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The government already handles sensitive information like tax records, census data and vehicle registrations because these systems are essential for running society. Health data is just another branch of what's already routinely done. Monitoring notifiable diseases like HIV and Hepatitis —and environmental exposures like asbestos and smoking— has been key for public health. Population-level surveillance drives prevention and progress, as seen in the dramatic reductions in HIV through targeted interventions. These existing disease registries show that sensitive data can be collected while remaining confidential, professional and neutral.
If the government uses this data for any sort of publication, researchers focus on population patterns, not individual stories. Data is anonymised early in the collection process, stripping out names and personal identifiers. If data mishandling is the concern, the solution is stricter penalties and better regulation, not abandoning research and potential solutions. I'd argue that personal privacy can be a significant barrier to societal progress, but that argument isn't even necessary here. It is entirely possible to defend personal privacy while recognising that responsible public health research can be performed.
Rates of autism spectrum disorder and ADHD, especially among children, have risen sharply. These are not simply lifestyle quirks but recognised medical diagnoses, often involving significant developmental impacts. Routine surveillance has long been the early warning system for public health threats. Environmental factors could very plausibly be contributing to rising ASD rates. Gathering and analysing broad health data increases the chance of identifying risks early and preventing harm for future generations.
Concerns about data misuse are understandable if you are a conspiracy theorist, but they collapse when you consider the reality of a government worker. If someone genuinely believes anonymised public health data can be used to cause harm, they should be able to explain exactly what harm would occur, how it would happen, how a government worker would have the power to enact it, how it would go unnoticed by their colleagues and why it would outweigh the public health benefits. Otherwise, the fear is just a conspiracy boogeyman. I don't think that everyone else should suffer worse health outcomes because of your phobias
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Your risk/benefit balance seems very skewed here. Just because there is one dodgy place doesn’t mean we should over-react and sabotage potential breakthroughs on a national or even global scale. If you snapshot the US right now, you would find a fraction of people driving under the influence of drugs/alcohol, but we don’t ban cars because of it. Why not just advocate for the closure of the JRC specifically rather than throwing the baby out with the bathwater?
From what I understand, the state isn’t exactly in favour of the JRC either. It seems to occupy a fringe position where its survival relies on legal technicalities and constant debate. When it has been under threat, parents and relatives of those in care have protested, suggesting that some people genuinely benefit from it. The JRC apparently handles the extreme cases where other treatment centres have failed. If someone is too challenging to be managed at a regular SEN school, they likely don’t have the capacity to make autonomous, informed decisions about their treatment. In such cases, best interest decisions are standard practice, even if that means using interventions the individual doesn’t enjoy. It’s not ideal, but it’s often the lesser evil compared to someone with severe mental illness roaming untreated and posing a danger to themselves or others.
The main controversy around the JRC is the use of electric shock therapy. Shock therapy tends to get a bad reputation from outdated films, but in reality it can sometimes be painless and helpful. I don’t know the exact methods used at the JRC, and it might well be problematic, but each patient’s case goes through a court review before treatment starts, which suggests there is some safeguarding in place (more than any other medical treatment I know anyway). For most medical treatments, you don’t see any real state oversight or gatekeeping. Things tend to get messy when non-medical people get involved in treatment decisions, as we’ve seen with abortion debates.
I’m not defending the JRC. I just think the focus should be on research and prevention so people don’t end up needing a place like that in the first place. If your problem is with the JRC, it doesn’t make sense to conflate that with routine health data collection. The mild-moderate autistic person reading the news and scrolling Reddit is not suddenly going to become cannon fodder for government experiments. Medical law already has plenty of safeguards when it comes to consent, institutionalisation and treatment.
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It's difficult to see one video without context and inside knowledge — then use this as justification to negate all the possible current/future benefits of nation-wide research.
The tapes don't immediately shock me. I've treated people with autism who will scream like that when they hear a sound they don't know in an unfamiliar environment. I'd say it's difficult to correlate the reaction to the severity of the stimulus unless you know the person as an individual. So while it looks shit, I don't feel it gives me any good read on the situation
I don't understand the treatment or why someone would perform it in a manner that is distressing. I would say it's against human nature to intentionally aim to cause pain to someone without a perceived benefit. Even if you find that kind of psychopath, it is then even more unlikely that you'd get them acting in a professional setting surrounded by several other people — without anyone whistleblowing, objecting or raising concerns.
I would want that reviewed formally with interrogation to see whether everything was performed in the correct manner. It seems there is good surveillance throughout and medical documentation can supplement. If it was performed as planned, ensure to review whether the treatment plan is actually appropriate. There are plenty of malpractice reviews and there's an established process for it. If there are medicolegal concerns, then changes are made and audited or whatever based on severity.
I get your concerns. I just think you have to jump through a few unlikely hoops to condemn that institution. And then you have to jump through many more hoops to justify why the 250 people in JRC, of which only 20% receive electric therapy, of which all cases have been court-reviewed — override the vast societal benefit of researching a surging mental health crisis and progressing prevention/treatment for everyone else. When we have robust medicolegal frameworks, consent/capacity/autonomy rules, whistleblower policies, surveillance, medical documentation, etc — it deserves quite thorough assessment show all of these safety netting those processes failed here, and continue to fail, despite their problems being known and under public scrutiny.
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JRC funding and practice
Location and Function
The Judge Rotenberg Centre is located in Canton, Massachusetts. It is a private facility operating as a residential school and treatment centre for children and adults with severe developmental disabilities or behavioural disorders. The institution is known for its use of aversive interventions, most notably electric shocks via a device known as the Graduated Electronic Decelerator (GED).
Population and Practices
Legal Status and Governmental Position
Federal Level
State Level (Massachusetts)
International Condemnation
Outcomes and Evidence Quality
Funding Sources
Source | Details |
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State and local government | Massachusetts has paid over $170 million to JRC over the past decade. |
Federal Medicaid | Residents funded via Home and Community-Based Services (HCBS) waivers. |
COVID-19 relief | JRC received $1.7 million in federal pandemic relief in 2020. |
Public funds continue to support the centre through legally permitted contracts with school districts and state departments, particularly where families and courts have authorised placements.
Mechanisms Permitting Continued Operation
Conclusion
The JRC remains operational and publicly funded despite international and domestic condemnation. This is due to legal authorisation frameworks, divided jurisdiction, failed legislative reform and judicial rulings that protect individualised medical plans. The centre operates within the bounds of current law but remains outside the bounds of accepted international human rights standards.
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Legal cases involving the JRC
The JRC has been involved in multiple legal proceedings concerning its use of aversive interventions, particularly electric shock devices.
1. FDA Ban and Legal Challenge (2020–2021)
2. Massachusetts Consent Decree Enforcement (1986–2023)
3. McCollins v. Judge Rotenberg Center (2012)
4. 2007 Incident and Subsequent Legal Actions
5. Contempt Proceedings Against State Agencies (1997)
6. Preliminary Injunction Against License Revocation (1986)
Summary Table of Major Legal Cases
Year | Case Name | Outcome |
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2021 | JRC v. FDA | FDA’s ban on ESDs vacated; JRC allowed to continue using GED devices. |
2023 | Enforcement of Consent Decree | Massachusetts court upheld the continuation of the consent decree. |
2012 | McCollins v. JRC | Case settled out of court; terms undisclosed. |
2007 | Criminal Charges Against Matthew Israel | Deferred prosecution; Israel resigned from JRC. |
1997 | JRC v. Department of Mental Retardation | Department found in contempt; receiver appointed; attorney’s fees awarded. |
1986 | Preliminary Injunction Against License Revocation | Injunction granted; JRC’s license maintained. |
These cases illustrate the complex legal landscape surrounding the JRC’s practices and the ongoing debates over its methods and oversight.
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