So here we go again, entering Ethan's 18th relapse. I can hardly believe he and we have gone through this 18 times. You think I would be used to this by now, but the pain of watching my son suffer is something I will never get used to. Ethan has been spilling protein since August 18th as soon as we dropped his dose to 5mg every other day. Now that we stopped the prednisone his protein has gone up the highest level and he has started to gain a pound of fluid a day. I called his Nephrologist today and the decision was made for him to start back on prednisone, although there is a twist.
They want us to start him back on 10mg every day until Monday, and then I am to call them and let them know how he is doing. If he continues to spill or there is no change then he will have to go back up to the full dose. The reason for this change is that they finally have the bone density scan results. It shows that he has Osteopenia, which means he has low bone density, but not yet full blown Osteoporosis. So this means that they really want to limit how much prednisone he will receive because of it's effect on his bones. With those results, they have decided that we will have to come in and discuss adding another chemotherapy drug to the mix. I will probably find out Monday when that will be. As you can imagine this is a lot of information to digest and I think I am still in shock that this is indeed happening again. I want to be strong for my son but the thought of having to go on chemotherapy drugs for the 2nd time is breaking my heart. Please keep us all in your prayers as we continue to digest this new information and wisdom for the doctors to know what the best options are for Ethan.
