We all love a bit of touch up, whether on a regular day or for an event. For millions of women across the globe, threading is a regular part of their beauty routine. From shaping eyebrows to removing unwanted facial hair, this grooming technique is practiced weekly or monthly and is widely considered quick, safe, and inexpensive.

But a recent video from a doctor turned influencer has caused a stir online by claiming that threading — like tattooing and body piercing — can potentially spread Hepatitis B, a serious liver infection.

What Did The Doctor Say?

In a video that has garnered over 400,000 views within two days, Dr Vishal Gabale, an internal medicine doctor from Navi Mumbai, narrates a case where three young women, all of whom had visited the same threading salon, tested positive for Hepatitis B with identical virus strains.

Dr Gabale says he investigated the case like a “medical mystery,” and found the common link between the patients was their visit to the same salon. Citing a 2022 World Health Organization (WHO) bulletin, he claims that Hepatitis B has been known to spread through tattooing, razor-sharing, and “even cosmetic procedures like threading.”

According to him, threading can cause micro-abrasions, and if contaminated tools or threads are used, the virus could survive for days — even without visible blood.

Medical Experts Respond with Skepticism

However, not all doctors are convinced. A dermatologist based in Hyderabad acknowledges that if threading causes skin abrasions, transmission is “theoretically possible,” but stresses that no confirmed case has ever been recorded.

“Tattoos are a different story — they break the skin and do carry a risk. But threading is far more superficial,” he said. “If threading was truly risky, we’d have seen documented evidence by now, considering how common the practice is.”

He also criticized the influencer’s decision to disable comments on the video, making it harder for experts to counter misleading claims.

Missing Evidence and Misleading Sources

Hyderabad-based neurologist Dr Sudhir Kumar also raised concerns. He pointed out a small disclaimer in the video saying it’s “only for educational purposes” and presents a theoretical risk — suggesting the doctor hadn’t treated any actual Hepatitis B cases linked to threading.

“The issue is that viewers may miss that disclaimer and assume the risk is real. But to date, not a single case report has linked Hepatitis B transmission to threading — that’s significant,” Dr Kumar explained.

About the WHO bulletin cited in the video, the doctor reportedly shared a screenshot of an unrelated 2010 article, which did not reference threading and wasn’t published by WHO.

Beauty Risks vs. Clickbait

Dr Kumar added that while there are documented links between Hepatitis B and procedures like tattooing, body piercing, manicures, or even shaving with unsterile equipment, threading has never been associated with such risk, reported The South First.

He warns against fear-mongering and called the video an example of “clickbait,” made worse by its origin — a doctor, not just an influencer.

“Threading doesn’t typically break the skin. Unlike tattooing or piercings, it doesn’t create the conditions necessary for virus transmission. We must focus on real risks — unprotected sex, reused medical needles, and poor hygiene in clinical settings — not unproven, hypothetical scenarios,” he said.

For many women with endometriosis, chronic and painful gastrointestinal symptoms are part of daily life, yet they often go untreated due to under-recognition by healthcare providers and a lack of evidence-based treatment options.

Endometriosis is a chronic, inflammatory gynaecological disorder affecting one in seven Australian women. It causes a range of unpredictable and often severe symptoms, including dysmenorrhoea (painful periods), pelvic pain (below the belly button and between the hips), and dyspareunia (pain during sexual intercourse). These symptoms disrupt daily life, impacting finances, relationships, mental health, and the ability to work, learn, socialise, exercise, and have children.

According to Jane Varney, Senior Research Dietitian at the Department of Gastroenterology, Monash University, gastrointestinal symptoms such as abdominal pain, bloating, distension, diarrhoea, constipation, and painful defecation affect more than three-quarters of sufferers. These symptoms often intensify during menstruation, occur regardless of bowel involvement, and overlap with irritable bowel syndrome (IBS), which affects between 10.6 per cent and 52 per cent of women with endometriosis.

Why current treatments fall short

Despite the high prevalence and burden of gut symptoms in endometriosis, treatment options are limited. Few treatments specifically target these gastrointestinal issues, and some, such as progesterone and opioid medications, can make them worse. Surgery can come with long waiting times, high costs, ongoing pain, and the need for repeat procedures, while hormone treatments and pain relief medicines are limited by modest effectiveness and troublesome side effects.

It is no surprise that many women turn to self-management strategies such as diet and nutritional supplements to help control symptoms and take an active role in their care. International data shows that more than 58 per cent of women with endometriosis have tried supplements, though only 43 per cent reported an improvement in pain. In Australia, three-quarters use fish oil, multivitamins, vitamin B, or vitamin D.

Dietary changes are also common. Surveys from Australia, Holland, the UK, and beyond reveal that between 27 per cent and 84 per cent of women with endometriosis use dietary modifications to manage symptoms, with many reporting benefits. Popular approaches include anti-inflammatory diets or avoiding red meat, gluten, dairy, lactose, FODMAPs, caffeine, soy, and alcohol. However, the evidence for most of these is limited or absent.

The EndoFOD study

The study was the first randomised controlled crossover feeding trial in this patient group. Thirty-five participants were assigned to a 28-day low FODMAP diet or a control diet based on Australian dietary guidelines, with both diets nutritionally matched except for their FODMAP content. After a washout period of at least 28 days, they switched to the other diet. Each diet began on the first day of a menstrual cycle to account for hormonal symptom fluctuations.

By the end of the trial, 60 per cent of participants responded to the low FODMAP diet, with significant improvements in gut symptom severity. Abdominal pain, bloating, stool consistency, and quality of life all improved. Changes were noticeable by week two, continuing steadily until the end of the intervention.

What it means for endometriosis care

What’s next for diet research

Epilepsy affects millions of people worldwide, yet it remains one of the most misunderstood neurological conditions. The disorder is marked by recurring seizures, sudden bursts of electrical activity in the brain , which can cause symptoms ranging from brief confusion and muscle twitches to severe convulsions.

While anyone can have a single seizure for a variety of reasons, epilepsy is diagnosed when a person experiences two or more unprovoked seizures. Experts say understanding the causes can help with both prevention and treatment.

Genetics Can Play a Role

In some cases, epilepsy runs in families, pointing to a genetic connection. Certain gene mutations can disrupt normal brain activity, making seizures more likely.

Genetic epilepsy can be inherited, but the link isn’t always straightforward, says neurologists. Different genes affect the brain in different ways, and researchers are still uncovering exactly how these changes lead to seizures.

Even without a family history, spontaneous mutations in a person’s genes can also result in epilepsy.

Brain Damage Can Lead to Epilepsy

Any structural damage to the brain can disrupt its electrical signalling, triggering seizures over time. This damage might be recent or decades old.

Common structural causes include:

• Birth complications that reduce oxygen supply to the brain
• Head trauma from accidents or falls
• Brain tumors
• Stroke or bleeding in the brain

“Sometimes the injury happened years earlier, such as during birth, but its effects on brain function appear much later,” says Dr Gabriel Martz, MD, FAES, writing for Hartford HealthCare, who is a neurologist and director of the Ayer Neuroscience Institute Epilepsy Center.

Infections and Autoimmune Conditions Can Be Triggers

Infections that cause brain inflammation, such as meningitis or encephalitis, can have long-term consequences. Even after recovery, scarring and other changes in brain tissue can increase the risk of seizures.

In other cases, the immune system mistakenly attacks the brain, a condition known as autoimmune encephalitis, which can also lead to epilepsy.

“These causes highlight why protecting brain health through early diagnosis and treatment of infections is so important,” specialist notes.

4Sometimes, the Cause is Unknown

Despite advances in brain imaging and genetic testing, many people with epilepsy never learn the exact cause.

“We don’t always get a clear answer,” Dr Martz notes. “Not knowing the cause can be frustrating, but it doesn’t make the condition less real or less treatable.”

This uncertainty means that in some cases, treatment focuses entirely on managing seizures rather than addressing an underlying trigger.

Lifestyle and Environment Matter

While lifestyle alone doesn’t cause epilepsy, certain factors can raise the risk by increasing the chances of brain injury or neurological stress. These include:

• Substance misuse
• Dangerous sports without protective gear
• Repeated concussions

“Protecting your brain is one of the best ways to reduce preventable risk,” doctor says. Wearing helmets, avoiding risky behavior, and staying away from drugs can make a real difference.

When to Seek Medical Advice

If you or someone you know experiences a first-time seizure, it’s essential to consult a doctor. Tests such as an MRI, EEG, or bloodwork can help identify potential causes and guide treatment.

Epilepsy affects people in deeply personal ways, not only in how seizures manifest but also in how the condition impacts daily life and emotional well-being. Understanding what lies behind it is the first step toward effective care and fuller, healthier lives.

Doctors are calling for a national strategy and a public awareness campaign to improve end-of-life care, warning that dying is often treated as an “unexpected” event or last-minute crisis, even when a patient’s condition has long been deteriorating.

The Royal College of Physicians (RCP) said healthcare systems tend to prioritize curative treatments, despite many patients living with progressive, life-limiting conditions such as frailty or advanced chronic illness. The college urged a “cultural shift” in both healthcare and wider society to recognize the value of palliative and end-of-life care.

Dr Hilary Williams, RCP’s clinical vice president, as reported by The Independent, described recognizing the end of life as “an act of clinical courage and kindness.” She stressed that early planning could improve comfort, dignity and choice for patients.

Most Deaths Are Predictable, Yet Families Unprepared

Citing earlier research, the RCP said around 70% of people die from long-term health conditions that typically follow a predictable course, meaning death can be anticipated well in advance. Despite this, many patients and families are left unprepared, missing opportunities for open discussions that could shift the focus from aggressive treatment to quality-of-life support.

The RCP has recommended that the Government:

• Launch a public campaign on end-of-life and palliative care
• Support professional education to improve recognition and delivery of such care
• Develop a national strategy, including workforce training

The college also warned of barriers such as social care challenges, funding gaps and workforce shortages that limit timely, compassionate care.

Need for Honest Conversations

Dr Williams said too often recognition that someone is approaching the end of life happens only in the final days or weeks, usually in acute care settings. She called for valuing continuity of care, experienced decision-making and time for clinicians to hold honest conversations with patients and families.

“With treatment options expanding, knowing when to start or stop interventions and when to focus on quality of life has become more complex,” she said. “These are skills rooted in expertise, and the system must value them.”

Support from Other Medical Leaders

Dr Nick Murch, president of the Society for Acute Medicine, as reported in The Independent said better planning could allow more people to die with comfort, dignity and in a place of their choosing.

Dr Suzanne Kite, president of the Association for Palliative Medicine, emphasized the need for a national strategy to guarantee access to high-quality palliative care at any time and location, supported by training and public dialogue, as reported by The Independent.

Charity Sue Ryder, which provides hospice and palliative services, backed the RCP’s call, noting that some patients die before hospice admission due to late referrals. The charity urged healthcare professionals to consider palliative care from the point of a terminal diagnosis.

Government Response

A Department of Health and Social Care spokesperson said the Government aims to ensure compassionate, high-quality care from diagnosis to end of life. Under its 10 Year Health Plan, more healthcare will move from hospitals into communities, with palliative care playing a central role. The department has invested £100 million in hospices, the largest such funding in a generation.

Separate from Assisted Dying Debate

The RCP clarified that its position on end-of-life care is separate from its stance on the assisted dying Bill. While acknowledging deficiencies in the proposed legislation, the college urged further safeguards to protect vulnerable patients and maintain trust in the doctor-patient relationship.