At long last, the federal government is considering moving toward a more sensible—and truly nondiscriminatory—blood donation policy.
In July, the Food and Drug Administration (FDA) announced it was seeking comments on the possibility of changing the ban on donations from men who’ve had sex with another man in the past year to an evaluation of individualized risk for determining blood donor eligibility.
If an individualized risk assessment based on the potential donor’s actual behaviors sounds familiar, that is because Lambda Legal has been advocating in favor of adopting this approach for years.
We are thrilled the FDA is finally seriously exploring this nondiscriminatory way of ensuring—and potentially improving—the safety of the blood supply.
Last Friday, Lambda Legal submitted comments, joined by several other advocacy groups, in response to the FDA’s request.
Our comments advocate for an assessment of the activities in which the potential donor has engaged that present a significant risk of HIV transmission, such as receptive anal sex without a condom, and a much shorter deferral period based on the ability of widely used tests to detect HIV and other blood-borne pathogens just a few weeks after exposure.
Because scientists know the level of risk presented by various activities with a fair degree of precision, the FDA could determine the specific point along the continuum of risk at which the line would be drawn.