PKD Foundation

I could just sit and read books all day.

We were connected through the PKD Foundation because you live with autosomal dominant polycystic kidney disease or ADPKD.

So I was wondering if you can just tell us a little bit about how you started on this journey.

I'm always interested in like what was the first thing that happened that when you look back now, you realize, okay, this was part of it.

And then I just tried to figure out what the next steps were in terms of like my own education.

You just like in the dark, it's kind of scary because it just takes you down a really dark path.

And then my mom, I told her about it and she reached out to PKD Foundation at that time.

I don't know if they still do it.