Calgary Apraxia
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    • Home
    • About
      • About Us
      • What is Apraxia
      • News + Media
    • Events
      • Events Calendar
      • CHAoS in the City
      • CHAoS in the City Clues
    • Sponsors
    • Camps
    • Resources
      • Financial Support
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      • PUF
      • FSCD
      • DTC + RDSP
      • IPP
      • Speech Buy & Sell
      • Downloads
    • GIVE
      • Volunteer
      • Donate
      • Sponsorship
  • Home
  • About
    • About Us
    • What is Apraxia
    • News + Media
  • Events
    • Events Calendar
    • CHAoS in the City
    • CHAoS in the City Clues
  • Sponsors
  • Camps
  • Resources
    • Financial Support
    • Speech Therapy
    • PUF
    • FSCD
    • DTC + RDSP
    • IPP
    • Speech Buy & Sell
    • Downloads
  • GIVE
    • Volunteer
    • Donate
    • Sponsorship

Program Unit Funding (PUF)

Overview

The Government of Alberta provides Program Unit Funding (PUF) to support the educational needs of children with a severe developmental disability or delay including Childhood Apraxia of Speech.


The funding is used to support children’s participation and learning in early childhood programs. 


Access to funding can be for up to 3 years, depending on need and when the child was approved. Children are re-assessed annually and the funding will cease at the end of kindergarten, regardless of how many years have been accessed. 

Eligibility

  • Children who are at least 2 ½ years of age and less than 6 years of age on September 1 are eligible.  
  • They must be enrolled in a preschool or kindergarten program
  • Qualification is determined by Alberta Education who evaluate the child's assessment and application

Alberta's PUF support is unlike anything available in other provinces. We were able to find a ECS provider that made a massive difference in my son's development.


- Chris W., Father of Child with Apraxia

Coding Criteria

Alberta Education uses a coding system to determine the severity of a child's condition. Depending of the severity of a child's Apraxia, they may fall into any one of these groups:

Code 44: Severe Physical or Medical Disability

Code 44: Severe Physical or Medical Disability

Code 44: Severe Physical or Medical Disability

An child with a severe physical, medical, or neurological disability is one who: 


  • has a medical diagnosis by a qualified professional of a physical disability, specific neurological disorder, or medical condition that severely impacts the child’s ability to function and learn in an educational environment 
  • requires extensive adult assistance and modifications to the educational environment to support their learning 


A clinical diagnosis by a registered medical professional specializing in the field of these disorders is required. However, a clinical diagnosis alone is not necessarily sufficient to qualify under this category. In addition to a diagnosis by a qualified professional, school authorities are required to have extensive documentation, completed by school staff, indicating the quality, nature, frequency, and severity of the impact of the disability/disorder within the educational environment. 

Code 47: Severe Language Delay

Code 44: Severe Physical or Medical Disability

Code 44: Severe Physical or Medical Disability

A severe language delay is assessed and diagnosed by a speech-language pathologist (SLP). The SLP uses a variety of formal and informal assessment instruments such as standardized tests, checklists, observational measures, and parental interviews resulting in an interpretive report that supports the diagnosis of a severe language delay. Eligibility for a severe language delay is based on a child’s overall speech/language development profile and assessment results, not on individual subtest scores. A child with a severe language delay is one who:


  • has been assessed and diagnosed with a severe language delay in expressive, receptive, or total language and the assessment report includes results, based on the assessment tool administered, either below the 1st or 2nd percentile in expressive, receptive or total language; or
  • has been assessed and diagnosed with a severe phonological delay; based on the assessment tool administered, is either below the 1st or 2nd percentile, AND with moderate to severe total language delay. 

Code 48: Moderate Language Delay

Code 44: Severe Physical or Medical Disability

Code 48: Moderate Language Delay

A child with a moderate language disorder: 


  • has been assessed by a speech/language pathologist with risk factors that are likely to persist into later childhood and have a functional impact on daily living that affects the child’s ability to participate in an ECS program; and
  • has been diagnosed with a moderate disorder or delay in expressive and/or receptive language; or
  • has been diagnosed with a moderate disorder or delay in expressive and/or receptive language and two or more mild or moderate delays in fine motor and/or gross motor development, vision, or hearing. 
  • Note: Moderate range 3rd to 6th percentile. 

How to apply

Step 1. See a Doctor

If you are concerned about your child's development, talk to your doctor first. If you do not have a doctor, use the Find A Doctor website. 

Step 2. Assessment referral

Upon seeing a doctor, you may be referred for further assessments. Often this assessment will come from AHS Speech and Language Services. 

Step 3. Connect with an ECS provider

If your child's assessments show a severe delay, your will need to connect to an Early Childhood Support (ECS) service provider. 

Step 4. ECS Provider applies on your behalf

Once you have selected an ECS provider and provided them with the necessary assessments and diagnosis reports, they will apply for PUF on your behalf.

ECS Providers and Delivery Methods

There are different delivery models of using PUF to support your child with CAS, below is an reference of some of them. You can see the websites for each of them to see more information, and we recommend contacting them to find out if they are a fit for you and your family. Every agency is unique, and have different methods/philosophy for working with children. 

1. Dedicated PUF Site

There are dedicated schools and centres in Calgary that deliver a preschool environment to children approved for PUF or other government funded programming and support. The school days are generally considered "half-days" (either morning or afternoon) and most of these include bussing to and from your home as well as lunch and/or snacks. There is no cost to the family for this delivery if a child has been approved for PUF and this option is generally the most robust in terms of support provided. Contact the provider directly to get more information on availability and registration.

2. Support via Community Preschool

Many preschools in Calgary offer screening and access to PUF. In this delivery of PUF, a third-party PUF provided would work with your child 1:1 at the preschool of your choice generally once every 1-2 weeks. The cost of the preschool is not covered in this delivery method but the therapy received is. The following is a list of PUF providers that come into your Community Preschool for therapy session. 

3. Support via School Board

Similar to the community preschool model, Calgary's various school boards (public, private and charter) can provide support via PUF however this is generally the most scaled-back delivery. Contact your school board for more information on what this would look like in Kindergarten. 


Copyright © 2025 Calgary Apraxia. All rights reserved.
Calgary Apraxia is a registered Canadian charity. 

Thank you for supporting families impacted by CAS

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