Skip to main content

Additional Learning Needs




I have never really liked the term ‘special needs’. Every child is special and every child has needs, so I therefore have previously used Specific Needs.

Just as I have never really liked the term ‘disabililty’. Ryan and I use and much prefer ‘diffability’; to mean Different Abilities.

Later in this post, I talk about the statutory assessment process that we went through with Ryan who now has a legally binding document setting out his specific educational needs. My original intent for the focus of this post was to go into greater detail on the 26-week assessment process and discuss Ryan’s statement, to offer advice to anyone embarking on a similar journey.     

I have, however, now changed my mind on the focus of this post and decided instead to discuss additional needs. I will therefore not to bore you with all the details of statementing for 2 reasons:

First, it is 16 pages long and secondly, from 2014, statements no longer exist. They have been/are being phased out across the UK and are being replaced with an alternative system “which is more flexible, needs-led and less bureaucratic” (Quote from council documentation) called Individual Development Plans (IDPs).

The term SEN - special educational needs has now also been replaced (yay) with ALN – additional learning needs.

There is lots of information about these new plans on various news sites if you do a quick Google search and the NAS has a very good pdf document detailing the new proposals.  I am no expert on this new system as Ryan’s statement will still continue for him. 

Children have additional learning needs if they have a learning difficulty, which calls for additional educational provision to be made for them.





This short definition emphasises the two key phrases that are part of the full legal description of special educational needs found in the Education Act.  The term SEN is no longer considered acceptable and ALN is now universally used in its place. 

Put simply, children with additional learning needs may find it harder to learn than most children of the same age, or have a disability, which makes it difficult for them to take part in school life. As a result they may need extra or different help to make the most of the learning opportunities offered by the school.

Learning difficulties can mean:
·        Difficulties in some or all areas of work.
·        Particular problems with reading, writing or mathematics.
·        Emotional, behavioural problems or organisational difficulties.
·        A physical disability.
·        A medical or health problem.
·        A sight, hearing or speech difficulty.
·        A general delay in development.
·        Expressing themselves and understanding what others are saying.

What is ALN provision?

ALN provision is the different or extra help given to children that face barriers to their learning. This provision can mean extra support in class, different strategies or approaches, small group work or individual help.  It can also mean individual or group work outside the classroom or additional help from specialists outside the school.

How many children have ALN?

20% of children on average have additional learning needs at some point in their school life.  Some children may have additional learning needs for a short time; other will require additional provision throughout school.  Children may have needs in particular curriculum areas or subjects, whilst others will require support in most aspects of their education.

Stage 1 – School Action.

The school with your assistance will coordinate appropriate help within the class such as: Different learning materials or equipment; Small group support or individual attention; Help from an extra adult; Different ways of teaching things; and create one or more of the following:
·        Individual Educational Plan
·        Behavioural Plan
·        Pastoral Support Plan
·        Personal Educational Plan
Which documents what the school will do to help your child and what is required from your child to help themselves. It will include: Short term targets for your child; Ways in which the teachers will work your child to achieve these targets; The additional support the school will provide through it’s own resources e.g. additional learning support time; How you can help your child achieve their targets at home e.g. reading with your child every day; A review date which should be at least twice a year. Ideally reviewed termly.

If you child does not make enough progress despite support from within the school setting, continues to make little or no progress in certain areas or continues to work at levels well below that expected of children at similar age, the teacher and ALNCo with you agreement may involve specialists from outside the school.

Stage 2 – School Action+

Outside agencies such as:
·        GP
·        Specialist Teachers
·        Educational Psychologists
·        Speech and language therapists or other health professionals.
·        SNAP

Will help with assessing your child’s needs and can provide the school with advise and strategies for new targets.

Stage 3 – Statutory Assessment

School action and School action+ have still not helped you child to access the curriculum or catch up to a level you would expect then a very small number of children with significant difficulties will require their needs to be considered in greater depth.  A statutory assessment can be requested by you as a parent or by the school or even better by both to the Local Educational Authority (LEA).  It is a very detailed investigation of a child’s Educational Needs and what additional support they require to meet those needs.  

Ryan was issued with a statement of educational needs in 2010, after I fought for 5 years to have his needs assessed.  He did go through all of the stages as I have previously told in our story to date.

It really helped all of the stages I have been through to keep a diary all of Ryan’s life detailing: illnesses; diet; exclusions; sensory issues; meltdowns; developmental stages, to name but a few.

The more you record the more evidence you will have and the more detailed, specialised, personalised assistance can be tailored for your child.

It is about knowing your rights and fighting for the rights of your child to receive a full inclusive education.

Tell me and I forget,
Teach me and I remember,
Involve me and I learn.
                                 

Benjamin Franklin

Comments

Popular Posts

Missing Education due to Illness

The Importance of Attendance If you read any news articles on education, correspondence from your child’s school, or are simply clued up on parenting then you will know the importance of school attendance. Schools place a great deal of focus on targets and will often offer incentives and competitions to encourage and increase attendance figures, but what if your child has a serious illness. What happens if they really are not well enough to attend school. What happens then? Attendance targets at Ryan's school are currently set at 95% attendance for the school year. Therefore realistically your child can only miss 10 school days due to illness. Medical appointments such as GP or Dentist do not count, but you are encouraged to make these appointments outside of the school day where feasibly possible. If your child consistently misses school, even if it is only one day a week, that equates to 39 days over the school year. Even missing one day in a week results in pressure on the ...

Questions to ask after Cancer diagnosis

Cancer Sucks I have shared with you Ryan's lymphoma journey where we have talked about the ups, the downs, the protocols for drugs, the side effects, but I realised recently I have never shared the questions. This post is all about what to ask when you receive a diagnosis of cancer. Receiving a cancer diagnosis is never ever going to be seen as good news. It can never be dressed up or made pretty. It is devastating, it is gut-wrenching, it is life-changing. There is so much information to process you will not think of the questions you need to ask or you will have hundreds of questions you want to ask all at once. These are just some of the questions you can ask once you have processed the news, in order to gain a better understanding of your fight ahead. General Information What type of cancer do I have? Where is it located? What are the risk factors for this disease? Is this type of cancer caused by genetic factors? Are other members of my family at risk? What lifestyle c...

Chemotherapy Cycle 5

What is Normal? With this being our penultimate cycle of chemotherapy I have had several family and friends comment to me “oh I bet you can't wait to get back to normal”. This has really thrown and upset me because it seems to come across that they have failed to comprehend the fact that we have 2-3 years of maintenance ahead and at least two more general anaesthetic surgeries. Not to mention physiotherapy as it is expected Ryan will take 12+ months to heal from the effects of being poisoned from the inside out. Normal is long way off yet. While everyone else appears to all be getting excited that Ryan is coming to an end of his chemotherapy protocol treatment, Ryan himself is becoming more and more tired with the cumulative effect of the onslaught of the chemotherapy drugs and is spending long periods of time in hospital after each cycle with infections due to his impaired immune system now as a result. Ryan is far from excited. Ryan is exhausted. We still have one more cycle t...

Peritonitis

Emergency Surgery On the morning of 25 October 2016 Ryan was complaining that his PEG feeding tube was unbearably painful. He was due for a review anyway that day at Velindre Cancer Centre and a PEG specialist nurse came for to look at Ryan. She said the site was a bit weepy and raw, she thinks he possibly caught or pulled it in the night. She is confident that it is fine and she also gave it another good clean.  A week on and we are back to square one. The district nurse came out on Monday 31 October 2016 to advance (turn) the PEG tube as is needed each week after the first month. The nurse was unable to move the disc and caused Ryan an incredible amount of pain. We ended up having to go to the Teenage Cancer Trust ward in Cardiff, where two gastro nurses met us and spent the best part of an hour, torturing Ryan while they 'forced' the PEG to move, which they eventually did. Or so they thought.  The following week, 7 November 2016, the district Nurse came again to the ...

Cancer Survivor Story

Cancer Doesn’t End When Chemo Does Ryan finished his chemotherapy treatment on his brother's 18th birthday in May 2017. The last two years and eight months were a blur of stress. Yet coming to the end of treatment coincided perfectly with Cancer Survivors Day on the first Sunday in June, each year, so what better way to mark this day than with our own survivor story. Ryan's weight at diagnosis was a staggeringly poor 42kg. He had lost so much weight not being physically able to eat due to the tumour in his throat, but with thanks to his own determination and the feeding tube that he had. Ryan's weight as we start his final chemo cycle....drum roll....prepare yourselves.... was an amazing 57kg. A year on in 2018 and despite going through treatment for the second time after relapse. Ryan weighs an impressive 65kg. Chemotherapy Cycle six Started on Monday, 1 May 2017 for hydration and the week went well without any drama. His final chemo took place on Friday, 5 May wh...