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IMS 2026 | Understanding the patient perspective in multiple myeloma disease management
Jenny Ahlstrom, HealthTree Foundation, South Jordan, UT, shares insights into key, underrecognized aspects of the patient experience, highlighting the importance of a single, patient-owned health record, as patients often have their data scattered across multiple electronic health record portals. She also emphasizes the value of patient participation in research, not only through clinical trials, but also by sharing clinical data and patient-reported outcomes. This interview took place at the 23rd International Myeloma Society (IMS) Annual Meeting in Glasgow, UK.
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