Showing posts with label application. Show all posts
Showing posts with label application. Show all posts

Monday, October 27, 2025

Microstory 2526: Middle Class Patient

Generated by Google Gemini Pro text-to-video AI software, powered by Veo 3
When the Foundation first made the rounds in the news, I both was skeptical, and didn’t think it applied to me. I exercise every day, even if it’s just a thirty-minute walk, and I always eat healthy. I get plenty of fiber, and the right ratio of my macronutrients. I’ve never had a problem with vegetables, even as a kid. Unfortunately, none of that mattered, because I was born with higher susceptibility to Hereditary Chorea. You can look up what that is, and what it does to your body, but it’s a genetic disease that there’s nothing you can do to stop it. It doesn’t matter how you live your life, or what exams and procedures you have done in your youth. You’re born with it, and only time will tell if you develop it. You can get tested to see if you have the gene, but you’re unlikely to even request such a test if you have no reason to suspect that it runs in your family. I was adopted by a very nice and soft-spoken man who I love very dearly, and the only thing I realized too late that I was missing in my life was the right kind of information. I never cared what happened to my birth parents. I was abandoned in a crackhouse as a baby, so family services had no idea who my mother was, let alone my father. I never had any interest in locating my birth mother, but looking back, I probably should have, for this reason, and this reason alone. I didn’t know that the disease runs in my family, and I still don’t know which side of the family it’s on. It could be both, for all we know. Had we thought to get me tested, I could have been better prepared for it. Very specifically, I would have chosen not to have children. Do not misunderstand me, I love my kids immensely, but I unwittingly placed them at risk simply by having them. That was the hardest part after the onset of my symptoms, worrying that one or both of them would suffer as I did when they got to be my age. I was so relieved when I started hearing proof that Landis was the real deal, and not some charlatan selling snake oil. I honestly didn’t think I would get the chance for a cure. I hoped that my children would have better chances when they were older. Then my thoughts darkened again, because I thought, what if Landis dies before my kids get the chance to be cured? How big is our window here? Then the news continued, and we found out about the panacea research, and I felt grateful again. If I died before they completed such research, I could leave this world confident that my young ones would likely grow up to a world with no disease. Obviously I applied for my own healing anyway, because I certainly didn’t want to leave them, and that’s how we’re here today. I put in a lot of work preparing my family for a future without me. Now I have to walk a lot of that back, and consider where we go from here. Not that I’m complaining. It’s a good problem to have.