“…In the area of clinical knowledge of sarcoidosis, classical reviews are still not outdated [ 27 , 28 , 29 ]. However, this knowledge is continuously proceeding by small touches, as illustrated by Catharina Moor’s paper, the main interest of which is to give a global picture of care of sarcoidosis patients, not limited to treatment via anti-sarcoidosis drugs but addressing all aspects of the disease, from clinical to economic and social life, thanks to the use of an ABCDE model (assess/backing/complaints and comorbidities/disease-modifying treatment/extrapulmonary specialists), without minimizing the unresolved questions concerning both the cause and best medical treatment of sarcoidosis [ 30 , 31 ]. Apart from well-known severe complications causing organ dysfunction and premature death [ 32 , 33 ], Quality of life (QOL) impairment, notably due to fatigue, depression, cognitive impairment, small-nerve neuropathy, familial and occupational life or due to reduced income, which have been insufficiently taken into account for a long time, are better recognized, as is the impact on familial partners.…”