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may 19 is the 10-year anniversary of my brother greg’s death. greg was a healthy, intelligent 31-year-old who had only told us of his potential diagnosis of testicular cancer days before. our family was shocked and devastated.
a major factor in my brother’s early death was canada’s poor health data infrastructure.
greg and his various health providers didn’t have access to all his health information. a red flag for testicular cancer was in his electronic medical record at one clinic but wasn’t available to the walk-in clinic doctor greg saw when he started having back pain. one of his doctors moved his practice, and the clinic didn’t have a process in place for follow-up. a specialist he was urgently referred to — via fax — was out of the office for an extended period and the referral sat there until greg finally called the office.
we made a lot of dangerous assumptions about health care
when my family wanted to learn what happened so we could help prevent it from happening again, we asked questions about how common cases like greg’s were. the system couldn’t provide what we thought was basic information. we asked for statistics on surgeries like greg’s and the frequency of blood clots for the hospital, region, province and nationally — which didn’t seem like a big ask at the time — and learned the information doesn’t exist.
since greg’s death, we’ve learned a lot about health care and have realized that we made a lot of dangerous assumptions.
in the first year after greg’s death, dr. ward flemons and the team at the health quality council of alberta investigated what happened, releasing the
continuity of patient care study. five years later, we partnered again to produce the film,
falling through the cracks: greg’s story. to date, it has been screened more than 470 times and we’ve participated in almost every screening’s post-film discussion. these conversations have been an opportunity to deepen our understanding of health care and refine what we believe is crucially important for its future.