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patient support professionals

Lisa M. Rose

Patient Support Professional
Instructional Designer/Project Manager
Raleigh, North Carolina, United States

Lisa M. Rose is the Executive Director at HOPE for SCD. She works with organizations to bridge the gap between technically complicated information and the broader, less informed target audience receiving the required education. As an Executive Director, she works in conjunction with the international medical community to identify gaps in education and develop curriculum to address current needs within the world of Sickle Cell Disease.

She also oversees development of chronic illness tools that focus on Adult Learners, including video based-education, pictorial modules, in person trainings and paper-based publications. Moreover, Lisa manages development and implementation of free education both in print and in person to people both living with and effected by Sickle Cell Disease and other related chronic conditions (such as chronic pain).

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