Introducing the Child & Youth Well-Being Plan and Outcomes Framework
The Child and Youth Well-Being Action Plan (PDF, 8 MB) and Outcomes Framework (PDF, 3.5 MB) are part of a long-term effort to improve how systems work together across B.C. to support children and families – including how services like health, education, and community supports connect in practice.
This discussion forum is an opportunity to hear directly from people about what’s working, where there are gaps, and where improvements are needed.
On this page
- What are the Action Plan priorities
- Why your feedback matters
- What to expect from this engagement
- Share your thoughts
What are the Action Plan priorities
The Action Plan takes a broad, system-wide view, focusing on key areas where change can make the biggest difference in peoples’ lives – from strengthening families and preventing violence to improving coordination across services and advancing Indigenous self-determination.
Rather than focusing on any one service or program, the goal is to better understand how different parts of the system fit together – and how they are experienced in real life.
To help guide this work, the plan focuses on five priority areas. These areas are deeply connected. In real life, people’s experiences often span across multiple parts of the system at once.
Click below to learn more about each of the areas and the actions government is taking.
Helping families access the basics they need to thrive – like food, housing, income stability, child care, and early supports – so children can grow up safe and supported.
What we are doing:
- Providing school food programs
- Improving access to child care
- Improving access to supports for children with complex needs
- Adding more mental health supports in schools and communities
Preventing violence before it begins and creating safety and support for those impacted by violence.
What we are doing:
- Supporting school programs that teach healthy relationships
- Improving how police, courts, and services work together
- Providing safe housing and counselling
Improving how services work together across systems so that children, youth, and families experience coordinated, connected support – especially during times of crisis.
What we are doing:
- Building tools to connect services across government
- Supporting crisis response groups that act quickly
- Creating teams that work across health, schools, and social services
Supporting Indigenous communities to lead and deliver services grounded in their own knowledge, cultures, and governance.
What we are doing:
- Working with First Nations and partners on funding and agreements
- Supporting Indigenous-led programs and services
- Strengthening cultural connections for children and youth interacting with the child protection system
Ensuring that children and youth who are most at risk – including those in care or involved with multiple systems – are safe, supported, and connected to opportunities.
What we are doing:
- Strengthening resources to support families to keep children and youth safely at home
- Helping youth with housing, school, and jobs
- Improving care and oversight for children in care
Why your feedback matters
We want to better understand how people experience services and supports in real life: what’s working well, where there are challenges, and how things could work together better.
You don’t need to be an expert to take part.
You’re welcome to share:
- Your own experiences
- What you’ve seen in your community or around you
- Ideas about what could make a difference
Even if something hasn’t directly affected you, your perspective still matters. People’s experiences don’t fit neatly into just one area – and that’s helpful. We’re interested in understanding how different needs and supports connect in real life, even if they don’t match one specific topic.
What you share here will help us build a clearer picture of what’s happening across the system. It will help shape future work over time.
What to expect from this engagement
This is just the first step. Over the coming months, we’ll be opening up more focused discussions on different areas of the Action Plan. We’ll also share what we’re learning along the way and check back with you to see if we’ve understood things correctly.
In the next phase, we will:
- Open more discussion forums for each of the plan’s priority areas, so you can share your thoughts on the topics that interest you most
- Launch a survey to better understand what matters most to people across B.C.
- If you’d like to take part in those future discussions, you can sign up for updates to be notified when they start.
Making this engagement accessible
We want this process to be as open and accessible as possible. If you need support to participate or want to share your ideas in a different way, please let us know – we’ll do our best to help.
A note on inclusion
This work recognizes that children, youth, and families across B.C. have different histories, experiences, and priorities – including Indigenous communities, who are leading their own approaches to well-being based on their cultures, knowledge, and governance.
Receiving feedback from a wide range of perspectives is important to building a better understanding of how the system is working, and where it needs to change.
Share your thoughts
To begin, we want to hear your first thoughts about the Plan.
We’re asking a few broad questions:
- What stands out to you about this plan for children, youth, and families – and why?
- Are there areas where small changes in services, supports, or how systems work together might make a meaningful difference, or where more understanding is needed?
- Are there areas where broad scale changes are needed?
You might also want to think about:
- Where things are working well
- Where there are gaps or challenges
- Where different supports or services are working well together
There are no right or wrong answers. People will come to this conversation with different experiences, and we want to hear from as many perspectives as possible.
Please look at our Moderation Policy and Terms of Use before participating.
I really appreciate that this plan recognizes the importance of prevention, family-centred practice, Indigenous partnerships, and better collaboration across ministries and services. These ideas aren’t new to those of us working with children and families, but it’s encouraging to see them reflected in a provincial plan. It’s also great to see recognition that children’s well-being is influenced by much more than health care or education. Housing, food security, transportation, caregiver well-being, and strong communities all play an important role.
From my perspective as an Infant Development Consultant, the challenge isn’t knowing what needs to be done—it’s having the time, people, resources, and systems to actually do it well. Families don’t experience government in separate ministries. They experience one system, and when that system doesn’t work together, they’re the ones left trying to figure it all out. They repeat their stories over and over, navigate complicated eligibility requirements, and spend countless hours trying to figure out who to call next.
One area where I think relatively small changes could make a big difference is improving communication between services. Families shouldn’t have to tell their story multiple times or go through duplicate assessments when that information already exists. Better communication, shared service planning (with consent), and clearer referral pathways would reduce frustration for families and allow professionals to spend more time supporting children instead of navigating systems.
Helping families understand and navigate available services would also make a huge difference. Many parents don’t know what programs exist, what they’re eligible for, or how different services connect. Families are often expected to become experts in a system they’ve never had to use before, all while caring for a child with additional needs.
I also think the plan could place even more emphasis on the earliest years of life. We know the first three years are critical for brain development, and early identification and intervention can have a lifelong impact. Investing in services like Infant Development Programs, speech-language pathology, occupational therapy, physiotherapy, Supported Child Development, and family supports is one of the best investments we can make for children and families.
Where I think bigger system changes are needed is around service capacity. Collaboration is important, but collaboration alone won’t shorten waitlists or fill vacant positions. Many families are still waiting months, sometimes years, for developmental assessments, pediatric specialists, therapy services, and mental health supports. Frontline professionals are doing their best while managing large caseloads, but there simply aren’t enough people or resources to meet the need.
Working in a rural community brings additional challenges that I don’t think are fully reflected in the plan. In many rural communities, professionals already work closely together because we know each other. The bigger barriers are recruiting and keeping specialized professionals, limited local access to services, long travel distances, and even transportation challenges like BC Ferries. Better coordination is important, but it can’t replace services that simply aren’t available or unreliable.
I like the focus on measuring outcomes rather than just counting how many services are delivered. At the same time, if agencies are expected to collect more data, they’ll also need the time, funding, administrative support, and technology to do that well. Otherwise, it means more paperwork and less time spent with children and families.
One thing I found myself looking for while reading the plan was more information about how all of this will actually happen. The vision is strong, but I wanted to see more concrete details and less pretty buzzwords. What are the timelines? What funding has been committed? Who is responsible for each part? What are the priorities over the next few years? Without those pieces, it’s difficult to know how these ideas will move from a vision into meaningful change on the ground.
Overall, I support the direction of this plan. It reflects many of the values and practices that those of us in early childhood have believed in for a long time. My hope is that the next step focuses on turning this vision into action by investing in the workforce, reducing wait times, strengthening early intervention, and giving frontline agencies the resources they need to provide the coordinated, family-centred support that children and families deserve.
you need to combine MCFD and MOECC together, it is expulsion to not do this as the services for the poor and disabled should not be set to the side, it should be an integrated part of the services for all families, then all of the barriers and the “reporting of,” all happens together and communities can use the resources invested in by their municipalities of schools to fully support children and families.
The Community Care and Assisted Living Act needs to apply to children every where at all times. It is a legal requirement under Canadian laws.
Community Care needs to happen for children and families as early as possible, We are a cooperative species and if we can give infants the experience of being in large cooperative networks rather than small families (Sarah Bluffer Hrdy has proven the nuclear family model is inadequate to realize full human potential, but it was a great start) We need to start this asap to stop the harm that comes to families when they transition their children in to Kindergarten. The families with children with diversity need it ASAP.
A plan and framework is only as good as the leadership, capacity and funds to maintain the high demands for children and youth. Unfortunately, The cost of education and cost of living is a huge barrier for building capacity to carry out this plan. There needs to be a process for hiring staff that tests their actual willingness to support and understanding for children, youth and families. There is currently too many employees in positions that require a specific skill “caring” and they don’t have it and are straight and narrow attitude I do my job you do yours, no working together, no networking to build supports for those they are supporting. Voluntary programs for youth is so disheartening to a family struggling to get supports for their child that deeply needs it. We need option where youth will have services that are not just voluntary, a system to look back at services provided not just individual stats for funding purposes. This includes those that are in the education, social services and community services fields.
The first thing I noticed when reading about the plan was the lack of direct reference to a major commonality with people who are directly affected by these services: poverty. The rates for regular assistance and PWD must reflect reality. The fact that this is mostly overlooked is why I feel that this plan is not going to succeed. When families are living in poverty the children and youth will not thrive. Period. The involvement of MCFD, Family Law, Police and RCMP, health care, housing supports will not address the most common and fundamental cause of family breakdown: poverty and the layers of consequences. Increase financial supports in meaningful amounts and watch violence, children entering care, homelessness, incarceration and adverse health outcomes reduce drastically. Raise the rates, institute a universal minimum income, make food and housing affordable and abundant. No family should ever go hungry.
Appreciate:
– cross-government collaboration and strategic partnership- reduction of silos and shared visioning across government organizations is the only approach that will truly make a difference for British Columbians
-addressing wellness from multiple factors and lens, recognizing that primary needs being met with allow for more foundational and sustainable change
– up-stream approaches that are not all reactive
-recognition that enhancing wellness for children and youth, families builds more robust, safer, healthier communities
Needs more attention:
– experience of refugee, immigrant families and strategies to support. We have a growing population of immigrants to BC who come with medically complex children, those who have experienced trauma, need support with adjustment to Canada etc. This is missing in this framework- more intention should be on focused on this area
– children with medical complexity- the systems that children with medical complexity continue to be siloed, with disparate services and vastly different experiences in decision making, access and allocation of services geographically. I am not certain the new system properly addresses the inequities or needs, but rather moves the same funding around to spread across more people.
– need for caregiver benefits for longer for parents with medically complex/palliative children are not worrying about finances while also caring for their medically complex children- again, the experience is grossly different geographically
– Enhancing benefits through At Home program for food, nutritional supplements and other common needs that are not currently covered will enhance health and reduce financial burden on families
– Transportation for medical respite- not currently covered but as the only medical respite for palliative children is in LM, consideration should be included
I’m also curious about family engagement and having families involved directly in the drafting, revising, execution and outcome measures. Compensating families so they can be at the decision making table will be a significant step forward for family empowerment, health and wellness
The word “addiction” is only stated once in this action plan. I’m interested to learn more about the plan to expand mental health and addiction supports for parents and families with young children. Specifically, the action to “Expand the Road to Recovery Initiative to help support parents struggling with substance use issues to access services”.
The plan speaks of children in care and parents actively seeking support, but I’m concerned about families that may not have a history of involvement falling through the cracks. Specifically, children and youth experiencing substance abuse in the home and not knowing how to navigate support or resources for help. Is the weight of recognizing when children and/or youth may be struggling with substance misuse or abuse in the home, on the shoulders of the education system? Currently, BC’s education system is experiencing staffing shortages, limited resources, and decreased funding.
My question is: How will multi-ministry supports work together to improve family planning and resources for children and youth living with caregivers with addiction? Specifically, Health, Mental Health & Additions, MCFD, and Education.
For decades, Guardianship, CYSN, and CYMH staff have worked together to build integrated teams that support young people and simplify service navigation. Right now, the most vulnerable children and youth—those involved in child protection, CYSN, and CYMH—are all served within a single Ministry. This structure makes collaboration easier and reduces the risk of young people falling through service gaps.
No evidence has been presented to show that breaking the Ministry apart would improve outcomes for children.
The risk is that fragmenting services (by dividing the Ministry up) could create the same isolation and segregation we are trying to prevent. For example, doctors within Health Authorities already report significant challenges navigating the child welfare system, often noting that children fall between the cracks. If CYMH were moved into Health Authorities, the gap between mental health services and the child welfare system would widen even further—making coordination harder, not easier, for the young people who need it most.
– Lack of clarity in the plan — It is unclear what is happening, when it will occur, and who is responsible for each component.
– Use of “tell your story once” messaging — The A Pathway to Hope tagline (“Families will only need to tell their story once”) is not realistic. Privacy legislation such as FOIPPA, FIPPA, and the YCJA restricts broad information sharing; staff cannot know “everything about everyone,” even with a shared IT system; and families do not want all government staff to have full access to their personal information.
– Information sharing already exists—with consent — Professionals can already share information when consent is provided. The plan does not make it clear whether consent-based sharing will remain a requirement.
– Unclear cross‑ministry roles and responsibilities — A Pathway to Hope was designed as a cross‑ministry initiative, yet Integrated Child and Youth Teams have faced criticism for lacking clinical clarity, operational clarity, and role clarity. It is not practical for every Ministry to be responsible for mental health—just as it would not be practical for every Ministry to be responsible for policing or road maintenance. Allowing each community to design its own ICY model also recreates the same issues CYMH faced before a provincial model existed: inconsistent services, unclear clinical frameworks, and wide variation in family experience.
– Need for structured accountability tools — Using tools such as a RACI framework would help define roles, responsibilities, and accountabilities across Ministries.
– Navigator roles are promising — Early Help Navigators appear helpful, and adding Complex Situation Navigators could further support families with high‑needs cases.
– Public confidence requires clarity about Ministry changes — As Ministries merge or shift (MCFD, SDPR, Health, Citz), public confidence would improve if government articulated how the new structures will differ from past models, what research informs the changes, and what will be done differently this time.
– Creating Lean processes and centralizing services such as IMIT is an enabler to service delivery. Centralizing services is not the same thing as “families only need to tell their story once” it is about efficient use of resources
There is alot of mention of initiatives provided through schools. What about autistic children who cannot attend school due to burnout and bullying. With no supplement, no guaranteed benefit and an inability to go out into the community to access community supports, I feel children like my son will fall through the cracks.
Disbanding AFU and gutting the At Home Program are going to cost a lot more down the road. Our health, education and judicial systems will be overwhelmed even more than they are now.
This is a massive mistake and will cost our province much more in a few years.
We need to keep AFU and also create a similar system for other disabled children.
There are only 1200-2000 Down’s syndrome children in BC that we need to help. 36% of those children already have access to the At Home Program and have access to $17000 for therapy throughout their childhood. Those kids will see a reduction of this support in the new system.
The new system will mean many families will have to have one parent leave the workforce which will mean less taxes paid.
Youth with Special Needs and intellectual disabilities need better transition supports that are NOT solely driven by their parents, but by system navigators whose job it is to ensure appropriate connection and support to community is maintained when they age out of CYSN and Disability Services. CLBC and MCFD need to work together for ALLyouth who qualify for CLBC service on reaching the age of majority, not just youth in care who qualify for CLBC funding and services. CLBC needs to come into the picture earlier, and MCFD needs to do more to ensure financial and social supports for youth with special needs. Disability does not vanish at 19, but services, supports, and connections certainly do. It’s absolutely deplorable that youth who don’t have strong advocates in place oten go unsupported by CLBC because they don’t have advocates. It’s also absolutely deplorable to expect burnt out parents and families to continue doing ALL the heavy lifting, advocacy and support when it comes to fighting for services to be engaged once their youth moves to CLBC. Case management needs to be reintroduced to CLBC because as it stands now, vulnerable adults are regularly falling through the gaps in the “service based” model. This is contributing to homelessness, substance use, increases in disability impacts, increased isolation, and growing mental health challenges for youth and adults with special needs across BC. It’s gut wrenching to watch families fall apart when funding and support from MCFD abruptly stops and CLBC does nothing to engage nor support, citing lack of funding.
The BC Coalition to End Youth Homelessness policy asks emphasize prevention, continuity of care, and systems alignment so that youth aging out of care and/or facing homelessness experience stability, connection, and a genuine sense of belonging rather than repeated disruption.
Issue
Youth aging out of care face intersecting barriers across income assistance, housing, health, and child welfare systems that undermine stability, continuity, and a sense of belonging—significantly increasing the risk of homelessness.
Why this matters now
• Youth homelessness is preventable with timely, coordinated policy interventions
• Current system misalignment creates avoidable costs across emergency housing, health, and justice systems
• Government has an opportunity to strengthen outcomes for youth aging out of care by addressing known policy barriers
BCCEYH priority policy asks
1. Remove employment disincentives by raising or eliminating earnings caps for youth and former youth in care on income assistance
2. Link mental health supports to education and employment for youth receiving income assistance
3. Improve coordination between SAJE and housing systems, including better data transparency
4. Expand Specialized Homes and transitional housing to ensure stable housing for youth aged 17–27 leaving care
5. Expand age appropriate transitional housing options for 17-18 year old’s within BC Housing or allow 17–18 year olds access to supportive housing
6. Update the definition of Affordable rent so that it is tied to an individuals income, cost of living and not determined based on market rents.
What success looks like
• Every youth leaving care has access to stable, affordable housing for 2–5 years
• Youth can pursue education and employment without losing income security
• Ministries coordinate around shared outcomes, data, and transition planning
What we are asking for
• Cross ministry engagement to advance these policy priorities
• Commitment to coordinated planning and data informed decision making focused on youth homelessness prevention
Generation Squeeze has an excellent analysis of budgetary spending that shows “province is working far harder to protect spending that benefits residents of retirement age than to invest in younger residents…. According to Budget 2026, medical care will receive another $3.2 billion in new annual funding by 2028 — more than double the $1.4 billion added to K-12 education, child care, trades training, and social services combined. ” (https://www.gensqueeze.ca/2026_bc_budget_analysis)
I’m concerned about a plan that aspires to provide the support that children need is situated in a context with decreasing k-12 public funding. The public education budget not only fails to keep up with inflation, the ratio of government spending on education is DECREASING. This is abhorrent and makes a plan like this impossible.
You cannot support learners when there are not nearly enough EAs in classrooms. You can force more literacy screening, but a child with dyslexia (like mine) will not be adequately supported…..because…inadequate funding. There are not enough non-enrolling teachers to teach him to read! There is not enough money to buy decodable readers/ books for children like him to use.
Why are only low-occurring disabilities funded? Districts are supposed to magically stretch funds dedicated to the needs of a tiny few towards the needs of the unfunded many. This makes no sense and is in direct contradiction to a Plan like this. You will never be able to support children with disabilities in schools unless schools are adequately funded. They have the RIGHT to be supported.
You will not attain any of these mental health goals as there are inadequate counselors and trained mental health workers in schools.
You will not recruit and retain teachers into an under-funded system. They are stressed and over worked because students are not receiving the in-school support they require and deserve. They are leaving because they are working in untenable situations in buildings with decades of deferred maintenance (poor air quality, decaying buildings).
You speak of wanting to prevent intimate partner violence or substance abuse before it starts. Guess where children are ALL to learn about this in rigorous and research/ outcome supported ways? The k-12 PHE Curriculum. But a system that is chronically and acutely under-funded cuts what 1st? Music/ Drama/ PHE. Devaluing PHE means that children are NOT receiving the health education they deserve. BC has an incredibly strong PHE Curriculum that is not adequately delivered because…there are fires to put out with a shoe-string budget.
The plan is quite broad and general. Lots of descriptions like “strengthen, enhance, streamline, etc “. It’s lacking in specifics and how these steps will be actionable, and outcomes measured.
There are some holes in the plan. With the first example of Cole – he gets priority access to skip to the front of the assessment wait list. What about the other 500 children who are now waiting longer? It also take a whole lot more than one assessment to include a student at school meaningfully.
The other observation is about how inequitable services and supports are around the province.
My own experience is of so many cyclical loops and closed doors trying to navigate health and education systems for two children with chronic health conditions. Attendance can be difficult for health reasons and in the past there were homebound teachers and programming, but that has been eliminated in some districts and kids get tossed out to online schools. Parents of children who are homebound don’t have access to income supports unless the child is critically ill. My family has lost one full time income because one of us must be home at any given time to care for our children, and organize the online learning program and take kids to appointments.
That also means I’m only able to provide part time hours as an early intervention therapist for other people’s children as a vacancy remains unfilled at our local CDC.
Almost all of the mental health supports and rehabilitation therapy we’ve accessed has been through private providers as my children don’t qualify for public supports. Also, much of the health care and medication has not been covered. Disability tax credit helps, but that was a process that took several years to qualify for. We look forward to the disability benefit in 2027 as we’ve never had any access to disability funding supports before.
Across the document, including the illustrative stories (e.g., “Cole” and “Jonah”), the system response is framed around building coordinated supports after difficulties become visible through school disruption, reduced attendance, or crisis escalation. While the intent is to improve coordination, the practical effect in the examples is that children are already experiencing significant exclusion or instability before meaningful intervention occurs.
The plan also relies heavily on concepts such as:
* “integrated response tables”
* “family navigators”
* “early help specialists”
* “wraparound supports”
However, there is limited detail on:
* who is delivering these roles (existing clinicians vs new hires)
* how staffing shortages will be addressed
* how services will be distributed equitably across regions
* what enforceable expectations exist for schools and districts
This creates a concern that the plan is strong on system design language but unclear on implementation capacity and accountability.
From a school perspective, it also stands out that exclusionary practices (e.g., reduced school days, partial attendance, or removal due to behaviour or overwhelm) are treated as existing conditions the system responds to, rather than practices the system is required to prevent.
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What stands out to you about this plan for children, youth, and families – and why?
What stands out is the emphasis on managing complexity through coordination rather than ensuring baseline access to services within core environments like schools.
In the school-focused examples (e.g., Cole’s story), the child’s reduced access to education is not prevented but instead becomes the starting point for layered intervention:
* expedited assessments
* navigators
* therapy referrals
* financial supports
* housing supports
This creates a pattern where the system response appears to focus on building supports around exclusion rather than preventing exclusion itself.
This is particularly concerning in relation to children with disability-related needs who experience:
* sensory overwhelm
* anxiety-driven school avoidance
* behavioural responses to unmet needs
* inconsistent school attendance due to lack of appropriate supports
In these situations, families are often already:
* advocating across multiple systems
* managing inconsistent school responses
* trying to coordinate care without system support
The plan’s emphasis on navigation and coordination may improve experience in theory, but without clear guarantees of in-school support delivery and prevention of reduced instructional time, it risks shifting responsibility onto families to navigate increasingly complex systems rather than ensuring accessibility at the point of education.
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Are there areas where small changes in services, supports, or how systems work together might make a meaningful difference, or where more understanding is needed?
Yes—there are several areas where relatively targeted changes could significantly improve the effectiveness of the plan without requiring a full redesign.
1. Clear trigger points for early intervention (before exclusion)
More detail is needed on when supports are activated, especially in schools.
For example:
* Does repeated absenteeism automatically trigger support before schedules are reduced?
* Are there thresholds where intervention must occur before exclusionary practices are used?
Without this clarity, support risks being activated only after breakdown.
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2. Clarity on Integrated Response Tables vs school accountability
The Integrated Response Table model appears useful for coordination, but it is unclear:
* whether it can intervene early in school decision-making
* whether it has authority to prevent or reverse reduced school attendance decisions
* how it interacts with existing school governance structures
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3. Diagnosis vs needs-based access pathway clarity
The plan states supports should be needs-based, but in practice examples:
* assessment still functions as a gate to higher levels of support
More clarity is needed on:
* what supports are immediately available without diagnosis
* what supports require assessment
* expected timelines for assessment completion
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4. Workforce implementation detail
More understanding is needed on:
* which clinicians are expected to deliver supports (OT, SLP, psychology, etc.)
* whether new staff will be hired or existing staff redistributed
* how rural and high-need areas will be staffed
Without this, integration risks remaining conceptual rather than operational.
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Are there areas where broad scale changes are needed?
Yes—particularly in relation to schools, accountability, and inclusion practices.
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1. Preventing exclusion, not responding to it
A key gap is the lack of explicit commitment to prevent:
* reduced school days
* informal removal from classrooms
* partial attendance as a default response to disability-related needs
Broad scale change is needed to ensure:
children are not moved out of full participation in education as a first-line response to unmet needs.
Instead, supports should be embedded within full-time school participation wherever possible, with clear accountability when this is not achieved.
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2. Accountability for educational access decisions
The plan emphasizes shared responsibility across systems, but does not clearly assign accountability for:
* decisions to reduce instructional time
* ongoing exclusion from full participation
* cumulative loss of learning time
Without clear accountability structures (e.g., school districts or designated roles), exclusion risks becoming diffuse and difficult to challenge.
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3. Strengthening IEP commitments
The reference to new or updated IEP guidelines is noted, but the plan lacks clarity on whether these changes will be:
* enforceable
* rights-based
* linked to minimum service guarantees
Key missing elements include:
* whether IEPs guarantee access to specific supports
* whether there are consequences for non-implementation
* whether reduced instructional time is tracked or limited
As written, the IEP changes appear procedural rather than structural, and may not meaningfully change access to education.
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4. Shifting from reactive integration to proactive access
While integration is a central theme of the plan, the current framing risks:
* improving coordination after children are already struggling
* rather than ensuring early, embedded supports that prevent escalation
A broader shift is needed toward:
embedding supports in everyday environments (especially schools) before crisis or exclusion occurs.
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Where things are working well
There are important strengths in the plan, particularly in its recognition that:
* families are currently navigating fragmented systems
* coordination across health, education, and social services is often difficult
* Indigenous-led and culturally grounded supports are essential
* early help and prevention are important system goals
The emphasis on reducing administrative burden on families and improving system navigation is also positive in principle.
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Where there are gaps or challenges
The most significant gaps include:
* lack of implementation detail (workforce, funding, staffing)
* limited accountability for school-based exclusion practices
* unclear triggers for early intervention
* reliance on crisis or breakdown scenarios in examples
* limited clarity on enforceable service entitlements in schools
* diagnosis still functioning as a practical access bottleneck in some pathways
For families with children who experience ongoing overwhelm, school avoidance, or disability-related participation barriers, these gaps matter because they determine whether support arrives early—or after significant disruption has already occurred.
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Where different supports or services are working well together
The concept of integrated response (bringing schools, health, mental health, and social supports together) is strong in principle.
However, its effectiveness will depend on:
* whether teams are properly resourced
* whether they have authority to act early (not only in crisis)
* whether they can influence school-level decisions directly
* whether families still carry the coordination burden
Without these conditions, integration risks becoming an additional layer on top of existing fragmentation rather than a replacement for it.
I am currently a social worker and a person with multi-generational lived experience in care. I offer this feedback from both a professional and deeply personal perspective.
Over time, I have observed a recurring pattern in ministry initiatives that raises serious concerns for me about how new programs are implemented in practice. For example, education supports such as tuition waivers and other post-secondary funding initiatives were introduced with the intention of improving access for youth in and from care. While these programs are important, eligibility has consistently been tied to specific criteria, such as being in care at the age of majority or meeting minimum “time-in-care” thresholds. In practice, this means that many young people with significant care experience, particularly those who leave care earlier or who are placed in less formal arrangements, still do not qualify for these supports.
Similarly, the expansion of “out-of-care” or kinship arrangements has been framed as a way to keep children connected to family and community, which is fundamentally or most important goal. However, these arrangements are often paired with significantly fewer financial and structural supports for caregivers. The result is that children who would previously have been fully supported within the system may now receive reduced support, while no longer being counted as “in care.”
From both my professional experience and my lived experience, this creates a concerning dynamic. Outcomes can appear improved on paper, such as fewer children in care, while the actual level of support available to those same children and families is diminished. This disconnect is particularly difficult to witness as someone who has lived in the system and now works within it.
As I reviewed the Child & Youth Well-Being Plan, I also noted that it places significant emphasis on the challenges families face in navigating the current system, as well as the existence of long waitlists. These are important and valid issues. However, the plan does not clearly explain how the proposed changes will meaningfully reduce those waitlists in practice.
Much of the proposed solution appears to focus on improving coordination across ministries and creating more integrated approaches to service delivery so that families can more easily navigate the system and experience more connected care. While improved coordination is valuable, it is not clear how this approach will increase the actual availability of services or reduce demand pressures that are driving waitlists.
The concept of supporting families through system navigation, such as through coordinated teams or designated guides is not new, and could be implemented within the current structure through targeted roles. In other words, there is little preventing the ministry from hiring and resourcing system navigators within existing services today. It is unclear why a large-scale structural shift toward a more centralized “mega ministry” model is required to achieve this outcome.
While integrated service models can improve access and reduce barriers in some cases, evidence suggests that they primarily reduce duplication and improve coordination rather than eliminate waitlists altogether, particularly when overall service capacity remains unchanged. Without clear and significant investment in frontline staffing and services, there is a risk that waitlists will persist, even if the system becomes easier to navigate.
With this context, I approach the new Child & Youth Well-Being Plan and Outcomes Framework with caution and I don’t mind admitting a significant amount of skepticism. I am concerned about how it will be implemented, particularly given broader organizational changes currently underway. These include increased reliance on AI in practice, encouragement of retirements, lateral transfers that may reduce staffing stability, and indications that positions may not be refilled.
It remains unclear how the ministry intends to expand into a more integrated, cross-government model while simultaneously reducing its workforce and shifting responsibilities in this way. Without sufficient staffing and meaningful supports, there is a real risk that this framework could repeat familiar patterns, achieving administrative or structural improvements without improving real outcomes for children, youth, and families.
I welcome the Province’s commitment to improving child and youth well-being through prevention, coordination, family support, Indigenous self-determination, and addressing the systemic barriers that affect children and families. The Action Plan reflects an important shift away from crisis-driven responses toward creating the conditions that allow children, youth, and families to thrive.
I encourage government to strengthen this work by explicitly grounding the Child and Youth Well-Being Action Plan and Outcomes Framework in the UN Convention on the Rights of the Child (UNCRC). Children’s rights and child well-being are not separate concepts. Rights provide the ethical, legal, and practical foundation that helps duty bearers understand their responsibilities and remain accountable for outcomes.
Well-being tells us what we hope children experience. Rights clarify what governments, institutions, professionals, communities, and parents are obligated to do to make those experiences possible. Without a rights framework, well-being risks remaining aspirational. Rights transform aspiration into shared responsibility, expectation, and accountability.
Child rights literacy also offers a practical pathway for parents and professionals to understand and enact well-being in everyday practice. It shifts the focus from controlling children’s behaviour toward supporting their development, participation, protection, identity, belonging, and agency. In practice, this means moving from questions of compliance (“How do I get children to behave?”) toward relational questions (“What do children need, and what are we responsible for providing so they can thrive?”).
This shift is deeply aligned with reconciliation.
For too long, systems of childhood in Canada have been shaped by transactional and compliance-based assumptions: that children are recipients of adult decisions, that “good outcomes” are produced through control, and that professional authority sits above lived experience. These assumptions have also shaped colonial systems of child welfare, education, and family support, often disconnecting children from culture, language, identity, and relational belonging.
A rights-based and reconciliation-aligned approach requires a different foundation, relationalism.
Relational childhood recognizes that children are not objects of intervention but participants in relationships, systems, and communities. It affirms that well-being is not produced through compliance or extraction of “desired behaviours,” but through relationships of care, responsibility, reciprocity, and belonging. This aligns directly with Indigenous worldviews that emphasize interdependence, kinship, and the responsibilities that exist between people, land, and community.
Child rights provide the explicit expectations that make this relational shift operational. They clarify that children are rights holders, not passive recipients; that families are knowledge holders and experts in their own lives; and that culture, language, and identity are not peripheral, but central to well-being. This reframes the role of duty bearers from managing behaviour to upholding conditions in which children and families can thrive.
I was encouraged to see the Action Plan recognize that “families are experts in their own lives.” I would encourage government to extend this principle further by explicitly recognizing that children are also experts in their own lives, consistent with Article 12 of the UNCRC, and that their voices must meaningfully shape the systems designed for them.
Finally, I encourage greater attention to children’s lived realities in digital environments, where identity, relationships, participation, learning, and belonging are now continuously formed. A comprehensive child and youth well-being framework must include children’s digital rights as core to modern well-being and clarify the responsibilities of duty bearers in these spaces.
Children’s rights literacy offers a practical and necessary foundation for reconciliation-informed, relational approaches to well-being. It helps shift systems away from transactional models of childhood toward relationships of responsibility, accountability, and care—where well-being is not something done to children, but something created with them.
As both a parent of young children with support needs and a professional working as a social worker, this plan resonates with me in some areas, but also raises significant concerns.
What stands out most is the strong emphasis on coordination, early intervention, and integrating services across systems. In principle, this is positive. We know families benefit when systems communicate and wrap supports around them rather than expecting them to navigate multiple disconnected services. This reflects what many families, including my own, experience day to day.
However, what also stands out is that the plan often builds layers of support around system gaps instead of addressing the root issues. As a parent, I am already navigating multiple professionals for my children (behavioural consultants, interventionists, speech therapy, occupational therapy, daycare supports). The idea of adding further coordination roles is helpful in theory, but in practice, it risks increasing complexity without addressing the underlying barriers families are facing.
From a professional perspective, I am concerned about feasibility. The plan proposes expanding access to professionals such as clinicians, therapists, and specialized service providers. At the same time, we are already experiencing significant workforce shortages across these sectors. Waitlists are long, and recruitment and retention of qualified professionals is an ongoing challenge. Without a clear strategy to address workforce capacity, expanding services may further strain the system, increase wait times, and place additional pressure on families and frontline staff.
There is also a broader system pressure to consider. When services are difficult to access in a timely way, families turn to emergency departments, crisis supports, and other parts of the health care system. This increases demand on already over-burdened services and contributes to longer wait times for everyone. From what I see professionally and personally, delays in accessing early supports often result in escalation, which the plan is trying to avoid, but may unintentionally reinforce if capacity is not addressed.
Another area where more understanding is needed is how the plan will support very young children. For families with children under school age, like my own, access to formal assessments can be limited due to age. Many systems rely on diagnosis, but early childhood often requires support based on observed need rather than formal diagnostic thresholds. More clarity is needed on how young children will be equitably assessed and supported within this framework.
In terms of gaps, there continues to be a disconnect between policy intentions and lived experience. Families are often doing the work of coordinating services themselves, advocating for access, and managing risk in the absence of timely supports. While the plan acknowledges these challenges, it is less clear how it will address system accountability in a meaningful way.
Where things are working well is when supports are already integrated at a local level, such as when daycare, intervention teams, and clinicians collaborate directly. These moments show what is possible when systems genuinely work together.
Broad scale changes are needed in how services are resourced and delivered. This includes:
* Addressing workforce shortages across health and social service sectors
* Ensuring timely access to supports without requiring escalation or crisis
* Reducing reliance on diagnosis alone, particularly for young children
* Improving accountability for service access and delivery across systems
Overall, the plan reflects the right direction in terms of values and intent. However, without addressing capacity, system barriers, and accountability, there is a risk that it will add complexity rather than reduce it for families who are already navigating an overwhelming system.
From both my personal and professional experience, families do not need more layers — they need timely, accessible, and sustainable supports that meet their children’s needs where they are at.
In Protecting and Uplifting the Most Vulnerable, there is mention of keeping kids at home, and improving care and oversight for children in care. Where does kinship care fit into this? It is not mentioned in the action plan or outcomes framework. Kinship needs to be better supported, including for private kinship arrangements made outside the child welfare system. Child in the Home of a Relative program needs to come back to keep kids with family.
There are many positives to the plan with key steps having already been initiated with other programs and initiatives.
One thing that may be helpful would be a family navigator who stays with the family the entire time and are the go to contact for the family who then advocates for services based on their understanding of services. they bridge the gaps.
One caution is the level of division of current services such as CYMH for example. CYMH is already responsible for school supports, health and psychiatry, eating disorders, substance use, Foundry, ICY, and direct services to children and families, children and families in care, and community support and education.
In smaller communities you may have one clinician working alone trying to manage the competing expectations with increased needs and complexity even with early intervention.