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Crucial Fact

  • His favourite word was donation.

Last in Parliament April 2025, as Conservative MP for Calgary Confederation (Alberta)

Won his last election, in 2021, with 46% of the vote.

Statements in the House

Job Losses in the Energy Sector February 8th, 2017

Mr. Speaker, that is a lot to talk about in five minutes. I was hoping to get some more questions as well from the opposition.

What the Liberal government has put in place with regard to policy, regulations, and taxes has kept industry out of Alberta. It has kept industry out of Canada.

I talk to the people in the industry daily. I go door-to-door, and I ask people what they do for a living. I would say that 50% of the time they indicate to me that they used to work, or they do work in the oil industry. They have brought their industry and their work down to quite a slow pace in the hope that the government will listen to them, and react in a way, so we can urgently and quickly develop the pipelines. They hope the government will talk to people like the mayor of Montreal, and convince Quebeckers, convince all Canadians that Alberta's oil is beneficial to every Canadian.

Job Losses in the Energy Sector February 8th, 2017

Mr. Speaker, I am very pleased to rise today to contribute to this debate on the Alberta jobs crisis.

The constituency that I represent, Calgary Confederation, is a riding located in the inner city of Calgary. It is smack dab in the middle, just north of the Bow River. It is a wonderful riding, and there are wonderful people who live there. They work hard and have great families. The population is approximately 112,000 people, and many of those people have been deeply affected by the downturn in the oil industry.

There have been massive lay-offs throughout my riding due not only to the price of oil but also due to the unnecessary taxation implemented by both the provincial NDP government and the federal Liberals on an industry that is already on its knees. The implementation of the carbon tax is an attack on an industry just trying to survive.

To understand the utter devastation that has taken place in the Alberta jobs market, one only needs to look at the Liberal government's record since taking office. While the national unemployment rate has remained steady at 7%, the unemployment rate in Calgary has risen dramatically to around 10%. Behind those unemployment numbers are real people, real families, and they are suffering. Even those with jobs today live under incredible stress not knowing if they will become one of the tens of thousands of laid-off workers in the oil industry.

My staff, in my constituency office, Lou and Pat, are on the front lines. They have been receiving calls that just tear me apart. It sometimes leaves them emotionally drained and visibly shaken.

There are parents, who are calling in, sobbing and telling of their children who have been sent away to family in other provinces, because they cannot afford to feed and house them in Calgary.

I went door knocking during the Christmas break, and I met one man who was ashamed to let me share his name. He told me of not finding work, depleting his family savings, losing his home, and still to this day cannot find work. He was so embarrassed by the situation that he sent his wife and three children to Manitoba to stay with his in-laws, so that he could shield the reality of his family's situation from his young children. Imagine being ashamed to be in front of your own children.

Another father almost had the same experience. He moved his wife and children to Saskatchewan, a province where at least the Saskatchewan Party and Premier Brad Wall get it. They strongly oppose a carbon tax, and I strongly applaud Premier Brad Wall for trying to convince the Liberal government otherwise.

Another constituent called into the office, and when we asked him his address, he gave us his licence number as his address. He lives in a car.

I have had two people mention suicide as an option if they do not get some help from the government.

The tragic stories go on, and the hope continues to fade. Hopefully, one day things will improve. We pray for the price of oil to go up again. We pray that the government listens to the people of Alberta, the people of Canada.

I implore all members to remember the people behind these unemployment numbers. Each person has a unique story, but they share the same challenges, putting a roof over their heads and food on the table. It is what every Canadian wants and every Canadian deserves.

The Liberal government must stop taxing Albertans into poverty. Let us stop destroying their primary industries. Better yet, let us stop ignoring them and their situation. Let us get Alberta back to work, and let us do it soon.

Petitions February 8th, 2017

Mr. Speaker, I am pleased to present a petition in support of my private member's bill, Bill C-316, which was submitted by Mr. Brad Arnold of Calgary. The petitioners are calling on this House to improve the organ donation system in Canada by making the process to register as an organ donor easier.

This would be achieved by adding a simple question to our annual tax returns. Mr. Arnold, a recipient himself, collected signatures from throughout Nova Scotia and New Brunswick, showing that there is indeed national support for this sensible change to our tax forms.

It is also my pleasure to rise today to present a petition in support of my private member's bill, Bill C-316. The petitioners are calling on this House to improve the organ donation system in Canada by making the process to register as an organ donor easier. This would be achieved by adding a simple question to our annual tax returns.

I would like to thank Don Axford for collecting all these signatures from around Calgary. There are 4,600 Canadians awaiting an organ transplant, who stand to benefit from his efforts.

Petitions February 1st, 2017

Mr. Speaker, it is my pleasure to rise today to present a petition in support of my own private member's bill, Bill C-316.

Petitioners are calling on this House to improve the organ donation system in Canada by making the process to register as an organ donor easier. This would be done by adding a simple question to the annual tax return.

I would also like to specifically thank Ms. Casey Amatto from Calgary for collecting all these signatures and showing she cares about the 4,600 Canadians awaiting an organ transplant.

Questions Passed as Orders for Return January 30th, 2017

With regard to credit cards issued to Ministers, Ministers of State and Parliamentary Secretaries: what expenses were charged to a government credit card, and not paid for by the government for the period of November 4, 2015, to September 23, 2016, including (i) the name of the vendor and the place of purchase, (ii) the date of the purchase, (iii) the value of the purchase, (iv) the due date of the statement, (v) the date on which the card holder provided reimbursement in full, (vi) the name of the card holder, (vii) the official job title of the card holder, (viii) the confirmation if that card holder is still an active holder of a government credit card?

Questions Passed as Orders for Return January 30th, 2017

With regard to credit cards issued to Ministerial staff: what expenses were charged to a government credit card, and not paid for by the government for the period of November 4, 2015, to September 23, 2016, including (i) the name of the vendor and the place of purchase, (ii) the date of the purchase, (iii) the value of the purchase, (iv) the due date of the statement, (v) the date on which the card holder provided reimbursement in full, (vi) the name of the card holder, (vii) the job title of the card holder, (viii) the department or agency of the card holder, (ix) the confirmation if that card holder is still an active holder of a government credit card?

Questions on the Order Paper January 30th, 2017

With regard to the list of chronic diseases maintained by the Public Health Agency of Canada: (a) why are Crohn's and colitis not included on the list; (b) when were Crohn's and colitis last reviewed for inclusion on the list; (c) what criteria do Crohn's and colitis not meet for inclusion on the list; (d) when will Crohn's and colitis next be reviewed for inclusion on the list; and (e) what is the full criteria used for determining whether a disease is included on the list?

Health December 7th, 2016

Mr. Speaker, I appreciate the information from the parliamentary secretary on what he and his government are doing in this country.

The problem is that 98% of illicit fentanyl is coming from China. Why are we not shutting off the tap from China, where this drug is coming from and killing many Canadians?

I appreciate the fact that the government is working on supervised injection and consumption sites and that an antidote, naloxone, is being distributed throughout Canada to help individuals who are overdosing on these particular drugs.

But again, why are we not focusing on China? Why is the Liberal government not talking to the Chinese government? Our Prime Minister should address this and talk to the Chinese officials. He is over there. He is talking with them. Let us deal with the issue.

Health December 7th, 2016

Mr. Speaker, I appreciate you sticking around for this late show tonight. It is my first late show, and I appreciate the pages and everyone in the room for sticking around when they want to see the Christmas lights being lit up outside here.

The reason I am here is, back on October 18 of this year, I asked a question in question period regarding the fentanyl crisis and I was not happy with the response from the parliamentary secretary to the minister of health, the member for Brampton West. She did not answer my question, basically, and that is why we are here today.

The fentanyl crisis is getting worse in the country. It is certainly a major national emergency in my mind. It is an epidemic. Just in B.C. alone, almost 1,000 people have died this year overdosing on fentanyl. In my province of Alberta, the numbers are not as bad as that, but certainly it is a crisis all over the country. We hear daily about the deaths that are occurring because of this drug.

It is because of the severity of this emergency crisis, that the Standing Committee on Health, of which I am vice-chair, postponed the study on the national pharmacare strategy that we were doing to address this national opioid crisis. We brought in many experts, doctors, nurses, ER staff, first responders, the EMS, the police, and officials from the fire departments around the country. We talked to pharmacists, social workers, and we even brought in recovering fentanyl and opioid addicts into our witness chairs to discuss with us the severity of this issue.

There were two particular presentations we received. One was from the commissioner of the RCMP and the other, the Canada Border Services. They indicated to us that 98% of illicit fentanyl is coming from China into our country. I had attempted in this meeting to have the Chinese ambassador appear before the committee to explain what his government is doing to help Canada tackle this deadly drug epidemic. I put the motion forward, and the Liberal government would not have a representative from the Chinese government come here to address this issue.

The Liberals are ignoring the obvious. China is the primary source of illicit fentanyl here in Canada, and the Liberals would rather deal with the deadly street drugs after they are in the hands of Canadians, instead of targeting the source, which is China.

Why is pleasing the Chinese government more important to the Liberals than saving the lives of Canadians? That was the question I had asked, and I would like a response to that question.

National Sickle Cell Awareness Day Act December 1st, 2016

Mr. Speaker, I am pleased to rise today to contribute to the debate on Bill S-211. The proposed legislation before us today will recognize June 19, on an annual basis, as national sickle cell awareness day.

Approximately 2,000 people living in Canada today have sickle cell disease. Increased awareness of their disease would be beneficial, given the low level of public knowledge at this time. It is a hereditary disease. It is not contagious. Carriers are usually not sufferers of the disease, but in combination with a carrier spouse, the disease usually becomes apparent in their offspring. This disease is most common among those with ancestors from India, Saudi Arabia, the Mediterranean, the Indian subcontinent, and the Sub-Saharan countries in Africa. However, it is still found in other cultures as well. Just to give people an idea, there are an estimated 43 million carriers, with 3.2 million people having the disease because both parents were carriers.

What is sickle cell disease? It is a group of red blood cell disorders. Those with the disease have abnormal hemoglobin. As many know, hemoglobin is the part of the red blood cells that carries vital oxygen throughout the human body. We know how important it is that tissues in the body receive a steady and life-sustaining supply of oxygen to work well. Hemoglobin takes the oxygen from the lungs to the parts of the body that need it. Normal cells are a disc shape, sort of like a donut. This shape allows the cells to be flexible. This flexibility and shape allow the cells to travel easily through blood vessels throughout the body.

Sickle hemoglobin is different. It forms stiff rods within the red cell, and this changes the cell's shape to something more like a crescent or sickle shape. As members can imagine, this creates enormous problems. The sickle-shaped cells result in blockages because the cells are stiff and unable to pass through the vessels easily. These resulting blockages mean that vital oxygen stops reaching the parts of the body that need it.

What impact does this have on the person with the disease? A lack of oxygen results in attacks of sudden and severe pain throughout the body. It is a horrible condition. These pains occur without warning, and often result in hospitalization. The pains usually last five to seven days. While not always the cause, it has been noted that pain crisis can be triggered by temperature changes, stress, dehydration, and even living in high altitudes. Of course, any infection that normally causes a rise the number of red blood cells triggers the disease as well.

Fortunately for most children with the disease, pain usually subsides between pain episodes. Nonetheless, many children known to have the disease take penicillin daily to help the immune system, and face a lifelong regimen of daily folic acid. For teens and adults, the pain is usually chronic. The effects of chronic pain are well known. They have a huge impact on the education, the employment, and the human mind of the sufferers.

Due to the lack of oxygen to vital organs on a regular basis, sickle cell disease often begins to cause long-term damage to vital organs. It is common for those with the disease to develop serious issues with their skin, their brain, their bones, their spleen, their heart, their kidneys, their liver, their lungs, and even their eyes. The spleen is particularly susceptible because of its narrow blood vessels and its basic job of clearing old red blood cells.

If this was not enough, there is another layer of cruelty to this disease. Normal red blood cells have a typical 90- to 100-day existence. Sickle cells last only about 10 to 20 days. Imagine what a toll this takes on the human body when it has to replenish red blood cells at 10 times the normal rate. When the body cannot keep up, which is often, there is a shortage of red blood cells and this results in the sickle-cell anemia. The most visible side effect is fatigue. As I mentioned before, this also adds to the pain, the long-term organ and tissue damage, and the toll the disease takes.

Sadly, this disease is a lifelong illness, and when I say “lifelong”, we must not kid ourselves. Lifelong is not a happy story either. Sickle cell disease shortens lives, but it depends greatly on where one lives and one's access to help.

In first world countries like the United States, life expectancy can range greatly, from 40 to 60 years. This is about four times longer than it was 40 years ago. Now, about 90% of those with the disease can expect to see their 20th birthday, and 40% of those will die by age 50.

Is there a cure? There is a treatment and it is called hematopoietic stem cell transplantation, or HSCT. HSCT is the best-known option at this time. Unfortunately, most people with the disease are either too old for a successful transplant or do not have a genetically matched person able to make the donation. The success of this type of treatment is heavily dependent on having a great match.

For HSCT to be successful we need an early diagnosis and good medical treatment. Those who are willing to donate bone marrow should consider the positive effects that their donation could have. Given the need for the best match possible, I specifically suggest that those in affected cultural communities help promote donation of organs and tissue, bone marrow, and blood.

In the meantime, the disease takes it toll. There are increased chances of stroke, infection, gall stones, joint pain, low immunity, erectile issues, bone infection, leg ulcers, vision problems, pre-eclampsia in pregnant women, and heart and kidney failure.

The pain of the disease often means that patients are prescribed opioids to deal with the pain. The good news is that addiction among sickle cell patients to opioids is not any higher than among the general population. However, that said, opioid addiction is a reality for many with sickle cell disease. We have heard a lot in the House recently about the effects of opioid addictions, and it is alarming. This type of addiction is often deadly, and even when it is not, it results in many other significant problems for patients and their families.

There are an estimated 5,000 Canadians living with the disease and the rate is increasing. There is prenatal screening, but with the knowledge comes the difficult decisions that parents must consider, which I cannot imagine.

The Sickle Cell Disease Association of Canada does a lot of advocacy and awareness work. I applaud it for its efforts, which have gone a long way toward bringing this disease into the fore and making it better known in our society. The association faces an uphill battle in finding a cure. Research dollars are not easy to come by, especially for a disease that is most prevalent in parts of the world that are not able to attract the attention of major pharmaceutical companies. It is still a disease that is very much not discussed, even within the communities most affected.

However, things are improving. There is an increase in research funding and awareness is slowly building.

Passing this legislation would go a long way to normalizing discussion about the disease. It would show those with the disease that we care and would help to educate those around them about their disease.

I will be honest that I knew nothing about this disease until I prepared for this speech. As I learned more about sickle cell disease and the thousands of Canadians who suffer from it, I wanted to share my comments with others. I applaud the hon. member for presenting this bill and the work that he has done on this. I give him my thanks. I am happy that I was able to talk a bit about it here today to help share awareness.

Let us support this legislation and keep spreading awareness and education.