There's been a trend in asking for ELCS after a previous traumatic birth due to secondary tokophobia (fear of birth after having previously given birth).
I've done a fair amount of reading on this as I had primary tokophobia (fear of birth having previously never had children).
There's similarities and differences between primary and secondary tokophobia which came up as I was doing my research.
My Consultant Midwife had a lot of experience with both. He reflected on it and the issue of control and did a lot of research. The primary group had certain pre-existing traits - they tended to be older, have a history of sexual abuse, issues with fertility and more likely to have gone through IVF etc. Research seems to show that if forced to have a VB anxiety seems to have had a physical effect and these women had poorer outcomes both physically and mentally.
The secondary group behaved differently. If given support and granted an ELCS in principle, a huge number changed their minds and had a VB in the end because that support and being listened to was such a massive thing and part of the problem. Because it was about control. It was about giving more involvement and choices and keeping patients informed as well as quicker access to pain relief if wanted. Stuff like that. So ultimately it was about standards of care and being in control of your own health.
The comments throughout the Liz Carr documentary therefore hit a nerve with me.
Disabled People are worried because of the effects on them from these changes and the implications for control of their own care.
What struck me was the complete absence of any disabled charity being supportive of assisted dying. Not one.
Then we get this narrative created by well and able bodied people which seems to suggest they are on the side of 'people who are suffering' but doing so by not amplifying the voices of the people in this position but instead talking about them or even over them.
The narrative of 'people who are suffering' is pointed out by Liz Carr to be fundamentally anti-disabled and I have to say I agree. It reeks of eugenics.
If you listen to people who have had life changing accidents or conditions it's interesting to hear the number who struggle terribly with depression before coming to terms with life being different to what they imagined but still worthwhile. And there being a period of coming to terms with it.
Once again it comes back to poor understanding and attitudes to mental health too and how we aren't providing adequate support and access to support where appropriate.
I, quite honestly, am going to tune out of all comments going forward from the most vocal on this thread who continue to engage with counter arguments and can't be bothered to watch the documentary. Because it says everything I need to know.
If you can not respond to and acknowledge the key arguments Liz Carr puts forward, then you are into eugenics as far as I'm concerned. If you do bother and respond accordingly, then I respect that. It's the total disregard for individuals who have chronic health issues who are genuinely (and with good reason) afraid of these changes that bothers me most. It's the arrogance of saying it's all about increasing MY choices without reflection of how that might reduce the option and choices of others that's tone deaf.