Interview with Jacqueline Franken from the Stichting Melanoom organization at the MPNE Rare 2017 conference
Meet Jacqueline Franken! In this brief interview shoot at the MPNE Rare 2017 Jacqueline Fraken talks about her personal experience as a uveal melanoma (UM) patient.
Lack of information remains one of the barriers to tackle when it comes to UM. At the moment, several patient organizations have been created to give emotional and scientific support to patients. You can find a detailed list here.