and while we tend to think of advocates as people who are “officially” affiliated with an organization, the term covers so many others, many of whom don’t even think of themselves as doing a “helping” job. so if you are a caregiver, if you have ever spoken out for someone who can’t do so for themselves or asked a tough question about your care or a loved one’s during a doctor’s appointment, then you too are an advocate. and you too are at risk of burnout.
so how can we protect those who advocate? it starts with acknowledging the value of advocacy, of course. it’s critical work that keeps us moving forward, ensures that people and systems are held accountable, and fills the many gaps that exist in health care. when organizations ask advocates to speak at their conferences, weigh in on their marketing decisions and share their lived experience with sales teams, this is consulting work and should be paid as such. and know that every time they tell their story it hurts, it brings them back to that hard thing that happened to them or someone in their community — that thing that they don’t want to ever happen again.
finally, let’s stop making it so difficult for advocates to get into the rooms where policy, spending and care decisions are made. let’s not be so quick to say no because nothing to do with fixing canada’s healthcare system and supporting patients and caregivers will happen without opening our minds to the possibilities that only lived experience can visualize.
if we can take this mission on and value those who speak up, both in terms of money as well as by acknowledging the emotional and mental cost of this work, and make it so there are more yeses — at least more maybes — than nos, perhaps we can weather the storm of burnout that currently threatens canada’s advocate community.
because, man, without our advocates, we’re screwed.