Mr. Speaker, sometimes we sit in the House of Commons and wonder if a day like this will ever arrive and today it has.
Before I begin I would like my hon. colleague from the Bloc to know that this is exactly what we are trying to do, to work with the provinces. It will be the provinces that deliver the treatment, and we know that, but what is required is some fiscal assistance from the federal government as well. That is part of the national autism debate.
We hope the Bloc Québécois will support the motion of the hon. colleague from Fredericton so we can actually have this debate. The health minister or the Premier of Quebec could sit down with the Prime Minister and other premiers and territorial leaders and discuss how we deal with this very important subject. That is really what we are debating today.
While I am here, Mr. Speaker, I have to tell you what happened on my road to Damascus conversion on the concerns of autism which happened a few years ago. While I was walking outside on Parliament Hill, I saw a gentleman named Andrew Kavchak who had a sandwich board sign. The curious person that I am, I spoke to him, which led to a very serious friendship. He introduced me to a woman named Laurel Gibbons who is the mother of a child with autism. Through her initiative, she has worked very diligently with all groups of people with autism. It does not matter whether it is the national autism group, provincial groups or the FEAT group, Families for Early Autism Treatment, and individual members of Parliament and senators, she will talk to anyone about it. Her dedication to not only her child but to other families with children with autism is unbelievable.
I know it is hard to believe but after that I met a certain gentleman from Ottawa who happens to be with us right now. I want to read his card. There are not many 12 year olds in the country who, because of a notice in a magazine in Ottawa, could be one of the top 50 people to watch out for in the future.
This young man is named Joshua Bortolotti. On his business card it says, “Autism Awareness Advocate and aspiring future Prime Minister of Canada”. By the way, he does not have autism but his little sister does. For Sophia Bortolotti, his sister, we should be able to tell young Joshua and his family and all the Joshuas of this world, the aspiring prime ministers, that this is the opportunity we get to tell this young 12 year old who is fighting for his sister and who I wish could have the opportunity to speak here in the House, what we will do today after this rather rational and very serious debate. Do we tell him that yes, maybe there will be the day that his sister and many other children like her across the country will have the opportunity to get the treatment that they require so they can live productive and normal lives in this country to the best of their ability? Or, do we tell them, because of crass politics and jurisdictional squabbles we are not able to do it?
I know many colleagues and friends of mine in the Conservative Party know this issue is very serious. I know many members of the Bloc and the Liberal Party also know it. I also know that Senator Jim Munson of the other place is a strong advocate for early intervention and cooperation between the federal, provincial and territorial jurisdictions to get this done.
When we speak of young Joshua Bortolotti, in the riding of the hon. member for Fredericton there is a school called the Leo Hayes High School, I believe, which has either a principal or a teacher named Greg Peters. I have received all kinds of tremendous letters from that school. This class of young activists, of all the causes that are out there, decided to take up the cause of autism. They have written to all of us, in both official languages, and they are probably watching the debate now, encouraging and watching all members of Parliament to see how we move this debate forward.
It is a tremendous day. It does not matter who moves the bill or what government does or whose name is attached to anything. This is the opportunity for members of Parliament to work together in a constructive manner to once and for all develop a strategy with the provinces, with various agencies and research firms and the providers of the care to actually say to those families with children with autism that here we go.
In my own riding, we have a military person who has a child who is a flight risk. Every single access to their house is locked. If that door opens just a crack, that little son of theirs will take off and run and run until physically he either drops or gets hit by something.
That is just one of the concerns about a child with autism. There are many of them who are voice challenged; they do not speak. Many of them react in ways that they do not fully comprehend or understand. The concerns for the families are not only the financial costs, but the emotional strain on families knowing that they give up their jobs, they sell their house, and they lose all possible equity. It takes money away from other children in the family. They themselves will pour all their resources into their child with autism.
Here, I believe, is where as Canadians we could something for those families. We all know, those of us who have been interacting with them and seeing them, that children with autism are some of the most beautiful children in the world. They are warm, they are generous and they are kind, but these people are just looking to us for indications of leadership, indications that we can work together, indications that they will not lose everything in order to provide the treatment their children need. We have that opportunity.
Recently I was in British Columbia with my colleague, the hon. member for New Westminster—Coquitlam, and we did a press conference with folks with autism. I met a young mother, and by the way, her sister happens to be my next door neighbour, which is quite a coincidence. She has two children with autism, not one but two, and the financial concerns are completely unbelievable. It is also the emotional strain on the families as well.
The hon. member for Fredericton is absolutely correct. We have the opportunity now to say to those thousands of families in this country, crossing all political lines, that we are going to step up to the plate. We are no longer going to wait for every single person in the country to agree to every single dot of the i's and crossing of the t's.
We have cross-political support on both sides of this chamber. We have tremendous numbers of people across the country who are saying that now it is time for government to move on this. In the era of tremendous fiscal surpluses, we are not asking the federal government to do this on its own. We would not do that because we understand the provincial jurisdictions.
The provinces themselves have challenges on this. I really compliment the province of Alberta because its treatment goes to age 18, while in my own province of Nova Scotia it is a sort of trial program. It is spotty. The province does not have anything constructive. In Ontario, treatment is until age 6, so what we are saying to families is that if they want treatment, maybe they should move to Alberta, but that puts tremendous strain on the Alberta economy.
What we are saying to the national government, working with provinces and territories, is to let us have the meetings that we need to take place to set the ball rolling. If we do that, then we are telling Laurel Gibbons, a mother with a child with autism, and we are telling young Joshua, who is arguing and fighting in such a great way for his little sister, Sophie, that yes, their advocacy has worked, and yes, their tireless efforts on behalf of her daughter and his sister have been noticed and mentioned. We would also be saying it to the school in Fredericton that has done tremendous work in taking on this issue.
It is a proud day as a member of Parliament, not just as a member of the NDP, but as a member of Parliament, with all my colleagues in the House, to stand here and give my thanks to the hon. member, to thank the Chair and to thank each and every one in this House for making this a reality and a possible ending to the concerns of families and children with autism.