logo
The real reason the rich and famous get lyme disease so often - as Justin Timberlake reveals he has the illness that also hit Justin Bieber and Kelly Osbourne

The real reason the rich and famous get lyme disease so often - as Justin Timberlake reveals he has the illness that also hit Justin Bieber and Kelly Osbourne

Daily Mail​18 hours ago
Justin Timberlake is the latest star to reveal he has been diagnosed with Lyme disease—and the former N*Sync singer is in good company.
The 44-year-old joins the likes of Comedian Miranda Hart, model Bella Hadid, singer Justin Bieber, actor Ben Stiller and TV personality Kelly Osbourne in having the tick-borne condition.
He revealed in an Instagram post: 'I've been battling some health issues, and was diagnosed with Lyme disease—which I don't say so you feel bad for me—but to shed some light on what I've been up against behind the scenes.'
Lyme disease is a serious bacterial infection usually contracted after being bitten by a tick, causing flu-like symptoms which can last for a few weeks, but for reasons not yet understood, some patients suffer for years.
The disease has seen an upsurge in prevalence across swathes of the US, and whilst latest figures show cases have fallen in the UK, experts warn the number of confirmed cases is likely an underestimate of the true burden of the disease.
So why does it seem like so many of the rich and famous are being diagnosed with it?
Professor Paul Hunter, an expert in infectious diseases from the University of East Anglia, told the Daily Mail there could be some factors that make celebrities more vulnerable to Lyme disease.
He said the stars' increased leisure time and typically greater access to the wilder outdoor areas where ticks reside could simply make it a numbers game.
'If there is a rich and famous or class bias in this, it's probably because they spend more time walking around in wooded parkland, more money to go out to those areas, or have big homes with these sorts of places,' Professor Hunter added.
The fact that celebrities are more likely to live in the US, where Lyme disease is more famously prevalent, could be another factor.
'As you're walking along the ticks jump on your legs and crawl their way up...have a blood feast and give you Lyme disease,' he said.
'If you go walking in these sorts of places the best thing to do is check, when you get home, that you don't have any ticks on you and if you have remove them safely.'
Mr Timberlake said: 'When I first got the diagnosis I was shocked for sure.
'But, at least I could understand why I would be on stage and in a massive amount of nerve pain or, just feeling crazy fatigue or sickness.'
His diagnosis came whilst he was on tour, which kicked off in April 2024, leading to a stream of criticism on social media which labelled his performances as lackluster.
More recently, fans have speculated that he looked more tired than usual and could be suffering ill health.
Mr Timberlake addressed the comments in his post, saying: 'I was faced with a personal decision.
'Stop touring? Or keep going and figure it out. I decided the joy that performing brings me far outweighs the fleeting stress my body wsa feeling. I'm so glad I kept going.'
He added: 'I was reluctant to talk about this because I was always raised to keep something like this to yourself.
'But I am trying to be more transparent about my struggles so that they aren't misinterpreted.
Addressing his fans he added: 'Not only did I prove my mental tenacity to myself but, I now have so many special moments with all of you that I will never forget.'
Professor Hunter said testing for Lyme disease is a complex, and sometimes controversial, topic with some tests offered by some private clinics not recognised by health authorities.
Clinicians have previously warned that some clinics are effectively offering Lyme disease diagnosis on demand for patients seeking an answer for symptoms, real or imagined.
This can particularly be the case for people who suffer 'chronic' or ongoing Lyme disease symptoms that can last for years.
Experts like Professor Hunter say some chronic Lyme disease cases are certainly real, but others are likely to be suffering from other conditions.
'There are people who do get longer term symptoms but probably not as frequently as people who believe they have,' he said.
'A range of symptoms, longer term, are headaches, neck stiffness, rashes, facial palsy which is partial paralysis of face muscles, arthritis and joint pain is a common one, intermittent pain in tendons, palpitations, dizziness, inflammation, nerve pain.
'The problem is all of those are quite common in the population in the whole, some people particularly as you get older get joint pain quite often which can just be wear and tear, rheumatoid arthritis, or Lyme disease.
'Distinguishing them, other than by definitive blood tests, is not easy.'
Mr Timberlake is not the first celeb who has spoken out publicly about their battle with Lyme disease in recent years.
Yolanda Hadid said that she had suffered deep depression amid a pileup of symptoms for the better part of a decade which she attributed to chronic Lyme.
'I can't begin to describe the darkness, the pain and the hell I lived through every day,' the socialite told British Vogue in February 2021. 'This disease brought me to my knees.'
Her daughter, Bella also last year described how she had undergone 100 days of treatment amid a battle with the condition that stretched nearly 15 years.
Musical artist Justin Bieber said, in January of 2020, that doctors had diagnosed him with Lyme disease after receiving nasty remarks about his appearance.
'While a lot of people kept saying "Justin Bieber looks like s***, on meth" etc. they failed to realize I've been recently diagnosed with Lyme disease, not only that but had a serious case of chronic mono which affected my, skin, brain function, energy, and overall health,' the Grammy-winning artist wrote on Instagram.
The first sign of the disease, which is also found in the UK and Europe, is a tell-tale bullseye rash that develops where the person was bitten, but this only appears on some people.
This rash can appear up to three months after the bite.
Sufferers then develop general flu-like symptoms, including fatigue, headache, swollen joints and a fever, which can last for a few weeks.
The delay between the bite, the rash which may not appear and the broad symptoms which could belong to a variety of other conditions, means patients can struggle to get a diagnosis.
Two blood tests that can diagnose Lyme disease are available, but the NHS warns they can be unreliable in the early stages of the disease.
A course of antibiotics is typically enough to treat most Lyme disease patients, though the process can take several weeks.
However, for reasons scientists are still exploring, some people with the disease can suffer ongoing symptoms for years.
The NHS warns that, as this form of the disease is still not understood, there is no agreed upon treatment.
Previous research has suggested the vast majority of people diagnosed with Lyme disease do not actually have the condition.
Experts from John Hopkins University in the US found that out of a sample of over 1,200 patients diagnosed with Lyme disease over 13 years, three-quarters were not affected, according to gold standard blood tests.
Publishing their findings in the journal Open Forum Infectious Diseases, they said this had led to patients being commonly given 'unnecessary antibiotic treatment'.
The UK Health Security Agency (UKHSA) is now reminding people of the steps they can take to protect themselves against tick bites this summer, as latest figures show there were 1,581 confirmed cases of the disease reported last year.
Whilst this is a 5.2 per cent decrease compared to 2023, experts warn the true figure could be much higher.
A rash
A rash is one of the most obvious signs of Lyme disease to look out for.
The erythema migrans (EM) rash, often referred to as a bull's-eye rash due to its red circular rings, should be treated straight away, says the charity Lyme Disease UK.
However, the rash doesn't always present in the same way, especially on darker skin, and a third of people do not develop a rash at all.
It can also not take on a ring shape and instead have a solid or bruise-like appearance.
The behaviour of any rash after a tick bite is the most important thing to be aware of, warns Lyme Disease UK.
An EM rash takes at least three days, and in some cases up to three months, to appear.
It generally isn't itchy, painful, or hot, and gradually spreads outwards.
However, if you have redness or itchiness immediately after a tick bite is usually a histamine reaction.
Flu-like symptoms
Not everyone develops a rash.
Some people experience flu-like symptoms.
Often likened to a 'summer flu', Lyme Disease UK says some people can get headaches, a stiff neck, muscle pain and fatigue.
Some small children may also have behavioural changes as they are unable to articulate how they are feeling, the charity adds.
If Lyme disease is left untreated or if it is not treated early on, weeks, months or even years later more serious symptoms can develop.
Pain and swelling in the joints, known as inflammatory arthritis, is one of the more serious symptoms that can follow Lyme disease, according to the government website.
Muscle and joint pain can also be felt just weeks or days after getting tick bite, the NHS says.
Facial paralysis
More serious symptoms can develop if Lyme disease is left untreated.
Drooping on one side of the face or a weakness of your facial muscles is another indication of an infection.
That's because the bacteria that causes Lyme disease can also damage the nervous system, including the facial nerve.
Weakness or a paralysis of the facial muscles can be seen in someone infected by Lyme disease and it usually affects on side of the face, according to the charity Facial Palsy UK.
This symptom is especially common in children, says Lyme Disease UK.
Some people can also experience shooting nerve pains.
This pain can feel sharp or prickly and follow the course of the nerve, according to the government website.
Memory problems
Being forgetful and struggling to concentrate are also later symptoms of the disease.
The bacteria that causes Lyme disease can not only cause numbness and nerve pain, but also memory problems and difficulty concentrating, according to the government website.
If the disease is treated early on it is less likely you will suffer with memory problems.
Eye problems
Blurry vision could be a sign of Lyme disease.
The Borrelia burgdorferi bacteria that causes Lyme disease can also change your vision, according to the charity Guide Dogs UK.
People can experience floaters and inflammation typically in the late stages of the disease.
However. this vision change can be temporary and can improve or resolve with treatment of the disease.
In the early stages the disease can cause conjunctivitis making your eyes bloodshot, irritated and swollen.
Due to the neurological effects of the infection, it can cause twitching anywhere on the body including the eyes.
The charity also highlights a more rare eye symptom, known as optic neuritis.
This is where the optic nerve becomes inflamed, which can lead to severe eye pain and vision loss, but experts say it is unclear how Lyme disease directly causes this to happen.
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Almost half of NHS England waiting list patients yet to have initial appointment
Almost half of NHS England waiting list patients yet to have initial appointment

The Independent

time35 minutes ago

  • The Independent

Almost half of NHS England waiting list patients yet to have initial appointment

Around three million people in England have had no further health care since being referred to a hospital waiting list, new data suggests. NHS England figures last month estimated 7.36 million treatments were waiting to be carried out at the end of May, relating to just under 6.23 million patients – with the analysis from MBI Health suggesting almost half of those have been left in limbo. Referring to the issue as a 'frontlog' that contributes to increasing NHS waiting list times, MBI said the problem 'has gone unchallenged for too long', with an estimated 2.99 million people waiting for their first clinical contact. MBI's analysis found that around 70% of referral to treatment pathways fall into the category of being 'unseen' since the patient's GP referred them to a specialist. Delays in making a first assessment can lead to late diagnosis, worsening symptoms and pressure on emergency services. The analysis found that ear, nose and throat (ENT), trauma and orthopaedics, gastroenterology, ophthalmology and gynaecology and obstetrics departments were consistently the specialist departments with the greatest number of patients not seen for the first time. As part of the Government's 10-year health plan, the NHS is expected to meet its target of carrying out 92% per cent of routine operations and appointments within 18 weeks by March 2029 – a target that has not been achieved for almost a decade. The latest figures show how challenging that target will be given an estimated one million of the three million unseen patients have already gone more than 18 weeks without receiving any care. 'If accurate, three million people are trapped in an invisible waiting list crisis, stuck without basic diagnostic tests of first appointments while their conditions worsen,' Rachel Power, the chief executive of the Patients Association, told the Guardian. 'The scale is staggering, as nearly half of all patients on a waiting list haven't been seen by anyone. That's not a healthcare service; that's a breakdown. 'These aren't just statistics. They're people checking their phones daily for hospital calls that never come, unable to plan their lives while their symptoms deteriorate.' Last month it was found people of working age are making up a growing proportion of those on the NHS waiting list for treatment in England. Data tables published for the first time by NHS England also show people in the most deprived parts of the country are more likely to wait more than a year to start hospital treatment than those in the least deprived. The figures, analysed by the PA news agency, showed 56.1% of those on the list at the end of June this year were of working age (defined as age 19 to 64), up from 55.8% a year ago and 55.0% in June 2022. At the same time, the proportion of people on the waiting list under the age of 19 has fallen, standing at 10.8% in June this year, down from 11.2% a year earlier and 11.9% in June 2022. The proportion who are over 65 has remained broadly unchanged at around 33.1%. People of working age are also more likely to have to wait more than a year to start treatment (3.0% of patients in this age group at the end of June) than those over 65 (2.5%). However, the proportion is the same as those under 19 (also 3.0%).

How I cut out ‘food noise' and lost 40lbs
How I cut out ‘food noise' and lost 40lbs

Times

timean hour ago

  • Times

How I cut out ‘food noise' and lost 40lbs

Over the past six years I've lost more than 40lb (almost three stone). It has been a long road to find 'peace' with food and my body, and at the age of 47 I have done it at long last. Healing a complicated relationship with food that involved years of binge eating and yo-yoing weight was difficult — but it is beginning to feel less of an achievement now that everyone else seems to be doing it with ease. Watching the pounds melt off people around me thanks to a relatively quick course of Mounjaro or Ozempic, I feel like someone who made careful investments and earned a modest amount of money just as others around me enjoy a lottery win. I've spent most of my life trying to manage my weight and now that I've finally done it, at a time when everyone seems to be getting teenier and teenier, it sometimes feels daft to have done it the 'hard way'. Perhaps it irks me because overcoming disordered eating and yo-yoing weight isn't something that just happens with an injection. It's a huge undertaking and for me it's a process that never really ends.

Jeannie Seely is dead at 85: Country music legend's 'dearest friend' Dolly Parton pays tribute
Jeannie Seely is dead at 85: Country music legend's 'dearest friend' Dolly Parton pays tribute

Daily Mail​

time2 hours ago

  • Daily Mail​

Jeannie Seely is dead at 85: Country music legend's 'dearest friend' Dolly Parton pays tribute

Jeannie Seely, the country music singer best known for her hit song Don't Touch Me, has died at 85. Seely died on Friday at Summit Medical Center in Hermitage, Tennessee, from complications brought on by an intestinal infection, according to People. Her death follows the loss of her husband Eugene Ward from cancer in December. Seely had been plagued by health problems since last year, and she announced in May that she had undergone multiple surgeries on her back to repair her vertebrae. The performer also said she had two emergency abdominal surgeries and developed pneumonia during an 11-day stay in the intensive care unit. 'Rehab is pretty tough, but each day is looking brighter and last night, I saw a light at the end of the tunnel. And it was neon, so I knew it was mine!' she said at the time. 'The unsinkable Seely is working her way back.'

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store