

Year and a half with diagnosed AGA - AMA!
Hi, guys!! I (27F) was diagnosed with AGA in October 2024 (at 25) after somebody on social media with a family history of it pointed it out to me on a public post in May of the same year. There were few AMAs around that time, especially among people my age who don't take oral supplements. I remember when I was first figuring things out, I was so scared. You hear things about the side effects of minoxidil or AGA progression and the like and honestly, you think you're doomed forever. And plus, it's a huge learning curve as a woman to learn that you are not your hair, even if it feels super cheesy. So two years later, now that I've been in a good place with it for a while, I'd love to help anyone who felt even remotely the way I did! Leave all your questions below and I'll try to answer them to the best of my ability!
Disclaimer: I am not a doctor. Not even close! I cannot diagnose and I cannot assign treatment. If you're wondering if you have it, please speak to a professional! If you look high and low and find a good doc, it's completely worth it, and I cannot recommend it enough.