BRIAN'S LAW (MENTAL HEALTH LEGISLATIVE REFORM), 2000 / LOI BRIAN DE 2000 SUR LA RÉFORME LÉGISLATIVE CONCERNANT LA SANTÉ MENTALE

ASSERTIVE COMMUNITY TREATMENT ONTARIO

LORI ANTIDORMI

ELIAS AND ASSOCIATES CONSULTING INC.

PARKDALE COMMUNITY LEGAL SERVICES

ASSOCIATION OF ONTARIO PHYSICIANS AND DENTISTS IN PUBLIC SERVICE

YVONNE JENSEN

CITIZENS COMMISSION ON HUMAN RIGHTS

DON BARBER

CONTENTS

Monday 29 May 2000

Brian's Law (Mental Health Legislative Reform), 2000. Bill 68, Mrs Witmer / Loi Brian de 2000 sur la réforme législative concernant la santé mentale, projet de loi 68, Mme Witmer

Assertive Community Treatment Ontario
Dr Ian Musgrave

Dr Lori Antidormi

Elias and Associates Consulting Inc
Dr John Elias

Parkdale Community Legal Services
Ms Peggy-Gail DeHal

Association of Ontario Physicians and Dentists in Public Service
Ms Debra Eklove
Dr Federico Allodi
Dr Michael Chan
Dr Bill Komer

Ms Yvonne Jensen

Citizens Commission on Human Rights
Mr Robert Dobson-Smith
Mr George Mentis

Mr Don Barber

STANDING COMMITTEE ON GENERAL GOVERNMENT

Chair / Président
Mr Steve Gilchrist (Scarborough East / -Est PC)

Vice-Chair / Vice-Présidente

Mrs Julia Munro (York North / -Nord PC)

Mr Toby Barrett (Norfolk PC)
Mrs Marie Bountrogianni (Hamilton Mountain L)
Mr Ted Chudleigh (Halton PC)
Mr Garfield Dunlop (Simcoe North / -Nord PC)
Mr Steve Gilchrist (Scarborough East / -Est PC)
Mr Dave Levac (Brant L)
Mr Rosario Marchese (Trinity-Spadina ND)
Mrs Julia Munro (York North / -Nord PC)

Substitutions / Membres remplaçants

Mr Brad Clark (Stoney Creek PC)
Ms Frances Lankin (Beaches-East York ND)
Mrs Lyn McLeod (Thunder Bay-Atikokan L)
Mr Richard Patten (Ottawa Centre / -Centre L)

Clerk / Greffier

Mr Viktor Kaczkowski

Staff /Personnel

Ms Margaret Drent, research officer,
Research and Information Services

The committee met at 1533 in committee room 1.

BRIAN'S LAW (MENTAL HEALTH LEGISLATIVE REFORM), 2000 / LOI BRIAN DE 2000 SUR LA RÉFORME LÉGISLATIVE CONCERNANT LA SANTÉ MENTALE

Consideration of Bill 68, An Act, in memory of Brian Smith, to amend the Mental Health Act and the Health Care Consent Act, 1996 / Projet de loi 68, Loi à la mémoire de Brian Smith modifiant la Loi sur la santé mentale et la Loi de 1996 sur le consentement aux soins de santé.

ASSERTIVE COMMUNITY TREATMENT ONTARIO

The Chair (Mr Steve Gilchrist): Good afternoon, I'd like to call the committee to order as we continue our deliberations on Bill 68, An Act, in memory of Brian Smith, to amend the Mental Health Act and the Health Care Consent Act, 1996.

We have a number of presenters already in attendance and I'd like to call the first one forward, Assertive Community Treatment Ontario, Dr Ian Musgrave. Good afternoon, welcome to the committee. We have 30 minutes for your presentation, and it's up to you to divide as you see fit between either a presentation or question-and-answer period.

Dr Ian Musgrave: Thank you very much, Mr Gilchrist. It's certainly a privilege and honour to be here today. I'm certainly very flexible with how my 30 minutes is used. I'll try not to ramble or talk too much to allow any questions that people would like to ask during this obviously very brief amount of time. I have had circulated a little bit of an outline of the things I'd like to speak to, which hopefully people have in front of them. I should also highlight that I've used the words "my opinion" on some of the things I'm going to speak to. I am someone who is directly employed by the Ministry of Health and Long-Term Care, but I do see my role as, in some ways, also being an academic thorn in the side to the government to continue to help inspire best practices of mental health services in Ontario. I wear that hat as liberally as I need to in order to inspire mental health reform etc in this province. I can't say I'm speaking on behalf of the ministry for a lot of the things I do for a living for them, including perhaps during this 30 minutes, but I'll do my best to help in any way I can to contribute to your understanding of the Bill 68.

Just by way of introduction, I'm a psychiatrist. I worked for the Brockville Psychiatric Hospital for about 10 years, primarily on services involved with very seriously mental ill people referred to that hospital for long-term care, and indeed was on the first assertive community treatment team in Ontario, which began approximately 10 years ago. For the last year and a half I've been seconded by the Ministry of Health and Long-Term Care to help in the implementation, site visits, nurturing, inspiring as well as accreditation of assertive community treatment teams since this ministry instilled a major public policy shift to involve assertive community treatment teams in the spectrum of care for the seriously mentally ill. We're also moving towards eventually evaluating these teams, and my job includes that mandate as well.

I have just a few very quick comments as to why, partly, we're here in this room today, I believe, some perspectives on the bigger picture of mental health services and why mental health acts are being amended in various provinces of Canada.

In 1962, there were approximately 60,000 patients in provincial psychiatric hospitals across this country. By 1995, there were less than 13,000 people involved in long-term stay. We had the advent of general psychiatry units in the 1960s but nowhere near the same kinds of bed numbers to supplant the provincial psychiatric hospital census. In other words, through a great deal of optimism, a great deal of greater attention to least restrictive environments, to civil liberties, also with a great deal of optimism towards what new medications could bring to patients who are seriously mentally ill, most governments around the western world have been on quite an agenda of downsizing their long-term beds and indeed their acute care service beds.

To make a Reader's Digest version out of what has happened during that 30 years or so, I would venture to say that many, many people with serious mental illness have been well served, and adequately served, by the kinds of programs and services that have been put in place. However, there are many people who have been left outside of any kind of community tenure with dignity and respect. A lot of people have grappled with that problem over the past 30 years and begun to truly struggle with the ways we can support individuals with such serious mental illness so that they don't just simply get dumped out on the street, they don't end up back with their families without adequate support, they don't end up in the criminal justice system inappropriately and they don't just simply become revolving door syndromes.

Ontario has been no stranger, like other places, to beginning to innovate and ask serious questions about this. In that sense, I truly honour and respect this current government's last several years of efforts to begin revamping services which truly begin to close the gap on that group of individuals whom we typically refer to as being heavy users of the mental health system. They can be variously defined, but I'm talking about individuals who have never yet had the opportunity to live outside of a long-stay institution, have been there for perhaps years and years, and also that group of people who are constantly in and out of general hospital psychiatric units, sometimes for much longer than 60 days in the last two years, which is a benchmark that's sometimes used to define people who are revolving-door-syndrome individuals.

In that respect, assertive community treatment teams do indeed form an important benchmark and backbone, if you will, for beginning to address that gap. We've talked about the principles of mental health reform in Ontario going back to the Graham report, and they are still echoed in some of the changes we're making. But it has really only been in the last several years that we've begun to truly bring about some major agenda changes. While people can be critical of just how ambitious the rate of bed closure has been, we can also praise the current government for the ambitious rate at which they're beginning to implement assertive community treatment teams.

One of my punchlines today is that we've now got cheques from Ms Witmer to the tune of about 50 assertive community treatment teams in Ontario, and a very conservative estimate of the number we probably need to have is at least three times that many, probably at least 150, to begin to epidemiologically close the gap on the number of people who likely deserve such services. I've seen no indication just yet that the government has intended to stop financing and resourcing these types of services. That delights me. I'm also delighted that it's caught up in the health rubric of evidence-based care paradigms, in other words, the ability for us to begin to set standards by which these teams operate, accredit them against those standards and to truly inspire best practices. That's a big new thing in health in general, and it's certainly a delight within bureaucratic circles of the Ministry of Health and Long-Term Care, to see mental health dollars going out with a great deal more accountability and desire to see how those dollars are accounted for. That's a two-way street. Obviously, we work very hard in Assertive Community Treatment Ontario to make sure that those teams, the public in general and those being served all have mechanisms to have their own feedback taken into account in these implementations.

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With respect to community treatment orders and changes to the Mental Health Act that are being envisaged for Ontario, off the top I'd like to say that I support the essence and principle of just about everything that I've seen in print with regard to those amendments. Indeed, a lot of what's captured is, as I was suggesting, being captured in many different jurisdictions' desire to truly not leave people outside the formal mental health system and not leave them outside the opportunity to receive necessary and needful treatment.

I'd like to speak specifically to just a few things and, as I say, try to keep my comments as brief as possible to entertain any questions you may have. It's a natural thing to wonder about what the potential relationship is between community treatment orders and ACT teams. So I'm not going to speak to the changes proposed in the Mental Health Act that have to do with the fourth criteria, if you will, of making it easier for patients to receive necessary treatment. I certainly support that issue and that's a by-the-by.

Point number 1 is the criteria overlap between community treatment orders and assertive community treatment teams. If you read who might be eligible for a community treatment order in the proposed legislation, it would not be that unlike who might be eligible for being entered into an assertive community treatment team. In fact, assertive community treatment teams have criteria that are a little bit heavier-duty often than what's defined in the CTO section of criteria. But more or less we're talking about the same clientele who are having an awful lot of trouble either staying out of the hospital or getting out of the hospital in the first place.

The second punchline of what I'd like to say to you is that by far the vast majority of people who you might think not only qualify for a community treatment order but who might be helped by a community treatment order in fact will simply be eminently helped by being admitted to an assertive community treatment team. By "vast majority," it's my best guess that we're talking about 95%. In other words, as soon as the state begins to provide the appropriate amount of resources for intensive, comprehensively based services, whose description is beyond the time we have to get into just now, you'll truly, in my opinion, have captured the greatest amount of good you could possibly do for those individuals you're most concerned about, who are typically, in most jurisdictions, left outside of benefitting from community reform.

That having been said, however, it's my hypothesis, it's my thesis that perhaps for every 100 people referred to services as intensive as assertive community treatment teams, about 5% of such individuals will not benefit from those services unless we enact mandatory, obligatory treatment in the community. In other words, there's quite a number of people who, through no fault of their own, by virtue of their illness, usually through a lack of insight into even knowing they suffer from a serious mental illness, will continue to revolve in and out of our mental health system, and even after months, if not years, of services from an ACT service would continue to revolve or continue to be found very unwell and returned to hospital.

By ACT services I mean people kindly and professionally dedicated enough to be visiting that person on a daily basis, to be bringing physician help and nursing help and all kinds of help in a treatment rehab and supportive kind of way, in a very intensive way, not being able to make a dent in some individual's life, where literally the families and many other components of society at large are begging you to be intervening and asking, "Is there anything else you could be doing to help this person's outcome?" More or less, the answer has sadly been no. We've usually been in the business of having to observe and watch such individuals extremely closely until they meet criteria for being "certified" and brought back to a facility to receive the necessary treatment at that time. So I really laud the opportunity that service providers in Ontario will have to address that small group of individuals, in both the context presumably of ACT services as well as the context of a variety of other mental health service providers in Ontario.

Point number 2 is the voluntary ethos of ACT teams. I'd like to emphasize that it's very difficult to help people who don't want to be helped. Indeed, that goes for health services of all stripes. We usually have a lot more emotional debate in mental health because sometimes the illness robs the person of appreciating that they may need help. Nonetheless, we really stress in a democratic society, obviously, the civil rights of individuals, even when they lack insight. We go to great pains to put in place all kinds of opportunities for substitute consent when that capacity is not there. Clearly this legislation addresses that as comprehensively as the former addressings of the Mental Health Act have. In that sense, I simply want to say that I support the legislation from the point of view that it's asking for people's consent. If they are not capable of giving consent, it's going after the consent of a substitute person mandated by law. It's in that context that I would see assertive community treatment teams being involved, because they are in the business of not pushing themselves on people who want nothing to do with them.

I'm going to skip to number 5. I've sort of covered 3 and 4 in stuff I've already said. I want to speak specifically to a variety of implementation issues in no particular order or importance. Some of these may apply to more than just ACT teams. But I'd be remiss if I didn't try to stress what I believe will be important implementation issues for us to sort out in the coming months if indeed this legislation is enacted.

I really like the fact that an issuing physician, who will have the responsibility to enact such an order, can't name third parties without their consent. A lot of people were concerned that there may be opportunity for community treatment orders to involve other parties. You may be aware that from time to time judges or probation orders etc have done that very thing, and it hasn't been terribly fair to the system as a whole not to be party to the kinds of undertakings that may be involved. That clearly applies to community treatment orders.

In fact, point number 2, I truly believe that the typical scenario for ACT teams will be that they'll likely be involved in initiating community treatment orders with their sister health-provider colleagues, from an in-patient setting for individuals whom they know very well. In other words, this is not an opportunity to round up or newly identify patients who haven't already usually been well known to the system. The good news about that is that there's a finite number of individuals who would qualify for such community treatment orders; it's not a black hole of need. Assertive community treatment teams, for example, will be in an eminently intimate and knowledgeable position to be able to identify individuals who might benefit from such enactments of a community treatment order where their previous services have not. So that, to me, would be the typical scenario for how a community treatment order would be initiated. It would not be, in my opinion, a very wise thing for a typical scenario to be for other people to be trying to initiate a comprehensive community-based treatment plan in the context of a CTO without involving individuals who truly have gotten to know the client him- or herself.

Point number 3, and this may be harder for you to appreciate at this point in time, I would truly stress that new assertive community treatment teams which are just getting off the ground ought not to feel any pressure to be taking on or initiating community treatment orders early on in their mandate. That is because a great deal of training and nurturing and start-up time has to take place for these kinds of teams to be truly running on all cylinders, if you will. They are already, in fact, under a fair bit of public scrutiny and scrutiny from within the mental health system as a whole. They are in the spotlight. There's a lot of pressure for them to be truly turning around a lot of people's lives, and I for one wouldn't want them to feel excessively burdened with a new pressure to be initiating CTOs as they are just finding their way. I think it's only a matter of time before services like this become well-acquainted with those individuals on their roster who they truly wish a better outcome for, where a CTO may be worth considering.

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My fourth point in implementation is that ACT teams will need to feel both clinically and ethically comfortable with their decision. There's no question we can't deny that there are a lot people who disagree even with the concept of community treatment orders on a personal ethics basis. That has led to a lot of emotional debate, as you know, and a lot of scrutiny of just what's entailed in a CTO. It goes without saying that a team will need to feel very comfortable to proceed with something as clinically complex on many occasions in dealing with individuals who may ultimately benefit from a CTO. For example, the physician on the team might feel a little bit or a lot more comfortable than certain health care providers on that team, but there's no way that physician could proceed to enact a CTO unless the team had come to a collective decision. That's captured in the changes to the act pretty well with this notion of a free consultative process to truly figure out what, in fact, would be such a plan. You won't want to deny teams of mental health care providers the opportunity to reach a consensus around how to proceed. It won't be helpful if this is in any way hammered home by an issuing physician, for example, where other members of the team who will be quite intensively implicated aren't at peace with the decision at all.

With regard to something the government set up with respect to ACT teams across Ontario, a technical advisory panel, I'd just like to advise you as well that we also will likely be organizing a system of monitoring ACT teams, especially with respect to their involvement or prospective involvement with community treatment orders. We've already spent a fair bit of time on a little subcommittee of that panel, beginning to understand community treatment orders, and will likely continue to want to take an active interest in that. As you know, other provinces have gone down that route of figuring out how best to do that.

That's my final point here, even though it's not within the specific agenda of the act itself. I think Ontario will do well to globally monitor and study the value and implementation of CTOs, with the capacity to refine and optimize their effectiveness from a variety of perspectives: first and foremost, those being served by them, their family members, from a caregiver perspective, and also study them from a point of view of measurements of an outcome nature, their clinical impact, how the rights protection mechanisms are working and how these kinds of changes to the Mental Health Act have truly integrated or not integrated with other aspects of the mental health system. We somehow have to be willing and able to proceed cautiously enough that we can make refinements and changes as we go along and find out things that we may need to change as time goes on. That probably doesn't mean the substance of the act itself, but more the nuts and bolts of how they're used and how they're implemented. Just like the current Mental Health Act has a cultural context, if you will, of how it's used, clearly we'll need to help guide and monitor how community treatment orders are used and how to monitor and study that so that citizens in Ontario benefit the most from them.

Enough of my ramblings. An opportunity, with the bit of time remaining, for any questions. I hope I haven't confused you more than-

The Chair: Thank you, Doctor. We've got about eight minutes, so we're going to have to ask everybody to try and keep it to about two and a half or three minutes each, if they could please, starting with the Liberals.

Mrs Lyn McLeod (Thunder Bay-Atikokan): Dr Musgrave, I appreciate the fact that you've said that, although we're making some progress with ACT teams, we only have a third of what we need to really provide more comprehensive assertive community treatment teams. So much of this is a matter of resources. There are a number of questions that I wish we had time to ask, like how we staff ACT teams with psychiatrists, given the shortage of psychiatrists, even if we had the dollars.

But I guess the question I'll ask you to focus on is, given the fact that we don't have all the community supports in place to deal with the full range of people who have serious mental illness in the community, are you concerned that the 5% who would meet the criteria for a community treatment order will end up bumping-and you said that the ACT team shouldn't be under pressure-will these 5% end up bumping the rest of the 95%? I guess I'm wondering, do you think it would be appropriate to not proclaim the community treatment orders of this act until we're satisfied that there are sufficient community supports for not only that 5%, but for the other 95%?

Dr Musgrave: Good questions. You're certainly thinking on some very valuable aspects. We clearly need to continue to progressively and deliberately put more and more community-based services truly intent and capable of addressing the needs of the most seriously mentally ill. That's by far the number one thing. And we're behind the eight ball like most western jurisdictions that were downsizing their beds for the last couple of decades. Ontario is no exception to that. So by far and away, I'd be just as happy to see us progressively and deliberately resourcing appropriately intensive and comprehensive community-based services without the advent of CTOs in the near future. That's probably a fairly reasonable thing to do.

However, there is no question we would be leaving some people without capacity to live a life of community tenure with dignity who otherwise would have had it. I don't think it's a question of there being necessarily a terrible competition between this vast majority who don't need them versus the few who do. They both merit more intensive and available and accessible services. We need to continue to advocate that this government or any government doesn't stop making sure it's got the right allocation of those services. But I, for one, am just as happy to see us begin to struggle with how to use community treatment orders and the other changes to the Mental Health Act now, as opposed to later.

In other words, we'll nonetheless gain by the experience of enacting them relatively contemporaneously, even though I've always been concerned that there's been just too much pressure on seeing some equation between ACT teams being enacted in order to justify another agenda of CTOs. Quite frankly, I don't believe that was ever the case at all. There isn't hardly even that kind of vision around where either of those were going. Most governments don't think that far in advance, from what I can see. It's usually a question of just a great deal of lobbying going on to see mental health reform move in the directions it should; some shaming process when they look at neighbours like Michigan and Wisconsin and Rhode Island and Vermont. Those are the kind of things that brought about the changes so that ACT teams were enacted. No doubt, for CTOs the big agenda is the perceived public safety issue, which is really not a huge agenda item for community treatment orders. As much as we would all like to hope and wish that safety will in some way be impacted upon by them, it's not really the huge issue. The issue is the ability to serve people in a community setting with a great deal more dignity and a whole lot less suffering than previously.

Ms Frances Lankin (Beaches-East York): Thank you very much. I truly appreciate your spending the time with us here today. Just a comment first. The remarks that you made about the need to monitor I agree with completely. In fact, of two of the amendments that we will be putting forward, one will look at a sunset provision that requires a review in order for the Legislature to receive a qualitative and quantitative review of the success of this program in order to continue it and/or refine it as necessary; the second, the establishment of a mental health advocate's office looking at systemic issues and conducting these kinds of reviews overall of the system. I think we're coming to the conclusion that this is going to be a necessary part of making this work.

Your description at the end of who CTOs may be helpful for, and the importance for that small group, I think we are collectively struggling with how to make the legislation bring effect to that. I personally don't believe the legislation does that as it's written. It's the intent-I believe completely it's the government's intent; I think it fails in terms of the actual language.

I was interested in a couple of things. You mentioned the ACT criteria are heavier than the CTO criteria. I'd like to ask you to address that. You mentioned that you're in the process of developing standards and I've talked about the need to have standards for CTOs. What are we talking about out there in terms of intensive community services? Any of the standardized and controlled studies in the States show that, for the majority of people, those who receive intensive community services, whether on CTOs or not, improve. It's not the CTO; it's the intensive community services. So, the criteria of the standards.

The last thing is, you said there's still about 5% of the ACT clients that you wouldn't be able to help, who would need a CTO. I'd like to know what it is you think the CTO will actually do that will help those clients, because I would like to get that crystallized and narrow the legislation to that aspect.

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Dr Musgrave: Another very good set of questions. We don't have time to get into them the way you'd like and the way that I would enjoy and like as well. As you probably appreciate at least as well as I do, the kinds of criteria for a community treatment order such as Ontario is proposing is much in keeping with most others. The evidence shows that nowhere near as many people end up getting served by them as could theoretically be served. That may not console you too much, but it's a state of fact that almost every jurisdiction that's bothered to study it that I've understood hasn't really used them anywhere nearly as much as they could. As I say, that's not necessarily a strong argument for trying to refine exactly who to make them serve, but it's worth at least bringing that up as a starter.

The fact that ACT criteria and CTO criteria may be similar also doesn't particularly bother me. There'll be no mad rush by ACT services to want to again, in any way, enlist the use of that opportunity, even for somebody who would qualify, when it's totally not necessary. I'm not concerned about that at all. I'm not sure what else you wanted me to comment on-the standards of ACT teams and stuff?

Ms Lankin: Well, just let me ask, what are CTOs going to do for that 5%? How will that make the difference?

Dr Musgrave: It's really hard to know how best to quickly put it in a nutshell, but as I was suggesting, for every 100 people I've served on an assertive community treatment team, I can name on one hand individuals who I've known and struggled with for years who have had the following scenario: When they're in the hospital with a major psychotic illness, they respond incredibly well to their treatment and the services provided. They leave hospital with every intention to continue that, and for whatever reasons, but clearly reasons tied up with their illness, they end up not being able to contain their well-being. We're talking about all kinds of services and intensity of service that pretty well approximates everything that's going on in that hospital setting.

Interjection.

The Chair: No more supplements.

Ms Lankin: I just want to know-

Dr Musgrave: Yes, I'm getting there. I'm just going slower than you'd like.

You go through that time after time after time again, year after year, month after month, if you will. What a community treatment order will do is allow you to intervene by virtue of the non-compliance with the treatment plan-I'm using jargon, I guess-by the person not being able or willing to live up to the covenant of the community treatment order, which will allow you to bring them back to a psychiatric facility by that virtue.

The sense of, "Is this worth the hassle?"-in other words, before, you would wait till they were reaching high-risk and dangerousness. Now you will be able to intervene in a far more a timely way, uphold the law on their behalf and help struggle with that patient to say, "You know, we're really wishing this to make a difference in your life." That in itself, according to North Carolina studies, shows that most people will say: "OK, if it comes to that and you really can intervene with that kind of sincerity on my behalf, even if I doubt your agenda or your motive, forget it, I'll take those medicines you've been so kindly offering." A lot of people would just be obviated by the hardship of this perpetual roller coaster ride of wellness and psychosis, just by virtue of having that in place. That's my sincere and honest feeling for a small handful of people I've been involved with. I've just cried with their families on behalf of the current outcome.

Mrs Julia Munro (York North): Thank you very much for coming here today and providing us, quite frankly, with a different perspective on this issue. I have a number of questions to ask you, but I realize the prerogative of the Chair. One quick question: In the sheet that you provided for us you mention something about new ACT teams ought not to feel any pressure to be taking on or initiating CTOs. I wonder if, in a couple of moments, you could give us some advice on that issue.

Dr Musgrave: We've got about 50 ACT teams. I'm convinced that some of them will be quite shy and ethically not as comfortable to be front lead and cutting edge of implementing community treatment orders. There'll be some others who, just by virtue of their personalities and the makeup and maybe the culture of the sponsoring agency, will be quite willing to get involved earlier. I'd welcome that kind of variety and that sense of just letting this evolve in a naturalistic way, without the teams that aren't feeling in any way-in other words, we'll all learn together. It'll be the subject of workshops, I can assure you, at conferences, and all kinds of other conferences as the years go on, and we'll clearly refine how best to serve clients with them. That's mainly what I'm referring to.

Mrs Munro: I think that's a really important notion in terms of professional education, if I might use that term. Does that cover what you're suggesting?

Dr Musgrave: It's frequently asked of me. I train, I visit all over the province nurturing new ACT teams. CTOs have been coming up now for the last many months and everyone wants to know your two cents' worth on it. By far and away you meet a lot of people who are less than comfortable with feeling that they need to feel supported in that. I'm convinced they're going to meet patients who they are going to struggle with ultimately and really wonder and consider whether a community treatment order may be in that person's best interests. That's what I'm referring to, as opposed to somebody saying, "You've got to do it now."

The Chair: Thank you, Doctor. We appreciate you taking the time to come before us here this afternoon.

LORI ANTIDORMI

The Chair: Our next presentation will be from Ms Lori Antidormi. Good afternoon, welcome to the committee. We have 10 minutes for your presentation.

Dr Lori Antidormi: We are the parents of Zachary Lawrence Antidormi. At the age of two and a half years, Zachary was murdered by our neighbour. Our neighbour was a 60-year-old woman with a long history of serious mental illness that went largely untreated. In addition, she was one of the small proportion of individuals with serious mental illness who also demonstrate violent behaviour. Under the current Mental Health Act, our neighbour remained in the community, untreated and a danger to others.

We are in full support of the proposed amendments to the Mental Health Act. In our view, the proposed amendments represent responsible action that balances the needs of patients with public safety. From our experience, it would seem that public safety has taken a back seat for far too long. In our personal experience, our safety was never considered, nor was it ever discussed. In the end, and sadly for Zachary, it became all too apparent that we were not safe.

At the inquest into Zachary's death, the Mental Health Act came under close scrutiny, especially the application of sections 15, 16 and 17.

Of particular relevance to our situation, and the section with which we have the most experience, is section 17 of the Mental Health Act regarding police powers. In our view, the proposed changes to section 17 are essential. One change relates to removing the requirement of the police office to personally "observe" disorderly conduct before acting to take a person in for assessment under section 17. The proposed change would allow police officers to intervene where they have reasonable and probable grounds to believe that disorderly conduct has occurred and where they have reasonable cause to believe that the person has threatened harm or behaved violently.

Evidence supporting the necessity of this change was heard at the inquest into Zachary's death. Several police officers at the inquest testified that they did not see any behaviour which would have allowed them to apprehend our neighbour. Sometimes this reflected a lack of understanding of the act and the word "disorderly." On other occasions, when the officers finally arrived at our home, generally several hours after the call was placed, our neighbour did not appear to be a threat to us or to herself, and she was often now behaving in a calm manner. This picture, however, was quite different from that reported by ourselves and by the daughter of our neighbour. Yet under the current Mental Health Act the police officers were restricted from taking our neighbour to a facility for assessment, as they did not directly observe disorderly behaviour or were not of the opinion that her behaviour was indeed disorderly.

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Through testimony at the inquest, we also learned that police officers are trained to use their discretionary powers while obtaining third-party collaboration to lay charges under the Criminal Code of Canada. It is our opinion that similar powers should also be applied when dealing with a person with a serious mental disorder to apprehend them under section 17 of the Mental Health Act.

Let me put it this way: The police did not observe Lucia Piovesan stab Zachary 10 times, yet they made an arrest. It is our opinion that if they had been able to act on reasonable and probable grounds, using their discretionary powers with third-party information, they would have been able to take our neighbour in for assessment and the situation would not have escalated to the murder of our two-and-a-half-year-old son, and Lucia Piovesan would have received the treatment that her family had tried so hard and so long to get.

Briefly, I would like to add that in addition to changes to section 17, we strongly support removal of the word "imminent" from the current committal criteria. As the jury at the inquest into Zachary's death revealed, this word is too easily, and hence too often, misinterpreted. As such, it represents a stumbling block to correct implementation of the Mental Health Act.

Lastly, I will suggest that successful implementation of the proposed changes requires sharing of information among those involved. At the inquest into Zachary's death, police officers testified that they did not share information with admitting physicians as they felt restricted by legislation regarding sharing of information. In order for the Mental Health Act to be effectively utilized, all those involved must feel able to share relevant information. Thus, in addition to the amendments which address guidelines for health practitioners and others who provide treatment under a community treatment order, we recommend the act include guidelines regarding sharing of information at the apprehension stage. More specifically, we recommend guidelines for police officers acting under section 17, and for admitting physicians making the initial assessment.

Making the Mental Health Act understandable, easy to apply and somewhat less restrictive is critical for public safety, and perhaps it is the first step in ensuring that individuals with serious mental illness, who often lack insight into their illness, are assessed so that they can receive the appropriate treatment they need.

In closing, I would just like to reiterate that, in Zachary's memory and in his honour, we support the minister's efforts and the proposed changes to the Mental Health Act. As the jury at the inquest into Zachary's death urged, it is necessary to implement these changes such that Zachary's death will not have been in vain.

The Chair: Thank you very much. That leaves us time for one question and the rotation up next would be the NDP. Ms Lankin, you have about two, two and a half minutes.

Ms Lankin: I thank you for coming today. I know how difficult it is, on a continuing basis, for you to face this issue, and your strength and your commitment to seeing change speaks volumes in honour of your son. We were talking out in the hall and I was saying to you that we are struggling, in a sense, to ensure that this legislation actually lives up to the expectations that you have and doesn't live up to the fears that many others in the community have put forward. That's the balance we hope to strike.

Many have said that the previous legislation, as it was written, actually struck the right balance, but we've heard from you and others that, whether the words did or not, the culture and the implementation of it didn't. Do you have any comments about how we should seek to make the language more understandable, plainer? For example, dropping the word "imminent." Some people have suggested replacing that with what the expectation always was supposed to be, a three-month period, actually saying "three months." Can we make this clearer? Because my concern is that as badly as the previous legislation was interpreted, the changes may be badly interpreted and we may still remain with the problem.

Dr Antidormi: I think the changes tried to make it a little simpler and more understandable and I guess, like we heard at the inquest, education around what those words mean. Michael Bay talked at length about what the words mean, and physicians and police tended to misinterpret, so maybe more objective or almost measurable types of words rather than abstract words like "imminent" might help in that regard.

The Chair: Again, thank you on behalf of all the committee. We very much appreciate your taking the time to join us and share your thoughts.

ELIAS AND ASSOCIATES CONSULTING INC.

The Chair: Our next presenter will be from Elias and Associates Consulting Inc. Mr Elias, good afternoon. We have 30 minutes for your presentation. Feel free to divide that between a presentation or question-and-answer period as you see fit.

Dr John Elias: I wish to thank your committee for inviting me to appear to comment on Bill 68. As I am from Saskatchewan, I consider this a privilege and respect your openness in calling on people from outside of Ontario to testify concerning this important legislation.

I support this bill and congratulate all who have worked to develop it. My only concern is that it doesn't appear to go quite far enough in establishing meaningful powers for providers of mental health services to provide involuntary treatment, either in in-patient facilities or in the community, to people in serious need who are non-compliant. I see obstacles and I'm going to identify them as I proceed.

I now have an independent consulting practice in organizational psychology, but for 20 years, until 1996, I served in executive management of Saskatchewan's mental health system and was extensively involved in the development of Saskatchewan's mental health legislation, including in 1993 when legislation was passed to enact community treatment orders. I am here presenting my own personal views. I'm able to relate some of our experience in Saskatchewan, but I am no longer employed by the government of Saskatchewan and am not in a position to make comments on their behalf.

On several occasions since 1994, I have been invited to Ontario to speak about mental health legislation, specifically about community treatment orders, and to testify at coroners' inquests in cases where deaths had occurred as a result of individuals suffering from psychotic illnesses living untreated in the community.

Failure of sound system.

Dr Elias: I had an opportunity to testify at inquests. The first one was in 1994, in Toronto. It was the inquest into the death of Lester Donaldson-

The Vice-Chair (Mrs Julia Munro): Excuse me. We'll have a short recess.

The committee recessed from 1618 to 1620.

The Vice-Chair: We will resume. Mr Elias, sorry. I must apologize for technical difficulties here. Please carry on.

Dr Elias: Fine. I had the opportunity to testify at several inquests in Ontario. The first inquest was in 1994 in Toronto, the inquest into the death of Lester Donaldson, which occurred in Toronto, I believe in 1992, after police were called to a rooming house to deal with a man with a serious psychotic illness who should have been under psychiatric treatment and who had become disruptive.

The second inquest was in 1997 in Ottawa, the inquest into the death of Brian Smith, which occurred in Ottawa in 1995 after the accused, Jeffrey Arenburg, had been living untreated in the community in a delusional state and considered the radio station where Mr Smith worked as a source of his troubles.

Another inquest was in 1997, in Whitby, the inquest into the deaths of two people, a six-year-old child, Jennifer England, and Marian Johnston, the 79-year-old mother of the accused, Ronald England, which occurred in 1996 in Bowmanville after the accused had been living in the community untreated for his psychotic disorder.

These three cases-and I understand a considerable number of other cases where I don't have detailed knowledge-raised serious questions about the provisions in the Mental Health Act and the Health Care Consent Act. At the time of the inquests, I had three main problems or issues as I saw them and I testified about these at these inquests.

First, I viewed the committal criteria as too narrow. Conditions to be satisfied before physicians, justices of the peace and police officers could initiate the process of psychiatric assessment and before attending physicians in psychiatric facilities could issue certificates of involuntary admission were overly concerned with dangerousness in the physical sense.

The second concern was that too often people were being detained in psychiatric facilities where there was no authority to provide them with treatment. Section 10 of the Health Care Consent Act provided that no treatment is to be given except with the consent of the person, if competent to give or withhold consent, or the person's substitute decision-maker, as defined in section 20.

As a result of this manner of obtaining or failing to obtain consent for treatment, as that's provided for in section 33 of the Health Care Consent Act, there appeared to be any number of possibilities for a person who is in need of treatment to be detained but not treated. This appeared to lead to many instances of either the absence of treatment for the person or the misuse of psychiatric facilities for detention only and not treatment or, thirdly, the discharge of persons in need of treatment because there did not seem to be much point in detaining them in hospital because it wasn't possible to give the treatment.

The third main problem, as I saw it, was that with respect to persons who were not being detained but who were outpatients or persons living outside of hospital, the situation appeared to be the same. There was provision for leaves of absence but no authority for treatment while in the community.

At these inquests, I made a number of recommendations which I have listed for you, and in the interests of time I'm just going to touch on them very briefly.

One recommendation was to broaden the reference to harm in the criteria to be used for both action to bring a person to examination and also to broaden the criteria for committal in a psychiatric institution. I advocated the integration of criteria regarding competency into the detention criteria so that the question of competency or capacity to consent is considered at the same time as the other criteria and that incapacity must be established before detention beyond the period of examination occurs.

Where incapacity has been established, I was recommending that you enlarge upon the powers under section 25 of the Health Care Consent Act to provide authority for emergency psychiatric treatment until such time as the question of substitute decision-maker is decided. Then also I recommended that there be more speedy decision-making procedures to get a substitute decision-maker established. I also recommended that where no consent for treatment is obtained, authority for the detention of the person be nullified. Finally, I made a recommendation to make provision in the Mental Health Act for community treatment orders.

Failure of sound system.

Dr Elias: I shall move on to more specific comments on Bill 68. Stop me if you need to.

As I read Bill 68, it accomplishes a great deal. I applaud those who have developed it. At the same time, I have some questions and concerns, and except for the recommendations which I had already submitted at the coroners' inquests mentioned above, I have not participated in the debate so I may be missing or misunderstanding some points. Nevertheless I make the following points.

First, Bill 68 proposes to broaden the criteria in sections 15, 16 and 17 under which physicians, justices of the peace and police officers, respectively, may act to require a person to submit to a psychiatric examination. It also broadens the committal criteria in section 20. It would remove the term "imminent" with reference to "serious physical impairment of the person" and also provides for a broader definition of "harm" to include the situation where a person "is likely to suffer substantial mental or physical deterioration or serious physical impairment." I consider all of these to be desirable changes. At the same time, I note that the definition of "harm" is still stricter than that found in many other similar statutes.

Secondly-and this is the biggest part of the bill-Bill 68 would make provisions in a new section, 33.1, for a community treatment order, or CTO, to be issued. Now I have a few specific comments. Most of these are very positive features.

The criteria in clause 33.1(2)(a) to be satisfied prior to the issuance of a CTO appear to be appropriate or at least defensible. It's interesting to me that your threshold criterion in subclause 33.1(2)(a)(i) is considerably broader than one adopted in Saskatchewan. You require only two or more previous admissions to hospital or a cumulative total of 30 days of hospitalization over the previous three-year period. It sounds like these admissions could be voluntary admissions. Any kind of admission would qualify under that criterion. In Saskatchewan, the threshold requires three previous involuntary admissions or a cumulative total of 60 days of involuntary stay in hospital over the immediately preceding two-year period.

I'm not arguing for differences of time frames, but I do question your use of any hospitalization or any period of hospitalization to meet that threshold criterion. It seems to me this would serve to discourage the voluntary use of hospitals or of health care providers by those people who need those services. I think it would be in your interest to limit that threshold criterion to refer only to involuntary hospitalizations or periods of involuntary stay.

(b) The requirement in clause 33.1(2)(b) that the physician, the person or his or her substitute decision-maker and others collaborate to develop a community treatment plan is laudable.

(c) The criteria in clause 33.1(2)(c) to be satisfied prior to the issuance of a CTO seem appropriate and consistent with the best thinking I've seen in the professional literature, except for one missing item, as I see it: that the person lacks the capacity to fully understand or make an informed decision. As I see it, CTOs should only be issued to apply to persons who lack this capacity. It may end up that way, but it seems to me that's what it should say.

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(d) The involvement of a rights adviser in advance of the issuance of the CTO, as required in another clause, appears to me a very progressive step.

(e) The consent of the person or his or her substitute decision-maker, as required in clause 33.1(2)(f), is clearly desirable, but I would question whether this might not be a serious stumbling block. Thinking back to the several cases leading to the coroners' inquests I mentioned, it seems to me that all three incidents would likely still have occurred as a result of the person or his or her substitute decision-maker withholding consent. It seems to me unreasonable that what I would consider veto power should be left in the hands of the person who has been found to be in need of a CTO. In my mind, CTOs should be issued only with respect to persons who lack the capacity to consent or withhold consent, as I already mentioned earlier. Making a CTO, that is, a so-called community treatment "order" subject to the consent of the person who's the subject of the order is no order at all but rather an agreement and one that the person can back out of at any time. This I see as a real weakness of the bill.

(f) The obligations of the person who is the subject of a CTO are similar to the obligations stated in similar legislation in other jurisdictions. I wonder, though, what powers exist to require that the person meet these obligations or comply with these requirements. As I read it, if the person does not comply, he or she may be required to be re-examined under section 33.3, but in the end there are no powers of enforcement. Furthermore, under section 33.4, the CTO may be terminated by the person or his or her substitute decision-maker simply by withdrawing consent. It seems to me all the power really is in the hand of the person who would otherwise be subject to an order, so I don't see this as an order all but rather an agreement that the person might enter into.

(g) The duration of a CTO for a period of six months, as provided in another section, is longer, I think, than provided in similar legislation elsewhere. In Saskatchewan the duration of a CTO is three months. Nevertheless I see this as defensible as long as the actual community treatment plan involves frequent contact between the attending physician, other caregivers and the person who is the subject of the order, so that there may be a withdrawal of the order, as provided in section 33.2, in appropriate circumstances.

I'll skip another point which is not so critical-I'll skip the next two. You might want to refer to the other comments, but I'll go to point (h).

(h) To the extent that I have studied the proposed changes concerning consultation, the sharing of information, reviews, appeals and matters of administration, they appear to me to be appropriate.

With respect to the third major area of change, Bill 68 proposes to makes changes in the Health Care Consent Act which are intended to streamline processes of dealing with persons who lack capacity to make health care decisions. This is an area rather more complicated than I feel I can fully comment on since I haven't studied it enough. I've just recently returned to this issue, but I will make a few general comments.

First, it still seems to me that the provisions in section 33 of the Health Care Consent Act will not permit the system to respond to the needs of people with serious disabling psychiatric disorders who are non-compliant. I appreciate the thrust of Dr Musgrave's testimony earlier and applaud all efforts at voluntary services, getting people to co-operate by making sure services are available, attractive and relevant. At the same time, there are a small number of instances where you're dealing with people who simply will not co-operate unless there are some meaningful powers in the right hands to be able to ensure they get treatment, whether they or their substitutes will agree or not.

In dealing with persons suffering from seriously disabling psychotic disorders, it is vitally important that psychiatrists and others be given the authority to provide treatment as quickly as possible. If the authority for treatment cannot be given by the person himself or herself, it should come quickly from someone else who is in a position to provide the authority. If there is no authority to provide treatment, in my opinion, except in rare instances of short duration, there should be no use of hospitals, physicians and other staff in the health care system to detain people. Health systems exist to provide health services. I do not consider it appropriate that hospitals and medical and related professionals be used to detain dangerous people who cannot be treated. In such cases, the public merits protection, but responsibility for this should be exercised by other institutions, not by the health system. I have to question whether section 33 contains-I think it's section 33 of that act-provisions that ultimately allow for all providers in the system, no matter how good their intentions are or how assertive they may be in their approach, to actually be helpful.

I will conclude now with very brief reference to some Saskatchewan data. I've said several times I'm from Saskatchewan. I had a hand in the development of the legislation there and know something of the experience up until recently. I can tell you that under the Saskatchewan system, where provisions for CTOs were enacted on July 1, 1996, there has been an average of 50 to 60 CTOs per year since that date. The numbers vary a little bit, but let me remind you that in Saskatchewan the maximum duration of a CTO is three months. If you take the number 60 and divide it into four, because you have four three-month periods in a year, that means that at any given time we have approximately 15 persons in Saskatchewan subject to CTOs.

If your experience were to be similar in Ontario, even with clauses having somewhat different provisions here and there, you would have something in the order of 150 in the province, grand total, at any given moment or a total of 600 actual-well, I don't know if you'd have 600 CTOs issued, because your duration is longer. But if the provisions were otherwise similar, you'd be having about 150 under CTO provisions at any given time.

Generally, people do not remain under CTOs for very long periods of time. Generally, there are one or two renewals after the first one is issued. We don't have people remaining endlessly under CTOs. It seems that once people have been under CTOs, they actually experience some success of living in the community in a treated condition, and they actually continue being compliant with treatment. It's no longer necessary to issue CTOs.

There has not been a formal evaluation of CTO provisions in Saskatchewan. There's been some research, some of which I've published, together with Dr Richard O'Reilly of London, Ontario, but there has not been an in-depth evaluation of that legislation.

In the end then, I would like to just make this statement: that mental health legislation needs to strike a balance between the rights of the individual, protection of society and the interests of caregivers, including family members, other primary caregivers and professional service providers. I do not hold to a dogmatic position favouring one of these three over the others. I have great respect for individual rights and would allow a wide margin of tolerance for privacy, idiosyncrasy and eccentricity. But I would draw the line at serious danger of harm to others, especially where danger is presented to people who are particularly vulnerable, especially children and others living in intimate relationship with a person or who are innocent bystanders. I personally favour strong powers for state authorities, police, courts and psychiatrists when providing health services and, simultaneously, serving a control function, coupled with strong safeguards against abuse of power, such as strict accountability, monitoring, reviews and appeals and so on. I see Bill 68 moving in this direction and applaud again those who have developed the legislation.

As important as mental health legislation is, it only provides a structure, a legal and policy framework within which people may act. To be effective, it must be accompanied by an adequate system of services which are accessible, responsive, accountable and delivered by qualified staff with compassion and commitment, intelligence and discretion, willing to do their duty and to go beyond the call of duty, even to take risks on behalf of the people whom they serve.

Thank you for the opportunity to make the presentation.

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The Vice-Chair: Thank you very much, Mr Elias. We certainly appreciate you coming here today to provide us with your commentary. My apologies for some of technical difficulties. We have however taken, even with allowing extra time-so I'm going to ask that we just have questions from one caucus. We are in rotation at the government members.

Mr Brad Clark (Stoney Creek): Two quick questions, Doctor, if I may. One deals with a comment you made regarding section 33.1 of the act. You suggested that perhaps we should be adding the terminology "has been an involuntary patient in a psychiatric facility on two or more separate occasions" etc. As opposed to not clearly delineating whether they're voluntary or involuntary, you're suggesting that they should be involuntary and remove the opportunity for voluntary.

The other thing I wanted you to address for me is, there was a North Carolina study that dealt with the reduction in victimization as a result of the use of outpatient commitment or CTOs. Do you have any comments about the reduction in victimization of mentally ill people who are actually on outpatient committal?

Dr Elias: I am not able to give you a real answer to that question on the basis of the Saskatchewan experience. The literature does state exactly as you have mentioned in reference to the North Carolina study. There are quite a number of other studies that are in the published literature that make exactly that same point. Unfortunately, in Saskatchewan there has not yet been a formal evaluation of it, so I cannot say honestly whether we've seen a reduction of victimization or harm.

Mr Clark: The other question was, you suggested we should clarify that it would be an involuntary patient.

Dr Elias: The recommendation I made was that the threshold criterion which is written into one of the sections of the bill be made more specific so that the threshold criterion in referring to number of previous hospitalizations or number of previous days in hospital refer only to periods of time when that hospitalization was involuntary. That is the point I'm making.

The Vice-Chair: Thank you very much for being here today to provide us with your insights.

Mr Richard Patten (Ottawa Centre): Can I ask through you, Madam Chair, if on behalf of the committee we might request-your research with Dr O'Reilly, I gather, is pretty recent, because we haven't seen it. Would you be prepared to share that with the committee? Not right now; I mean send it to us.

Dr Elias: Most certainly. I'll be happy to send that either to Mr Patten or to the clerk.

The Vice-Chair: Through the clerk's office would be the appropriate thing.

Dr Elias: I'd be happy to do that. I shall send a copy.

The Vice-Chair: Thank you very much for coming today.

PARKDALE COMMUNITY LEGAL SERVICES

The Vice-Chair: I'd like to call on Parkdale Community Legal Services. For the sake of our technical difficulties here, I'm going to ask you to use one of the microphones on that table there. Thank you very much and welcome to the public hearings. You have 20 minutes to give your presentation.

Ms Peggy-Gail DeHal: My name is Peggy-Gail DeHal. I'm a community legal worker representing Parkdale Community Legal Services. I'd just like to let you know that I will submit a copy of what I'm speaking about today at the end.

I come here today as a representative of Parkdale Community Legal Services, an anti-poverty clinic servicing those with low income in the Parkdale area. Because we're an agency that provides free legal services to the poor, we frequently work with many individuals living with mental illness. This is probably due in large part to the province's largest psychiatric facility being located in our community.

During the 1970s, there was a movement to deinstitutionalize individuals by helping them re-enter the community with the introduction of medications. This created a spilling of many individuals into a community that was ill-prepared with resources. The issues of housing, poverty, unemployment and mental illness became bred as social problems without an easy or quick fix.

It is our agency's mandate to work as legal advocates for those marginalized in our community by poverty. Unfortunately, many of these individuals are also living with mental illness, emotional distress and, for some, the everyday strains of living in the margins of their community.

Today, I not only represent Parkdale Community Legal Services but the number of psychiatric survivor and consumer-survivor groups we work with in the Parkdale community. I stand here today as an advocate for those living in mental institutions, mothers whose ill children have been reduced to guinea pigs, five-year-old children lethargic and vacant from Ritalin.

Mental illness does not just happen. Susceptibility requires a stressful trigger, such as deprivation, abuse, violence, incarceration or a history of psychiatric drug use. Today, an excitable child or one who exerts too much energy is given such labels as "learning disabled," "attention deficit disorder" or "hyperactivity" while frustrated and tired parents agree to psychiatric medications as behavioural control without fully understanding or knowing of the damaging side effects. How can a small body, full of life and requiring a special kind of love and patience and understanding, start consuming deadly chemicals that alter their developing minds and stay trapped in their small organs? The statistics are staggering. You only need to check how many prescriptions drugstores fill a day, a week, a year. Take notice of the many psychiatric prescriptions filled by drugstores for children in poor communities. How can we not advocate and provide other resources when there is such a fine line between mental health and mental illness?

Most people who have gone through the psychiatric system do not just wake up one day and feel like their soul was sick. Many end up there because of a lack of resources, knowledge and general acceptance of illness that can so drastically alter behaviours. I am referring to those on our streets, in our hostels, whose poverty limits their options and forces them into the system, forcibly consuming medications whose side effects guarantee a chemical dependence so that they cannot be here to speak for themselves today. This is the kind of advocate I appear as today.

Parkdale Community Legal Services endorses the views of the No Force Coalition, the Psychiatric Patient Advocate Office, the Canadian Mental Health Association, family groups and medical professionals who are opposed to the amendments proposed to the Mental Health Act, in particular the introduction and implementation of community treatment orders. Our agency feels that any legislation seeking to take away an individual's choices is a violation of our rights under section 9 of the Charter of Rights and Freedoms.

We believe the existing Mental Health Act addresses the issues of treatment for those unable to make decisions for themselves. Because there is a process of certifying an individual through forms, the problem is the understanding and use of the act. There already exist provisions for detention as a patient can be certified for three months while in the community in section 27 of the act. The Substitute Decisions Act will provide an individual the opportunity to decide the nature of treatment they desire in times when they are deemed incapable of making such decisions themselves. If the Substitute Decisions Act and consent to health care act were used effectively, community treatment orders would not be necessary. Forcing people into locked facilities until they are medicated and paroling them in the community is criminalizing those most vulnerable.

Dr David Goldbloom, physician in chief at the Centre for Addiction and Mental Health, states, "The problem is not the current act itself but the understanding of the act and the use of the act...." If it was better understood, if it was less cumbersome to use, it would be used more. The form 1, which any physician in Ontario can fill out to bring someone to psychiatric hospitalization for up to 72 hours, is a terribly constructed form. It is almost guaranteed in its crafting to be filled out incorrectly.

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We support the right of consumers and psychiatric survivors to make their own decisions about health care. We oppose the treatment of mental illness as different from the right of individuals to make informed choices about life-threatening illness or accidents. We strongly believe that a vital part of making a safe and healthy choice about one's care would involve real choice: the ability of diverse resources in the community, not legislation that takes away an individual's rights because they refuse to be medicated, and because they refuse to take medication that often has damaging and immobilizing side effects or provokes a state of lethargy.

Community treatment orders constitute arbitrary detention, offending an individual's right as permitted in the Charter of Rights and Freedoms. This legislation does not recognize that forced medication is chemical incarceration, whether in a psychiatric ward or in the community. The side effects can be damaging, particularly for someone who has been exposed to multiple psychiatric medications over a period of time. Community mental health services must include the provision of alternative options to neuroleptics that have brain-damaging effects such as clozapine, zyprexa and Haldol.

Families should not be put in the position to make choices for loved ones when the options are limited to psychiatric drugs, unavailable hospital beds and limited or non-existent resources. Families need services that work towards better mental health while maintaining an individual's rights and dignity and assist in resolving social inequalities they experience as a result of their illness. The existing health care system has put families already in a state of exhaustion where it is easier to accept quick fixes so their loved ones are spared from being demonized because of their mental illness.

Resources need to be put into the community to provide real options for those who are mentally ill or in need of emotional intervention. This government has cut so many services and social provisions for cost-effectiveness while the proposed ACT teams cost a disproportionate amount of money and can only service a limited number of individuals in need. Those same dollars can be spent opening up a number of services, enhancing training programs, providing people with social assistance programs so they can be adequately housed and fed. If this is not about dollars, then it has to be about social cleansing. This government must invest in community resources, not in chemical compliance. Forced treatment violates the rights of the individual.

I have spent the last seven years as a front-line worker for homeless youth and men and women who have been in conflict with the law. It is easy for me to make the connections around how systemically people can be driven to mental illness if they are susceptible, as I have seen how single families and individuals have been reduced to homelessness, unemployment and illness. Suicidal thoughts have been an increasingly common response to these circumstances. In our society, particularly the laws that criminalize the poor and homeless, are worded and legislated separately, yet so many of the same individuals are recipients of multiple doses of legislation that hide them from visibility in prisons and on psychiatric wards.

Most individuals are not homeless because they are mentally ill; they are mentally ill while being homeless. The proposed community treatment orders target the most marginalized population in our communities, people who are isolated from supports and who are living in transience.

During my time as a front-line worker I saw the increasing impact legislation has had on those living in poverty. The National Council of Welfare says the poor are more likely to be arrested, charged, denied bail and convicted than other people. They are more likely to appear in court without a lawyer. The city of Toronto food and hunger action committee's preliminary report finds a growing food crisis in our city, with 20% of Torontonians unable to afford basic needs and facing difficult choices such as paying rent or buying food. The report identifies that cuts by senior levels of government to social programs and a serious lack of affordable housing are seen as pushing hunger to a critical point in Toronto.

Instead of solving problems, this unnecessary legislation panders to public fear and ignorance regarding mental health.

In a report on the consultative review of mental health reform in the province of Ontario, Dan Newman suggests that while moving ahead to reform the mental health system our government must use the following guiding principles:

Our government should focus mental health reform on the quality of life of individuals with serious mental health problems;

Our government should recognize the importance of a holistic approach to the mental health system, one that addresses the broader determinants of health, including housing, education, jobs and income support;

Our government should focus on creating an integrated and comprehensive system of mental health services which provide a continuum of care for those who need it, from prevention to community and in-hospital treatment.

What conflicts here with proposed amendments to the Mental Health Act is that these amendments to the act will not enhance the quality of life for individuals with serious mental health problems. Forcing human beings to be drugged without choices violates their rights. Those with disease and physical illness are given the choice whether to take medications with damaging side effects or not, just like those charged with a crime are given a fair trial and a release date at the time of sentencing.

Community treatment orders are unnecessary. As the Canadian Mental Health Association points out, "The Health Care Consent Act and the Substitute Decisions Act, if used properly, permit treatment of a person found incapable of consenting to treatment." If both these acts were made available and accessible to those at concern here, they would be able to participate in their own treatment and care.

Many will agree that successful treatment depends on the consented participation of the individual. How can such an act enhance the quality of life for individuals when there is no requirement for doctors to inform their patients of the deadly side effects some of these medications can have? Further, what about the enormous profits to be made by pharmaceutical companies that will gain guinea pigs served up by the state?

The importance of a holistic approach is also at issue here. How can we trust that this government shares the same notion of holistic approach as the community does? The very community agencies that service marginalized individuals have been struggling for years under increasing reduction in program and staff funding at the same time there has been an influx of people with mental health issues in their offices.

The resources to service this influx are not there at the community level, at the academic level or at the medical level. Colleges and universities do not offer full-time diploma programs focused on community mental health. How can Mr Newman propose a holistic approach when communities have seen decreases, not increases, to program resources?

In recent years, the introduction of Ontario Works and Ontario disability support programs disentitled many from financial assistance who were in need. When, reluctantly, this income is granted, the recipients are policed and criminalized for needing it.

At the same time that hundreds of people were disappearing from the system and moving into hostels and on to the streets, the government took away rent control, landing many people in a cycle of homelessness, transience or below minimum standards of accommodation. If the maximum general welfare cheque is $520, then one can only afford unpleasant accommodations in a boarding room in Toronto.

Given the restrictions to social assistance, there are very few people who would choose to remain dependent on the system on a long-term basis. They cannot go to the community for help, because reductions in social spending and community-based programs have long waiting lists, burnt-out staff, inadequate resources and are busy competing for the few dollars that have been waved before them. If they happen to lay their head on a street corner or beg for food or money, they are thrown into jail under the Safe Streets Act. I am not willing to participate in stripping people of their dignity because of illness or distress.

This is a legislation that has controversial implications. It can be presented as a resource for families and individuals, but when all other options are non-existent there are limited choices, especially in the midst of a crisis.

We at Parkdale Community Legal Services do not see this legislation as an isolated form of social control. We couple it with changes to rent control, social assistance, workers' compensation and employment insurance provisions, as well as the depleting funds of vital social services in our communities across the province. The increase in deaths due to cuts to hospital beds and cost-saving measures is no longer invisible.

To this end, once again we raise concerns about the violation of an individual's rights under the current proposed legislation, since we believe the existing act makes provisions for care decisions, supervision, apprehension and detention in a psychiatric facility.

It is of importance that this government recognize their systemic dismantling of resources and how this has contributed to homelessness, increased poverty, unemployment, inaccessible education, health care that can kill you and the violation of an individual's rights in the name of public safety.

Have you been held accountable for the state of poverty you have created and have you stood trial for the lives you have taken in order to shift these dollars to the private sector? We all know you have not and you probably will not. That is not why I am here today. I speak for those frustrated, affected, marginalized and criminalized because of oppressive legislation that targets the working class, the poor and some of society's most vulnerable individuals.

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The Chair: Thank you very much. That leaves us with about two and a half minutes for questions. This time I'll give the time to the Liberals, in the rotation.

Mrs McLeod: I'm very appreciative of what you said during the course of your presentation about homelessness and the mentally ill, and very aware that certainly in my community in northwestern Ontario it's as true as it is in Toronto-maybe just of a different magnitude in Toronto-that we do not have the affordable housing, let alone the supportive housing, that's needed to provide the living conditions that would be much more optimal for those with mental illness.

I wanted to ask you, in your experience, do you feel there are people who, because of their illness, would not be able to access whatever housing support or even treatment supports that would be there? I know we don't have all of this, but even if we had all of the community supports-the housing, the treatment supports-there would be people, who, because of their illness, couldn't access that, couldn't even stay in a supportive housing situation?

Ms DeHal: Part of what we've noticed is that people's inability to afford accommodation that they choose has become an issue. There are certain kinds of housing accommodation available for somebody who is on ODSPA or Ontario Works. Unfortunately, the provisions for rent do not allow for acceptable housing, and a lot of times these very same people do have to move out.

Of course, there are the issues that happen with an individual who can't keep their housing because of their illness. We feel, however, that the lack of resources-and this has been noticed by many other front-line workers whom I have worked alongside with, and we've done this work on the streets as counsellors and in various sectors all over the city. A lot of us have noticed in the last five years an incredible number of people who are mentally ill and are being kicked out of their apartments. Many of their rights are being violated by their landlords, though, because they can and because they are vulnerable.

Sure, we'll never be able to provide the right of amount of resources, but if we could at least provide intervention services to be able to facilitate healthy living, we might be able to assist people in making some choices when they are well. Not eating food every day, having to go out to the food bank once a month, producing ID to get that food, and often that food at the food bank isn't-people don't give away fresh food, and we know that. A lot of people in our community are dependent on food banks and can't find jobs and don't have ID at times and go into hospitals services, and because they've been there so many times, they get kicked out by emergency staff or they don't receive beds.

So it's more than a revolving-door cycle; it's about a lack of resources and people's understanding of what mental illness is. We want to understand what we see, and it is very horrible what we have seen on our streets over the last couple of years. Yes, there have been some violent implications of the lack of resources; however, these are individuals in our community whom we have as much accountability to as we do to do those who are living in private accommodation.

The Chair: Thank you very much for coming before us this afternoon. We appreciate your taking the time to be part of our proceedings.

ASSOCIATION OF ONTARIO PHYSICIANS AND DENTISTS IN PUBLIC SERVICE

The Chair: That takes us to our next presentation, the Association of Ontario Physicians and Dentists in Public Service.

Good afternoon, welcome to the committee. We have 20 minutes for your presentation. You can divide that as you see fit between presentation or question-and-answer period. Perhaps at the outset, as you're probably planning to, you could introduce yourself for the purpose of Hansard.

Ms Debra Eklove: I thank the committee on behalf of the association for giving us the time to present to you. My name is Debra Eklove. I'm the executive director of the association. With me are members of the association who are all psychiatrists working in the psychiatric hospitals. To my far right is Dr Bill Komer from St Thomas, Dr Michael Chan from Kingston, and Dr Federico Allodi from Queen Street, which is now the Centre for Addiction and Mental Health. Dr Allodi will begin our presentation.

Dr Federico Allodi: First of all, I would like to make a general statement and then we'll go into specifics.

The Association of Ontario Physicians and Dentists in Public Service would like to express its support for the proposed legislation, because it is in favour of providing and improving the care of the severely mentally ill patient, and particularly those patients who are not covered by the present section 15 of the Mental Health Act; namely, those people who, because of their mental illness, pose a physical danger to themselves or to other persons, or because they put at risk, imminent risk, their bodily health, and yet these people who do not comply with treatment may endanger and deteriorate in their mental health. Those are basically the people this bill, the legislation proposed by this Legislature, is addressing. We support that.

We support it for two reasons. First, although a mechanism already exists to provide service to those patients who do not fit any of the three main criteria already existing in the Mental Health Act, they still pose a risk for deterioration in their mental health. The mechanism that exists is cumbersome, distressing to the patient, involves the patient within the judiciary and correctional system and is dilatory in the treatment of the patient and costly to the community.

I will not go into the details of how we have to wait, psychiatrists or physicians sometimes, until the family, for some reason-and sometimes after a year or two of persuasion on our part-will consent to criminally charge this mentally ill young man or young woman because they have taken the car without permission and driven to California, to end up in disaster and waste. Then we persuade them to charge these mentally ill persons so they can come into the judicial system and then the judge can make a decision to provide for these people a parole system on condition that they obtain psychiatric treatment under a psychiatrist. It is only through this manner of circumvolution we manage to provide psychiatric treatment for these patients.

The new act intends to bypass this costly and distressing mechanism. The evidence that it will be so is first in our cumulative experience as psychiatrists, and on the research evidence provided by the North Carolina group and other groups, including Dr O'Reilly, from whom I have received information. It is indeed a mechanism that will reduce mental hospital admissions from 50% to a five or six time reduction. The evidence is very considerable that it will be effective in providing treatment and reducing admissions.

On the specifics of the proposed legislation, we have looked at the section tending to modify and, in our belief, improve section 15 of the act. In fact we see that what is added is a new or fourth criterion, the criterion of compelling or assisting these mentally ill persons to receive treatment on an outpatient basis on the grounds that non-treatment will increase the risk of deterioration of their mental health. This is a new criterion, and we are satisfied that the conditions for the application of this criterion are wise and sensible, both permitting the implementation and respecting the freedoms and rights of the individual patient.

There's much less, we have to say-we in our association agree with the Ontario Medical Association position that this new service should be implemented with adequate resources. By "adequate resources" we mean they have to be appropriate to the intended program.

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We do not believe that we have to delay or that we should ask you to delay the implementation of the legislation until all resources are in place and to the satisfaction of everybody. We would be satisfied that a clear mechanism for responsibility and the delivery of resources and a statement of commitment to deliver the resources be made. By "resources" we mean mostly staffing, training of the personnel, supervision by senior and experienced physicians, material equipment when necessary and the sufficient and necessary administrative support. This is what in general terms the association would like to state. Thank you.

The Chair: Is that the extent of your comments or would you like to open up to questions now?

Dr Michael Chan: If I could just make a few brief points?

The Chair: Please.

Dr Chan: Just to continue on, I think this is a long-overdue and necessary legal tool. I think this will be the linkage or the glue that will make the community resources or services link up with patients, especially non-compliant or refusing patients who are so ill that they are unable to seek out the necessary help themselves and to get it. I think this legislation will provide the necessary continuity of care of patients as they move through the system from the hospital into the community and ensure continuing treatment. The research from North Carolina and also Iowa has supported that you need a six-month time frame to really begin to see benefits, and I think that six-month time frame is an important one.

My own background in Kingston is in the forensic system. People have called us a parallel framework for ensuring continuity of care, and I've seen it work and work well. Once people are hooked up and linked in with the system, once linkages are there, the services can flow smoothly and the patients are usually very grateful.

I would agree with previous speakers who emphasized the need for community resources to make this framework successful. The literature clearly has also stressed that.

One other point that the literature has made, and Mr Clark raised that, was that the Swanson study, coming out of North Carolina and reported a month ago in the British Journal of Psychiatry, made the very strong conclusion that it reduces victimization and it reduces criminal recidivism in the community. Really, with an ideal and properly resourced psychiatric system, the forensic system would perhaps go out of business, an important point to make. The forensic system reflects inadequacies elsewhere in the system.

The community treatment order model I think has to be clear and has to be easily implementable, with clear entry points, clear mechanisms for care pathways and also a way of enforcing it should it break down with respect to compliance. I believe that the procedural safeguards with respect to rights advice and appeal mechanisms to the review board are adequate. I've also seen those appeal mechanisms significantly delay much-needed treatment of people already on the in-patient side.

In general I would be very supportive and I would say this is long-overdue. Our neighbours to the south have been ahead of us, and I would strongly urge this Legislature to proceed with both the changes to the commitment criteria and to section 33 on the community treatment orders.

Dr Bill Komer: I just have a couple of points to add, just to emphasize again that I think the legislation is long overdue. Since about 1960, we've seen the numbers of individuals in psychiatric hospitals significantly decrease, and the provision of treatment is more in the community than it is in the hospital. The Mental Health Act, however, has not kept pace with that change and typically provides a framework for treatment and management of patients inside of a hospital. It does not have any framework for management outside of the hospital. I think in default, because the legislation hasn't evolved as the treatment has evolved, we've seen the Criminal Code acting as that Mental Health Act last resort, so we've seen individuals being criminalized.

Just as a general point, I think you should try to have the legislation as simple as possible so that the practising front-line physicians and clinicians can understand it and use it practically.

I want to emphasize again the issue of resources. One wants to have a framework in place but one also wants to make sure the resources are there so that these orders are actually made.

The Chair: Thank you very much. That leaves us with about seven minutes for questions. This time the rotation will start with Ms Lankin.

Ms Lankin: Thank you very much. I appreciate your presence here today.

If we started from a premise that we all agree with the intent of getting help to that very small population that a lot of people have talked about that currently is falling through cracks, I think we would also agree that we want to make sure that the actual words in the law we're passing do that. I want to put to you a concern that I have with the words, not the intent. I'm not going to differ with anything you've said. I just want to see if you have any similar concerns with how we get to the end goal.

The law as it's written, as I read it, allows a doctor in the community to determine that a patient meets form 1 criteria, simply that that person meets the criteria that could compel them to be taken for an assessment. They don't have to fill out a form 1, they don't have to send the person for an assessment, a psychiatrist doesn't have to be involved, no assessment has to be done, and the person would be put on the community treatment order if they meet those criteria and some other criteria.

Some of those other criteria are things like, they have been in a psychiatric facility before, not even detained in, as in the Saskatchewan legislation, involuntarily detained; they've gone voluntarily. If they've been in before, that helps meet some of the criteria. Surely-let me not prejudice this. In my view, I don't think that describes the population you're talking about.

I'm interested in ensuring that we have someone get a psychiatric assessment, that a psychiatrist is involved in building a plan, that they are involved in the assessment that says this person first of all warrants committal, that this is a less restrictive way and this person can be successful in the community with these conditions. I feel that the current steps that are set out are too broad in some ways and too narrow in other ways. Have you looked at the detail-you say you support the legislation-the detail words? Are you comfortable with that process I've described in the legislation, or is it the intent that you're saying that you support?

Dr Allodi: It is basically the intent, but also, without being a lawyer, I'm familiar with this form of procedure and am satisfied, as far as I can see, that it's adequate.

Your specific concern with the criterion or the necessity of being a mental hospital admission not necessarily involuntarily I think is adequate in the sense that mental hospital admissions are very rare these days for people who have not a very severe mental illness. Then they may shorten the necessity to select carefully the patient for admission to a mental hospital. I would say that almost all of them are severely mentally ill and need admission because of severe crisis and severe disruption of their mental function in the community life. So the fact that it is simply an admission, not necessarily a previous involuntary admission, nowadays doesn't make a great deal of difference. The thing is that it's strong criterion still.

The fact that it is an MD, not a specialized psychiatrist, who would be able to certify a patient is balanced by the fact that it's are only three days, which go very quickly, and immediately, in fact the same day, a psychiatrist will be consulted upon the admission of this person.

The Chair: Ten seconds. We've already gone well into the time of the other parties.

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Ms Lankin: In fact, what I'm telling you is that the legislation does not compel the person to go for three days to see a psychiatrist. It's simply saying, if I think as a doctor that you meet the criteria that I could send you for an assessment, I can put you on a CTO without the assessment or a psychiatrist being involved.

Dr Allodi: But if the patient refuses the alternative information-

The Chair: Thank you, Ms Lankin. We have time for very brief questions from each of the other two parties. Mr Clark.

Mr Clark: A brief question. Section 33 of the act proposed-this question has come up before and I'm wondering if we can get a comment from you-states that "a physician may issue or renew a community treatment order under this section," and then it goes into a number of clauses. The question that has come up before is, do physicians, general practitioners, have the capabilities and understanding of mental illness? Do they have that ability to issue that community treatment order? The act simply states that a physician may do it. So should it be a qualified physician, that there should be some, I don't know, certification process that a physician would have to take in order to be able to do it, or can a general practitioner do it? A comment from you folks?

Dr Komer: I think ideally you want to have a psychiatrist, but there are going to be situations throughout the province where you're not going to have a psychiatrist, and one would not want to have this treatment order not be available to a person who needs it because there's not a psychiatrist. But I would agree; I think by and large a psychiatrist is the most trained to do that. There are some family physicians who have much more of an interest in mental health issues and there are some that do not. That's why I think one should try to keep it as simple as possible for people to understand the forms and to complete them.

I wanted to pick up on a question that's related somewhat, because it is about section 33. I think one doesn't want to get too complex. I think 33.1(2)(a)(i) talks about the patient previously, over the last three years, having been in hospital. I think that gets a little too specific and arbitrary. I think it would be important to look at mainly the criteria that are in (b) and (c) and below that deal with the person's need to be on this order. My reading of it is that a physician needs to at least do an assessment and come to an opinion that this person needs to be on this order because of certain needs of that person. I think there are the safeguards that you are concerned about. At least it says in there that there needs to be the opinion of the physician that the person has a mental disorder and needs treatment.

The Chair: If I could ask you to keep your answer fairly brief, please.

Dr Allodi: The current application of the Mental Health Act, if anything, really shows how shy physicians and psychiatrists are in applying that section. Last month a family physician who knew this patient very well for many years, and also a group of physicians who do emergency visits, both refused to visit the patient in their home and issue a certificate of involuntary admission. If anything, this new procedure is going to be used very rarely. If the physician is unwilling because of lack of familiarity, he or she will seek a consultation or refer the case to a psychiatrist, which is the usual mechanism. On the other hand, we should not underestimate the new training of medical school students, in which I have participated over the past 20 years. In resources, we should make sure this is adequately covered in the finishing year of the medical students.

Mr Patten: Thank you for coming today. I'll have to be quick because we're running out of time, but I want to establish one thing: Those who are against this legislation continue to say that there are provisions already, that section 27 provides the option. There was a quote this afternoon referring to Dr Goldbloom. I have a paper by Dr Goldbloom, who is the physician in chief at the Centre for Addiction and Mental Health, where he says, in applying section 27 in his particular institution, that it was reviewed by a board hearing at the centre and was not upheld as being used as a community-based treatment of a certified patient, which is one of the motivations, in fact, to attempt to deal with this. But that mythology continues to perpetuate in the community, especially for those working on a community basis. Would you comment on that, please.

Dr Allodi: I must add, and question the date of that document of Dr Goldbloom's, because Dr Goldbloom changed his mind after that paper and was in favour after he conducted with a colleague of his, Dr Zipursky-

Mr Patten: This is that paper. I'm saying he's-

Dr Allodi: You say he supports it.

Mr Patten: I'm saying he's supporting the CTO or CTA of whatever you want to call it on the basis of the leave not being permissible. Section 27.

Dr Allodi: Section 27 leave of absence is rarely used and not fully utilized. Correct.

Mr Patten: That's right. OK.

Dr Allodi: The only mechanism I am aware of that has a similar continuity of care is the forensic system, which is based on the federal Criminal Code. To enter that system you have to be criminalized. You have to go through the criminal justice system, be incarcerated sometimes and eventually get across to the psychiatric end of the system. It's a very costly way to go about it. I think if there is a direct link into psychiatric services, and not necessarily going through the criminal justice system, that's the way to go. I think that's what this is about.

The Chair: Thank you very much, gentlemen and madam, doctors all, for coming before us. We very much appreciate the expertise you brought to these hearings.

YVONNE JENSEN

The Chair: Our next presentation, Ms Yvonne Jensen. Please come forward. Good afternoon and welcome to the committee. We have 10 minutes for your presentation.

Ms Yvonne Jensen: I'd like to begin by saying that I have worked at what used to be called the Queen Street Mental Health Centre for a total of 16 years. I have worked in the capacity of psychiatric nurse, clinical instructor in psychiatry for nurses and as the chaplain. As you see, I am also a survivor. When I first decided that I wanted to address this issue, it was for that reason, because if CTOs had been in effect in 1971, I would not be here today, nor would I have had the chance to continue with my education. I am grateful for this opportunity.

About a year ago, I took a leave of absence from that institution, Queen Street, where I was working as the chaplain, because I had a great deal of difficulty with feeling that I was part of legitimating that institution. I was visiting every week a woman on a ward who was receiving treatment against her wishes and who died on the table receiving ECT. She was revived and she continued to receive ECT against her wishes. I visited her every week and said, "I will see you next week." The woman sat in terror from one week to the next, saying, "If they don't kill me this next time, you will see me." To me, it is unthinkable that anyone should be sitting that way week after week, month after month, fearing for their life.

James Hillman, a very famous psychologist, has said we have had psychotherapy and we have had psychiatry "for a hundred years and the world is getting worse." Psychiatry has become the gatekeeper for society. Psychiatry decides who is in and out and has the status and prestige of a science. But the way diagnostic categories are arrived at is not scientific, and mistakes are made all the time. This is well documented-there is a mistake in the reference-by Paula Caplan in her book They Say You're Crazy: How the World's Most Powerful Psychiatrists Decide Who Is Normal.

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However, once a person has been diagnosed and is prescribed treatment, it's very rarely without drugs, because people who refuse drugs when seeking help and/or admission are often asked, "If you don't want medication, why are you here?" I have heard this; I worked for five years in the admitting department of Queen Street Mental Health Centre: "We are the experts. If you won't follow our advice, why are you here?"

The patient is administered drugs which are often dangerous and once into the treatment process, there is no way to correct the situation. People are trapped in the treatment process with no possibility of reassessment. I'm not saying a person isn't regularly reassessed; they are. But once they receive these debilitating drugs, they are no longer the person they were.

In 1971, I had one of these injections, my first and last. I was discharged, and after two weeks when the medication wore off the hospital phoned me up and said, "Unless you come back and receive another injection, you will become very ill." But that was the very worst two weeks of my life. I could not imagine how I could not kill myself because of the way that drug felt.

I had to hide from the system for years. It was lonely, and it was frightening. I am speaking here today because I am afraid that with CTOs in effect, many people are not going to seek treatment. They are going to be afraid to seek treatment to discuss what kinds of thoughts and feelings they are having. We're just going to create a whole underground of people who cannot access the resources that the taxpayers think they are paying for in order to protect the vulnerable. Also, there are dangerous physical side effects of psychotropic drugs, which I'm sure you are well acquainted with at this time.

In Touched With Fire, a book that talks about people with mood disorders, there are numerous accounts of our most famous artists, musicians, writers and poets, all diagnosed with mental illness, all of whom could have been medicated, in which case we would not now be enjoying the fruits of their labours. Schubert, Van Gogh, Emerson, they're all in there. You name the artist and you can almost be sure they are in there, and you can read that for yourselves.

Some patients commit suicide because their lifestyle becomes such that life isn't worth living. One patient managed to get better, to the point where he was ready to start his own business, creating and selling fine jewellery. He had a relapse related to his environment and was restarted on neuroleptics. Neuroleptics inhibit right-brain function. They decrease creativity, they decrease motivation and they inhibit the ability to imagine. This man ended his life. These are just a very few cases. There are many, many people who are victimized like this.

The violence myth: The media would have us believe-every time there is a mentally ill person who commits a violent act, it says in the newspaper, "This person was mentally ill." But in all other cases of violence reported in the newspaper, when the person is not diagnosed with a mental illness, the newspaper does not say, "This person was not mentally ill." I would suggest that we start asking, "What kind of a society are we that generates so many people who simply cannot adjust to our society?"

The fact that violence among the mentally ill is a myth, or that there is a greater danger there, has led me to question the motivation behind this proposed legislation. I think it's political rather than rooted in deep compassion and a real desire to help people who are mentally ill.

Mentally ill people know what they need and are asking for what meets their needs, but we're not asking them, "What do you need?" because once a person has been diagnosed with a mental illness, they are already a write-off. Their judgment is off, and they are not taken seriously. People need adequate housing, food, meaningful work, the right to education and mutual respect, just like all the rest of us.

In Recovery from Schizophrenia-and this book is used as a textbook at the University of Toronto, the School of Social Work-Dr Richard Warner, medical director of the Mental Health Center in Colorado and associate professor at the university, argues: "We have been too pessimistic about the cause of untreated schizophrenia, and overconfident about the benefits of modern treatment. Despite the increased use of new anti-psychotic drugs and massive annual investment in the treatment of schizophrenia, the outcome from the illness in modern industrial society is no better than in the Third World. Much of what is called community treatment is, in fact, the antithesis of treatment, resulting in people with psychosis living a life in which even the basic needs, such as food and shelter, are not met"-and such as security. Any one of us has only to visit some of the boarding homes over in Parkdale that I have had the privilege of visiting people in while I worked as a chaplain.

Since the media have targeted mainly the schizophrenic person, the following recommendations will address this population. We have far to go before schizophrenic persons are welcome in our society and before they can view themselves as equal, useful members of society. Until such a time, schizophrenia is likely to be a malignant condition. We have the knowledge to render this condition benign.

The recommendations are on the front page. We need to address concerns around psychiatry as a scientific profession. They make mistakes in diagnosis, with ensuing dangerous drug treatment. We need to look at the effects of medications. We need to treat the acute phase of the illness in small, domestic, non-coercive settings which reflect the humane principles of moral treatment. We need to ensure adequate psychological and clinical support in the community, including a full range of independent and supervised, non-institutional accommodation, and give recognition and support for the care offered by the schizophrenic person's family and provide family education and counseling.

We need to provide jobs and training for the mentally disabled, work which is neither too demeaning nor too stressful. We need to establish economic incentives to work and a more gradual reduction of disability benefits for disabled workers and wage subsidies for the severely handicapped. We need to encourage economic and social advancement through consumer-cooperative business, housing and services. We need to fight for the rights of people with schizophrenia and their families to participate as fully integrated members of our society, taking the issue before the public through the media, and then to use the anti-psychotic drugs as a supplement to all these measures, not-as often happens these days-as a substitute for all these measures.

The problem is so much bigger than focusing on the people we call the mentally ill, because if we were going to do all these good things for people with schizophrenia, we would also have to do them for all those people we call the poor people. We really all have the same needs, and if we did all those things for the poor people, then we wouldn't have an increase in people being labelled as mentally ill. We wouldn't have such a need for these CTOs even to be under discussion.

I have worked, as I said before, at the hospital, and I think the word "imminent" should definitely be left in the Mental Health Act. I think that if a person is imminently at risk we should intervene, but if they are not imminently at risk, we should ask them what they need.

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Parts of this plan would be expensive, but overall it may cost little more than our current vast expenditure on treatment and support of schizophrenic people and on the associated disruption, crime and imprisonment which result from inadequate care. Our society is inherently unequal, however, and to provide such a quality of life for the person with schizophrenia is scarcely feasible since such a large proportion of the population, including an army of unemployed, would be left in worse circumstances. To render schizophrenia benign, we may in essence have to restructure our provisions for all of the poor.

In ending, the recommendation I would make for all poor people, for all people in distress-it has worked for me; this is very personal, and this is why I am a chaplain-is prayer and a faith in a transcendent, merciful, benevolent being. A hope for the coming of that kind of life moved by those sentiments on the earth is what helps most of all.

The Vice-Chair: Thank you very much for coming here today. You have taken the time that is available, and we certainly appreciate the insight that you've been able to bring to our deliberations.

CITIZENS COMMISSION ON HUMAN RIGHTS

The Vice-Chair: I'd like to call on the Citizens Commission on Human Rights, Robert Dobson-Smith and George Mentis. Thank you very much for coming here. I would just ask, for purposes of Hansard, that you would introduce yourselves.

Mr Robert Dobson-Smith: My name is Bob Dobson-Smith. I'm the president of the Citizens Commission on Human Rights. This is Mr George Mentis, who is the executive director of the Citizens Commission on Human Rights. I'll begin.

The Ontario government has introduced Bill 68, known as Brian's Law, an act to amend the mental health and informed consent laws of this province.

One official speaking for the government at a recent public consultation on this hill in Toronto stated that this bill was intended to affect 60 to 70 people at most in Ontario, yet its ramifications are far-reaching. Bill 68 will affect everyone in this province, in all sectors of society. Moreover, Bill 68, which includes the introduction of community treatment orders, will lead to widespread abuse of civil liberties and fraud.

At the root of community treatment orders are involuntary commitment laws. In addition to the violations of civil rights that such laws facilitate, there is ample evidence which shows that involuntary outpatient commitment does not lower hospitalization rates, nor does it result in increased public safety. A study done in New York City on December 4, 1998, by Policy Research Associates for Bellevue Hospital found that outpatient commitment had no statistically significant effect on rehospitalization rates or days spent in hospital. The study also found that outpatient commitment did not improve compliance with medication and continuation of treatment or reduce the number of arrests or violent acts committed.

The Bazelon Center, a clearing house on mental health issues based in Washington, DC, describes the New York City study as one of the most comprehensive and best designed studies of outpatient commitment released to date. The study sought to answer whether an outpatient commitment order contributed to any additional beneficial results when compared with patients who received intensive services without such an order. The findings, which the Bazelon Center describes as conclusive, found no additional improvement in patient compliance with treatment, no additional increase in continuation of treatment, no differences in rates of hospitalization, no differences in lengths of hospital stay and no differences in arrests or violent acts committed.

In the only released controlled study of the subject, it was found that individuals given the option of enhanced community services did just as well as those under commitment orders who had access to the same services.

Closer to home, when we examine the data from Ontario, we see a steady increase in people involuntarily committed to provincial psychiatric hospitals from 1990 to 1995. In 1990, some 13,365 people were involuntarily committed to psychiatric hospitals. By 1995, that number ballooned to 16,817. This translates into 48 people a day being locked up against their will in a psychiatric hospital. It is estimated that currently there are more than 70 involuntary commitments across Ontario every day. These statistics show that under the current legislation an alarming number of citizens are being committed, which contradicts the argument that stronger legislation is needed.

A basic assumption of Bill 68 is the fallacy that psychiatric drugs emptied the institutions and hospitals. Lacking any other evidence, this assumption-and it is nothing more than that-is relied upon to demonstrate the efficacy of these psychotropic substances. This proposition is a myth. It is true that psychiatric patients were sent out of psychiatric hospitals; what is not true is that this was caused by the efficacy of the drugs. What actually happened is that the media, human rights groups and others exposed widespread abuses in institutions across the country, and the psychiatric community found itself vulnerable. After all, before that time, patients were warehoused, heavily medicated, electroshocked, experimented on and worse, all without the slightest hint of public scrutiny.

Instead of cleaning up their act and providing medical treatment, psychiatrists moved patients into thousands of group homes across the province, like the homes for special care. Whether for-profit or non-profit, these facilities earned a lot of people a lot of money. There were approximately 21,000 psychiatric patients in Ontario prior to the homes for special care program being implemented. Afterwards, around 14,000 were transferred to approximately 2,500 of these private homes. Psychiatrists implied that these patients benefited from treatment, yet what occurred is that patients were taken out of regulated facilities and placed in ones where they were virtually out of sight.

These homes were, and are, little more than human warehouses for patients who are rarely seen by a health care practitioner and who are constantly kept in a heavily drugged state so that they will not be a management problem. This reduces costs and increases profits. After all, the highest expenditure in any health facility is labour. The Queen Street Mental Health Centre promoted a few years ago that they had a re-admission rate of 75%. If patients cannot be cured in a major psychiatric institution with tens of millions of tax dollars in funding every year, how will they be cured in a private home with nothing more than mind-altering drugs?

"We do not know the cause of even one major psychiatric disorder nor can we cure in a reliable way those people who suffer psychiatric illness," stated Dr Paul Garfinkel of the Clarke Institute in 1996.

Dr Fred A. Baughman, a board-certified neurologist, said so-called biochemical disorders of the brain are a "fraud." Dr Baughman has discovered real neurological diseases and had his findings published in peer-reviewed medical and scientific journals.

"The fact that psychiatrists do not perform physical or neurological examinations by which diseases of the brain and nervous system are diagnosed make their claims of diagnosing and treating `biologically-based' brain diseases unbelievable, a fraud. There is no physical or chemical abnormality to be found during life or at autopsy in `depression,' `bipolar disorder,' `attention deficit hyperactivity disorder' ... or in any other `mental illness.'"

The Charter of Rights and Freedoms protects from discrimination on the basis of age, colour, sex, religion and mental or physical disability. Clearly, Bill 68 is a revocation of this charter and will undoubtedly generate numerous legal battles, as it has in the US. The United States Supreme Court has ruled that involuntary commitment to a psychiatric hospital is "a massive curtailment of liberty." The court also emphasized that "involuntary commitment to a mental hospital, like involuntary confinement of an individual for any reason, is a deprivation of liberty which the state cannot accomplish without due process of law." Moreover, the court has clearly stated that there is "no constitutional basis for confining such persons involuntarily if they are dangerous to no one and can live safely in freedom." Interestingly, the US decision is extremely similar to the Canadian Charter of Rights and Freedoms, which we're all familiar with.

1750

The proposed Ontario legislation wants to eliminate the "imminent danger" criteria from the Mental Health Act, based on the assumption that psychiatrists can somehow predict future dangerousness. This couldn't be further from the truth.

Whether the assessment of imminent danger is done by a police officer or a mental health worker, even the psychiatric profession admits that predicting dangerousness involves nothing more than a craps shoot. A brief filed by the American Psychiatric Association before the US Supreme Court stated that "such predictions are fundamentally of very low reliability." If, as the APA states, predictions of dangerousness are not reliable, this contradicts the whole basis for community treatment orders legislation, which is based on the premise that psychiatric patients must be forced to take medication or they will become violent.

According to a prominent US professor of psychology, Dr Margaret Hagen, who wrote the book Whores of the Court, the predictions of psychologists in court are wrong two thirds of the time, a statistic significantly worse than that of the general population.

In a case documented in 1977 by CCHR, a man in his late 40s was picked up by three members of an assertive community treatment team from his home in Scarborough and taken to the psychiatric ward of a local general hospital. Without explaining anything to him-this is a mentally competent man-the man was forcibly injected with a mind-altering drug by a psychiatrist. Upon leaving the room he told the patient, "There's not a court in the world that can touch me."

It is important to note that these are not just isolated incidents being complained about by victims and advocates. Illegalities have been known to the authorities for years as being widespread.

A case in point: In 1997, the Provincial Auditor of Ontario exposed abuses at the Whitby Mental Health Centre. His report, submitted to the Ontario Legislature, stated:

"From a sample of patients considered capable of consenting to treatment, we found that: the assessment of mental capacity to consent to treatment was not documented in 76% of the clinical records we reviewed; informed consent was not documented in 88% of the cases we reviewed; 60% of the capable patients we interviewed stated that no one at the centre had explained the side effects of their medications before they were asked to take the medications, another 13% did not know whether they had received explanations, and 39% of the capable patients we interviewed did not know the medication they were taking and 41% did not know what would happen if they did not take their medication. Many of these patients stated that there would be no change if they stopped taking their medication." To date no one has been charged, although this violated the informed consent regulations.

According to the law, a patient must be informed about the nature of the treatment, expected benefits, risks, side effects, alternative courses of action and the consequences of not having the treatment. Yet this is violated as a matter of routine, in both the public and private mental health sectors and other areas, such as our schools.

The Vice-Chair: Excuse me. I see the light flashing. We will take a recess. The committee will continue after our vote.

The committee recessed from 1754 to 1822.

The Vice-Chair: Ladies and gentlemen, sorry for the interruption. You have five minutes remaining.

Mr Dobson-Smith: I have eight minutes, I think.

The Vice-Chair: I have you beginning at 5:40.

Mr Dobson-Smith: No, we started at 5:45, actually. The other fellow ran on. We have 20 minutes, I understand.

The Vice-Chair: Yes, you do. Continue.

Mr Dobson-Smith: Thank you.

I was explaining when we left off, just to refresh your memory, about the report of the Provincial Auditor of Ontario and giving you the various statistics. I basically said that there had been no informed consent in many circumstances at the Whitby Psychiatric Hospital, with 76% of the cases and 88% of the cases etc, and that these people did not understand their medications, whether they should take them or not and what would happen if they didn't take them. To date, because there was no informed consent in this vast number of individuals, no charges have ever been laid; no one has ever been brought to say why this occurred.

According to the law, a patient must be informed about the nature of the treatment, expected benefits, risks, side effects, alternative courses of action and the consequences of not having the treatment. Yet this is violated as a matter of routine, in both the public and private mental health sectors and other areas, such as our schools.

Earlier this year, at a small school near Brantford, a couple was shocked to discover that their son had been sent for a psychological assessment without their knowledge. They discovered that the school had a policy to prevent disclosure to parents. The policy, known as "referral process," stated, "Do not get a signed consent form from parents."

In conclusion, every aspect of the community treatment order initiative will lead to abuse of patients and taxpayers. A real solution would include changing mental health laws to better protect patients. As an example, Ontario could implement videotaped consent procedures. This low-cost measure would ensure that patients are given proper informed consent in accordance with the law.

There should also be a written information sheet for every single psychiatric treatment and medication that will provide a standard minimum level of information to a patient in lay, understandable terms. This would protect every patient and it would also protect every practitioner.

Another valuable amendment would be mandatory medical testing to pre-screen for physical ailments, as it is known that many physical illnesses manifest symptoms that appear to be of the mind, yet they are of the body. This would help ensure that whatever condition the patient is suffering from would actually be addressed.

After all, if a psychiatrist does not diagnose without thorough testing, he or she cannot really be sure what is wrong, as without a full, searching, medical examination, a medical practitioner cannot establish the nature of the illness and thus provide a truly informed consent.

We firmly believe that a truly informed consent means the patient and/or his substitute decision-maker, his family member, fully understanding any medical condition that could be manifesting these things also, which is why a medical examination is necessary. Often, the patient is just looked at, and he's considered to have a bipolar disorder or whatever with just cursory observation.

In closing, I would like to say that if informed consent is not being applied in this province after more than two decades of it being written into law in the Mental Health Act, how can we ever expect psychiatrists not to abuse the vast powers granted to them with community treatment orders? Community treatment orders will do nothing more than legitimize the illegalities and abuses occurring in psychiatric facilities in Ontario every single day. Every single week we get calls.

The Vice-Chair: Thank you very much. We have about two minutes. Mr Clark, do you want to begin?

Mr Clark: I'll defer to Mr Patten.

Mr Patten: So I gather you support the legislation. No, I'm just kidding, obviously.

Mr George Mentis: We do support amendments to it.

Mr Patten: You do, OK. By the way, the Citizen's Commission; are you connected with the Church of Scientology?

Mr Mentis: Yes, we were established by the church in 1969.

Mr Dobson-Smith: We're currently separately incorporated.

Mr Patten: You're separately incorporated. Because this is twice; I had a group called this as well, but they didn't disclose that until they arrived in the office. Can I ask you-

Mr Dobson-Smith: Are you suggesting there's something improper about-

Mr Patten: No, not at all. I'm just saying, why is it that there isn't an upfrontness about saying that you are connected-

Mr Dobson-Smith: We're not connected.

Mr Patten: So you're no longer connected with them.

Mr Mentis: It's not that, sir. That's like someone coming up here and you asking them questions such as, what is their religion? I myself am a Scientologist; however, we are an independent body.

Mr Patten: No, I mean there are church councils who come; there are different groups. Anyway, I don't want to dwell on that.

You cited a lot of pieces of legislation, some I'm familiar with. I'd review that Bellevue piece of legislation as well, in saying that if indeed there was an analysis done by two completely different populations that showed that there was no distinguishable difference between the record of voluntary treatment and people who indeed were far more severely ill, I would arrive at a positive conclusion.

However, in your own particular minds, are there circumstances under which people who may be offered services, may have access to services, but in fact do not have the mental capacity at a particular time? Are there circumstances under which you would support involuntary treatment?

Mr Mentis: Yes, yes. There are clear circumstances where a person does need to be restrained. If a person is a danger to themselves or other people, obviously for the good of the person, his family and everybody around him, that person would need to be restrained. However, having said that, it's also very important to note that a very careful review of the past 400 cases of public violence-in each case, including the Taber shooting, the Columbine school shooting etc, psychiatric treatment preceded the crime. That was the only common denominator in every single instance. So although, yes, I will say that someone has to be restrained, other than the period of danger, once the danger subsides we should go into a regimen of standard medical treatment. Otherwise you're feeding the same thing.

Some of these drugs, as has been exposed in the media-for example, some people brought up this North Carolina study. If one examines what has gone on in North Carolina just in the past 12 months, as has been exposed on 60 Minutes, you'll find that a lot of the patients in these psychiatric facilities are horrendously abused.

A case in point is Charter Medical Corp, which was the largest provider of mental health services in the entire country, where you had in one facility alone 24 deaths which were as a result of restraint. In case after case in the medical records it would say "death due to asphyxiation." However, what would actually happen in a lot of the cases is that the person, the kid, the adolescent, whatever, would be on a psychiatric drug, they would be normally overdosed, and then when a physical restraint would occur, what normally would not kill that person, in this particular case would. As a result, as I speak, the US government is now reviewing restraints in facilities across the country.

The Vice-Chair: Thank you both for coming here today. We appreciate your comments.

1830

DON BARBER

The Vice-Chair: Our last presenter is Don Barber. Welcome, Mr Barber. You have 10 minutes in which to make your presentation.

Mr Don Barber: In expressing my concerns about Bill 68, I would like to address the issue from two points of view: the general negative trends in our society and my personal life. I am among the many who believe this bill will lay the foundation for Canadians to be wrongfully arrested more often.

In 1994, I started for the first time to become involved in government as a community representative and to try and save a local, old-growth urban forest, the Cawthra Bush in Mississauga. My main focus and efforts were more on human and democratic rights than environmental and to get the facts to the public and then to try to get the right for the community to make an informed decision by way of vote. Over the years, I came to a new understanding about how Canadian law was enforced regarding human and democratic rights. Unlike many apathetic Canadians, I came to see that our country was not so great that politicians couldn't ruin it, if we let them.

Some of the first-hand examples provided are while dealing with Hazel McCallion, a politician who doesn't care how she wins, just as long as she wins, and should be used by this committee while reviewing the possible negative side effects of Bill 68. Many abuses of this bill will be by the government, but members of the public, bullies generally speaking, will also find uses for this bill which are not the intentions of lawmakers.

First of all, what has been lost by governments of the day? That is, what is a human being and what does the human animal need for a quality life? This is the most basic question that is not asked. There's no single body of work the government can point to and say, "That is our best understanding of our kind and its needs." Why should it exist? Because to make quality decisions in government you need to know who you are making them for and what people really need.

The mentally challenged belong in our society, just as much as the elderly do. They are a part of the world we are created to live in, and it is dehumanizing for all of us to try and purge the streets of their existence. Governments have often made hard decisions regarding what people want and what is best. The wisdom of the ages has guided many. It is better to err on the side of caution and often the truth is the exact opposite of the popular perception.

In the case of human beings, the best overall statement to make is our lives should be as close to the balance between chaos and order as reasonably possible. Too much of either can destroy not only the individual life but whole societies as well. To say to a government that too much order can destroy the quality of a person's life, their culture, society, if not the very country they live in, is a hard sell.

Another important element in good government decisions should be made understanding there are acceptable losses in our society, or how many people are we willing to lose before action is taken? To put that another way, if you try and save everyone, you have to try to control everyone. Over-control leads to its own losses. Human and democratic rights come at the cost of human lives. We should try not to be motivated by do-gooders who overreact to events, start up a media-driven bandwagon to influence our emotions and ignore the intellect. The role of good government is to be far-sighted and to understand that the loss of a few should not be used as a power grab in our lives while grandstanding for votes.

Once laws are passed, they have a habit of growing, linking with other laws and legal precedents to become even more intrusive. With the whole body of human history to review, let us look at a good example of how some of these principles have been applied in other governments, some that they thought were too big to fall as a result of them, such as the USSR, a country that thought ruling from the centre would be the best way to do things, with a grand list of laws enforced by unaccountable bureaucrats. The USSR did label those who disagreed as mentally ill in many cases, and there is reason to believe the same would happen in Canada. The use of this bill begins the same process. Under the guise of doing good, a political weapon is created against the most important group to a dynamic society, and those who would oppose are threatened.

Good government depends on accountability. The current government has downsized that factor and removed it in the case of the police complaints process. The possibility of taking a police officer to court has been removed and a tribunal of persons the government selects, some of whom have made large donations to the current government, replaces trained legal professionals. In general, bureaucrats are very unaccountable and the police are little more than gun-carrying bureaucrats.

Members of the public have often been bullied by the government because they are poor or lack the knowledge to stand up for their rights. Added to this, the poor can't fight back, a fact known by the poor and recently reported by the National Council of Welfare. Our legal system discriminates against the poor from start to finish. This is the most important point, as many would boast that there are laws to protect Canadians' rights. The truth is they have to be bought. You have to buy justice in Canada. If you can't afford lawyers to fight back, our lives are just flushed.

The bill is about making the public more accountable to doctors and police, but nowhere does it try to make doctors and police more accountable to the public. There's no effort for a balance here. With the creation of newly privatized or privately run facilities like prisons, it would appear the government wants to fill them at our expense.

One of the key elements for accountability in regard to police, doctors and bureaucrats is that they make interpretations regarding events and then force them on members of the public. The only way it can be challenged is in court. If there is no money, it can't be challenged. The bureaucratic mindset is one that builds like records and reports on top of existing ones. Rarely does a bureaucrat stand out from the crowd by saying records in the past are wrong and should not apply. Often wrong interpretations are made because it is known the person can't afford court or any legal method to fight back. Nowhere does this government address this fundamental failure of our legal system. Instead, it passes new laws that only the well-off can afford to avoid-the old idea of a class system.

To use events in my life, I hope to show how dangerous it is to be poor and how unaccountable and unjust government can be towards a stand-up kind of person, as well as the politically active. When I tried to used the freedom of information act to get city of Mississauga records for the public's use, the mayor personally stepped in and shut down the act. I was poor and could do nothing. In time, they accused me of being a frivolous and vexatious abuser of the freedom of information act. In the inquiry that followed, the Canadian Environmental Law Association bent their own rules to make a submission, as it recognized the importance of the issue I was appealing, but a bureaucrat knowingly made a wrong decision, knowing I couldn't appeal. This injustice will stand until I can find thousands of dollars to fight it.

The next point is one of the most important ones that I've been trying to make. Next, city politicians sent the police to my door because they didn't like my demeanour-nothing else. Not only was it direct harassment against me, but the same politicians who enlisted the police made a point of telling the public the police had been sent to my door in an effort to publicly discredit me. Again, I am poor with no chance to fight back. This is the way of the future: politicians abusing the law and their power, knowing the public can't fight back.

As I have made a point of not backing down, even when the police are present, when it comes to standing up for my rights-and it is based on what I have read in their notes about the event and whatnot and what they had said at the time-it is very clear to me that if this bill had been in place they would have arrested me for a bad attitude towards politicians.

Another example is the matter of a sadistic bully who uses the law as a weapon against me. This person-

The Vice-Chair: Mr Barber, I just want to inform you that you have about 30 seconds left in your 10 minutes.

Mr Barber: OK. Thirty seconds? Can't get two minutes or anything?

The Vice-Chair: No, sorry. If you'd just give us a few final comments.

Mr Barber: Basically, the idea is that bullies use the law as a weapon against you. The police are then faced with individuals who are consummate liars and manipulators and you actually have to prove your innocence.

I'll have to submit the rest in writing. Generally speaking, this law opens up the opportunity for a great many more people who are not the target of the bill to become vulnerable just simply because there are more laws for people to be arrested. I'm very concerned that if politicians can send the police to your door because they don't like your attitude, this bill will be simply extended to arresting people whose attitude they don't like.

The Vice-Chair: Thank you for coming here to our committee. We stand adjourned.

The committee adjourned at 1842.