Professional FASD practice

What should professionals understand about FASD in a kinship family?

FASD-informed practice combines neurodevelopmental understanding with the realities of kinship care: incomplete history, caregiver load, trauma, school transitions and long-term system navigation.

Grandmother and granddaughter working together

Part of our For Professionals resource series. See the main For Professionals guide for the wider topic and related resources.

Information reviewed September 2026. Assessment pathways, services and program rules can change, so use the linked official source when a current process matters.

Do not use FASD as shorthand for a behaviour problem.

FASD is a lifelong disability affecting the brain and body, and individual profiles vary widely. Public Health Agency of Canada guidance lists possible differences in learning, memory, attention, communication, motor skills, emotional regulation and physical health. Most people with FASD do not have obvious outward signs.

Canada: About FASD

Ask what function the behaviour is serving.

A professional response should consider receptive language, working memory, sensory load, executive functioning, fatigue, trauma, anxiety and environmental demands before concluding that a child is simply refusing to comply.

Support the caregiver as a source of functional knowledge.

CanFASD guidance for health providers notes that caregivers often know which communication style, sensory adaptations and routines help the child function. In kinship care, the caregiver may also be reconstructing developmental history from incomplete records, so professionals should help organize information rather than treating gaps as caregiver failure.

Use consistent, concrete communication.

  • One idea or instruction at a time.
  • Concrete language instead of metaphor or vague time concepts.
  • Visual or written support where possible.
  • Check understanding by asking the person to show or explain the next step in their own way.
  • Build predictable follow-up and avoid relying only on verbal reminders.

Design the environment for regulation.

CanFASD healthcare guidance recommends reducing sensory stimulation where possible, using quieter spaces and involving caregivers in understanding what works. Similar principles can help in schools, court waiting areas, community services and appointments.

CanFASD: Tips for healthcare providers

Diagnosis should lead to a plan, not just a label.

The practical question after assessment is what changes in school, health care, daily living, mental health, supervision, benefits and transition planning. Professionals should tell the caregiver what happens next and who owns each referral.

Watch the transition points.

Starting school, changing school, adolescence and the move into adult services can increase stress for both the individual and caregiver. CanFASD's CARE Study has identified life transitions and the sustainability of supports across the lifespan as major caregiver concerns.

Protect against stigma toward both the child and birth parent.

FASD should not become a moral label for the person with the disability or the parent who used alcohol during pregnancy. Public Health Agency of Canada notes that alcohol use during pregnancy can occur in the context of trauma, poverty, isolation, violence, depression, unplanned pregnancy or alcohol use disorder.

For schools

Use concrete instruction, visual structure, predictable transitions and functional support rather than escalating punishment for repeated skill failures.

FASD at school

For health & community services

Reduce sensory and communication barriers, clarify authority, and use warm referrals when several systems are involved.

Warm referral standard