Patients must be able to give adequate informed consent Able to give informed consent TREATMENT: Patient able to give informed consent Patients must be able to give informed consent Patients who are able to give informed consent Able to give informed consent Donors must be able to give informed consent Able to give informed consent Able to give informed consent Subjects must be able to give informed consent Be able to give informed consent Able to give informed consent Patient able to give informed consent Be able to give informed consent TREATMENT: Patient able to give informed consent DONOR: Able to give informed consent Able to give informed consent Able to give informed consent patients who are able to give informed consent Able to give informed consent Able to give informed consent Able to give informed consent. Able to give informed consent Patients must be able to give informed consent Patients must be able to give informed consent Able to give informed consent Subjects must be able to give informed consent Able to give informed consent ELIGIBILITY FOR ENROLLMENT/SCREENING (ARMS AND ): Patients must be able to give informed consent Able to give informed consent Patients must be able to give informed consent Able to give informed consent. Be able to give informed consent Able to give informed consent Patient must be able to give informed consent Able to give informed consent Able to give consent Able to give informed consent PARTNER: Able to consent to the study Able to give informed consent Able to give informed consent Able to give informed consent Are able to give consent Participants are able to give consent Participants are eligible if they are able to give consent Are eligible if they are able to give consent Patients able to render informed consent and to follow protocol requirements Able to give informed consent Subjects are able to give informed consent Able to give informed consent Able to give informed consent Able to give informed consent Able to give informed consent Able to give consent Able to consent for the study All subjects must be able to give informed consent Patients/subjects able to give informed consent Patient is able to give informed consent for this study Subject is able to give informed consent for this study Able to give informed consent Able to give informed consent Able to give consent Women who are not able to give consent The patient must be able to give informed consent