We enjoyed reading Hendrick et al's important article entitled "Age Distributions of Breast Cancer Diagnosis and Mortality by Race and Ethnicity in US Women" 1 and the accompanying editorial by Yaffe. 2 We write, however, to point out several important errors in the editorial by Seewaldt and Bernstein. 3 They incorrectly cite Stapleton et al 4 as stating that "for Black, Asian, and Hispanic/Latina women, the diagnosis of invasive breast cancer peaked at the age of 40 years (vs the mid-60s for NH-White women)." The actual statement is that "the median age at diagnosis was 59 years for White (IQR, 51-67 years), 56 years for Black (IQR, 49-65 years), 55 years for Hispanic (IQR, 48-64 years), and 56 years for Asian patients (IQR, 48-64 years) (Figure 1)." Figure 1 shows that the "peak" is in the mid to late 40s for Women of Color.Citing an advocacy website, 5 they also incorrectly state that "all 50 states in the United States have enacted legislation requiring radiologists to inform women of all races and ethnicities who have high breast density that they 1) are at increased breast cancer risk and 2) may benefit from supplemental breast cancer screening modalities, such as whole breast screening ultrasound." The federal law passed in 2019 ensured that the Food and Drug Administration process of updating postmammography reporting requirements for both patients and referring physicians would move forward. To date, the Food and Drug Administration has not introduced a federal standard. 6 Individual state "inform" requirements are still accomplished through individual state laws. Currently, 38 states and the District of Columbia 7 have active density inform laws, but they vary in the depth and breadth of information required to be provided to women. For instance, not all mention increased risk or supplemental screening or even require mammography facilities to inform a given woman that she has dense breasts. The outcomes of breast cancer in women with dense breasts are, in fact, worse in the cited analysis of Gierach et al 8 with an excess of late-stage (II and III) disease. The relatively short mean follow-up of 6.6 years was insufficient for an accurate analysis of mortality after screening.