We are examining the evolution and delivery of palliative care to patients with pulmonary hypertension (PH) and pulmonary arterial hypertension (PAH) in this issue of Advances in Pulmonary Hypertension. This is an important topic since many of our patients have either reached a point at which quality of life is limited (either by the disease itself or by complications of the medications), medical therapy is no longer effective, or transplantation is not an option. Yet, we, like physicians in other areas of medicine, often wait too long to consult our palliative care colleagues, thereby depriving our patients of