 So yeah, I found out that I was pregnant. It was absolutely amazing. My perspective changed. It's not about me anymore. It's about this little person that I have to take care of. So I was so excited. I was like, my dream come true. I have the boy and my two girls. I wasn't one of them. The doctor came and said that have you considered your daughter have Down syndrome? What? He told me that's not true. And she said, yeah. What's going to happen? She's going to be OK. How are we going to deal with this? Looking back at our appointment with Dr. Finn, she kind of looked at us, and she saw that we were not beat down, we wanted no more. We really want to be an advocate for our daughters. And that's when she says, you know, we're forming a research bank committee. We would love for you to be a part of. We jumped to our seat and says, yes, we want to be a part of this. The Kaiser Permanente Research Bank collects blood from the members of Kaiser to be able to study those blood samples, to hopefully be able to find cures or treatments for diseases. For me, what's personal, it's important for us as a minority community, they get our blood. That's the only way that they can find out what's going on in our community. The only way they find out something is from us with our blood, and they need us. And they need us now. Anything we can do to help our daughter, our other kids, other people, yeah, we're all in. Through the process, I've learned that Janela has come to us as a gift. And we love her for that gift that she is. And it's been quite an interesting journey, for sure. You can experience the most wonderful love. I think it's the most rewarding experience. If you want to help your future generation, your kids, kids, they need us. And it's our responsibility as a human being to help.