I have asked my ivf clinic many times to do further investigation in order to know why am having implantation failure he never bothered himself and blamed it on age
So I went to see another doctor for second opinion and suggested to check lupus anticoagulant
Am so devastated all these embryos and the money spent was wasted
I don't know how they treat lupus I have to check with my GP now
So sad
Written by
LadyMM
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I have it too. But mine was only picked up after having three miscarriages. I had two missed miscarriages last year after ivf treatment. It didn’t stop me getting pregnant. In fact the consultant said that blood thinners are fine to be started around 6 weeks. Having said that, I’m on blood thinners from the clinic now in preparation for my transfer tomorrow and I was on them for my last fet (which was a negative despite the heparin and aspirin). It does seem a bit of a shock when you first find out I know xx
Hi LadyMM. Usual treatment is using some sort of anti-coagulant such as Clexane/low dose soluble aspirin are the usual drugs of choice during IVF. Still no guarantees, but they are definitely worth trying. I hope you have a satisfactory meeting with your GP. Diane
I already had lupus- diagnosed as a teen- so was put on clexane and aspirin from the day of egg collection. Got my BFP on the 1st round but think it was only because of this. I hope you get it resolved xx
I have just found a very faint raised lupus but the next tests came back as negative. It is a very sensitive test apparently. Anyway, I have put myself on baby aspirin and I fully expect a positive outcome next time xx
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