Hello, thank you for sharing information about this topic. In Spain, people have no idea that this genetic mutation exists and that it can affect you so much in the long run. Doctors never test your homocysteine levels, and if you finally manage to convince one to order it in your bloodwork, they don't know what to do with the results afterwards. It’s unbelievable!! I believe in preventive medicine... I've suffered from migraines since I was 20, and my mother was diagnosed with cognitive decline 10 years ago. Ever since then, my search for answers began... and in the end, I had to diagnose the genetic mutation myself, researching and studying on my own. That's how I found you on Instagram and later on Skool. I have finally managed to get a hematologist to order the genetic test; I had it done yesterday, Tuesday, and I will have the results soon. I am already supplementing and managed to bring my homocysteine down from 53 to 30... but I still have a way to go. Thank you for all the valuable content you provide on this blog. Best regards.