Developmental coordination disorder and dyspraxia

What is DCD?

Developmental coordination disorder (DCD) is the term used to describe a range of difficulties 6-8% of children experience with posture, movement and coordination, without there being a specific medical reason for these difficulties. These difficulties are severe enough to adversely affect their everyday function and school activities.

There are a number of other terms or labels used for the difficulties experienced by children including low muscle tone, minimal neurological disorder, and clumsy child syndrome.  The trouble with each of these labels is that make an assumption about the cause of the difficulties the child has - whereas the underlying cause is not known.

What is dyspraxia? 

The term dyspraxia is sometimes used as an alternative term for DCD.  
There are no formal criteria for a diagnosis of dyspraxia.  This makes it very confusing: different people use the term dyspraxia in different ways.  

It is also the reason why a diagnosis of dyspraxia is not recognised by many pediatricians and school authorities. 

The information provided by the dyspraxia support group websites tend to list a range d by a child who has been diagnosed as having dyspraxia, including poor emotion regulation, attention, short-term and working memory and other cognitive difficulties.

Including all these different developmental difficulties into one diagnosis has its drawbacks because it prevents clear thinking about the different factors contributing the everyday difficulties the child is experiencing. 
5y 3m outdoor walking.jpg

What causes DCD? 

DCD is not really a single disorder with a known cause, a typical developmental pathway or known outcome.
it is now generally accepted that children with DCD have atypical brain development that affects the way they learn new skills. They appear to have difficulties forming internal representations (also called internal models) that  form the basis learning, planning and coordination of motor skills.  
In addition children with a diagnosis of DCD often have difficulties related to self-regulation, anxiety, attention and working memory which impact on their learning of new skills.
Together this means that in order to help a child with DCD it is necessary to understand all the factors that contribute to poor motor performance so that a suitable plan of action can be implemented to help the child. 
4y carrying bucket.jpg
Why a DCD child has
poor motor control 
DCD and anxiety 
Helping a child with DCD New DCD and hypermobility
 DCD and attention difficulties DCD and low muscle tone 
A whole gamut of co-occuring difficulties   

Why a child with DCD has poor coordination 

DCD is a specific motor learning developmental disorder

It is now generally accepted that children with DCD do not create internal representations of the subroutines involved in performing everyday actions in the same way as typically developing children do. 

Internal representations are the blue prints within the brain that link information from the body sensors (muscles, joints, eyes) with the motor commands for activating muscle contraction at the right time, in the right order with the right amount of force for an action. 

Children with DCD do not make effective use of everyday experience for building a large bank of internal representations to guide and plan movements. They often require additional guided practice to learn new skills in order to develop the internal representations / models that will form the basis for future performance of the skill.   

The many representations needed for an everyday task

Take for example picking up a plastic beaker of water to take a drink. This looks like a fairly simple task - reach, grasp and lift.

But think about it carefully.  The amount of pressure you apply to the beaker and the speed that you lift it all depend on making judgments about how flexible/soft the beaker is and how full it is. 

If the beaker is made of thin plastic, it is important not to grip the sides too hard. If it is full you need to lift it more carefully so as not to spill the water, and you also need to adjust your grip so that it does not slip out of your hand. 

Each of these aspects of pick-up-and-drink-from-a-beaker action is controlled by an internal representation.

Cutting out a circle with a pair of scissors

Many children with DCD / dyspraxia have difficulties cutting out a circle with a pair of scissors. 

The pictures below show how one child's skill at this task improves over time. In the first frame she is 4 years old and having difficulties positioning and holding the paper. One year she cuts out a circle with confidence - mostly because she has learned to to hold the paper closer to the line of cutting. 

Two things have happened in the intervening year and many hours of cutting experience. The first is that with age and experience her ability to plan her actions so that the two hands work together to cut along the line.

The second is that at 5 years she expects to produce a good end product. She now pays attention to outcome and uses her mistakes to improve her accuracy each time she cuts out a circle. 

Read more: Cutting with scissors: refining control through experience


R 3y 9m scissor cutting 24.jpg R 5y 3m  cutting circle 3.jpg

Helping a child with DCD

Research has shown that providing a child with additional guided practice improves performance of everyday and school related tasks. In other words, individualised coaching in the learning of new tasks pays off. 

Parents play a vital role in such coaching. Some coaching will require setting aside specific time for practice. But in many instances it can and should form part of a family's everyday activities.

Once you understand the requirements for a task and why a child has difficulty performing a task, building help into your interactions with your child pays off in terms of your child's ability to be independent, self-confidence and ability to participate with peers in the playground. 

More about understanding and coaching motor skills

How Nick practises walking through the house without bumping into things - an example of parent coaching

Children with DCD and dyspraxia often have hypermobile joints and associated muscle weakness

About 20% of people have joints that are more mobile than usual. This is because the capsule and ligaments that hold the joint together are more pliable (they can be more easily stretched) than usual. The muscles are also more pliable and more easily stretched than usual. The body parts are only loosely held together which means that the muscles have to work harder to hold the body steady and move it against the ever present downward pull of gravity. 

Joint hypermobility affects the way a child learns to move and often results in the child developing inefficient pattens of movement and posture. Although the child's joints and muscles are very flexible, some muscles such as the hamstrings and iliotibial band may be very tight and this affects sitting posture and also hampers the child's performance of agility and balance tasks.

Children with joint hypermobility also often have poor endurance.

The muscle weakness and tightness and the poor endurance can be substantially improved by a programme of exercises tailored to meet the child's specific needs and abilities.

Children with DCD and dyspraxia also often have a diagnosis of “low muscle tone”

Children are said to have low muscle tone when they have poor posture and difficulty sitting erect and keeping the trunk steady when moving the arms.

In most cases the cause of these difficulties is muscle weakness and poor endurance usually associated with joint hypermobility.

It is important to recognise the muscle weakness as this can improved by a programme of exercises to strengthen weak muscles, improve endurance and train more effective postural control.  

Read more about low muscle tone

roan 5y eagg and spoon.jpg 4y transferring soil into a bucket.jpg

DCD often co-occurs with other developmental disorders 

Children with DCD frequently have co-occurring developmental difficulties which impact on the child's everyday function and capacity for learning. 

Recognizing each specific area of difficulty  and how it impacts on learning of movement skills, attention and behaviour in general is very important.  It makes it easier to understand the child's behaviour and also allows parents and teachers to address each area of concern in an appropriate way. 

Co-occurring difficulties include:

  • Attention difficulties: these may be related to anxiety and poor emotional self-regulation. 
  • Poor emotion self–regulation: which is often related to having an anxious nature 
  • Poor working memory which makes it difficult for the child to remember instructions and keep a goal in mind.
  • A very cautious nature which is associated anxiety and hypersensitivity to sensory stimuli, and often allergies and asthma 
  • Joint hypermobility and associated weakness with associated muscle weakness "low muscle tone" and poor levels of fitness
For more on related difficulties see CanChild: DCD Related Disorders

Movement difficulties a child with DCD may experience  

Usually a child is given a diagnosis of DCD because he or she is having difficulties with the control, organization and planning of posture and movements.

However, these children often have associated difficulties with the attention and thinking skills needed for organizing themselves, staying on task, persisting with a task, and remembering and learning a new task. .  

Together these difficulties impact on the child's ability to complete everyday tasks and learn new skills, such as:

  • Balance and agility activities - such as hopping, skipping, climbing on the jungle gym
  • Ball skills - catching, throwing and kicking
  • Getting dressed - particularly buttons and laces
  • Sitting still and upright at a table
  • Eating with a knife and fork
  • Building with construction toys
  • Handwriting is slow and untidy, the child complains of discomfort in the shoulder and hand and dislikes writing, complains that it is boring
  • Slow to learn to ride a bicycle
  • Slow to learn to swim
  • Games and PE at school - tires quickly, cannot keep up with the other children

What is the cause of DCD?

In many cases the reason why a child develops DCD is not known.  The cause may lie in atypical development of the brain. 

The effective control of all our actions and thoughts depends on the different areas of the brain working together in a coordinated fashion.  In the young baby the connections between the different parts of the brain are present, but not well developed. Over time, as the child’s brain grows and develops these connections become much more clearly defined and specific, and as a result child becomes able to perform more complex tasks which involve doing more than one thing at a time.

The richness and complexity of these connections is influenced by the particular way in which the individual child’s brain develops and the way in which the child engages and interacts with the social and physical environment. Our brains are shaped by the variety and range of our experience.  

Some researchers believe that children with DCD do not create these links between the different brain areas in the same way as typically developing children – everyday experience is not enough, they seem to require additional help.   

There may also be a genetic connection. DCD sometimes runs in families  – there is often  a parent, an aunt or uncle in the family who had difficulties with balance, coordination and motor planning as a child.

Some children born very early also have movement difficulties as a result differences in brain development caused by the pre-mature birth. 

Children on the autistic spectrum sometimes have poorly developed motor skills – possibly also related to atypical brain development.

A child who has hypermobile joints with related muscle weakness (sometimes called low muscle tone) often has difficulty acquiring movement skills in the usual way.

Temperament also plays a role in the development of movement-based skills. A child with a very cautious temperament may avoid activities that are new and appear difficult and require that require mental and physical effort. This affects their ability to learn new skills in the usual easy way. 

Can DCD be cured? 

Children with DCD can learn to perform most everyday tasks given the right opportunities and support.  It just takes more practice and learning to pay attention in a special way to compensate for the way in which their brains learn new skills. 

But even when a child with DCD has learned to perform a task quite well, it might take more effort than usual and require added attention and more time. This needs to be remembered particularly in school tasks where time demands can have a very negative impact on a child's ability. 

Some skills that require a great deal of co-ordination make remain a problem - but then these need not be part of the child's life. Team sports and learning to ride a bicycle on rough terrain are examples of activities that can be avoided. 

Handwriting is the one school activity that can cause long term issues, and the child may need access to a keyboard for school work.  

General fitness can be improved and can make a big difference to how the child perceives his or her abilities. Being able to keep up with the other children in the playground is important and running fitness and coordination can usually be improved with a bit of effort. 

Therapy for children with DCD

Children with DCD are often referred for physiotherapy and / or an occupational therapy.  Although there is a lot of overlap between these therapies, each profession tends to focus on certain aspects of the child’s function. 

Physiotherapists tend to focus on posture and gross motor skills as well as strength, flexibility, agility, endurance. 

Occupational therapists usually pay more attention to fine motor control, hand function, handwriting, perception and daily activities.

However, depending on the therapist's interests, skills and training a therapist may cross these boundaries.

Common intervention approaches include:

CO-OP is a cognitive based approach which has been well researched. The Canchild website has more information on Co-op as well as some good information on DCD

Sensory Integration Therapy (SIT) is an the approach commonly used by occupational therapists. The assumption in SIT is that the problems experienced by children with DCD/Dyspraxia are due to an underlying disorder of the ability to process sensory information.

Neuromotor task training, an approach developed and used in the Netherlands has provided some evidence for its effectiveness.




for the most 
up to date, evidence based information on DCD


Developmental Gym Approach 

The Developmental Gym approach assumes that there are many different factors that impact on the learning and performance op movement tasks - and that all these factors need to be considered when planning physiotherapy intervention for children with movement difficulties.

It differs from other programs in that it does not view a child's thinking, emotional and movement skills as separate entities - but approaches the child as a complex being with a range of needs and functioning in a family environment.

It also differs from cognitive approaches, such as CO-OP in that physical factors such as strength, endurance and flexibility that may be limiting a child's are addressed at the same time as addressing cognitive, emotional, attention and movement planning issues that are hampering a child's movement performance.

It differs from traditional physiotherapy approaches in that the physical factors limiting task performance are not addressed in isolation from the emotional and thinking aspects of movement performance.

Children with DCD often need encouragement to engage in the effortful physical activity needed to be fit for the classroom and playground and able to keep up with their peers.  

The Fit for Action Webspace provides parents with a range of ideas for improving a child's strength, endurance and flexibility, based on the Developmental Gym approach. 




HI MY SON IS 2yrs old and has coordination disorder ....very hard FOR HIM TO DO THINGS..HE JUST GIT
DENIED Ssi ..I try ed every doctor out there for my son still no new no body knows what really
Wrong with my son

Encourage your toddler to be active


I am sad to hear that you do not have access to a good child development service which can give you the information you need about your son's developmental delay. 

Perhaps you can locate a physiotherapist or occupational therapist who specializes in children to do an assessment and perhaps refer you to a specialist pediatrics clinic. 

In the meantime, your son will benefit from being encouraged to be as active as possible - start with the things he can do and then see if you can get him to do a little more. If he can walk, encourage him to walk in different places, on soft surfaces, in sand, in puddles, on rough surface, in the garden or park.  If he can only sit - well then let him sit on the floor and play with him there so that he has to reach and turn and move across the floor to reach you or the "toys" that you can find in your home - plastic cups and bowls, cardboard boxes,  plastic bottles etc etc.  toddlers like to make towers, unpack, pack up, throw, knock over, push and pull things. The trick is to find out what your child likes doing and then spend time playing with him.





Tremor in right hand

Hi I work with a grade two boy with a slight tremor in his right hand. His handwriting is acceptable when writing short paragraphs but the tremor is more visible and his writing speed much slower when writing longer one and two page stories. Do you have specific advice or exercises that may be beneficial? Many thanks.

tremor in right hand

Hello and thank you for your question. 

There may be a number of reasons why a child has a tremor but the most common one is an essential  tremor. This runs in families and can effect one or many parts of the body. I hope the child has been seen by a paediatric neurologist to establish the underlying cause. It is important that everyone - the child. family,  teacher and occupational therapist all understand that the child cannot control the tremor. 

If it is a familial tremor there is nothing much you can do about the tremor itself. it tends to get worse when the child is tired or stressed. It  may be useful to start thinking about the use of a keyboard and a referral to an occupational therapist is useful to assess this, 

 Children with a tremor tend to use more force on the pencil to control their movements - and this is one of the reasons they get tired and the quality of the writing gets poorer. 

 It helps to ensure that the child is using an effective pencil grip that allows for finger action to move the pencil tip. This will provide the best starting point for helping the child use the fingers as effectively as possible even when applying additional pressure,  But remember that an effective grip is not always a perfect dynamic tripod grip!




Sorry moderators, I forgot one IMPORTANT question in my last post that I submitted, so please would you ignore my previous post, and post this amended version - thank you and sorry for any inconvenience caused.

My son is 13 and has had difficulties all of his life. He has diagnosed ADHD, over-sensitive hearing, hypermobile joints, significant difficulties in processing and modulating all senses (auditory, visual, vestibular ..... ) and the emotional responses to these, fine motor skill difficulties. He has an upcoming appointment for an Aspergers assessment (grandparent has diagnosed Aspergers). School said he has fine motor skill difficulties and shows OCD tendencies. Primary school said he showed autistic tendencies (but I do not have that in writing unfortunately).
He has shown all of these difficulties all of his life.
I started to try to get help for him. Then his dad got involved in a lengthy court case over custody. He said I was "labelling" my child and used this against me in court, so I had to back off getting help for my child as it was EXTREMELY frowned upon in court.
10 years on my son is in secondary and having ENORMOUS difficulties.
School have not even written down all of his medical difficulties, so teachers are unaware.
He is an intelligent person, but is not reaching his full potential and is getting EXTREMELY frustrated and his attitude has changed to school - now he has a "can't be bothered attitude". He has been moved down groups and now is not challenged enough and is bored, and his marks in the groups he has been lowered down to are now getting even worse.
Went to doctors for referral for dyspraxia. She sent us to an OT service that only cater for up to 11 years old (even though I told her that before she sent us there!, as I had done some research).
Assessment went ahead, and OT did NOT do FULL assessment, and has NOT even written in all of the information that both my son and me provided to her.
Result is her report (which school are waiting for), is NOT an accurate reflection of my son. There are numerous errors in it and important stuff has been left out. It is also badly phrased and open to interpretation.
I contacted OT, had a meeting to explain things: I provided a printed copy of what report should contain (based on what did actually happen at assessment). OT (who says one thing and does another) said she would talk to her manager and get back to me.
She also stated "me and my team have worked hard to make reports short so that we can see more children".
5 weeks later !!! she got back to me and said "I've spoken to my manager and she said my report is ok". I have changed some things.
Picked up report ... its the same! (apart from one part about him having difficulty "opening" taps).
Also found out OT "went behind my back" so to speak and sent doctor a letter summarising our meeting when I had asked her to change things, and stated to doctor that I had bought all new evidence along.

Situation is this: report is NOT accurate. Son still needs help. He has a GCSE in June this year, as his school do their first GCSE English paper in Year 9. School are NOT helping. They say he should use an Alphasmart, but he FORGETS to ask for one because he is forgetful. I've asked SENCO to reserve one for him and she says "I can't there's not enough to go around and also people with sprained wrists need them". This has been going on for a long while. I have now managed to BORROW an OLDER version of an alphasmart from outside school.

I have asked the SENCO for my son's IEPs (as he is on School Action Plus) and was told "we don't do IEPs in secondary school". Another time the SENCO said to me "We have no legal obligation to do IEPs". I feel so in the dark about my son's special educational needs - the school are NOT helping even though they get a budget and also get a pupil premium. NO support WHATSOEVER has been provided or is provided for my son for the past 2 and a half years.

I have been writing about some the problems my son has been having in his Homework Diary and the SENCO saw the notes, and photocopied them all. Next day I got a phone call from the Head of Year saying "you obviously have a lot on your chest, you need to come in and discuss things". I asked who with. He said "with the Deputy Head and myself". I said "I'd like the Head there". He said "I'll go back and tell the Deputy that you are not willing to come in and have an appointment then". I said (which is totally out of character because I am normally really timid) "I did not say that, I said I would like the Head there". He said "you'll have to wait a lot longer to see her, she is really busy" (trying to put me off I believe). I said "OK".

I feel I need to explain that the Head of Year and Deputy Head cover things up and sweep things under the carpet (I have experience of it already, and they have already found my son guilty of something that I CATEGORICALLY know that he would not have done).

Since the Head of Year rang I have tried to contact other teachers, and now NO teachers are ringing me back. Effectively they have gone into lock-down so to speak ... another tactic of the school, which I have previous experience of.

When my son sat for the entrance exam to get in the school, the primary SENCO asked for extra time and a separate room for him due to his medical difficulties. These were granted.

Now my son is in secondary, he is NOT getting any of these reasonable adjustments. Yet, he sees others getting them (including another boy who was in the separate room with him when they both did the entrance exam). He knows the boy and the boy has ONE of the difficulties that my son has.

This is all such a mess and we really need help. I just don't know what to do.

These are my 3 questions:

Question 1:
How do I get this INCORRECT OT report amended, as I cannot pass it on to school (who are waiting for it because they know of its existence because the OT phoned them) nor can I pass it on to anyone regarding any future assessments.

Question 2:
Who is the BEST person to do a FULL assessment for my son re dyspraxia, bearing in mind my son is 13 (nearly 14). We are in Hertfordshire, and have been told they do not assess in this area between the ages of 11 to 18.
PALs advised us getting referred to Gt Ormond St Hospital. Can I ask the doctor to arrange that?
My son DOES need a FULL assessment done - I KNOW he shows numerous symptoms of dyspraxia. School are NOT listening.

Question 3:
What do I do about the school? How do I get the help that my son needs? Bearing in mind my child is already in Year 9 and is doing a GCSE in 4 months time! (He needs extra time and needs a separate room)
Parent Partnership have been suggested, but I understand that they do NOT speak up on your behalf. Unfortunately I need someone who will because I am rather timid (I have my own difficulties too), and also I am not clued up enough about Education Law and entitlements re Special Educational Needs.

Please help because this is having HUGELY detrimental effects on my son's ability to learn, his self-esteem and our family life to the point that I want to take him out of the school that he worked so hard to get in (through academic tests). But I know that this is not a sensible option because he has difficulty making friends and has difficulties dealing with change. Home life is unbearable - it is INCREDIBLY stressful. Homework takes an eternity and causes so much friction.

Please help - thank you :)

I have been where you are

My son has had an horrendous time at high school. I ended up getting him a Statement of Special Needs. The senco used to say we don't do IEP's but as soon as the Local Authority issued a Statement, surprise surprise we had an IEP. Please don't give up and go straight to your Local Authority and ask for a Statutory Assessment to be done on your son. Keep all correspondence from schools, doctors, paediatrician etc and use that as evidence to say that the school aren't listening. My sons school hate us because we proved the SENCO wrong and it has been so hard but keep going. If you need any help/advise contact national autistic society and they will also help. They were absolutely brilliant. Good luck. The stress will be worth it in the end. I had a breakdown from all the stress but I am now going through it all again with my younger son but it has made me a stronger person and more determined than ever that my ASD children will never have to suffer at school again.

Hi My name's Sue and I am mum

Hi My name's Sue and I am mum to H who is 8 who I also believe is dyspraxic and struggles terribly at school, socially, emotionally etc. etc - the reason I am writing is because we are identical to you. First of all a big hug to you - it is tough with a child with all these difficulties - exactly the same as my son and no-one understands this until they are dealing with it. I'm going to share my experience with you in brief, as I can feel your pain - at times it is desperate I know I've been there and go there frequently. As far as schooling is concerned if the school won't support you - you can request a statutory assessment yourself - I did this I was refused initially but then County agreed (we are in the same area as you) and the results were devastating - H is very far behind. I have an 11 page Notice in Lieu presently but I want H statemented - we have a hearing in November. Medically we have all the same issues too - I am on my third paediatrician's opinion - we've now been referred to Great Ormond Street where H will be seen by a paediatrician specialising in neurology. We were referred by our paediatrician but I had to fight for it as I have done to get all of the support I currently now have for him. I don't think the doctor can refer it needs to be a paediatrician but look at GOSH's website under Neurology. H has counselling - he struggles like your son with anxiety, low self esteem etc. and suffers from stomach ache every day. I am happy to share my experience with you - you could be claiming DLA for your son and become his full-time carer - I'm H's carer as a consequence of which I am able to claim Legal Aid for lawyers fees to achieve for him the education he is entitled to.My email address is [email protected] - email me if I can help you I will.

Thank you for provding much needed moral support

Hi Sue

Thank you for responding to Me4ourhealth's post and offering much needed moral support.  It can be very demoralising when one has to fight each step of the way to get support for a child who is being failed by the school system. 

Parents like you pave the way for others. Us professionals also need to listen to mums who say there is something wrong and that something needs to be done about it - because in my experience they are usually right.



Knowing your rights and the rights of your child in school

I am a SENCo in a primary school. I feel very disheartened to hear about the problems you are facing with your child's school. We SENCos are meant to try to alleviate some of the whole family's distress and find ways to overcome barriers to learning for children. Hopefully I can help by providing you with information as to your rights and the school's responsibilities.

Firstly, all schools in the UK must have a SENCo. That SENCo is responsible for coordinating with your son's teachers and finding out how his needs can be met. We do this by assessing the child to see where there academic, physical and social problems lie, then try to set short term, measurable and realistically achievable targets which, with intervention, we can reasonably expect the child to meet. The time scales are important here - good practice is no more than 10 weeks before a current intervention is reviewed to see what, if any, impact this has had on the child's capabilities. If the intervention is working, great, it may continue for a while. If it's not working, we review to see if we can find a different approach to help the child. At his point a child is probably likely to be on School Action. After a couple of terms, if the interventions are not making enough difference, and several different approaches and strategies have been tried (hence a bit of a time delay), we then need to consider putting a child on School Action Plus. At this point, what we are really saying is that staff need the expert opinion of an external agency to come and help us to assess this child, with a view to getting extra help or advice (or training for staff) into school.

Your child's school is legally obliged to ensure this happens. You should know whether the school have requested an external agency to help with your child, as they need you to sign a form to allow them to do this. Your son should have an Intervention Plan - this is a legal requirement for all schools (even secondary) and this must be updated every term. You should be invited into school to discuss this IP with the SENCo and a copy of the IP should be given to you. You have a legal right to this document. Schools also have to provide evidence to the Local Authority about how the pupil premium is spent to benefit each child in receipt of one. Perhaps a phone call to your Local Authority Special Needs advisor would help.

If you are really concerned, you can contact Ofsted about your concerns. I think you can do this via their website.
Finally, I would take the bull by the horns and WRITE to the Head requesting a meeting within two weeks of the date on the letter. In the letter, request that all of your son's IP's are copied and sent to you in advance of the meeting. You could request for the SENCo to be present too. When you attend this meeting, make sure you have a list of questions that you want to be addressed. If they can't answer your questions straight away, write down what you want them to find out and agree a timescale, then request that they sign the paper. Ask if they can get it photocopied so you both have a copy and make it clear that you are now keeping records of all correspondence and conversations, in case the Local Authority request it when you contact them. Tell them that you really want to work with them, for the benefit of your child, but if you don't feel this is happening, then you are your child's voice and you will have to fight for his rights through other official channels, starting with contacting the Inclusion team at your Local Authority.

Hope this helps. Good luck!

getting the school system to work for a child


You certainly seem to be running into all sorts of blocks and frustrations. 

Here are some suggestions that might help you find the assistance you need to negotiate the system.

Join the UK based yahoo group Dyspraxia families This provides great parent-to-parent support online. 

Join a local Dyspraxia Foundation group - again for support and advice.

If you are in the UK, I think that there are special people within the school system whose job is to assist parents with children who have special need. Make enquiries - the Dyspraxia Foundation people should be able to help you with this. 

Best wishes 





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