Recurrent Miscarriages

[Lifeafterloss22]

Hello,

I was hoping to reach out to others that are currently going through investigations following loss. I had my third consecutive miscarriage in May of this year. I’m 27 years of age with no living Children.

Currently under Professor Quenby at Coventry Hospital. I’ve also paid for NK cell testing with Professor Brosnen.

Is anybody else going through investigations? Has anything been found? I had my biopsy on Friday along with all the generic blood testing. It should take around 3 weeks for my bloods and 5 weeks for NK results. I’ve had progesterone prescribed for any future pregnancies, but at the moment we are taking a break whilst we have tests.

I would love to hear from others ☺️ Just a bit of moral support really and somebody singing from the unfortunate same place!

Hi @Lifeafterloss22

I've took a bit of a break from mumsnet following my third miscarriage in June so didn't see your post. Thought I'd reply anyway even though it's been a while!

I'm just had my 3D scan (normal apart from PCOs) and bloods done by St Mary's in London, hoping to get the blood results on the 25th of October. Haven't looked into the NK cells yet.

I got my GP to do some blood tests that Tommy's recommended while waiting for my appointment with St Mary's and discovered I have Coeliac disease which might be what has been causing the miscarriages. However, we won't know until I'm gluten free for a while longer and start trying again. I've been gluten free for 3 months today (yay!). I'd like to wait until 6 months to try again and get the all clear from St Mary's.

I'm a bit older than you, 35. We started trying just over a year ago.

Where are you in your journey now? Anything show up from your test?

xxx