plenty of questions...and do as much research as you possibly can....you need to "inform yourself"....and ask questions...then ask them again.
Hi, Kristen. Good luck with all your tests!
Let me second Phil's very important advice above.
Never assume you're being told everything you need to know. Not only about long-term risks, etc. Even about instructions for testing and so forth. For example, remember to ASK in advance if you're supposed to show up for testing on an empty stomach. It would be a shame to lose a testing date because it wasn't made clear to you that you're mean to be fasting. And--coming from someone who's done the 24-hour urine collection six times--double-check if they expect you to keep the urine refrigerated during and after the collection. You don't want to do it for nothing.
On a more general level, this board is indeed an unbelievably good resource for information and support. People are incredibly kind and helpful. To get another perspective, you might want to take a look at another site (
http://sirencristy.blogspot.com/), run by a kidney donor who had a bad experience. Although some of her judgments might appear harsh and overly cynical, she has some interesting things to say about the limitations of the organ donor system, including weaknesses in reporting/collecting of data on the long-term health of kidney donors. Just realize her blog is
not set up to guide or encourage you through the donation process. Still, it's not a bad idea to be aware of some of these issues: it's your body, and your health. It's also, at least meanwhile, your kidney.
Be well, Snoopy