After our MMC last week, I have been at my wits end trying to understand what went wrong, or what I did wrong. Half the time, I think I’m still in shock. It doesn’t help waiting around for my period start before we can get ready for FET #2.

With that said, we met with our RE today to plan out our next transfer. Having had already genetically tested our babies over the summer, it is more than likely bad luck that our little one didn’t survive. Having had 1 MMC from a natural pregnancy, and now this MMC with a PGS babe, she’s changing our protocol and running extra tests to put us all at ease:

-Updated SIS (make sure no polyps/fibroids appeared)

-Updated hormonal bloodwork

-Blood clotting panel

-Endometrial scraping

-Antihistamine protocol (Prednisone, Pepcid, Claritin)

We opted against an updated HSG, testing for dna fragmentation and ERA.

Looking at either transferring first week of Dec or first week of Jan 💕🤞🏼