Katie Price is ‘dicing with death' as she undergoes ‘riskiest surgery yet', warns surgeon
Click to share on Facebook (Opens in new window)
A SURGEON has warned Katie Price is 'dicing with death' as she undergoes 'riskiest surgery yet'.
It comes as media personality Katie, 46, recently revealed her plans to have a fourth BBL surgery.
Sign up for the Entertainment newsletter
Sign up
4
A surgeon has warned Katie Price is 'dicing with death' amid plans for a risky surgery
Credit: Getty
4
Katie is no stranger to going under the knife
Credit: Katie Price
4
Dr Gerard Lambe shared his advice to the media personality
Credit: Reflect Clinic
Standing for Brazilian Butt Lift, the procedure entails injecting fat from other parts of the body into the bottom to give a more rounded or lifted look.
According to Dr Gerard Lambe, one of the UK's leading plastic surgeons and head of Reflect Clinic UK, the star has major factors to consider.
Dr Lambe told New Magazine: 'Katie needs to be aware that she is putting her health and body under extreme pressure with the now countless number of procedures she's had done in the last year alone.
"BBL is one of the most dangerous surgeries anyone can undergo and it has the highest mortality rate – it's one of Katie's riskiest surgeries yet. She is dicing with death."
He added: "When injecting deeply, the fat can enter veins that are large and the fat can travel to the heart or lungs, and in severe cases this can be fatal.
"It is also necessary to follow strict post-op protocols.
"The human body needs long rest periods between any essential surgeries, never mind cosmetic ones.
"She is putting her heart and organs under considerable pressure and not allowing the vital healing period between surgeries."
Katie previously told fans on Instagram: "So yeah, got the volume in the lips and now I'm gonna see the surgeon about my butt.
"So yeah, if there's anyone who, you know, instead of having surgery you want your butt done, obviously all your lips or this is the place for you.'
Katie Price undergoes new 'age reversing' procedure in bid to turn back the clock - despite fans begging her to stop
In her caption, Katie confirmed her plans: '@THE_CLINIC_CLUB BBL PENDING WITH NEW SURGEON.'
Back in February, Katie insisted she would not be undergoing further surgery to make her bum bigger.
She had planned another BBL but, in a shock u-turn, decided she would enlarge her behind through hardwork instead.
Speaking on The Katie Price podcast, the star revealed: 'I'm starting the gym next week.
'I've decided my bum I'm not going to have filler or implants, I'm going to work my a*** off at the gym.
'I'll do before and after pictures mind you it will probably take a year to get my bum to where I want it.'
Katie Price's Surgery: A Timeline
1998 - Katie underwent her first breast augmentation taking her from a natural B cup to a C cup. She also had her first liposuction
1999 - Katie had two more boob jobs in the same year, one taking her from a C cup to a D cup, and then up to an F cup
2006 - Katie went under the knife to take her breasts up to a G cup
2007 - Katie had a rhinoplasty and veneers on her teeth
2008 - Katie stunned fans by reducing her breasts from an F cup to a C cup
2011 - Going back to an F cup, Katie also underwent body-contouring treatment and cheek and lip fillers
2014/5 - Following a nasty infection, Katie had her breast implants removed
2016 - Opting for bigger breasts yet again, Katie had another set of implants, along with implants, Botox and lip fillers
2017 - After a disastrous 'threading' facelift, Katie also had her veneers replaced. She also had her eighth boob job taking her to a GG cup
2018 - Katie went under the knife yet again for a facelift
2019 - After jetting to Turkey, Katie had a face, eye and eyelid lift, Brazilian bum lift and a tummy tuck
2020 - Katie has her 12th boob job in Belgium to correct botched surgery and a new set of veneers
2021 - In a complete body overhaul, she opts for eye and lip lifts, liposuction under her chin, fat injected into her bum and full body liposuction
2022 - Katie undergoes another brow and eye lift-and undergoes 'biggest ever' boob job in Belgium, her 16th in total
2023 - Opting for a second rhinoplasty, Katie also gets a lip lift at the same time as well as new lip filler throughout the year
2024 - Katie has her 17th boob job in Brussels after revealing she wanted to downsize. She performed at Dublin Pride just days later and surgeons warned the lack of recovery posed a risk of infection
While last year, Katie revealed she wanted a 'bubble butt', adding to her already extensive list of procedures.
She said: 'I've just had my consultation to get my bum as big as my lips.
'I'm getting it done in Janaury but this time they've got an ultrasound which means it'll be much safer.
"Get used to the big lips because soon I'm going to have a bubble butt. Wahey!"
Hashtags
Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Daily Record
an hour ago
- Daily Record
Mum with MND dies after starving herself to 'protect her children'
The news of Dignity in Dying campaigner Emma Bray's death was shared in an emotional post on social media. A mum with motor neurone disease has died after she made the heartbreaking decision to starve herself to death to 'protect her children' from witnessing her die suddenly from choking. Emma Bray, 42, previously spoke of her intention to move into a hospice and stop eating and drinking voluntarily. The mum-of-two from Barnstaple, North Devon, was devastated she could not hug her children or dry their tears due to the progression of her condition, but wanted to fight for the law to change on assisted dying to help others in similar situations, the Mirror reports. On Monday, July 14, she shared a final message on her @stupid_mnd Instagram page, along with a picture of her lying in her bed in the hospice. She wrote: 'If you are reading this then I've finished my final spin round the sun. 'I've lived a very good life, surrounded by love, music and laughter and I want this to continue in my memory. Rather than shed a tear (or whilst you do) please plant a tree or call a friend, do a random act of kindness or take time to watch a sunset. 'For moments of doubt please ask 'what would Emma do?' and run with that probably inappropriate answer. Hug everyone a little tighter and love openly. 'Please surround those who were closest to me with love, time and patience. And to quote Frank Turner - Remember you get to dance another day but now you have to dance for one more of us. Love you, bye.' Just days before, she had gone to see Alanis Morrissette in concert with friends, ticking an item off her "bucket list". She said at the time: 'After 29 years of true love I wasn't going to let a little inconvenient terminal illness let me miss this.' At the end of May this year, the former charity worker, who had supported hundreds of domestic abuse victims and homeless people, revealed she wanted to protect her "amazing" children, aged 15 and 14, from witnessing her potentially "brutal" death. She said: 'I've had four different health professionals tell me I've got the worst disease possible.' Join the Daily Record WhatsApp community! Get the latest news sent straight to your messages by joining our WhatsApp community today. You'll receive daily updates on breaking news as well as the top headlines across Scotland. No one will be able to see who is signed up and no one can send messages except the Daily Record team. All you have to do is click here if you're on mobile, select 'Join Community' and you're in! If you're on a desktop, simply scan the QR code above with your phone and click 'Join Community'. We also treat our community members to special offers, promotions, and adverts from us and our partners. If you don't like our community, you can check out any time you like. To leave our community click on the name at the top of your screen and choose 'exit group'. If you're curious, you can read our Privacy Notice. Emma did not want her children to watch her suddenly choke to death, instead wanting a "calm and peaceful death", and had also planned her funeral and written her eulogy. She added: 'My last bit of parenting I can do is to limit the suffering and trauma they have to witness. 'I made a promise to myself that I wanted to wait to see my daughter finish high school and my son grow up a little so I can picture the man he will become.' She chose to die using the practice of voluntarily stopping eating and drinking (VSED). According to Compassion in Dying, this involves an adult 'with mental capacity to decide to do so and in the absence of control or coercion', decides to hasten their death by completely restricting all food and fluids. They say dying as a result of VSED can typically take between 10 and 14 days. Emma had also travelled to London to show her support for the Assisted Dying Bill. She wanted other families in a similar position to avoid having to make decisions between two "painful and potentially horrific" ways to die. She said: 'This bill will have offered me protectio n for those I love who have already spent two years living with anticipatory grief and watching me suffer. 'Imagine seeing your children crying and upset and not be able to hug them or curl up in bed and wipe their tears away. This is hands down the thing I hate the most about motor neurone disease. It's taken my children's mum from them little by little.' Speaking to the Mirror using her eye gazing machine, she continued: 'I now feel I am at the stage where my quality of life is very affected, I can no longer use any of my limbs. My talking is severely affected and I struggle to eat and it's getting harder to breathe. I am only really comfortable in bed and social visits are exhausting. 'I have carers multiple times a day, can't be left alone overnight and can no longer do any basic tasks. I can't scratch an itch, push up my glasses, move a bed sheet if I am too hot or cold. I feel like I am losing the essence of me, I am still so loved but I can't be myself and I see that grief on everyone's faces. 'This whole journey has been brutal but I have still been able to be a parent and I now realise I can't be a bit of the parent I need and want to be. Watching your children grieve you and not be able to hug them is the most painful feeling ever. This disease takes from everyone and it will take the children's mother from them bit by bit.' Emma told us: 'VSED is not an easy death but with the current law in England this is the only way I can have control over my death. 'I want to protect my children from seeing me choke and struggle to breathe. I don't want to die but I am going to and have come to terms with my impending death and I know I want to die surrounded by loved ones, music and laughter not in an emergency way after further decline.' '...My end of life wish is to be at the hospice surrounded by my friends and family. I want to have music playing, to hear people laugh and watch them playing card games over me.' Honouring her children, Emma said: 'My children are amazing and have spent so much of their childhood witnessing me decline. 'They watched me crawl around the floor for a year before diagnosis, they help me with everything as I have no working limbs, they live in an environment where there is a constant flow of carers coming into our home. 'They are obviously struggling. They struggle watching me fade, they are already grieving for the mum I once was. How they are still attending school and laughing astounds me and is a credit to what amazing people they are. 'They have a village of people around them but I know they desperately miss me. They are living in limbo land, they know they will have to move house to live with their dad but they don't know when and that uncertainty is hard for them. 'I can see their pain and grief on a daily basis and I would do anything to take that away from them. They are desperate for a hug from me and that hasn't happened in years… 'There is never a good time to lose your mum but all my maternal instincts want to make that horrible reality as easy for them as I can. 'I urge MPs to realise that this bill will not end my life, motor neurone disease is doing that but they can help me and others with less than six months to live to die with peace. '
Daily Mirror
2 hours ago
- Daily Mirror
'I was diagnosed with cancer three weeks after clear mammogram'
Louise Butcher said she only picked up her lobular breast cancer because she was doing such a thorough check Louise Butcher, a 52-year-old charity worker from Braunton, Devon, discovered she had lobular breast cancer after performing a self-check at home, despite a mammogram three weeks earlier showing no signs of the disease. Although it came because she struggled with health anxiety, Louise's vigilance paid off when she noticed a 'thickening' in her left breast, leading to an ultrasound that revealed a 5cm tumour. Diagnosed in April 2022, Louise underwent a mastectomy and later chose to remove her right breast as well. This week, campaigners have been pressing Health Secretary Wes Streeting for increased research into this type of cancer, which often evades detection on mammograms. Louise said: "I did a self-check at home. There was a weird feeling - a thickening like it was attached to something else. "It doesn't feel like a lump - more like a spider's web. I had never heard of it [lobular cancer]." Louise credits her thorough self-examination for detecting the cancer, noting that while growth near the nipple can cause inversion and dimpling of the skin, she experienced none of these symptoms. At present, there is a lack of national standard treatment or guidelines specifically for lobular breast cancer, with it being treated similarly to other forms of invasive breast cancer, despite being the second most prevalent type. Following her diagnosis, Louise chose to have a double mastectomy and opted against reconstructive surgery, instead learning to accept and love her new body. She explained: "I couldn't cope with just having one. I was too scared - if you can't see it I'm going to be scared all the time." Louise also decided against conforming to societal expectations of undergoing reconstructive surgery, adding: "I didn't feel the need to stick with social norms and get reconstructive surgery. I accept the way I am - and it's something I've learnt to control, despite what others think." Louise is a strong advocate for increased research into lobular cancer, highlighting the complexities and uncertainties surrounding the disease: "You never know what's happening with it. It's not so simple." The campaign is urging the government to pledge £20m over five years to fund research into lobular cancer. Louise has also written a book, 'Going Topless', and can be followed on Instagram @louisebutcher39.
Daily Mirror
3 hours ago
- Daily Mirror
Brave mum Emma Bray's final days after deciding to starve herself to death for sake of her kids
Dignity in Dying campaigner Emma Bray has died after making the heartbreaking decision to starve herself to death. Just last month, she spoke with the Mirror about her poignant hopes for her final days A courageous mother has shared a heartbreaking message from beyond the grave after making a difficult decision. Emma Bray, who lived with Motor Neurone Disease (MND), previously spoke with the Mirror about her plans to voluntarily stop eating and drinking after moving into a hospice. The Dignity in Dying campaigner explained that she wanted to shield her 'amazing' children, aged 15 and 14, from the 'brutal' and "terrible" death she faced, in what she regarded as her "last bit of parenting". Now, an Instagram post has revealed that the 42-year-old has sadly died, just one month after she opened up about her wishes for her final days. The pre-written message was accompanied by a photograph of Emma lying in her hospice bed in Devon, looking out over a tranquil tree-lined view. Expressing gratitude for her time on this earth, Emma, from Barnstaple in North Devon, wrote: "If you are reading this, then I've finished my final spin round the sun. "I've lived a very good life, surrounded by love, music and laughter, and I want this to continue in my memory. Rather than shed a tear (or whilst you do), please plant a tree or call a friend, do a random act of kindness or take time to watch a sunset. "For moments of doubt, please ask, 'What would Emma do?' and run with that probably inappropriate answer. Hug everyone a little tighter and love openly. "Please surround those who were closest to me with love, time and patience. And to quote Frank Turner - Remember you get to dance another day, but now you have to dance for one more of us. Love you, bye." Back in June, Emma, who helped hundreds of domestic abuse victims and homeless people through her career as a charity worker, reflected on how she'd like to spend her final days. She shared her longing for a 'calm and peaceful death', and revealed that she'd already planned her funeral and written her eulogy. Emma continued: 'VSED is not an easy death, but with the current law in England, this is the only way I can have control over my death. 'I want to protect my children from seeing me choke and struggle to breathe. I don't want to die, but I am going to and have come to terms with my impending death, and I know I want to die surrounded by loved ones, music and laughter, not in an emergency way after further decline.' "My end-of-life wish is to be at the hospice surrounded by my friends and family. I want to have music playing, to hear people laugh and watch them playing card games over me.' As per Compassion In Dying, VSED is a process whereby an adult 'with mental capacity to decide to do so and in the absence of control or coercion, makes a decision to hasten their death by completely stopping the oral intake of all food and fluids'. Death can take between 10 to 14 days. Emma was first diagnosed with MND two years ago. She told us: 'I've had four different health professionals tell me I've got the worst disease possible." MND is a terminal neurological condition that affects a person's brain and spinal cord, resulting in muscle weakness and wasting. As her condition progressed, Emma was left unable to hug her two children or wipe away their tears, and she was left fearing the possibility of choking to death in front of loved ones. The devoted mum, who spoke with the Mirror using her eye gazing machine, discussed the severe difficulties she was facing day to day, stating: 'I now feel I am at the stage where my quality of life is very affected, I can no longer use any of my limbs. My talking is severely affected, and I struggle to eat, and it's getting harder to breathe. I am only really comfortable in bed, and social visits are exhausting. 'I have carers multiple times a day, can't be left alone overnight and can no longer do any basic tasks. I can't scratch an itch, push up my glasses, or move a bed sheet if I am too hot or cold. I feel like I am losing the essence of me. I am still so loved, but I can't be myself, and I see that grief on everyone's faces." Expressing her support for the Assisted Dying Bill, Emma said: 'This bill will have offered me protection for those I love who have already spent two years living with anticipatory grief and watching me suffer. 'Imagine seeing your children crying and upset and not be able to hug them or curl up in bed and wipe their tears away. This is hands down the thing I hate the most about motor neurone disease. It's taken my children's mum from them little by little… 'I urge MPs to realise that this bill will not end my life, motor neurone disease is doing that, but they can help me and others with less than six months to live to die with peace. '
