Every year, World Toilet Day is observed to raise awareness about the global sanitation crisis and encourage action to solve it. The goal set by the United Nation is to achieve safe toilets for all by 2023, as a part of their Sustainable Development Goals.
The UN also states that 3.5 billion people live without proper sanitation and many children also lose their lives due to poor sanitation and unsafe water. This is why World Toilet Day is observed to raise awareness on this issue.
This year, the theme for World Toilet Day 2024 is "Toilets - A Place for Peace'. This focuses on the growing threat to sanitation that is caused by conflict, climate change, disaster and neglect. When there is a threat to using toilets, it can lead to many health risks.
Not using toilets for too long may lead to Urinary Tract Infection or UTI. For many who do not have access to clean toilets do not drink enough liquid or hold pee for too long. Doctors suggest that holding in pee for too long can cause bacteria to multiply and lead to UTI. By not drinking enough water, your bladder fails to tell the body to pee often, and can cause the bacteria to spread through the urinary tract, which can lead to infection.
Holding in pee for too long can also cause your bladder to stretch, making it difficult or even impossible for the bladder to contract and release pee normally. It can also damage your pelvic floor muscles or could lead to kidney stones.
To prevent such conditions, it is important that everyone has access to clean and safe toilets. In terms of history, the day was established in 2001, by the World Toilet Organization (WTO), which was founded by Jack Sim. However, it was officially recognised by the UN in 2013. The Government of Singapore worked with WTO to create the first UN resolution called Sanitation for All.
India too promotes safe and hygiene toilet through its Swachh Bharat Yojna.
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The XFG COVID-19 variant is driving a rise in cases and hospitalizations in the UK and France, while some US regions are also reporting increases.
XFG, nicknamed ‘American COVID’ or Stratus, is a recombinant SARS-CoV-2 variant from the Omicron lineage, formed from LF.7 and LP.8.1.2. The WHO recorded the earliest documented XFG sample on January 27, 2025, and designated it a variant under monitoring in June 2025.
The NHS has advised infected people to stay home to limit spread. The UK is rolling out COVID vaccination, while France is expected to begin its campaign next week.
COVID and flu symptoms can overlap, including cough, fever, sore throat, headache, runny nose and fatigue.
In France, the estimated number of people with COVID consulting GPs for acute respiratory infections rose to 13 per 100,000, from nine the previous week, according to The Connexion. This translates to around 8,806 new cases, up from about 6,000.
In England, hospital PCR positivity rose from 5.9% to 7.0% in the week to September 20, while hospital admissions increased from 0.81 to 1.20 per 100,000. Overall activity remained low.
US CDC data from September 29 showed cases rising in some states while falling or remaining stable in others.
Also read: ‘American Covid’ Strain Drives 50% Surge in UK Hospital Admissions: XFG Symptoms to Know
HealthandMe spoke to experts who said the UK-France rise does not necessarily mean India will see a similar increase.
“The rise in COVID-19 cases in the UK and France does not necessarily mean that India is headed towards a similar increase,” said Dr Suranjit Chatterjee, Senior Consultant, Internal Medicine, Indraprastha Apollo Hospitals, Delhi.
XFG is being monitored because it has become more common in some countries, but available evidence does not indicate that it causes more severe illness than other circulating variants.
“For India, the more relevant question is whether XFG is increasing locally and whether this is translating into a rise in symptoms or hospitalizations,” Dr Suranjit told HealthandMe .
Dr Amit Prakash Singh, Consultant - Internal Medicine, CK Birla Hospital, Delhi, said the spread of XFG highlights the need for continued surveillance as SARS-CoV-2 evolves.
“Yet at present there is no evidence to indicate that the XFG variant causes more severe disease than the other Omicron-lineage variants,” he said.
However, the “main concern for India would be a greater rate of transmission, especially among older people, those with comorbidities and the immunocompromised, should the variant become more common in the country”.
Read More: COVID-19 Cases Rise In France, Vaccination Campaign Set To Start Next Week
Dr Amit told HealthandMe India should continue genomic surveillance and monitor hospitalizations and severe disease rather than focusing only on case numbers.
Dr Suranjit said international travel can introduce new variants, but their impact depends on community spread and existing immunity.
“At this stage, there is no reason for people (in India) to be unduly concerned or change their daily routine.”
He added that continued surveillance, timely testing when symptoms occur and sensible precautions during respiratory infections remain appropriate.
XFG-specific vaccines have been developed and are either in use or authorized in several countries. The US and UK have opted for XFG-targeted formulations for the 2026–27 season.
In India, an XFG-specific vaccine should be considered available only after regulatory approval and commercial supply.
The WHO continues to stress that vaccination should not be postponed while waiting for an updated formulation.
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The Supreme Court, on Thursday, asked the Centre to form a panel to form statutory regulations against unethical practices by pharmaceutical companies. This includes gift giving, hospitality, and other incentives offered to doctors.
A bench of Justices Vikram Nath and Sandeep Mehta issued the direction while hearing a petition seeking stronger regulation of pharmaceutical marketing practices.
The court wants the committee to recommend whether, and how, the unethical interactions between pharmaceutical companies and doctors should be brought under a legally enforceable framework.
The matter will resume in court on January 29, 2027, when the Centre is expected to show compliance with the directions.
The court's order follows earlier concerns about whether the existing system is equipped to prevent unethical pharmaceutical marketing.
Justice Sandeep Mehta, reading out the order, said, “We have directed the Union of India to constitute the committee and give its recommendations in terms of our previous directives and observations.”
The committee will examine the representations received and make recommendations to the Union government on the need for statutory regulation.
The Court had reserved order after Solicitor General Tushar Mehta informed the Court that the Union government is to form a three-member committee to assess whether a statutory framework is needed to regulate unethical practices by pharmaceutical companies.
The case was filed by the Federation of Medical and Sales Representatives' Associations of India (FMRAI), which has sought accountability for alleged practices such as expensive gifts, foreign trips, hospitality and other benefits used to promote medicines to doctors.
It said, “This has led to over-prescription of drugs resulting in a serious infringement of the right to life and the right to health of the citizens.”
Also read: Russia Denies Second Plague Case As WHO Seeks Answers On Lab Death; Trump Says It’s Not A Bioweapon
Pharmaceutical companies use various marketing strategies to promote their products to healthcare professionals. These can include gifts, hospitality, sponsored travel, benefits related to conference and other promotional incentives.
The concern before the Supreme Court is not just an ordinary interaction between drug companies and doctors, but whether financial or material incentives can unethically influence drug-prescribing decisions.
India already has the Uniform Code for Pharmaceutical Marketing Practices (UCPMP), 2024, which lays down rules concerning gifts, physician samples, brand reminders, continuing medical education and other promotional activities. However, questions remain over whether the framework has adequate statutory regulation.
The Centre has previously said the UCPMP is functioning, but agreed that the question of giving pharmaceutical marketing regulation statutory backing should be examined separately.
The Centre, in its response, said, “The Department of Pharmaceuticals has issued the Uniform Code for Pharmaceutical Marketing Practices (UCPMP), which is applicable to Pharmaceutical Companies, medical representatives and agents.” The code clearly prohibits pharmaceutical companies from offering gifts, travel facilities, hospitality, cash or monetary grants to physicians or their family members, it added.
The biggest concern is that a prescribing decision could become influenced by factors other than clinical need, evidence, safety, and cost. If incentives influence prescribing, patients could potentially face:
These concerns have previously been raised before the Supreme Court in relation to alleged pharmaceutical marketing practices. The issue, therefore, goes beyond ethics for patients. The doctor-pharma relationship can directly affect what medicine a patient receives, how long they take it, and how much they pay.
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Artificial intelligence (AI) is moving deeper into biological research, with Meta, Google DeepMind, the US government and other partners backing a $1.8 billion effort to build AI-ready biological datasets and predictive models of life that could help scientists better understand, predict and treat diseases.
Mark Zuckerberg and Priscilla Chan-backed nonprofit Biohub first announced the Virtual Biology Initiative in April 2026 with a $500 million commitment.
The five-year effort aims to generate large-scale, multimodal biological data that could help scientists develop AI models capable of predicting how cells respond to different interventions — potentially accelerating disease research, drug discovery and the development of new treatments.
The initiative has now expanded through partnerships involving the US Department of Energy, National Institutes of Health, Meta, Google DeepMind and Isomorphic Labs, bringing the total commitment to $1.8 billion.
“An accurate predictive model of biology could dramatically accelerate scientific discovery by enabling scientists to perform experiments digitally. The insights that come from this could unlock a far greater understanding of disease and open up completely new paths for cures,” said Biohub Head of Science Alex Rives.
“Because of this potential, the creation of a virtual cell is one of the most important challenges for the next era of science. It will require coordinated data generation efforts at a national and international scale, which is why these partners are coming together. We invite the worldwide scientific community to join us in this project,” he added.
Also read: Anthropic, OpenEvidence Expand Clinical AI Globally: WHO Warns of Ethics Risks
The Virtual Biology Initiative aims to coordinate biological data generation across institutions and scientific disciplines, creating open, AI-ready datasets that can support predictive models of life.
The broader goal is to build increasingly accurate models of the complex workings of cells, allowing scientists to investigate biological mechanisms and understand how diseases develop. Such models could allow researchers to ask and test questions digitally at a scale and speed that would be difficult to achieve through laboratory experiments alone.
If successful, the approach could help accelerate scientific discovery, identify potential biological targets and support the development of therapies for complex diseases.
Of that commitment, $400 million supports technologies designed to expand what scientists can measure, including cryo-electron tomography to resolve near-atomic details inside cells, microscopy capable of imaging millions to billions of cells in living tissue, and engineering tools to build and perturb biology at molecular, cellular, tissue and whole-organism levels. A further $100 million supports research outside Biohub.
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