Well ladies i am back from my appointment at the john radliffe .......... and i feel deflated!!!
I did actually see a doctor which i was surprised about on a saturday, but we werent in there long and i felt it was really rushed!
He started by giving me the bad luck/chromosome speech!!!
I wanted to leave there and then..... then i showed him some bloods i had done at the doctors, he said they were fine, asked when the mc were, how old i was n if id had erpc etc.
He said hed arrange some bloods for both of us, but we needed to come bk when the are open which is a pain because its a good 45min drive. He said the 1 that checks both our dna takes 6 weeks and to chase him if i hadnt heard in 8 weeks! They are also doing cd3 bloods for me and the rest of the clotting 1s i hadnt had at docs, but he pretty much said he didnt expect to find anything wrong there, looking at what id already had!
Also going to arrange an ultrsound to look at uterus, but he finished by saying they probably wont find anything! Carry on as normal in the meantime.
I brought up the nk cells test, and he shook his head and said no straight away! I said i could go somewhere and have it done and he said dont pay for tests privately theres alot of money to be made at fertlity clinics by exploiting people and nothings been proven, i said but i keep reading that crohns disease is an autoimmune disease and there could be a link, but he dsmissed it, then said some1 at oxford is doing work on nk cells, and if i meet the criteria then he will get her to call me.
Anyway sorry for the long post just thought id fill u in.....feeling fairly crap and down and just know im gonna miscarry again, im actually starting to think thats it for me, no baby......
Hi to all the new ladies xx