This week was hard. Really hard. And I was grumpy pretty much all week. Really grumpy.
Early in the week, I was a bit frantic, but felt like things were mostly under control. My in-laws were in town for the week, and Steve and I had to work more than we'd planned, but we were treating it just like any other normal Christmas week. I found myself being mildly envious of the people I knew with recognizable physical conditions--a bad knee; a slipped disc--that let them just lie on the couch and do nothing, as that was pretty much what I felt like doing all week. But of course, we hadn't told Steve's family, so they were left wondering why, exactly, I was being such a bitch.
I like to think that the week would have been perfectly manageable, if not for my RE follow-up appointment on Tuesday. I woke up in a terrible mood on Tuesday, and it was only mid-way through the day that I realized why: I really didn't want to go to that appointment.
Steve and I went together, leaving Andrew with my in-laws, and taking a plate loaded heavily with my homemade cookies and candy. They waved us into the ultrasound room (a bit of a surprise; had I expected it, I wouldn't have worn my horrid Christmas socks under my boots) and a quick ultrasound showed that my uterus was now utterly, completely empty. They gave me a lab slip for an HCG test, to make sure that my levels were decreasing appropriately. (The Christmas Eve results: 23. Spreading Christmas cheer!) They told me that the results for the genetic testing on the embryo were not back yet, but should be soon. Finally, I talked to the nurse, briefly, about what we wanted to do next.
Not miscarry was my first thought, but they wanted a little more specificity than that. We talked briefly about my general fertility--three pregnancies in a calendar year, we agreed, was pretty close to normal rates of fertility--and then a bit about that nasty miscarriage business.
The nurse mentioned, as my doctor had months previously, the possibility of IVIG therapy, given my diagnosis of antiphospholipid antibody syndrome, and the fact that the heparin/aspirin treatments don't seem to be helping much. She gave me the information for a local doctor who has performed the therapy for some of their patients, and suggested that I talk to him to see if he thought it would help, and also to get a sense of how insanely expensive it would be.
When I got home, I googled the therapy to see if it was as witch-doctory as it sounded. I recalled, from looking into it three years ago, that at the time it was seen as pretty far-fetched and scientifically unsound.
All of my googling this time, however, led me to this study on IVIG therapy for secondary recurrent miscarriage, which looks like it would pretty much fully answer my questions about whether or not this therapy would be helpful to me. Of course, (a) it's not enrolling new subjects; and (b) they haven't published their results yet. They're supposed to complete the study in 2010, but the "primary completion date" is January 2009, which they define as the "final data collection date for primary outcome measure." I am hoping that means that I might be able to contact them next month and see if they would be able to give me a sense of whether I should even try to follow up with this.
Meanwhile, I'm just a bit adrift--waiting for my HCG levels to drop to 0, waiting for another cycle to start, waiting to see if the genetic testing yielded any results. Waiting, and hoping that this next year is just a bit easier.