Are you looking for an event to raise awareness of dyspraxia and sponsorship for the Dyspraxia Foundation? Is our usual British 10k event overwhelming and ...
We are pleased to announce a brand new conference for Friday 3rd March 2017. The new location is the Keepmoat Stadium, home of Doncaster Rovers! An ...
We are very happy to announce the start of the Dyspraxia Foundation Unity Lottery! We've partnered with Unity, the nation's charity lottery, to offer you the ...
Don't delay, join thousands of others and become a member of the Dyspraxia Foundation today!
NEW: Dyspraxia Keyring Card added to our online shop only £2.00 inc p&p. A keyring card with a simple, clear overview of dyspraxia to help others ...
Did you know that whenever you buy anything online - from your weekly shop to your annual holiday - you could be collecting free donations ...
Why not raise money for the Dyspraxia Foundation at absolutely no cost to yourselves or your company by making all your restaurant bookings with ChariTable Bookings. Simply ...
The Dyslexia / SpLD Support Project is funded by the Department for Education and will run until 31st March 2017. It is led by the British Dyslexia ...
We are delighted to have our helpline available to help you with problems and issues you may encounter; offering help and advice to people with dyspraxia, parents, carers and families about or on the subject of dyspraxia. The helpline is available Monday to Friday, 9 am to 5 pm.
Charity launches appeal for urgent funds #dyspraxiaappeal
Due to a declining membership and with current funding coming to an end, we launch an urgent campaign to raise funds to ensure our services continue until we are able to secure long term sustainable funding. We have successfully managed a three-year Big Lottery Fund project providing a helpline service and awareness raising campaigns; supported membership, local groups and research projects whilst reaching almost 40K on our social network pages. The charity is staffed by a few long-term employees and supported by volunteers of parents of children and adults with dyspraxia, health, education, PR and employment experts. Together, we offer help, advice, support and work to raise awareness of this still poorly understood condition.
See full press release below
You can donate here: http://campaign.justgiving.com/charity/dyspraxia/appeal
Or simply donate via Text
Text DYSX16 (space) £5 or 10 to 70070 to donate to Dyspraxia Foundation and make a difference today. JustTextGiving by Vodafone.
Example DYSX16 £5
PRESS RELEASE: DYSPRAXIA FOUNDATION LAUNCHES CAMPAIGN FOR LONG-TERM FUNDING The Dyspraxia Foundation, the UK’s only national charity providing information and support on dyspraxia, has launched a campaign through JustGiving to secure long-term funding.
Dyspraxia, also known as Developmental Coordination Disorder (DCD), is a common condition affecting fine and/or gross motor coordination in children and adults. It can also affect short-term memory, spatial awareness and speech. It affects 5% of the population – that is generally 2 children in every classroom. With the right support and understanding, the challenges associated with dyspraxia can be managed well. However, many people with dyspraxia/DCD struggle to get the recognition and help they need at school and in the workplace. The Dyspraxia Foundation is committed to raising awareness to ensure it is not a barrier to opportunity and fulfilment. More funds are urgently needed to continue offering support to people with dyspraxia/DCD through their helpline service, local groups and research projects.
Eleanor Howes, Dyspraxia Foundation Chief Executive Officer, said:
“Due to a declining membership and with current funding coming to an end, we launch an urgent campaign to raise funds to ensure our services continue until we are able to secure long term sustainable funding. We have successfully managed a three-year Big Lottery Fund project providing a helpline service and awareness raising campaigns; supported membership, local groups and research projects whilst reaching almost 40K on our social network pages. The charity is staffed by a few long-term employees and supported by volunteers of parents of children and adults with dyspraxia, health, education, PR and employment experts. Together, we offer help, advice, support and work to raise awareness of this still poorly understood condition.”
‘The information provided was invaluable to me. Knowing that the issues my son faces daily could be acknowledged and support given that would lessen the impact keeps me fighting the ignorance.’ Helpline Caller
Please help us continue this vital work to support people with dyspraxia and their families by donating today!’
Donations can be made using Justgiving at the following address: http://campaign.justgiving.com/charity/dyspraxia/appeal
Dyspraxia/DCD can occur alongside other neurological conditions such as dyslexia, A.D.H.D and Aspergers Syndrome, or alone.
For more information, please contact: Eleanor Howes, Chief Executive Officer on 01462 455016 or email [email protected]
Send Review Guide – A school-led approach to improving provision for all
The SEND Review Guide, part-funded by the Department for Education and produced by teachers and school leaders, is now available to download for free from LLS-SEN-Review-Guide-v21. The SEND Review Guide was created in partnership with over forty outstanding special and mainstream schools and parents/carers of children with SEND as well as organisations such as Contact a Family, Ofsted, the Council for Disabled Children, the Institute of Education and the Teaching Schools Council. It is powered by the London Leadership Strategy (LLS), a not for profit organisation created by school leaders for school leaders to transform schools and improve outcomes for children.
The Review Guide is based on the Pupil Premium Review and can be used by all schools to audit their own SEND provision. It is, however, most powerful when used as part of a programme of school-to-school support. A direct response to the increasing gap in outcomes between students with SEND and their peers, the Review Guide was created with the purpose of empowering schools to improve their SEND provision. It is made up of a paper-based audit, examples of good practice, guidance on how to carry out a review of SEND provision and self-evaluation templates. The Review Guide is free for schools to use and schools are able to partner with other schools to use the Review Guide with minimal costs.
The aim of the Guide is to ensure that children and young people with SEND are:
- Visible in their school
- Supported in their learning
- Included in decisions about the teaching they receive.
Based on a school-to-school support model and with a focus on improving outcomes for all pupils, the Review Guide will continue to embed a culture of inclusion, collaboration and support within education.
David Bartram, LLS’s Director of SEND and co-author of the Review Guide, said: “There has always been a wealth of expertise in our schools and this Guide draws on some of the best practice in SEND that already exists within the system. Our aim has been to produce a practical framework for schools to self-evaluate their provision and promote purposeful, focused collaboration between schools in the area of SEND.”
Maria Constantinou, Deputy Headteacher at St. Mary’s Primary School in London and SEND Leader, said: “Supporting another school has had an immense impact on me as a practitioner. The coaching dialogue with colleagues has always aimed to be pragmatic, positive and empowering, resulting not only in reflection about other schools’ practice, but also on the nature of SEND practice in my own setting”. To find out more information or request a white label version of the Review Guide, please visit www.thesendreview.com or email [email protected].
Free Teacher Training on Neurodiversity
Dates announced for FREE teacher training on Neurodiversity around the country – see posters below for full details. Please ensure your child’s school is aware of this resource. This is an exciting opportunity for all schools to participate in some free and comprehensive training relating to neuro diversity! To book your places please visit http://www.eventbrite.com/o/a-department-for-education-funded-consortium-10928767586
The Dyspraxia Foundation is thrilled to be involved in a new Department for Education funded project that will help teachers and support staff across the UK to better understand dyslexia and other specific learning difficulties and to help equip them with the tools and knowledge that they need for best practice teaching for those with learning difficulties
With a healthy uptake there is the potential to influence the practice of some 360,000 teachers and support staff in their response to dyspraxia/DCD and other co-occurring conditions. This in turn could positively impact on the experience and outcomes of those with Dyspraxia/DCD in the classroom and throughout life
Please share the news and this flyer with your schools and sign up today…..
Awareness Week Employment Survey
In preparation for Dyspraxia Awareness Week (9th – 15th October) we are carrying out a survey to find out about the employment experiences of people with dyspraxia/developmental coordination disorder (DCD). This information will help us produce a ‘press release’ highlighting the challenges experienced by employees with dyspraxia/DCD, the benefits that people with dyspraxia/DCD bring to the workplace and the strategies that enable people with dyspraxia/DCD to be successful.
The survey will also help us to identify how we can best help our adult members and provide us with evidence that will be useful when we are talking to government and businesses.
We welcome responses from people with dyspraxia/DCD who are employed, volunteering, unemployed, self-employed or retired. Please follow the link below to start the survey which closes on 12th August 2016.
If you are interested in being a Case Study to help us raise awareness of dyspraxia/DCD in the workplace during our Awareness Week campaign, please email [email protected] for a copy of our Case Study form.
Thank you for supporting the Dyspraxia Foundation!
Fundraising for Dyspraxia
Collabro and our very own celebrity patron Jamie Lambert raising funds for dyspraxia in our home town! Support the Dyspraxia Foundation and have a fabulous evening with the most popular Britain’s Got Talent winners and their special guest Catriona Murray in our beautiful St Mary’s Church on Saturday, 30th July!
ONLINE study about quality of life of families of children (5-18 years) diagnosed with Dyspraxia or DCD
A researcher at the University of Texas at Arlington (USA) is conducting an ONLINE study about quality of life of families of children (5-18 years) diagnosed with Dyspraxia or DCD.
To participate, please complete a survey that can be found here (it only takes 10-15 minutes!): https://uta.qualtrics.com/SE/?SID=SV_2nUY763hSyP0Mnz
We are looking for 500 participants and have about 85 so far – if we can get to this number, we might be able to make a case for interventions that involve helping children overcome their difficulties and include quality of life of the whole family, hopefully at a local and international level.
THANK YOU SO MUCH FOR YOUR TIME!
Priscila Caçola ([email protected])
New film raising awareness of dyspraxia/DCD and its impact
Dyspraxia Foundation are pleased to have supported Dragon Fire Films in the making of a new film raising awareness of dyspraxia/DCD and its impact on young people, families & schools. “With the backing of the Dyspraxia Foundation and the help of experts and teachers, Dragon Fire Films looks at what the condition is, how it affects people and what can be done to help. Ideal for teachers and parents this film shows what it can be like: Living with Dyspraxia” http://www.dragonfireschools.co.uk
Dyspraxia Foundation Spring Ball
£18,367.00 raised at the Dyspraxia Foundation Spring Ball on Saturday, 14th May in London! A fantastic amount towards supporting the helpline thanks to the hard work of the organising committee Michele Lee, Eleanor Howes, Jane Trowbridge, Bernie Mohan, Sophie Kayani, Marilyn Owen, Jacquie Hall, Shirley Stevens and Silja Turvill. We certainly could not have raised such a fantastic amount without the generous support of our donors, bidders and guests and the help of our fantastic team of volunteers on the night who made it all run smoothly.
Special thanks to The Royal Garden Hotel for a wonderful venue, excellent service and food, our live band ‘Hot Stuff’ for getting everyone up and dancing, to Stephanie Guidera who not only sang like an angel but took the time to talk about her dyspraxia and the importance of the helpline, to Del Boy and Patsy for being Absolutely Cushtie, to our Auctioneer Martin Pope for whipping up the bids and to National Casinos, Smartpics, Give Smart and all our supporters for contributing to the success of the event. It’s not too late for you to give generously to help save this vital resource! Just go to the link on this page and Donate Now!
Don't delay, become a Dyspraxia Foundation Member today!
The Dyspraxia Foundation membership year runs from 1st April to 31st March each year. Please do become a member and join us as we continue to raise awareness and understanding of Dyspraxia and support those affected by the condition. The Foundation depends entirely on membership subscriptions and donations to survive. Download your Membership form here Membership 2016-17 Standard/Professional members paying by Standing Order receive a £2 discount download the Membership Standing Order Form here. Please complete your details and return the form to us for processing. We look forward to hearing from you. Alternatively , membership can also be purchased from our webshop http://dyspraxiafoundation.org.uk/shopping/shop/search-products/?min_price=1&max_price=49
The application of Reasonable Adjustments for working adults with Dyspraxia and employment tenure outcome
The purpose of this research will be to gather details of Reasonable Adjustments offered to adults with dyspraxia by employers; to ascertain how useful participants felt these were; to capture bespoke adjustments valued by those with dyspraxia and to share these with others with dyspraxia. The aim is to enhance employment tenure for those with dyspraxia through education regarding useful Reasonable Adjustments.
I am seeking 100 adult Dyspraxia foundation members who have experienced employment, with the aim of obtaining a cross-section for gender, age, ethnicity, origin and occupation to capture unbiased data.
This survey will be open for 4 weeks, closing on Friday 17th June.
Opportunity to participate in DF approved research project
Research Participants Required
A RESPONSE STATEMENT ON THE GUARDIAN DYSLEXIA AND SPERM BANKS STORY
Maxine Roper, Dyspraxia Foundation Press Officer
Statement from the Dyspraxia Foundation following the Guardian’s story on dyslexia and sperm banks (December 30 2015)
We are concerned by reports that a leading sperm bank is turning away donors with neurological conditions, which include dyspraxia, as well as dyslexia, A.D.H.D and autism.
Despite being a neurological disorder dyspraxia can bring many strengths as well as some challenges. Those with neurological differences have a lot to offer society. They are often determined, resilient and creative. Employers increasingly recognise this, with some organisations such as GCHQ specifically advertising for applicants with dyspraxia and dyslexia. Many people with dyspraxia are very intelligent and with the right support difficulties associated with the condition can be managed well. If sperm banks are discriminating against donors with dyspraxia, it is deeply saddening and regrettable. There is no basis to exclude these conditions any more than excluding someone with asthma or diabetes which are also genetically-based conditions.
Although those with dyspraxia lead happy and successful lives, many also struggle to get the recognition and help they need. As with dyslexia, there is no NHS funding for adult assessments for dyspraxia, and a private assessment can cost up to £500. For those who are not high-flying managers or entrepreneurs, affordable support is vital.
Dyspraxia, also known as Developmental Coordination Disorder (DCD), is a common disorder affecting fine and/or gross motor coordination in children and adults. It can also affect short-term memory, organisational skills, spatial awareness and speech.
The Dyspraxia Foundation is the UK’s only national charity providing information and support on dyspraxia.
For more information please contact: Dr Sally Payne c/o Dyspraxia Foundation, 8 West Alley, Hitchin, Herts SG5 1EG.
Tel: 01462 455016/Email: [email protected]
Congratulations to dyspraxia supporter Emma Lewell-Buck MP
Emma openly talks about her dyspraxia to help raise awareness and improve understanding of the condition and is a staunch supporter of the work of the Dyspraxia Foundation.
Speaking of her condition, she explains: “I can’t wear eyeliner, because you’ve got to have a steady hand. Every time I try, I end up with a big line down my face.”
“If I got hair straighteners, you can guarantee I would burn myself.”
Speaking of her school days, she said: “I was struggling, but stuff like this wasn’t on the agenda when I was at school, so I often got dragged into misbehaving.
“Really it was a way of saying, ‘I can’t do this and I don’t know why because no one is helping.”
Penny Bellis represented drivers with dyspraxia at a recent consultation on new driving test
On behalf of the Dyspraxia Foundation, on Thursday 12th November 2015, I attended a disability consultation by the Driver and Vehicle Standards Agency at the Driver Training Academy at Cardington, Bedfordshire.
I enjoyed meeting both the DVSA staff and the other delegates. The presentation was given by driving test examiners, who were good company and very approachable. The other delegates were from organisations representing people with cerebral palsy, the deaf, autism and chronic regional pain syndrome.
The consultation was about the development and implementation of a new DVLA driving test. It began with a presentation about the proposed changes given by Paul Halbing, followed by a demonstration of both the current test and the proposed new test by Neil Wilson, Neil Smith and Graham O Bryan. The main change was an extension of the current ten minute independent drive to twenty minutes, to be facilitated with a satellite navigation system………..
Dyspraxia: Dyspraxic Adults Surviving in a Non-Dyspraxic World: A Dyspraxia Foundation Adult Support Group Publication [Kindle Edition]
A review received within 24 hrs of publishing
“Brilliant book, excellent read, really useful and interesting.
Truly recommend x”
This book, written by and for adults with dyspraxia offers a wealth of information and practical strategies to address the daily challenges experienced by adults with dyspraxia in all areas of life. Previously considered a disorder of childhood, dyspraxia (also known as developmental coordination disorder) is now recognised to affect individuals across the lifespan. Despite this, awareness and understanding of dyspraxia in adulthood is limited. To address this gap in knowledge the editors of this book, who both have dyspraxia, set up an on-line discussion group for adult dyspraxics to share their experiences and coping strategies. Their aim was to write a book that focused on the issues that matter to adult dyspraxics, share coping strategies and provide reassurance to other adult dyspraxics that they are not alone in experiencing life as they do.
Research Participants Required Nottingham University
An Interpretative Phenomenological Analysis of the experiences of children with Dyspraxia in UK secondary schools
The aim of my research is to find out what the experiences of secondary school aged children with Dyspraxia are in the UK. In order to do this, I hope to speak with children with Dyspraxia who are aged between 11 and 17 years old about their everyday experiences in school and how they feel their Dyspraxia affects them. As little is known about how a child experiences their Dyspraxia, and even less is known about how they experience school, it is hoped that this project will contribute new knowledge about how it is for children in the UK who have Dyspraxia….
Dyspraxia Foundation launches NEW resource: Managing Anxiety - Advice Sheet for adults and teenagers
Anxiety is a common and recurring theme amongst people with dyspraxia – a Dyspraxia Foundation survey in 2014 found that 40% of people with dyspraxia aged 13-19 years felt anxious ‘all the time’. Anxiety is the term we use to describe feelings of unease, fear or worry. It is a normal response to a frightening or unknown situation such as attending a job interview or preparing for exams. Feelings of anxiety can range from feeling slightly nervous to something completely debilitating unless it is recognised and managed appropriately……..
download this free resource here Managing Anxiety for teens and adults
Dyspraxia Awareness Week launch at Parliament
Host a reception in the Thames Pavilion, Houses of Parliament
On Wednesday, 14th October to mark
Dyspraxia Awareness Week (11 – 17 October 2015)
Dyspraxia – is it a battle of the sexes?
Guest speakers: Emma Lewell-Buck MP and Pat Glass MP
The Dyspraxia Foundation extends its appreciation to our sponsors Norton Rose Fulbright
New Dyspraxia Foundation logo incorporates DCD
The Dyspraxia Foundation updated the definition of dyspraxia in 2015 to incorporate the current terminology of Developmental Coordination Disorder (D.C.D.) used internationally by researchers and in the medical profession. The Trustees felt that the Dyspraxia Foundation should use the term within the logo to ensure consistency and to reflect the fact that the terms are often used interchangeably.
Incorporating DCD will also ensure that when people are searching DCD on a web browser, the Dyspraxia foundation will feature in their findings, thus increasing our visibility to the wider world……….
The Dyspraxia Foundation launches NEW factsheet in response to a nationwide survey
Some issues are different for girls than for guys. As each person with dyspraxia has a unique profile of strengths and difficulties, the strategies that work will vary from individual to individual.
We hope you find some new ideas here!
Dyspraxia Awareness Week (11-17 October) - A message to the press from celebrity patron, Jamie Lambert
Most people take for granted the fact that they can do simple tasks such as walking up and down stairs, getting dressed, throwing a ball or even mastering the art of handwriting! However, for the thousands of adults and children in the UK living with Dyspraxia/Developmental Coordination Disorder, day-to-day life can be a real struggle.
Dyspraxia (or, DCD) is a very misunderstood condition. Once cruelly (and incorrectly) labelled ‘clumsy child syndrome’, it affects up to six percent of the UK population – that’s around 2 children in every class.
However, it shouldn’t get in the way of you achieving your goals! I believe that I’m example of this, as I am proud to be part of the band “Collabro” who won ITV’s prime entertainment show ‘Britain’s Got Talent’……….
Dyspraxia Foundation Launches Survey Results
DYSPRAXIA – “IS IT A BATTLE OF THE SEXES?
Urgent call from national charity for greater awareness of dyspraxia among females as new survey shows they may be “slipping through the net”
New findings released today [Monday 12 October 2015] have revealed a significant gap in the diagnosis – and therefore, treatment – of dyspraxia, otherwise known as developmental co-ordination disorder (DCD), amongst young women and girls.
The nationwide poll1 , commissioned by the Dyspraxia Foundation, reported that over half (53%) of all female respondents said that their primary school teachers were unaware of their difficulties (compared to just 39% of the males questioned). 47% of teenage girls reported the same situation in secondary school, as opposed to 32% of males.
Experts from the Dyspraxia Foundation – the only national charity in the UK dedicated to raising awareness of the condition – believe such findings may reflect teachers’ perceptions of dyspraxia as a largely “male” disorder, leaving girls often overlooked in the classroom. It may also be possible that girls with dyspraxia are simply better at masking their difficulties by putting in extra effort and recruiting the assistance of friends to help them cope……..
Dyspraxia Awareness Week Blog Spot
Awareness Week has prompted many of our supporters to reach for their pen/laptop and share their experiences with us – if you have any to add, please let us know [email protected]
Rosie Edmondson: Dyspraxia Awareness Week 2015 – So what is dyspraxia?
Natalie Williams: Dyspraxia Awareness Week – 10 facts about dyspraxia
Misspraxic (an anonymous university student with Dyspraxia and other hidden specific learning difficulties) ; Dyspraxia Awareness Week 2015 – being at university with dyspraxia and how you can support a friend
Robert E Hodge: Dyspraxia & DCD Awareness Page
Alice Hewson: Dyspraxia Awareness Week 2015: Organisation and the transition from University to the world of work
Rachel Stratton Canwell: Herding Moggies – A Life With dyspraxia: Awareness why raise it??
Rosie Edmondson with Kerry and Phoebe Pace: reframing dyspraxia more positively
Rosie Edmondson: Dyspraxic Women, chaotic world
Alice Hewson: DYSPRAXIA AWARENESS WEEK 2015 BLOG 2: GROWING UP AND NOT FITTING INTO THE YOUNG ADULT STEREOTYPE
Andrew Weston, INTO THE OPEN: CHARITIES AND DYSPRAXIA
Eben Fletcher-why they need to know 4 sports coaches
Local charity gives its “stamp of approval” as it pledges to post out new book to over 200 schools
The Dyspraxia Foundation teams up with local Rotary Club to distribute specialist book to promote awareness of the condition
Hitchin-based charity, the Dyspraxia Foundation is delighted to announce that over 200 schools in the Hertfordshire area will be receiving a free, educational resource for the start of next term!
The delightfully fun yet touching and insightful book, “You’re so clumsy, Charley” (written by Jane Binnion – an author who herself has been diagnosed with dyspraxia) will be mailed out to 225 primary schools thanks to a grant from Hitchin Tilehouse Rotary Club, with a further £1,000 matched funding from the District Rotary Foundation.
The cartoon-style book – which follows the daily challenges of Charley, young boy with dyspraxia – has been developed for children in Year 1 and 2 (ages 5 – 7) and the Dyspraxia Foundation advises that a copy is kept by the school’s SENCo (Specialist Educational Needs Co-ordinator). As well as reading it together as a class, teaching staff could also use the new resource to prompt a discussion with a parent who has raised concerns about their child.
Charity adds a new voice to its cause as it announces its first ever “Celebrity Patron” ahead of Annual Awareness Week
Jamie Lambert from award winning “classical boy band” unveiled as new patron for the Dyspraxia Foundation.
The Dyspraxia Foundation – the only national charity in the UK dedicated to raising awareness of dyspraxia and championing the needs of people living with the condition – is hitting the high notes this week with the news that it has recruited its first ever celebrity ambassador!
26 year old Jamie Lambert (originally from Tyne and Wear) is a founding member and “one fifth’ of the acclaimed all male singing group, Collabro, who shot to fame last year after winning ITV’s prime time talent show, ‘Britain’s Got Talent.”
Jamie, who along with his fellow band members stole the hearts of the nation with their winning rendition of, ‘Stars’ from Les Miserables, invited the team at Dyspraxia Foundation to announce his new role to all delegates at the charity’s recent summer conference……….
Research Participants Required
How can you help spread the word?
We are fast approaching the end of year 2 of our 3 year project. ‘Dyspraxia Diffusion’ funded by the Big Lottery Fund to employ a full time Information Officer and offer a vital Helpline Service. Lisa McCarthy and trained volunteers are busy answering calls and emails from 9 -5, Monday to Friday but there are still parents, adults with dyspraxia, health and education professionals and employers who do not know we are here ready to help. You can help by downloading an A4 Poster or A3 Poster and putting up in your local school, surgeries, hospitals, parent groups, places of work, or anywhere people will see it.
contact us for copies if you could use a supply in your area.
[email protected] or call us on 01462 455016
'Dyspraxia - The Foundations' Now available in Kindle format
A comprehensive introduction to dyspraxia with quick and easy e- links to relevant information on the Dyspraxia Foundation website. The book covers, diagnosis, what dyspraxia is and isn’t, its impact, movement difficulties, family issues, visual learning difficulties,support strategies and more. This is an excellent and inexpensive book for those starting out on their journey with dyspraxia, but equally is excellent additional information for anyone interested in the condition, with prior knowledge, or who supports someone with the condition. It avoids complicated jargon and is a really accessible book which can be read as a whole or dipped into as needs arise. It is the only book to date with a detailed chapter on visual learning difficulties written by an expert in the field. Available from the Amazon Kindle store – Dyspraxia – The Foundation by Gill Dixon Also available free to members through the Members Only section, join today
How can you help!
Every donation helps us to improve the lives of people affected by dyspraxia, if you would like to help please use the button below.
Are you looking for an event to raise awareness of dyspraxia and sponsorship for the Dyspraxia Foundation? Is our usual British 10k event overwhelming and daunting? Or just looking for something the whole family can take part in? Then why not come join us on Sunday 3rd September in London’s Queen Elizabeth Olympic Park for the Parallel London event. In 2016 trustee Matt, his girlfriend Rosie, youth member (and blogger) alongside Natalie, youth member (and blogger) and her dad took part in the first event. All reported back on how wonderfully inclusive the event is, people of all ages, abilities and disabilities took part across a variety of events from 100m to 10km! There is no time limit, everyone is allowed to complete their distance and the pace that suits them! Note that pushchairs, wheelchairs and all other mobility devices are fully allowed, when they say all-inclusive they really mean it!
There is also an amazing event village, last year everyone could have a free slice of cheese on toast and there was a choice of free ice cream for everyone – this includes the spectators! The event village also has lots of accessible activities to take part in and the chance too visit a wide range of exhibitors!
The key point to remember is that Parallel London is for all ages and abilities; anybody can take part in one of five distances (10km, 5km, 1km, Super Sensory 1km, 100m) set in the majestic Queen Elizabeth Olympic Park to raise awareness and generate funds for the Dyspraxia Foundation.
To find out more, and see more from the 2016 event – and to register to take part in the 2017 event, visit the Parallel London website today! – and after you register make sure you tell us you are taking part via Twitter, Facebook and remember to drop an e-mail to us at firstname.lastname@example.org so we can share your stories and fundraising links across social media and in our monthly members newsletter!
Add the 3rd September to your diary now and join us and a range of runners at Parallel London!
A rare opportunity to come join us at the Dyspraxia Foundation has become available. We are looking for a fundraising coordinator to work in partnership with the Chief Executive and the Fundraising Committee to coordinate, manage and expand the existing fundraising programme covering large grant applications, trust funds and community fundraising, and to contribute to the delivery of the Fundraising Strategy.
Identify, develop new opportunities, co-ordinate and be responsible for generating the fundraising income in support of the Dyspraxia Foundation core operations as well as for specific projects which will enhance and improve the wellbeing of those with dyspraxia/DCD.
Please send your current CV and covering letter outlining why this role is of interest to:
Eleanor Howes, Chief Executive Officer, Dyspraxia Foundation, 8 West Alley, Hitchin, Herts. SG5 1EG or by email to email@example.com.
Closing date for applications: Wednesday, 1st February 2017
Interviews for this role will be held week commencing Monday, 6th February 2017
The University of Surrey is conducting research looking to understand the mental health and thinking abilities in adolescents with and without Developmental Coordination Disorder (DCD)/Dyspraxia.
In the study, parents will be asked to complete some questionnaires about their child’s motor ability and thinking abilities (e.g. planning and memory). Your child will also be asked to complete a questionnaire about their mental health. We may also ask to visit your child at home to administer a short assessment of vocabulary and reasoning skills.
Your child can take part if he/she is aged between 12 and 16, and has a diagnosis of Developmental Coordination Disorder / dyspraxia.
If interested, please email Serif at firstname.lastname@example.org for more information.
This study has received a favourable ethical opinion from the Faculty of Health and Medical Sciences Ethics Committee, at the University of Surrey