Triple Negative Breast Cancer

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Hi,

I am posting this on behalf my mum.

She is 55 & has just been diagnosed with triple negative breast cancer, although the lump has been removed and she is awaiting chemo the stats online for this particular cancer returning seems higher than some of the other breast cancers which is terrifying her.

Is there anyone else out there with triple negative breast cancer? 

Or anyone who has recovered and surpassed the 5 years?

Hope to hear from you soon.

  • ohhhhhh the info now is making more more anxious...defo talking to mcmillan nurse tommorow.  heal good . and happy ur daughter is with you. wish mine was she lives in Norway and is semi disabled. not a good traveller either. maryoma. 

  • Sending you big hugs all the way from sunny Spain.  Have a good old chat tomorrow, they’ll be able to reassure you.   Baby steps xx

  • hya ocho ...well I eventually had my savi yday ..app supposed b 10am . I was seen around 1200. out for 1300 and in bed for 1400. ....I shudnt have got worked up about it coz fear of it was worse than the actual savi insert. I have now got another op date which is this Thursday.  all going on now. 

  • I’m glad it all went well.  It’s the waiting that’s the worst.  My mind runs away with me.  Take it easy, big day on Thursday.  Keep me posted.  My stitches out today.   Onwards and upwards xx

  • Hi, 

    I was diagnosed with triple neg in October, had a lumpectomy in November and started chemo early December. It's quite a journey, but I can honestly say it's better than I had feared. More good days than bad and the bad days I am getting through with the love and support of family and friends. Keeping positive isn't always easy but it does help. My breast care nurse told me that TNBC now has about the same recurrence rate as other cancers because treatments are improving so much. There is a lot to be positive about. Some great advice a friend, who is a cancer survivor, gave me us that it's a journey, never a nightmare. I always remind myself of that when I'm low or gave grotty side effects.

    Be there for your Mum every step of the way and encourage her. She will get through this. Good luck on the journey

  • I’m at that in between stage, op over and not sure next steps.  I’m glad it’s not as bad as you feared.  I’m trying not to think too much about it.  Also good to hear about reoccurrence rates.  Yes quite some journey we have ahead of us.  Is your treatment plan, chemo then radiation??

  • Yes, radiotherapy 6 weeks or so after end of chemo. I found it easier once I knew the plan and got started. Good luck

  • hya all the build up to op was terrible but the actual op no probs ...im 3 days post op now and only tapes under my arm where sentinel node was taken . they are rubbing my under arm coz I've got very sensitive lately in that region . post op consultation in 2 weeks and results of biopsy. 

    wats best pain blockers only been told 2x500 codocodomol every 4hrs but the pain is back b4 the 4hrs is up. 

    any advice appreciated.  

  • well I've had the op. not as bad as the build up to it.. 3days post op today and tape under arm is rubbing that's all though. surgeon really was great . she's kept the insition to a minimum ....no stitches to come out they're dissolvable.  just tired and still shakey but think as they say I had plenty morphine. 

    2 weeks for biopsy results till then restveat sleep Zzz