My husband does home hemo-dialysis. After spending nearly a year now trying to inform and educate family/friends on ESRD and dialysis, we are STILL hearing the following remarks being repeated: "why is he still working and not on disability?" "his doctor can put him on a registry to get a new kidney" (he doesn't want a transplant and we've both explained in length all the reasons why). We've also been told these gems: "certainly you are not implying that only wealthy people can get transplants, are you???" One family member asked "any chance you'll get your old life back?" while another calls dialysis "analysis". Yeah, that's right. We analyze his kidneys at home five nights a week.