Giving a voice to individuals with apraxia of speech
Childhood Apraxia of Speech
Acquired apraxia of speech
Primary Progressive Apraxia of speech

Childhood Apraxia of Speech
Acquired apraxia of speech
Primary Progressive Apraxia of speech


Childhood apraxia of speech, acquired apraxia of speech, primary progressive Apraxia of speech and non verbal oral apraxia, global information, advocacy and support organisation. Join over 10,000 members worldwide.
Services we offer-
Advice from a team of specialists
Showcase research and recruit participants
Parent/Carer +Professional networks
Research/CPD
Events/training
Newsletter
Therapy App reviews
Extensive resource gallery.
Therapy information
Information on living with speech apraxia
Speech Apraxia International is part of the Speech, Language and Communication Alliance and the Inclusive Literacy Alliance
Our aim is to empower, inform, and support people with apraxia of speech. Thank you for joining our Speech Apraxia International community
Ruth Rowntree MSc, BSc (Hons), DipHE, HCPC Reg, MRCSLT
Speech and Language Therapist
Founder of Speech Apraxia International
Website Index
Most sections include information for Childhood Apraxia of Speech (CAS), Acquired Apraxia of Speech (AOS), and Primary Progressive Apraxia of Speech (PPAOS).
Home – https://speechapraxia.co.uk/ – News, events, training, resources, and information about Speech Apraxia International. Meet our team.
Diagnosis – https://speechapraxia.co.uk/diagnosis – Symptoms, diagnosis, assessment tools, and diagnostic resources for CAS, AOS, and PPAOS.
Therapy – https://speechapraxia.co.uk/therapy – Evidence-based therapy approaches, treatment programmes, and practical resources for children and adults.
Resource Hub Resource Hub – Information & Support School, Work, Finances, helpful organisations, books, films,driving, reading and other
Meet others Meet Others with Apraxia of Speech – Personal Stories & Support Personal stories, podcasts, videos, and opportunities to connect with others affected by speech apraxia.
Co-occurring Conditions Co-occurring Conditions with Apraxia of Speech – CAS & AOS –– Information on neurological, developmental, and genetic conditions commonly associated with speech apraxia.
Our organisation provides advice, information and advocacy. All our services are provided without any significant cost barrier making them accessible for all.
Our community helps each other with support, guidance and practical assistance. See how this has helped one parent, Sarah to navigate Childhood Apraxia of Speech which effects her son Ron.
Get our newsletter
Hear about events
Get the latest news
Join special interest groups including parent/carer, professional, researcher
Your membership enables us to
Use this link
https://forms.office.com/r/Vdzhfjb37X?origin=lprLink
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Updated often
Loads of specialist content on Speech Apraxia

Acquired/primary progressive apraxia CPD Events Wed, Sep 23, 2026, 9:30 -12.30
Acquired Apraxia of Speech and Primary Progressive Apraxia of Speech CPD
Wed, Sep 23, 2026 9.30-12.30

Childhood Apraxia of Speech CPD event FREE (min donation £1) Mon, Sep 14, 2026, 9:30 -12.30
Karen Massey (SLT) -Exploring the unique intersection of Autism and Childhood Apraxia of Speech
Hazel Shaw (SLT) -Treating childhood apraxia of speech in practice
Elina Csapo - Lived Experience- Growing up with CAS
https://www.eventbrite.co.uk/e/1989153004182?aff=oddtdtcreator

Meet Ruth Rowntree and team members , chat about speech apraxia over coffee
Speech Apraxia Virtual Conference 2027- Practice and Focus today in working with Apraxia of Speech
14th May 2026
https://www.eventbrite.co.uk/e/speech-apraxia-international-conference-2027-tickets-1990528184383?

Research events are open to all. We have some top researchers in the field talking about their research. Come and join the discussion whether you are interested in digging into the process of doing research or interested in the end results.

Fantastic opportunity to learn and train in the evidence based therapy
Rapid Syllable Transition Treatment and be taught by the lead researcher from Australia! This is a unique opportunity that is only available once in the UK!
When?
Around the date of the 17th June 2027. We are presently securing a a date.
Where?
Birmingham
How do I register?
Follow Speech Apraxia International on Eventbrite and you will get notified.
Here is a recent podcast https://www.patreon.com/SpeechApraxiaInternational/posts/what-happens-of-165497307?utm_medium=clipboard_copy&utm_source=copyLink&utm_campaign=postshare_creator&utm_content=join_link

To join our Global Professional Speech Apraxia Network just the following
link.
https://buy.stripe.com/9B65kD6xLg07189b52dAk06
Why join
No need to use Eventbrite Joining links
Exclusive Events
All Speech Apraxia UK CPD events are accredited by Speech Apraxia UK, You can receive a certificate if you are a member of the Global Speech Apraxia Professionals Group,

Online, peer-led discussion space for Speech and Language Therapists working with speech apraxia. Sessions focus on shared clinical reasoning, differential diagnosis, ethical decision-making, and complex motor speech cases.
This is a reflective, non-hierarchical forum for SLTs to think together about real practice challenges.
🗓 Online
Book via Eventbrite
All Speech Apraxia UK events are by donation (minimum £1) to keep them accessible to all
Suitable for qualified SLTs with an interest in motor speech disorders.

Oxfordshire SEND parents/carers Group
SOAS University of London
UCLAN
Aprex Ability Conference
Saltroad SSD CPD group
New Zealand Speech Therapy Association
Apraxia Kids
To book an event fill request form
Training is FREE -Donation for larger events

Childhood Apraxia of Speech CPD event FREE (min donation £1) Mon, Sep 14, 2026, 9:30 -12.30
Karen Massey (SLT) -Exploring the unique intersection of Autism and Childhood Apraxia of Speech
Hazel Shaw (SLT) -Treating childhood apraxia of speech in practice
Elina Csapo - Lived Experience- Growing up with CAS
https://www.eventbrite.co.uk/e/1989153004182?aff=oddtdtcreator
Wed, Sep 23, 2026, 9:30 -12.30
Acquired Apraxia of Speech and Primary Progressive Apraxia of Speech CPD
Wed, Sep 23, 2026 9.30-12.30

The films on the front page of our website were made by the amazing film producer Rae Wiltshire! He is a Guyanese filmmaker, playwright, cinematographer and Chevening Scholar who is an ardent student of cinema. As the founder and creative director of the Georgetown Film Festival, he is devoted to telling and showcasing films about Caribbean people. www.georgetownfilmfestival.org/our-team

Ruth Rowntree -CEO of Speech Apraxia International has been invited to present at the Apraxia Kids Conference on Childhood Apraxia of Speech: How Much Knowledge and Experience do Clinicians Have and What it Means
To book your place visit National Conference - Apraxia Kids

Speech Apraxia International is one of over 50 organisations to support the Invest in SLT compaign c oordinated by the RCSLT and Mikey’s Wish Foundation) (founded by activist and campaigner, Mikey Akers). Invest in SLT campaign letter delivered to Downing Street | RCSLT Invest-in-SLT-Letter-to-PM_-22March26.pdf

📣Research Opportunity - help us understand Dyspraxia/DCD📣 🧬Researchers at the University of Surrey are exploring the genetic influences on Dyspraxia/DCD, through the GROW-DCD (Genetic Research Of Walking and Developmental Coordination Disorder) study🧬
Who can take part?-
Anyone aged 18 or over with a diagnosis of DCD or who suspects they may have Dyspraxia/DCD
- Who lives in England, Wales or Northern Ireland
What does participating involve?
-Completing a short online questionnaire
- Providing a saliva sample from home using a kit sent to you
🎁As a thank you, you'll receive a £20 Amazon voucher once you've completed the study
🎁 To take part, use the QR code in the attached flyer or follow this link: http://bit.ly/3UdPNRZ
Any questions? Please contact Judith (j.gentle@surrey.ac.uk)#dyspraxia #DevelopmentalCoordinationDisorder #research

The Speech, Language and Communication Alliance has been formed to ensure that the UK Government, and national and local policymakers are focused on the issue of speech, language and communication, and the potential impact of these on all children and young people when developing or reviewing policy, legislation and services.
Speech and language therapist;Laura Cookson
"The Speech Apraxia UK website has been very helpful in providing advice and information quickly when I made a query. I have also heard from parents of children with CAS who have found some of the podcasts and signposting on the website useful and informative"

Visiting the House of Commons with the Speech Language and Communication Alliance raising awareness of Speech Apraxa International meeting Members of Parliament Jen Craft, Saqib Bhatt and Helen Hayes

The RCSLT have a fantastic range of support and resources and it was a privilege to meet with CEO Steve Jamieson and talk about our organisation. www.rcslt.org

Speech apraxia can have a direct impact on children's access to literacy support. We are proud to stand alongside organisations such as Teach Us Too, the ACE centre and Communication Matters in this powerful alliance.

Over 5000 members! To join click on www.facebook.com/groups/1058131123104807



Having fun at the London Speech Apraxia International Social!















Our amazing team of SLTs/SLPs the ‘Friends of Speech Apraxia’ are here to help. They’ve generously offered their time and expertise to answer your questions. Use this form to reach out for information, support, and friendly advice https://forms.office.com/r/1T5mpuw5JS

We can offer training or personal experience talks. These are FREE if online to a non-funded group. Otherwise there is a small charge to cover our running costs.https://forms.office.com/r/aJS92UAjFq


Currently Speech Apraxia UK is mainly unfunded. Most of our services are FREE. We provide extensive support, information, and awareness around Speech Apraxia. If you would like to contribute, it would really help. 'Buy us a coffee' with this link https://buymeacoffee.com/speechapraxia

Working with the New Zealand Speech Language Association to spread international awareness over speech apraxia. Communication Matters Issue 63 – Autumn 2026 page 11-12

Speech Apraxia UK- a global organisation

Listen to our NEW official podcast Talking Speech Apraxia, a heartfelt, insipiring show featuring a range of experts in speech apraxia, (Pictured is Alonna Bondar form Bondar Speech who did a fantastic podcast anwering your questions on treating speech apraxia)


Extensive resources
Professional Networks
Training providers

https://forms.office.com/r/9SGYnivJav
Have a go and develop your knowledge

https://forms.office.com/r/cej9fNkMht
Quick check to see what you know

https://forms.office.com/r/UE6yQ64ZR1
Review your understanding

We have a busy parent and carer support group running. You are welcome to join, just complete our Speech Apraxia membership form above.

Every year we don't just keep our organisation going but believe in supporting others. Mikey's Wish Foundation is our charity of the year. Please do consider helping them with their important work.

We are keen to collaborate with other organisations doing excellent work in supporting individuals effected by speech apraxia such as the , Stroke Language and Communication Group and 1Voice.
10A Station Road, Kirkham PR4 2AS England
info@speechapraxia.co.uk Facebook @speechapraxia

Alternative name-Developmental Verbal Dyspraxia. It is a label used for a specific type of speech sound disorder in which the planning and/or programming of the movements to produce speech is inefficient.

Speech disorder, which is acquired after a stroke (or other neurological disorder) , It affects the ability to plan and coordinate the movements necessary for speech.

Primary Progressive Apraxia Of Speech is a neurological disorder that affects the ability to plan and coordinate the movements necessary for speech sounds, leading to significant communication difficulties over time

SEND / EHCP guidelines + support
Bullying
Making school accessible
Reasonable Adjustments

Going to work or employing someone with speech apraxia, find information and support.

Whether it is the law over discrimination, financial help, or support while studying, we have you covered.

We have loads of support available
Resource Hub – Information & Support
Regular online meetings
Meet Others with Apraxia of Speech – Personal Stories & Support
Directory of helpful organsiations

Why not become a member of Speech Apraxia UK (FREE)
Book us to deliver (FREE*) training
Send us some research or an article
Take our online quizzes
Advertise with us
Have us impartially review your product for FREE

Our website has extensive information and resources, from recommended books to the latest research. We have a whole section on related conditions.

We cannot spread awareness alone.We work with many people with speech apraxia, organizations, professionals, and parents, including:
Charities/SLCN organisations
New Zealand Speech Language Therapy Association.
RCSLT
Selective Mutism Information & Research Association (SMIRA)
Elliot's Voice
From Stuttering to confidence
PROMPT Institute
Nuffield Association
RADLD
Universities
Newcastle University Students' Union
The University of Sydney: One of Australia’s top universities
Companies
SLPFlow AI - Best AI for SLPs | SLP
Researchers
Murdoch Children's Research Institute.
Sick Childrens Hospital-research group
Chris Kamara admits, 'I'm no longer the person I used to be' and reveals deep regret. Sky Sports star Chris Kamara's life was turned upside down in 2022 when he was diagnosed with apraxia of speech (AOS), which also affected his balance and coordination.
Chris, 67, flew to Mexico for treatment in a bid to reverse or slow down some of the effects of the neurological disorder, which include difficulty when speaking. However, despite initial success, the machine that transmitted radio frequency and magnetic fields into the body similar to an MRI became less effective, resulting in Chris stopping treatment(Mirror, 2025).
We were absolutely delighted to share that Professor Emeritus Anita van der Merwe globally respected leader in the field of motor speech disorders — has shared warm praise for our new website.
In her message, Professor van der Merwe wrote:
“Congratulations on your website for apraxia of speech for people in the UK and elsewhere; it is a great website!”
She even wrote a special guest piece for the site, focusing on apraxia of speech and approaches to speech motor treatment.
We’re truly excited and honoured to welcome her voice to the website.

Join our Facebook community to discuss all things Apraxia of Speech - Facebook
From a kitchen table laminator to schools, parks & even fire stations — Kendra Frank turned her son Elliott’s CAS journey into Elliott’s Voice. Her organization, which she founded in 2023, aims to provide accessible visual supports to children and adults who are nonverbal or have limited verbal abilities,
Did you know joining Unique is completely FREE?
If you have a rare chromosome or gene disorder you can join our membership to access our support, expertise and get connected with other families affected by the same condition. We'd love to have you join our supportive community.
https://rarechromo.org/join-us/


Laura Brown (spinningworldofautism) who has a son with autism and CAS has created two short Google Forms to gather experiences: one for families and one for both NHS and independent Speech and Language Therapists.
The aim is to collect lived experiences from families of autistic children, as well as from therapists who have supported autistic children.
If you could please complete the form relevant to you and also share it with families or colleagues who may wish to contribute, She would greatly appreciate it. If possible, it would also be very helpful if you could share it within your WhatsApp groups or networks.
Form for families: https://forms.gle/D7BbsQPyqvGgbErcA
Form for NHS Speech Therapists: https://forms.gle/nQqCJkLQqewcH4B8A
Form for Independent Speech Therapists: https://forms.gle/YexT3CHNvnsDrRkw8
Chris Kamara ITV.com

While we strive to provide accurate and up-to-date information on this website (www.speechapraxia.co.uk), the content is not intended to replace professional medical advice, diagnosis, or treatment.
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Copyright © 2025 Speech Apraxia Interantional - All Rights Reserved. Speech Apraxia International is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn fees by linking to Amazon.co.uk and affiliated sites. As an Amazon Associate, we earn from qualifying purchases. Other goods or services promoted by us may also earn us a small commission withich is vital to keeping our services going.
Website Index
Most sections include information for Childhood Apraxia of Speech (CAS), Acquired Apraxia of Speech (AOS), and Primary Progressive Apraxia of Speech (PPAOS).
Home – https://speechapraxia.co.uk/ – News, events, training, resources, and information about Speech Apraxia International.
Diagnosis – https://speechapraxia.co.uk/diagnosis – Symptoms, diagnosis, assessment tools, and diagnostic resources for CAS, AOS, and PPAOS.
Therapy – https://speechapraxia.co.uk/therapy – Evidence-based therapy approaches, treatment programmes, and practical resources for children and adults.
Resource Hub Resource Hub – Information & Support School, Work, Finances, helpful organisations, books, films,driving, reading and other
Meet others Meet Others with Apraxia of Speech – Personal Stories & Support Personal stories, podcasts, videos, and opportunities to connect with others affected by speech apraxia.
Co-occurring Conditions Co-occurring Conditions with Apraxia of Speech – CAS & AOS –– Information on neurological, developmental, and genetic conditions commonly associated with speech apraxia.
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