When preg with DS, i didn't know at first. Suspected, did a test and confirmed with doctor. They sent me for a dating scan and I was nearly 14 wks. I was ecstatic to be pregnant. I was "bullied" into having the blood tests by midwife and friends/family, even though I said I would want a baby no matter what - Downs didn't bother me etc. they said "you'd want to know if something was wrong", dp said if it's disabled then we should think about abortion cos it's not fair on baby or him as he would have to bring it up, not just me (although we agreed from the start I would be a fulltime SAHM). Apparently his family was of the same opinion, and my family think disabled kids should be "put in homes". I refused to have an amnio (didn't want to know, risk of m/c, painful etc.) and did not have an anomaly scan until nearly 22 wks. They then changed my dates again. If they had found anomalies, I would have been pressurised into aborting and could not have lived with myself. Thank god he was fine. If I had had to have an abortion, it would have been OVER 24 wks possibly and a very hurried decision.
I hope to god I never find myself having to make a choice like that, for any reason.
When pg with dd, I refused all tests, and I was constantly pressurised to have them, but stuck to my guns, was very anxious at scan but luckily everything again OK.
If they lower the limit, then maybe other women will not be put into that situation.
Everyone is different and has their own reasons for abortion, early or late, but it should be their choice and not doctors, governments, partners, family etc.
I have heard of cases where scans are wrong and the aborted baby is actually fine, but it's too late then.
Makes me shudder.