Paclitaxel & Trastuzumab

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Hi All, After a long summer of surgeries (3 in total) finally saw my Oncologist today,  I am going to be having weekly chemo for 12 weeks with Herceptin (Trastuzumab) because I am HER+ no sure how I feel about weekly Chemo but I guess It kind of gets it out of the way quicker.  I have been given a long list of side effects, just hope I dont get them all.   Feeling a bit anxious today having been given the percentage rates for survival for my grade 3 Her2+ cancer, although 89% survival rate over 10 years if pretty good I guess?  However 15% chance of recurrence which again the Onocology said are very low!  Still feeling a bit numb but at least now I know what is what and my path to getting on with it.   

Any advice if anyone had this Chemo would be greatly appreciated. 

Take care everyone and thanks for  listening. 

xx

  • HI Somersetlass, sorry to hear you have BC but you are in the right place for advice and support.  You don't say which chemo you are having but most chemo's aren't as bad as thier press and with modern drugs most side effects can be controlled.  Love from Ann

  • hello, i finished my Paclitaxel chemo 10 weeks ago , i used to have every week for 12 weeks plus Trastuzumab every three weeks and still continue. I used cold cap all chemo period to save my hair and it worked for me.I had very mild side effects but not up to week 5-6 and they was very mild. This chemo very manageable, my cancer also her2 positive grade 3. I worked true chemo period just week 12 i started feel more  fatigue and it continued for a while. Otherwise i was absolutely fine . I hope you will be ok and if you have any questions feel free to ask. Good luck xxx

  • Thanks Annna for your reply, that gives me a lot of comfort.  I can't use the Cold Cap as my hospital are not allowing it at the moment due to Covid and risk of Infection so that is not an option for me but I have kind of got my head around that now.  Its nice to hear of someone else on the same journey as me.   I just wondered why I was having it weekly and didn't ask Oncologist Yesterday but I am presuming its because its manageable weekly?  Which hospital are you with? I'm with Taunton Musgrove. Take care and thanks for your reply. x 

  • How you getting on with chemo?

    Did you get paclitaxel (taxol) weekly?

    I have been given options and one of them is weekly taxol, herceptin and perjeta.

    Would be interested to hear your experiences??

    Sending u healing vibes and hope you're OK there. 

    Ps i use to live in Somerset also near Frome. Now in Wiltshire 

    C x