I'm sorry you are going through this OP. I'd TTC 4yrs before finally getting pregnant. Unfortunately the baby had trisomy 13, patau syndrome, so I chose TFMR. I'd paid for the NIPT early, so had the procedure at 12 weeks. I was also told I'd need medical management. Obviously follow the medical staff advice, but here are some things I wish I'd known at the time.
-Go to the loo before they put the tablets inside. They should have massive pads you can put on (like a nappy) otherwise use the largest maternity pads you can find
-I laid down for about 1hr, then started getting cramps so walked around and moved.
-The pills will commonly cause diarrhoea, nausea, vomiting and a high fever. My face looked like a beetroot and I was burning up. These are not allergic reactions, just common side effects. Ask for paracetamol and pain relief before it gets bad. It didn't last too long, but did feel awful at the time
-When you use to loo, you might see a whole tablet come out or a white/grey/pink paste when wiping. They will still work so don't worry.
-Being only 12 weeks, I never considered that I'd have waters break. I realise that sounds silly, but had just never thought about it so wasn't expecting it
-The might take hand/foot prints for you to keep. You will likely also get time with your baby. Some hospitals offer a special, cool crib to take babies home, but you'd have to ask if that was an option if you wanted to do that.
-I was kept overnight on a gynae ward. Sorry if TMI. The following day I met with a genetic counsellor and also someone asking what I'd want them to do with the baby after the autopsy. I was told I could pay to have a private funeral take the baby home or he'd be part of a group cremation with his ashes scattered in the Garden of Angels section. This was the first time I broke down because I hadn't even thought about funerals etc. DH and I hadn't discussed it so its something to keep in mind.
-DH and I were given karyotyping blood tests a few weeks later to check it wasn't a translocation
-Depending on your babies condition, there might be a facebook group you could link in with
Remember OP that this isn't your fault and you aren't alone. If you have any questions, I'm more than happy to answer. Or PM me if you prefer xxx