Today was an exciting day! On the Jeremy Vine Show (Just to confuse matters slightly, Paddy O’Connell was sitting in for Jeremy today), Lottie Jenkins, alongside Dr Sarah Jarvis talked, and raised awareness of Dyspraxia, which included many people phoning in afterwards!
We are delighted to confirm that our London Conference / AGM takes place on Saturday 24th June 2017!
Starting at 10.00am, all members of the Dyspraxia Foundation are invited to attend our AGM. This will be followed by a day of talks for parents, carers, young people (16—25) and adults with dyspraxia, professionals in health and education, teachers, SENCos, Learning Support Staff, employers and anyone with an interest in neurodiversity.
The Dyspraxia Foundation 2017-18 annual membership is here! Join, or renew, your membership for the next 12 months to add your voice to ours to support and raise awareness of Dyspraxia/DCD.
New for this year, we have set up Direct Debit payments to make renewal even easier so please do visit the website here to use this facility.
Today we are pleased to announce that we are launching our brand new ‘Friends of Dyspraxia’ monthly donation scheme – via direct debit!
Demand for our services is increasing, and at the heart of what we do, we aspire for a world in which all those affected by dyspraxia/DCD are enabled to achieve their full potential in life. We cannot achieve this goal without the generosity of people like you, and that’s where our Friends group can make a real difference.
University of Surrey are looking for adult participants for a study they are running. Please find all the information we have received from them following. Should you have any queries, please do contact Shiloh Grant Smith at the email given in the text. Please note that this is not a Dyspraxia Foundation run study.
Did you attend a residential special school/college in the UK as a child? Are you the parent/carer of someone who attends (or who attended) residential special education in the UK?
Update: This survey has now closed, thank you to everyone who submitted a response.
It’s that time again! Why not come join Team Dyspraxia and run around the amazing British 10K route around London on Sunday 9th July! By joining us you will receive:
Run with us for an amazing experience. We’re with you every step of the way.
Kindle Edition only £7.99 or read with free app
Essential reading for parents/carers of children who have dyspraxia/DCD, for parents/carers of children who are waiting for an assessment, and for parents/carers who are concerned about their child’s motor/organisational development and who want to do something ‘while they wait’ for professional assessment or support.
Yesterday, ITV News Yorkshire played out a video on dyspraxia! Including an apperance from our very own trustee Gill Dixon!
‘Growing up, I got the sense that people thought I was a bit slow – they thought he’s not quite as smart or clever as everyone else. Even though I am.’
Today is #TimetoTalk day, a national day by Time to Change (http://www.time-to-change.org.uk/) asking everyone to talk about mental health. The Dyspraxia Foundation believes that the views of people with and affected by dyspraxia/DCD are important. In 2016, feedback from a consultation by the Dyspraxia Foundation with young adults with dyspraxia found;