I've had 4 mcs following having my dd by emcs. We've been through all the tests at St Marys and had no diagnosis, no chromosomal or clotting disorders.
We have a follow up appointment next week but I'm not expecting any treatment plan.
Our other option is to go to Prof Quenby for NK testing. However I don't know if my patter of mcs fits with it being a nk cell problem:
Mc1 twin pg, mmc diagnosed at 8-9 weeks, 1 hb but passed away the week later.
Mc2 spontaneous at 5 weeks
Mc 3 mmc diagnosed at 8 weeks, no hb ever seen
Mc4 mmc diagnosed at 10.5 weeks, good hb seen weekly up to 9.5 weeks
Can anyone advise?
Thank you 