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Rizzy Akanji's avatar

This was an important piece. Thank you for taking the time to document what so many people with sickle cell experience but rarely see reflected in the media. These stories aren’t exaggerations, they’re the day-to-day reality of a system that still isn’t built to treat this condition with the urgency it demands.

Appreciate the clarity, the reporting, and the willingness to highlight an issue that’s been ignored for far too long. I'm also committed to pushing this conversation forward and pushing for the structural changes that patients and clinicians need.