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Tony Holohan will not run for president to protect family from campaign ‘abuse'

Tony Holohan will not run for president to protect family from campaign ‘abuse'

Irish Times14 hours ago
Former chief medical officer
Tony Holohan
has announced he will not now seek a nomination to run for the
presidency
because he wants to protect his family from the 'personal abuse' of a campaign.
Prof Holohan said he could not expose his family to 'distress, criticism or abuse at a time when we are all still rebuilding our lives'.
He had been strongly considering trying to enter this year's presidential race, after a poll commissioned by his supporters last week put him at 15 per cent.
But in a statement to The Irish Times, Prof Holohan said that, 'after a lot of careful consideration and reflection, I have decided not to seek a nomination to contest the election'.
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'While a number of different factors have influenced my decision, my overriding consideration has been my wish to protect my family from the kind of personal abuse which is becoming increasingly normalised in Irish politics generally and in presidential elections in particular,' he said.
'I understand the very tough nature of modern politics and, while I am more than capable of defending my reputation and the decisions which I have taken over a long career during challenging times in public service, my family is not. I cannot now expose them to further distress, criticism or abuse at a time when we are all still rebuilding our lives.'
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Covid, CervicalCheck and the Trinity job: questions for Tony Holohan if he launches a presidential run
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Prof Holohan said he 'earnestly' hopes the upcoming campaign will be marked by 'civilised and respectful debate'. He wished the next president success, and said they will have his 'full support'.
Meanwhile, Fine Gael will meet on Monday to consider the
presidential election
campaign as support grows inside and outside of the party for
Heather Humphreys
to run.
The former minister has said she is giving the matter '
very serious consideration
'. She had ruled out the possibility in May.
Ms Humphreys, who did not contest last year's general election, has emerged as the favourite to replace former MEP
Mairead McGuinness
, who on Thursday announced she was stepping down as the Fine Gael candidate on
health grounds
.
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Can you have too much democracy?
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A number of Independent politicians have come out in support of Ms Humphreys running to succeed
Michael D Higgins
. Ministers of State
Michael Healy-Rae
,
Noel Grealish
and
Seán Canney
have said they would support her candidacy, noting her 'broad' appeal and ability to 'bring a lot of people together'.
Ms Humphreys is also understood to be the preferred candidate for a number of senior Fine Gael ministers.
Fine Gael MEP
Seán Kelly
, a former
GAA
president, on Saturday said he was weighing up his options about seeking the party's nomination after this week's news about Ms McGuinness.
He said last month that he would not run, describing it as the 'most difficult decision' of his political life, but on Saturday told
Newstalk
'the goalposts have changed'. Mr Kelly said the discussion within Fine Gael on who it would now run as its candidate 'hasn't started really' out of respect for Ms McGuinness.
'I think next week will be time enough to reflect properly on that and take action. There's no rush,' he added.
Fine Gael MEP Regina Doherty, a member of the national executive, said there should be a contest if Mr Kelly and Ms Humphreys both put their names forward.
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I'm in constant pain after hearing big crack at base of my skull but doctors say there's nothing they can do
I'm in constant pain after hearing big crack at base of my skull but doctors say there's nothing they can do

The Irish Sun

time17 minutes ago

  • The Irish Sun

I'm in constant pain after hearing big crack at base of my skull but doctors say there's nothing they can do

A NEW virus is spreading that feels a little reminiscent of the Covid-19 pandemic. Chikungunya is a mosquito-borne infection that can cause severe joint and muscle pain, headaches, sensitivity to light and skin rashes. 4 Dr Zoe Williams helps Sun readers with their health concerns The UK Health and Security Agency reported 73 cases this year to June, a 100 per cent increase on 2024. These were travellers returning from abroad (the mosquitos that spread the virus are not found in the UK). Outbreaks have been reported in 16 countries, including China, France and Italy. The last major one was 20 years ago, affecting 500,000 people. Most people recover in a couple of weeks, but for some the joint and muscle pain can persist for years. In rare cases, chikungunya is fatal. UKHSA says check the Travel Health Pro Website before you go abroad for the latest advice on your destination. Here's a selection of what readers have asked this week. Is little-known hMPV virus ravaging China the NEW Covid? So low over neck pain Q: ABOUT three years ago, while playing snooker, I looked up to take a shot, when there was a big crack right at the base of my skull. The pain was incredible and I now get pain whenever I look up. 4 A reader is suffering from pain at the base of their skull Credit: Getty My doctor suggested I might ­benefit from physio, but when the therapist massaged my neck, I got a sharp pain in a different area of it and I told her to stop. Since then, I have a constant pain in the place she massaged. It radiates down my neck, across my shoulder and down my left arm to my elbow. The pain is unrelenting. The doctor said there was nothing they could do. I feel abandoned and don't know what to do. A: That sounds incredibly distressing – both physically and emotionally – and it's understandable you would feel abandoned when you're living with constant pain and not ­getting clear answers or relief. It sounds like there may have been an acute injury at the time, to a ligament, joint, disc, or nerve involvement, due to the 'crack'. Then, ongoing pain when looking up might indicate nerve compression or irritation in the cervical spine (neck). The pain that radiates from the neck to the shoulder and arm would also fit with nerve root irritation or compression (possibly cervical radiculopathy). Of course, I can't diagnose you, but given your symptoms started with a traumatic event and are now persistent, radiating, and worsened by a prior intervention, I would push to make sure you're referred for further assessment and likely imaging (X-rays, MRI scans, ultrasound). Most hospitals have a 'musculoskeletal (or MSK) service' which is often run by advanced practice physiotherapists. They are highly skilled at assessing and managing musculoskeletal conditions, including ordering imaging and referring on to orthopaedics, rheumatology, neurology or pain clinics if needed. The fact your symptoms worsened after physiotherapy means something may have been aggravated, and 'nothing can be done' is not an acceptable answer when your quality of life is being severely affected. If your pain changes suddenly – especially if you get weakness, numbness, trouble walking, or bladder/bowel changes – that's a medical emergency and you should go to A&E immediately. Tip of the week GPs see neck, back and shoulder pain all the time. Sometimes the fix is to adjust your sitting position, especially at a desk. Sit back against your chair, with your feet flat on the ground. Use a supportive cushion to fill the gap between your lower back and the chair if needed. Q: l AM 69 and am very healthy, except l have been asthmatic all my life, though it has always been managed well. After my last check-up at our asthma clinic, the nurse took my reliever inhaler (Ventolin) off my repeat prescription and said just to use the preventative (Fostair) when needed from now on. 4 A healthy reader opens up on being asthmatic Credit: Getty Seems OK so far, but I wondered why this has happened. Is it a money-saving exercise, do you think? A: I am really glad that you have asked this as there is a lot of confusion regarding the recent changes to the asthma guidelines. Firstly, what your nurse has done is correct and secondly, it is not a cost-saving exercise. In fact, the Fostair inhalers cost more. The change is more about safety and aligning with modern best practice. The only 'cost-saving' aspect is indirect – preventing serious asthma attacks by keeping inflammation under better control. For decades, the advice was to take your preventer every day and use your reliever (bronchodilator), which helps open up the airways, when you get symptoms. But research showed that relying on the reliever alone for these episodes can increase the risk of sudden asthma attacks. People who felt 'fine' could still have ongoing airway inflammation, and frequent bronchodilator use was linked to worse long-term outcomes. Your nurse has switched you to a 'single inhaler maintenance and reliever therapy' (MART) plan. It means Fostair is now doing both the jobs of your preventer and reliever. Fostair contains beclometasone (steroid) and formoterol (long-acting but also quick-acting bronchodilator). So you will use it daily for maintenance, and if you get asthma symptoms, you can use this same inhaler to get instant relief and anti-inflammatory treatment in one puff. You can use Fostair 'as needed' and it will work just like Ventolin to open up the airways, but also treat the inflammation immediately. For people with mild, well-controlled asthma, this approach can reduce flare-ups and hospital visits. If you're using it more than two to three times a week as a reliever, it might mean your asthma isn't as controlled as it could be, and it's worth having an asthma review. What's causing unsightly leg veins? Q: OVER the last few months, I have developed these unsightly spider-type veins in my right ankle. The area they cover seems to be expanding. They are not painful, but I just wondered if you might know the cause and also if they are harmful. 4 One reader has developed these unsightly spider-type veins in my right ankle Credit: Supplied I had a liver problem three years ago but I'm now OK. I take medication for slight portal hypertension. A: Thank you for sending me this picture of your ankle, which shows small red blood vessels (capillaries) visible on the surface of the skin in a web-like pattern. These could be one of two things – spider veins or spider naevi. Spider veins (also called telangiectasias or thread veins) are small, dilated blood vessels that look like thin red, blue, or purple lines, often in a web-like pattern. These are very common, usually appearing on the legs and sometimes the face. Causes include increased venous pressure, valve weakness in veins, prolonged standing, hormonal changes, or sun damage. They are not dangerous. Spider naevi (also called spider angiomas) can be distinguished by a central red dot (feeding arteriole) with thin radiating vessels like spider legs, which extend out from the centre. The most common locations for these are the face, neck, upper chest, and hands, but they can also appear on the legs. Doctors are more interested in these, because if there are three or more in adults, this can point to underlying liver problems or hormonal imbalance. If I could examine you, I'd do a simple test to help differentiate between the two, because from the picture you have sent, and with your history of liver disease, yours really could be either. The red spot of spider naevi with radiating blood vessels blanch (go pale) when pressure is applied (such as with a glass) and rapidly refill with blood from the centre of the spider outwards. This distinct pattern is a key diagnostic feature.

Downing Street warns Sally Rooney she risks prosecution if she donates to Palestine Action
Downing Street warns Sally Rooney she risks prosecution if she donates to Palestine Action

The Journal

time2 hours ago

  • The Journal

Downing Street warns Sally Rooney she risks prosecution if she donates to Palestine Action

NORMAL PEOPLE AUTHOR Sally Rooney risks committing a terrorist offence if she funds banned organisation Palestine Action, Downing Street has warned. The award-winning author said she will donate her earnings from her books and BBC adaptions to support the group, which was recently proscribed as a terrorist organisation in the UK. Downing Street said 'support for a proscribed organisation is an offence under the Terrorism Act' and said no-one should be backing the group. The Co Mayo native said that if that backing Palestine Action 'makes me a 'supporter of terror' under UK law, so be it'. Writing in the Irish Times over the weekend , Rooney said she will use the proceeds of her work and her public platform to continue her support for Palestine Action and 'direct action against genocide in whatever way I can'. Palestine Action was recently proscribed under terrorism legislation in the UK, but not under Irish law. Advertisement The BBC has broadcast adaptations of Rooney's novels Normal People and Conversations With Friends in recent years. But she has never been on the broadcaster's staff and it is understood the corporation is not working with her on any upcoming projects. Dr Jilan Wahba Abdalmajid, the ambassador of the state of Palestine in Ireland, said today: 'Sally Rooney is using her voice to call out international law and human rights violations in Palestine. 'I hope these calls result in practical actions that will stop the horrors we're witnessing carried out by Israel in Palestine; to stop the genocide and forced displacement and end the Israeli occupation.' In Westminster, Keir Starmer's official spokesperson would not comment specifically on the author's comments, but said: 'There is a difference between showing support for a proscribed organisation, which is an offence under the Terrorism Act, and legitimate protest in support of a cause.' Asked what message No 10 would give to people considering giving money to the group, the spokesman said: 'Support for a proscribed organisation is an offence under the Terrorism Act and obviously the police will, as they have set out, they will obviously implement the law within the law as you'd expect.' The spokesman said Palestine Action was proscribed 'based on security advice following serious attacks the group has committed, following an assessment made by the Joint Terrorism Analysis Centre'. In a statement, a BBC spokesperson said: 'Matters relating to proscribed organisations are for the relevant authorities.'

'My life is on hold. It has been a kick in the balls' - Colin Hawkins opens up
'My life is on hold. It has been a kick in the balls' - Colin Hawkins opens up

Irish Daily Mirror

time2 hours ago

  • Irish Daily Mirror

'My life is on hold. It has been a kick in the balls' - Colin Hawkins opens up

His day began in a waiting room, a real-life purgatory. The clock ticked past nine when he took his seat. He recalls the noise of the water cooler; the rise and fall in volume as people passed along the corridor. Otherwise there was silence, which is not an uncommon thing on the seventh floor of the Mater Hospital, where cancer patients get their treatment. Read more: AZ Almaar manager's snappy response to question about Troy Parrott's future Read more: Shock report suggests Manchester United and Liverpool are eyeing up Ireland star And on this sunny Friday morning, this was where Colin Hawkins, one of only 20 Irish footballers to win a medal at an official World Cup event, went to discover if the cancer drug they'd given him would save his life. The clock ticked on. It was just after ten when he left his chair to take in the view from the seventh floor window; Croke Park to the right, Dalymount Park to the left. It was Dayler where Hawkins played when he was 25-years-old and considered the best defender in the League of Ireland. 'You felt invincible,' he says of his days as a professional footballer. But no one ever is. Still, at that stage of his life, the midpoint of a professional career, it is no exaggeration to say he was among the country's healthy elite. Now, as a 47-year-old man, his feelings of invincibility are over. So he sat back down for his appointment and waited, every second feeling like a minute, every minute an hour. Time passed. Time didn't heal. He thought about his upbringing. He was one of ten children, the only one of his siblings to become a professional athlete, a four-times winner of the League of Ireland, later a player with Coventry City in England's Championship, Europe's fifth best attended league. 'I probably took my health for granted,' he says. 'Put it this way, it was a big shock to my nine siblings that I was the one who got so ill. 'It can't be you, you are the sports guy', they said.' But it was him because cancer is a democratic illness. Anyone can be diagnosed with it. A King of England died from it. It doesn't discriminate against rich or poor. 'It is two-and-a-half years since I was first diagnosed,' Hawkins says. 'And the thing you learn about this life is that you don't know when your time is (up). 'I don't feel punished or whatever. It is just unlucky. Still, if you ever want a wake-up call about why you should enjoy every day of your life, go into the Mater every Friday. 'Walk to the seventh floor. Go into the waiting room where you receive your treatment. You are handed a number. A person sits to your left, another to your right. 'I keep asking, 'how is this place so busy? Are more and more people getting cancer than ever before?' Their answer is actually reaffirming. 'No,' they tell me, 'more and more people are surviving.' Colin Hawkins is drawing the positives from life. (Image: ©INPHO/Donall Farmer) By now it was 11am. He still had the ticket in his hand. It resembled a small raffle ticket, a beige colour. He waited and thought back to 2023 when he started to feel unwell. By the time he discovered he had cancer in his blood, the pain became practically unbearable. He subsequently needed surgery on his neck and his back. 'When the myeloma is alive and active, that is when your bones break,' he says matter of factly. 'When it is gone and under control, all that pain is gone.' Good news came. He received stem cell treatment and entered remission. Then terrible news followed. His wife, Elaine, was diagnosed with breast cancer. Telling their three children this news was the hardest day of their lives. Better days came after that. Elaine's treatment worked. She, thankfully, is in remission. Life returned to normal for a while until his old pains resurfaced. He visited Dr O'Gorman in the Mater to review a new drug he had been on for six weeks. 'Your numbers have gone through the roof and your myeloma has gone crazy again,' he was told. 'We need to take you off this drug and get you on a new one.' That was three months ago. He had to check into the hospital that night and ended up staying for a month to see if he could deal with the side-effects of the drug. He got pancreatitis. There is pain and then there is pain. Pancreatitis was hell. But this feeling he had on that Friday morning was way worse, sitting on a blue chair, holding a beige-coloured ticket, staring at the clock, waiting and wondering. If the news was good, if he was told the drug was working, then life would go on. He'd return to work 'to CPM, the best employers in the world who have looked after me while I have been ill'. But if this drug wasn't working, what then? Was there a fifth drug they could try? He hadn't asked. 'Sitting in that room, waiting for that news was the first time I was seriously worried. Three treatments had failed. 'I had my bloods taken the day before. I had scans. As the clock ticked towards noon. I was waiting to be told if my numbers had improved or got worse. 'I have always fought it (his cancer) head on. This was the first time when I realised this was a trial drug; so if this doesn't work then what the hell is the next treatment?' The stem cell transplant he had received was supposed to give him ten years in remission. 'For the cancer to come back after 18 months was kind of unheard of for my age. I was obviously nervous waiting for the result.' Nervous waiting for a result! He remembers the first time he issued those words, back in 1998. He was a St Pat's player then. They won that year's League of Ireland title on the last day of the season, beating Kilkenny City away. But to become champions, they needed Dundalk to defeat their rivals, Shelbourne. So they waited for a result from Oriel Park. They got the news they wanted. The following year something similar happened, Pat's beating Bray on the final day of the season to win back-to-back titles. Consumed by the game, he worked to make the most of what he had, reaching an incredibly high level, representing his country at underage level, winning bronze at the 1997 Under 20 World Cup. And when he spent a month in the Mater Hospital over Easter, all those players from all those teams came in to visit. Brian Kerr, his Ireland manager in 1997, checks in at least once a week. Brian Kerr, the former St Pat's and Ireland manager, is still a regular at Saints games (Image: ©INPHO/Tom Maher) 'Brian has been incredible,' Hawkins says. 'He has such a big heart. Football people, they're great. They don't forget. They remember the big nights, you being there for them on the pitch. "This time they were there for me. All these years later and the dressing room spirit is still strong. It's why football is special.' Yet now all those characteristics which made him such a winner were being put to the test. He says: 'My life is on hold. Thursday I get the bloods done, Friday my treatment. It has been a kick in the balls. That is where my life is at the moment. 'I am not working because I don't have the energy. My immune system is really low. I kind of feel I have a permanent flu or a chest infection.' Yet he isn't feeling sorry for himself because he has spoken to people in the chair next to him in that waiting room, swiftly realising if they have no hope. And on this Friday morning three and a half hours elapsed before Dr O'Gorman called. And that was when the man who played in a World Cup U20 semi-final for Ireland, got up off the blue chair and walked into a doctor's office. In those steps, the fact he had been a champion footballer on four different occasions ceased to matter. He was just another number, waiting to hear if his cancer drug was helping. 'It is,' said Professor O'Gorman. 'You are responding well.' That was eight weeks ago. Today Colin Hawkins is in remission. This champion football player has just won the biggest prize of his life. Get the latest sports headlines straight to your inbox by signing up for free email .

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