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It was a cold, typically rainy Manchester evening, October 1993, when Michael Spencer Jones set out to meet a new guitar band he had been commissioned to photograph.

The weather was miserable, he didn’t know their music, wasn’t totally in the mood. “I had to drag myself from home, thinking: is it going to be worth the trouble?”

On the drive to the Out Of The Blue studio in Ancoats, on the outskirts of the city centre, a song he’d never heard before came on the local radio station. “It was like, wow, what is that?” The track was Columbia, by Oasis, the band he was on his way to meet.

He started to get excited.

Oasis star Liam Gallagher. Photo: © Michael Spencer Jones
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Liam Gallagher at the Out Of The Blue studios in October 1993. Photo: © Michael Spencer Jones

Spencer Jones had previously met Noel Gallagher during the musician’s time as a roadie for fellow Manchester band Inspiral Carpets. But not Liam.

“As a photographer, obviously, the aesthetic of a band is massively important,” he says as he recalls that first shoot. “I’m just looking down the camera lens with a certain amount of disbelief.”

In front of him was a 21-year-old, months before the start of the fame rollercoaster that lay ahead. And yet. “I was looking at a face that just seemed to embody the quality of stardom.”

Liam Gallagher pictured in one of the outtakes for the Be Here Now cover shoot. Pic: © Michael Spencer Jones
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Liam Gallagher pictured during the shoot for the cover of Be Here Now. Photo: © Michael Spencer Jones

‘Success was inevitable’

It was the start of a partnership that continued throughout the band’s heyday, with Spencer Jones shooting the covers for their first three albums, their most successful records, and the singles that went with them.

“You work with bands pre-fame and there’s always that question: are they going to make it? With Oasis there was never that question. Their success was inevitable.”

There was a confidence, even in those early days. “Incredible, intoxicating confidence. [They were] not interested in any kind of social norms or social constraints.”

It wasn’t arrogance, he says, of a criticism sometimes levelled at the Gallaghers. “They just had this enormous self-belief.”

Spencer Jones was one of several photographers who followed the band, capturing the moments that became part of rock history.

Oasis in Paris on the banks of The Seine in 1995 (L-R). Pic: Jill Furmanovsky
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Tension on the banks of The Seine in Paris in 1995. Photo: © Jill Furmanovsky

‘Noel had an uncanny intuition’

Jill Furmanovsky, who started working with Oasis towards the end of 1994, a few months after the release of debut album Definitely Maybe, says Noel always seemed aware their time together should be documented.

“An uncanny intuition, really, that it was important,” she says. “I think Noel has been aware right from the start, because for him that’s what he used to look at when he used to buy his Smiths records or Leo Sayer or whatever, he would stare at the covers and be fascinated by the pictures.”

Contrary to popular belief, Furmanovsky says the brothers got on fairly well most of the time, “otherwise they wouldn’t have been able to function”.

Oasis around the release of Be Here Now in 1997. Pic: Jill Furmanovsky
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This image was taken around the release of third album Be Here Now in 1997. Photo: © Jill Furmanovsky

She picks one shoot in 1997, around the release of their third album, Be Here Now, as one of the more memorable ones. Noel had shared his thoughts about the band on a chalkboard and “they were having such a laugh.”

But when things did erupt, it became significant. “There were tensions in some shoots but they never started hitting each other in front of me or anything like that. I used to complain about it, actually – ‘don’t leave me out of those pictures where you’re really arguing!’.”

In Paris in 1995, tensions had boiled over. “It’s one of my favourites,” she says of the shoot. “It reflects not just the band but the family situation, these brothers in a strop with each other.”

What is notable, she says, is that they were happy for photographers to take candid shots, not just set up pictures to show them “looking cool”. Pictures that on the surface might sound mundane, showing “what they were really like – tensions, mucking about, sometimes yawning… This was the genius of Noel and [former Oasis press officer] Johnny Hopkins.”

Furmanovsky also notes the women who worked behind the scenes for Oasis – unusual at a time when the industry was even more male-dominated than it is now – and how they kept them in line.

Read more on Oasis:
A high-five and the briefest hug: Oasis – the first reunion gig
Cool Britannia: Life in the UK in the ’90s
It felt like it would never happen – but now, finally, Oasis are back

Oasis stars Liam and Noel Gallagher during a break from the Wonderwall video shoot September 1995. Pic: Jill Furmanovsky
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The brothers pictured during a break from the Wonderwall video shoot September 1995. Photo: © Jill Furmanovsky

“They got on well working with women,” she says. “Maggie Mouzakitis was their tour manager for ages and was so young, but she ruled. For a band one could say were a bunch of macho Manchester blokes, they had a lot of women working in senior positions.”

This is down to the influence of their mum, Peggy, she adds. “Absolutely crucial.”

Furmanovsky has been working with Noel on an upcoming book documenting her time with the band, and says she initially wanted to start with a picture of the Gallagher matriarch. “Noel said to me, ‘Jill, you do know she wasn’t actually in the band?'”

Oasis stars Noel and Liam Gallagher in Portland Street, Manchester, in August 1995. Pic: Kevin Cummins
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The Gallaghers in Portland Street, Manchester, in August 1995. Photo: © Kevin Cummins/ Iconic Images 2025

Touring with Oasis – ‘the journalist had to take a week off’

Kevin Cummins was commissioned to take pictures when Oasis signed to Creation Records, and it “kind of spiralled out of control a little bit”, he laughs.

“I photographed them for NME, gave them their first cover. I photographed them in Man City shirts because we were all Man City fans, and City were at the time sponsored by a Japanese electronics company, Brother. It seemed a perfect fit.”

The early days documenting the band were “fairly riotous”, he says. “They were quite young, they were obviously enjoying being in the limelight.

“I remember we went on tour with them for three days for an NME ‘on the road’ piece, and the journalist who came with me had to take a week off afterwards.

“I dipped in and out of tours occasionally – I’ve always done that with musicians because I cannot imagine spending more than about seven or eight days on tour with somebody, it would drive you nuts. They’re so hedonistic, especially in the early days. It’s very, very difficult to keep up.”

Photos of Oasis taken by Kevin Cummins are on display at Wembley Park throughout the summer. Pic: Kevin Cummins/ Iconic Images 2025
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Photos of Oasis taken by Kevin Cummins are on display at Wembley Park throughout the summer. Photo: © Kevin Cummins/ Iconic Images 2025

Cummins says the relationship between Noel and Liam was “like anybody’s relationship, if you’ve got a younger brother – he’d get on your nerves.”

During the shoot for the City shirt pictures, he says, “Liam kicked a ball at Noel, Noel pushed him, Liam pushed him back. They have a bit of a pushing match and then they stop and they get on with it.”

Another time, following a show in Portsmouth, “as soon as we got [to the hotel] after the gig, Liam threw all the plastic furniture in the pool. Noel looked at him and said, ‘where are we going to sit?’ And he made him get in the pool and get all the furniture out. So there were like attempts at being rock and roll, and not quite getting it right sometimes.”

Cummins says he has “very affectionate” memories of working with Oasis. “I’ve got a lot of very sensitive looking pictures of Liam and people are really surprised when they see them,” he says. “But he is a very sensitive lad… it’s just he was irritating because he was younger and he wanted to make himself heard.”

Photographes taken by Kevin Cummins are on display at Wembley Park throughout the summer
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Photo: © Kevin Cummins/ Iconic Images 2025

Getting ready for the reunion

All three photographers have yet to see the reunion show, but all have tickets. All say the announcement last summer came as a surprise.

“There was an inkling of it, I suppose, just in the thawing of the comments between the brothers, but I still wouldn’t have guessed it,” says Furmanovsky, who has a book out later this year, and whose pictures feature in the programme. “It’s wonderful they have pulled it off with such conviction and passion.”

Cummins’ work can be seen in a free outdoor exhibition at Wembley Park, which fans will be able to see throughout the summer until the final gigs there in September.

“I think the atmosphere at the gigs seems to have been really friendly… I like the idea that people are taking their kids and they’re passing the baton on a little bit,” he says. “Everyone’s just having a blast and it’s like the event of the summer – definitely something we need at the moment.”

Noel and Liam Gallagher returning to the house where the cover for Definitely Maybe was shot. Pic: © Michael Spencer Jones
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The Gallaghers returning to Bonehead’s former home, where the cover for Definitely Maybe was shot. Photo: © Michael Spencer Jones

Spencer Jones, who released his second Oasis book, Definitely Maybe – A View From Within, for the album’s 30th anniversary last year – adds: “They really seem to be capturing a new generation of fans and I don’t think a band has ever done that [to this extent] before. Bands from 20, 30 years ago normally just take their traditional fanbase with them.”

But he says his first thought when the reunion was announced was for the Gallaghers’ mum, Peggy. “I think for any parent, to have two children who don’t talk is pretty tough,” he says. “It’s that notion of reconciliation – if they can do it, anyone can do it.

“The fact they’re walking on stage, hands clasped together, there’s a huge amount of symbolism there that transcends Oasis and music. Especially in a fractured society, that unity is inspiring. Everyone’s had a bit of a rough time since COVID, battle weary with life itself. I think people generally are just gagging to have some fun.”

Brothers: Liam And Noel Through The Lens Of Kevin Cummins is on at Wembley Park until 30 September. Definitely Maybe – A View From Within, by Michael Spencer Jones, available through Spellbound Galleries, is out now. Oasis: Trying To Find A Way Out Of Nowhere, by Jill Furmanovsky and edited by Noel Gallagher, published by Thames & Hudson, is out from 23 September.

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‘Living with a death sentence’: NHS cadaver implant leaves woman with one of world’s rarest diseases

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'Living with a death sentence': NHS cadaver implant leaves woman with one of world's rarest diseases

A woman infected with an incurable brain disease due to an NHS operation when she was three years old has told Sky News she is “living with a death sentence”.

Natalie Bralee-Brett was born with spina bifida, a birth defect caused by a gap between the brain and spinal cord.

In 1975, her mother Maureen was told by doctors at Great Ormond Street Hospital that Natalie would have an improved and prolonged life if they operated on her using a new procedure. 

But this, unknown to Maureen at the time, involved taking membrane taken from dead bodies and inserting it into Natalie’s spinal cord. Now nearly 40 years later this treatment is the very thing that could kill her.

Natalie Bralee-Brett was born with spina bifida
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Natalie Bralee-Brett was born with spina bifida

It has caused microbleeding on her brain, leading to memory loss. Natalie, 53, is also falling over constantly and suffers debilitating headaches. 

It also means Natalie is at high risk of dementia and could suffer a catastrophic stroke at any time. 

“Living with a death sentence, this is the only way I could describe it,” Natalie told Sky News. 

“Because every day, if you get a headache, you’re thinking ‘is this a sign of an episode that is linked to this problem? Is it a stroke?'” 

“I want to know why I’ve got this problem. And that probably makes me more angry than actually having to deal with this condition.”

Search for answers

Sky News has been following Natalie’s case for more than a year, and we have spoken to experts around the world to try to help Natalie get answers.

Natalie was given a dura mater graft in 1975. This is a piece of membrane collected from dead bodies. Its use is intended to protect the spinal cord and prevent fluid from leaking.

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Cadaver surgery leaves patient with incurable disease

Natalie as a child
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Natalie as a child

But over years, proteins already in the membrane can build up and cause plaques, leaving patients at high risk of diseases like Alzheimer’s. It can also make them vulnerable to strokes and brain haemorrhages. 

The procedure was common in the 1970s in the UK, across Europe and the US.

It’s thought tens of thousands of patients around the world might have undergone the procedure, but it is not known how many might be suffering the same life-limiting and potentially fatal consequences today. 

Natalie was diagnosed with a brain tumour in 2009, aged 37. A year later it was confirmed she had epilepsy. But it wasn’t until 2022 that Natalie was diagnosed with iatrogenic cerebral amyloid angiopathy (ICAA). 

Her family have now suffered another devastating blow.

Natalie’s brother Neil, who also had surgery for spina bifida in 1980, was diagnosed with ICAA in July. He’s no longer able to work and is suffering from Alzheimer’s.

Natalie and Neil with their mother Maureen
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Natalie and Neil with their mother Maureen

Natalie and Neil as children
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Natalie and Neil as children

The siblings were born with the same condition, underwent the same procedure, and are now infected with the same incurable brain disease. 

Natalie and Neil, 45, are the only siblings identified on the international ICAA register, which has just 52 confirmed cases.   

Natalie says her mother Maureen is “heartbroken”. 

ICAA cases ‘a heartbreaking tragedy’

Cases of ICAA have been identified in the Netherlands, Australia, Japan, Croatia, Austria, Italy, Spain, Slovenia, and the US.

Explained: Why cadaver implants are causing brain disease

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How cadaver graft caused incurable brain disease

Harvard Professor Steven Greenberg is one of the world’s leading ICAA experts. 

“We hope and believe the numbers will be limited,” he said. “The hope is that we’re talking hundreds.”

But for those who are impacted, “it is a heartbreaking tragedy, and we feel it very much as the healthcare providers taking care of them”.

ICAA is caused by a medical examination or treatment, relates to the brain, involves amyloid proteins that can stick together and cause a range of problems for major organs – and that is a disease of the blood vessels. 

Doctors believe there are three possible causes of the illness: cadaveric material introduced into a body during surgery, the use of human growth hormones containing cadaveric material and surgical tools not sufficiently sterilised. 

Professor Greenberg explained: ”When I was in medical school, one of my professors said ‘the I stands for I, the doctor caused the problem’.

“And in the case of iatrogenic CAA, this is kind of a heartbreaking echo of an era when it appeared that a good neurosurgical procedure was to use tissue from human cadavers to close defects in the nervous system.

“And I am not a surgeon and I certainly wasn’t practising at the time. But my understanding is that it appeared to be good natural biological material for closing up areas and then had this unexpected and tragic effect of introducing some kind of protein that would later cause disease in the brain.”

Prof Greenberg hopes cases of ICAA are restricted to hundreds
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Prof Greenberg hopes cases of ICAA are restricted to hundreds

‘I deserve answers’

Natalie’s health is steadily deteriorating. The bleeding on her brain is causing memory loss, and she dreads what the next few months will bring. 

“The pattern seems to be every time I go for a scan, I’m being shown to have more bleeding,” she said.

“And the last scan showed that I also had inflammation. It’s always hanging over you because you get a headache, and you think ‘is this going to turn into something worse?’

“And because of being at risk of a stroke it’s constantly there, and it’s a condition that is going to get worse.”

Natalie’s agony is further compounded by the lack of information.

She wants to know more about the donor of the diseased membrane implanted into her brain. But there is no record of where the dura mater came from.

And most of the time these grafts were made up from more than one body.

Natalie said: “I think I deserve answers. And if you’ve got something wrong with you, you want to know it’s human nature. You want to know why you’ve got this problem.”

Diagnosing ICAA has only become possible due to advancements made in MRI scanning.

Specialists including Professor Greenberg have set up the international register so any neurologist suspecting ICAA can flag cases to their peers.

This isn’t the first time cadaveric dura mater grafts have infected patients.

The World Health Organisation advised against their use in 1997 after it was discovered they had been giving patients Creutzfeldt-Jakob disease (CJD) which at the time was also being spread by eating cattle infected with BSE or ‘mad cow disease’.

There were 228 of these confirmed cases worldwide.

Dura mater grafts were used in more than 20 surgical procedures over 25 years, with the last known use in the UK in 1992.

Natalie Bralee-Brett says she is 'living with a death sentence'
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Natalie Bralee-Brett says she is ‘living with a death sentence’

‘Something is seriously wrong’

Simon Stratford was only 34 and a father of four young children when he died in April 2003.

That was nearly 16 years after having surgery to remove a brain tumour. During the operation a Lyodura graft was inserted into Simon’s brain. The membrane was infected with CJD and a coroner’s inquest found that it was this procedure that caused Simon’s death.

Simon Stratford with three of his children
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Simon Stratford with three of his children

Speaking exclusively to Sky News, his widow Colleen said she warned doctors treating her husband that she knew he was dying.

“I kept saying to the doctors he’s getting worse and something seriously is wrong, and you know, Simon did say to me at that point he thought he was dying.

“He had a brain tumour removed which saved his life and then was given a life sentence. They said it was the Lyodura dura mater that took his life.”

Colleen Stratford said she warned doctors treating her husband that she knew he was dying
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Colleen Stratford said she warned doctors treating her husband that she knew he was dying

Sky News asked B. Braun, a major German manufacturer which made Lyodura, to help with our investigation. They declined to comment on the link between dura mater grafts and ICAA.

For more than a year we have been speaking to experts around the world. Scientists in Europe declined to be interviewed. Natalie’s own medical team in the UK also refused to be interviewed.

The risks posed by the grafts are being better understood but the scale of the damage they have caused is not.

Some specialists who spoke to Sky News but did not want to be named are keen to stress that surgeons who carried out operations using these grafts were acting on the best available medical evidence to improve the length and quality of patients’ lives.

Natalie had her operation at Great Ormond Street Hospital. It’s likely, at least hundreds of patients would have undergone the same procedure.

Sky News has been speaking to experts around the world about cadaver implants for more than a year
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Sky News has been speaking to experts around the world about cadaver implants for more than a year

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Following our investigation, its medical director Dr Sophie Varadkar told Sky News: “We understand that this situation may be deeply worrying for former patients who believe they could have been affected.

“At the time, this type of product was commonly used in surgical procedures worldwide, and sadly, the risks associated with it were not yet understood.”

“For any of our former patients who think they may be affected, we will support you with getting access to your medical records to allow you to discuss your concerns with your current doctors.”

The Department of Health told us concerns around ICAA – including new forms of transmission – were being investigated.

“The Advisory Committee on the Safety of Blood, Tissues and Organs is currently considering this issue with a view to providing further advice to the Government,” a spokesperson said.

“We encourage anyone with concerns about historical treatment to speak with their GP or specialist healthcare team for appropriate support and guidance.”

Do you have a story to share with us? Contact NHSstories@sky.uk

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‘Critically ill with one of the world’s rarest diseases in a remote corner of British Isles’

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'Critically ill with one of the world's rarest diseases in a remote corner of British Isles'

Paddling in a bay on the tiny Channel Island of Sark, I suddenly felt very sick and cold.

Less than 48 hours later, I was being emergency evacuated to the intensive care unit of a London hospital via cart, tractor, lifeboat, private jet and ambulance.

Ultimately, an incredible team of doctors, nurses, and volunteers saved my life – for a second time, though falling ill with one of the rarest diseases in the world while in one of the remotest corners of the British Isles was an unfortunate first.

Deborah Haynes covers some of the biggest foreign stories around the world. She also hosts The Wargame podcast
Image:
Deborah Haynes covers some of the biggest foreign stories around the world. She also hosts The Wargame podcast

I have something called atypical Haemolytic Uremic Syndrome (aHUS) that – when triggered – affects my immune system, destroying blood cells and harming other vital bodily functions.

Classed as “ultra-rare”, there is only around one new incident of aHUS per two million people every year. And an attack can be fatal, so the speed of diagnosis is key.

In my case, I already knew about the condition as I first fell ill with it eight years ago.

When it happened a second time, the heroic efforts of Sark’s only doctor, a group of volunteer rescuers and the medics at University College Hospital (UCH) meant I was raced from the middle of the English Channel to an intensive care bed in just over 11 hours – enabling rapid and effective treatment.

Now back home and expected to make a full recovery, I thought I would share my experience to help raise awareness about this little-known disease as today is aHUS Awareness Day.

Deborah Haynes in ICU after falling ill with atypical Haemolytic Uremic Syndrome (aHUS)
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Deborah Haynes in ICU after falling ill with atypical Haemolytic Uremic Syndrome (aHUS)

‘I was feeling increasingly wretched’

My husband and I had planned to spend a few days in August on Sark – a beautiful island in between the UK and France that is a designated “dark sky” area because of an absence of light pollution.

There are no public streetlights on the territory.

More relevant to this story, cars and regular ambulances are also banned.

Instead of driving, Sark’s just over 500 residents and ferry-loads of tourists either walk, cycle or sit on the back of carts towed by horses – and on occasion tractors – to visit beaches, coves and other attractions.

A some 100-metre-high ridge connects the rock islands on Sark. File pic: AP
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A some 100-metre-high ridge connects the rock islands on Sark. File pic: AP

I started to feel queasy on the ferry that took us to Sark.

We initially thought it was seasickness.

But the nausea lingered as we walked from the port to our hotel to dump our bags.

Thinking a swim might make me feel better, we trekked down a steep path to the beach and ventured into the sea, which is when my body decided to break.

I came out of the water, shivering uncontrollably and thought I was going to faint. After getting myself dry, we tried to return to the hotel, but I started vomiting violently on the side of the path – much to the disgust of a family that was trying to overtake us.

Once back at the hotel, I collapsed into bed, only leaving it to be sick.

We speculated that it must be food poisoning and hoped it would pass within a day.

But 24 hours later, while I had stopped vomiting, I was feeling increasingly wretched and beginning to wonder whether it could be aHUS again.

The 'ultra-rare' condition is caused by part of the immune system becoming overactive
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The ‘ultra-rare’ condition is caused by part of the immune system becoming overactive

‘The onslaught is like an invisible storm’

The only other time I have been struck down by the disease was in January 2017, while working as the defence editor at The Times.

On that occasion, I took myself to my local hospital in Kent to be told that I had acute kidney failure and my bloods were “deranged”.

Fortunately, the haematologist on duty had been aware of aHUS – then a new acronym for me – and had me rushed to University College Hospital in London, which has a specialist team that can treat the condition led by Professor Marie Scully, a world-renowned expert.

I soon learnt that aHUS is caused by part of my immune system – called the complement system – becoming overactive and attacking my body rather than targeting bugs.

This “friendly fire” – likely linked to a genetic glitch that, in my case, had thankfully lain dormant for the first 40 years of my life – can be activated by infection, pregnancy or food poisoning, though sometimes the cause is unknown.

The subsequent onslaught is like an invisible storm that destroys a patient from the inside, shattering red blood cells, damaging small blood vessels and causing tiny clots.

The clots clog up kidneys and trigger acute renal failure.

If left untreated, other organs can also collapse, while the risk of a stroke or heart attack rises.

Without intervention, the prognosis is dire.

Between 10 to 15% of patients die during the initial illness, while up to 70% of patients develop end-stage renal failure, requiring a lifetime of dialysis.

Since 2013, however, patients in the UK have had access to a drug called eculizumab, which effectively turns off the malfunctioning part of the immune system. It is expensive – at many thousands of pounds a shot – but it saves lives, including mine.

An aHUS attack can be fatal, so the speed of diagnosis is key
Image:
An aHUS attack can be fatal, so the speed of diagnosis is key

‘My protein levels were off the scale’

Lying in bed in Sark more than eight years on from the first episode, I did not want to believe my body had turned on itself again.

But after a little over 36 hours, with no improvement, my husband decided to get help.

His action likely saved me from even graver kidney damage or worse.

He set out to find Sark’s only GP, Dr Bruce Jenkins.

Blood tests are the best way to diagnose aHUS, but they were not an option on the island.

Instead, Dr Jenkins did a urine test, which is a good alternative.

Any trace of blood or protein in the urine is a sign that a person’s kidneys are in trouble.

My protein levels were off the scale of the test.

Upon seeing the result, Dr Jenkins instructed my husband to go back to our hotel and pack our bags – I was still floundering in bed – while he coordinated an emergency evacuation.

On Sark, given the lack of vehicles, this meant mobilising an ambulance cart towed by a tractor, which is operated by a team of Community First Responders – all volunteers.

The Sark medical team who helped save Deborah's life
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The Sark medical team who helped save Deborah’s life

The GP also contacted the main hospital on Guernsey, a larger Channel Island, which provides a marine ambulance service to rescue anyone with a medical emergency on Sark.

While all this was happening, I called an emergency number for the aHUS medics at University College Hospital to warn them I was likely suffering a relapse.

By chance, Professor Scully was on duty that day – a Friday – and over the weekend. She and her team sprang into action, contacting Sark and Guernsey to help.

Speed was key as my condition was worsening.

‘I asked a doctor if I was going to die’

Within minutes of the alert going out from Dr Jenkins, a tractor, pulling a white ambulance cart, arrived at our hotel, and the first responders guided me and my husband onboard.

They took us to the port to wait for the “Flying Christine”, an ambulance boat carrying two paramedics and operated by St John’s Ambulance and Rescue Service.

That team transported us via sea to Guernsey hospital before we were transferred to a specialist medical plane to be flown to Luton airport.

The last leg was a more conventional ambulance drive to UCH, where critical care doctors, as well as Professor Scully and her colleagues, were poised to start the treatment.

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This quick response by the NHS and a network of volunteers meant I was taken from my sickbed in Sark to life-saving treatment in London in barely 11 hours.

By this point, the aHUS attack had caused my haemoglobin and platelet levels to drop, and my kidneys were failing.

The main treatment was the eculizumab drug – administered intravenously – but I also needed blood transfusions and to be put on a machine that acts as a form of dialysis.

The relief of being in the best possible place for my condition was immense, but the next few days were still frightening as my body took time to respond.

At one point, I asked a doctor if I was going to die – she assured me I was not.

Deborah has now been discharged and says she is 'on the mend'
Image:
Deborah has now been discharged and says she is ‘on the mend’

On another occasion, pumped full of medication, hooked up to various machines and drifting in and out of sleep, I dreamt I was under missile fire – an occupational hazard of being a journalist who covers war – and tried to leap out of bed to an imaginary shelter, prompting the nurse who was looking after me to spring into action and make sure I stayed put.

Gradually, though, the treatment started to work.

After nearly a fortnight in hospital, including one week in intensive care, I was well enough to be discharged.

Today, I am on the mend and incredibly grateful to everyone who helped to save me from myself.

Deborah Haynes and Professor Marie Scully will be on Sky News from 8.30am to speak about aHUS Awareness Day.

What is aHUS?

Atypical haemolytic uraemic syndrome is an ultra-rare disease that affects between 2.7 and 5.5 people per million population worldwide. It has an incidence rate of about 0.4 people per million a year and can occur at any age.

The disease affects part of the immune system called the complement system. It starts to destroy the body’s own cells, especially those that line blood vessels. This leads to clots forming within small vessels. The kidney is most commonly impacted, but all organs can be harmed.

AHUS is typically linked to a genetic fault in the complement system or a group of proteins meant to regulate it.

The trigger for an attack can be infection, pregnancy or food poisoning.

Symptoms can include feeling unwell or tired, becoming confused, blurred vision, shortness of breath, high blood pressure, nausea and vomiting, diarrhoea and abdominal pain.

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Boris Becker ‘shocked’ by drug use and overcrowding during his time in UK prison

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Boris Becker 'shocked' by drug use and overcrowding during his time in UK prison

Former tennis star Boris Becker has told Sky News he was “shocked” by widespread drug use and overcrowded conditions during his time behind bars in the UK.

Becker claimed there weren’t enough officers to manage nearly 2,000 inmates at London’s Wandsworth Prison, where he was jailed for hiding £2.5m of assets and loans to avoid paying his debts.

The 57-year-old German told The UK Tonight With Sarah-Jane Mee: “Who’s controlling who? It’s just so overcrowded.”

In his new book about life on the inside, he says the “wardens are in charge until they weren’t”.

He told Sky News: “Mine was a white-collar crime, as they say, but my next-door cell neighbour was a murderer, opposite was a paedophile and on the right there were people smugglers and serious drug dealers.

“Everyone is together, so naturally there’s friction.”

Boris Becker at London's Southwark Crown Court for his trial in April 2022. Pic: Reuters
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Boris Becker at London’s Southwark Crown Court for his trial in April 2022. Pic: Reuters

‘You could get pretty much everything’

The former sportsman, who won Wimbledon three times, was in HMP Wandsworth for several weeks as part of his sentence and was released from jail in December 2022.

He served just eight months of a two-and-a-half-year jail term but was deported afterwards despite having lived in the UK for a decade.

Becker said it was an eye-opener that it was possible for some prison inmates to get hold of contraband.

“I didn’t know you could get pretty much everything inside,” he said.

“I’m talking about the drugs, talking about small phones, talking about food – whatever you wanted. Even a bit of alcohol on the weekends.”

“That shocked me,” he admitted.

“The most common drug on the inside was called spice, I’d never heard of it before,” said Becker, adding: “Everyone knows who’s doing what, it’s just a lot of people choose to look away.”

Spice is a synthetic drug that is incredibly strong and addictive, and has been a problem in prisons for a number of years.

It is understood that there were 240 prison officers available for duty at the time Becker was in prison in Wandsworth. He was one of about 1,500 prisoners at the jail.

A Ministry of Justice spokesperson said: “The government inherited a prison system in crisis overcrowded, crumbling infrastructure and our hard-working prison staff at risk of violence and harm.

“We have already taken action to improve safety, security, and conditions at HMP Wandsworth. We have deployed specialist staff and will redirect £100m to be spent over five years.”

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