 Iwer Johnnie started in Dundee at Nine Wales Hospital. We had to go for IVF and the IVF was successful and we found out that we were pregnant after 14 days. And as far as I knew as a first-time mother, the pregnancy was going fine, everything was well. Everything just seemed to be fine. For a 20-week scan, which is the anomaly scan. We got taken into our room and that's when we got told that Jessica had spina bifydda. So, we just heard spina bifida. And when you hear spina bifida, you take all the negatives. So, we're thinking, oh my God, my baby's got spina bifida. Oh my God, my baby's not going to be able to walk. Oh my God, my baby's not going to be able to do this, not going to be able to do that. I was overwhelming, really overwhelming. It was like, you know, you just wanted the whole, like a whole to open up and for you to fall in this hole and I was distraught. I mean I was really upset and I thought it's my fault. I didn't do the right thing. I've not taken enough folic acid or I've done all the wrong things. But the field medicine team reassured me that it's not anybody's fault. It's a one in one thousand chance. We didn't know for sure what kind of spina bifida she was going to have until she was born. So, the doctor at the Sick Kids Hospital, Mr Tuller, he told us to go and have a look at his spina bifida association website. We were introduced to Becca and Becca's became our case worker. Becca's lovely. She's helped us a lot. It's been really good and the fact that they've introduced us to people that have got spina bifida has helped with the accommodation at the hospital. Giving us information about how to fill out forms, how to seek medical attention if we need it, just to listen to us, just to be there. They have given me the support going from being distraught, being upset, feeling alone, feeling like the only one in the world that's got a child with spina bifida. To give me the confidence to be able to talk about spina bifida and knowing that just because Jessica's got spina bifida doesn't mean that she isn't going to be able to walk. She's became our own little person. She's not categorised now as a baby with spina bifida. She's a person. She's Jessica. She's a baby that has spina bifida that can overcome anything that she puts her mind to. I think the spina bifida association has taught us that, but Jessica could turn out to be a surgeon that's dealing with people that have spina bifida. So it's given me hope that I know she's going to be fine. We've still got a long path to go, but I think she is doing really well and I think she's going to flourish and be the person that she wants to be. But I'm biased. I'm her mother.