Children very quickly learned how to avoid the stress that might trigger the light-headedness." -From Leenhardt's seminal report on the first pediatric CPVT cohort (1)T he practice of wise physicians recommending activity restriction in the setting of heart disease is woven into the fabric of cardiology.Until quite recently, "bed rest" was standard care for many common conditions, including myocardial infarction, rheumatic fever, and Kawasaki disease.Three decades ago we learned that patients with heart failure were best off with beta-blocker-induced "bed rest" after inotropic and adrenergic stimulation in heart failure not only failed to improve outcomes but also placed patients in harm's way. In the realm of adrenergically triggered arrhythmias, immense emphasis has been placed on ultracautious prevention of triggers that lead to events (2), arguably more so than on the development of rigorous evidence to titrate and deliver effective medical and interventional therapies to protect patients and liberate them to be more active.It has been just more than a decade since a group of experts came together to deliberate on exercise recommendations across a broad range of cardiac conditions, armed with very little data on which to base understandably conservative recommendations (2). Dr. Ackerman coauthored the Bethesda recommendations stating that "Symptomatic patients (with catecholaminergic polymorphic ventricular tachycardia [CPVT]) have a poor prognosis unless treated with an implantable cardioverter-defibrillator (ICD), and all such patients are restricted from competitive sports with the possible exception of minimal contact, Class 1A activities" (2). Since then, Ackerman and his team have been working to temper this edict with data. In this issue of JACC: Clinical Electrophysiology, Ostby et al. (3) report their experience with a cohort of patients diagnosed with CPVT, one-third of whom chose to continue with athletic participation after consultation at the renowned Mayo Clinic's specialized inherited heart rhythm clinic. We do not have all the details we would likeabout the population, such as whether the patient is the proband or a symptomatic relative, whether this is a "reassigned" diagnosis, whether the patient is seeking a review of athletic exclusion, or what is meant by "clinical risk profile." However, we can glean that the population is primarily referral based with a consensus statement-supported diagnosis of CPVT at a mean age of 16 years. At the time of the retrospective analysis, 79% of the group was highly treated with beta-blockers, and 35% were treated with flecainide; 32% had an ICD and 30% had previous sympathetic denervation. The temporal management of medical therapy is not described in response to intake or subsequent clinical status, but we are provided with helpful specifics about drug selection and titration.