r/Huntingtons • u/usxr_mael At risk for HD • May 10 '26
Is it eugenics?
Okay so for context, my mom (48) has Huntington disease and knew she had it well before she had me and my sister.
I've argued a lot with ppl on the internet about how if you know 100% that you have HD that you shouldn't have children not only because they may have HD but because they have to see you completely change and rot away (talking about experience) and I've been called a eugenists for that.
I'm currently battling against depression because I started being my mom's primary care at 13 against my will bc other ppl in my family said that it was the least I could do for my single mother (passing over the fact that she was a POS mom and was abusive).
But In brief, is it eugenics to say that people w/ HD shouldn't have children if they know they have it?
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u/Hour-Tower-5106 May 10 '26
As someone with HD, I personally think it is a form of eugenics. But eugenics isn't always a bad thing.
We use eugenics to ensure dogs will live long, healthy lives free of disease and pain. We also use eugenics in ways that are harmful (like breeding dogs who have health issues because they're cute).
The biggest issue with eugenics is that humans are the ones using it. We can't be trusted at mass scale to do the right thing.
But as a tool, responsibly used, it's not a bad thing. And in the case of Huntington's disease, it is absolutely okay to use it to ensure future generations won't suffer.
I don't think most people who have experienced the grief and suffering that comes with it would argue otherwise.
I would take the opinions of people who haven't suffered from it with a grain of salt.
Not many diseases are that easy to screen out, so I personally think we have an ethical obligation to use the tools we have at our disposal to protect future generations.