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High Risk, Strong Family History, +PASH?

Hi there. I have a very strong family history of BC (gene negative). Grandmother twice, Mother twice, 1st cousin at age 31…

Anyways, because of this I alternate Mammos and MRIs. Just had an MRI biopsy (not my first one) that came back benign with a foci of PASH. I'm reading all I can about this but I'm curious if anyone has specifically had this diagnosis and been in a similarly high-risk category like I am and what you did about it? Do you just let it go since it's benign? Did this make you more proactive in doing something prophylactically? Thanks for any advice !