Department of Health And Human Services Updates Its Guidance For Gender To Comply With Trump's Executive Orders

Updated Feb 20, 2025 | 10:00 AM IST

SummaryThe guidance reiterates the Trump administration's stance that only male and females can be sexes and that it cannot changed.
Gender Ideology

Credits: Canva

Ever since the 47th President of the United States, Donald Trump's inauguration, a lot has changed in the health sector. With his executive orders and DOGE programs, new regulations, cost-cutting and many more new policies have been introduced. The latest update is the US Department of Health and Human Services or the HHS issuing guidance updating its official definition of terms like sex, female, and male on Wednesday following President Trump's executive orders. These orders also limited transgender rights as they denied to identify any other sexes except that of male and female.

The guidance thus reiterates the Trump administration's stance that only males and females can be sexes and that it cannot changed. This guidance is one of the first actions taken by Robert F Kennedy Jr. after his confirmation last week as the Secretary of Health and Human Services.

“This administration is bringing back common sense and restoring biological truth to the federal government,” Kennedy said. “The prior administration’s policy of trying to engineer gender ideology into every aspect of public life is over.”

Why Is This Health Update So Important For the Trump Administration?

On his Inauguration Day, Trump said, "It will henceforth be the official policy of the United States government that there are only two genders - male and female", which will end the "gender ideology" as per the President. While Trump denies to identify the existence of the transgender population, the data says otherwise. As per the US Census Bureau Household Pulse Survey, 1.14% of the nation's adult population or around 3 million Americans are transgenders.

However, their rights have become a heated topic of debate in politics, especially in recent years. In fact, many Republicans too have campaigned to reverse their rights and the laws that safeguard their rights. It is in this backdrop, that a number of executive orders were signed which ended a range of policies promoting and protecting trans rights, and the rights of LGBTQ+ people.

What Does The Guidance Say?

While the guidance has now updates two only two sexes, male and female, the definition of female reads: A person of the sex characterized by a reproductive system with the biological function of producing eggs. For males, it is: A person of the sex characterized by a reproductive system with the biological function of producing sperm.

The sex of a human, female or male, is determined genetically at conception (fertilization), and is observable before birth,” notes the guidance.

HHS also confirmed to comply with Trump's order to prevent the "chemical and surgical mutilation" of children. This refers to the hormonal or surgical treatment of those who wish to change their gender assigned at birth to their own gender identity. This also refers to gender-affirming care, and puberty-blocking medications, which have also been in the scene of heated row.

While the HHS confirmed complying with the President's executive orders, it did not specify which orders they were taking action on. Reuters reports that a federal judge has temporarily blocked health agencies from enforcing the order.

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Foundayo: US FDA Approves Eli Lilly’s GLP-1 Weight Loss Pill

Updated Apr 2, 2026 | 01:31 PM IST

SummaryFoundayo’s approval comes after the US FDA in December last year approved Novo Nordisk’s Wegovy pill — the first-ever GLP-1 pill for weight loss. The Danish drugmaker rolled out the pill in January this year.
Foundayo: US FDA Approves Eli Lilly’s GLP-1 Weight Loss Pill

Credit: iStock

American drugmaker Eli Lilly’s first oral pill for weight loss, Orforglipron, marketed as Foundayo, has been given the green signal by the US Food and Drug Administration (FDA).

Lilly is also known for injectable drugs like Zepbound for obesity and Mounjaro and Trulicity for diabetes.

Foundayo’s approval comes after the US FDA in December last year approved Novo Nordisk’s Wegovy pill — the first-ever GLP-1 pill for weight loss. The Danish drugmaker rolled out the pill in January this year.

Novo Nordisk was also the first to launch oral GLP 1 Rybelsus to treat type 2 diabetes. It was approved by the US FDA in September 2019.

Also Read: World Autism Awareness Day 2026: Can Cell Therapy Be The Future Of Autism Treatment?

In a statement, the US FDA said that "Foundayo has been approved for use in combination with a reduced-calorie diet and increased physical activity. The pill is targeted to reduce excess body weight and maintain weight reduction for the long term in adults with obesity or overweight".

Lilly said that the drug will be available from April 6 through its its direct-to-consumer platform LillyDirect at a cost of $149 per month for the lowest dose for self-pay customers — on par with Novo's pill. "Shortly after” it will be available through retail pharmacies and telehealth providers in the US.

"Today, fewer than 1 in 10 people who could benefit from a GLP-1 are taking one, held back by access, stigma, perceived complexity, or the belief that their condition isn't serious enough for treatment. We believe Foundayo can help level the playing field for those living with obesity or who are overweight and living with weight-related complications," said David A. Ricks, chair and CEO of Eli Lilly and Company.

"As a convenient, once-daily oral pill that delivers meaningful weight loss, this is obesity care designed for the real world," he added.

Foundayo: A Meaningful Reduction In Body Weight

The US FDA approved Foundayo after two randomized, double-blind, placebo-controlled trials in adults with obesity or with overweight showed benefit.

Also Read: Foundayo: US FDA Approves Eli Lilly’s GLP-1 Weight Loss Pill

In these trials, 72 weeks of treatment with Foundayo, in combination with a reduced-calorie diet and increased physical activity, resulted in a statistically significant and clinically meaningful reduction in body weight.

Foundayo: US FDA Approves Eli Lilly’s GLP-1 Weight Loss Pill

Deborah Horn, Director of the Center for Obesity Medicine at McGovern Medical School at UTHealth Houston, stated that Foundayo “delivered an average of 12.4 percent weight loss at the highest dose in clinical trials – addressing both the clinical realities of obesity and the practical challenges patients face every day."

In addition, Foundayo also led to reductions in many markers of cardiovascular risk, including waist circumference, non-HDL cholesterol, triglycerides, and systolic blood pressure across all doses, Eli Lilly said.

How Foundayo Works

Lilly licensed Orforglipron, the main ingredient in Foundayo, from a Japanese pharmaceutical company in 2018.

As with the injectable forms of GLP-1s, Foundayo is available in six doses, ranging from 0.8mg to 17.2mg.

In consultation with their doctors, patients start with the lowest dose and gradually work up to higher doses; not everyone may need to reach the highest dose.

Also read: Eli Lilly's Experimental GLP-1 Pill Shows Promising Weight Loss

Unlike the Wegovy pill, people taking orforglipron do not need to restrict food or drink after taking the pill. Orforglipron is a small molecule that the body can absorb quickly and get into the blood, where it reaches the necessary tissues.

Foundayo: Side Effects

Foundayo is not safe for use in children and has an increased list of side effects, such as tumors in the thyroid, including thyroid cancer.

The drugmaker urged watching for possible symptoms, such as

  • a lump or swelling in the neck,
  • hoarseness,
  • trouble swallowing
  • shortness of breath.
Other common side effects of Foundayo include

  • nausea,
  • constipation,
  • diarrhea,
  • vomiting,
  • indigestion,
  • stomach (abdominal) pain,
  • headache,
  • swollen belly,
  • feeling tired,
  • belching,
  • heartburn,
  • gas,
  • hair loss.

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New Zealand Launches Surveillance After Spotting Dengue, Zika-carrying Mosquito Larvae

Updated Apr 2, 2026 | 12:31 AM IST

SummaryHealth officials confirmed that the larval species were 'Aedes aegypti'. ​​As New Zealand does not normally have the mosquito species, the larvae detected were counted as "exotic". ​The mosquito species did not cause any outbreak, but were spotted during a routine surveillance program in Auckland.
New Zealand Launches Surveillance After Spotting Dengue, Zika-carrying Mosquito Larvae

Credit: Canva

New Zealand has stepped up surveillance after the first detection of a dengue and Zika-carrying mosquito larvae in the country.

The larval species was confirmed as 'Aedes aegypti' — known to carry diseases including dengue fever, yellow fever, Zika, and chikungunya, across the globe.

As New Zealand does not normally have the mosquito species, the larvae detected were counted as "exotic".

The mosquito species did not cause any outbreak, but were spotted during a routine surveillance program in Auckland.

"The National Public Health Service has commenced a heightened surveillance and interception programme following mosquito larvae being collected from a routine surveillance trap at Queens Wharf, Auckland, on Monday 30 March," Health New Zealand said in a statement.

Health New Zealand reported that exotic species were occasionally found at ports and airports.

Not A Public Threat Yet

The health body noted that the larvae were not considered a public health or biosecurity threat yet because there was no indication they had become established.

But the agency aimed to continue "intensive monitoring for at least three weeks".

"The monitoring would take place within a 400m radius of the site where the larvae were identified. Health Protection Officers would place mosquito traps in the survey area," the statement said.

"These have been hidden away from plain sight so they are not disturbed, for example, in old tyres, bushes, or pools of water. We ask members of the public to avoid touching or disturbing these traps if they find them, as it may disrupt our monitoring and trapping efforts," medical officer of health Dr David Sinclair said.

Sinclair said New Zealanders were most at risk from diseases transmitted by mosquitoes when travelling overseas, including to Pacific Island countries and territories where dengue fever was known to be present.

Dengue Surging In 17 Countries

The US Centers for Disease Control and Prevention recently issued a travel alert of dengue outbreaks across 17 countries.

The CDC alert issued on March 23 identified 17 countries reporting an increased number of cases of dengue. These include: Afghanistan, Bangladesh, Bolivia, Colombia, Cook Islands, Cuba, Guyana, Maldives, Mali, Mauritania, New Caledonia, Pakistan, Samoa, Sudan, Timor-Leste, Vietnam, and the United States territories of American Samoa, Puerto Rico, and the US Virgin Islands, where local transmission is already common.

Also read: Long-term Exposure To Air Pollution Increases Fatality Rates In Dengue: Study

What Is Dengue?

Dengue is a disease caused by a virus spread through mosquito bites. It is transmitted through infected mosquitoes, primarily the species Aedes aegypti.

The breakbone fever is caused by an infection with any of four different dengue viruses. These include:

• Dengue virus type 1 (DENV-1 or DEN-1)

• Dengue virus type 2 (DENV-2 or DEN-2)

• Dengue virus type 3 (DENV-3 or DEN-3)

• Dengue virus type 4 (DENV-4 or DEN-4)

Also read: New dengue vaccine over 80% effective, prevents severe disease for up to 5 years

Common Symptoms of dengue include:

• Sudden onset of high-grade fever.

• Intense headache

• Severe muscle, joint, or bone pain.

• Skin Rash that often appears 2–5 days after the fever starts

• Nausea and Vomiting

• Minor bleeding

• Fatigue.

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COVID Cicada variant: Are Children More At Risk? How To Safeguard?

Updated Apr 1, 2026 | 10:30 PM IST

SummaryExperts explained that due to 75 mutations to the spike protein, the body’s antibodies will take a longer time to fight the Cicada variant.However, there is no evidence yet that it is likely to cause more severe disease.
COVID Cicada variant: Are Children More At Risk? How To Safeguard?

Credit: iStock

The COVID Cicada variant, currently circulating in 23 countries, is likely to affect children more than the previous variants.

Children have largely escaped severe illness from the SARS-COV-2 virus.

However, the new Cicada variant with around 75 genetic changes in its spike protein is likely to disproportionately affect children, as per an expert, who noted its presence in the UK.

“Some people have done analysis on this, suggesting it may be more prevalent among young children. Children get infections all the time, but this might be something to do with the fact that they have never been exposed to Covid vaccines," Prof Ravindra Gupta, of Cambridge University, who advised the UK government during the pandemic, was quoted as saying to The Mirror.

“So this is something we’re looking at in the lab to try and work out why. The problem with this is that it is an infection that spreads fast. Eventually, it ends up in someone vulnerable," he added.

Key Symptoms

Symptoms seem to be similar to those of other recent variants and include

  • sore throat,
  • cough,
  • congestion,
  • fatigue,
  • headache
  • fever.
According to the US-based Centers for Disease Control and Prevention (CDC), the Cicada variant is also likely to raise gastrointestinal issues such as nausea or diarrhea.

Also read: Cicada Variant: Will The Current COVID Vaccine Provide Protection?

What Do The 75 Genetic Changes Mean?

Cicada, a descendant of the Omicron variant that emerged in 2021, was first detected in South Africa in 2024. However, it disappeared soon after, only to emerge early this year.

Prof Gupta told the publication that “the Cicada variant developed the 75 mutations to escape immunity, and it evolved by incubating a single patient for over a year”.

"This 'patient zero' would have been unable to clear the virus due to a compromised immune system," due to HIV or anti-cancer drugs.

Further, he explained that due to 75 mutations to the spike protein, the body’s antibodies will take a longer time to fight the Cicada variant.

However, there is no evidence yet that it is likely to cause more severe disease.

Will The Cicada Variant Cause Severe Illness?

The Cicada variant is particularly concerning as it provides no immune protection to people with previous infection or even vaccination.

Yet, the World Health Organization and health experts advise that existing COVID vaccinations can help prevent severe illness and hospitalization.

"It would appear that all the protections we have from our experience with the virus and with vaccines probably offer more limited—not zero—but more limited protection against this strain," Dr. William Schaffner, professor of infectious diseases at Vanderbilt University Medical Center, was quoted as saying by Time.

Also read: COVID Variant BA.3.2 Spreads To 23 Countries: Is The Variant Under Monitoring A Cause Of Worry?

How To Safeguard

Dr. Sai Balasubramanian, a doctor and healthcare strategy executive, writing in Forbes, stressed the need to follow COVID practices such as masks and hand hygiene.

"Healthcare professionals recommend taking general precautions, similar to those used to prevent most viral transmission: get vaccinations when appropriate, wear masks in crowded areas or indoors where there is a high risk of transmission," he said.

He also urged “avoid individuals who have known illness or infections, wash hands frequently, and continue to stay apprised of local community guidelines and the infection spread”.

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