
Дружина Лесика підтвердила його отруєння і висловилась, хто це зробив: “Дуже ненавидить його”

A LOTTO winner hilariously hit back at a troll who body-shamed her by wiping fake tears with £20 notes.
Olivia Love, of Glasgow, scooped £10,000-a-month for a year alongside hubby Kevin last month.
After the first installment dropped in her bank account, Olivia went on a huge shopping spree and enjoyed her “Pretty Woman moment” spending £750 in Victoria’s Secret.
The 36-year-old’s also been able to quit her job at a local supermarket, and hire a cleaner and gardener.
And thanks to her massive tax-free win, she hopes to build her dream career in wedding content creation.
Since going public with her win, Olivia has been speaking out about the life-changing cash in more detail on TikTok.
Many social media users have flooded her with supportive messages, but the mum-of-four has still faced cruel comments from trolls.
In a video, she said: “You see things like ‘looks like she needs a PT’, I’m assuming personal trainer. Or when they say things like, ‘my bro’s only with her for the money’.
“And when they comment on the things that I’ve spent the money on. It’s pretty soul destroying to have this kind of bullying.
“Now I realise that I went public, so I’m kind of bringing this on myself. But I didn’t realise that in announcing a lottery win [and] trying to change our lives by using the money for good, would end up with this.
“It’s 2025, why are we still commenting on a woman’s body?
“This is a happy time for my family. We’re overjoyed, we’re so unbelievably happy. And it has changed our lives for the better.
“But these people, with their jealousy and nastiness, are determined to bring me down. I’ve got a relatively thick skin, I’ve been through a lot of s***. And I’ve done my best to come out the other side of it.”
Olivia made an example of one hateful message by responding with a hilarious video.
She wiped fake tears from her eyes with £20 notes she pulled from a Kleenex box and joked that she “cried all the way to the bank” while looking at a comment which read: “£750 in Victoria’s Secret? For her? She’ll look like a smoked ham in a thong.”
Her clip quickly racked up 30,000 views with people left in stitches over her good humour.
One gushed: “Omg that has made me howl, perfect response.”
“You deserve every penny”, a second insisted.
A third echoed: “I hope you win even more money!!!”
A fourth wrote: “This is such a good reaction to this comment. AHAHHAHAHA.”
A fifth said: “Love this reply!! Sod the haters. Enjoy your winning.”
Meanwhile, a sixth added: “Best response!”
We told earlier how a simple email from the National Lottery team at 12.33am on May 16 changed everything for Olivia.
Before this, the mum-of-four was earning just £800-a-month working in a supermarket’s customer service kiosk.
She was on Universal Credits to subsidise her eye-watering £1,800-a-month childcare costs and “dreaded” her council tax bill coming through.
She said: “My husband and I claimed Universal Credit because we needed help with the cost of childcare.
“Now, obviously, because I’ve won £10,000 a month for a year, I’m no longer entitled to that which, you know, quite right.”
Olivia and Kevin won the second-tier prize on The National Lottery’s Set For Life on May 15 after matching five main numbers.
The winning numbers in the draw were: 03, 27, 42, 45, 46, plus Life Ball 06.
‘Set For Life’ offers a top prize of £10K a month for 30 years when the five main numbers and the Life Ball are matched.
Players can also win £10K a month for a whole year by matching the five main numbers.
GARDAI carried out a controlled delivery of firearms to Carlow gunman Evan Fitzgerald after being tipped off by the FBI about attempts to buy them on the dark web.
Senior sources told the Irish Sun that the 22-year-old’s obsession with firearms, which was only discovered after his arrest, underlined the validity of the initial operation against him.
Fitzgerald caused mayhem at the Fairgreen Shopping Centre in Carlow on the evening of June 1.
He discharged a number of shots in the air before turning the shotgun on himself after armed officers arrived at the scene and declared who they were.
Labour’s Alan Kelly this week raised questions over the “proportionality” of the gardai’s actions in March 2024 when they carried out the controlled delivery of firearms.
He asked if they could have looked at alternative interventions given Fitzgerald was not involved in organised crime and had “some issues.”
The Irish Sun understands that the controlled delivery was carried out by gardai in the wake of a tip off from the FBI in the US.
It followed a €2,700 payment being allegedly paid over for the acquisition of firearms and ammo.
Controlled delivery is a common methodology used by police forces worldwide.
It sees a handover of illicit items to a suspect, who has sought to get them, by an undercover police officer.
A senior source said: “Gardai were correct to act in the initial case last year and act on information passed to them.
“Controlled delivery is a very common method used by police forces worldwide.”
In a statement on the matter, a spokesperson said: “An Garda Siochana is precluded by law from commenting on protected disclosures.
“An Garda Siochana does not comment on matters before the courts.
“In general and without commenting on any specific case, An Garda Siochana use a range of internationally recognised investigative techniques when tackling serious crimes such as the sale and supply of drugs and procuring of firearms, either of which could then be used to cause significant harm to the public.
“One of these is controlled deliveries. In controlled deliveries if any material is used it is made safe by the law enforcement agency before being used, ie firearms are deactivated.
“Following these allegations being published by a national newspaper in May 2025, the Garda Commissioner referred these allegations to Fiosru for independent examination in line with the ‘incidents of concern’ provision in the Policing, Security and Community Safety Act, and relevant material was provided.
“As stated by the Commissioner, Fiosru has informed An Garda Siochana that it would not be taking any further action on the matter.
“The individual involved was charged following independent evaluation of the Garda investigation by the Director of Public Prosecutions.”
During Fitzgerald’s first court appearance, gardai initially objected to his bail but then acceded to it under strict conditions which the accused had stuck to until the day of taking his own life.
Another source explained that Fitzgerald did not have any criminal history, which made it difficult to prevent him from getting bail when charged last year.
This source added: “There are a number of factors that the gardai could object under, such as being a flight risk, interference of witnesses or the risk of committing a serious offence while on bail or the seriousness of the alleged crimes.
“But this all has to be backed up by examples and facts.
“The fact is that this man had no criminal history whatsoever to back up any such concerns.”
The Irish Sun last week revealed how cops probing Fitzgerald’s death seized a USB stick found taped to his friend’s bedroom window.
They are now examining its contents in a bid to get answers behind his actions.
PARENTS of children suffering from a rare muscular disease are pleading with the government to speed up the approval of a new miracle drug that could help them live longer and retain the ability to walk.
Duchenne Muscular Dystrophy is a rare condition that mainly affects boys and causes progressive muscle loss as they grow older.
The life-limiting disease – which effects fewer than 200 children in Ireland – results in kids losing the ability to walk and use their muscles as it progresses.
There is no cure for the disease but a new drug has been invented that significantly delays the progression of the disease and gives children more time.
Eilish and Mark O’Sullivan, from Co Donegal, have two boys with Duchenne Muscular Dystrophy.
The family were told that their oldest son Nathan would lose the ability to walk by 12 and may not live past the age of 18.
However, the GAA-mad youngster was admitted to a clinical trial in the UK for the miracle drug Givinostat and is now 21 years old and still able to walk.
Nathan’s younger brother Diarmuid is nine years old and is not able to access the same drug because it has not yet been approved in Ireland – despite already being rolled out in other countries across the world.
Mum Eilish and dad Mark joined around 100 people at a protest outside Leinster House today where families are pleading with Health Minister Jennifer Carroll McNeill to step in and speed up the approval of this drug in Ireland.
Eilish told the Irish Sun: “When Nathan was diagnosed, we brought him over to Newcastle in the UK for a clinical trial back in 2016.
“He’s been on the drug ever since. He was previously told he wouldn’t be able to walk by 12 and he could possibly lose his life by his 18th birthday.
“He is now 21 and he does the score board for all the Donegal GAA matches in MacCumhaill Park in Ballybofey and climbs up and down the steps to do it. It is a miracle and we put that down to the drug.”
The loving parents brought a dose of Nathan’s miracle medicine to the protest today to highlight the heartbreaking situation where one of their sons can access this drug while his younger brother can’t.
Dad Mark said: “We’ve seen what this drug can do in one boy and yet in the same home the other boy doesn’t have the same opportunity.
“That is hard to explain to him because when the time comes and he asks ‘how come my brother is 21 or 22 and I’m nine, ten or 11 and I can’t walk but he seems to be doing OK.”
The roll out of the drug in Ireland is incredibly time sensitive for children with muscular dystrophy as it has only been approved for use by the European Commission for children who are still able to walk.
Several parents at the protest today told the Irish Sun that they fear the HSE will take so long to approve the medicine that their sons will no longer be able to walk and will no longer be eligible for the treatment.
Little Dean Thompson, eight, and his brother Conor, 10, both live with Duchenne Muscular Dystrophy.
Conor has started using a power wheelchair as the muscles on his legs deteriorate while his younger brother is still without the need for a chair.
Dad Jamie told the Irish Sun: “This drug slows down the progression of Duchenne. We know it’s not a cure.
“But every day our boys go without this drug, our boys lose a little bit more muscle and they will not get that back.
“This will change lives. It is the difference of the lads staying on their feet for another few years and that is huge.”
Mum Karen added: “Conor and Dean are amazing little boys. They are full of love for life. They make us laugh every day.
“We want them to live their best life for as long as they can. They enjoy life. They have great pals in school and friends.
“They love swimming and playing with their brothers and gaming like all kids. They are so caring, thoughtful and loving and we just want to hold onto them as long as we can.
“We really really need this drug. They need to approve it as soon as possible because our boys don’t have time to wait. Every day is a day lost.
“They are using this in other countries already all over Europe. There are early access programmes. There are compassionate access programmes.
“It is not fair to make our boys wait. They need it now.
“We don’t have time. If Conor has to wait another year, the chances are he won’t be eligible for this.”
“We’ve seen what this drug can do in one boy and yet in the same home the other boy doesn’t have the same opportunity.”
Mark O’Sullivan
Little Fionn Brogan is nine years old from Dublin and was diagnosed with Duchenne six years ago.
Mum Maeve told the Irish Sun: “Fionn is incredibly stubborn and determined. He’s really behind the campaign because he wants people to see how strong boys with Duchenne are.
“We call them our warriors because they have to keep fighting.
“Fionn is at the stage where he is really struggling with things and finding steps and stairs hard.
“He is on the edge. If this drug takes too long to get through then he could miss out on it.”
Dad Michael is pleading with the Health Minister to step in and set up a pilot programme immediately to enable children like Fionn to get access to this drug in the coming months.
He said: “We want a very concrete plan. I want to see the commissioning of a pilot programme to expedite the rapid access of the drug.
“It is likely that it could take up to two years to approve in our system here. We can’t wait that long.
“There’s no reason why the Minister can’t intervene here immediately and introduce a pilot programme to roll out the drug now.
“I’ve spoken to the clinicians who would be involved in rolling out such a programme and they said they are willing and able to do it.”
Fianna Fail Senator Teresa Costello told the Irish Sun that she has written to the Health Minister to ask her to intervene with the situation and speed up access to the medicine.
She said: “It is out of the government’s hands at the moment as the manufacturer has to put in their application and I’ve engaged with the drug company and they said they are going to apply to the HSE so that should be in for July.
“I’ve written to the Health Minister to ask that this drug is made available through an early access programme because these families can’t wait that average time of over 600 days for approval.”
The HSE today told the Irish Sun that they are aware of the plight of patients with Duchenne Muscular Dystrophy and are waiting on the drug company to apply for approval here.
They said: “The company must now apply to the HSE for the treatment to be reimbursed through the public health system.
“If the company, Italfarmaco SpA, chooses to submit a pricing and reimbursement application, the HSE will give fair consideration to the application with consideration for the criteria detailed in the 2013 Act.”
The Irish Sun contacted the Minister for Health and the drug company Italfarmco SpA for comment.
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