Just wondering if anyone has had the same or similar or are medical professionals that can give advice
Currently 30+1 with #2. This pregnancy in a nut shell is:
- essential hypertensive
- asthmatic
- previously Cin3 cells
- #1 was born at 33 weeks with 42ml of blood due to a silent, pain and blood-less Fetomaternal haemorrhage.
- only symptom I had with my son's FMH was reduced then absent movements
- I have Cw antibodies
Have previously failed 17 hours of CTG's between 26+6 and 28+4.
Always failed on:
- no episodes of high variation
- long term variation in high episodes below acceptable level
This was put down to immaturity.
Hospital trust appear fixated on the STV variation being an acceptable level. And as long as that's okay, it's just repeat in 12 hours/repeat in 24 hours.
However - at 30+1 I went in with RDF/absent sessions and have failed on the same 2 criteria... but it can't be put down to immaturity. So now they've gone for "loss of connection" which equates to 1m 59 seconds within the 60 minute period! 🤦🏻‍♀️
I'm kinda at a loss now 🤷🏻‍♀️