Hi All, nice to meet you!
I have very sadly been referred for recurrent miscarriage by my GP and I am currently waiting to undertake the first batch of blood tests at the Leicester Royal Infirmary. As I am sure a lot of you are aware of, it’s a long and very distressing process that will take two months just to have the first responses and then further tests and investigations might be needed either to confirm a diagnosis or to investigate further if nothing is found.
During other more generic blood tests the doctor order me and were performed within the surgery they have found my vitamin D level is a bit low. To make a long story short I have come to this forum searching on line any information on a correlation between mc and vitamin D deficiency and I found out there are other tests available that are not normally offered within the NHS recurrent miscarriage investigation such as research of NK cells in the uterus, intrauterine investigations … I have also see someone mentioning progesterone supplementation to support implantation and the first trimester of pregnancy. Now, I don’t know whether this could be my case but at the Leicester Royal Infirmary they told me they don’t investigate in it because there is not enough prove that progesterone supplement will help you carry on your pregnancy (whereas it appear that some other hospital will consider this www.cmft.nhs.uk/media/1425169/recurrent%20miscarriage%20service%20november%202016.pdf ), nor they will look into NK or any autoimmune syndrome other than the standard testing for Antiphospholipid Antibodies. However I have read one user mention this in this forum here www.mumsnet.com/Talk/miscarriage/2628310-Recommended-recurrent-miscarriage-clinics . None of the doctors I have spoken with seemed to have any consideration for this aspect and I am a bit nervous because I would like it to be investigated as well in order to rule out all possible scenarios.
I have read, in the same topic, that the Implantation Clinic in Coventry does test for uterine NK cells. Does anyone her have an experience of rmc investigations with them? Do you know whether they would look into the NK only or progesterone deficiency and other tests are taken into account?
I am based in the Midlands but I am willing to travel as long as I can find someone thorough that will look into all possible causes and will offer assistance in case of a future pregnancy will be a possibility.
Thank you so much for taking the time to read this, whilst I hope to find some help and advice I wish none of you had ever experienced such a heart-breaking time, or at least had a positive and happy ending to this nightmare
.
xxx