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Decentralized Democracy

House Hansard - 175

44th Parl. 1st Sess.
March 29, 2023 02:00PM
Context: House Hansard - 175 - Mar/29/23
Mr. Luc Berthold (Mégantic—L'Érable, CPC)
Madam Speaker, I wanted to speak to Bill C-215, sponsored by my colleague from Lévis—Lotbinière, because I have had experience with some really difficult situations involving the duration of EI sickness benefits. The people I know, as well as the people who came to my office, did not ask to have to deal with these terrible illnesses one day. I am mainly going to speak about cancer because that is what most of these people were dealing with. These people never expected that one day, they might have to choose between focusing their full attention on healing and slowly dying while trying to heal because they could no longer afford their treatment. For some, the treatments are very long. I was listening to the speech given by my colleague, who had a lot of empathy and compassion for people in such situations. Unfortunately, the government could have granted a royal recommendation and allowed this bill to be voted on so it could finally be passed after many years of trying. I will have the opportunity to speak to that in my speech. The fight to help people with these serious illnesses get access to money from employment insurance has been going on for years. Most of these people contributed their entire lives to a system that is supposed to be there to protect them. Unfortunately, when the time comes for some people to be able to benefit from it, the system simply does not meet their expectations. I wanted to commend my Bloc Québécois colleague from Salaberry—Suroît, because she has worked very hard on this file. She talked about Normand Chevalier, who was listening to her speech and may have been patient enough to listen to the other parliamentarians until my speech. I want to say hello to him. I can tell him that there are people working very hard on this issue, as my colleague from Lévis—Lotbinière has been doing ever since he had the opportunity to introduce this bill. There are people working very hard to change things. Unfortunately, as we have seen, things are not changing. I am directly and indirectly involved in the Relay for Life. Every time I participate in a Relay for Life event, I am always amazed to see that a town as small as Plessisville has the largest Relay for Life in Canada. This shows how willing people are to support cancer patients and survivors. It is heartbreaking to walk the Relay for Life route and see the thousands of little luminaries lit for people who have cancer or survived cancer, or for families and people who have lost a loved one to cancer. Everyone should come to Plessisville to see how big this event really is. Luminaries line the entire two-kilometre route, creating a mosaic of light, and each and every one of those luminaries is dedicated to someone. How many of these people had to make a difficult choice between treatments and work? The answer is too many. I do not want to get into a fight over numbers. We do not need to argue about whether it is 23% or 30%. Either way, it is too much. Nobody knows how long treatment will take. Nobody knows how to cure each of these diseases. Nobody knows how each person is going to respond to treatment. One thing is certain. These people are forced to choose between devoting themselves 100% to their recovery or devoting themselves 50% to their recovery and 50% to their work, because they have no income and they cannot go through such an ordeal without income. This can affect young people, but it often affects women or men, mothers or fathers. It can affect people who have a family to support, whether they are men or women. There are not many Quebeckers or Canadians who can afford to go an entire year without earning a cent. That is why I think the right thing to do would have been for all parliamentarians to finally pass Bill C-215. The government had promised on several occasions to agree to this request, which came in particular from two people whom I would like to salute today. Marie‑Hélène Dubé started a petition that was presented here in the House. It was signed by over 600,000 people and calls on parliamentarians to set aside their differences and partisanship and finally recognize the needs of people with cancer who have to undergo treatment so that they can focus on getting well. Ms. Dubé has helped draft many bills. She herself has had cancer several times and she has never given up, but I think that she is a bit discouraged that parliamentarians have not yet found a solution. I have never spoken to her, but I saw her in the media. I looked at her website. I saw everything she has been doing to try to convince parliamentarians. There is always a parliamentarian who is ready to take up the torch. When one party is unable to introduce the bill because of the way the lottery draw for private members' bills goes, someone else takes up the torch. This time, it was my colleague from Lévis—Lotbinière. He and the member for Salaberry—Suroît both worked very hard on this bill. I want to recognize the work of Ms. Dubé, who has not given up, even though she may be a bit discouraged. Today, I read her most recent post on the website 15weeks.ca. I will read it even though it is not that recent. We are currently on the 14th bill to amend the act to increase benefits to more than 50 weeks, after 13 years of vigorous campaigning. If you can believe it, this campaign that I have been waging by myself since 2009 has been going on so long that I have qualified for my first FADOQ card. That's crazy! I was 38 years old when I gathered the first of the 619,000 signatures… I am honestly so exhausted, but I could never abandon you. My colleagues are applauding her and I think she deserves it. How far will we have to go? How long will we have to wait? There have been committee studies and unanimous motions adopted in the House, where all parliamentarians said they agree with the principle of 50 weeks. However, no government has made a move to change things. It is not a matter of money, because we can make it happen by using the EI fund. It is not a matter of politics, because everyone knows someone, like a family member or a friend of a friend, who has had to go through a difficult situation because of EI benefits. I know there is not much time left, about 15 minutes, but perhaps someone on the government side will hear this final appeal from Ms. Dubé, from my colleagues and from all those who have championed this bill and its previous versions. I hope that the bill will finally receive a royal recommendation so that these people can focus on their recovery. It will send a message of hope to their loved ones. Let us send hope to all those who have had this disease and survived and to the many others who will one day have to deal with this terrible disease.
1271 words
  • Hear!
  • Rabble!
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