Each transplant center is required to keep data on donors for 2 years post transplant. Most centers do a one month, six month, one year and two year follow up. If we do not have data for donors it is very difficult to assess how kidney donation effects donors. If you live far or find it difficult to go to your transplant center, ask them for a form so that you can have blood work done (may still be covered under recipient's insurance) at your local primary care doctor and make sure they receive this information so it can be documented. Sadly, most centers do not spend time trying to locate donors and just check "lost to follow up". If something does change in our health status, such as you develop high blood pressure, protein in your urine, problems with incision or anything else that may be significant, you should alert them so that this data can be collected.
Good luck at your appointment and hope you are feeling well.
Sherri