This Conservative government must support our Ontario NDP legislation and pass the Patient-to-Nurse Ratios for Hospitals Act. Thank you to our health critic from Nickel Belt. This act is a life-saving piece of legislation. There are simply not enough nurses in our hospitals to take care of patients with often complex needs.

As we once said, we need at least 22,000 more nurses here in this province. This government spoke of nurses as “health care heroes” during the pandemic, yet they didn’t even ensure they had the appropriate PPE to keep all of them alive. Some of our health care professionals died on this government’s watch. In fact, nurses were taken to court by this government. And I don’t need to reiterate the disaster that was this government’s Bill 124 on nurses—racialized and women, predominately, in that sector, I might add—and other public sector workers.

This government has sat idle while over a thousand emergency room closures last year happened. This is simply not good enough. Over 3,200 different studies have been conducted proving that a lower nurse-to-patient ratio is necessary to save lives and prevent burnout of our nurses. This piece of legislation is a win-win. It’s a win for the government, it’s a win for the official opposition, but most importantly, it’s a win for the nurses, their patients and their families.

One such report was WeRPN’s latest survey of over 1,300 registered practical nurses. The 2024 report found that “unsustainable workloads, wage compression, pressured working environments and a lack of support have continued to drive RPNs out” of the profession. The current nurse-to-patient ratio directly impacts patient care. Today, this government can turn the page and do something positive for a change that will directly impact all of our nurses, all of the nurses who have been advocating day in and day out over the last six years, begging this Premier to stop his privatization-of-health-care schemes.

I want to thank Joyce, my local community member and an RPN, for expressing her concerns to me via email. I echo every single one of them:

—introduce nurse-to-patient ratios to reverse deteriorating patient care and ensure workplace safety for nurses and patients;

—pay nurses what they’re worth;

—establish a fair and professional level of compensation for RPNs that reflects their knowledge; and, yes,

—reduce reliance on for-profit nursing agencies that are siphoning out our nurses, yet another way of prompting up this government’s privatization scheme.

So absolutely, we need this patients-to-nurses ratio legislation passed today.

Some 689,000 people in Ontario have eating disorders and they disproportionately impact women and girls. Sherri is one of them. Sherri has been waiting for a publicly funded adult in-patient bed since 2021. Why? Because there are only 20 publicly funded beds in Ontario. People who cannot afford to pay $30,000, $50,000, $60,000 for private care are dying on wait-lists. Last we spoke, she was still on a wait-list that was closed. I don’t want Sherri to die.

My question is to the Premier. Will this government increase adult ED beds, address the specialized staff shortage, make the temporary 14 pediatric beds permanent and create billing codes to ensure ED survivors and families aren’t paying out of pocket for the physical and mental health care they so desperately need?

This Conservative government claims its privatization of health care bill, Bill 60, will give Ontarians more access to health care they need when they need it. The reality is, only those who can afford to pay to play will get the care they need in private clinics and private hospitals. Bill 60 leaves vulnerable patients without deep pockets in dangerous situations where diseases will go undiagnosed and surgeries will be delayed, all while they live in chronic pain and depression as their illnesses get worse.

Speaker, my question is to the Premier. Why does this Premier believe that access to health care should depend on one’s ability to pay?

Karen Bender is a 73-year-old senior in my community, and she needs eye surgery. She has been told that she’ll be waiting eight months to a year and that her vision will get worse, if not completely untreatable, the longer she waits. Karen knows of other seniors who were upsold in private clinics, and she’s also aware that the Premier and the Minister of Health admitted that their profitization of health care bill has nothing in it to protect patients like her from extra charges.

So my question is back to the Premier: What advice would this Conservative Premier give Karen and others without deep pockets waiting and desperate for surgery, while they’ve left our publicly funded surgical operating rooms empty and unstaffed in our province?

I’m rising on behalf of our wonderful community from Toronto–St. Paul’s. A special shout-out to Liza Butcher and other St. Paul’s community members who are living with EDS, and also the ILC Foundation and thousands of others across Ontario who have reached out to our office.

This petition 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 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” at least “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.”

Speaker, I support this petition, and I affix my signature.

I know this is an issue that has actually impacted former PC MPPs’ own family members. So I hope they’ll get it right this time.

I’m going to hand it over to Havana for tabling.

I’d like to thank the ILC Foundation and my local constituent Liza Butcher, along with hundreds of other folks across Ontario for their staunch advocacy for the EDS community. I’m glad to join them in amplifying their call to action. This petition 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 ... 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 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.

Thank you to the EDS advocates in St. Paul’s and across Ontario. I sign this petition and will hand it to Julien for tabling with the Clerks.

“Petition to the Legislative Assembly of Ontario:

“Whereas Black, Indigenous, and racialized people are often subject to race-based hair discrimination, including experiencing racism in schools and the workplace—resulting in negative impacts on their lives such as school-based bullying and harassment which impacts academic performance and economic impacts such as job discrimination and reprisal in the workplace for so-called ‘unprofessional’ hair styles or texture;

“Whereas physical presentation, which includes textured hair maintenance and protective styles, is directly linked to physical safety, mental health and sense of identity, self-esteem and confidence;

“Whereas Black, Indigenous and racialized performers with natural textured hair often arrive in their workplace of film/TV and theatre sets with professional hair stylists who have received insufficient training for working with their hair type—risking permanent damage to their physical appearance and therefore earning potential;

“Whereas hairstyling training in Ontario currently only focuses on cutting, designing, permanent waving, chemically relaxing, straightening and colouring hair, but does not have any instruction or practice to ensure every hair stylist can service Black people’s natural hair or the textured hair of many Indigenous and/or racialized community members, whether performers or otherwise;

“Therefore we, the undersigned, petition the Legislative Assembly of Ontario to immediately pass MPP Andrew’s motion ... calling for the government of Ontario and Ministry of Labour, Training and Skills Development which regulates the hairstyling trade profession in Ontario to amend the hairstyling program standard to mandate culturally responsive training, specific to Black and textured hair in hairstyling education and practice across Ontario.”

I 100% support this petition and thank the folks of St. Paul’s, the folks of ACTRA, and many performers and otherwise across Ontario who have signed this. I’m tabling it with Karma.

To the Premier: Bill 7 is a give-consent-or-go-broke government bill. It is poised to strip ALC patients and families of their dignity by allowing seniors and patients with disabilities, among others, to be forced into long-term-care homes some hundreds of kilometres away without consent. Through Bill 7, patients could be forced into for-profit long-term-care homes, which we know are more likely to be understaffed and underfunded. During the pandemic alone, for-profit private homes have accounted for thousands of patient deaths, far outnumbering those of publicly funded and operated homes.

My question is to the Premier. Does this government think their plan to strong-arm seniors, patients, away from family and community-based services is best for their physical and mental health? Is this what the doctor ordered?

My question—Speaker, through you—is back to the Premier: Why does this bill not make any reference to home care, the number one choice of seniors and advocates like TAIC, SPRINT Senior Care, Seniors for Social Action (Ontario), the OVCO seniors’ working group, the Reena Foundation, Community Living Toronto—I could go on and on—folks who want seniors to receive care while aging in place in their homes and communities for as long as possible? Why does a bill saying that it’s going to do better care not include home care? Why is home care absent?

My question is to the Minister of Health. Our public health care system is in crisis because this government refuses to respect and protect our front-line health care workers, like Ashley and Laureen right in St. Paul’s—and the Ashleys and Laureens across Ontario. Our nurses are run off their feet. Their mental and physical health is crumbling. The official opposition; ONA, here today; RNAO; nurses in my riding; patients have sent this government solutions, and we have been ignored.

My question is to the minister: Will this Conservative government repeal Bill 124 and help save our public health care system and the lives of our nurses and their patients once and for all? Will you?

My question is back to the minister: Will you stop the privatization—yes, the privatization—of health care by investing in public sector workers, patients and families and repealing Bill 124? It’s what we’re all asking for. Forget about the official opposition; ONA is asking for it, nurses and patients. Yes or no, will you repeal Bill 124?