To the member who spoke so eloquently about why housing is necessary in his community and about the experience of that retired PSW: Can you explain what types of infrastructure you’d also like to see the government committed to in terms of making life better for Ontarians, for your residents? Obviously we need affordable housing. Can you speak to the benefit of other things like community centres, like libraries, like transit that works?

We know right now that Metrolinx has been dragging their little feet a little bit long in terms of the Eglinton LRT construction. We know that the community in Mount Dennis that’s relatively near to your community as well is also feeling left out of the consultation process with Metrolinx with this government.

What would you like to see in terms of infrastructure, and what is the benefit of infrastructure to housing in your community?

Speaker, 2.3 million people in Ontario do not have a family doctor. That’s 2.3 million Ontarians who cannot access the basic humane right of seeing someone whose expertise is in taking care of sick people. Many of those 2.3 million people have ended up on the doorsteps of our already understaffed, underfunded and overburdened emergency rooms—some of which have experienced shutdowns under this Conservative government due to its ongoing health care privatization scheme.

The goal should be to keep people out of ERs as much as possible, for as long as possible, but to do that, people need access to family doctors, so they can manage their physical and mental health needs. Statistics show that those without access to primary care are more likely to receive late diagnoses, which directly impacts both short- and long-term health outcomes. Without family doctors, if you need a specialist appointment, good luck on that journey, because you’re out of luck.

Every Ontarian deserves access to care. I say this as an MPP representing my community of St. Paul’s, I say this as a family member of folks in my own family who don’t have family doctors, and for many in this community—and many are racialized, let me tell you that. Many are in communities that are already underserved; many are rural; many are northern.

Today, we, the Ontario NDP official opposition, are giving this government yet another opportunity to help patients, to put them first. We are giving this Conservative government a solution to help our doctors get back to what they do best, that is, seeing patients, not having to fill out 19 hours a week of necessary, critical administrative work and paperwork. Help patients access more doctors by reducing the amount of time doctors spend on administrative work. That’s what we’re asking, Speaker. Help patients access more doctors by reducing the amount of time doctors spend on administrative work.

We are calling on this government to invest in administrative support staff and integrated health teams. By doing so today, we can add the equivalent of 2,000 more family doctors here in Ontario and help up to two million additional Ontarians get the help they need.

This should not be a partisan issue, Speaker. Saving lives should be about humanity. The NDP has put forth a solution. The government has the opportunity today to save people’s lives. Will the government accept our proposal today? Yes or no?

This petition comes from Ontarians. Thousands of Ontarians have been putting this petition forward now for months. It is to the Legislative Assembly of Ontario:

“Whereas the Canada Health Act requires provinces to fund medically necessary treatment for Canadians; and

“Whereas a growing number of people in Ontario suffering from Ehlers-Danlos syndrome (EDS) have to seek out-of-country treatment at their own expense because doctors in Ontario don’t have the knowledge or skills to understand EDS symptoms and perform the required delicate and complicated surgeries; and

“Whereas those EDS victims who can’t afford the expensive treatment outside of Ontario are forced to suffer a deteriorating existence and risk irreversible tissue and nerve damage; and

“Whereas EDS victims suffer severe dislocations, chronic pain, blackouts, nausea, migraines, lost vision, tremors, bowel and bladder issues, heart problems, mobility issues, digestive disorders, severe fatigue and many others resulting in little or very poor quality of life; and

“Whereas despite Ontario Ministry of Health claims that there are neurosurgeon doctors in Ontario who can perform surgeries on EDS patients when surgery is recommended, the Ontario referring physicians” often “fail to identify any Ontario neurosurgeon willing or able to see and treat the patient;

“We, the undersigned, petition the Legislative Assembly of Ontario as follows:

“Require the Minister of Health to provide funding to hire one neurosurgeon who can and will perform neurosurgeries on EDS patients with equivalent or identical skills to the international EDS neurosurgeon specialists, including funding for a state-of-the-art operating room with diagnostic equipment for treatments for EDS patients; and meet the Canada Health Act’s requirement to afford equal access to medical treatment for patients, regardless of their ability to pay for out-of-country services.”

I want to thank St. Paul’s and the folks across Ontario who are surviving with EDS. I’m glad to see this petition here, and I look forward to supporting them further. I affix my signature and will pass it—

This petition is entitled “Support Ontarians Living With Long COVID.” I just want to thank Lesley Stoyan, who is an amazing local community organizer in St. Paul’s and is also a certified therapist and movement wellness coach. She does many things, but a lot of it has been impacted by long COVID.

“To the Legislative Assembly of Ontario:

“Whereas the impacts of long COVID are extensive and devastating, which include migraines, dizziness, vertigo, brain fog, loss of smell or taste, and mental health conditions such as depression and anxiety;

“Whereas socio-economic analyses on long COVID project significant negative impacts on the economy through its effects on the labour market, gross domestic product, as well as added costs in health care and social supports;

“Whereas 1.4 million Canadians or approximately 500,000 Ontarians are suffering the devastating health impacts of long COVID;

“Whereas adequate treatment options for those suffering from long COVID are mostly limited to private clinics and can cost as much as $5,000 a month in order for them to continue in their day-to-day lives through gainful employment, parenting, and overall life enjoyment;

“Whereas the Ontario government has failed to properly address and support the escalating crisis of long COVID and how it is devastating the lives of an increasing number of Ontarians;

“Therefore we, the undersigned, petition the Legislative Assembly of Ontario as follows:

“To immediately allocate funding to support fair, equitable, accessible, and appropriate treatment for the complicated symptoms of long COVID and implement a cohesive and comprehensive funded support system for those suffering from the disease.”

I couldn’t agree more. Again, thank you to Lesley Stoyan and all of those in St. Paul’s who have signed this. Thank you. I’m going to sign it and pass it over to Kian.

This petition is entitled “Support to Ontarians living with long COVID.” The petition is,

“To the Legislative Assembly of Ontario:

“Whereas the impacts of long COVID are extensive and devastating, which include migraines, dizziness, vertigo, brain fog, loss of smell or taste, and mental health conditions such as depression and anxiety;

“Whereas socio-economic analyses on long COVID project significant negative impacts on the economy through its effects on the labour market, gross domestic product, as well as added costs in health care and social supports;

“Whereas 1.4 million Canadians or approximately 500,000 Ontarians are suffering the devastating health impacts of long COVID;

“Whereas adequate treatment options for those suffering from long COVID are mostly limited to private clinics and can cost as much as $5,000 a month in order for them to continue in their day-to-day lives through gainful employment, parenting, and overall life enjoyment;

“Whereas the Ontario government has failed to properly address and support the escalating crisis of long COVID and how it is devastating the lives of an increasing number of Ontarians;

“Therefore we, the undersigned, petition the Legislative Assembly of Ontario as follows:

“To immediately allocate funding to support fair, equitable, accessible, and appropriate treatment for the complicated symptoms of long COVID and implement a cohesive and comprehensive funded support system for those suffering from the disease.”

I absolutely support this petition. I want to thank Lesley in my community of St. Paul’s for her leadership and advocacy on supports for long COVID. I have affixed my signature and I will hand it to Ryan for tabling.

Just before I started, I want to express to anyone watching or to those who aren’t familiar with the government’s Bill 60, the profitization and privatization of health care, which the member from Eglinton–Lawrence spoke so proudly of: Make no mistake, the excess service that this bill claims to provide Ontarians is only provided to those who have the pockets, the money, the finances to purchase. It’s very, very problematic when procedures that should be covered and are covered by your OHIP are all of a sudden being covered by credit cards, courtesy of Bill 60. I just wanted to clear that up so that folks got the reality check of what Bill 60 is.

Anyone with a prostate can get prostate cancer, and this includes cisgender men, trans women and nonbinary people. I wholeheartedly support this motion, and I’m calling on the Ford government to follow the lead of eight other provinces and fully cover the prostate-specific antigen PSA test under OHIP when prescribed by a doctor.

I must also note that this motion, put forth by our outstanding member from Niagara Falls, is a fiscally responsible piece of legislation that calls for investing now to help save lives, as opposed to not covering the PSA test, which has been known to act as a deterrent for those who may have limited financial means. A cost for diagnostic tests will deter people from seeking answers early, and with prostate cancer, early detection is key. If prostate cancer is left undiagnosed and unchecked, the cost to our health care system would be tenfold. As the saying goes, prevention is better—or, I might add, cheaper—than the cure.

The cost of a test should never be a prohibitive factor, especially for groups in society who have felt the disproportionate impact of health inequities. This is especially true for many Black men, who are disproportionately impacted by prostate cancer. Black men, as we have heard, have almost double the risk of developing prostate cancer compared to non-Black men. They’re also more likely to have prostate tumours that grow and spread quickly. Black men are also more likely to die from prostate cancer compared to other men.

I want to read into the Hansard a quote from Mr. Ken Noel, the president of the Walnut Foundation: “Prostate cancer disproportionately impacts Black men in this province, according to a recent study co-authored by the Walnut Foundation and published in the Canadian Medical Association open journal. The Walnut Foundation, a prostate cancer awareness and support non-profit organization targeting the Black community, encourages Black men to be more involved in their personal health, get the facts, ‘know your numbers’ and that ‘early detection saves lives.’ However, men are thwarted by having to pay for a simple blood test in Ontario. We need to minimize barriers to early diagnosis and getting the PSA test funded by OHIP will improve outcomes for those most impacted by this disease. Remember Black men are 76% more likely to be diagnosed and 2.2 times more likely to die from prostate cancer.”

The name of that study, and I would encourage everyone to read it—it is a study that was led by Dr. Aisha Lofters. It is titled Prostate Cancer Incidence among Immigrant Men in Ontario, Canada: A Population-Based Retrospective Cohort Study.

I of course also want to give a shout-out to Mr. Henry as well. Thank you for your leadership and your advocacy—and your research, at that.

The Walnut Foundation’s annual Walk the Path Walkathon to help raise awareness about prostate cancer is taking place on June 3 this year. I also want to give a shout-out to Ivan Dawns, who has been named the honorary campaign chairperson of this year’s walk. Ivan Dawns is the first Black union representative with the International Union of Painters and Allied Trades, and recently received the Ontario Black History Society Dr. Anderson Abbott Award for his leadership and advocacy. Dr. Abbott, born in 1837 in Toronto, Upper Canada, was Canada’s first Canadian-born Black person to be licensed as a doctor.

The Ontario NDP has long called for the collection of race-based socio-demographic data in health to prevent worse health outcomes for racialized Ontarians. If we see where the disparities are, we can address health inequities through a full systems approach. According to the Black Health Alliance, “Although there are some conditions that are inherited at greater rates in some ethnic groups, such as sickle cell disease”—which we’ve also raised legislation for in this House—“the majority of chronic illnesses have many different contributing factors including—social determinants of health such as access to health care, support networks, education and stress.”

Lastly, “One ongoing stressor is anti-Black racism, which we believe is a major contributing factor to many of the disparities in health that Black people experience.” Experiencing everyday systemic and even internalized racism intersecting with class or socio-economic barriers and disparities, according to evidence-based research, has been shown to worsen illness and health outcomes for many within Black, Indigenous and racialized communities.

I couldn’t support the member for Niagara Falls’ legislation more, and I hope that this government passes it and saves lives.

I’d also like to welcome the fine folks from Forest Hill in St. Paul’s. Welcome to your House.

My question to the government: I’m wondering how the government feels that this piece of legislation is going to build trust in community with regard to the environment when we have seen this government slash the Environmental Commissioner of Ontario. We have seen this government sell off or attempt to sell off parts of the greenbelt. We have seen this government not support nature in a way that actually allows our upcoming generation of leaders to be safe without climate crisis anxiety. What is there in this piece of legislation that’s going to ensure that Ontarians can actually trust what this government has to say about the environment?

Thank you to our member for that wonderful presentation. The government seems to think that privatization of health care gives Ontarians choices. But really, it gives choice to those who have the deep pockets to be able to take advantage of private care. I’m wondering if the member can express how this broadens the gap between the haves and have-nots in terms of access to health care, where it seems that the healthy and the wealthy are at the front of the line. They’re at the top. But where are those who don’t have? Where are they?

I’m glad to be able to share some points on Bill 39 and Bill 23, government bills. They’re pretty much “waste” bills, frankly, to use millennial language.

I’m wondering why the government is using immigrants as scapegoats—because no immigrant comes to Ontario asking to live on the greenbelt, asking to live on wetlands.

This government doesn’t understand that their notion of affordability is driving Ontarians into poverty. The average Ontarian does not make $130,000 a year.

So can the Brampton North member tell me which house anyone making $39,000 or $35,000—or ODSP recipients. Which house can they afford to build on Bill 39, Bill 23, or any of the other crap they’ve brought in the Legislature this year?