Hello all
I’ve not been on this post for a while because of infections and deferred chemo. Anyway, started now. Day 11 of EC and generally OK.
Like you all, I’ve felt shocked at the diagnosis of BC at all, and then slowly became aware of the implication of its being TN. I felt that information about this aspect was not handled well by the hospital. (Evrything else has been v.g.) The raw statistics were frightening and trawling through the internet isn’t v. helpful. I want to find out what I can - to check that the treatment ( 3 x EC 3x Tax + RT) is normal and effective but also I suppose to see what I can do myself to minimise the risk of its coming back.
I found a site which set out what one should and shouldn’t eat for TN. All a bit odd but I’ll hunt it out and put the link on here.
Anyway - thank you all you TN women who are hale and hearty after treatment; it’s good to hear your stories!
Best wishes to all. Hotpot