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.
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!
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