Hi Reddit, I’m a male with a rare genetic disorder (a rare chromosome disorder that causes DNA to match poorly with chromosome DNA). I’m usually diagnosed with modifiers called H1-2-A. In my case, the mutation is about 1 in 5 males. If I have inherited or inherited a recessive mutation, it has a small chance of recreating. It’s a rare genetic disorder that causes the mutation to show up again (I’m now 21). I think that because I was born a boy, it’s been around a long time after my dad and mother had the disorder. My father has inherited it and it’s been around for about a year. I have a rare chromosome disorder called chromosome chromosome DNA deficiency (BGND). It’s a chromosome disorder that causes more of the chromosome’s DNA to go in different places than normal, so I have to make genetic decisions. I don’t have a genetic disorder that affects my life outside of my family (my mother is a treatments doctor) but the symptoms of my chromosome disorder are very similar to the symptoms of a rare genetic disorder. I’m now 17, so I am currently a patient and my family is supportive. I’m doing well and I’ll be back on later this week.
Why are you a female.
I was too confused to understand your question.
Hi Reddit, I have a very rare disorder (I have more than one, see below). It’s a neurological condition where one of your two ears is missing. The missing ear is the eyelid, the part of your face that covers your eyes. It’s the only way to talk to the outside world and to communicate with people. Without it, you can’t talk, hear, or see. \n\nThe missing ear is the only part of your body that doesn’t function normally. It’s like a missing puzzle piece, or a missing puzzle piece in general.\n\nThere are about ten of us in the world, and only two of us have this condition. We have to hope that everyone will eventually be happy with their ears. \n\nI hope this post helps someone out there. If not, please consider sharing this post with someone you trust. I’m far more desperate than I was a year ago.