Tuesday, 29 July 2014

Moving on up… “Transition from Senior School to College/University” by  Dyslexia Dublin CETC © 2014

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Have you experienced a transition from your normal routine?... changing job or moving home perhaps?  This change can affect your structure and stability and can also be very stressful for many.  Multiply this and that is how a child with additional/specific learning needs feels every time he or she has to face even the smallest change.
The stress and anxiety doesn’t just stop with the student either … the parents will worry for the child/young adult and themselves about the early days in the new environment, knowing full well this has already been a problem with less challenging changes like moving desks, teachers and classes in the past and now we are talking a whole new environment in an adult world, where most of the direction has to come from the student.
All change is challenging and comes at a price, so transition needs to be gentle.  Why more schools don’t allow students to go to the next level for tasters (visit the college for a couple of days to allow students sample courses before deciding which to enrol for) is beyond me… this is achieved by few and yet a wide range of tasters and courses are offered by so many third level colleges… certainly in the UK and something that would be worth looking into at any college you’re considering.
Flexibility is king in accommodating the transition process when a child/young adult presents with SPLD.  There are guidelines for schools and colleges to follow, but many parents will be unaware of this at the point it’s required.  It’s vital to maintain communication with tutors and/or special needs department, both prior to and after transition to make sure everyone is aware of the individual’s needs.  Senior schools should communicate with both parent and college/universities to compile the information necessary to be able to accommodate the child’s needs (IEP).  Parents need to be made aware of points reductions where statements can back up a specific learning need, such as in Ireland there is the DARE scheme…this allows for a reduction in entry points required and many colleges subscribe to this.
Guidelines in the UK:
“To comply with the terms of the Equality Act, students with dyslexia and other specific learning difficulties should not be penalised for poor spelling, grammar or sentence structure.
Students registered for dyslexia/spld support are given blue cards to attach to their work to alert the marker to their dyslexia/spld so that appropriate concessions can be made.
For further information about marking the work of dyslexic/spld students, please see:
For modules where academic standards would be compromised by applying dyslexia/spld marking concessions, exemption may be requested. This is normally likely to apply only to modules specifically testing use of language – for example foreign language modules.”  Quote from Oxford Brookes University.

Guidelines in Ireland:
DARE is a College and University Admissions Scheme (Disability Access Route to Education) that offers places on reduced points to school leavers with disabilities, apply early.

Who is DARE for?
Dare is for school leavers (Under 23yrs as at 1 January 2013) who have a disability and who may not be able to meet the points for their preferred course, due to the impact of their disability.
Apply Early: apply to the CAO at www.cao.ie

Discuss the history of your child/young adult with the college/university to make sure you are all singing off the same hymn sheet… reasonable accommodation should be afforded in certain instances (students with dyslexia, dysgraphia and dyscalculia), such as :

 Voice Recorder.
 Writer present - to be able to sit their exam away from the main exam room (less distraction).
 Exemption from spelling and grammatical components in language subjects (waiver).

The key to reduced stress lies in preparation… I will always remember the old saying “fail to prepare, prepare to fail”. Be pro-active and less problems will occur… transition is, as it says, a period of smoothness from one thing to another.  This should happen very early on in the final year/sixth class and below I have made some suggestions that can be used by both parent/child and school.

Transition without the Stress – Hints to help from Second Level School to college/university:

Get the College to demonstrate an understanding of your child’s condition.

Talk with the students on a one to one basis about the different structure and the increased formality they might face at third level.

Introduce a mentor from the present first year to ease in the new student… this will grow the network for the incoming students.  Avoid older students as they could draw the incoming students out of their comfort zone.

Try to get the College to offer lockers that are easy accessible and away from the hustle as young adults with learning needs can become nervous in crowds and all fingers and thumbs.

Most will realise that they will have a variety of teachers, possibly one or more per subject… it’s important that their year tutor informs the others of your child’s needs.

Parents/carers should teach their children/students how to write out and also read prepared timetables and it helps to colour code and replicate with text books…e.g. 1st lecture on Monday is yellow so put a yellow sticker on the relevant book and the timetable…they will have far more free self-directed study periods at third level and need guidance to discipline themselves with this strange routine.

Students need to know about acronyms… for example, Exam bodies like Edexcel and RSA …these will be used far more in third level.
Make sure you avail of every opportunity to visit the new place of education… it’s worth driving past there occasionally, especially at busy times.  Let them know about shortened lesson times and moving to different classrooms for each lesson (orientation is so important).  Also, they need to know meals will be at different times, depending on their timetable… is there a cafĂ© or will they take food?  Maybe show them the college website and they can check out the gallery of photos. Take them along to as many open days as you can and talk to course tutors, etc.

Make sure your child decides on whether they want their college/friends to know they have learning needs… not all children are comfortable with this and the college cannot tell others as you are protected under data protection. I have found from experience that there is great support from those that know, at this higher level of education.

You should be in possession of a valid statement in order to show the new college/resource department for the provision of resource hours, laptops, etc.  Most have really great facilities in their learning resource rooms and can help with essay/assignments, etc.

Make sure they are aware of toileting, etc… I recently spoke to my son’s teacher about his transition from primary school last year and asked if they understood about his dyspraxia and the answer was ‘yes’.  However, in the next sentence they mentioned that he was spotted going to the toilet less than 20 mins after the start of the first class of the day and surely he knew he wanted to go (inferring he should have gone before lessons started)… so did they fully understand dyspraxia?... no is the answer.  Also, they might well have quiet rooms if your child gets stressed or make arrangements for time out if your child feels threatened by an activity.

Parents need to be prepared for colleges to call them if meltdowns happen… it might be wise for you to take time off work during the first week at least so you can collect them from their new environment, have a coffee and let them talk about their early experiences. It’s also advisable in case you are called by the college.

 Keep an eye out for bullying (change of mood, disturbed sleep, confused and reluctance to get going, wanting to change courses after a few weeks  and maybe even a  return to bed wetting…  these can all be  indicators).  Find out who they spend breaks with… listen out for names and check to see that they are in the same year, as quite often older boys will use them to do things they shouldn’t be doing, like leaving the college to go to the shop or start trouble on their behalf.  Watch out for people trying to influence smoking/drinking or drug taking.
Try to be all positive and avoid pressure in relation to performance until they are settled.

Get to meet their new friends and encourage them to visit... this will help them gel and stay in the loop, thus preventing isolation.
Make sure you attend parent evenings and get a direct line to your child’s course tutor and make sure they have all the relevant information in course files. Get dates from them for exams and project deadlines and make sure you chase them about accommodation for exams ahead of time to avoid upsets.
I will say, third level are far more pro-active than first or second level in this regard, as they are funded on outcomes in most cases and not student numbers.
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All our articles are for information only and guidance… professional advice should always be sought. Toby Lee, Dyslexia Dublin CETC © 2013
‘Dyscalculia - (revised) The Why’s And How To Spot Some Of The Signs’ by  Dyslexia Dublin CETC © 2014

Do you as an adult, or maybe your child, have problems with immediate number recognition?   This article has been penned to give you an idea of what dyscalculia is all about and some helpful tips to improve things along the way.
 Dyscalculia can be described as an innate specific learning disability (in the mind) that prohibits various levels of understanding in mathematics.  It is very similar to dyslexia and, in some cases, children/adults can have both (co-morbidity).
Maths as we all know is a core subject and therefore has to be studied, but there are ways that it can be improved by becoming number fluent… we suggest and use a very visual/kinaesthetic approach to improving fluency and improving mental imagery, and visualisation is all important. Those of you who share dyslexia and dyscalculia, as I do, will know that we are constantly told we have a great imagination… can you imagine how many football players or snooker players would have never reached the height of their profession without great imagination? It is a great asset and if we can apply this to our studies, we will truly fly! Numbers for many is tiring, unless you are an accountant or extremely rich and spend all your time calculating your wealth
We have great results from many that at one point shook just hearing the word maths, it needs to tuition needs to take into account all the various learning styles.

There are very few centres that work with dyscalculics, if you would like to discuss this further then you can visit our website at www.dublin-cetc.com

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There are many variants with dyscalculia, which can include a difficulty in understanding numbers, ie. 5 back to front and getting sums reversed (54 x 4 can be read as 45 x 4), learning how to manipulate numbers, learning maths facts and a number of other related symptoms, such as recognising the letters/words side of maths (dyslexia) and even down to reconstruction of the sum onto to your workbook (dysgraphia) and number alignment, which is key to totalling sums correctly.  As with dyslexia, Maths disabilities can also occur as the result of some types of brain injury (apraxia), in which case the proper term is acalculia, to distinguish it from dyscalculia which is of innate, genetic or developmental origin.
Although maths learning difficulties can be genetic, occurring in children with low levels of academia, dyscalculia also affects people from across the whole IQ range (Einstein had dyslexia) and sufferers often, but not always, also have difficulties with telling the time and measuring (eg. cooking).
 Many find counting numbers going forward in a particular pattern straightforward, however they have problems with reversing numbers, especially those that have a sequence involving 2's and 3's.  Very few develop islands… by this I mean number platforms like 5-10-15 or 3-6-9… this alone can improve calculating as many use their fingers and count from the base line of say 1-10-20, so 20 + 8 becomes 21-22-23-24-25-26-27 and finally 28, instead of platform 25 and 26-27-28, much easier and quicker too.

Estimates of the population with dyscalculia range between 3 and 6%.  Around 50% of those with dyslexia have dyscalculia and those who don’t are generally quite good at mathematics.
Dyscalculia can cause problems with the written maths and indeed for those with dyslexia and dyscalculia, algebra can cause particular problems as the calculations and written word become entwined… however, not so with physical maths (eg. counting with fingers or an abacus) as this is visual.  Learning Maths through the visual channel is very important (games, etc.).  Also, I find that some, but not all, children are no longer being taught by rote (ie. memorising through repetition)… children with specific learning needs would benefit from this method also as it creates rhythm and provides another method of learning. As I’ve mentioned in previous articles, over learning is so important, ie. a variety of ways of learning a subject and lots of repetition.

Children suffering from visual stress and those with dysgraphia can also have a problem with writing down sums, as they have a problem in forming columns and rows.
Symptoms of dyscalculia could be if you throw down a number of coins or counters in a random fashion the child/adult would have difficulty in arriving at the correct value/number.  They would have a far greater chance of accuracy if they were in rows.  This, in itself, can be a problem if your child goes into a shop to buy something.  If, for example, you ask them to buy milk in the shop and get something for themselves, it’s helpful to give the money for both separately so they know which is which and don’t get confused.  It can also be useful to let them pay the cashier when you’re with them, counting the money out loud, to help them get used to the values of different notes and coins.  As they get more confident, you could get them to calculate the supermarket shopping, adding each item as you put it in the basket either on a calculator or by writing and adding the numbers in their maths copy book (squared).  All these things help to build greater number recognition.
Also, with varied objects, ie. one of each… cow, pig, horse, dog for example… they would then use their visual image side to great effect and gain the correct answer and with increased speed too.
Reading a clock is also difficult, especially analogue as opposed to digital… again, games can speed this up.  Also, going in up in 5’s is good (5, 10, 15 mins) again using platforms and try, for now, to avoid introducing the ‘to the hour’, just use past the hour, ie. 10,20,30,40 mins past, etc. ‘Quarter past/to’ and ‘half past’ can be introduced later on.  Also. time keeping can be a problem – it’s beneficial to use minutes when giving instruction, ie. we’re going out in 10 minutes, it’ll be time for bed in 20 minutes… as they will find this easier to understand.
As with Dyslexia, left and right is a problem - with map reading people often turn the map towards the direction they need to head.
Other symptoms are an inability to process multiple requests, difficulty in multi-tasking. Also, problems with reading music and with visualisation in general.
Many adults with dyscalculia have learnt to adapt their world to allow them use their strengths. Being creative for the most part, many become writers and artists.

Software intended to intervene and improve children and adult’s academic ability is now widely available.
Multi-sensory educational therapy is a very effective way of increasing academic (ability) age up to a person’s chronological age range.
Need resources to support those struggling with maths?... then visit our online store at www.dyslexiadublin.ie
 NB. This information is from personal experience and research and also partly sourced through the work of others.  It is purely for improving the understanding of dyslexia and to offer helpful advice.  Toby Lee, Dyslexia Dublin CETC © 2013

Sunday, 27 July 2014

Troubled Sleep in Children with Specific Learning Needs by Dyslexia Dublin CETC © 2014

A sleep disorder can be temporary or more long term/habitual.  This can be known as somnipathy, which is a medical disorder that affects our sleep patterns.

Disturbed sleep can cause the same problems if it persists and this can lead to somnipathy and it may be severe enough to interfere with a person’s normal physical, mental and emotional functioning! Meltdowns/tantrums could well be the result of lack of sleep.

There are very strong links between childhood sleep disorders and behaviour, lack of concentration and mood swings. Sleep disorders that are directly caused by behavioural factors (eg. sleep-onset association disorder) can present in some children with specific learning needs. Invariably, sleep deprivation increases the chances of  meltdowns and this can have a major impact on the entire family.

Some sleep disorders are serious enough and known to interfere with physical, mental and emotional routines.  In cases that are causing noticeable problems, a sleep study/test (Polysomnography Test) can be recommended by your GP/Consultant.

Insomnia can also cause problems, due to falling asleep at times when you are feeling at ease (symptoms however need to go beyond 4 weeks before the GP will intervene) and then at the allotted time you cannot sleep due to things flooding the mind. This, however, is more apparent in adults.

What is a reasonable amount of sleep required to carry out normal routines in childhood? Children of 5–13 years require about 10 hours sleep, and those aged 14–18 years need about 8 hours. These levels are the minimum required and if involved in physical exercise, they should take more rest.
The amount of sleep a person needs will vary from individual to individual, but most people require around eight hours.

We don’t fully understand how we came to require around seven to eight hours of rest per night (just to add, catching up is a bit of a fallacy). It is thought by many professionals in this field that it is down to build, muscle size and fat stores. We tend to go into partial hibernation in the winter months and spend longer sleeping. A lot takes place in these hours of rest, children’s growth hormones become very active, as do our repair and replenishment function (skin replacement and general healing).

So, what causes our sleep to be disturbed? Not winding down is one and this can be caused by the run up to bed time…home work should be well finished by tea time, any revision after this point will lead to the mind being occupied and the chance of a good night’s rest will be compromised, making the following day more challenging.

SPD (teeth grinding) is another possibility, along with dehydration and lack of air…many children with dyspraxia tend to breathe through their mouths which dries the mouth out and can also cause snoring. This may also result in headaches (drink a good few glasses of water a day).
Sugar is another cause of hyper activity and lack of sleep. Caffeine (stimulants) should not be consumed after 17.00.

Children, like adults, need to unwind and creating a relaxed, noise free atmosphere is a must. Let them chat about their day and also encourage them to keep a reflective diary, as this will dump information into their long term memory. Try to avoid giving them information about special occasions until the day…how many children have trouble sleeping before a birthday or Christmas?!

Sleep could be, and often is, thrown out of sync due to lack of a stable routine and the body clock being altered through certain habits, such as allowing  a child to routinely fall asleep watching telly during the day (with exceptions like illness).  For example, a parent might be working night shifts and nods off and the child relaxes and does likewise (eg. on the couch with the parent). Also, getting up late in the day becomes self-perpetuating, this will lead to difficulties in getting to wind down and sleep in the evening or can even cause problems due to being in a light sleep and waking during the night. Even during school holidays the routine should still be in place, stability and regularity are one thing that are needed to correct and maintain good sleep patterns.

By around the age of two, if a child wakes in the night it should have the ability to be self-soothing and able to settle again. Separation anxiety can also lead to sleep disorders and it is always a good idea not to share your child’s bed or let them share yours. You can wean a child off this and one good way is to substitute you with a favourite teddy or doll…allow the surrogate to share the meal table, watch TV with you and even go out on family trips. A trust will build very quickly and when the child has to separate from you for socialising or sleep, it will bring a great feeling of security. This will also help with children that have recurring bad dreams…it’s no harm to record dates and details of the bad dreams or broken sleep patterns and try to identify triggers or see if a pattern emerges…watching adult TV/movies is a big factor.

All this has a knock-on effect on the ability to maintain concentration and discipline during school time…this is something the school might not pick up on as they may only notice lethargy or bad behaviour and not lack of sleep. 

Teenagers have a greater problem in this area and their lifestyle so often exacerbates poor sleep routines. Social networking means that teens can communicate with their friends well into the night and many would never see this as the cause of their lack of motivation during school times and even the weekends.

The problems tend to increase in the summer due to the bright evenings and increased noise which travels greater distances through the thinner air.

Conditions have to be right for all children to sleep… young children don’t have the ability to regulate temperature until they are around eight years of age, so room/body temperature can be a problem.

Maintain a good sleep routine, even during holidays.
Keep your children hydrated during the day and reduce sugars and caffeines.
Make sure the bedroom has plenty of air and is noise free.
Use blackout curtains and, if needs be, acquire a soothing night light.
Wind your children down…don’t let them play with gaming machines just before bed.
Avoid homework in the evening, this should all be finished by tea time.
If they are young, read a story and one that will relax them.
Don’t share their bed, sit on the edge or in a chair.
You can also use specialist relaxation CD’s. http://dyslexiadublin.mygostore.co.uk/mindfulness-matters-cd.html

Record disturbed sleep patterns and try to see if there is a trigger.
Don’t let them share your bed…if they can’t settle, stay in their room until they do.

Make sure they eat well.
If you want to reduce tantrums/meltdowns, etc. persevere and they will very soon get back into a settled sleep pattern.

Don’t be fooled by a child that has his or her eyes shut, they could be sat up the second they think the coast is clear!

Sleep is vital for restoring mental energy. We spend all day learning, thinking and creating, this all helps to deplete our energy reserves. And during our hours of sleep we process this information, for the most part in a harmless way (dreams) and sometimes the opposite…(nightmares).

You and your children’s bodies are like a well-oiled machine and rest is required by each and every one of us. We don’t know for sure exactly how much sleep we all need, but we sure know the consequences if we, or our children, have too little.

 This article was written for guidance purpose only and, as with all things that cause concern professional advice should always be sought.

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Friday, 11 July 2014

How is Confidence and Self Esteem affected by Dyspraxia, (DCD), Dyslexia and other specific learning needs by  Dyslexia Dublin CETC © 2014 Revised on the 11.07.14

Confidence and achievement is everything… we can all do our own personal SWAT (strengths, weaknesses, opportunity and threats)… just take a look what you are good at, what do you struggle with? Can you do everything you need to do?
How easy is it to lose your confidence… imagine yourself down a hole and every time you stick your head out, someone hits it with a stick or shouts at you.  How many would still continue to pop their head up?
Many with dyspraxia have days, weeks, months and years like this and children with dyspraxia dealing with learning needs, maturity and skill building have these problems to face.
Dyspraxics generally have reduced ability when it comes to co-ordinated skills (gross and fine motor) such as sport and dance and this in itself multiplies the time required to carry out a given task that can be mastered by others in the shortest (one or two attempts) period of time.  Quite often we, as parents, fail to recognise this as a problem and fall short in time/tolerance required to help our children develop the required skill or skill sets.  Our parent's may considered spending the same amount of time teaching us how to ride our bike, as they would with siblings (brother sister), whereas in fact we often  require up to four times longer to grasp that particular concept.  It’s important for parents not to tire and make sure to give their children this extra time and remember… praxis makes perfect! It would be similar for those with dyslexia as we utilize areas of the brain that process all learnt material (instruction) our processing speed is known to be much slower, hence the required prolonged lessons and practice.
How does this impact on our child’s confidence and low self-esteem?
How do we go about assessing this lack of belief?
How do we address this area and encourage self-belief?
How can we make them feel good about themselves without feeling patronised?

Gross and Fine Motor Skills, Motor Planning and Organisation of Movement.
For a start we need to give due importance to the area of gross/fine/motor/organisation by taking time to work on these areas. This is a real issue and affects self confidence in most of our daily lives as a dyspraxic and also for those with SPD and hyper mobility.
DCD can confuse many, from Ed Psych’s, friends, teachers and even close family members, all can appear fine for the short time we are in others company and this can be a problem in itself.   Quite often we seem just like those without DCD when we are sitting or are relatively stationary… however, the very second we  have to carry out a task we fall apart… for example, walking with a cup and we drop it, or walk into someone.
We are all aware that DCD (dyspraxia) is a motor, planning and co-ordination disorder.
The disorder can range from mild to severe.  It runs in families and can be co-morbid, which often means many will have elements of hyper mobility, dyslexia, dysgraphia (writing/comprehension), dyscalculia (maths) sensory processing, social communications disorder (DSM5).  Most will have poor memory and memory recall.  Others may present with mild dyspraxia and no other traits.
Presentation of DCD is so variable in its spectrum and has a very wide range of limitation/delay in co-ordination, planning and motor skill.  It can range from very moderate to severe… some would be good at sport and others would struggle, the same would be the case for academia.
The child could be fine in the early stages with limited concern shown by the parent, especially if they happen to be the first born so there is no benchmark set and familiar milestones hit by an older sibling, ie. walking, talking, eating, kicking and catching a ball.
We can also see problems with speech and language... quite often we witness a delay in speech which can so often slow the introduction to reading/spelling and indeed writing, into the early years of school.
Dyspraxia (DCD) affects around 1 in 8 school-age children and likewise adults, around the world.  There is a variation to this, so I am going with an average figure.  We also know that it affects far more boys than girls… statistics show around 80% are boys, although in my personal opinion, I feel the gap may well be closer in reality.  The reason I feel this to be the case is that boys tend to show frustration and meltdown whereas girls tend to internalise and just get on with it, which can result in more boys being diagnosed. 
So what do we do to keep confidence and self-belief high?
Firstly I want to say don’t give praise where it is not due… it must be genuine.
Take everything that has to be learnt very slowly and then praise, praise, praise!
During the early days put them in a baby walker, as this helps develop leg movement (gross motor skill).
Spend time helping them to crawl and walk by letting them mimic you.
When they start to feed themselves encourage this but give them easy things to eat (nice bright carrot stick)… pieces of apple will help with fine motor skill… feed them every other piece to reduce frustration.
Make lots of funny faces to encourage smiling and always use a cup and then a straw to drink through, as this will help facial muscle tone and early speech.
Try and get them to improve core muscles by getting them on their tummies and looking up… this will strengthen their back and shoulders.  This will also help posture when they start sitting more frequently.
When they are ready to play, roll a ball to them… this will help eye hand co-ordination.
All of the former is important. Make sure you check out their dominant side too… how do they move? Is it left hand or right first (crawling)? Which leg leads, if already walking? It is so important to figure out their dominant side to make writing etc. easier later on… many pick up the pencil in both hands and often use their non-dominant side to write with (less control)!
We also find placing things in order or stacking difficult, due to the planning/processing side of the condition.
With the singular focus that we have as a result of being dyspraxic, we struggle with multi co-ordination on a variety of fronts, like climbing stairs, running, hopping, and jumping, co-ordinating limbs to dress (shirts, trousers, socks, etc.)
We can also have difficulty chewing solid food, due to hyper-sensitive gag reflex (tough meat and fibrous fruit like pears and fish too) and sensory processing problems.
There is a high incidence of ambidexterity in dyxpraxics and this could be down to planning/processing at an early stage (dyspraxic children often pick the pen up with the nearest hand and proceed to write or draw… this could then become ingrained). This often leads to indifferent writing techniques and poor writing skill.  Let your child know you make mistakes also...none of us are perfect, laugh at your mistakes by all means bur don't laugh at theirs.
This all leads to problems performing daily activities and many of our personal routines like getting dressed.
Due to required repetition, a far greater time is required to master new skills and skill sets (tying shoelaces, fastening buttons, zips, etc).
Tripping and falling due to lack of concentration and poor balance, even standing still and the occasional wobble, can all make us look very clumsy.
We tend to have a far slower rate of maturity due to most of the above and this can lead to voluntary and involuntary isolation.  If we are on our own we feel less pressured to perform and no one witnesses our mistakes.  However I must express this is not a good thing. As a result, we tend to hand around or play with children much younger than us.
I have written many articles on anger and frustration and this all goes alongside dyspraxia. It’s no surprise we beat ourselves up over the slightest mistake and also as a result of being constantly pulled up and criticised by our peers/family members.
We have a very singular focus and this in turn causes poor concentration and listening skills… we also find it hard to follow verbal and written instruction, it is much easier to watch and learn or follow pictograms.
In adulthood this can often be the case with D.I.Y… we would prefer to follow the picture on the box than read the instructions inside (right brained).
It can cause problems with learning to drive (see article on Learning to Drive with Specific Learning Needs by Toby Lee).
Anger and frustration.
If you suspect any of the symptoms of dyspraxia, I would recommend you seeing an OT or Ed. Psych.  II would stress it is important to get a good assessor, as one that doesn’t know dyspraxia could miss some of the signs or might not apply the correct conditions to show that your child has dyspraxia.
You could also find during the assessment your child might have dyslexia/dysgraphia or dyscalculia…these are co-morbid conditions that can also shadow dyspraxia…ADD…ADHD and ASD.
It is so important to be prepared before you see anyone for a diagnosis… observe your child and draw up a list of issues, make a note of milestones like walking/talking, etc.
 Motor problems of children with DCD persist at least into adolescence, although it weakens as we come to terms with routine and we no longer need to be competitive, like running around the school yard or taking part in sport. 

All our articles are written to give guidance only and we would suggest that all of our readers seek the required professional guidance Check out our new look website at www.dublin-cetc.com