The Cutaneous Lymphoma Foundation's CEO, Susan Thornton talks about what it is like to be diagnosed with cutaneous lymphoma and how the Foundation helps through its mission of promoting awareness and education, advancing patient care, and facilitating research.
Overview of how to navigate health insurance concerns when living with cutaneous lymphoma - information is U.S. based - presented at the Chicago 2-Day Patient Conference in June, 2016.
Social worker and cutaneous lymphoma patient, Ricky Kitchen shares recommendations on how to live with cutaneous lymphoma at the Chicago 2-Day Patient Conference in June, 2016.
Individuals diagnosed with cutaneous lymphoma share their stories and their experience starting patient networking groups in their local communities at our Chicago 2-Day Patient Conference held in June, 2016.
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