Between 2017 and 2020, British Columbia’s Ministry of Education convened interest holders, appointed review panels, held consultations, and produced reports examining how the province funds inclusive education. Teachers, parents, trustees, and advocates spent hundreds of hours analysing proposals, documenting concerns, articulating alternatives. The Funding Model Review dominated education policy discourse for nearly three years.
The review asked: Should BC move from designation-based funding to prevalence-based funding?
The review avoided: What would it cost to adequately fund inclusive education?
Executive Summary
- Between 2017 and 2020, British Columbia’s Ministry of Education conducted a comprehensive review of how inclusive education is funded. The Funding Model Review presented itself as a choice between designation-based and prevalence-based funding for students with disabilities and diverse learning needs. It excluded the determining question: what it would cost to adequately fund inclusive education.
- Instead, the review evaluated two administrative mechanisms for managing scarcity.
- Under the current designation-based system, individual assessment is the gateway to support. Funding follows formal designation. Families with money, time, and institutional knowledge are more likely to secure assessments and services; families without these resources are far less likely to do so. Refusal is structurally easy. Denying support requires no justification or oversight, while granting it requires sustained advocacy, documentation, and exhaustion. The result is systematic under-identification: many disabled students remain unrecognised, managed through behaviour interventions or exclusion, and absent from official data. This undercounting allows the province to claim it funds “all identified students” while unmet need remains invisible.
- The proposed prevalence model appeared more equitable by allocating funding based on assumed population rates rather than individual designations. However, once identification no longer affects funding, assessment becomes administratively irrelevant. Over time, diagnostic infrastructure degrades, designation rates decline, and official data show “falling disability prevalence” despite continued exclusion. Measurement erosion becomes the justification for funding reductions.
- Designation-based funding organises denial through gatekeeping. Prevalence-based funding would organise denial through the degradation of measurement. The mechanism differs; the function does not. Both enable chronic underfunding while sustaining a narrative of responsiveness.
- By framing the issue as a technical choice between these models, the Funding Model Review avoided the question of adequacy altogether.
Table of contents
What the review actually evaluated
The Funding Model Review presented itself as a choice between two funding models for students with disabilities and diverse learning needs. The choice was framed as technical, administrative, procedural—a question of allocation mechanics rather than political commitment.
The current designation-based system requires individual assessments to access support. Funding follows formal designation. Students whose families can afford private assessment and navigate bureaucratic requirements may receive additional resources. Students whose families cannot, do not.
The proposed prevalence model would allocate funding based on statistical assumptions about disability rates in the population. Instead of funding individual designations, districts would receive block grants calculated from total enrollment multiplied by expected prevalence. Assessment would theoretically continue, but would no longer drive funding.
Both systems were presented as viable approaches to inclusive education. Both were described as responsive to student need. The debate focused on which model better served students, families, teachers.
This framing obscured what the models shared: neither was designed to adequately fund inclusive education. Both were mechanisms for managing scarcity while appearing responsive to need.
How designation-based funding organises denial
The current system rations support through access barriers.
Formal designation requires assessment. Assessment requires money, time, cultural capital, knowledge of system navigation, ability to sustain advocacy through bureaucratic delay. These requirements function as a class filter. Wealthy families purchase private assessments, hire educational consultants, retain lawyers when districts deny services. Poor families wait for underfunded school-based assessment that may take years, accept partial schedules and behaviour plans in place of support, watch their children excluded.
This is a system designed for denial: refusing accommodation is the path of least resistance, the default outcome, the architecturally embedded response to requests for support. Saying no requires zero justification, zero documentation, zero oversight, zero consequence. Saying yes requires families to overcome multiple redundant barriers, satisfy gatekeepers who are accountable to budgets rather than students, prove need to parties professionally invested in skepticism, and exhaust themselves navigating processes deliberately constructed to produce abandonment while performing consideration.
The system produces systematic undercounting. Many disabled students go unrecognised. They remain in classrooms without adequate support, managed through behaviour intervention, excluded when they struggle, disappeared from official counts of need.
This undercounting serves a political function. The Ministry can claim it funds “all identified students” while systematically under-identifying. Unmet need remains invisible because unrecognised students disappear from data. The gap between funding and need vanishes when need itself escapes measurement.
Denial distributes across thousands of individual cases. Each family experiences their child’s exclusion as unique failure—their inability to afford assessment, their failure to advocate effectively, their child’s particular struggles. The pattern becomes visible only in aggregate, and the current system produces zero aggregate measure of unmet need.
Administrative discretion operates at every level. Districts decide what “counts” as need requiring designation. Schools decide which students to refer for assessment. Individual administrators decide whether behavioural struggles indicate disability requiring support or defiance warranting punishment.
This discretion is described as flexibility, responsiveness to individual circumstances, professional judgment. In practice, it functions as denial management shaped by budget constraints.
The current system is underfunded, and it is politically sustainable. Harm distributes invisibly. Families blame themselves. Teachers absorb impossible contradictions. Children learn that access to education depends on how much suffering adults will witness before intervening.
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Protecting the ledger over the learner: operationalising scarcity in BC School Districts
British Columbia’s public schools are mandated to provide inclusive education for all students, but they do so in a context of chronic resource scarcity. Scarcity in education means there are not enough funds, staff, skills, or services to fully meet all student needs. School districts…
How prevalence funding would reorganise denial
The proposed prevalence model carried different risks that would produce similar outcomes.
Prevalence funding establishes a population-level assumption: X percent of students have disabilities requiring support. Districts receive funding based on total enrolment multiplied by this rate, regardless of how many students are formally identified.
This approach initially appears more equitable. It removes the financial incentive for districts to deny or delay assessment. It provides funding for students who need support but lack formal designation. It shifts from individual gatekeeping to population-level planning.
Teachers and advocates identified the flaw: prevalence funding delinks resources from identified need. Once funding becomes independent of formal designation, assessment becomes administratively irrelevant. Why invest in expensive diagnostic infrastructure when identification stops affecting the budget?
Over time, assessment capacity atrophies. Formal designation rates decline—the system stops facilitating recognition even as students continue struggling. Students still struggle. Teachers still request support. Official counts show “declining disability rates.”
The Ministry can then point to this decline as evidence that less funding is needed. “Our data shows the prevalence rate is falling. We’re adjusting allocations accordingly.” What appears as responsive resource management is actually manufactured justification for cuts enabled by measurement erosion the funding model itself produced.
Prevalence funding would make underfunding visible initially—there would be a clear gap between the prevalence rate used for funding and the actual population need. That visibility degrades over time as the administrative apparatus for measuring need disappears.
The mechanism of denial shifts from gatekeeping to measurement erosion. The function remains the same: enable chronic underfunding while appearing responsive to need.
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The budget is the behaviour
These responses do not aim for diplomacy. They carry the clarity earned through harm. Most families hold them quietly—unspoken but vivid—because many relationships still require us to perform gratitude after exclusion. These sentences arise from moments when a decision was made to withhold…
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The ABCs of engineered scarcity
A learning module for educators, caregivers, and community members resisting austerity logic in public systems. Engineered scarcity operates like a slow haemorrhage, draining public education of the resources it owes every child while masking that attrition behind soothing administrative dialects; this primer sets…
What adequate funding would require
The third option remained off the table throughout: population-based funding sufficient to actually support inclusive education.
This approach would establish population-level measurement with ongoing assessment infrastructure. All students would be counted. Disability would exist as a collective responsibility first—a population fact that districts must plan for and fund regardless of how many children secure formal designation in any given year.
Funding would be sufficient to provide universal design, proactive identification, publicly funded assessment, and individualised support. The system would include enforceable standards, regular adequacy reviews, and consequences for non-delivery. Assessment infrastructure would be public, accessible, and universal—privatisation and rationing would end.
Most critically: adequate funding would make denial visible and politically costly. The gap between population need and service delivery would be measurable. Underfunding would require explicit defense rather than operating through distributed administrative decisions.
This is why adequate funding remained excluded from serious consideration during the Funding Model Review. The review was designed to reorganise scarcity management, avoiding any determination of what inclusive education requires and any commitment to providing it.
Prevalence threatened to make underfunding visible by establishing a population baseline the Ministry would need to defend cutting. Opposition to prevalence gave political cover to abandon even that minimal constraint.
What remains enables maximum flexibility to underfund while avoiding accountability for doing so.
What complaint-responsive funding would require
Complaint-responsive funding treats exclusion as the primary accountability signal and funds its reduction.
It requires mandatory, transparent tracking of events that already produce harm and documentation: room clears, exclusions, partial schedules, reduced instructional time, behaviour plans that remove rather than support, parent complaints, teacher documentation of unmet need, Human Rights Tribunal filings, Ombudsperson complaints, and FOI requests related to exclusion.
Funding escalates automatically when harm persists: when complaint levels remain elevated over time, when exclusion increases in any category, or when advocacy labour intensifies. All data are published quarterly, compared against baselines and reduction targets. Missed targets trigger explanation, third-party review, and further escalation.
The objective is not better measurement but fewer exclusions. Zero tolerance exists for redefining harm out of existence.
Complaint becomes the funding signal. Reduction becomes the outcome.
Why this works: complaint as method
Sara Ahmed shows that complaint is how institutional violence becomes visible. Families already complain. Teachers already document harm. Students are already excluded.
The current system treats complaint as disruption to be managed. A complaint-responsive system treats complaint as data about institutional failure.
This approach works because it uses information that already exists, makes advocacy labour count, removes diagnostic gatekeeping as a precondition for response, and ties funding to lived harm rather than promised inclusion. It cannot be gamed through definitional shifts. A room clear cannot be rhetorically softened into accommodation.
Complaint makes denial legible. Publication makes it political.
Design vulnerabilities
There are some downsides to complaint-based funding, potentially, though it could be combined with other methods to get results.
Complaint suppression
Institutions are skilled at suppressing complaint. They discourage formal filing, exhaust families through process, retaliate subtly, redirect responsibility, isolate complainants, and reframe exclusions through language. Suppression is already a core cost-containment strategy.
Any model that ties consequences to complaint must assume suppression attempts and design against them.
Complaint-responsive funding does so by tracking multiple channels simultaneously. Suppressing parent complaints does not erase teacher documentation, exclusion events, tribunal filings, Ombudsperson complaints, or FOI records. Exclusion produces paper trails for liability reasons. Patterns across families, schools, and districts are harder to erase than individual complaints.
Transparency exposes anomalies. Sudden complaint drops without corresponding improvement trigger review. External audits, whistleblower protections, and mandatory publication make suppression itself visible and costly.
The complaints already exist. This model does not create vulnerability so much as surface existing suppression.
Strategic complaint inflation
A second vulnerability is incentive distortion: districts might benefit from higher complaint volumes if complaints trigger funding.
This risk is real and structurally limited.
Complaints are not administratively generated signals. They are costly, adversarial, reputation-damaging, and legally risky. Districts cannot fabricate them without tolerating sustained public evidence of exclusion, failure, and rights violations.
Complaint-responsive funding does not reward complaint. It responds to documented breakdown and demands its reduction.
Escalated funding is paired with timelines, outcome targets, and oversight. If complaint does not decline, funding escalation continues alongside audits, intervention, and political cost. A district attempting to game the system would be choosing sustained exposure, tribunal risk, and public documentation of failure.
That is not an advantage. It is a liability.
Why the vulnerabilities do not defeat the model
Complaint-responsive funding works only if suppression and inflation are harder than addressing harm.
This requires multiple data sources, automatic triggers, inter-district comparison, external oversight, and consequences for both exclusion and suppression. Designed this way, the path of least resistance becomes actual inclusion.
The current system already incentivizes suppression and denial. It simply does so invisibly.
Complaint-responsive funding makes those incentives legible, contestable, and costly. Even imperfectly implemented, it replaces hidden harm with public accountability.
That alone marks a structural improvement over systems that fund exclusion while pretending inclusion exists.
The system BC actually chose
By October 2019, working groups had completed their reports. Those reports noted that recommendations on inclusive education funding “would require extensive work to ensure there would be zero negative, unintended consequences for students.” When the Ministry announced phase one implementation in March 2020, prevalence funding was conspicuously absent. It had been deferred to “phase two”—a timeline with no specified endpoint.
The deferral was presented as evidence of responsive stakeholder engagement: government had heard concerns and would proceed cautiously. Four years later, phase two remains unrealised. Prevalence funding remains perpetually “under consideration.”
Instead of either strengthening the designation-based system or implementing prevalence funding, British Columbia introduced a hybrid that combines the worst features of both.
In March 2020, the Ministry implemented a new Priority Student Supplement, described as making operating funding “better represent the number of vulnerable students in B.C. schools.” The supplement covers children in care, students with mental health challenges, and students from low-income families. Disability—the population central to the prevalence debate—was explicitly excluded.
The supplement adopts population-based rhetoric while operating entirely through local discretion. There are no population rates, no transparent formulas, and no enforceable standards. Funding is provided “based on local needs,” preserving full administrative control over what counts as need and whether support is delivered.
This is prevalence funding’s language without its constraints.
Designation barriers remain fully intact for disabled students, preserving class gatekeeping through assessment access. At the same time, the system introduces a discretionary supplement that mimics population-level recognition while eliminating population accountability. Procedural accountability was added—districts must engage parents, monitor outcomes, and report publicly—while accountability for adequate resourcing was explicitly avoided.
The result is a configuration worse than either prevalence funding or a strengthened designation system. It combines:
- the class gatekeeping of designation-based funding, where only families with resources secure recognition for disability
- the accountability-free discretion associated with prevalence funding, without any population baseline to defend
- the exclusion of both the population visibility prevalence would create and the enforceable rights a properly resourced designation system could provide
Each component enables chronic underfunding through a different administrative mechanism:
- Designation-based funding makes recognition expensive, undercounts need, and allows government to claim it funds “identified students” while systematically under-identifying.
- Prevalence funding would make recognition irrelevant to funding, degrade assessment infrastructure over time, and justify cuts as official rates decline.
- The priority supplement uses population rhetoric while operating through discretionary allocation, producing zero accountability for adequate support.
What makes the current system uniquely harmful is not any single element, but their combination: designation barriers are preserved, administrative discretion is expanded, population accountability is eliminated, and a discretionary supplement creates the appearance of responsiveness while enabling denial.
The Funding Model Review avoided asking what adequate funding would require. It asked instead how scarcity could be reorganised to make underfunding more politically sustainable.
The answer was operational, not accidental: preserve designation barriers, defer prevalence indefinitely, introduce a discretionary supplement with population language, and add procedural accountability without funding requirements. The result is maximum flexibility to deny support while appearing responsive to need.
Comparing funding models
The Funding Model Review presented a choice between designation-based funding and prevalence-based funding. Both were described as viable approaches to inclusive education, differing only in administrative mechanics.
This framing obscured what matters: under conditions of systematic underfunding, both models function as mechanisms for organising denial while appearing responsive to need.
A third option—adequate population-based funding with enforceable accountability—remained excluded from consideration throughout.
A fourth option—complaint-responsive funding that treats exclusion itself as the measure requiring response—was never considered, despite complaint data already existing and advocacy labour already being performed.
The table below compares these four approaches across key dimensions. The systems differ in how they ration support, who bears the burden of advocacy, and how visible they make underfunding. What designation, prevalence, and the current hybrid system share is the capacity to enable chronic under-resourcing while claiming responsiveness to student need. What adequate funding and complaint-responsive funding share is that both make denial visible and politically costly—which is precisely why neither was seriously considered during the review.
Comparison of funding models for inclusive education in BC
| Dimension | Current designation-based system | Proposed prevalence model (deferred to “phase two”) | Adequate population-based funding | Complaint-responsive funding (Sara Ahmed model) |
|---|---|---|---|---|
| How disability is counted | Individual assessments required for each student | Statistical assumption based on population rates | Population-level measurement with ongoing assessment infrastructure | Tracked through exclusion events, complaints, advocacy labour, documented harm |
| Who gets recognised | Students whose families can afford/navigate private assessment | All students assumed to exist at population rates (initially) | All students, with proactive identification and universal design | Students whose exclusion generates complaint—then the complaint itself becomes the measure requiring response |
| Funding mechanism | Per-student amounts tied to specific designation categories | Block grants based on total enrollment × prevalence rate | Sufficient base funding + targeted supplements based on demonstrated population need | Funding increases automatically when complaint levels rise; decreases only when exclusion demonstrably falls |
| What happens to funding over time | Undercounts need through access barriers; appears “responsive” while systematically under-resourcing | Assessment infrastructure atrophies → official rates decline → funding cut to match “declining need” | Funding grows with enrollment and population-level indicators; regular review ensures adequacy | Funding must increase until complaint drops to 2% of baseline within 3 years; sustained complaint triggers automatic funding escalation |
| Class dynamics | Wealthy families buy access to designation; poor families go without | Initially more equitable access, but declining assessment means declining recognition for everyone | Universal access through publicly funded assessment and supports | Complaint is already distributed across all classes; tracking makes that labour visible and compensable; poor families’ complaints count equally |
| Administrative discretion | High (districts decide what “counts” within categories) | High (districts decide how to allocate block grant) | Constrained (funding tied to enforceable standards and population accountability) | Zero—complaint level determines funding; districts must reduce exclusion or explain publicly why complaint persists despite resources |
| Visibility of underfunding | Invisible (unidentified students disappear from data) | Initially visible as gap between prevalence rate and funding; becomes invisible as rates artificially decline | Visible through gap between population need and service delivery | Maximally visible—every complaint is tracked, published, attributed; harm becomes the metric government must address |
| Assessment infrastructure | Privatised, expensive, inaccessible | Becomes irrelevant to funding → degrades over time | Publicly funded, proactive, universal | Less relevant—exclusion itself demonstrates need; complaint removes burden of proving disability before receiving support |
| Accountability mechanism | Zero (only identified students “count”) | Weak (can point to prevalence rate but zero enforcement) | Strong (population-based targets with consequences for non-delivery) | Strongest possible—districts accountable for reducing actual harm, measured through complaint; failure triggers automatic intervention and funding increase |
| Primary function in practice | Rations support through access barriers | Rations support through measurement erosion | Actually funds inclusive education | Makes harm politically costly; converts advocacy labour into accountability data; forces system to address exclusion or face escalating public documentation of failure |
| Who benefits | Wealthy families (can buy designation); administrators (discretion to manage budgets) | Administrators (flexibility without accountability); government (declining rates justify cuts) | Disabled students and their families | Students currently being excluded; families already doing advocacy labour; teachers documenting harm; system becomes accountable to those experiencing violence |
| What it enables government to say | “We fund all identified students” (while making identification inaccessible) | “We fund based on population rates” (while allowing those rates to artificially decline) | “We fund inclusive education adequately” (and can be held accountable when we fail to) | Zero evasion possible—government must say “complaint is falling because exclusion is falling” or admit failure publicly |
| Mechanism of denial | Gatekeeping through cost and bureaucracy | Measurement erosion (disincentivise assessment → rates fall → cut funding) | Zero—denial becomes visible and politically costly | Impossible—complaint itself is the measure; denial requires explaining why harm persists despite resources |
| Long-term trajectory | Chronic undercounting + growing gap between need and recognition | Declining official disability rates used to justify funding reductions | Funding keeps pace with population need | Complaint-driven escalation until exclusion becomes rare; system must actually solve problem or face permanent documentation of ongoing harm |
| Political vulnerability | Low (zero population baseline to defend) | Medium (must defend cuts to established rate) | High (cuts are visible and attributable) | Extreme—every excluded child, every complaint, every room clear becomes public accountability data; government cannot hide behind measurement disputes |
| What it costs | Underfunded but politically sustainable (harm is distributed and invisible) | Underfunded and politically sustainable (appears responsive, enables managed decline) | Adequate funding (politically difficult but necessary) | Whatever it takes to reduce complaint to 2% of baseline—cost is determined by actual harm reduction, not administrative convenience |
| What it measures | Designation (bureaucratic category) | Prevalence (statistical assumption) | Population need (measured capacity gap) | Harm (complaint, exclusion, advocacy labour, documented violence) |
| Who does the work | Families (navigate assessment, prove need) | Districts (allocate block grant) | System (proactive identification and support) | Families already doing advocacy—but now that labour counts as data requiring systemic response |
| Current status in BC | ✓ This is what we have (with added discretionary “priority supplement” for some vulnerable populations, excluding disability) | Proposed 2017-2020, deferred to “phase two” in March 2020, remains unrealised four years later | Excluded from consideration throughout the Funding Model Review | Theoretically possible using existing complaint data; would require transparent tracking and automatic funding escalation triggers |
Designation-based funding sustains itself because it distributes denial across thousands of individual cases and produces zero aggregate measure of unmet need. Prevalence funding would eventually become sustainable as assessment infrastructure degrades and official rates decline, providing justification for cuts. Adequate funding creates political difficulty because it makes the cost visible and creates enforceable obligations. Complaint-responsive funding creates maximum political difficulty because it makes harm visible, attributable, and automatically escalating—which is precisely why it remained unthinkable within the review’s framework.
Different measurement tools identify different disabled populations. Change the measure, change who is recognised, funded, supported, denied. Change the population, change obligation itself.
This describes measurement design operating as intended under scarcity. When commitment to fund actual need is absent, measurement becomes the mechanism through which governments decide which needs to make visible and which to systematically erase.
Complaint-responsive funding threatens this logic. It makes erasure impossible. The harm is the harm. The exclusion is the exclusion. The complaint cannot be defined away.
The Ministry of Education understood this. That is why it advanced prevalence funding without releasing concrete formulas, consulted without providing the models being evaluated, withdrew the proposal without strengthening the alternative, and proceeded with a system that maximises administrative discretion while minimising accountability. That is why complaint—despite being the most direct measure of institutional failure—was never considered as an accountability mechanism.
What disability advocates warned
Every critique of prevalence funding that emerged during the review was grounded in evidence, experience, and analysis of how these systems operate elsewhere.
Teachers warned prevalence would delink funding from need and enable long-term underfunding. They were correct—the Ministry deferred it rather than implementing safeguards.
Parents warned designation barriers exclude poor families and make recognition inaccessible. They were correct—those barriers remain fully intact.
Disability scholars warned that measurement shapes obligation and that elimination of population accountability would shift all burden onto individual advocacy. They were correct—the new priority supplement operates through the same discretionary mechanisms it was meant to replace.
These warnings were specific, documented, repeatedly communicated. The BC Teachers’ Federation published detailed analysis in October 2019 titled “No Model and No Mandate,” documenting how consultation proceeded without access to concrete proposals and how the Ministry refused to provide the formulas, data, or assumptions that would allow meaningful assessment of implications. Parent groups testified at consultations. Advocates submitted written briefs outlining exactly what would happen under each scenario.
The Ministry responded by implementing new accountability measures. Districts must now “engage parents, caregivers and community members in the development of school district strategic plans,” “continuously monitor and publicly report on student outcomes,” and “ensure strategic plans and financial decisions are focused on improving student outcomes.”
These requirements mandate process while guaranteeing zero resourcing. Districts must engage parents—while retaining discretion over whether to fund the supports parents request. They must monitor outcomes—while retaining discretion over whether students receive services. They must focus on student needs—while remaining constrained by existing budgets.
This is accountability theater. It creates the appearance of responsiveness through procedural requirements while avoiding accountability for the only thing that matters: whether students actually receive adequate support.
The Ministry heard the warnings. It had access to research on how prevalence funding operates in other jurisdictions. It understood that designation-based funding without adequate assessment infrastructure produces systematic exclusion. It understood that discretionary supplements without enforceable standards operate as denial management.
It proceeded with the configuration that preserves maximum flexibility to underfund: designation barriers intact, prevalence deferred indefinitely, discretionary supplement introduced, procedural accountability implemented, adequate funding perpetually excluded.
The outcome was structural, predictable, designed.
Also see:
BCEdAccess – May 2018 submission https://bcedaccess.com/2018/05/01/thoughts-on-the-funding-model-review/
- Key quote: “changing the funding model alone won’t change much if the funding level itself isn’t adequate. The resounding consensus from the many submissions we have read to date make it clear, as it is to us, that more money is needed, not simply a new model.”
InclusionBC – January 2020 https://inclusionbc.org/proposed-education-funding-model/
- Highlighted concerns about lack of concrete model, need for economic modelling transparency, risks to individualized needs
BCTF – October 2019 “No Model and No Mandate” https://www.bctf.ca/news-and-opportunities/news-details/2019/10/02/no-model-and-no-mandate-bc-s-flawed-funding-model-review-for-public-education
- Damning critique: “Consultation with education system stakeholders has ended without the Ministry of Education revealing a concrete model of the proposed changes”
BCTF – January 2019 “A Recipe for Inequity” https://www.bctf.ca/news-and-opportunities/news-details/2019/01/01/report-of-the-funding-model-review-a-recipe-for-inequity-for-students
Patti Bacchus (former Vancouver School Board chair) – November 2018 https://www.straight.com/news/1162331/patti-bacchus-bcs-education-funding-review-headed-trouble
- Key quote on class dynamics: “parents who have the means to get their kids privately assessed…are able to use that information to advocate for their kids…That’s a major equity issue, and I fear a shift to a prevalence model could make that a whole lot worse”
- Critique of lack of transparency and inadequate funding
From measurement to exclusion
When disability recognition is unstable and funding discretionary, the gap between need and support fills with crisis.
Children attend classrooms whether or with recognised disability status. When supports are denied or delayed, strain manifests elsewhere. It appears as behaviour that teachers must manage without adequate resources, as learning gaps that widen without intervention, as social exclusion that intensifies without support, as children in visible distress that schools lack capacity to address.
The system creates impossible conditions, then holds individuals accountable for them. Teachers are evaluated on classroom management and student outcomes while managing need that exceeds available support. Students are disciplined for behaviour that expresses unmet need. Families are blamed for their children’s struggles and told to accept partial schedules, behaviour plans, or placements elsewhere.
When inclusion is inadequately resourced, exclusion becomes the path of least resistance. This too is designed for denial—exclusion requires minimal justification, operates through distributed administrative decisions, generates zero visibility in aggregate data. Inclusion requires fighting bureaucracy, justifying every accommodation, proving need repeatedly, sustaining advocacy despite exhaustion. The system makes saying no easier than saying yes at every level.
Shortened school days. Behaviour intervention plans that demand conformity rather than provide support. Suspensions for disability-related conduct. Pressure on families to withdraw children who “aren’t a good fit.” Room clears that remove students from learning environments they have a right to access.
These practices are predictable outcomes of funding architecture that makes support discretionary while making exclusion administratively simple. The current system produces the conditions that make them appear necessary, even inevitable.
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Engineered famine in public education
In British Columbia schools today, we are not facing a behaviour crisis—we are facing a famine of care. This essay weaves together personal memory, systemic critique, and deep empathy for teachers and families alike to ask why our schools are starving the very…
The choice that was made
British Columbia chose to preserve administrative discretion rather than constrain it. The government refused to limit its own flexibility.
The Funding Model Review made this choice explicit. Teachers warned what designation barriers produce. Parents explained how the absence of population accountability shifts burden onto individual families. Disability scholars describe how measurement creates obligation—and how scarcity transforms every measurement system into a rationing device.
The Ministry responded by deferring the recommendations that would have imposed constraints, however imperfect, on administrative discretion. Prevalence funding was pushed into a “phase two” with no timeline and no commitments. Four years later, it remains unrealised.
What was implemented created the appearance of population-level responsiveness without population accountability. The Priority Student Supplement was framed as funding that “represents the number of vulnerable students,” while operating entirely “based on local needs.” Population language was adopted; population constraints were not.
Procedural accountability was added without resourcing accountability. Districts must consult, monitor, and report. They retain full discretion over whether to fund the supports those processes identify as necessary. The system mandates process while guaranteeing no obligation to act on its findings.
This configuration serves administrative flexibility rather than student need. Designation barriers remain intact. Discretion expands. Population baselines disappear. Enforceable standards never materialise. Scarcity is preserved while responsibility is diffused across thousands of individual decisions.
These constraints are not inevitable. The province could fund inclusive education adequately. It could establish population-level accountability. It could invest in public assessment infrastructure. It could create enforceable obligations for service delivery.
It chooses otherwise. The Funding Model Review revealed that choice with unusual clarity.
When interest holders demanded adequate funding, the Ministry offered a choice between mechanisms for managing scarcity. When teachers warned about prevalence risks, prevalence was deferred indefinitely while a discretionary supplement was introduced that mimics population-based funding without its constraints. When parents demanded accountability, officials implemented procedural requirements while avoiding accountability for adequate resourcing. When advocates documented systematic exclusion, the Ministry pointed to record spending while exclusion continued.
The pattern is consistent: advocacy is answered by reorganising denial, while adequate funding remains excluded from consideration.
Clarifying district behaviour and spending
It is important to be explicit about what this system produces at the district level. Districts are not reliable advocates for additional funding, nor are they consistently spending the resources they already receive on inclusive education—even amid widespread exclusion.
District leadership is evaluated on budget compliance, not inclusion outcomes. Unspent funds signal fiscal responsibility, not unmet need. Asking for additional resources requires districts to demonstrate failure, risk audit scrutiny, and invite political conflict with a Ministry that has made clear it will not fund adequacy. In this context, restraint is rewarded. Demand is penalised.
The result is a system where exclusion can coexist with underspending. Students are removed from classrooms. Supports go undelivered. Families escalate complaints. Meanwhile, districts report balanced budgets and return funds at year’s end, reinforcing the narrative that existing allocations are sufficient or even generous.
Procedural accountability does not correct this. Consultation, reporting, and engagement requirements generate documentation without obligation. They surface need without triggering funding. Districts may acknowledge exclusion in reports while remaining structurally disincentivised from responding to it with spending.
This is precisely why population accountability matters. Without a population baseline, districts are never required to defend the gap between exclusion and expenditure. Under-spending becomes evidence of efficiency rather than evidence of harm.
In this system, neither the Ministry nor districts are required to ask the most dangerous question: if students are excluded and funds remain unspent, what is the funding actually for?
What this reveals about inclusion
The language of inclusive education saturates provincial policy. The Ministry affirms commitment to diversity, belonging, and student-centred learning. Districts publish inclusion plans. Administrators attend professional development. Teachers implement differentiated instruction in classrooms that lack the resources to support it.
Meanwhile, disabled students are excluded at rates that would constitute crisis if applied to any other identifiable group. Families exhaust themselves securing supports that should be guaranteed. Teachers manage harm they did not create and cannot remedy within existing constraints.
The gap between inclusion rhetoric and exclusion practice is not accidental. Rhetoric provides legitimacy. Practice manages scarcity. The funding architecture ensures these can coexist indefinitely.
Inclusion becomes something the system describes rather than delivers. Exclusion occurs through dispersed individual decisions rather than explicit policy. Accountability becomes impossible because commitment is expressed in language rather than operationalised through funding.
This is governance without population accountability: organised abandonment administered through routine discretion and justified by resource constraints that are themselves political choices.
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The economics of abandonment
When districts exclude children from school, the funding does not follow the child home. The money remains captured within institutional accounts, redirected toward students who attend, while parents absorb the cost of providing education systems are legally required to deliver. I’ve reduced my…
The question still refused
The Funding Model Review is complete. Phase one was implemented in March 2020. Phase two—where inclusive education funding reform was deferred—remains perpetually forthcoming.
As long as reform is described as “in progress,” the current system can be framed as transitional rather than structural. Exclusion can be attributed to implementation gaps rather than design. Advocates can be told to wait for a phase that has no endpoint.
The review’s central debate—designation versus prevalence—was resolved through indefinite deferral, paired with a discretionary supplement that gestures toward population-based funding without accepting its obligations.
The question still refused is simple: What would it cost to adequately fund inclusive education in British Columbia?
A related question remains equally unasked: What if complaint itself were treated as a measure of institutional failure and funded accordingly?
Until adequacy is addressed as a political commitment rather than a technical problem, every measurement debate will serve the same function—reorganising how denial operates while avoiding accountability for choosing denial as policy.
Teachers know this. Parents know this. Disabled students and their families know it because they are already filing complaints, documenting exclusions, and performing the advocacy labour that an accountable system would make unnecessary.
The choice stands between adequate funding for inclusive education and continued reliance on funding architectures designed to make inadequacy politically sustainable.
British Columbia made that choice during the Funding Model Review. Everything since confirms it.
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How public schools tax disabled families twice
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