* lisa *

Lisa Machado

Patient/caregiver advocate | Journalist | Speaker | Supporter of lived experience

Hi! Thanks for coming to check me out. I am a communications expert, healthcare strategist and patient advocate with 20+ years of experience helping organizations and communities improve how people experience care in Canada and internationally. As a senior leader who drives mission-aligned change through communication, advocacy, and strategy, I’ve led national and regional initiatives that translate complex health challenges into human stories, align stakeholders around shared goals, and move systems toward more equitable, compassionate care.

My background in journalism, including years as a financial reporter and a national health columnist, have shaped my belief that stories change systems. Whether it’s social media, media relations, or comms strategy, I use that lens to help organizations build trust, turn data into insight, and communicate in ways that inspire action and accountability.

As the founder of the Canadian CML Network, I built a national community for people living with cancer that influenced drug access policy and strengthened the patient voice in cancer care. Through my consulting work, I’ve partnered with government, health agencies, and nonprofits to develop engagement frameworks, policy communications, and awareness campaigns that deliver measurable impact. I’m recognized for leading with empathy, building trust across sectors, and turning strategic vision into tangible outcomes.

I also teach in the Liberal Arts department at Toronto’s George Brown College and I am currently designing a new course in Healthcare Management at Humber College that will look at the value of patient engagement.

Areas of leadership:
• Strategic communications & knowledge translation
• Patient and stakeholder engagement
• Health policy & systems transformation
• Mission-driven organizational strategy
• Advocacy leadership & public voice

And in case you are wondering how I got here … I was born into advocacy. My younger brother had hemophilia, a condition that prompted my parents to create an organization to support families living with what was — at the time (70s) — an extremely life-affecting condition that no one seemed to know a lot about. Fast forward a decade and he, along with hundreds of other hemophiliacs, were infected with HIV and Hep C during what would become known as Canada’s Tainted Blood Scandal. In 2021, he died of an aggressive form of liver cancer as a result of the damage caused by Hep C. This, just two years after my dad passed away from dementia. These difficult experiences, plus my own health challenges, have given me unique and thought-provoking insights into what it means to be a consumer of health care in Canada, why caregivers are essential to any health care team, why the voice of lived experience must be embedded in everything, from clinical trials to healthcare administration, as well as the challenges facing patients as they seek the best health outcomes.



Some stories Lisa has been sharing…

September 2025 – Healthy Debate Patient Perspectives: Telling our stories is critical to improving care

August 2025 – Narrative-Based Medicine Lab, Temerty Faculty of Medicine, University of Toronto 3 Questions with Lisa Machado: Making Room for the Patient Experience

April 2025 – The Globe and Mail When caregiving ends, how does my life begin again?

March 2025 – We are all just one stroke of bad luck away from being homeless

January 2025 – Healthy Debate Is patient experience finally having its moment?

November 2024 – Healthy Debate Dementia patients deserve more than coloured balls and matching games

August 2024 – Patient Voice: It’s time to acknowledge that survival and quality of life are not the same thing

August 2024 – WATCH: Quality of life while living with cancer

July 2024 – It’s time to stop equating survival with quality of life

April 19 – Will ‘symptom science’ make it easier to live with cancer?

April 12, 2024 – There are a lot of reasons for missed cancer diagnoses, lack of access to screening should never be one of them

April 5, 2024 – Holding leaders accountable is the only way we’ll see the change we desperately need

March 29, 2024 – Long-term care is not OK

March 24, 2024 – Is anything worth more than making life better for others?

March 15, 2024 – Alberta’s failed lab privatization deal is another costly example of governments not listening to those who know best

March 8, 2024 – The trauma of a scary diagnosis isn’t something you just ‘get over’

March 2, 2024 – We need to stop blaming people for their disease

Feb 26, 2024 — Telling your ‘sick’ story isn’t always a way to make friends

Feb 16, 2024 — Empathy is good for us and for healthcare professionals. Yet, here we are

Feb 9, 2024 — Survival predictions are based on math, science and past experience — but they aren’t always accurate

Jan 26, 2024 — It’s struggling, but there’s a lot about universal healthcare that works

Jan 19, 2024 — We can’t let stories of overcrowded ERs, burned out staff and doctor shortages lose their sting

Jan 12, 2024 — The mess that is Canada’s healthcare system is proof of what happens when we ignore lived experience in favour of cost

Jan 6, 2024 — Stop inferring that financial support from pharma means that advocacy groups are ineffective, biased or puppets