This is an FYI for anyone else interested. If you have a close relative that has/had breast or ovarian cancer, most insurance companies pay for the genetic testing for the mutation. The 1st level test is BRCA 1 and second level is BRCA 2. Then there is a more in depth test that does a lot sequencing and permutations to look for those rare mutations. This extra test is not covered and costs $700.
I had the BRCA 1 & 2 down and both came back negative for mutations. These were covered by my insurance. I'm trying to decide if I should spend the extra $$ for the additional testing.
My history includes:
Aunt had breast cancer 20 yrs ago and she is still a survivor.
Mom had ovarian cancer...found early and she survived long time (died from Alzheimer's)
Paternal grandma** died from ovarian cancer at age of 49 (before I was born)
My CA 125 (blood test for ovarian cancer) was monitored for 15 yrs and when it began to rise ...out came the ovaries...but ther are lots of parts that still can get "ovarian cancer"
I have had two different breast biopsies that turned out neg.
Docs kept suggesting I have the genetic testing done. So, I did. The first level is negative. I just have to decide if it is worth $700 to find out if I have one of the rarer forms.
** I didn't know about my paternal grandma's ovarian cancer until I started doing some genealogy and ordered a copy of her death certificate. She died before I was born and my dad died when I was 5.