Patient experience

Surviving sepsis: A life and career changing experience

Before my near-death experience, I had no idea what the word sepsis meant. And I certainly didn’t know what the long-term effects would be for my family and me.

Viral response to alcohol guidelines highlights need for harm-reduction messaging

Highlighting the harm reduction aspects of the new alcohol intake guidelines could go a long way in helping consumers make better choices and help bridge the gap between patients and clinicians.

Cancer survival rates have significantly improved. Now we must pay attention to rehabilitation

Cancer survivors should not be left to feel like they need to manage their impairments on their own. There are models for cancer centres across Canada that can provide timely and comprehensive rehabilitation services.

Making time for love and compassion in clinical encounters

What if we were to look at the five love languages in the context of the doctor-patient relationship. What if we replace the word “love” with “compassion?” How might this look within our dealings with patients?

Paying tribute to the good in our health-care system

There is immense work to be done in our fragile health-care system. But in honor of this World Health Worker Week, one patient living with bipolar disorder wants to pay tribute to all the goodness in health-care workers' hearts.

Emergency brain surgery showed me the best of Ontario health care – and the worst

It’s true that when faced with a crisis, some of the best health-care professionals in the world are available to care for us. But that system is at its breaking point.

Team-based care key to alleviating primary-care crisis

Primary care is in crisis and there aren't enough doctors to go around. Done right, team-based care can expand the capacity of family doctors to care for more patients.

Having breast cancer impacts sexuality: Why don’t we talk about it?

It's common for women to struggle with sexual health issues after breast cancer. But it isn’t just our bodies that change; the experience of cancer changes our relationship with time, aging and even the arc of life that we imagine for ourselves.

Give me a primary-care provider who understands me

What do Canadians want in a primary care doctor? The OurCare survey results highlight that an ongoing relationship between a clinician and patient is key.

Virtual care must be integrated into public system, not driven by profit

Virtual care is here to stay. But how it should be used and who should own the services are important to patients, OurCare survey shows.

Comparing health-care systems – a personal journey

During my professional career, my family and I lived in four different countries (including Canada). Each country has significant differences in the delivery of health care and how it is paid for. This is an essay about my experiences in each of those countries.

Addressing a blind spot in care for patients living with diabetes

The sudden decline in diabetes screening as a result of the pandemic has put a significant number of Ontarians in danger of vision loss. Unchecked, this problem is associated with a massive cost for the government and society. But this can be avoided with a proactive screening strategy.

OurCare survey highlights lack of access to primary care

A nation-wide survey on the state of primary care in Canada illuminates pressing issues facing our health system. Dr. Tara Kiran and a team of collaborators with the OurCare project have launched an online dashboard with the findings.

The good people that give me hope – my journey with Parkinson’s

Every day on this Parkinson’s journey, I am genuinely amazed at how supportive the community has been as a whole. I know my family and friends have got my back, but having a perfect stranger go above and beyond is humbling and comforting.

The Treadmill

"Now the treadmill makes my steps uneven. One foot moves faster or slower than the other, and I stagger like a would-be dancer who wasn’t taught the choreography before the show."

Groundbreaking research into ME/CFS a pandemic ‘silver lining’

ME/CFS is a misunderstood complex chronic illness affecting more than 600,000 Canadians. For decades ME/CFS patients have been left without proper medical support. But now, with the wave of new post-viral illnesses from the COVID-19 pandemic, ME/CFS patients might finally see some answers.

The Faces & Phases of COVID-19

The Faces/Phases Project is a portrait of the COVID-19 pandemic in Canada. Through a series of data visualizations, we cover the first two years of the pandemic.

Ten health literacy principles cancer patients need to know

A medical oncologist describes ten health literacy principles to help cancer patients be informed participants in important treatment decisions.

Virtual care is here to stay. But what are patients’ expectations?

As we redesign a better primary care system coming out of the pandemic, we need to consider the role of virtual care and what patients will expect.

Take the survey: What are your priorities for primary care?

What trade-offs are acceptable to you? Do you currently have a family doctor or nurse practitioner? How important is it that every person living in Canada has a relationship with a family doctor? These are some of the questions we ask in the OurCare/NosSoins nation-wide survey.