Classic re-issued to mark its 60th anniversary still resonates
By MITA MISTRYJun 23, 2021
THE greatest literary classics have a timeless quality, which enables them to connect to different generations, and some like Sunlight On A Broken Column are so special that their underlying message has the same impact decades later.
The unforgettable classic, first published in 1961, is getting reissued on July 15 to mark its 60th anniversary and is remarkably one of only two books written by hugely influential author Attia Hosain, who was in her eighties when she passed away in 1998, with the other being a collection of short stories.
The coming-of-age story set in the lead up to the turbulent Partition of India revolves around an orphan girl from a distinguished Muslim family brought up in her conservative grandfather’s house, where she is made to keep a purdah and then her move to a liberal autocratic uncle’s guardianship.
Then she gets the first taste of freedom at university but is torn between centuries old tradition and a world quickly heading towards modern culture. There is also conflict as people begin to take sides ahead of Partition, which mirrors her own inner struggle.
It is no surprise the novel continues to be admired 60 years after publication. The absorbing story beautifully brings 1930s India to life with lovely descriptions and contrasting lives of different communities by a writer who was obviously connected to that time. That authenticity in all things, including mannerisms, setting and political turmoil, adds weight to the story but also gives modern day readers an interesting insight into an important period in history.
The protagonist is from a different era, but is wholly relatable and touches upon issues
and emotions that are relevant even today. The novel marks 60 years and will likely power on in the decades ahead. The only downside is that author Attia Hosain didn’t write another novel because this one is so good.
Singer Jessie J has announced she was diagnosed with early-stage breast cancer in April, sharing the news with her fans via an emotional video posted to Instagram. The 37-year-old artist revealed that she had been undergoing medical tests for the past two months while continuing to perform and release music.
“I was diagnosed with early breast cancer,” said Jessie J, whose real name is Jessica Cornish. “Cancer sucks in any form, but I’m holding on to the word ‘early’.” The Price Tag singer explained that she had been “in and out of tests” since her diagnosis, while still managing her music career and public commitments.
Balancing health and career
Jessie J said the diagnosis came shortly before the release of her latest single, No Secrets. She is scheduled to perform at Capital’s Summertime Ball at Wembley Stadium on 15 June, after which she plans to undergo surgery.
“I am going to disappear for a bit after Summertime Ball to have my surgery,” she said. “And I will come back with massive tits and more music,” she added, using humour to manage what she described as a deeply challenging experience.
Despite the serious nature of the diagnosis, Jessie J said she was choosing to focus on the fact it was caught early and expressed gratitude that it had been identified in time for treatment.
Opening up about timing and emotions
She also reflected on the timing of the diagnosis, which coincided with the promotional rollout for songs including No Secrets and Living My Best Life. Both singles were prepared in advance of her diagnosis, making the coincidence especially poignant.
“To get diagnosed with this as I’m putting out a song called No Secrets right before a song called Living My Best Life… you can’t make it up,” she said.
Jessie J explained that she needed time to process the news, and decided to speak publicly as a way of confronting the reality of her illness and to reach out to others going through similar experiences. “I just wanted to be open and share it,” she said. “Selfishly, I do not talk about it enough. I’m not processing it because I’m working so hard.”
Support from fans and friends
After her announcement, fans and fellow celebrities expressed their support in large numbers. TV presenter Gaby Roslin commented, “Sending you so much love and enormous hugs,” while others offered similar messages of encouragement and solidarity.
One follower wrote, “God is already busy healing you. You give us so much kindness. It’s time for the universe to give back some of that light.” Another said, “You are not alone. May your recovery be gentle, peaceful, and full of healing. Sending you a tight hug and all the love my heart can carry.”
Jessie J later shared on her Instagram story that she was still emotionally processing the situation. “Honestly, I need to process it and talk about it. I need a hug,” she said.
Ongoing health struggles
This is not the first time Jessie J has had to face serious health issues. She was diagnosed with a heart condition at the age of eight and suffered a minor stroke at 18. In 2020, she experienced a brief period of hearing loss, and in 2021, she went through the trauma of a miscarriage.
The singer welcomed her first child, son Sky Safir Cornish Colman, in May 2023Getty Images
In May 2023, she gave birth to her first child, a son named Sky Safir Cornish Colman, with her partner Chanan Safir Colman, a retired Danish-Israeli basketball player. Sharing her journey as a new mother has formed part of her recent online updates, as she balances her personal life with her return to the stage.
Tour still planned
Despite her diagnosis and upcoming surgery, Jessie J has not postponed or cancelled her planned tour dates. The European and UK No Secrets Tour 2025 is still scheduled to begin later this summer, with the opening show set to take place in Amsterdam.
While there may be adjustments to her schedule in the coming months, the singer has indicated she remains committed to performing and sharing new music with fans.
Spreading awareness
By sharing her diagnosis, Jessie J has once again demonstrated her openness with fans and her willingness to use her platform to raise awareness. While she acknowledged that she has not always taken time to fully process her own experiences, she said that hearing from others going through similar struggles has helped her feel less alone.
“It breaks my heart that so many people are going through so much similar and worse—that’s the bit that kills me,” she said.
With her tour on the horizon and treatment ahead, Jessie J continues to face her health challenge with strength and honesty—qualities that have long defined her music and public persona.
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This variant has raised concern due to its increased transmissibility.
A new strain of Covid-19, named NB.1.8.1, has been identified in the UK and several other countries, more than five years after the initial outbreak of the virus. While the variant does not appear to cause more severe illness, it has raised concern due to its increased transmissibility.
Where has NB.1.8.1 been detected?
The variant NB.1.8.1 has been confirmed in parts of the UK, including Northern Ireland and Wales. Globally, cases have also been reported in the United States, Australia, Thailand, and across China and Hong Kong, where it is currently the dominant strain.
According to the World Health Organization (WHO), NB.1.8.1 now accounts for over 10 per cent of all Covid-19 cases worldwide. The WHO has classified it as a “variant under monitoring”, meaning it is being closely observed but is not currently listed as a variant of concern.
How is NB.1.8.1 spreading?
Experts believe NB.1.8.1 has a growth advantage compared to previous strains, which may explain its increasing presence in different countries. It appears to infect cells more efficiently than earlier variants, potentially making it more transmissible.
A WHO spokesperson explained that the variant dynamics have shifted significantly in recent months. At the beginning of 2025, the most prevalent variant globally was XEC, followed by KP.3.1.1. However, XEC’s circulation began to decline in February while another strain, LP.8.1, became more common in March. Since mid-April, the presence of LP.8.1 has slightly decreased, with NB.1.8.1 emerging as one of the most detected variants.
What are the symptoms of NB.1.8.1?
The symptoms of NB.1.8.1 are broadly in line with previous Omicron subvariants. These include:
Fatigue
Fever
Muscle aches
Sore throat
Some cases have also reported gastrointestinal issues such as diarrhoea, nausea, and constipation, which are less commonly associated with Covid-19 but have been observed in certain Omicron infections.
Despite its increased transmissibility, there is no evidence that NB.1.8.1 causes more severe illness than earlier strains. “Data indicates that NB.1.8.1 does not lead to more severe illness compared to previous variants,” said Professor Subhash Verma, a microbiologist at the University of Nevada, speaking to CBS News.
Are Covid vaccines effective against this variant?
The symptoms of NB.1.8.1 are broadly in line with previous Omicron subvariantsiStock
Existing Covid-19 vaccines are expected to remain effective in protecting against serious illness from NB.1.8.1. Health authorities continue to recommend vaccination as the most effective way to prevent severe outcomes from Covid-19, including hospitalisation and death.
Monitoring and challenges
The actual number of cases may be underreported due to a decline in routine testing. As fewer people are tested for Covid-19, public health experts caution that official figures may not accurately reflect the spread of the virus.
Nonetheless, global health agencies are continuing to monitor NB.1.8.1 and other emerging variants to assess any potential impact on public health measures, treatment, and vaccine efficacy.
As Men’s Health Week 2025 (9–16 June) approaches, UK-based charity Lepra is raising awareness of hydrocele, a largely overlooked condition that significantly impacts men’s lives. A complication of lymphatic filariasis (LF), hydrocele causes fluid to accumulate in the scrotum, resulting in extreme swelling that can hinder mobility, limit income opportunities, and affect personal relationships.
Despite the availability of a simple surgical fix, many men suffer in silence due to social stigma, lack of awareness, and barriers to treatment.
A personal struggle: Arjun’s story
Arjun, 38, lives in a rural village in Odisha, India, with his wife, four children and father. As the family's main provider, he worked as a labourer until, six years ago, he began experiencing swelling and pain in his scrotum. The condition gradually worsened, leaving him unable to work effectively. Arjun endured daily discomfort, emotional distress, and increasing isolation due to embarrassment about his condition.
Post-surgery, Arjun experienced a significant improvement in his physical healthLepra
His family, unaware of the cause, worried about the financial burden of treatment. The turning point came when Arjun was screened by a Lepra programme and diagnosed with hydrocele.
Understanding hydrocele and its causes
Hydrocele is a common long-term effect of lymphatic filariasis, a neglected tropical disease transmitted by mosquitoes, usually during childhood. According to the World Health Organization (WHO), LF often remains asymptomatic for years while silently damaging the lymphatic system. As men age, this damage can manifest as chronic conditions, including lymphoedema, elephantiasis, and hydrocele.
Hydrocele can cause significant pain and immobility. Married men may struggle with intimacy, while single men often face social exclusion. In many cases, the stigma surrounding the condition leads to isolation, low self-esteem, and mental health challenges.
The simple solution: Hydrocelectomy
Hydrocele can be completely cured through hydrocelectomy, a straightforward surgical procedure with a recovery period of just two weeks. Yet access to this surgery is limited in many areas due to a shortage of trained surgeons and the stigma that prevents men from seeking help.
Following his diagnosis, Arjun received counselling to help him cope with the emotional toll of his condition. Although initially hesitant, he agreed to undergo surgery. After the operation, Arjun’s physical health improved dramatically. He regained the ability to work, restored his independence, and began reintegrating into his community.
The wider problem: Underreported and undertreated
It is estimated that up to half of men who contract LF in childhood will develop hydrocele in adulthood. In 2023 alone, WHO recorded a 258,886 increase in reported hydrocele cases globally, while only 7,380 surgeries were carried out, a stark reminder of the treatment gap.
Although hydrocelectomies are available for free in public hospitals, long waiting lists and inadequate surgical capacity prevent many from accessing timely care. In response, Lepra arranges private surgeries at a cost of just £100 for men unable to wait or travel for public treatment.
Lepra’s ongoing efforts
Lepra not only facilitates surgery but also works with local governments in India and Bangladesh to expand training for hydrocelectomy and improve access to care. The charity also runs community support groups led by trained volunteers who play a crucial role in awareness campaigns and pre-screening education.
These networks help break down stigma by informing communities about LF and the importance of early diagnosis. They also address common fears around surgery and travel, encouraging more men to come forward before the condition worsens.
About lymphatic filariasis
Lymphatic filariasis is classified by the WHO as a neglected tropical disease. It is caused by filarial parasites transmitted through mosquito bites. While infection usually begins in childhood, the consequences can appear much later, affecting the lymphatic system, kidneys, and immune response. Chronic conditions linked to LF include lymphoedema, elephantiasis, and hydrocele.
About Lepra
Lepra, originally founded in 1924 as the British Empire Leprosy Relief Association (BELRA), has been known simply as Lepra since 2008. The organisation works in India and Bangladesh, diagnosing and treating people affected by leprosy and related neglected diseases. Alongside medical care, Lepra tackles prejudice and discrimination through education, rehabilitation, and advocacy.
The charity operates under the patronage of His Majesty King Charles III and has His Royal Highness The Duke of Gloucester KG GCVO as Vice President.
To find out more or support Lepra’s work, visit:www.lepra.org.uk
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Food items can still be sold on TikTok Shop without providing any ingredient or allergen details
TikTok users are reportedly selling food items without declaring allergen information, posing potential risks to consumers, according to a BBC investigation.
The BBC found several listings on TikTok Shop in which sellers failed to mention whether the products contained any of the 14 main allergens that food businesses in the UK are legally required to declare. Following the findings, TikTok removed the highlighted listings and stated that the platform is “committed to providing a safe and trustworthy shopping experience”.
Despite this, the investigation revealed that food items can still be sold on TikTok Shop without providing any ingredient or allergen details.
Among the sellers identified was Mega Buy UK, which offered a Squid Game-themed sweet product but listed ingredients and allergens as “not applicable”. Another seller, The Nashville Burger, promoted a burger-making kit that included milk and wheat, both of which fall under allergens that must be declared by law. However, on TikTok Shop, the allergen information was reduced to “spices”, and the ingredients were simply described as “flour”.
Allergy charities have raised concerns over the findingsiStock
A third seller, UK Snack Supply, was advertising crisps and lollipops without any listed ingredients or allergen information.
Although TikTok removed the specific adverts highlighted by the BBC, the accounts belonging to the three companies remain active on the platform, continuing to sell products, many still without comprehensive allergen details. The BBC contacted all three sellers for comment but could not independently verify whether they are UK-based.
Allergy charities have raised concerns over the findings, saying the safety of consumers should not depend on the geographical location of a seller. Simon Williams, chief executive of Anaphylaxis UK, urged caution: “If the ingredient and allergen information isn’t there, don’t buy it. You’re putting your life in grave danger.”
TikTok responded by stating it has policies in place requiring sellers to comply with safety standards. “We will remove products that breach these policies,” a TikTok spokesperson said.
Kate Lancaster, a TikTok content creator known as The Dairy Free Mum, regularly shares advice related to allergies. Her two children have milk allergies, and she expressed serious concern over the lack of regulation. “It’s completely unacceptable and really worrying. Failing to provide ingredient information is potentially very dangerous, and it feels like a complete disregard for the safety of those living with food allergies,” she said.
The issue is particularly sensitive in the UK, where the death of teenager Natasha Ednan-Laperouse in 2016 after consuming a Pret a Manger baguette containing undeclared sesame seeds led to the introduction of Natasha’s Law. The legislation requires full ingredient and allergen labelling on all pre-packed food made on the premises and sold directly to consumers.
Tanya Ednan-Laperouse, co-founder of The Natasha Allergy Research Foundation, said TikTok must ensure sellers using its platform follow UK food laws. “TikTok is responsible for ensuring that all their UK food sellers meet legislative requirements to sell food products on their app. Any that don't should be immediately removed from the app and investigated, but ideally this should not happen if their checks and balances are rigorous and in place,” she said.
Kate Lancaster also believes TikTok is allowing sellers to bypass basic safety regulations. “Since Natasha’s Law has come into effect, I feel that, in general, allergy labelling has improved, but it’s frightening that a huge platform like TikTok does not have adequate measures to ensure that labelling is in place,” she added. “The thought of someone with a food allergy, or an allergy parent, buying items that they assume are safe, when in fact they may not be, is really scary.”
Concerns remain about whether current safeguards are adequate to protect consumers with allergiesiStock
The Food Standards Agency (FSA), which oversees food safety in England, Wales, and Northern Ireland, stressed that food businesses must be registered and follow legal requirements, including the provision of allergen information both online and on packaging. Dr James Cooper, deputy director of food policy at the FSA, stated: “Wherever people buy their food, it needs to be safe and what it says it is. All food businesses have a legal responsibility to sell safe food and provide allergen information.”
The FSA also points out that for “distance selling”—which includes online and telephone orders—businesses must provide allergen details at two stages: first in the product listing, and again on the packaging, to ensure buyers have clear access to essential safety information.
Simon Williams from Anaphylaxis UK emphasised that while the ultimate responsibility lies with sellers, TikTok should do more to protect users. “At the moment it’s being used as a platform to sell things that may not be safe. They [TikTok] do need to do more,” he said. “There’s a lot of people making a lot of money—great side hustle—but they’re putting people at risk.”
As TikTok Shop continues to grow as a marketplace, particularly for food trends and viral snacks, concerns remain about whether current safeguards are adequate to protect consumers with allergies.
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Simran’s project reflects a growing shift towards mindful fashion choices
Delhi-based content creator Simran Anand has captured widespread attention on social media after she upcycled a 20-kilogram patchwork bedsheet into a unique and eye-catching lehenga. Sharing the process with her followers on Instagram on 1 July, Simran highlighted the creative transformation of a traditional decorative textile into a fashionable statement piece.
The striking fabric was discovered during a casual visit to Janpath, one of Delhi’s popular street markets. The bedsheet, although heavy and originally intended for home décor, featured intricate hand embroidery, mirrorwork, and patchwork – elements commonly found in festive wall hangings in regions like Gujarat and Rajasthan.
“These types of embroidered textiles are usually hung as tapestries or used as festive décor,” Simran noted. “But I saw fashion in it,” she added, referring to the moment she decided to turn the bedsheet into a garment. Inspired by ideas on Pinterest, she took the fabric to a local tailor and collaborated with him to create a custom lehenga.
The result was a bespoke outfit that retained the charm of the original patchwork while embracing a modern silhouette. The lehenga quickly gained attention online, with many social media users praising her creativity and the craftsmanship involved. One commenter wrote, “Love a smart woman with an amazing fashion sense, love this on youuu.” Another applauded the tailor’s skill: “Lucky bhaiya is so skilled ❤️.” A third user even suggested exploring more pieces: “A blazer out of this would have been so good too, another one!!”
Patchwork has increasingly emerged as a trending element in fashion, blending sustainability with style. Simran’s project reflects a growing shift towards mindful fashion choices and showcases how traditional or overlooked fabrics can be reimagined into statement garments. Her approach not only highlights individual creativity but also promotes the value of upcycling and working with local artisans.
Transforming a 20kg decorative item into wearable fashion underlines the evolving nature of design today, where vision and innovation are often found outside conventional fabric stores. As fashion continues to explore sustainable practices and cultural references, creations like Simran’s patchwork lehenga demonstrate how inspiration can come from the most unexpected sources.