I did look into the Down’s syndrome side of things, a lot of leaflets, and sort of got in touch with various, I think the Down’s Association I got in touch with. But that was quite difficult, I found, because I actually spoke to the hospital and I asked if I could speak to somebody that had a Down’s baby, and they didn’t feel that it wouldn’t be beneficial. And at the time I was a bit sort of, ‘Well, I don’t understand that. But in hindsight now, I can understand it a bit more.

And so I did look into that quite a bit, but mainly leaflets really. The hospital gave me a lot of leaflets on congenital heart disease and so I did read up on bits of that. But I must admit I didn’t actually contact any organisations. I didn’t actually physically speak to anybody. At the time I don’t think I wanted to – I did and I didn’t.

I think maybe if somebody had contacted me, I’d have probably quite happily chatted away and asked them lots of questions, but at the time I didn’t feel possibly strong enough or confident enough to actually contact them.