I don’t really know how to talk about the next bit because, without wishing to sound overly dramatic, I don’t know what the legal implications are of writing about my clinic and what they did or didn’t do, without giving them a chance to respond to what I’m saying. And I know I’m anonymous and I know I haven’t named them but I’m still wary. So I’m going to try to use quite broad brushstrokes.
I’d felt that there had been communication issues between us and the clinic for a while. Questions going unanswered, inexplicable delays and a lack of a sense of urgency, me having to request tests that I thought they should have already organised, information not being passed on. But I’d kind of sucked it up because everything up to this point hadn’t really been about me, it had been about our donor. I didn’t feel as if I could force issues because maybe there were other things at play. Maybe the delays were down to the donor (which I was totally fine with). Maybe the lack of information was a privacy issue. Maybe, maybe, maybe…
This strange feeling of detachment persisted. We knew what day the donor would be donating because B had to go to the clinic to wank into a cup (it is what it is, so let’s not dress it up as anything else) so her eggs could be fertilised. And while I wanted to know how many eggs they’d got from her, how many had been fertilised, how many had got to day 2, day 5, how many blastocysts, I didn’t have that same desperate-for-the-phone-to-ring anxiety.
Maybe it was that I still felt quite detached from it, but I think a lot of it was also because I feel more sanguine about the whole process. More aware that there’s nothing I can do that will change the outcome so whether I know at 10am that day how many embryos looked healthy, or whether I don’t find that information out until seven hours later makes no odds.
But once bitten, twice shy and all that. We said yes to the agency, we signed paperwork, we paid sums of money for treatment, but I felt very detached from it all. I just didn’t really engage with it. It was all taking ages, there were tests for her, tests for me, tests for B – the tests went on and on, the weeks and months went by. The process of getting our donor to the point where she could actually donate, that we’d been told would take three months, dragged on and on — if this were a film or TV programme, this is the point at which you’d see the leaves on the trees changing colour from autumn to winter to spring to denote the passing of time.