Being blessed with “the gift” of a
moderate form of dyspraxia has meant and still means having to
navigate the challenge of social engagement and getting my use of
language on-point. When I was younger I used to be quite shy when in
a group scenario, especially at school because I was afraid of saying
the wrong thing or using incorrect grammar. I have been known to swap
words around in a sentence and adding fillers into my speech when not
really necessary, usually to allow my brain some time to bring a
conversation back on topic. Using the same adjective or adverb
several times during the course of a conversation is a defence or
coping mechanism for me- a way of indicating I have understood what
has been said by an interlocutor or a way of eliciting a response
without being too overt about it. “Absolutely” seems to be one of
my favourite go-to adverbs to demonstrate my understanding of a topic
or agreement with a statement. When used alongside a low pitch/tone
of voice and affirmative facial expressions and eye-contact it can be
way of sounding confident even when you may not feel confident
inside.
My level of self-confidence, as I've
blogged about countless times has been up and down. It can be
affected by negative conversations and being put into uncomfortable
or unfamiliar situations: for example, if I'm talking to a group of
young people about a topic I have knowledge of and passion for- like
raising awareness of dyspraxia, I tend to feel less tense, less needy
of crutch words and behaviours and more able to structure sentences
to get my point across. However, when I am speaking to a group of
high-powered professionals, who may not have much understanding of
neurodiverse conditions or may have expectations of listening to a
flawless presentation (or at least how I perceive flawless to be, as
no presentation ever happens without incident), I have been known to
get tongue-tied, avoid eye-contact and nervous for the questions that
follow.
Young people with dyspraxia, otherwise
known as Developmental Coordination Disorder or DCD for short
regularly experience dips in self-confidence as a result of engaging
in presentation delivery. Pratt and Hill (2011) conducted research
with young people with DCD and found that they “experience high
levels of ‘panic anxiety’ when faced by a task that they have
previously found challenging (Pratt and Hill 2011), leading to
avoidance behaviour”
(https://dyspraxiafoundation.org.uk/wp-content/uploads/2017/02/Dyspraxia-Mental-Health-Consultation-March-2016.pdf).
I found speaking about scientific subjects much more difficult than
talking about poetry, prose or plays in the first years of secondary
school so I would try and avoid taking part in class discussions in
Science, Technology, ICT, Maths and Graphic Design by taking notes
and avoiding eye-contact with the teacher. When I was asked to
deliver a presentation I would use the PowerPoint presentation I
created as a prop to keep my speech on track but I'd often digress
onto different subjects, which must have been quite frustrating for
some of my peers! Thanks to working with my English, Drama and Modern
Foreign Language teachers I managed to build my self-confidence to
the point where I could speak without being prompted but the
digression element really hasn't gone away! The extra effort required
to get to that point was draining and I never would have managed it
without tailored support and my parents and friends willing me on.
This feeling of being overwhelmed seems to be quite common amongst
children and young people with DCD: Missiuna, Moll et al (2007) found
that parents of children with DCD have reported that their children
have felt overwhelmed “because of the expectations and work
required of them and ‘mask’ their problems by putting in extra
effort so that that their difficulties weren’t noticed”
(https://dyspraxiafoundation.org.uk/wp-content/uploads/2017/02/Dyspraxia-Mental-Health-Consultation-March-2016.pdf).
Anxiety has been a mental health concern that has dominated much of my life. I get anxious over the most silliest of things – if I forget a pen to make notes at a meeting I'm worried about forgetting everything at that meeting and if I don't note nearly everything down I think I'm going to forget what was said or misinterpret it and upset someone. I'm perpetually worried about missing buses and trains and tripping up on the steps or getting stuck in the door. Fear of getting the wrong bus or train or missing the last train or bus has meant I am more reluctant to attend events outside Lincoln alone.
I've thought so many times that I'm
blocking everyone's way by standing awkwardly or sitting in the wrong
place and when I do get something wrong I can focus my attention on
reflecting on that action for far longer than is necessary. I don't
want to feel like a burden but when you've felt like you are being a
burden to others you care about for so long, it's difficult to shake
that feeling off. It makes you feel like shit and it's in those
moments you need to have friends and family around to talk to.
I experienced social isolation
throughout my teenage years and young adulthood, partly as a result
of not having been pro-active and going out to clubs, taking part in
leisure activities and joining societies, partly as a result of
socio-economic circumstances and the stigma associated with that (I
think Universal Credit advisors need to continue to promote
volunteering, participation in job clubs and taking part in free
events in the local area to challenge that sense of
self-stigmatisation) and partly as a result of fearing what
circumstances I could have found myself in. I have been fortunate to
meet some amazing, non-judgmental folks over the past few years but
it's been a hard journey. Young dyspraxic people living in rural
Lincolnshire must have found and continue to find it tougher to
engage in social activities due to public transport issues and/or
socially conservative attitudes of their parents, guardians and
carers and I do worry about overall levels of youth social isolation
and loneliness. Social media plays it part in keeping young people
connected and there are YouTube videos and stars that young people
can turn to for advice and guidance for when they do feel lonely but
I've met young people who still feel incredibly lonely. One young guy
I met who is dyspraxic felt that he couldn't meet up and play
football with his schoolmates because he didn't want to be judged for
not being able to catch the ball (he said he often finds himself put
in the goalie position at school so that he doesn't “wander all
over the place” or “slow the game down”). Teachers, pastoral
care staff, professionals with knowledge of neurodiverse conditions
and parents, guardians and carers all have a role to play in reducing
social isolation and improving inclusion of neurodiverse young people
in sports and creative activities. This includes teaching young
people about neurodiversity in Science and in PSHE lessons. The
Dyspraxia Foundation undertook a Youth Mental Health Consultation
back in 2016 and the report found that young people with dyspraxia
often felt that lack of understanding about dyspraxia “added to
their sense of feeling different”
(https://dyspraxiafoundation.org.uk/wp-content/uploads/2017/02/Dyspraxia-Mental-Health-Consultation-March-2016.pdf).
If young people understand to some extent what their peers with
dyspraxia are going through, the anxiety they face and the extra
effort they put in to participate, they may adapt slightly the sports
and creative activities they engage in (e.g. slowing down the
football game slightly or reminding their friend to bring pen and
pencil grips for drawing) so they can be inclusive.
When I was growing up I never knew
anyone who had been diagnosed with dyspraxia as early as me (I was
diagnosed initially aged 6 following consultation with educational
psychologists and following an referral by my primary school
psychologist). Nobody openly discussed having dyspraxia and I never
read about anyone who was dyspraxic or saw anyone on TV or in films
who said they were dyspraxic. It was almost like it was a condition
you had to avoid talking about for fear of being singled out. I
really hope that will change in the future, with more fictional book,
TV and film characters being created who happen to be neurodiverse
and with more documentaries being produced on neurodiverse conditions
and I'd be more than happy to give advice on this (wink wink, nudge
nudge shameless plug).
Even when I was at mainstream secondary
school and no longer needed a SENCO or Occupational Therapist to
support me on a daily basis I felt different. At times during Year 7
and 8 I felt like I didn't belong in the school at all; that somehow
my acceptance had been a fluke and that I consistently and
consciously had to show grateful thanks to the teachers for allowing
me to have a space and pretty much take on board what they said as
gospel truth. I remember my Mum telling me that my Year 7 RE teacher
said that my chances of getting a Grade C in English and Maths at
GCSE (Grade 4/5 nowadays) was pretty much non-existent let alone
getting one in RE and yet through sheer hard graft and hours and
hours of studying after-school I ended proving him wrong, getting my
A* in English Lit and RE and going on to study both alongside English
Language, French, German and General Studies at A-Level and then
studying English and Philosophy at the University of York. Believe
me, with tailored support and the determination to succeed, you can
achieve. I still think of Mr Year 7 RE teacher with a wry smile and
utter a “you were wrong” under my breath. I really try not to
gloat or revel in other people's mistaken beliefs but sometimes I
just can't help it. We're only human after all.
As the years went on I began to
realise that what made me different was far more than my dyspraxia
and my gender and actually that it was OK to be seen as different, as
unique. The anxiety was still there, I was still pretty much socially
isolated outside the school grounds and yet there was a rebellious
sense of freedom I could latch onto. These days I am much more attune
to and revel in my rebelliousness because it's a refusal to conform
to gender expectations and semantic structure expectations. I wear
what I want within the confines of the law and I accept that I won't
be the Jacob Rees-Mogg type of rhetorical speaker (Thank God!) I can
own my own truth, try and phrase things in the way I know how and
happily invite others on the journey with me. Being a confident
communicator means embracing semantic and grammatical differences. If
someone uses “and” to start a segment of lecture once in a
while....it may not be seen as “Standard” English but so what!
Being a confident listener means embracing the challenge of
understanding different modes of speech delivery; if a young person
uses “Absolutely” 10 times during the conversation because they
may happen to be nervous about meeting you for the first time...No
Big Deal! Listen to the overall content of the conversation and
appreciate how much effort that young person may have made to come
and talk to you in the first place.
I hope that more young people with
dyspraxia will receive the support they need, especially with regards
to reducing levels of anxiety and social isolation. It starts with
professionals being open to finding out more about neurodiverse
conditions.
There are several ways of finding out
this information :
- Accessing websites run by specialist organisations containing information and advice on supporting young people with dyspraxia- e.g. Dyspraxia Foundation - http://www.dyspraxiafoundation.org.uk/
- Reading textbooks and guides published by experts working with neurodiverse young people-
- Understanding Dyspraxia – A Guide for Parents and Teachers by Maureen Boon (https://www.jkp.com/uk/understanding-dyspraxia-2.html)
- Caged in Chaos by Victoria Biggs about her life as a dyspraxic teenager (https://dyspraxiafoundation.org.uk/shopping/product/books/caged-in-chaos-a-dyspraxia-guide-to-breaking-free/)
- Can't Play Won't Play by Sharow Drew and Elizabeth Atter which contains a number of strategies to encourage children with dyspraxia to engage in physical activities through socialising
- Discover Yourself by Gillian Dixon – a book aimed at primary school students to help them understand more about dyspraxia
- Booking training on dyspraxia and other neurodiverse conditions delivered by qualified and experienced professionals
- Dyspraxia Foundation may have funded training sessions available or they can be approached to deliver training sessions in schools/colleges/universities/workplaces
- Dyspraxia UK has training sessions for teachers and teaching assistants and occupational therapists (https://www.dyspraxiauk.com/generalinformation.php)
- Booking professionals onto online CPD training courses
- AC Education has an online course in Understanding Dyslexia and Dyspraxia (https://www.ac-education.co.uk/online-course/understanding-dyslexia-dyspraxia/)
- Communicate-ed, a specialist education training organisation offers an online course specifically on supporting students with dyspraxia (https://www.communicate-ed.org.uk/courses/supporting-students-with-dyspraxia).
Young people with dyspraxia can be some
of the wittiest, academically bright young people around. By
understanding some of the challenges they face, like dealing with
unfamiliar social situations, professionals can offer the right
amount of support for those young people to cope whilst empowering
them to pursue their aspirational goals. To young people reading my
blog, I say this: you can and will achieve great things. Reach out
when you think you need additional support. Never give up and
remember it's OK not to be OK sometimes. You know what's best for
you.