Our Bridging Connections team helps by:

  • Providing supports and advocacy before, during, and after assessment
  • Linking Métis Albertans with cultural supports and resources
  • Connecting individuals to FASD Networks, resources, and information
  • Supporting the navigation of community resources and systems
  • Informing and supporting the MNA citizenship process
  • Offering cultural training to professionals who work with the Métis community

Who is eligible?

  • MNA citizens and self-identified Métis people living in Alberta
  • Must be diagnosed with or someone who may have FASD

Take the first step today by filling out the Bridging Connections intake form! Email your completed form and any questions you have to fasd@metis.org, or call 780-455-2200 to have our program staff walk you through the process.

Let’s cross this bridge together.


The Children & Family Services Team

FASD Caregiver Connect Night

Our FASD Caregiver Connect Nights are a safe space for parents and caregivers raising children / youth / adults with Fetal Alcohol Spectrum Disorder to gather for support and to discuss hard things. We want you to know you are not alone!

FASD Caregiver Connect Nights are held on the second Wednesday of every month 6 – 7 pm on Zoom. Each month we will briefly discuss one key issue pertaining to FASD then open up the discussion to parents/caregivers to talk about their struggles and their successes.

Upcoming Dates:

  • March 13, 2024: Register Here
  • April 10, 2024
  • May 8, 2024
  • June 12, 2024

You will receive the Zoom invite after you have registered for the FASD Caregiver Connect Nights.

For more information or to suggest a topic for a future FASD Caregiver Connect Night, please email fasd@metis.org.

FASD Information Session

The FASD Information sessions will focus on a variety of topics including Living with FASD, Healthy Pregnancy & FASD Prevention, FASD & Sensory Integration Issues, and more. These sessions are held bi-monthly with a different topic for each session.

Upcoming Dates:

    • March 26, 2024

FASD Survey

FASD – why does it matter?
Fetal Alcohol Spectrum Disorder (FASD) is a common disability that impacts approximately 1 in 25 Albertans of all ages. FASD is a medical condition that impacts people from all walks of life. In fact, you may know people with FASD at work, in your community, or in your family.

It is our hope that by openly talking about FASD, we can reduce the stigma associated with this disability, build skills, promote wellness, and prevent FASD. We would like to hear from you about FASD, even if you do not know someone with it. Sharing your experience and perspective will help us shape FASD supports, services, and resources for Métis Albertans.

Your privacy will be protected and all answers will be anonymous.
If you require assistance to complete this survey please call 780-455-2200 or email fasd@metis.org. We will be happy to assist.

Fill out the survey link!