My 2nd DC was born with a very rare condition that is typically found in 2 syndromes. When the paediatrician told us, within hours of birth, my overriding thought was ‘it doesn’t matter’. We had to wait days for confirmation it wasn’t part of the syndromes and then a further 6 weeks for confirmation the condition didn’t need surgeries. During those hours & weeks we didn’t particularly think of what our lives were going to be like with DC - they were here and loved, we would deal with it.
But, I knew during those first hours (and still to this day mainatin) that if DC had been diagnosed invitro with the syndromes I would have terminated. I saw that DC’s life would have been difficult for them, our older DC and what would happen to them after DH and I were gone? I never thought of the impact on mine or DH’s lives - DC was here, loved & would be cared for.
My DC took years of fertility treatment, but I would still have terminated had we had proof during pregnancy. Thankfully DD is fine, not impaired by the condition but does fear it being seen (she’s currently a teenager and self concious) and I too feared her being ridiculed during those early years in school.
While it isn’t your job to advise your DD of what she should or shouldn’t do, if it were me and my DD, I would be discussing the practicalities of life with a new born, toddler, teenager, young adult and adult with needs.
God bless you all.