 I'm sorry. So, whenever you're ready, Wadi. So, I was originally diagnosed with kidney cancer. I had a tumor on my kidney and it was greatly advanced. So, I had an effrectomy. They took my renal blend out and my spleen and they thought they got it all three months later. They diagnosed it as metastasizing to my lungs. Tell us a little bit about how you came to your treatment. I went to several hospitals trying to find a cure to combat this and I don't know if you want to know this part. I went to one prestigious hospital in the city and they gave me literally months to live and I wouldn't buy that. So, I went to a few other hospitals. One wanted to do some kind of experimental procedures and I didn't want to do that. I met up with Dr. Dutcher and my brother found her online somehow and took a liking to her, trusted her and went with her diagnosis. She suggested it, which was IL-2. Can you tell us a little bit about the treatment process? How do you take IL-2 in the hospital? So, the process of taking IL-2, we go into the hospital for a week at a time. The first week, the first morning, they give you an IV, I guess. And you get three treatments a day, every eight hours, that's a drip. And you get sicker and sicker gradually throughout the week to the point where Friday you're at that store almost. You're vomiting, you have diarrhea, you have to chill, fever. My blood pressure would drop to where I would practically black out. And I got a bad skin rash, which I would have to take oatmeal baths for. So, anyway, you do that for a week, you go home, take a week off and you would feel much better and you go back and do another week. And when you start up again that first drip on Monday, you're right back to where you were two weeks ago on Friday. So, it's like having the flu they say 100 times over, but I wouldn't compare it to that. I can't compare it. It's been 14 years that I'm cancer-free and I try to block it out of my mind. I can't really remember that it was as bad as it was, but it was tough. But I still feel like I cheated not only death but all cancer survivors, especially those who go through chemo and stuff, because I didn't feel bad. I didn't lose my hair, I didn't lose a lot of weight. It was just that week of suffering, I guess. How long after taking IL-2, did your doctor know that it was working? From what I can remember, about three months, maybe a few weeks, you'd have to talk to my doctor. I can't really recall. I think it may be four or several weeks I got another CAT scan and she could see that the nodules in my chest were going down. And then I think three months at a time I'd get CAT scans and within a year I think I was told that I was cancer-free and it never recurred. It was three to four weeks, several weeks after my one cycle of Enter-Lukin-2, which consisted of the first week was three days, because I couldn't take the high dose IL-2. So they sent me home. I came back a week later, took a full week of the low dose, which I couldn't take at all because I was getting such reactions. And then I went home for a week and came back. So that was my cycle, about two and a half weeks within a month. And after several weeks, she had a CAT scan and the results showed that my nodules had been getting smaller. And then within a year, cancer-free, knock on wood. Perfect, yes. That's great. Okay, I do have one more question. I just want to know if you could, you know, I know the side effects are bad, if you could tell us just a little bit about the side effects. And then if you could also say a little bit about how the staff managed the side effects? The side effects are not filed to consist of low blood pressure. Mine would drop considerably. They have a medicine for that, but they would give it to me after the first couple days, after I passed out. Luckily, I know my body and can feel what's going on. And I would ask for that medicine when I could feel my blood pressure going down. So they would give it to me earlier and then I would black out. Before I think you get the chills. I mean, you're freezing and you're sweating. So you're covering up and I mean shaking and then you're taking everything off because you're sweating. Diarrhea, gas, weak and tired. And the worst part for me was I would get a skin rash. I would be itching all over. And that continued for six months to a year after I took it, which I took as a sign that it was in me working. But that was the hardest with the rash because if someone would touch me, it would make my skin react. So I would take oatmeal bags. The nursing staff at the hospital were fantastic. They would just monitor me and if I needed anything, they were there. It's been, like I said, 14 years. I can't remember details. But I had that button and I would press it and they would come running in and take care of me. But the main thing was the blood pressure going down and the diarrhea and again, the chills. We got a wrap up. So just one last question. Can you just tell us, you know, why an event like this is important? What it means for you with these events? Give me a little bit closer, John. How do I repeat that? So say, you know, events like patient education events are important to us. Patient events like this are important, I'm sure, mostly for those who are suffering from it now. I just came back today for the first time in 14 years to talk to, in a setting like this, actually to repay my doctor. There's not enough money in the world to repay him.