Hmm. So I didn't have I didn't even know I was having I'd had this condition until I was 18 or 19. So what happened with me was like, you know, I was missing things like because with retinitis pigmentosa, the scope of the vision starts reducing gradually. In my case, it was coming down from the outside to the centre. So I started missing things like you know, missing a foot on the pavement or missing an overhanging branch or like like that, when I see someone who's out a hand to shake my hand, I wouldn't be able to see their hand. So that's when we started noticing that something is like something's not right with the sight. And the diagnosis of retinitis pigmentosa did not happen immediately. But it was but at least I understood there was a condition with my retina. That's all I mean, that's how we understood at the beginning and I was about 80 As I said about 1918 at that And when these things started happening, but in my case, by the time I was 23, I was totally blind. The progress was very, very, very quick. So I hadn't, in a way, it was good for me, because I had been able to see a sighted world for a long time, so many things I can understand, because I've seen those things. And, and then it wasn't like, since I was just in my early 20s, you know, I had, I was studying chemistry, it's my, that was something that I wanted to do. But I had to drop out of university at that time, because I couldn't continue that particular field. I couldn't continue any more. And, but still, as I said, No, I was lucky enough that it was not in the big does not like somewhere in the middle of my career, this is the beginning of the career. So I could change tracks, and I could redo a lot of things. So another thing that happened to me at that time was like, you know, how do I say this? Okay, we lost, I mean, we lost her mother, she was struggling with cancer. And so it happened almost at the same time. So it didn't, maybe because of that I didn't have too much time to, to think about myself, you know, because our family as a unit was going through a lot. And so we all had to be there for each other. So, so that was that was supporting in a way, like I didn't sit down and mope for a long time about myself, I had to look, you know, like, get up and be a part of that group, which was going together. So I learned so at that time, like. So I learned to cook and I learned to do these things. And then I also thought, like, you know, I don't want to, I do not want to sit at home, you know, all my friends. But as I said, we all were just beginning our lives and careers, everyone had a job, and people are moving around. And I didn't want this vision loss to stop me. So I kept asking, like, you know, how do I want to how do I do? What do I do? Like? How do I cope with it? Because medically, I knew there was no solution, there was no cure. So the whole thing was like, How do I cope with it. So it took me about a couple of years to find people who could guide me. And so then I learned about a place where they were teaching company where there was a computer course, where we could learn how to use this with screen readers. And I got some of and when I went there, I met a lot of blind people. And they taught me how to use a white cane and how to move about. And so once I got my mobility, and I understood how to use technology, then I was able to, I was able to even finish my I was able to graduate and do I mean go further. And then I got a job, I was able to do all the things that I wanted to do.