Thank you, Mr. Chair.
I have several questions. Some of them are really easy, so I just need quick answers.
First, is there any restriction on who can be a witness to the consent?
Second, the education material that is to be created by the agency or is the responsibility of the agency, given that they have a fairly large budget and not an active board, but lots of money that we seem to have approved last week or the week before...I'm wondering if some of that work has been done currently and whether there's anything we could actually look at.
Third, I want to follow up Dr. Bennett's comment. It's one thing to have education and awareness material “available”. I don't know how I know it's available. If I've gone to a private clinic, are they going to say to me, here's the 1-800 number you call and there will be a trained, experienced person on the other end of that? And how many languages will this line be available in, because that's a major concern across this country these days?
I've come into this a bit late, and this may be a foolish question, but when somebody signs an organ transplant card, is there any way that sperm is included under organ transplant? I'm just curious. I'm wondering if under those circumstances, if the donor is dying and we talk about a donor who has died or is dying...I'm not sure how one actually goes about getting consent for how sperm can be used.
My last question, and I think the chairperson was getting at this point, is if you're going to run a stem line or create a stem line using the in vitro, does it say somewhere in the consent how far you can and cannot go with that stem line and with those stem cells in terms of research that will produce--and maybe it's covered off by the word “reproduce”--a human being? So is there something that says the research can only go this far if you're running a stem line and collecting stem cells?
Thank you, and maybe they weren't so easy.