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Sheep Mops for Killarney National Park

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An ingenious system to reduce the prevalence of ticks that carry Lyme disease, in Killarney National Park, has been put forward by Fianna Fáil Councillor, Michael Cahill at this month's meeting of Kerry County Council.

Councillor Cahill has proposed that the Minister for Agriculture urgently investigate the effectiveness of a scheme introduced in the Scottish Moors, whereby sheep, having been regularly dipped to eradicate the ticks that carry Lyme disease were allowed graze there.

"This would reduce the spread of these dangerous ticks to humans," he said.

“These ‘Sheep Mops’ as they are known, could be used in Killarney National Park as a method of preventing this horrible, debilitating disease.
A man, who describes himself as a ‘Lyme Survivor’, recalled t when there were 3,000 sheep in the National Park. I believe it could be a very simple, cost effective project to introduce and apparently it has been an amazing success on the Scottish Moors."

“Dr John Lambert, who is an expert in the area of Lyme disease in Ireland, informed me that many GP's are not aware or informed of the symptoms of Lyme. He said that the HSE do not keep records of those effected in this country, in the United Kingdom, in Germany or any other known location. Dr Lambert said that the figure may be as high as 2,500 affected every year but we don't know,” said the Rossbeigh based Councillor.

“The figure is 70,000 in both Germany and France every year. Testing is not perfect and there is not a good understanding of it. Dr Lambert said that prevention and early intervention is critical. He said that wooden ‘Beware of Ticks’ signs should be erected in all Parks and areas where deer are present”, added Cahill.

“Finally, I would like again to call on the HSE to introduce testing and treatment at University Hospital Kerry as the numbers of cases are continuing to rise in both Kerry and Cork and from what we know the figures are higher in the Southern part of Ireland than the rest of the country," he told the meeting.

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New nursing unit to open by end of March

Killarney’s multi-million euro Community Nursing Unit is finally expected to open its doors by the end of March 2025, bringing an end to years of bureaucratic delays. The 130-bed facility […]

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Killarney’s multi-million euro Community Nursing Unit is finally expected to open its doors by the end of March 2025, bringing an end to years of bureaucratic delays.

The 130-bed facility on the grounds of St Finan’s Hospital. which began construction in 2022 as part of a national Public Private Partnership, was officially handed over to the HSE last year.
The Health Service Executive is currently in the final stages of the registration process with HIQA.
A “courtesy pre-registration visit” was conducted in late January, and the HSE is now addressing minor recommendations before submitting the final application.
The state-of-the-art unit includes 30 dementia-specific beds and will replace the aging facilities at St Columbanus’ Home and Killarney Community Hospital.
Once the transfer of residents is complete, it will clear the way for further healthcare developments in the town, including a proposed Minor Injury Unit at the St Columbanus site.
Bernard Gloster, CEO of the HSE, recently told the Oireachtas Health Committee that the opening is a priority for the first quarter of the year.
Mayor of Killarney Martin Grady confirmed the timeline.

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Father despairs as “voiceless” cast aside in Health Centre dispute

The father of a nine-year-old Killarney girl with profound disabilities has spoken out against the “needless turf war” and “parish pump politics” he believes have stalled the development of a […]

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The father of a nine-year-old Killarney girl with profound disabilities has spoken out against the “needless turf war” and “parish pump politics” he believes have stalled the development of a primary healthcare centre in the town.

Steve O’Mahony, whose daughter Alexis requires round-the-clock care, issued a stinging open letter following the decision by local councillors to reverse the inclusion of a HSE-run facility at the Áras Phádraig site.
The move followed a period of significant public backlash regarding the use of the town-centre location.
Alexis lives with Pyruvate Dehydrogenase Deficiency, a rare metabolic condition that causes brain abnormalities, alongside cerebral palsy and epilepsy. For the O’Mahony family, the lack of a centralised hub means navigating cramped, scattered facilities or undertaking difficult journeys to Tralee, Cork, and Dublin for vital appointments.
The “voiceless” dismissed
In an open letter seen by the Killarney Advertiser, Mr O’Mahony questions why no one has properly investigated the function of a primary care centre, which he describes as “a lot more than a physical building.”
He argues that the focus on the Áras Phádraig site as being “for the people of Killarney” is a rhetoric that fails to recognise that those with disabilities are also citizens with immediate needs.
“I am a father of a child with complex medical needs who turns 10 years this April,” Mr O’Mahony wrote. “I have ten years of experience of navigating the health system both locally and nationally. It is not always a pretty picture especially when it is mixed with politics, most notably parish pump politics. I do know one thing more than anything and that is that those with a disability are the voiceless. As a father it is my civil duty to speak about this and the whole sorry saga which in my humble opinion has been led by fear and mistrust and shown the voiceless being cast aside yet again.”
He added that the phrase “the Áras Phádraig is for the people of Killarney” is “an insulting phrase that completely dismisses the immediate needs of the most vulnerable in our society.”
A call for urgency
Mr O’Mahony expressed frustration that Killarney is at risk of rejecting €16 million in targeted funding due to the dispute.
He believes the opinions of those who would actually use the services including the elderly, young parents, and people with disabilities were never specifically sought during the public consultation.
“The silence is deafening,” he noted, referring to the lack of follow-up since the initial public outcry subsided. “If half the energy devoted to this story was reinvested in the need for such a centre in our town we would all be smiling.”
As the wait for a modern facility continues, the O’Mahony family remains focused on the daily realities of Alexis’s care.
Over the years, the community has rallied to support the ‘Let’s help Alexis’ fund, helping to provide a wheelchair-accessible vehicle and essential equipment.
However, Mr O’Mahony says the town now needs a proactive approach from its leaders to provide the long-term health infrastructure that children like Alexis depend on.

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