As a physician, I am an advocate. I am an advocate for my patients individually and collectively, and I am an advocate for my field: pediatric rheumatology. My own experiences as a patient drive me to integrate my patients’ perspectives into my medical decision making, and although my academic training has prepared me to best care for my patients, I have sought out opportunities to broaden my impact.
Unique Challenges Require Collaboration
Pediatric rheumatology poses unique challenges that make advocacy crucial. Physicians alone cannot tackle all the challenges of caring for our complex patients. A therapeutic alliance between patient, family and physician, built longitudinally, allows for optimal care for children with chronic illness. Despite their best efforts to advocate for themselves, patients and families often rely on their physicians to magnify their voice. Yet we, too, must collaborate with key stakeholders to create meaningful change. Legislators write and implement policies that dictate healthcare access, delivery and research funding.
Purple Cupcakes & FITs
A recent encounter with one of my patients highlighted how meaningful individual advocacy efforts can be. She is a precocious 10-year-old girl with lupus. Unlike some of my older patients, she has already learned all about her disease, and knows the names and dosages of all of her medications. After educating herself, she decided to educate others. She baked cupcakes with purple icing (to represent lupus) and walked door to door in her neighborhood. She met each of her neighbors, passing out her purple treats and explained about her illness. She asked each of them to sign a petition acknowledging their understanding.
My patient’s efforts reminded me of RheumPAC.