Articles About Children, Adolescents and Adults
Autism in Ireland
I suppose there are a few countries in the world where it is harder to access services, be treated with kindness, decency and get useful information about autism than Ireland but they are few and far between. The plight of parents to access therapeutic and educational services for children on the autistic spectrum is a nation scandal no one wants to talk about.
I read with interest that the Green Party has manipulated the government into rescinding cuts in the education budget. But I do not see one single item, unless I have missed it, that relates to the cuts in special education. So once again the children with the greatest need receive the poorest service.
If you child has autism this is the situation you are likely to face:
I know there are exceptions to the above. At primary level things have improved greatly and teachers in our primary schools really do care about these children.
I know this to be a fact because I have trained, worked with and spoken with thousands of them. There are privately funded support groups offering help to families of people with autism. But despite these advances and pockets of support things are bad and could get worse.
9 Responses to Autism in Ireland-The Harsh Truth
paula
October 15th, 2009 at 6:18 pm
that sounds about right all of this can occur on a daily basis in my house due to having two on the spectrum and another with special educational needs. it can only get worse now with the budget to look forward to, thanks dr. Carey
bill domican
October 15th, 2009 at 9:28 pm
Yes, sadly all of the above is as it is. It’s worth noting that some of the precious ”funding” that went into special needs and autism during the boom was absorbed by the creation of a new raft of useless public servants called SENOs (or saynos as described by most parents). The purpose of these gems seems to be to block services for children in need and to prop up archaic educational practices just to tow the government line and hamper evidence based intervention practices. I do not know of any parents out there who have any good to say of SENOs and many worry when theres a mention of one getting involved where their child is in a school placement and has access to services. Our government has got so many things wrong.
lisadom
October 16th, 2009 at 8:13 am
I’ve linked you.
Emma Roe
October 16th, 2009 at 12:35 pm
A National Disgrace is exactly what this is. Getting the diagnosis is a walk in the park when compared to what comes next…accessing services and education is an absolute nightmare. Agree with Bill entirely regarding SENO’s another complete waste of public money and don’t get me started on Beechpark Services! What are these people doing with the money that is given to them to run their service??? A child’s right to an education is a fundamental basic human right….not in Ireland apparently ….It’s sickening.
bill domican
October 16th, 2009 at 8:18 pm
Emma, Thanks for you support. And yes, I know what you mean. All that crowd want to do is hold meetings about meetings. They are never happier than when they put a ” learning disability” tag on a child and hence exclude same child from speech therapy and other services. I have never heard of a case where they assessed a child and recommended an intensive programme of ABA supported by speech and occupational therapies. Total wasters. They’re looking top cut home support hours at present. Be forewarned and forearmed. We are not a soft touch.
Milena Venkova
October 18th, 2009 at 12:57 am
Posted this on the IAA website first:
Thanks very much Dr Carey for outlining the absurdity of educational provision. To add my pennyworth – my son was assessed to be on the spectrum, and with IQ of 78 it was recommended he attends a mainstream school. Which means he is denied occupational therapy and speech and language therapy by Beechpark on the basis they provide services only for children in their special units. We got a letter last week stating clearly that if we want to avail of those services, we should take him out of his school and put him in one of the units they support. So, if a child is estimated (however erroneously) to have an IQ under 70, he/she is not allowed into a special unit. If, on the other hand, he/she is above 70 and thus able for mainstream, they are recommended to go into a special unit so they get services?! I assume the ideal situation will be when no children are enrolled into the units so they are closed down
Barb Harlow
October 28th, 2009 at 4:40 pm
I am an early childhood special education teacher in America and am interested in teaching in Ireland. Please know that your frustrations about children with autism receiving services and the government cutting funding for those who need it the most is not specific to Ireland. Here in the states more and more young children are being denied services because government beaucrats move the money elsewhere. Not only do familes and children who have special needs suffer, it also puts a lot of pressure on teachers. We are being asked to provide premier service with less and less tools to do our job. What are some other resources I can find on the internet to help me learn more about special education in Ireland and teaching opportunities?
Ruth Stribblehill
January 18th, 2010 at 1:09 pm
I have a 10-year-old son with Asperger Syndrome, which was diagnosed in the UK, before we moved to Ireland. Over there, he received psychotherapy and occupational therapy, and we had the ongoing support of a multi-disciplinary team, led by a consultant psychiatrist at our local CAMHS. Now, after an 18-month wait for a CAMHS appointment here, we’re told he has no mental health issues, so they can’t help us. There is no access to OT, either through CAMHS or community-based. Beechpark was mentioned, but I’m certain it wouldn’t be appropriate for my son to be in a special school. The only useful thing to come out of our recent meeting with a CAMHS psychologist was the suggestion that we look into the Centre for Talented Youth.
My son’s school is doing what it can, and I have to say that his teacher is very good, but with the best will in the world, they have neither the expertise nor the funding to meet all his needs.
Maya Bailey
August 29th, 2010 at 6:29 pm
there has been no permanent cure for autism yet but i think stem cells could also help**’