The Canada Northwest FASD Partnership (CNFASDP) is an interprovincial/territorial alliance formed in 1998 to advance evidence-based policy development and service design in FASD prevention, diagnosis, and support through the sharing of resources and expertise.

The current CNFASDP member jurisdictions are Alberta, Manitoba, Northwest Territories, Nunavut, Saskatchewan, and Yukon.

The CNFASDP supported the establishment of the Canada FASD Research Network in 2004-2005, and is proud to provide continued operations funding support for the Canada FASD Research Network.

Watch the Story Behind the Canada Northwest FASD Partnership

Darren Joslin, a founding leader of the Partnership, reflects on how decades of collaboration, shared knowledge, and evidence-based action have shaped FASD policy, research, and support across Canada and beyond.

Watch now to learn more about how the Canada Northwest FASD Partnership drives meaningful change—and how you can be part of it.

Strategic Priorities 2024-2027 

Indigenous Led Work and Supports

Supports and services for Indigenous people with FASD must be Indigenous-led and incorporate traditional Indigenous wisdom and practices to ensure programs are inclusive, culturally relevant, and reflective of Indigenous approaches. Aligning with the commitments outlined in the UN Convention on the Rights of Persons with Disabilities (CRPD), the UN Declaration on the Rights of Indigenous Peoples (UNDRIP), and the Truth and Reconciliation Commission (TRC) Calls to Action. Together, these frameworks emphasize the importance of Indigenous self-determination, equal access to culturally safe services, and the need for healing that addresses health inequities and respects Indigenous governance and practices.

Outcomes: 

  • FASD programs and services are person-centered, more inclusive to Indigenous approaches, informed by and reflect Indigenous ways of knowing and being

Housing Needs of Individuals with FASD

Individuals with FASD often require a continuum of housing supports to address their significant risk of homelessness.  Jurisdictions are trialing different housing models.

Outcomes: 

  • Information on current evidence-based housing models and practices that support adults with FASD, and their families/caregivers is shared between jurisdictions.

Resources: 

FASD Training

Enhancing the understanding and knowledge of FASD among service providers enables them to more effectively address the specific needs of individuals with FASD, leading to improved outcomes. Providing targeted training opportunities is essential to increasing the confidence and competence of those supporting individuals with FASD, particularly through practical, FASD-specific skills training and support for individuals who use substances during pregnancy. It is imperative that such training is validated by individuals with lived experience to ensure its relevance, authenticity, and effectiveness.

Outcomes: 

  • Increase access to FASD training to support the competencies of community service support workers and caregivers who directly support individuals with FASD.
  • Increase access to FASD training for a broad range of stakeholders in all levels, from government policy officials to direct service providers.
  • Share information on FASD training and education initiatives between jurisdictions.

Resources: 

  • Online Learning – Flexible online learning opportunities for you or your team, from CanFASD
  • FASD Training and Education – Learn about Fetal Alcohol Spectrum Disorder (FASD) through online training, videos and publications. From the Government of Alberta.

Mental Health and Addictions

The majority of individuals with Fetal Alcohol Spectrum Disorder (FASD) also have a concurrent mental health diagnosis, yet they are often not adequately supported by existing mental health and addictions services. It is crucial for service providers to be FASD-informed to ensure they can offer appropriate supports or refer individuals with FASD to services that address their unique needs effectively.

Outcomes: 

  • Service provider knowledge of mental health and addictions supports is FASD-informed to enhance service delivery.
  • Mental Health Resource and Practice Guide are distributed and evaluated widely to maximize its impact.
  • Tailored resources are developed for service providers on mental health and addictions services and programs specifically designed for individuals with FASD, including targeted supports for pregnant individuals and Indigenous communities.

Resources: 

Supports and Services

Supporting individuals with FASD and pregnant individuals who use substances requires a multi-faceted approach that integrates current best practices, research, and compassionate care.

Outcomes: 

  • Best practices, tools and resources in incorporating culturally safe and trauma-informed approaches are shared with service providers, policy makers and communities.

Resources: 

FASD Prevention Messaging

A shared common approach to FASD prevention messaging across jurisdictions can significantly enhance the effectiveness of efforts to reduce alcohol use during pregnancy. When jurisdictions—whether at the national, provincial, or community level—align their strategies and messaging, it ensures consistency, maximizes reach, and builds public trust.

Outcomes: 

  • Increase common FASD prevention messaging between jurisdictions and share this common messaging through other disability related forums and committees to increase awareness of a united FASD prevention messaging.

Resources: 

Enhancing Cultural Safety in FASD Diagnostic Clinics

FASD diagnostic practices must prioritize culturally safe approaches to ensure that assessments are inclusive and respectful of diverse backgrounds. It is essential that these approaches are tailored to the unique needs and contexts of individual communities, including Indigenous communities, which have distinct histories, experiences, and cultural values. By adapting diagnostic methods to local circumstances, healthcare providers can offer more equitable and sensitive care that aligns with the cultural traditions and experiences of the people they serve. This personalized approach is critical in fostering trust and improving health outcomes in FASD diagnosis and care.

Outcomes: 

  • Establish best practice guidelines and resources towards delivering culturally safe diagnostics process to persons with FASD.​

Resources: 

The Canada FASD Conference is coming to Edmonton, Alberta from November 16-18, 2027. The event will welcome researchers, caregivers, individuals with lived experience, policymakers, and professionals from across Canada and abroad to share knowledge and perspectives on FASD.

Canada Northwest FASD Partnership – Q&A

How did the Canada Northwest FASD Partnership form?

In 1998, the governments of Alberta, Manitoba and Saskatchewan formed the Prairie Province Partnership on Fetal Alcohol Syndrome (FAS). In 1999, the Partnership expanded to include Northwest Territories, Nunavut, and the Yukon, and in 2001, British Columbia joined the Partnership. In 2003, the name of the Partnership changed to the Canada Northwest FASD Partnership to reflect the expanded membership.

What is the mandate of the CNFASDP?

Ministers:

  • Collaborate with Ministerial colleagues in advancing the profile of FASD prevention and support across the Partnership and in their respective jurisdictions.
  • Approve the funds to be contributed annually by each jurisdiction to support the work of the Partnership and the CanFASD Research Network.
  • Approve the strategic priorities of the Partnership every three years.

Deputy Ministers:

  • Implement the direction of the Ministers through the Steering Committee.
  • Provide direction to the Steering Committee as required, examine issues pertaining to FASD and share best practices and information on initiatives occurring in their jurisdiction.
  • Approve agenda items for virtual or in-person meetings of Partnership Ministers.
  • Foster and facilitate the exchange of information and discussions on policies and programs pertaining to FASD among jurisdictions.

Steering Committee:

  • Implements the direction of the Deputy Ministers.
  • Examines issues pertaining to FASD and shares best practices and information on initiatives occurring in their jurisdictions.
  • Provides program and policy advice to the Deputy Ministers by identifying priority areas for discussion and collaborative action.
  • Fosters and facilitates the exchange of information and discussions on policies and programs pertaining to FASD among jurisdictions.
  • Ensures that progress on work plan deliverables is sufficient to warrant productive Deputy Minister and Minister meetings.
  • Recommends agenda items and develops materials for virtual or in-person meetings of Deputy Ministers and Ministers.
  • Organizes and determines the schedule of Partnership-sponsored events (webinar, symposium, conference) and which partner jurisdiction will be the host and/or lead of each event on behalf of the Partnership.
  • Collaborates with CanFASD to set research priorities.

How much do CNFASDP jurisdictions pay?

CNFASDP membership requires annual contributions to the CNFASDP Trust Account to fund learning events and initiatives that advance the CNFASDP’s strategic priorities. Each provincial partner contributes $20,000 annually, and each territorial partner contributes $6,500 annually. CNFASDP jurisdictions also contribute core annual operational funding to CanFASD, according to a population-based formula. This funding includes partner jurisdiction membership in CanFASD.

Can other governments participate in the CNFASDP?

Yes. The CNFASDP welcomes partnership from other governments in Canada.

We will see improved outcomes from advancing the diagnosis, prevention, and the intervention of FASD, and the care and support of individuals affected by FASD, the more coordinated we are across the country. This will lead to enhanced learning and responsiveness to the needs of people living with FASD, their families, caregivers and service providers.

What is the connection between the CNFASDP and the CanFASD Research Network?

In 2004-2005, the Partnership formed the Western/Northern FASD Research Network to address the urgent need for research on FASD and best practice guidelines to inform and guide work on diagnosis, prevention and intervention.

The Research Network quickly evolved to what is now the Canada FASD Research Network – a national Canadian charitable organization whose vision is to support Canada’s leadership in addressing the extraordinary complexities of FASD.

The Partnership invested in research to answer the critical questions arising from on-the-ground efforts to prevent FASD and support individuals with FASD. In turn, researchers were, and remain, very interested in being a part of a network with direct links to program practitioners and policy makers who are eager to translate research findings into practice.

CNFASDP creates a Strategic Priorities Plan every three years, incorporating the priorities of the Partnership jurisdictions. CanFASD supports the CNFASDP Steering Committee towards the advancement of these priorities and ensures CanFASD research priorities are in alignment.

How did CNFASDP create the Research Network?

At its inception, the Western/Northern Research Network was formed in a phased approach. Phases included:

  • Phase 1: Consultation and Leadership Development
  • Phase 2: Establishing the Network
  • Phase 3: Implementing the Research Plan

CanFASD is governed by a Board of Directors that aims to include representatives from its jurisdictional members (including CNFASDP jurisdictions). A member of the CNFASDP Steering Committee sits on the board as an ex-officio member.

How does government partnership benefit the FASD community?

  • Creates a forum for sharing information, collaboration and support on FASD initiatives.
  • Supports capacity to share educational/training sessions through conferences, symposia and videoconference links.
  • Establishes links with a variety of researchers associated with the CanFASD who can provide advice and assistance on province- or territory-specific research.
  • Enhances and streamlines ready access to up-to-date research findings on FASD.
  • Creates and facilitates opportunities to engage in discussions with researchers to better understand the implications of research for practice.
  • Provides the opportunity to influence the research agenda on FASD.
  • Supports a higher profile for and interest in FASD and FASD research.
  • CNFASDP’s leadership benefits all regions in Canada through cross-government integration and through the CanFASD’s work in knowledge development, research and translation.

What are the benefits of the Partnership to governments?

Collaboration and Shared Commitment

  • The Partnership serves as a mechanism for effective cross-jurisdictional collaboration and a coordinated approach to FASD policy, programs and services across western and northern Canada.
  • The Partnership can facilitate provincial engagement with the federal government on FASD issues when considering policy and program development, including past consultations with Health Canada and First Nations and Inuit Health.
  • It invites participation from other partner jurisdictions where applicable (i.e. webinars, prevention research, workshops and conferences).
  • Collaboration on FASD at the ministerial and officials’ levels is invaluable as jurisdictions continue to develop and implement provincial and territorial FASD strategies to improve the lives of Canadians living with this disability.
  • The Partnership serves to strengthen and sustain provincial/territorial commitment to FASD prevention, intervention, services and support.

Maximizing Impact

  • The Partnership serves as a forum for effectively leveraging provincial resources.
  • Each jurisdiction contributes a modest amount of funding, which is used collectively to support significant initiatives such as major conferences and symposia that help inform future policy and program development in partner jurisdictions.
  • Relatively few financial and human resource commitments are required to benefit from the expertise developed by other members of the CNFASDP.

Sharing Evidence-Based Knowledge and Best Practices

  • The Partnership provides excellent learning opportunities regarding best practices related to FASD. Partner jurisdictions with FASD strategies and action plans provide examples of best practice and approaches for prevention, intervention and support. This enhanced knowledge transfer supports service development and improvement within and across Partnership jurisdictions.
  • It provides opportunities for citizens in partner jurisdictions to participate in community-based research, such as Prevention from a Women’s Health Determinants Perspective. This research has informed the development of effective programs and policies related to FASD.
  • It shares diverse program approaches and organizational structures FASD prevention, intervention and support, helping to strenghten links between program areas and strategies.
  • The Partnership continues to benefit from the work of CanFASD, which delivers evidence-based research that supports the development of sound, clinical, and preventive practices.
  • Through the Partnership’s support, diagnostic processes and protocols have been enhanced. As a result of accessing research related to the diagnosis of FASD, partner jurisdictions, like Saskatchewan, have developed enhanced diagnostic capacity and expertise and follow-up supports post-diagnosis.

What types of activities is CNFASDP involved in?

Conferences

  • When the CNFASDP started hosting conferences on FASD, there were few other opportunities for people in western and northern Canada to come together to learn about FASD.
  • Now, there are a number of governments and groups offering FASD workshops and conferences on a regular basis.
  • To make the best use of resources without duplicating efforts, CNFASDP started alternating conferences with smaller symposia, designed to bring practitioners together for learning.
  • The Partnership aims to co-sponsor a FASD conference every four years, open to individuals and families with lived experience, service providers, researchers, educators, and government officials, to advance topics identified in the Partnership’s strategic priorities plan.

Symposia

  • The Steering Committee endeavours to host a symposium on FASD in one of the intervening years between FASD conferences.
  • The purpose of a symposia is to provide a smaller forum where professionals from across Partnership jurisdictions can come together to discuss issues specific to their area of practice and/or research and that focus on topics identified in the strategic priorities plan.

Webinars

  • The Steering Committee supports a policy webinar series focusing on strategic priorities of the Partnership in the intervening years of conferences and symposia.
  • Webinars serve as a forum for discussions and sharing of evidence-based knowledge with policy makers and government officials as the target audience.
  • Themes usually link to CNFASDP’s Strategic Priorities or address emerging issues that warrant focused attention.

How can I learn more about the CNFASDP?

If you are from a CNFASDP member jurisdiction, contact your provincial/territorial government steering committee representative. Please refer to the CNFASDP Steering Committee contact information.

CNFASDP Steering Committee Member Contact Information

Partner Jurisdiction Representative Email Website
AB Dana Robinson
Manager, FASD and Disability Initiatives
Ministry of Assisted Living and Social Services
dana.robinson@gov.ab.ca Fetal Alcohol Spectrum Disorder (FASD) | Alberta.ca
Kyra Tuff
Director, Statutory Oversight and Reporting/Disability Initiatives
Ministry of Assisted Living and Social Services
kyra.tuff@gov.ab.ca
MB Melanie Muehling
Manager, FASD Programs & Policy
Department of Families
melanie.muehling@gov.mb.ca Province of Manitoba | fs – Fetal Alcohol Spectrum Disorder (FASD)
Ken Lamoureux
Program and Policy Consultant, FASD Intervention
Department of Families
ken.lamoureux2@gov.mb.ca
NT Cygni Brown
Health Planner, Continuing Care
Department of Health and Social Services
cygni_brown@gov.nt.ca Fetal Alcohol Spectrum Disorder | Health and Social Services
Karin Bucher
Director, Seniors and Continuing Care
Department of Health and Social Services
karin_bucher@gov.nt.ca
NU Margaret Piercy
Health Promotion Specialist
Department of Health
mpiercey1@gov.nu.ca Fetal Alcohol Spectrum Disorder | Government of Nunavut
Zan Tao
Health Promotion Specialist
Department of Health
ztao6@gov.nu.ca
SK Denise Grad
Director, Continuing Care Branch
Ministry of Health
denise.grad@health.gov.sk.ca Fetal Alcohol Spectrum Disorder Services in Saskatchewan | Health Services for People with Disabilities | Government of Saskatchewan
Darla Boyle
Senior Program Consultant, Continuing Care Branch
Ministry of Health
darla.boyle@health.gov.sk.ca
Maud Amoafo Senior Project Manager, Continuing Care Branch Ministry of Health maud.amoafo@health.gov.sk.ca
YT Wendy McIntire-Cowx
Manager, Disability Services
Department of Health and Social Services
wendy.mcintire-cowx@yukon.ca Prevent fetal alcohol spectrum disorder | Yukon.ca
Stephanie Nobecourt
Policy Analyst
Department of Health and Social Services
stephanie.nobecourt@yukon.ca