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ASYLUM SEEKERS LIVING in Direct Provision for more than two years by the end of 2020 should be allowed remain in Ireland for five years, a report drawn up by former Secretary General of the European Commission Dr Catherine Day has said.
An Advisory Group, chaired by Dr Day, has made a number of sweeping recommendations in its report, which is due to be published today, including a once-off grant to people who have lived in the current system for more than two years. It also recommends increasing access to the labour market.
Direct Provision was set up in 1999 in response to a sharp increase in the number of people seeking asylum in Ireland.
The system has been repeatedly criticised by migrant rights groups due to the length of time people remain in centres while their asylum applications or appeals are processed, the conditions of centres as well as the psychological effects on those living in these centres.
Over €1 billion has been paid to private contractors and businesses since the system was established.
It’s understood the report recommends that any person who has been living in Direct Provision for more than two years be granted leave-to-remain for a period of five years – pending security vetting.
There should be an option to renew this under a once-off case-processing approach which should be put in place by January in order to clear the current backlog of asylum applications.
Leave-to-remain is granted to people who have been refused refugee or subsidiary protection but are not deported for humanitarian or other reasons.
Day’s report was commissioned by former Justice Minister Charlie Flanagan. The Advisory Group first convened in November 2019 and presented its findings to Government in recent days.
The current system of accommodating asylum seekers should be ended and replaced by a three-stage system of State-run accommodation by mid-2023, the report recommends.
The new reception system outlined in the Advisory Group’s report would see accommodation provided to people at State-owned centres for three months, according to the report.
On-site services should also be available at this stage to assist applicants in accessing services such as health and social welfare.
After three months at a reception centre, applicants should be helped to move to own-door accommodation through a housing allowance model.
A payment similar to the Housing Assistance Payment (HAP) would also be made available as well as a weekly allowance under this new system. It’s understood Housing Minister Darragh O’Brien has been briefed on the report, which calls for a mix of solutions to accommodate protection applicants.
If a person receives International Protection or permission to remain in Ireland they should be provided with support for up to 18 months afterwards, according to the report.
Application process
Dr Day’s report was drawn up in consultation with a number of NGOs, including Nasc, the Irish Refugee Council and Movement of Asylum Seekers in Ireland (MASI) as well as current and retired senior civil servants.
The report calls for a “whole-of-government” response to replacing Direct Provision.
Dr Day previously described the current Direct Provision system as “unsatisfactory” and “largely reactive”.
In addition, “binding targets” for different stages of the protection process should be introduced – to come into effect from 2023 – including a six-month deadline for the International Protection Office to make a first instance decision and a six-month deadline for the International Protection Appeals Tribunal to make a decision on an appeal.
This should be supported by an increase in resources for the Legal Aid Board to ensure that protection applicants have access to legal advice and support from when they arrive in Ireland, it’s understood.
The report also makes provision for increasing access to the labour market by making permission to work available within 3 months of lodging an application for protection.
The report calls for the new system to be in place by mid-2023.
The report, which is not legally-binding, will now inform the Government’s White Paper for replacing the controversial system of accommodating asylum seekers in Ireland, which is due to be published by January.
Responsibility for administering Direct Provision accommodation transferred last week from the Department of Justice & Equality to the Department of Children & Youth Affairs, as part of an agreement under the Programme For Government.
The report and its recommendations will now be considered by a committee overseeing the drafting of the White Paper.
The Advisory Group’s report also makes a number of short-term recommendations while the current Direct Provision system remains in place.
Vulnerability assessments should be introduced as soon as possible and be offered to asylum seekers within 30 days of their arrival by 2023.
In addition, it is recommended that the Health Information and Quality Authority (HIQA) carry out inspections of Direct Provision centres around the country.
Inspections have previously been carried by the Department of Justice & Equality and private contractor QTS.
I was diagnosed when I was 20. Now 33. My first medication didn’t work and I was getting worse so I changed to another medication. Thankfully it has slowed down the progression so to look at me you’d think I was grand. I have ongoing problems like constant headache, bladder issues (h have peed meself countless times) and trembling of hands and pins n needless and so on.
The most difficult part of ms for me is the mental side. It’s a lifelong illness so it’s always there BUT I never give up. It’s an awful disease but it is what it is. Always talk to somebody about your mind and h how you’re computing the daily madness of ms.
@Gareth Wogan: well done you are a strong man, eat a healthy diet and paced exercise, your still a young man and hopefully there will be a treatment for this auto immune illness
@nick mullen: my mistake I meant strong woman (in my case a senior moment)
@nick mullen: well I think I’m a man!!!!
Beautiful words. I have been diagnosed almost 5 years ago here in Ireland. it was hard because I wasn’t in my own country and English isn’t my mother language. I was a long time in hospital and after they sent me to rehabilitation. MS life is not easy, many hard day’s but never let it put you down you are beautiful and strong. Whishing you a great life full of happiness. You are not alone.
Huge kiss
Thank you for sharing.
Wonderful writing Rosie, brought a tear to my eye.
Wishing you two a long and happy life together.
A terrible disease, with somewhere between three and four times more women than men affected, but normally more aggressive in men. My brother was diagnosed a few years ago and it is a very tough battle.
Beautiful
I’ve no knowledge whatsoever about MS & am not remotely qualified to make a comment but from what I’ve just read now; just wanted to say thanks for sharing a bit about your life living with it: without sounding too corny, you’re an inspiration, woman.
Many, many years of happiness together ahead.
Good luck Rosie
Since been diagnosed myself I and others in the same boat understand yours and ours predicaments.
I hope you and your husband have a long and fruitful life.
I was diagnosed with Multiple Sclerosis (MS) in October 2011, at the age of 55. I woke up one morning with numbness in my lower back and legs, I couldn’t feel my feet touching the floor. I saw my doctor and had an MRI to see if I had a disc problem, it was negative and she told me she feared MS. I was sent to a neurologist, had two more MRIs, and was told that night that I have four lesions on my spine MS. I tried every shots available but nothing worked. In 2015, my neurologist and I decided to go with natural treatment and was introduced to Natural Herbal Gardens natural organic MS Herbal formula, i had a total decline of symptoms with this treatment, the numbness, terrible back pains, stiffness, body weakness, double vision, depression and others has subsided. Visit Natural Herbal Gardens official website ww w. naturalherbalgardens. com. This treatment is a breakthrough for all suffering from Multiple sclerosis, i am strong again!
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