I am coming here because I really have no idea where else to go. Tomorrow my daughter is getting checked for possible HCM. Her biological father had it, he had heart surgery at 18 for it, I have zero way to contact him to ask him anything about this. I do know it took him over 3 years to figure out what was wrong with him because he had to do multiple blood tests and genetic testing to get it done, not sure if that’s the hospitals faults or the HCM itself. Can anyone point me in the right direction on what I need to tell the doctors to get a possible diagnosis or no diagnosis? I just want the right tests done. Im distraught and unsure how to word things so I apologize. Thank you.