS. Twin pregnancy type is normally identified by early ultrasound, with physicians being able to track future complications from inception.
Twin pregnancies, even without the presence of TTTS, entail a variety of health risks to the mother as well as infants:
Over 60% of twin pregnancies end in premature delivery, with birth usually taking place before 37 weeks. Premature infants can have immature organs and need neonatal intensive care (NICU) assistance to assist with breathing, feeding, and infection fighting.
Pregnant women with multiples are at increased risk of having high blood pressure during pregnancy. This, if left untreated, can result in preeclampsia, a serious complication of pregnancy that can result in damage to organs, preterm labor, and in some cases, maternal or fetal death.
Pregnant women carrying multiples are twice as likely to experience anemia, a condition where the body does not produce enough healthy red blood cells. This can lead to fatigue, dizziness, and complications during delivery.
According to John Hopkins Medicine, multiple birth babies are twice as likely to have congenital abnormalities compared to single births. These can include heart defects, neural tube defects, and gastrointestinal issues.
When twins have to share a placenta, they are more likely to have polyhydramnios (excess amniotic fluid) or oligohydramnios (not enough amniotic fluid). Both result in distress to the babies during fetal development and can result in premature labor.
Twins are at increased risk of excessive postpartum hemorrhage because their uterus is larger and there are greater blood supply needs.
Jesy Nelson's openness about her challenging experience is raising awareness for TTTS, a condition that few individuals—let alone expectant mothers and fathers—might be aware of. Through her tearful video, Nelson stressed the significance of knowing about twin pregnancies aside from the thrill of having multiples. "We had no idea that this type of thing occurs when you're having twins. We just desperately want to make people aware of this because there are so many people who aren't aware."
Her case reminds us of the intricacies involved in twin pregnancy and the significance of early identification and medical management. For mothers carrying twins, frequent ultrasounds and vigilance can become a life-and-death issue for early detection and better outcomes of both babies.
Through constant medical attention and care, she and her partner Zion Foster remain positive and get ready for their babies to be born. In other parents whose situations are no different, the story of Nelson highlights awareness, medical progress, and emotional encouragement in handling complicated pregnancies.
The expecting parents of twin siblings are advised to discuss TTTS screening and possible interventions with their physicians to give their babies the best chance.
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The US Food and Drug Administration has approved a new breast cancer treatment that aims to act on signs of treatment resistance before the cancer starts progressing.
The US FDA has granted accelerated approval to Etcamah (camizestrant), in combination with a CDK4/6 inhibitor, for adults with hormone receptor-positive, HER2-negative locally advanced or metastatic breast cancer whose tumours develop an ESR1 mutation while being treated with an aromatase inhibitor and a CDK4/6 inhibitor.
The new approach uses a blood test to detect circulating tumour DNA (ctDNA) carrying an ESR1 mutation. If the mutation is detected, doctors can switch treatment to camizestrant rather than waiting for visible disease progression on scans.
The FDA described this as its first cancer therapy approval guided by detection of a resistance mutation in circulating tumour DNA before imaging shows progression of the disease.
Also read: Have Dense Breasts? What Women Should Know About Their Breast Cancer Risk
The approval was based on results from the Phase III SERENA-6 trial, which included 315 patients with HR-positive, HER2-negative locally advanced or metastatic breast cancer.
All participants were receiving an aromatase inhibitor plus a CDK4/6 inhibitor as their initial endocrine based treatment and had no evidence of disease progression when an ESR1 mutation was detected through blood testing.
Patients were randomly assigned to either switch to camizestrant while continuing their CDK4/6 inhibitor or continue their existing aromatase inhibitor with the CDK4/6 inhibitor.
Survival period without progression was 16 months with camizestrant compared with 9.2 months with standard treatment. The risk of disease progression or death was reduced by 56% with the camizestrant combination.
Also read: Alcohol-Linked Cancer Deaths Doubled In US: Colorectal Leads In Men, Breast Leads In Women
ESR1 mutations are one way hormone receptor-positive breast cancers can adapt to treatment. According to the FDA, fewer than 5% of patients have an ESR1 mutation when HR-positive metastatic breast cancer is first diagnosed. After disease progression on an aromatase inhibitor, however, the mutation is found in nearly 40% of patients.
This means that detecting the mutation earlier could potentially give doctors a chance to change treatment while the cancer is still controlled.
Dr Kevin Kalinsky, an investigator on SERENA-6, said, "The approach allows doctors to change treatment at an earlier opportunity ahead of disease progression rather than waiting until the cancer becomes harder to treat."
The FDA approval is accelerated, meaning continued approval may depend on confirmatory studies that will verify clinical benefit.
The regulator specifically noted that it has not yet been established whether intervening when an ESR1 mutation is detected, before radiographic progression, ultimately translates into a meaningful overall survival benefit.
The FDA has simultaneously approved the Guardant360 CDx blood test as a companion diagnostic to identify patients whose tumours carry the relevant ESR1 mutations.
The significance of the approval therefore goes beyond a new drug. It represents a shift toward using molecular clues in the bloodstream to detect treatment resistance and change therapy before cancer progression becomes visible on a scan.
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Illegal horse trade across the US-Mexico border are raising fresh concerns among US officials and ranchers as the country tries to contain the spread of New World screwworm, a flesh-eating parasite that can cause severe and possibly fatal wounds in animals.
According to Reuters, horses and other animals are continuing to cross the border outside regulated channels, bypassing veterinary inspections designed to detect diseases and parasites.
There is no confirmed link between individual smuggled horses and specific screwworm cases, but experts warn that uncontrolled animal movement creates a gap.
Unlike ordinary maggots that generally feed on dead tissue, screwworm larvae feed on living tissue, creating wounds that can become severe as more larvae develop. The parasite can infest cattle, horses, pets and wildlife and, more rarely, humans. An untreated infestation can cause serious tissue damage and death.
The US had previously eradicated the parasite through a decades-long campaign involving the release of sterilised male flies. But New World screwworm has been moving northward through Mexico and is now threatening US livestock again.
Also read: Wegovy & Zepbound Are Not Approved By US FDA For Children Under 12: So Why Are Prescriptions Rising?
Animals entering the US through legal channels undergo veterinary checks and must meet health requirements. Smuggled animals can bypass those safeguards.
Reuters reported that authorities in Presidio County, Texas, have intercepted more than 50 smuggled horses over two years. Some were reportedly moved through remote areas along the Texas-Mexico border, making them difficult to monitor.
That matters because an infected animal can potentially carry screwworm larvae or adult flies into new areas.
USDA officials have described animal trafficking as a biosecurity concern. However, authorities have not established that illegally transported horses are responsible for particular screwworm infections in the US.
The parasite was previously eliminated from the US, making its recent return a major agricultural concern.
The USDA says New World screwworm is a devastating pest capable of causing serious, often deadly damage to livestock. It can also affect pets, wildlife and, in rare circumstances, people.
The economic consequences include potential damage from a major Texas outbreak at up to $1.8 billion, reflecting losses to livestock and related industries.
The threat comes as the US is also navigating the difficult balance between controlling screwworm and maintaining livestock trade with Mexico.
In August, the US began a phased reopening of Mexican cattle imports after a more than year-long suspension linked to the screwworm threat. Mexico has simultaneously been releasing sterile flies and other containment efforts along its northern border.
One of the main tools is the sterile insect technique. Large numbers of male screwworm flies are sterilised and released into affected areas. When they mate with wild females, they produce no viable offspring, helping reduce the population.
As of September 4, the agency said the current risk to animals and people in the US remained very low, and stressed that screwworm is not a food-safety issue. But illegal animal trade complicates those efforts.
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The use of GLP-1 medications weight-loss medications among children under 12 in the US has risen in recent years, according to a new study. This has raised questions about how these drugs should be used in younger children and what is known about their long-term effects.
Researchers studied health records from more than 3.5 million children aged 8 to 11 with obesity and found that prescriptions for GLP-1 medications increased more than 300-fold between 2019 and June 2026.
In 2019, only about 0.03% of children in the study group had been prescribed a GLP-1 drug. By June 2026, that figure had risen to 9.3%.
The medications included drugs like Wegovy and Saxenda, made by Novo Nordisk, and Eli Lilly's Zepbound.
The researchers used data from Epic Cosmos, a large electronic health-record database covering patients across the US. Epic was not involved in the study.
Also read: The New Nutrition Gap: Why Knowing What To Eat Doesn't Mean We Actually Eat It
The rise does not appear to represent routine prescribing for children who are simply above a healthy weight.
Among children receiving GLP-1 medications, 94% had severe obesity, while about 65% had obesity-related health conditions, including high blood pressure or sleep apnea.
Childhood obesity can increase the risk of metabolic and cardiovascular problems. Hence, along with lifestyle changes, doctors are increasingly looking for treatments.
One of the major concerns surrounding the findings is that the GLP-1 medications included in the study are not formally FDA-approved for weight management in children younger than 12.
However, doctors can prescribe medicines off-label when they believe there is a medical reason to do so. Clinical guidelines can also support the use of obesity medications in certain circumstances involving younger children.
The study therefore does not necessarily mean that doctors are prescribing these drugs indiscriminately. Instead, it shows how rapidly their use has expanded among children with obesity.
Also read: The Postpartum Nutrition Gap: Why New Mothers Often Neglect Their Own Health After Delivery
Dr Babak Orandi of NYU Langone Health, one of the researchers, highlighted the importance of long-term monitoring as these medications become more widely used in younger children.
He said that while the absolute numbers of children under 12 receiving GLP-1 treatment is still low, the study shows that GLP-1 use is accelerating rapidly among that age group. Orandi also said that long-term safety monitoring is needed to ensure the drugs remain safe and effective for children.
Additionally, children from higher-income households were 55% more likely to be prescribed the drugs than lower-income communities. This suggested emerging disparities in access, according to the study published in the journal Pediatrics.
"Physicians and health policymakers alike have a responsibility to ensure ... these valuable and sometimes costly treatments become available to more than those who have access to health insurance and can afford to visit pediatric clinics," said Allan Massie, co-author of the study and associate professor of surgery at NYU Grossman School of Medicine.
So even if these medicines prove to be useful for treating severe childhood obesity, access may depend partly on a family's ability to obtain the medicine, insurance coverage and treatment.
GLP-1 drugs can cause side effects like nausea, vomiting, diarrhoea and constipation. But questions around prolonged use during childhood extend beyond short-term side effects, including how treatment may affect growth, development and nutritional health over time.
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