We enter 2021 with a new series, Conversations With.... talking to members of the Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD) community, from all around the world, living with different types of EDS and of HSD, about life, relationships, physical and mental health, diagnosis, coping, and hopes for the future.

President and CEO of The Ehlers-Danlos Society also lives with EDS, and here talks to Jenni of the UK who has hypermobile Ehlers-Danlos syndrome (hEDS), Anne of Finland who lives with HSD, Annie in the USA who has vascular Ehlers-Danlos syndrome (vEDS), and Sabra in the USA who lives with hEDS.