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FASD Service Coordination

Contact Brant provides Service Coordination support to families of children and youth who have FASD, or possible FASD.

Fetal Alcohol Spectrum Disorder (FASD) is a diagnostic term used to describe impacts on the brain and body of individuals prenatally exposed to alcohol. FASD is a lifelong disability. Individuals with FASD will experience some degree of challenges in their daily living, and need support with motor skills, physical health, learning, memory, attention, communication, emotional regulation, and social skills to reach their full potential. Each individual with FASD is unique and has areas of both strengths and challenges.

Understanding FASD

FASD is the leading developmental disability in Canada, affecting 4% of Canadians

Consider a child’s developmental age not their actual age – expectations need to match the developmental age.

FASD is a “Disability of Thinking”.  Create thinking-free days with routines, repetition, and consistency.

It is NOT that children with FASD WON’T, it is because they CAN’T.

Make getting help or receiving support a “good thing” – encourage supported independence.

When things are not working – step back, reduce expectations, increase supports, and focus on the child/youth’s strengths.

Provide

Information and strategies through an FASD lens.

Connect

To community services and the Brant FASD Caregiver Support Group.

Develop

Service plans that best fit the family’s needs.

Educate

To build capacity with families and community professionals.

Eligibility for FASD Service Coordination

  • Ages 0-18 or,
  • Ages 18-21 and still attends school, and
  • Diagnosed or suspected of having FASD.

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