
Children's Rights Alliance calling for €50 million more funding for child protection services
The organisation's announcement comes ahead of a public event on Tuesday, June 24, at which the Minister for Children Norma Foley will deliver a special address and Kate Duggan, CEO of Tusla, the Child and Family Agency, will speak to current challenges the agency is facing to meet demand.
Tanya Ward, Chief Executive of the Children's Rights Alliance said: "Since 2019, referrals to Tusla have increased by 70pc. They have doubled in the last ten years.
"The impact of the Covid-19 pandemic and the sudden withdrawal of services is increasingly evident in the complexity of cases and challenging circumstances reported by services on the frontline.
"Last year's budget allocation was largely to provide for existing levels of service. However, existing levels of service cannot meet the demand and need that exist.'
Ms Ward highlighted 'persistent staffing issues and an acute lack of appropriate residential and foster care placements'.
The organisation's call out follows reports earlier this month that approximately 30 children in Tusla's Separated Children Seeking International Protection service were missing and unaccounted for in January and February this year.
Additionally, 27 other children were unaccounted for at different stages of the inspection and returned to the centre.
Ms Ward added: 'The infrastructure and personnel must be there to support the root and branch reform that is needed in the system.
"This will mean the Government needs to secure funding for at least 300 social workers and social care workers, additional foster carers, as well as capital funding for Tusla to acquire enough appropriate residential facilities.
'We know from children directly of the transformative effect timely interventions, the support of a key professional and appropriate care placements can have.
"However, we also know what happens if we fail to deliver these. For too long, Government investment in our core child protection services and wider family supports has been below the level needed to provide safe and appropriate care for children and young people who have no choice but to depend on the state. This cannot continue.'

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Irish Examiner
3 hours ago
- Irish Examiner
Surge in older population poses major funding challenge for Ireland, ESRI warns
A phenomenal rise in the number of older people in Ireland has left the Government facing a major funding challenge to provide long-term nursing home beds and home help hours, research has found. The Economic and Social Research Institute (ESRI) said the number of long-term residential care beds and home supports for older people will need to increase by at least 60% by 2040 to meet demand. It found that long-stay bed requirements will grow from 29,579 beds in 2022 to between 47,590 and 53,270 beds by 2040, a growth of between 61% to 80%. Furthermore, short-stay beds may need to rise from 3,745 in 2022 to as high as 7,265, which would be an increase of 94%. Home help hours, meanwhile, are projected to grow from 28.7m hours annually to up to 54.9m annually by 2040, a growth of up to 91%. ESRI senior research officer Brendan Walsh: 'Ireland has experienced tremendous improvements in life expectancy' which means there will be a much larger population 'who require long-term care services to support them at home, or within residential facilities.' Picture: ESRI The steep rise in demand is being driven by the steady increase in the size of the older population, according to the ESRI. By 2040, one in five people in Ireland will be over the age of 65. The population aged 85 and over, who use a large proportion of nursing home beds and home support, will be more than double what it is now. ESRI senior research officer Brendan Walsh said: 'Ireland has experienced tremendous improvements in life expectancy in recent decades, driven mainly by reductions in mortality at older ages. This means there is, and will be, a much larger population at older ages who require long-term care services to support them at home, or within residential facilities. 'Therefore, plans and policies are needed for long-term care to ensure the health system is in a position to meet the increasing care needs of the older population. Our findings provide policymakers with an important evidence base to help develop these plans and policies.' The research body said that healthier ageing in future may reduce the requirements for long-term beds while the expansion of home support services could also be of benefit. However, the sheer numbers of people who will be aged 65 and over who require such care may offset these changes. Regional projections of where services will be needed must also be prepared, the research said. Health minister Jennifer Carroll MacNeill said the programme for government pledges to build more public nursing home beds, create a homecare scheme to help people stay in their homes longer, and increase home care hours. She said: We are already making progress in increasing both residential care capacity and home support hours for our older population. "This is shown by the €4m allocated in Budget 2025 to staff and open 615 new community beds. 'The Department of Health and the HSE are also working on a new Long-Term Residential Care Additional Capacity Plan, to be published in 2025.' Minister of state Kieran O'Donnell, who has responsibility for housing and older people, said that the ESRI research would be 'invaluable' for capacity planning for residential care and home support. 'It is evident that significant action will be required by Government in order to ensure that the appropriate care services are available for our older population and to deliver on programme for government, Sláintecare, and Project Ireland 2040 commitments,' said Mr O'Donnell. 'I am absolutely committed to ensuring that this capacity planning is advanced in 2025.'


The Irish Sun
10 hours ago
- The Irish Sun
My daughter, 22, was diagnosed with rare tumour after earache – now she's in horrendous pain & needs life-saving op
WHEN Maeve Duffy began experiencing a "persistent" earache, she never imagined it could be a rare and aggressive tumour that would leave her in "unimaginable pain". The "beautiful" young Co Advertisement 2 Maeve Duffy was diagnosed with a rare tumour when she was just a teenager Credit: Collect 2 Maeve and her loving family are doing everything they can to ensure the life-saving surgery takes place Credit: Collect Maeve, who is now 22-years-old, was diagnosed with facial nerve schwannoma when she was just 17. The rare benign tumour grows on the nerve that controls facial movement and sensation and can result in facial paralysis, facial spasms, dizziness, balance problems and hearing loss. And after exhausting every treatment available in Ireland - including radiation and years of delays and consultations - her doctors have told her that the tumour is inoperable here. But there is hope. Advertisement READ MORE IN HEALTH Specialists in Maeve's desperate mum Siobhan is doing everything she can to raise the funds needed for the operation to ensure her little girl can return to her life. Speaking to The Irish Sun, Siobhan told how the Covid-19 lockdown forced a surgery that could have removed Maeve's tumour to be cancelled. She said: "It started with an earache which we thought was just an earache. Then they said it was what they thought was a polyp. Advertisement Most read in Health "They tried to remove it, then went for surgery and when they did surgery they discovered it was a tumour and we were sent from Waterford to Dublin to Beaumont and she had all her scans and was scheduled for surgery in Beaumont. I was diagnosed with breast cancer after noticing small mark - I'm not giving up, I'll give treatment all I've got "Unfortunately lockdown happened the day before her surgery and it was cancelled. "So actually 14 months later we got back to Beaumont and they redid all the scans and they decided it was inoperable at that stage." Maeve was just 17-years-old when this took place and was worrying about her schoolwork and the impact this may have on her dreams to study biomedical science. Advertisement Siobhan explained: "She was doing her Leaving Certificate, she knuckled down with her study and tried to put it to the back of her mind. She wanted to go to college. SYMPTOMS WORSENING "We were worried about it but there was a lot happening at the time and she really did just want to get it sorted and get her Leaving Cert done and move to college. "Maeve is obviously very bright and she wants to do biomedical science but this has all put her studies on hold. "She's not been able to study or go to college or actually do anything because of the pain and because of the side effects of the drugs. Advertisement "The drugs are almost as bad as the growth." In 2022, as Maeve's symptoms started to worsen, the brave young woman underwent five rounds of aggressive radiation therapy, the maximum safe dose. The goal of this was to stop the tumour's growth and relieve her symptoms. However, heartbroken mum Siobhan told us how, after the radiation, Maeve admitted: "Mam, I just can't stick the pain, it's horrendous". Advertisement The side effects of Maeve's radiation were severe and the tumour did not change as a result of the intense treatment. Instead, she developed necrosis, triggering constant, excruciating pain. She's 22 and she wants to socialise and go to college but can't because of her constant pain, nauseousness and dizziness. It's just not possible for her." Siobhan, Maeve's aunt Maeve was placed on high-dose steroids and Pregabalin - the side effects of which are immense. And Siobhan described the drugs as "debilitating", telling how her daughter has been battling the fierce side effects of the medication for two years now. Advertisement She explained: The side effects are not good, her quality of life has been reduced to a minimum. "Maeve will never get off those tablets or drugs as long as that tumour is there. "Our only hope to get her back is to get the tumour removed and that is not going to be done in Ireland - there is no one to do it." Siobhan told how the Duffy family was "so lucky" to get into contact with specialists at the International Neuroscience Institute in Hanover, Germany, renowned for treating complex cases like Maeve. Advertisement The family met the team and within weeks it was confirmed that surgery to remove Maeve's tumour could be performed. Siobhan's mum said the team of medical experts have no fear of facial paralysis or any side effects of the operation and believe that, within a few months of the surgery, Maeve can be taken off all the medication she is currently taking. The surgery can be completed as soon as July 8th - but the family has been forced to put the operation on hold until they raise enough to cover the staggering €107,000 price. HOW CAN YOU HELP? MAEVE'S family has set up a GoFundMe page to raise enough money to cover her surgery in Hanover, Germany. At the time of writing, over €50,000 has been raised to support the family - but they need the full amount in order to go through with the operation. Writing on the page, Maeve's family and friends said: "Their surgical team has the expertise to give Maeve a real chance at recovery. But the cost of this surgery is over €107,000, and time is critical. "We're doing everything we can to raise the funds to get Maeve to Germany for this life-changing surgery. "If you're able to donate—no matter how big or small—it would mean the world to Maeve and all of us who love her. "And if you can't donate right now, sharing this page with your friends, family, or on social media would be a huge help." You can Siobhan said Maeve is "really looking forward" to getting the surgery over and done with so she can return home and follow her dream. Advertisement The young woman has a deferred place in a biomedical course in Maynooth University. Siobhan said: She's very eager to get back to college and study, and she's also got job offers that she can't even think about at the moment. "It's just to get the surgery over to get her life back so she can plan her future." Siobhan said the family is remaining strong for Maeve, adding: "We need to carry her." Advertisement FAMILY'S PAIN Siobhan's sister Margaret told how the situation is "very hard" on the family, including Maeve's two younger brothers. She said: "It's hard on them to see her suffering and not being able to go to college, not being able to do the things she wants to do. "She's 22 and she wants to socialise and go to college but can't because of her constant pain, nauseousness and dizziness. It's just not possible for her." Speaking about Maeve, Siobhan described her as a "beautiful person". Advertisement She told The Irish Sun: "She's a really sweet kid. She's beautiful, a beautiful person, so kind. "I would say a little on the old fashioned side as in she's not your average trendy 22-year-old. "She's never been that person, she's always very simple. She's just, you know, she's really sweet." And speaking about the whopping €50,000 that has already been raised for Maeve since the GoFundMe was launched just over a week ago, Siobhan said the support from people has been "unbelievable". Advertisement She said: "It's just been unbelievable. People have just come out of the woodwork. It's amazing."


Irish Examiner
17 hours ago
- Irish Examiner
Terry Prone: Memory of late Thalidomide victim Jacqui Browne should be honoured
Just under a year ago, Jacqui Browne stated her grim certainty. That certainty was that the Government was simply waiting for Irish Thalidomide survivors to die. This week she died, her death not probative of such an intent, but a reproach to the system, nonetheless. She held that certainty even though, this time last year, the Government was indicating that it would take a new approach to solving the problems caused by doctors prescribing a morning sickness drug to pregnant women, those doctors unaware that it would cause grievous damage to their unborn babies. Long after that drug had been removed from sale in other countries, it lurked on the shelves of pharmacies here, ready to maim and disfigure. Jacqui Browne, front, with other members of the Irish Thalidomide Association arriving at Government Buildings in 2022 for one of many meetings where they sought long-overdue justice for survivors of the Thalidomide drug. File picture: Sam Boal/Rolling News Kerry woman Jacqui Browne was one of the babies born disastrously damaged by Thalidomide. Her hands and forearms were shortened. Her hearing less than normal. Her speech impaired. When most toddlers are learning to play and explore, Jacqui was being poked and tested, torn from her family for special education in a school for deaf children in Dublin. The first of 35 major surgical operations was done to the little girl when she was a tiny five-year-old. Big surgical interventions continued throughout her life. And yet, she forged a career for herself, internationally, as a disability equality consultant. Intrepid yachtswoman She had a life; becoming a yachtswoman who survived a shipwreck near Java. The Cork Clipper — with Jacqui Browne among the crew — leading the fleet out of port at the start of Race 3 from Rio to Cape Town in the 2010 Clipper Round the World Race. File picture: Clipper Ventures/PA One of a group competing in the Clipper Round the World Yacht Race 15 years ago, when their boat went aground, she and the rest of the crew managed to get to a place where they could survive until rescue boats came. Despite the never-ending problems caused to her life by Thalidomide and the corrective surgeries that never seemed to be complete, she was a self-confessed optimist. 'I'm always happy,' she confirmed. 'I have wonderful friends and great family support. But I do find physically there is so much I can't do.' Along with the other 40 survivors (together with some people who the Thalidomide Association believe to justify adding to that number), she went public in recent years to ask the powers that be to apologise to the mothers who have blamed themselves all their lives for the hurt to their children caused by the 'miracle' drug. What emerged last year aggravated, rather than assuaged, the anger of the survivors. It was an expression of sympathy rather than a straight-up apology. In its aftermath, another mother died. The Thalidomide survivors, Jacqui front and centre among them, have for years asked the State to revisit the issue, pointing out that, just as polio victims suffer post-polio syndrome decades after they thought they were done with the sequelae of the infection, victims of Thalidomide enter new levels of suffering as they enter old age — for different reasons. 'When you have impairments due to the thalidomide drug, you're all the time compensating,' Jacqui pointed out. You're doing things maybe differently to how somebody else might do them, but you're actually overusing one side of your body. So that too becomes inflamed and sore and painful because you can't use the other side. Paying tribute to Jacqui, Irish Human Rights and Equality Commission chief Liam Herrick talked of mourning the loss of a 'colleague, advisor, and friend'. Her Thalidomide Association colleagues — 39 of them now left to continue the fight they shouldn't still be fighting — talk of losing a warrior. Her family will experience the loss differently: They grieve a family member, a beloved sister. The Taoiseach and Tánaiste — each of whom has at various times expressed understanding of the issue and a wish to solve the remaining problems — might honour the memory of Jacqui Browne by kicking life into an administrative process that's almost one sadly unproductive year in business this month.