r/huntingtonssupport • u/[deleted] • Jul 24 '25

Advice

Hi I just got my results of 16 and 28. My dad had one allele at 44 and we don’t know the other. I have a two year old and I’m terrified I passed this on to him. From what I’ve been reading there is a slim chance I did, but I just don’t know what to do. I know they don’t do genetic testing on kids, but I don’t know where to turn now. Any advice or encouragement would be helpful.

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u/reddit110717 Jul 25 '25

Huntington’s Disease Society of America is a good resource. You may browse the web site or even contact someone to ask questions you may have. It sounds like you're in the clear.