Hi,
I'm 22 years old I recently decided to do 23andme because I was experiencing liver issues. Along with a genetic link to my liver issues, I found that I am a e3/e4. I panicked at first, but am very glad to have found this website. I feel optimistic that this does not mean I am guaranteed to develop Alzheimer's. I was wondering if anyone has been to a genetic counselor? I am interested in meeting with one but don't know how to go about it or if my insurance would cover it? Also I am of Native American/East Asian ancestry and a woman and I saw some articles saying that these factors could increase my chances of developing AD. Can anyone could give me some insight into this, or what I should do to help counter these factors. I have read the introduction and the things I can do for prevention (many I am doing already to help my liver). I am adopted so I don't know anything about family history. I do have 2 biological first cousins who are around my age, but neither of them have done 23andme. Any insight would be helpful, thanks!