 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 we want to be ahead of the curve, not behind. We don't want to be reactive. We want to be proactive. And that's when she says, you know, we're forming a research bank committee. We will look for you to be a part of. We jumped 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, it was personal. If somebody asked me if the research bank and Kaiser Permanente is safe, can I trust? If I donate my blood, I definitely will say yes. One of the things that was very fascinating to me was that there was a company like Kaiser that was willing to actually meet with you, meet with people. I mean, they were transparent about it. It's like, this is what the research bank does. We were taken even to the facilities to see what the bio bank is and did an explanation of what it was so that then we could go to the committee and say, this is what they're doing. We are able to bring our voice. We, as part of the faith community, as Hispanics, we're able to actually come and bring the concerns about or the questions that our communities might have. And so it feels good, actually, to be a part of this and for us to say, OK, this plan and this strategy that Kaiser has, we've been part of it. It's important for us as a minority community they get our blood. That's the only way that they come to find out what's going on in our community. They need us to be able to find out why, for example, Hispanic community is getting diabetes. 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 Janella, Janella 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.