HER2 breast cancer with mets to liver & brain

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Hello to all of you affected by  HER2 Brest cancer.
. I just wanted to give you an insight-and hopefully, something positive to read. I was diagnosed with HER2 with mets, in November 2013. I have had 145 three weekly treatments and have never missed one. 
briefly -I am living with Cancer. At first this was very worrying but I have adapted and accepted that, whilst I have incurable cancer, I must live my life as fully as I’d possible.

Last year a new drug replaced Herceptin and Pertuzumab and that was concerning. The new drug  is an injection in my leg only takes a  few minutes -replacing the 3 hours!! It used to take. 
things haven’t been plain sailing for me though because in 2028 it did spread to my brain and my eyesight is now damaged. 
But -I am still here and making the most of what I can do. 
so - please try to be as positive as you can be, keep as as fit and outgoing as you can and I really hope the drugs work well for you. 

Wishing you All the Best

Sheila C

  • Amazing ! I had breast cancer 15 years ago , returned as her2 positive in my bones at start of lockdown- I had 6 docatexel chemo with herceptin and other drug intravenous- I am also now continuing 1 year later with 3 weekly injections of phesgo - presume this is same as you?

    It’s lovely to hear a positive voice living with cancer, I am active also apart from spinal problem caused by delay in start of treatment, but I am coping well and try to do everything as normal.

    Take care everyone and I agree take each day as a good beginning and enjoy every minute.

  • Very encouraging long May it lastxxxx

  • FormerMember
    FormerMember

    Well done Sheila C!  Do you have any side effects from your treatment? I am also secondary HER2+ (liver mets), I have had 33 3-weekly treatments so far...I think I have a worse reaction to the new injectable drug (Phesgo) or maybe its just the toxicity that has built up through use over time?  After every treatment I get a massive head ache, diarhhea, a rash and feel so tired I go to bed for a couple of days.  My onc has suggested I take steroids alongside the phesgo, but I've taken dexamethasone before with chemo and I hate it! He also suggested taking anti-histamine but that has had no effect.  We are going to discuss moving to 4-weekly treatment to see if I tolerate it better. First a round of tests to see if there is anything else going on. I'd be interested to hear if anyone else gets side effects with phesgo??

  • Hi Sheila, it's really nice to hear your positivity! My mum was diagnosed with HER2+ Breast cancer in 2019, she became very poorly with her chemotherapy so only had 3 sessions. Her breast cancer has returned and spread to her liver. We found out in April 2022 and she has just started chemotherapy again. We have been told this is a gentler form. She is on Docetaxel chemo and is given it every third week for 6 sessions then this will be reviewed. She is also on Herceptin and Pertuzumab. We don't know how severe the cancer in her liver is yet as she is awaiting a CT scan. We are trying to stay positive!