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THE NEW US owners of the 400-acre Cherrywood site on Dublin’s southern outskirts have said they want to build new homes on the vacant land as “quickly as possible” because of the city’s housing crisis.
Hines Ireland, the local arm of the US-based global property developers, has finished its buyout of the land for a reported price of over €270 million.
The site, the biggest land parcel ever sold in Ireland, has approval for a new town shopping centre, 3,800 apartments and houses, and permission to expand the nearby office park to 3 times its existing size.
Hines Ireland senior managing director Brian Moran said building homes would the company’s immediate priority because of the “pressing and urgent requirement” for accommodation in the Dublin region.
We aim to deliver houses and apartments into the market as quickly as possible, and where permissible, sooner than currently planned under the (zoning rules),” he said.
The site sits on the M50 near the N11, and is also the end point for the Luas green line. The existing offices, built by now-failed developer Liam Carroll, already have tenants that include Dell and med-tech firm Covidien.
What’s the plan?
The majority of the land has already been earmarked for fast-track residential development, although the plan also includes parks, schools and a health centre.
The plan includes staggered development of three “growth areas”, all of which come with requirements that road upgrades and other infrastructure need to be built along with the new homes.
Hines already has interests in the Liffey Valley shopping centre at Clondalkin, in Dublin’s west, the Bishop’s Square office block near the city centre and at Spencer Dock.
The company said it was now managing assets worth over €1 billion in Ireland and the total amount it had invested was more than €500 million.
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why would we be any more susceptible to intermarriage than say Faroe islanders or Icelanders .
Quick open the borders .
@Before its too late: Same reason Nationalists can’t find a woman outside their gene-pool apart from cousins or sisters.
@John McQuaid: I think you might need to read up on who are the main victims of birth defects and congenital birth defects in Britain , here’s a hint , their not Nationalists , Your eminence .
@Before its too late: *They’re. Enjoy your downloaded .pdf of Mein Kampf!
@Before its too late: who says we are more susceptible? We’re actually slightly less due to our Viking, Norman, Flemish and Anglo-Saxon admixture. However, there are particular diseases which, through our isolation, have become more prevalent in the Irish gene pool, cystic fibrosis and Crohn’s disease included. The Faroese people also have the same problem with hereditary diseases, although with different diseases such as GSD type III and Parkinson’s, which are far more common among them than in other populations. Icelanders have to deal with an elevated risk of Hereditary Cystatin C Amyloid Angiopathy which causes strokes and dementia.
@John McQuaid: Wow , great response , I am truly burnt .
The usual resort to name calling , as if people are bothered anymore with those tactics .
You’d be the first on here to defend Palestinian nationhood , yet for some reason find Irish Nationalism a cause for ridicule .
The hypocrisy is strong in this one .
@Before its too late: Nationalism is for imbeciles, you won’t find me defending any nationalist movement. Bubble burst!
@John McQuaid: What do you defend?
@George Hogan: turf wars eh! think planet.
@George Hogan: Caliphates ?
@Before its too late: they have their issues also. MS for example. Intermarrage is a simplistic answer anyway. There are many other reasons that could be explored such as the age of the population, their diet, etc.
Was diagnosed 10 years ago.
Had no symptoms – my brother was diagnosed so had tests which proved my diagnosis.
25 phlobotomy response over the coarse of the first 12 months and my iron count was down to the accepted level – 50 – 60.
Now I do phlobotomy four times a year as part of the maintenance programme.
Would strongly urge everyone to get themselves checked.
@Charles Alexander:
Phlobotomy ‘response’ should read ‘sessions’.
@Charles Alexander: Me two. However my iron build up is very low, so I only go for 1 max 2 venesections a year. I knew something was wrong but just did not know why. After a few different doctors, one finally diagnosed it. No fan of the needle though that they use to drain the blood. Jaysus you could pipe water through it. Glad yours was caught in time. Any idea if the ibts accept it yet, seems like a lot of perfectly good iron rich blood going to waste.
@Charles Alexander: you might have to demand it from your doctor though, its not taken seriously enough by most.
@Charles McCarthy:
That’s good going on the iron build.
Mine normally increases by about 100 per quarter which is odd since I’m a vegan. But then, as my GP says ‘ that’s biology for you’.
I’m almost certain the IBTS accept blood but check with them.
Don’t get me started regarding the needle.
Good luck
@Paul A Whelan:
I think it’s more to do with the lack of awareness.
I know of people who went through over 2 years of tests before they were eventually diagnosed.
I was fortunate because my brother was diagnosed so my GP knew what to look for.
I think things are a bit better concerning awareness then they were 10 years ago but more needs to be done.
Ten years ago a GP would give up trying to find out what was wrong and would eventually refer you to blood specialist.
I blame Guinness
The inference here is incorrect. There is a suggestion that the high incidence in Ireland relates to ‘ inter- marrying’.
In fact it is explained by the principle of natural selection.
One gene for haemochromotosis confers a degree of protection against TB which was v prevalent in Ireland, it is this that gives rise to a population with a higher number of carriers.
Obviously when that poulation marries there is a higher incidence of couples who each have one gene and it is in their children that the condition is expressed.
The term ‘ inter-marrying’ suggests ‘inbreeding depression’which is incorrect and has a negative connoctation
Ironing has ruined many a marriage or is that irony. Don’t we all get our iron from Guinness?
@David Dickson: no we all get the tarmacadling the Jax leon trotskys from Guinness!
I didn’t bother reading this article as I find the tumble drier gets rid of most wrinkles so I rarely use the old iron, never mind overload it
That’s hilarious most of the people I know are iron deficient but then again I don’t know 83 people. Probably need to get out more.
@sinead casey:
Don’t you have 3897 close friends on Facebook like the rest of us?
@sinead casey: I was only 10 days away from a knee replacement op when the pre op blood test results showed an iron deficiency. Op postponed, went on an iron supplement … knee is in good shape now, op cancelled !!
I am doing my best to prevent this by marrying an Asian woman.
@Jimmy O’Brien: i’m doing my best to say No to Asian women … it it’s difficult…especially here in Thailand … 555 !
@Terry Cahill: are you sure they’re women!
Reading the comments, some are funny some not so much. There are a few inaccuracies, the blood bank do take the blood in Stillorgan and dolier street. The hospitals get paid a lot of money to carry out the Phlobotomy but they do dump the blood. We need more blood banks to keep the blood. It is crazy the hospitals are profiting from this and not at least keeping the blood. They are the ones complaining about the lack of blood donations. If you are concerned about it talk to your GP. The test is a simple blood test. I have it by the way and I send my shirts out to the laundry to get ironed. It is too dangerous in my condition
The trolls are out in force re this article,due to lack of understanding
Its the doctors who need to be aware of it. They treat it too casually if they even consider it. It leads to serious symptoms more than this article even suggests such as liver failure, severe arthritis, diabetes 2 and heart arrhythmia. People die a long slow death from it due to these disorders. Very very serious indeed.
@Paul A Whelan: Spot on Paul! A lot of Doctors and nurses are not up to speed on correct protocol of diagnosis and treatment!
Just send the ironing to the laundry or wear t-shirts and Speedos to work.
‘3 or 4 blood takings a year’
Shouldn’t people just be encouraged to donate blood?
@Ciara Jones: They just dump the blood.. Totally stupid I know but that is what is done.
@Ciara Jones: the blood bank won’t use blood from people with the condition.
@Niall Connolly: What “condition” would that be?!?
@Niall Connolly: not true..you can give blood
@Ciara Jones: the use the blood in Australia. Its absolute madness in Ireland throwing it all away. Blood banks are crying out for donations, Ireland has a huge amount of people who have no choice but to donate to stay healthy, and then we throw it all away. Its a joke.
@Siobhán Ni Mhurchú:
Correct, sufferers can give blood as it is used for transfusions due to its high iron content particularly mother’s who require transfusions after childbirth.
@Kate Flaherty: I’m sorry but you are wrong there . For yrs I donated blood & had a very high hemoglobin count , so much so that they used mine for hemophiliacs ,,,, in hindsight it should probably have been investigated further but it wasn’t , fast forward 30 yrs & I had 2 heart attacks in a wknd because my blood wasn’t carrying enough oxygen & I was constantly tired . On medication now to thin my blood ,,, Xeralto
@Niall Connolly: You’re correct, but that looks like it will change soon. It’s ridiculous as there is nothing wrong with the blood. It is not a blood disorder but a metabolic disorder.
Icelanders have an app for inbred checks.
Ireland should follow suit.
http://mentalfloss.com/article/76323/app-keeps-icelanders-dating-their-relatives
Irony is..even though we are more prone here than our European neighbor’s.. testing for it is done in Wales ..
People also need to be aware of how dangerous iron overload is in pregnancy. My mother and I both nearly died as she has high iron levels,nand naturally passed those onto me. As a premie, the levels were so severe I wasn’t expected to survive. When it turned out I would, doctors realised that if my levels didn’t drop naturally, I would need a full body blood transfusion. Luckily that didn’t happen. I do have higher than average iron, but not to the point of hemachromatosis yet.
My mum has had to reduce her dietry intake of iron after realising that she was setting off the metal detectors at airports with her blood!
Not to mention all the creamy pints of Guinness had by all
It’s very easy to find out from a regular blood test. Ask your doctor to request a test for Ferritin as well as the usual HDL/LDL tests. HIgh levels of Iron in Ferritin may indicate you have haemochromatosis. This can be controlled easily if you donate blood a few times a year.
We’ve Nailed it at last
It’s in our culture, boss. Oh crap we’re all part of the group.
Moral: only have intimate relations with foreign (living) bodies…
I wonder what the web address of the Irish Haemochromatosis Association is? Didn’t see it in the article.
Donating blood 4 times a year can help the condition.
… sister, it’s just kiss away, kiss away …
Only in laois
Should not have to pay 80 euro for every visit to get pint of blood off
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