Any long term survivors who have TNBC

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Hi all

I have a bad feeling that there aren’t many w TNBC and mine is now a few bone mets, not even 2 years after diagnosis. Curious if anyone is stage 4 TNBC and doing well? I have a 5 year old and hope can be with him for 20 years. Thanks all. Got lots of wonderful stories from those that aren’t TN. Appreciate all the info and positive stories. Sending big virtual hugs to all of you (((hugs)))

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  • KSkier
    KSkier Member Posts: 467
    edited March 2020

    Triple negative here. Dx'd w/Lung mets in 2009. I had a one year old and a four year old at the time: now they are teenagers!

  • dlittkemann
    dlittkemann Member Posts: 234
    edited March 2020

    @Kskier you Have no idea how badly I needed to hear that today. I cannot thank you enough for letting me know definitely helps me keep my hopes up. What treatments were you given? Or maybe it’s in your bio. I didn’t look but I will. Thank you so much. Glad you are well (((hugs)))

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