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The real reason you feel ghastly when you catch a cold

Tuesday, October 28, 2014

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An astounding number of germs lurk invisibly everywhere we look or touch
An astounding number of germs lurk invisibly everywhere we look or touch
An astounding number of germs lurk invisibly everywhere we look or touch: on door handles, computer keyboards and kitchen counters.
With all these disease-causing bugs around us, you might be excused for thinking it's a wonder any of us are still alive. Well, it is a wonder: a wonder called the immune system.
We have multiple layers of defence against illness - from 'good' bacteria in the gut, to 'memory' cells that remember diseases we've had.
This intricate system operates silently in the background, only becoming noticeable when things go seriously wrong. Here are seven ingenious things you didn't know about your immune system . . .
WHY YOU FEEL ROTTEN WHEN YOU'RE ILL
Often when we have an infection, the invading viruses or bacteria aren't all that harmful - it's the immune system's overreaction that is the major cause of our symptoms.
Consider the cold virus. It's actually one of about 200 different kinds of virus, which all cause similar symptoms such as a sore throat and sneezing.
But the cold viruses themselves contribute almost nothing towards these symptoms: they're the result of the inflammatory response by your immune system. Inflammation occurs when immune cells send chemical distress signals to recruit more resources to fight the infection.
Blood vessels near the infection site become more permeable, allowing more cells and substances to flood the area. This means there is suddenly more aggressive stuff intent on killing the virus. For us, this means a blocked nose or sore throat, because that's where the virus tends to hang out. The inflammation also irritates the nose, making you sneeze.
WHY SOME BUGS LAY YOU LOW FOR DAYS
Many bugs are eliminated by the immune system minutes after entering the body. When the pathogen (any micro-organism that can cause disease, such as a virus or bacteria) enters the body, a cocktail of enzymes and antimicrobial molecules try to attack it.
First, proteins known as the complement system stick to the intruder's surface and try to kill it. If this doesn't work, bacteria-gobbling cells called phagocytes try to swallow the pathogen whole, digesting it with chemicals.
Often, this is enough to bring an infection under control in a couple of hours. This system is called the innate immune system.
The adaptive immune system tailors its response to the individual infection. This takes days to take action
The adaptive immune system tailors its response to the individual infection. This takes days to take action
However, sometimes intruders are too numerous or cunning - for instance, the bacterium that causes tuberculosis, Mycobacterium tuberculosis, can survive inside our bacteria-gobbling cells without being digested and killed. In these scenarios, the adaptive immune system takes over.
Unlike the innate immune system, which fires the same attack all the time, the adaptive immune system tailors its response to the individual infection. This takes days - rather than minutes - to take action.
The adaptive immune system is mostly two kinds of white blood cell: T cells and B cells. T and B cells only take action against illnesses they are designed to fight.
When they meet a pathogen they know how to fight, they multiply rapidly and attack the infection. B cells do this by releasing proteins called antibodies into the blood, which latch onto the pathogen and stop it from functioning.
Some types of T cell work by poisoning cells infected by a pathogen with toxic chemicals. But as these T cells only respond to individual pathogens, most remain unactivated and unused for the duration of your life.
 One study found just looking at pictures of sick people caused our immune system to become more active
HOW VACCINES PROTECT YOU
The immune system remembers its own history. After an attack by a pathogen, B and T cells produce copies of themselves, which act as 'memory' cells, hanging around in our bodies in case the same pathogen returns.
This is how vaccinations work. When a doctor injects you, they introduce a small amount of a pathogen into your body - not enough to be harmful, but enough to trigger the B and T cells into action to create the 'memory' copies of themselves. This means when the pathogen next attacks, the body can react more quickly.
It seems some diseases are easier to remember than others.
Recently, researchers discovered the immune system has a short-term and long-term memory. Short-lived memory B cells and short-lived memory T cells stick around the body for a few weeks after infection; long-lived memory cells can stay for decades - even indefinitely. Vaccine developers are now taking this into account.
BREASTFEEDING CAN BOOST YOUR BABY
A recent suggestion is that breastfeeding provides a way for a mother and child's immune systems to 'talk' to each other.
When a baby suckles, it draws out milk through ducts around the nipple. Some of the baby's saliva will find its way into these ducts.
The mum's immune system then analyses the saliva, which contains clues as to what's going on in the baby's body - and her milk changes accordingly, generating and delivering a specific immune response to any illness the baby may have; in effect acting as the baby's immune system while its own is maturing.
The immune system responds to anything it detects as 'foreign'
The immune system responds to anything it detects as 'foreign'
TAPEWORMS BEAT ALLERGIES
A possIble reason for the marked rise in allergies over the past few generations could be how successful we have been at eradicating disease caused by parasites such as tapeworm.
Our immune system has different types of response for different types of pathogen. One of these is an inflammatory response - where a surge of infection-fighting substances are released.
Allergies are caused by the immune system overreacting when it comes into contact with a harmless substance - such as pet fur or pollen - triggering this inflammatory response. However, the inflammatory response is not enough to cope with larger invaders, such as parasitic worms.
So, instead, when the body is infected with a parasite, the immune system deploys specialised white blood cells, known as eosinophils, to try to kill it. But activating eosinophils at the same time as the inflammatory response uses a lot of energy, so the body uses only one at a time.
If eosinophils are activated, the inflammatory response is dampened down. In less-developed countries with high levels of disease from parasite, there are substantially lower rates of allergies.
The thinking is, if the body is busy fighting parasites, it won’t waste resources on an inflammatory response against a harmless allergen.
Scientists are now trying to find out how to use this knowledge to dampen down the inflammatory response without actually having to swallow a tapeworm!
HOW FRIENDLY BACTERIA HELP
The mainstream way of thinking about the immune system is that it responds to anything it detects as 'foreign' - the body's notions of what is part of our body and what is foreign are largely fixed by the time we're a few months old.
But the body changes over our lifetime. Pregnancy, lactation, puberty - all produce molecules that weren't there when we were infants, yet our immune systems don't react. Why?
Some immunologists argue it isn't simply a case of the immune system hunting down anything 'foreign' - instead, it responds to intruders only if they actively damage our cells.
For instance, we all harbour so-called commensal bacteria - 'friendly' bacteria that live in or on our body without causing harm, which the immune system leaves alone. It may be the same with foetuses, food, or any other foreign element that finds its way into our body: it will be tolerated as long as it behaves nicely.
WE'RE HARD-WIRED TO AVOID DIRT
It's not just our cells that protect us from illness - washing our hands or brushing our teeth is, arguably, another layer of immunity, sometimes called the behavioural immune system.
It is difficult to know how much of our behaviour is learned, and how much is down to our genetic make-up. But some things do seem to be hard-wired into us.
For example, one study found that just looking at pictures of sick people caused our immune system to become more active.
More speculative, contentious studies have suggested that some of our cultural attitudes are also under the influence of these inbuilt immune responses.
Could it be instinct that makes you shy away from the dirty, smelly stranger on the bus with the hacking cough, who looks like he might be harbouring something nasty?
Adapted by JENNIE AGG from Why Aren't We Dead Yet? The Survivor's Guide To The Immune System by Idan Ben-Barak (Scribe, £12.99) published on November 6. 

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Joey Essex Expains how to keep fit Simple and penniless

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Joey does 50 press-ups, 250 crunches and 150 sit-ups every single morning
Joey does 50 press-ups, 250 crunches and 150 sit-ups every single morning
Former The Only Way Is Essex star Joey Essex, 24, answers our health quiz.
HOW DO YOU KEEP FIT? 
Each morning I do 150 press-ups, 250 crunches and 150 sit-ups. Sometimes when I get home from work I do the same routine again. I aim for at least 40 minutes of exercise every day. I also go for a 3.5-mile run three times a week. I don't use public gyms, as it's difficult to train when people recognise me and want to talk. I prefer exercising in my bedroom.
GET YOUR FIVE A DAY?
I eat enough veg, especially broccoli and asparagus, but not as much fruit as I should, apart from a banana with my porridge every morning. Apple gets stuck in my teeth so I prefer blueberries and raspberries. I eat chicken or fish most days, and red meat about once a week. Although I'm not a very good cook I prefer eating freshly cooked meals than ready-made ones. I've never dieted - I'm about 11 st and just under 6ft.
BIGGEST VICE?
I love milk chocolate and feel guilty when I have it. I like a drink - my favourite is vodka with slimline tonic or soda and lime. My mates take the mick out of me, asking if I'm on a diet. I avoid sugary fizzy mixers with alcohol.
WORST ILLNESS OR INJURY?
I had a mild form of pneumonia when I was 14. One of my lungs filled with fluid and it really scared me as it was extremely painful. Antibiotics sorted it out. When I was nine I was showing off on my bike by cycling hands-free until I fell off and broke half of my front tooth, which involved a visit to A&E.
HAD ANYTHING REMOVED?
Years ago I had a painful tooth abscess which was removed under general anaesthethic.
WOULD YOU HAVE PLASTIC SURGERY?
I'd never say never, though I'm not looking to at the moment. Some of my family and friends have had work done, for instance if they weren't happy with their nose. I don't see anything wrong with it. I don't even notice when a girl has hair extensions, never mind anything else!
He loves milk chocolate and fry-ups on a hangover but feels guilty for it
He loves milk chocolate and fry-ups on a hangover but feels guilty for it
POP ANY PILLS?
I take fish oil and evening primose oil, for the brain and eyes. I also drizzle omega-3 and omega-6 oil on my salads, for general health and keeping cholesterol levels normal.
FAVOURITE HANGOVER CURE?
Going for a 30-minute run or a cooked breakfast - although an hour after the breakfast I always feel guilty for eating it. I also recommend porridge, or scrambled egg, smoked salmon and tomatoes.
WHAT KEEPS YOU AWAKE AT NIGHT?
I'm always chatting on my phone to my manager or mates late at night, and usually go to sleep around 1am. Due to my hectic lifestyle and frequent travel, my body clock is never right. Strangely, if I've had more than seven hours' sleep, I'm tired throughout the day.
BIGGEST PHOBIA?
It sounds stupid but until about five years ago I was scared of the dark and slept with the telly on. Even now, if I'm sitting in the dark, I often switch on the light on my phone to check there's no one around! I also have a fear of moths and bugs, and hate it when an ant crawls on me, as I think they have germs.
LIKE TO LIVE FOR EVER?
Yes - I could do everything I want to do without rushing.
Educating Joey Essex: Reem Halloween, is on ITV2 at 9pm on Friday. 
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Woman who lost part of her leg to cancer has new knee joint made using her FOOT

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A young woman who lost her leg to cancer had a new knee joint created using her left foot - which was then attached backwards.
Jordon Moody's bone cancer meant her thigh had to be amputated - with her lower leg then moved up in the place of her thigh.
The 22-year-old from Hull, East Yorkshire, now has her foot in the place of her knee, but rotated 180 degrees. 
This leaves her toes twisted backwards and her heel at the front - providing the most natural 'downwards' angle to how a normal knee bends.
She is now waiting to be fitted with a new artificial lower limb, which will be attached to the joint created from her foot.
Jordon Moody, 22, lost part of her left leg to bone cancer. She now has her left foot in the place of her knee, but rotated 180 degrees. This leaves her toes twisted backwards and her heel at the front, creating the  most natural 'downwards' angle to how a normal knee bends, ready for a prosthetic to be attached 
Jordon Moody, 22, lost part of her left leg to bone cancer. She now has her left foot in the place of her knee, but rotated 180 degrees. This leaves her toes twisted backwards and her heel at the front, creating the most natural 'downwards' angle to how a normal knee bends, ready for a prosthetic to be attached 
She needed the radical surgery after her bone cancer returned for the second time. She underwent the op at the Royal Orthopaedic Hospital in Birmingham in July and is now adapting to life with her new limb
She needed the radical surgery after her bone cancer returned for the second time. She underwent the op at the Royal Orthopaedic Hospital in Birmingham in July and is now adapting to life with her new limb
She needed the radical surgery after her bone cancer returned for the second time. She underwent the op at the Royal Orthopaedic Hospital in Birmingham in July and is now adapting to life with her new limb
Miss Moody needed the operation after being diagnosed with bone cancer for a second time.
She had been studying performing arts in New York when doctors first discovered she had the disease in her thigh.
She stayed in America for the next year, undergoing chemotherapy and an operation to remove the tumour.
After being given the all-clear, she returned to England to the home she shared with her parents and two sisters.
But during a visit to her godmother in Germany last year, she suffered excruciating pain and was rushed to hospital.

WHAT DID THE SURGERY INVOLVE?

Miss Moody's bone cancer meant her thigh had to be amputated - with her lower leg then moved up in the place of her thigh.
The 22-year-old from Hull, East Yorkshire, now has her foot in the place of her knee, but rotated 180 degrees.
This leaves her toes twisted backwards and her heel at the front - providing the most natural 'downwards' angle to how a normal knee bends.
She underwent the surgery at the Royal Orthopaedic Hospital in Birmingham in July and is adapting to life with her new limb.
She is now waiting to be fitted with a new artificial lower limb, which will be attached to the joint created from her foot. 
She flew back to England and was taken to St James's Hospital in Leeds for more tests where doctors confirmed the cancer had returned and she was facing the amputation of her leg.
The 22-year-old said: 'The pain was worse than ever and I just couldn't move it.
'It was so scary, especially in light of the fact that the more times you get cancer, the less likely chemotherapy is going to work.
'In all honesty, you just have the fear that you are going to die.
'It's there in the back of your mind all the time.'
Doctors then told her she could either have a leg completely amputated or undergo the rotationplasty. 
She underwent the surgery at the Royal Orthopaedic Hospital in Birmingham in July and is now adapting to life with her new limb.
She is now waiting to be fitted with a new artificial lower limb, which will be attached to the joint created from her foot.
Miss Moody said: 'At first after the surgery, it was awkward-looking so it was a real shock.
'It took some getting used it but now, it seems totally normal to me.
Miss Moody, pictured with her parents, Ivory and Lieca and her sister, Tanika, is now waiting to be fitted with a new artificial lower limb, which will be attached to the joint created from her foot
Miss Moody, pictured with her parents, Ivory and Lieca and her sister, Tanika, is now waiting to be fitted with a new artificial lower limb, which will be attached to the joint created from her foot
'They told me they could get rid of my thigh and use the bottom part of my leg to replace the top part and my foot would become my knee.
'They would have to turn it 180 degrees because of the way the foot bends so it would bend the same way as a knee.
'It was really hard to hear.
'When they told me I had an option to keep my leg, this wasn't what I wanted to hear.'
Miss Moody said: 'It seemed like I would have a better quality of life as I could have a prosthesis fitted.
'I have been on crutches since I had the first operation so it's been a couple of years now.
It is hoped Miss Moody will be walking unaided again before Christmas
It is hoped Miss Moody will be walking unaided again before Christmas
'That's my main way of getting around and I use a wheelchair.
'Hopefully, before Christmas, I will be walking unaided again.'
She added: 'I've always been independent and I hate to feel dependent when I'm in a wheelchair or having to use the walking aids.
'There's not so much going out now but I will be able to walk unaided if I get a prosthesis so that's my aim now. That's my goal.' 
Mr Lee Jeys, an orthopedic oncology surgeon at the Royal Orthopedic Hospital, Birmingham, carried out Miss Moody's procedure.
He said: 'Jordon had already had treatment in America for a thigh tumour and unfortunately we needed to remove the whole of her thigh bone.
'Instead of leaving her without a leg, we connected her shin bone to the remaining thigh bone, creating a knee joint from her foot.
'The idea of the operation is where we turn the foot around and move it up, so Jordon could have a below the knee prosthesis.
'Otherwise she would have had to have an amputation and would have been left with no leg at all.
'It is very technical surgery and I perform it about three a year- usually on young patients.
'The aim of the surgery is so the patients can walk, and in clothes will look completely normal.
'Of course, out of clothes it looks a little unusual but we do it to offer patients the best functionality they can. Most patients will eventually be able to walk unaided.'

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Beautiful Selfies

Tuesday, October 21, 2014

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Beautiful Selfies
Beautiful Selfies
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The REAL Sleeping Beauty

Monday, October 20, 2014

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Teenagers are known for their ability to sleep for hours on end.
But one young woman suffering from a rare condition gets up to 22 hours of shut-eye a night.
Beth Goodier, 20, suffers from Kleine-Levin Syndrome, also known as 'Sleeping Beauty' syndrome, which dominates her life.
The neurological condition - which began when she was 16 - means she sleeps, on average, for 18 hours a night.
Beth Goodier, 20, suffers from Kleine-Levin Syndrome, also known as 'Sleeping Beauty' syndrome
Beth Goodier, 20, suffers from Kleine-Levin Syndrome, also known as 'Sleeping Beauty' syndrome 
Speaking on BBC Breakfast this morning, she described how the condition triggers episodes every five weeks. The condition is characterised by periods of excessive sleep of around 20 hours a day
When an episode strikes, typically every five weeks, she can sleep for anything between one and three weeks - and requires 24 hour care. 
Even when she wakes, she can be in a child-like state, confused and not able to tell the difference between reality and dreams.  
It's thought only around 1,000 people worldwide suffer from the disorder, 70 per cent of them male. 
It is not clear what causes it and there is no cure.  
Miss Goodier, from Stockport, Greater Manchester, appeared on BBC Breakfast this morning to discuss her situation, which triggers episodes every five weeks.
Discussing her frustration at the situation, she said: 'I spend half of my life in bed. The onset for most people is adolescence, when you are at college, university, getting a job, finding out who you are.
'It [Kleine-Levin Syndrome] takes all that away from you at a crucial time. My life is on hold.'
She added: 'I only remember snippets of an episode, so it's like half of my life disappears.' 
Miss Goodier was accompanied by her mother, Janine, who added: 'When she's up, all she does really is, she's either in bed or on the sofa and she'll watch telly, often the same things over and over again as she likes predictability.'
Upon eventually waking, Miss Goodier can be in a child-like state, confused and not able to tell the difference between reality and dreams. It means she must be constantly supervised by her mother Janine (pictured)
Upon eventually waking, Miss Goodier can be in a child-like state, confused and not able to tell the difference between reality and dreams. It means she must be constantly supervised by her mother Janine (pictured)
Mrs Goodier explained to Breakfast presenters Bill Turnbull and Louise Minchin how the family tries to make the most of the time between the Kleine-Levin episodes 
Mrs Goodier explained to Breakfast presenters Bill Turnbull and Louise Minchin how the family tries to make the most of the time between the Kleine-Levin episodes 
Patients return to normal between episodes, however they may become depressed as a consequence of the condition.
Mrs Goodier, who has been forced to give up work to care for her daughter, explained the family tries to make the most of the time between the episodes.

WHAT IS KLEINE-LEVIN SYNDROME? 

Kleine-Levin Syndrome is a neurological condition that starts during adolescence, and sometimes begins after an infection or illness.
It is characterised by periods of excessive sleep of up to 20 hours a day. Episodes can come on very quickly and last between a few days to a few weeks.
During such an episode a sufferer may be irritable, childish, disorientated and want to eat excessive amounts of food.
Patients return to normal between episodes, however they may become depressed as a consequence of the condition.
Around 1,000 people worldwide suffer from the disorder, which is commonly known as Sleeping Beauty Syndrome. Two-thirds of sufferers are male.
There is no known cure for the sleeping disorder, and the main treatment is watchful waiting at home by loved ones.
Research suggests episodes decrease in frequency and intensity over the course of 8 to 12 weeks. 
'On the odd time she's well we don't say any more, "We'll do that next week". 'We do it now when she's well because that might be the only time you get.'
Kleine-Levin Syndrome has had a devastating effect on Miss Goodier's life, stopping her from moving out of home or attending university, the BBC website reports. 
Because the condition causes her to often be in a child-like state when awake, she must be supervised by her mother.
During such an episode a sufferer may be irritable, childish, disorientated and want to eat excessive amounts of food. 
The disease tends to strike at a key time of life - during adolescence - and sometimes begins after an infection or illness.
Episodes can come on very quickly and last between a few days to a few weeks.
There is no known cure for the sleeping disorder, and the main treatment is watchful waiting at home by loved ones.
Eventually, the condition tends to 'burn out' after 10-15 years, doctors say. 
Miss Goodier added: 'I want to be able to do something productive in the time when I'm well.I want to productive for society,' she said on a programme aired tonight on BBC Inside Out North West. 
However she hopes by talking about her illness, she can raise awareness.  'There are Facebook groups, which have really helped. ' 
Miss Goodier's story features on BBC Inside Out North West tonight (Monday) at 7.30pm and will be available for 30 days on iPlayer after that. 
For more information on Kleine-Levin Syndrome, click here. 

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Sugary drinks could age the body as much as SMOKING, scientists warn

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Fizzy drinks appear to speed up the rate at which cells in the body age, a study has found 
Fizzy drinks appear to speed up the rate at which cells in the body age, a study has found 
Sugary soft drinks may accelerate ageing as much as smoking, new research shows.
Experts found the damage fizzy drinks cause to health goes beyond making people fat - they also appear to speed up the rate at which cells age.
The research showed that people who drank the equivalent of two cans of cola a day had DNA changes of cells 4.6 years older.
Campaigners have blamed sugary drinks for contributing to the rise in obesity and the number of people with type-2 diabetes, but this is the first piece to research to link soft drinks with premature ageing.
Scientists analysed thousands of DNA samples to find that people who regularly reached for a fizzy drink had shorter telomeres,
These are tiny structures that protect DNA from damage and are an indicator of health.
Found at the ends of chromosomes, they protect the DNA in them from damage, much like the caps on the ends of shoelaces prevent fraying.
As we get older, our telomeres get shorter and shorter, leading to DNA becoming damaged and raising the odds of age-related illnesses such as Alzheimer's, diabetes and heart disease.
Shorter than average telomeres are seen as a sign of ill health and premature death.
Studying telomeres, the scientists found people who regularly drank sugar-sweetened fizzy drinks had ‘significantly' shorter telomeres than those who did not.
Professor Elissa Epel, from the University of California at San Francisco, said: ‘Regular consumption of sugar-sweetened sodas might influence disease development, not only by straining the body's metabolic control of sugars, but also through accelerated cellular ageing of tissues.
‘This is the first demonstration that soda is associated with telomere shortness.
‘This finding held regardless of age, race, income and education level. 
'Telomere shortening starts long before disease onset.’
While she only studied adults, Professor Epel warned it is possible that drinking fizzy drinks is linked to telomere shortening in children, too.
Scientists analysed thousands of DNA samples to find  people who regularly consumed fizzy drinks had shorter telomeres (illustrated). These are tiny structures that protect DNA from damage and are an indicator of health
Scientists analysed thousands of DNA samples to find people who regularly consumed fizzy drinks had shorter telomeres (illustrated). These are tiny structures that protect DNA from damage and are an indicator of health
However, she stressed the study shows a link between soft drinks and ageing, but doesn't prove drinking fizzy drinks causes the ageing of cells.

HOW WORK CAN MAKE YOU STAY YOUNG FOR LONGER 

Working keeps you young, according to a study published last summer.
The research linked unemployment with premature ageing. It is thought that the financial and emotional stress of being jobless makes its mark on the body's DNA. 
Men who had been out of work for at least two of the three years before their blood was taken were more than twice as likely to have short telomeres as those who had been in continuous employment.
Researcher Jessica Buxton, of Imperial College London, said this suggests that the financial and emotional stress associated with being out of work was to blame. 
She said: 'Stressful life experiences in childhood and adulthood have previously been linked to accelerated telomere shortening.' 
In the study, the scientists measured telomeres in the white blood cells of 5,309 participants aged 20 to 65, with no history of diabetes or heart disease.
They found drinking two cans of cola a day – 20 fluid ounces – was linked to 4.6 years of ageing, based on telomere shortening and that one in five of the study’s participants fell into this category.
Drinking a small soft drink daily, equivalent to eight fluid ounces, was associated with telomere shortening equivalent to 1.9 additional years of ageing.
The effect on telomere length was similar to that of smoking, the researchers wrote in the American Journal of Public Health.
Dr Cindy Leung, also of the university, said: ‘It is critical to understand both dietary factors that may shorten telomeres, as well as dietary factors that may lengthen telomeres.
‘Here it appeared that the only beverage consumption that had a measurable negative association with telomere length was consumption of sugared soda.’
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I tried to kill myself with a bag of nuts says wife of Hasting Scott

Sunday, October 19, 2014

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On the face of it, Jenny Hastings looks like she has everything – a celebrity husband, a comfortable lifestyle, two talented children, and the slender figure of a twenty-something, the result of her years training as a swimmer and triathlete.
But the reality is that Jenny, the wife of Scottish rugby icon and Sky Sports commentator Scott Hastings, has spent the past two decades struggling with periods of mental illness which, although brief, have had a devastating impact.
Now both husband and wife have decided to break years of silence about the debilitating condition – including revealing the extraordinary moment just a few months ago when Jenny attempted to kill herself by eating a bag of peanuts, imagining her nut allergy would lead to a rapid death.
Laughing themselves back to happiness: Scott and Jenny share a light-hearted moment at home
Laughing themselves back to happiness: Scott and Jenny share a light-hearted moment at home
Jenny has even been driven to undergo controversial electric shock treatment – ECT – in a failed bid to cure her depression.
And she admits that in her distress she has tried to ‘marry off’ her husband to friends, believing he would be happier with someone else.
At their home in Edinburgh, she says: ‘We come from a generation that didn’t talk about the “D word”, so I’ve never felt able to talk about it publicly before. It was too personal and I felt too vulnerable.
‘I felt people would judge me if they knew and, at my worst moments, I felt useless enough as a wife and mother, even as a human being, without anyone adding to it.
‘People have said: “Jenny’s got everything, why on earth would she be depressed?”
‘But the reaction to my “coming out” has been absolutely amazing. I can’t believe how kind and supportive people have been. I’m touched by the love I’ve been shown.’
But just four months ago her depression reached a terrible nadir.
As she quietly explains: ‘I bought a bag of mixed nuts in Marks and Spencer, drove to South Queensferry and parked up the car, before eating a peanut. I’d left no suicide notes. No explanations. I just wanted to die and end it all.
Legend on the pitch: Scott Hastings in his rugby heyday playing for Scotland
Legend on the pitch: Scott Hastings in his rugby heyday playing for Scotland
‘I’m absolutely ashamed looking back, now that I’m well again, at what I almost did to Scott and our children. But at the time I thought I was doing them a favour and they would be better off without me.’
It’s clear the couple have developed a black sense of humour on the subject. Indeed, Jenny struggles to control her laughter as she describes how, after sitting in the car for hours with no reaction, she decided to drive home.
She recalled: ‘But when I reached the house, I started to be violently sick. I went into anaphylactic shock. Scott grabbed the EpiPen adrenaline shot and injected me in the leg. We didn’t know if we were using it properly, so he stabbed me in the other leg to make sure.
‘Then the doorbell rang. But it wasn’t the paramedics – it was the delivery man with the new bike I’d ordered. Honestly, you couldn’t make it up.’
At the time I thought I was simply doing them a favour
Her problems seem to have started with a bout of post-natal depression after having her second child. But she believes the latest trigger for was turning 50 in May and the prospect of ‘empty nest syndrome’ as their daughter, now 18, prepared to leave school and go off to university.
Jenny says: ‘I was in it again before I realised and all I can think of was it was a landmark birthday and Kerry-Anne was about to leave home. Sounds crazy that that would do it, right? But this time, it was the worst ever. I was in a very dark place, full of self-loathing.’
It was Scott, 49, a former British Lion and one of Scotland’s most capped rugby players, who cautiously suggested she should make her depression public, and they are speaking out in the hope it will help others feel less alone about the condition.
His first experience of the illness was in 1996 when he went off with the Scotland squad to New Zealand on a six-week tour and came back to find Jenny ‘in bits’, unable to cope with newborn Kerry-Anne and their young son, Corey, then three.
Suicide attempt: Jenny tried to kill herself by eating a bag of peanuts, imagining her nut allergy would lead to a rapid death
Suicide attempt: Jenny tried to kill herself by eating a bag of peanuts, imagining her nut allergy would lead to a rapid death
He adds: ‘In the beginning, I don’t mind saying now, I found it embarrassing when she was diagnosed with a mental illness. It was such a taboo subject.’ Jenny is clearly hearing this for the first time and asks incredulously: ‘Did you? You’ve never told me but then, I suppose, how could you?’
The rugby star replies: ‘It wasn’t the kind of thing I was going to start talking to anyone about. No one talked about mental health then. Thankfully we’ve come a long way but we could still go so much further.’
It may have become easier to talk about, but dealing with Jenny’s manic bouts at home – she’s had five in total – when they are in full flow can still be challenging.
Scott adds: ‘It’s like a slide, you can’t stop it. She goes off the edge into the precipice. It doesn’t matter what you say, there’s no pulling her back from it. She withdraws from life. She doesn’t like going outside and worries about everything.’
Scott, who nowadays runs a sports marketing and hospitality agency, laughs as he recalls how Jenny tried to ‘marry him off’ during her latest breakdown this summer to two of her friends because she thought he would be happier with someone else.
Embarrassed, Jenny explains: ‘I didn’t see how he could love me any more in the condition I was in, so I thought he should find someone else. He just looked at me like I was crazy, which I was.’
After a short spell in hospital after her suicide attempt, Jenny agreed to try six sessions of electroconvulsive therapy two months ago in the hope she would be one of the 93 per cent of people suffering from depression whose condition improves.
I’m proof that anyone going through this can get better 
The idea of treating a psychiatric illness by passing a jolt of electricity through the brain is one of the most controversial in 20th Century medicine, with critics branding it barbaric and ineffective.
Jenny says: ‘I was desperate. The hardest part was that every time I came round, I was an absolute blubbering mess. I felt like I was being traumatised more than ever. I wouldn’t put anyone off it. It works for some people, just not for me.’
For now, she’s content with life again, helped by the fact she has finally been given an official diagnosis of depression after a complete review of her case history.
She says: ‘I’m proof to anyone going through this that you can get better if you get the proper support. Scott has been a real rock for me.
‘And for me, this time feels different. I never say never and it’s early days but I’m quietly confident I’m not going back to that dark place again and the fact I’m able to talk about it for the first time ever, gives me a new confidence that everything’s going to be all right.’
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Truvada the Wonder drug' which can reduce HIV risk by 92%

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An HIV 'wonder drug' could be made available on the NHS, in what has been hailed as the most significant breakthrough against the virus in a generation.
A landmark trial in England is to be sped up after interim analysis of the the drug Truvada found it to be 'highly protective against HIV'.
Campaigners have urged the NHS to offer the medication – which has been approved for use in the U.S. since 2012 – to vulnerable groups as soon as possible.
A 'wonder drug' which can reduce the risk of contracting HIV by 92 per cent could be offered on the NHS, as a landmark trial into the drug's use could be sped up
A 'wonder drug' which can reduce the risk of contracting HIV by 92 per cent could be offered on the NHS, as a landmark trial into the drug's use could be sped up
U.S. guidelines say the tablet offers up to a 92 per cent reduction in the risk of contracting HIV - if taken every day. 
Truvada is a drug which provides 'pre-exposure prophylaxis' (PrEP).
This involves giving antiretroviral drugs - usually prescribed to treat HIV - to people who don't have the virus but are at a high risk of exposure to it.
NHS England have now set up a group looking into the viability offering Truvada on the NHS, as it is already known PrEP effectively protects against HIV.
As part of the trial, Truvada was prescribed to 407 men taking part in a study in Brighton, London, York, Manchester, Birmingham and Sheffield.
A further 138 men who were on the 'deferred arm' of the trial, originally due to receive the drug in a year's time, will now be offered it immediately. 

WHAT IS PRE-EXPOSURE PROPHYLAXIS? 

Pre-exposure prophylaxis, or PrEP, is a way for people who do not have HIV but who are at substantial risk of getting it to prevent HIV infection by taking a pill every day. 
The pill (brand name Truvada) contains two medicines (tenofovir and emtricitabine) that are used in combination with other medicines to treat HIV. 
When someone is exposed to HIV through sex or injection drug use, these medicines can work to keep the virus from establishing a permanent infection.
When taken consistently, PrEP has been shown to reduce the risk of HIV infection in people who are at high risk by up to 92per cent. 
PrEP is much less effective if it is not taken consistently.
PrEP is a powerful HIV prevention tool and can be combined with condoms and other prevention methods to provide even greater protection than when used alone. 
But people who use PrEP must commit to taking the drug every day and seeing their health care provider for follow-up every three months.
 Source: Centres for Disease and Control Preventions
Lead researcher Dr Sheena McCormack, from the Medical Research Council Clinical Trials Unit at University College London, who led the PROUD study told MailOnline: 'It’s the first HIV prevention trial of this scale that’s ever been done in the UK.
'To fast-track the trial is completely unexpected. When we started we didn't expect we would achieve a result in this number. 
'We were just seeing if we could recruit enough men.
'This is a real key piece of evidence that the policy group will put forward to make the case for the drug to be available on the NHS.
'These are great results, but we really want to understand them.
She added that a national trial could provide more information that would help NHS England make its decision.
She said: 'The early adopters might be very good at taking the tablets
'A national study might find people might not be so good at taking them.
'We need to look at how long people stay on it, do people carry on taking it?'
She added: 'A HIV test only gives you the results for your status six weeks ago. So you could leave the clinic today with a HIV negative and be highly infectious.
'So PrEP has a key role for people in between HIV tests.
'It’s really exciting, and I’m not going to give up. You don’t do research if you don’t want it to be put into clinical practice.'
The results of the trial will be published early next year and it is hoped that it could be rolled out nationally in 2017.
The study includes HIV-negative gay and bisexual men and transgender women who reported having anal sex without condoms recently.
All participants were offered regular testing for HIV and sexually transmitted infections, condoms and safer sex support.
Researchers hope to answer questions such as whether PrEP will lead to a reduction in the use of condoms and its impact on the spread of other sexually transmitted diseases.
Truvada has been approved for use in the U.S. since 2012, and is recommended for groups at high risk of exposure to HIV, such as non-monogamous couples and people who inject drugs
Truvada has been approved for use in the U.S. since 2012, and is recommended for groups at high risk of exposure to HIV, such as non-monogamous couples and people who inject drugs
Dr Rosemary Gillespie, Chief Executive at Terrence Higgins Trust, said: 'This is potentially the most exciting development in HIV prevention in some years. 
'For a trial to be fast-tracked in this way is rare, and shows just how much confidence researchers have in PrEP as a tool to reduce the spread of HIV. 
'A number of questions remain unanswered, including how PrEP will be made available and who will be able to access it. 
'The PROUD study has accelerated their part of the process. 
'We will now be looking to the NHS to match that pace, and act swiftly to ensure those most at risk of HIV in the UK can access PrEP.' 
U.S. studied found participants who took TRuvada every day reduced their HIV infection risk by up to 92 per cent
U.S. studied found participants who took TRuvada every day reduced their HIV infection risk by up to 92 per cent
Yusef Azad, director of policy and campaigns at NAT (National AIDS Trust), said: 'The announcement that the PROUD study has already shown such a significant benefit in preventing HIV transmission is exciting and welcome news. 
'HIV transmission in the UK remains far too high, especially among gay men, and we need to add to the prevention options available. These encouraging results provide powerful evidence that PrEP should be accessible to all who need it as soon as possible.'
At the end of 2013, 35 million people were living with HIV, according to World Health Organisation statistics. 
In May this year, the Centres for Disease Control and Prevention in the U.S. recommend that PrEP be considered for people who are HIV-negative and at substantial risk for HIV.
This includes gay or bisexual men who have had unprotected sex in the last six months, men who do not regularly use condoms, someone in a relationship with a person who is HIV- positive and people who inject drugs.
The decision followed from studies which found that taking Truvada daily reduced the risk of HIV by an average of 44 per cent when compared with a placebo. 
A quarter of participants who took Truvada every day reduced their HIV infection risk by 92 per cent compared with a placebo, although researchers warned this could be an overestimate, as people who took their drug many have also reduced the risk in other ways. 

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Send your child to school - even with tonsillitis!

Monday, October 13, 2014

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Send your child to school - even with tonsillitis! Parents outraged by new guide that tells them pupils should take 'zero days off' if they get range of conditions 

dular fever should carry on going to school, a new health guide tells parents.
The booklet says pupils should take ‘zero days off’ if they get a range of conditions during term time, which also include head lice, conjunctivitis and threadworm.
And children should take just five days off for chicken pox, whooping cough and mumps, and four days off for measles.Parents were outraged by the guide.
'Zero days off': Children with tonsillitis should carry on going to school, a health guide tells parents. (File image)
'Zero days off': Children with tonsillitis should carry on going to school, a health guide tells parents. (File image)
Father-of-two Gareth Whittle, from Cardiff, said: ‘I thought it was a joke. I think as parents we are responsible enough to know when and for how long we should keep our children away from school.’
Another parent said: ‘There are no hard and fast rules when a child falls ill – but each child is different and you get worse cases of mumps or chicken pox.
‘I don’t know who writes this rubbish, have they got children themselves?’ 
Pauline Jarman, a governor at Mountain Ash Comprehensive School in South Wales, said: ‘When I had glandular fever I was too run down to function.
‘I am inclined to trust the judgment of the parent or guardian.’
A spokesman for Rhondda Cynon Taf Council, one of the five local authorities in Wales to hand out the booklet, said the advice was taken from the Health Protection Agency in conjunction with the Royal College of Paediatrics.
The guide also urges parents to seek advice from NHS Direct or their GP before removing children from school.
Rules: Parents were told that children should not take any days off for head lice or conjunctivitis. (File image)
Rules: Parents were told that children should not take any days off for head lice or conjunctivitis. (File image)

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Sore after the gym? Get off your backside: The best way to beat pain is to move MORE, doctors say

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If a tough weights class has left you with sore muscles, you might want to relax on the sofa.
But moving around will stop the soreness more than resting, doctors have said.
Resting, using ice packs, anti-inflammatory drugs and and painkillers like ibuprofen actually delay a person's recovery from exercise rather than speeding it up, says the doctor who came up with a well-known technique for treating minor injuries 36 years ago.
Dr Gabe Mirkin came up with the RICE acronym, the most popular technique for recovering from muscle soreness, pain and injuries in 1978.
Moving around will help muscles recover after intense exercise more than resting, doctors have said
Moving around will help muscles recover after intense exercise more than resting, doctors have said
RICE stands for Rest, Ice, Compression, Elevation and describes the process he formerly recommended for treating minor injuries.
This involved resting the injured muscle, putting an ice pack on it followed by a compression bandage and then elevating the muscle to reduce swelling.
Now he has warned that the 'rest' and 'ice' elements should be scrapped as they could actually slow down the healing of sore muscles.
Writing on his blog, he said: 'Coaches have used my "RICE" guideline for decades, but now it appears that both Ice and complete Rest may delay healing, instead of helping.'
He added that athletes can begin moving a day after their injury, if it is a minor injury like muscle soreness.
He said: 'With minor injuries, you can usually begin rehabilitation the next day. You can move and use the injured part as long as the movement does not increase the pain and discomfort. 
'Get back to your sport as soon as you can do so without pain.'
His advice comes as new recommendations from the American Physical Therapy Association (APTA) advise that heat patches and ice packs could actually harm patients and stall their recovery. 
These remedies 'discourage patients from becoming active', which makes the time it takes for them to recover longer, and increases the risk of eventually needing injections or surgery, the recommendations said.
Muscle soreness is caused because muscles become damaged after intense exercise.
To heal damaged muscles, the body's immune system sends inflammatory cells and proteins to the tissue to promote healing.
The inflammatory cells - called macrophages - release a hormone called Insulin-like growth Factor (IGF-1) into the damaged tissues, which helps muscles and other injured parts to heal.
Ice packs could delay muscles from healing as they constrict blood flow to the injury, doctors advised
Ice packs could delay muscles from healing as they constrict blood flow to the injury, doctors advised
But Dr Mirkin says that applying ice to reduce swelling actually delays healing by preventing the body from releasing IGF-1.
Applying ice to damaged tissue causes blood vessels to constrict and shut off the blood flow that brings in the macrophages that will heal the muscles.
Dr Mirkin added that this shutting off the blood flow can cause the tissue to die and can even cause permanent nerve damage.
A previous review also found that using an ice pack might reduce pain but it also interferes with the athlete's strength, speed, endurance and coordination.
Dr Mirkin said that anti-inflammatory medicines like cortisone and pain-relieving medicines like ibuprofen, also reduce's the body's immune response and so will also delay muscles from healing.
Dr David Nieman, a professor at Appalachian State University told Outside Online magazine that people who take ibuprofen regularly have some cell damage, especially in their colon.
'That allows bacteria to escape in small amounts into the blood stream, augmenting the inflammatory response' he said.
He advised that the best way to avoid sore muscles is to eat properly; preferably 30 to 60 grams of carbohydrate an hour, or half a banana every 15 to 30 minutes.
He added that eating plenty of fruits and vegetables can help the speed up the healing process ad they contain flavonoids which protect the body against inflammation.
He said: 'Tissues with high levels of flavonoids can help the body protect against the inflammation and oxidative stress all of us go through all of the time just being living, breathing humans.
'It'll help make your body's natural defenses a bit better.'

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The little boy with cleft FEET whose mother can't find any shoes to fit him

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A mother has spoken of her despair at not being able to find any shoes that fit her son, who was born with a rare deformity.
Jack Duncan-Hale was born with cleft feet, which appear as though they are split down the middle, with his toes protruding outwards to the sides.
Due to the extent of his condition, the four-year-old cannot wear ordinary footwear. 
Jack has three toes on each foot which vary between a size 12.5 and 13.5, and he needs specialist footwear which is individually moulded for him. 
Jack Duncan-Hale (with his mother, Kim) was born with cleft feet, which appear as though they are split down the middle, with his toes protruding outwards to the sides
Jack Duncan-Hale (with his mother, Kim) was born with cleft feet, which appear as though they are split down the middle, with his toes protruding outwards to the sides
The four-year-old has three toes on each foot which vary between a size 12.5 and 13.5, and he needs specialist footwear which is individually moulded for him.
The four-year-old has three toes on each foot which vary between a size 12.5 and 13.5, and he needs specialist footwear which is individually moulded for him.
He has now outgrown a pair of orthopaedic shoes he was given when he was much younger, and needs specially made footwear so he can walk and play.
But Jack's desperate mother, Kim Hale, cannot afford to pay the £2,000 she has been quoted by a specialist cobbler.
Ms Hale, of Podsmead, Gloucester, said: 'I have been trying to do everything and I am just going around in circles.
'He has no shoes at all. He did have orthopaedic shoes but he cannot wear them any more as they don't fit him.
'You have to see his feet to believe it - this is such a rare condition.
'When he was younger it didn't really affect him but now he is walking a lot more his feet swell up.'
She is now appealing to the public to help her find an alternative.  'He needs special shoes but I can't get funding anywhere. 
'My GP has done everything he can and the school I can't thank enough because they have been trying their hardest.'
Cleft foot is a rare congenital anomaly that causes the affected foot to have missing toes, a V-shaped cleft and other anatomical differences.
The condition is generally thought to have a genetic cause. It can occur by itself, or with a cleft handIt is very rare, affecting fewer than 1 in one million babies.
To help with the family's problem, email david.shepherd@glosmedia.co.uk
Jack has now outgrown a pair of orthopaedic shoes he was given when he was much younger, and needs specially made footwear so he can walk and play
Jack has now outgrown a pair of orthopaedic shoes he was given when he was much younger, and needs specially made footwear so he can walk and play

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Thats awful;Man with 'agonising' 17-hour erection claims he had three pints of blood drained from his penis (and 24 injections).

Saturday, October 11, 2014

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Man with 'agonising' 17-hour erection claims he had three pints of blood drained from his penis (and 24 injections)

A man with a 17-hour erection had to have three pints of drained from his penis to relieve the problem.
Jason Garnett, 23, described the situation as 'pure agony' and said he could only watch in horror as a doctor stabbed a cannula into the side of his manhood.
He was diagnosed with a condition known as priapism - caused by a blockage of the blood vessels that empty the penis. 
Doctors told him they would have to draw off blood to reduce the pressure.
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Jason Garnett, 23, could only watch in horror as a doctor stabbed a cannula into the side of his penis
Jason Garnett, 23, could only watch in horror as a doctor stabbed a cannula into the side of his penis
'Seeing them stab my penis with a needle was horrible - like something out of a horror film,' said Mr Garner, a hotel worker from Harrogate, North Yorkshire.
'They were injecting me with adrenalin - and had to do it 24 times.'
Doctors had warned that if the injections failed to work, they would have to operate. 
The incident occurred last week after he spent the drinking heavily before sleeping with a female friend - and not taking Viagra, he insists.
'I got home went to sleep for a bit,' he told MailOnline. 'I woke up at 9am and it was there, but lots of guys have that in the morning.'
But by midday, the began to get concerned. 'It started to get really sore, and I looked on the internet to see what it could be.

WHAT IS  PRIAPISM?

Priapism usually affects men but in rare cases, can affect women too.
The condition is where a penis or clitoris becomes engorged with blood, causing a painful, long-lasting erection.
It is caused by a blockage of the blood vessels that empty the penis.
Also, a number of medications can sometimes disrupt the normal workings of the nerves that help trigger an erection by widening the arteries in the penis.
The nerves essentially ‘forget’ to narrow the arteries after the feelings of sexual arousal have passed, leading to priapism.
Those that have been linked to priapism include anti-depressants, erectile dysfunction medication and some recreational drugs.
'I was in so much pain when I arrived at the desk that I can't remember exactly what I said - but I made the staff laugh,' he recalled. 
Two hours later, a urologist arrived from another hospital to treat him. 
'He warned me he would have to draw the blood out by stabbing the side of my penis with a cannula.
'At that point I thought "just hurry up" - it really, really, really, really hurt.' 
The doctor drained two pints of blood - and the remainder was left to drip out onto an absorbent pad. 
'I think in total there was about three-and-a-half pints that came out,' said Mr Garnett.
'The urologist said he had never seen anything like it.'
Even after the blood had been drained, the erection remained.  It was only at 2am that the problem subsided - after 24 injections. 
Such was the extent of his blood loss and the effect on his blood pressure of the adrenalin injections, Mr Garnett had to spend Friday to Monday in hospital. 
Fortunately, he has been reassured there will be no long-term damage. But doctors can't rule out the problem occurring again. 
'I'm not worried about it, though,' said Mr Garnett. 'The girls will love it.' 
Due to the amount of blood he lost, and the effect of the adrenaline shots on his body, Mr Garnett had to stay in hospital for three nights 
Priapism usually affects men but in rare cases, can affect women too.
The condition is where a penis or clitoris becomes engorged with blood, causing a painful, long-lasting erection.
It is caused by a blockage of the blood vessels that empty the penis.
A number of medications can sometimes disrupt the normal workings of the nerves that help trigger an erection by widening the arteries in the penis.
The nerves essentially ‘forget’ to narrow the arteries after the feelings of sexual arousal have passed, leading to priapism.
Those that have been linked to priapism include anti-depressants, erectile dysfunction medication and some recreational drugs. 
Mr Garnett was diagnosed with a condition known as priapism - where the penis becomes engorged with blood, causing a painful, long-lasting erection
Mr Garnett was diagnosed with a condition known as priapism - where the penis becomes engorged with blood, causing a painful, long-lasting erection



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