However, the wishes of individuals not to be so informed shall be observed” (Council of Europe 1997). In opposition to a presumption of this right, some have proposed that the right is activated through explicit choice (Andorno 2004), meaning that a family member must state their desire not to know before the patient

is obligated to not inform them. Potentially, trying to discern preferences without guidance from the family member can create a dilemma for the patient: by not disclosing the patient might be observing this right, but they would also fail to fulfill the “need for the provision of information sufficient to allow people to make meaningful choices” (Laurie 1999). In addition, by trying to determine a relative’s wishes, the patient might have to disclose

the existence Daporinad clinical trial of a potential risk (e.g., by asking “do you want to know your genetic risk?”) so that the purpose of the right not to know is defeated (Laurie 1999). For these reasons, the personal responsibility to communicate genetic risk information should be tempered by a more informal observance MK-1775 in vivo of the right not to know. This would permit a well-grounded decision not to inform without an explicit refusal by a family member, if the patient reasonably believes that the family member would not want to receive the information: “patients can reach a decision after a careful process based on the sharing of thoughts, beliefs, and desires in the family” (Gilbar 2005). This is not a perfect solution, as patients will not always know the wishes of others in their family and poor intrafamilial relationships could create additional difficulties. However, considering the complexity raised above concerning the deciphering of a family Sinomenine member’s wishes without explicit statements, granting patients’ discretion to disclose or not or to gain more

information from family members regarding their wishes is perhaps the most realistic solution. Points to consider: personal responsibility to communicate genetic risk to family members 1. Disclosure of genetic risk by patients to their families should be a personal and voluntary obligation, as the practical implication of a personal responsibility is to create an atmosphere that encourages and promotes voluntary disclosure. 2. The decision to disclose should be made by the patient, following guidance from a health professional when needed. 3. Patients should be informed of the familial nature of genetic information and their obligation to communicate this information to family members as part of pre- and posttest genetic counseling. 4. Children, when sufficiently mature, should not be automatically excluded from this website parents’ efforts to inform family members of genetic risk, as they have at least as much interest in the information as other members of the family. Genetic risk information can be both valid and useful for children to know and can permit them to incorporate behaviors that lessen risks.