Thanks Primek. Where we have a family history and non BRACA1&2, we just may be
amongst the 80% for whom a gene has not been found. There are studies being done on
cell methylation. (A bit complex for me) but im longing for Liquid Biopsy to become available. I cant understand why PET cannot be done to see if the cellular activity is still
abnormal. Sophisticated scans seem to be done when the disease is self evident.
Ive concluded, the only early detection is public mammogram screening! We just
wait for the next event... All rather contradictory given early detection is the best intervention at whatever stage.. Thanks for encouragement and knowledge..
Go gently and well...