Apraxia Kids

Apraxia Kids The leading nonprofit that strengthens the support systems in the lives of children with apraxia.
(442)

“I learned so much for my son and have already gone back to advocate with the research and classes I took. The classes w...
06/19/2026

“I learned so much for my son and have already gone back to advocate with the research and classes I took. The classes were great but most of all the people I have made friendships with are priceless! I went to the conference alone and nervous but came out with so much more than I could ever ask!”

Learn more and register today: https://www.apraxia-kids.org/apraxia-kids-national-conference/

The Apraxia Kids National Conference is the only major conference on the speech, language, learning, and life needs of c...
06/17/2026

The Apraxia Kids National Conference is the only major conference on the speech, language, learning, and life needs of children with apraxia. The National Conference brings together parents, professionals, researchers, and others who are seeking the most up-to-date and in-depth learning opportunities available.

Learn more and register: https://www.apraxia-kids.org/apraxia-kids-national-conference/

06/17/2026

If you are a returning attendee, you know the level of expertise our speakers bring to the conference. For first time attendees, we hope you will consider joining us for evidence-based learning, engagement with the professional community, along with making new friends who are on a similar journey.

Learn more and register: https://www.apraxia-kids.org/apraxia-kids-national-conference/

06/16/2026

Mikey Akers, from , has been recognised in the with an MBE for services to special educational needs.

Mikey, 25, lives with the lifelong, neurological speech disorder, childhood apraxia of speech (CAS), previously known as verbal dyspraxia.

Louisa, Mikey’s ‘proud’ mum, told : “He was diagnosed with CAS when he was just 2 years old. Growing up with CAS was a lonely and isolating experience, as Mikey never met anyone else with the diagnosis, so at the age of 13, he decided to set up a page, Mikey’s Wish - Verbal Dyspraxia Awareness https://www.facebook.com/share/1bz1i7ysiS/?mibextid=wwXIfr, and share his story in the hope of ensuring that no other family would feel as alone as his.

“Due to his speech, language and communication needs, Mikey also struggled in school so he started fundraising to support children in schools with CAS and SEND. Donating more than £20,000 to his local primary school over the years.

“Mikey has also travelled to America to talk at the Apraxia Kids National Conference four times to give parents hope for their child’s future, he has given talks in schools, at SEND Conferences, head teacher conferences and he is an ‘expert by experience’ at Birmingham City University where he gives talks to student speech and language therapists.

“In 2022, Mikey started working with his MP, Saqib Bhatti, and the RCSLT to raise awareness in parliament. Mikey tabled a petition calling for more investment in speech and language services that was debated in January 2025 and from that he had a meeting with Stephen Kinnock (Health and Social Minister at the time) who promised Mikey and the ‘Invest In SLT’ team an action plan on speech and language.

“Mikey also founded the registered charity, Mikey’s Wish Foundation, where Mikey and the team of trustees are improving the lives of people with childhood apraxia of speech by providing resources, holding events to bring people together, supporting children in school and helping them access the essential support.

“When Chris Kamara was diagnosed with acquired apraxia of speech, Mikey and the Mikey’s Wish Foundation trustees supported Kammy and he then agreed to become the charity’s patron.

“He does all this alongside working full time as a child specific teaching assistant at his local school, supporting children who like him have additional needs.”

The annual Apraxia Kids National Conference is the longest-running and only major conference focusing on the speech, lan...
06/15/2026

The annual Apraxia Kids National Conference is the longest-running and only major conference focusing on the speech, language, learning, and life needs of children of all ages with childhood apraxia of speech (CAS). This unique event brings together families, professionals, researchers, educators, SLPs and future SLPs, young adults with CAS, and others who are seeking the most up-to-date evidence-based information from renowned speakers from around the world.

Learn more and register: https://www.apraxia-kids.org/apraxia-kids-national-conference/

"When our daughter was diagnosed with childhood apraxia of speech, her school-based speech therapist pointed us to Aprax...
06/14/2026

"When our daughter was diagnosed with childhood apraxia of speech, her school-based speech therapist pointed us to Apraxia Kids as a trusted resource. Through that connection, we found incredible speech therapists who have truly changed the course of her journey.

Receiving this diagnosis opened our eyes and challenged us to view the world through Mia’s unique lens. As parents navigating what felt like uncharted territory, Apraxia Kids has been an incredible source of guidance and support.

There was a time when we quietly wondered if we would ever hear her say her name or tell us “I love you.” Now, we hear “My name is Mia” “I love you, (mama/dadda)” and even “I can’t help, I’m busy”—words (and sass!) we once only dreamed of.

The right resources and specialized therapy make a world of difference for children with apraxia. Progress doesn’t happen by chance—it happens with the right support, knowledge, and people who truly understand this diagnosis.

Apraxia Kids gave us connection, direction, and hope when we needed it most. Supporting this organization means helping more families access life-changing care and giving more children the chance to find their voice—one word at a time."

~Karly, Apraxia Awareness Month Ambassador, Apraxia Kids

Address

Pittsburgh, PA
15233

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Telephone

+14127857072

Alerts

Be the first to know and let us send you an email when Apraxia Kids posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Organization

Send a message to Apraxia Kids:

Share