Madam Speaker, I am pleased to speak today to Bill C-268.
This bill picks up a tiny portion of the extensive and important debates on medical assistance in dying that took place on Bill C-14 in the previous Parliament in 2016 and again on Bill C-7 in this Parliament. I want to start today by restating the principle that has guided the New Democrats through these debates.
We believe that medical assistance in dying is an important tool for helping to end unnecessary suffering for patients facing end of life issues and for avoiding the unnecessary suffering of their families, who have to accompany them on this journey. This is the reason the New Democrats will always defend the right of access to information about MAID and access to the service for all those who qualify for assistance and choose to proceed.
In the debate on Bill C-7, many issues arose concerning the challenges Canadians face at the end of life, some of which Bill C-7 addressed and some of which have not yet been addressed. Two important concerns were front and centre, and these, for me, were very important. The first was to help alleviate unnecessary suffering by eliminating the waiting period, which was a cause of great concern for patients who feared loss of capacity before they could complete the waiting period, as this would make them ineligible for medical assistance in dying. The second was allowing a waiver of final consent, which deals with the same issue. It was often known as “Audrey's amendment”. This is a provision that I knew quite personally, as a friend of mine chose to go earlier than she would have liked because of a brain tumour and her fear that she would lose capacity to consent at the last moment. Bill C-7 would make some important improvements on eliminating suffering at the end of life.
A second challenge was debated: How do we preserve as much autonomy as possible for Canadians who are dying? Most of the issues related to this still have to be dealt with at the special joint committee on medical assistance in dying that will begin its work next Monday. This includes questions of advance directives and whether protections for people with disabilities from being pressured to seek MAID are adequate. I was disappointed that Conservative senators spent a lot of time holding up the establishment of this new joint committee. It was very frustrating because the five-year statutory review of Bill C-14 was supposed to have started over a year ago. However, it is good news that this committee will commence its first regular meeting next Monday and will deal with the outstanding issues that were not dealt with in Bill C-7.
A third challenge that came up in the debate on Bill C-7 was access to services at the end of life. We learned there are a great many gaps in services in our Canadian health system for those who are facing death. There are gaps in diagnostic and treatment services, depending on where one lives, whether it is in a major city with excellent facilities or in a rural and remote area. We learned of important gaps in palliative care. Again, depending on where one lives, access to palliative care is highly variable. Of course, we also learned of gaps in the ability to access information about medical assistance in dying and the ability to access the service.
There are some very important questions here about the absence of services in rural and remote areas, about the inadequacy of services and about the shortage of trained professionals. Very important to me was the testimony we often heard about the complete absence of culturally appropriate services for indigenous Canadians and for new Canadians from different cultural backgrounds.
However, instead of addressing these challenges, the challenges of autonomy and the challenges of access to services, Bill C-268 is about something else. What this bill would do is override a patient's right to access information about, and to have access to, legally provided medical services, based on the personal beliefs of a service provider.
Let us put that in plain language. Let us suppose there are a variety of treatments available to a patient. It does not really matter in this case what they are. If a medical professional believes that one of them should not be available, this bill says there is no obligation to make sure patients find out all the options available to them. Professional organizations like colleges of physicians and surgeons and colleges of nurses have found this to be unethical behaviour, so they have required doctors, to varying degrees, to refer patients to someone who is supportive of those services and is accessible to them.
This requirement to refer, as mentioned in a previous speech, has been upheld by the courts. That is the main reason I cannot support this bill. It would result, on a practical basis, in the denial of access to necessary health services for many Canadians.
Many communities have a very limited number of doctors, and if one of those doctors, or even more than one of those doctors, is unwilling to let their patients find out about medical assistance in dying, then we are condemning those Canadians to suffer at their end of life in ways that other Canadians would not have to suffer. No health care professionals are, in fact, required by the law to participate. It is the professional associations who require some form of referral. Whether a referral is actually participation, I will grant to author of this bill, is debatable. I do not really believe it is.
An equally important reason for opposing this bill is the dangerous precedents that this bill would set. Its role as a potentially precedent-setting bill has already been noted by anti-choice advocates who have been vocal in their support of this bill. They recognize it would provide a precedent for denying referrals for access to contraception and abortion services. I want to point out that denials of service and denials of information are very real in our existing Canadian medical care system.
Just this year, Providence Health Care, which runs St. Paul's Hospital in Vancouver and is building a new hospital with $1.3 billion of public money, announced that in this new facility, abortion and contraceptive services will not be provided, nor will medical assistance in dying. I find this particularly problematic. I know of several cases in Vancouver where those who wished to access medical assistance in dying were forced to leave the hospital where they were being cared for and transfer to another facility, at a time when they and their families were already in a great deal of distress.
This bill would also be a very bad precedent for the current attempts to deny trans minors the counselling and medical services they need to affirm who they are. Without access to the services that others may think are appropriate, this will leave families with trans minors struggling to find the information and support their kids need. If this kind of precedent is allowed, medical professionals would not have to provide a referral to someone who would be providing a medically necessary service.
As a gay man who lived through the AIDS epidemic, I am also concerned about any precedent that allows the denial of access to medically necessary services. The AIDS crisis was generally ignored by the public, and treatment for those suffering from HIV and AIDS was regularly denied to members of my community, who quite often suffered very painful and tragic deaths as a result of that.
As I approach the end of my comments today, I cannot end without mentioning yet another unfortunate precedent set in this bill, and that is its use of inflammatory language. I have no doubt, as I said in my question to the sponsor of this bill, of her personal convictions and their strength.
However, as sincere they may be, the language used in this bill conjures up a spectre of the use of violence to intimidate medical professionals, something of which there is no evidence of happening in Canada. Using the kind of language that involves violence is certainly not conducive to an informed debate on the real principles that are in question here.
I will close my comments today by restating that on principle, New Democrats are opposed to any legislation that would limit access for Canadians to medically necessary services based on the personal beliefs of others, no matter how strong the beliefs the others hold are. There is a right in this country to access legal medical services, and that right can only be effective when, as professional organizations have recognized, doctors who do not wish to participate make referrals to doctors who will provide those services.
There is no doubt that the end of life is a difficult moment for all families and medical assistance in dying, I still believe, is an important way of ending unnecessary suffering, both for patients and families at the end of life. I would not like to see anyone denied access to the information they need to make a choice that protects their own autonomy about how their lives end.
