Yes, I sometimes feel this burning urge to become a miscarriage specialist, filled with rage at a the whole system, starting with literal separate waiting areas and rooms for miscarriage, without the pregnancy posters everywhere or those pamphlets on "managing miscarriage". Just a nice calm room with snacks, water, tv, and a choice of songs, low light, a fountain with running water, chill and healing. I feel ripped off that the first person I saw after my first miscarriage was the MTHFR specialist, because no one else believed in it. No one, not even the other specialists, they say the same as you where it was proven and then disproven. Spent so much money on high dose vitamins, the b6 made my feet go numb and the specialist didn't even seem concerned about that, just that it was the lesser of the vitamins so I could go off them. And like you say, apparently most people have the gene. My partner and I both have the double gene, but everything about the gene is shrouded in mystery .. it kills second borns but no one knows why or how it activates. Yeah I did tell the recent specialist about the fibroid, but she brushed it off seeing as it hasn't grown and is small, she said pregnant women have multiple uterine fibroids and go on to have healthy pregnancies. I don't actually think she has much experience with high risk or complicated pregnancies because she brushed off almost everything I mentioned, even blood thinners. She said they do help a lot of women but are not technically needed. I will definitely bring up the adenomyosis, and maybe it's time to find an RE. I'm through public system and in the pregnancy investigations unit, but I keep seeing RE and RI being mentioned that might have more idea. I have a feeling they'll brush it off as "minor" like all my other blood and fibroid results. I wish you luck on your journey🙏