Madam Speaker, I would like to inform you that I will be sharing my time with the exceptional member for New Westminster—Burnaby, who is sure to shed a great deal of light on this fundamental issue.
I would like to take 30 seconds at the beginning of my speech for something more personal. Today is October 31. A year ago, my partner's mother, Debbie Djevahirdjian, passed away. Today is the anniversary of her death. I just wanted to highlight her life and all the love she gave to her family and loved ones. We still miss her dearly.
I also wanted to talk about my grandmother Alice, who did not have an easy life. She had to flee a home where she was being mistreated and malnourished. She had to leave home when she was about 14. She was fortunate to meet my grandfather, who was in the army at the time. They had a child, a son, who is my father.
Alice had a very difficult start to life, and she also had an extremely difficult end of life with Alzheimer's disease. We saw her wither away before our eyes for years and years. My father wrote a book on Alzheimer's called La mémoire des mots that recounts the end of life of my grandmother, Alice Boulerice. This book also speaks to hundreds and thousands of families across Quebec and Canada.
We all have end-of-life stories from family and friends. We all have stories of people who have experienced the end of life of someone they loved very much and who, over time, ended up unable to recognize their spouse, husband, children or friends. It is extremely painful and extremely difficult. To witness this, even as a child or teenager, is something that leaves a mark.
This means that one day, in our own lives, we would like to have the opportunity to influence this, whether in research, science or medicine in general. It can also be through legislative measures that could mean that a person does not have to see themselves wither away and lose awareness of their own existence or the existence of the people they love. In short, we would like to do something about it.
Today I have the opportunity to rise in the House to talk about it. It is such a fundamental issue because it affects the dignity of human life. We know that we are all going to die one day. We hope it will be in the best conditions with as little suffering as possible, surrounded by our loved ones.
The law currently does not allow advance requests for medical assistance in dying. MAID has been the subject of great debate in society, in Canada and in Quebec, for many years now. In Quebec, there is a certain consensus on the fact that this assistance was a way to help people, to respect their will and respect their wishes to leave this world in dignity and with as little suffering and humiliation possible. For example, Alzheimer's disease or other degenerative diseases can be extremely difficult.
Not everyone is going to want to ask for medical assistance in dying. It is a choice that is extremely personal, that involves the will of each person and how they see life according to their own values, religious or otherwise.
I mentioned my wife's mother earlier. Debbie had a good friend named Janice who had MS. Janice always wanted to live right up to the end. For her, asking for medical assistance in dying was never an option. We need to respect that.
Science and medicine have evolved when it comes to this issue, as has the societal debate. Now, we can say that people are beginning to agree that medical assistance in dying is acceptable and that we need to respect each person's decision. To date, medical assistance in dying has been allowed when the person's death was foreseeable in the very near future. It has not been allowed in the case of cognitive degenerative disease, such as Alzheimer's.
The Quebec government has decided to authorize advance requests. A person of sound mind who has been diagnosed with a serious and incurable illness will be able to sign a document outlining their wishes and establishing the criteria, timing and symptoms that will indicate when they are no longer capable of making a decision because they have reached a level of advanced cognitive impairment.
Now, we find ourselves in an absolutely impossible situation because, as of yesterday, Quebec law allows advance requests for MAID, which contravenes the federal Criminal Code, all because the Liberal government has failed to act for months and years. It is mind-boggling to see that the only thing the Liberals want to do on this issue is align themselves with the Conservatives by saying that they are not going to do anything, not going to move forward. It takes the Supreme Court to force them to make decisions and change laws. It takes the Quebec Superior Court to force them to make decisions. I have never seen a government with so little leadership on such a fundamental issue that affects every Canadian, every family in this society.
Now we find ourselves in this absolutely absurd situation. Because of their ineptitude, their inertia and the fact that they are dragging their feet, we are stuck in limbo. This Liberal government's response is to say that consultations will be held and that a major national conversation is needed. However, the Quebec law has been in force since yesterday. What are we going to do about it? The Liberals have known about this for months. A joint House of Commons and Senate committee has studied the issue and made recommendations. What did the Liberals do? They did absolutely nothing.
Now we find ourselves in this impossible situation, while the Quebec law is giving people hope, the hope of having a dignified end-of-life experience that respects their wishes. People do not want to see themselves waste away. I understand that completely. I would not want to see myself waste away like that either. I think most people probably feel the same, and we have to be able to respect that.
There is someone in Quebec who has become something of a spokesperson for people who receive this kind of diagnosis and want to decide for themselves when to depart this world and on what terms. Her name is Sandra Demontigny. She has been very active in the media and has touched a lot of hearts. Her message is that we need to move in this direction, and she hopes that the Quebec Government's legislation will spare her the worst when she reaches the end of her life. Ms. Demontigny, who has a genetic type of early onset Alzheimer's, has been advocating for this right for a long time. Naturally, she was very pleased by Quebec's decision. Her wishes are clear. According to an article published yesterday in La Press, she said the following:
I don't want to be a prisoner of my own body. I want to keep my dignity and independence. That's where I'm coming from. It's quite a privilege to be able to set my own limits and not have them forced on me.
There are clear rules. An advance request cannot be made by just anyone at any time. Guidelines have been established to support health care professionals in their discussions with patients who have received a diagnosis and, under the law, those professionals can only authorize MAID under very specific circumstances. MAID is regulated and scientific. Professionals, witnesses and third parties the person trusts are involved. It can be administered only when the patient has specific symptoms and when the disease and the person's conditions have progressed to a certain point, so I do not see why the current Liberal government is incapable of taking action. It is putting Quebec doctors in an impossible position right now. Their concern that they could be sued for abiding by the Quebec law and the patient's wishes is a legitimate one.