When more people share their story, more power goes into the hands of patients.
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Like Anita, many of us are dependent on what the doctor tells us, and we don’t ask questions:
“I had no pain, I had nothing, nor did I have knowledge of what a fatty liver meant. So, I did not question my doctor as to what a fatty liver was, nor did my doctor indicate to me what changes in my lifestyle I had to make…”
—Anita, Fatty Liver Disease/Liver Cancer (HCC) PatientCHMConnect partners with underrepresented communities to develop life-saving educational programs on conditions that disproportionately impact People of Color. Our team is made up of survivors and supporters from the underrepresented communities we serve, and we are 100% minority-owned.