Hello,
I'm hoping I might get some support from anyone who has been through or is going through something similar to me. I have one healthy 2 year old daughter but this year, I have had two consecutive missed miscarriages. I am now 39 years old so I assumed it was age related but my husband and I decided to go ahead with tests to see if there is an obvious underlying cause. Today I had an internal scan and bloods done and I was floored to be told I have endometriosis! I had no idea and i will have had it for years. Today I have been put on Estradiol Valerate (oestrogen) and in 2 weeks I start Norethisterone (progesterone) so as to bring on a period. I haven't bled yet since my miscarriage and my endometrium is very thin. I will be having a endometrium biopsy in 3 weeks time. My husband has also had his sperm tested and we are waiting for results.
I feel a bit overwhelmed by everything. Really, I could have done with more time to get over the miscarriages but I just don't have time to wait at my age. We have had to go private for these tests because the NHS waiting list is a year. I also found out today that I have diminished egg reserves but I expected that at 39.
The three times I have got pregnant, it has happened in only 1 cycle of trying. Conceiving is not the issue. It seems my immune system is in overdrive and I'm attacking the embryos which was so disheartening to hear.
Has anyone had any success stories with endometriosis? Is anyone else going through these tests for recurrent miscarriages? I'm feeling really alone at the moment.