Hi everyone,
I hope that this is the right place to post this question. My mother began experiencing extreme migraines nearly twenty years ago. She had an MRI and was diagnosed with a CCM in her left temporal lobe. She also had an EEG performed and was diagnosed with epilepsy despite being asymptomatic.
Since diagnosis, she has not sought out any medical care or advice despite many prevailing symptoms. Some of her symptoms include migraines severe enough to impair all functioning 2-3 times per month, mild epilepsy, and recent visual changes. She also has severe mood disturbances, but I do not know if this is due to the CCM or other causes.
I am not trying to push my mother into treatment because that is her decision to make. However, the genetic possibility of CCM is something that may affect me. I would like to be aware if I am predisposed to developing CCM and if this is something I should take into consideration when planning to have children.
Does genetic testing seem to be a reasonable option for me? Is this something that is feasible even if I do not have any specific medical information about her condition? I understand I need to speak to a doctor for true medical advice, but this forum seemed like the best place to start with my questions.
Thanks in advance!