Molly
“One big challenge I’ve had throughout my life is dealing with cystic fibrosis. Cystic fibrosis was initially super exciting to me, because it was how I learned about biology and I felt like I was my own case study. I spent a lot of time learning about immunology and how it influences the lung. Eventually, I had that ‘Ah-ha!’ moment of ‘Ok I get it, that makes sense,’ but on a day-to-day basis, I don’t want that to define my life. I think there’s a lot of benefit of being able to compartmentalize this piece of who I am with my daily life, in terms of work, or what I do for fun. Studying cystic fibrosis would be such an all-encompassing thing, that it would be really difficult for me to see it for the piece of my life that it is, and not the defining factor of who I am as a person.
It was harder at first, but there’s a lot of pride that comes with being able to have a conversation with someone very frankly about the experience of examining your mortality throughout your life. I think most people have some big challenges not easily seen from the surface and it’s important to be able to talk about the times when it’s hardest. Being able to step back from it and come to terms with adversity in a way that helps you be a resource for other people going through it, is a really cool feeling and is probably the thing I’m most proud of myself.
Right now, I’ve been thinking a lot lately about what I want to do with this education that we’re getting and the value of this experience. We don’t have to pay for this, and we’re in a very protected little bubble for the next six years. I’ve been trying to rationalize the privilege of getting that, while also thinking about how to use it to improve things for other people. I’ve been focusing on the challenge of making this experience worth it, not only to myself but in a way that gives back to other people.”