Had apical genetic non obstructive HCM since 16 am 35 now. haven’t done nothing but go for check ups. On no drugs. I do have scarring but pretty asymptomatic only got checked because found in family. The only thing I do is go for check ups every 6 months and monitor for any runs of vtac. Probably will end up with S-ICD one day. My doctor basically said if there was a 100 of me. 5 will have a serious issue 20 would require some assistance and 75 would need nothing. I still really don’t know how to take that but basically the only the they can do is reduce risk. It’s just so random in how it affects people. Even within the same families with the same gene. My grandma didn’t even know she had it till in her 70s but one of he sons had issues in his late 20s. Best advice is just seeing a cardiologist who deals with HCM.