Hi everyone
Not posted on here for a while. I'm now about to start the next step in my journey, chemo which starts on Friday. I had a bilateral mastectomy 15th Jan and it has seemed forever for my oncologist appointment to come around. I remain to still not have my full histology report 8 weeks after surgery!?! The last time I knew they still hadn't located the cancers ( 2 in my right, one in my left) but could tell me that my lymph nodes were clear.
My treatment plan is to have 3 x EC 3 weekly then to have Paclitaxel weekly for 12 weeks. When I heard how long this was going to be I had my first wobble since diagnosis back at the end of November. I've pulled my big girl pants back up and I'm now back to the 'let's get on with it' mode.
I'm wondering if any of you ladies have got/had the same treatment plan as me. I know we are all individuals and none of us will have the same exact side effects but if any of you can give me a heads up particularly how you were with Paclitaxel the weekly cycles.
Love to all xx
Me, I have just fiinished my 3 x EC (every 3 weeks), it was a very hard but i am glad that is over. i am due to start my Paclitaxel plus targeted therapy tommorrow. Ill let you know how i feel after Paclitaxel. We dont know much about it right now just that they said there won't be as many side effects as EC. it feels like chemo is going on forever but i am thinking after it i will be better. I haven't had surgery yet so chemo then surgery.
xx
Thank you xx
Hope for your remaining cycles you stay relatively OK....its just the stepping into the unknown that's the scary part xxx
Hi this is my first post or reply on here but I am having my 4th (and last) EC tomorrow then in 3 weeks I will start Abraxane for 4 cycles (every 3 weeks). My first 2 cycles of EC were bearable but I felt awful last time so my consultant is reducing my dosage for tomorrow to see how I fare. I kept thinking to myself that this was the worst part and then I'd be onto different drugs but now I'm equally as worried what side effects they will have too.
I then face lymph node removal surgery and radiotherapy - I already had a mastectomy and reconstruction on one side last November.
I'm trying to see a positive that I'm halfway through, so any other positive replies will be very appreciated.
Good luck to everyone currently on this treatment journey. I naively thought that with being 37, the side effects wouldn't affect me so much so I've found it very hard accepting that I can't do everything (some days not a lot at all).x
I've had 3 x EC and am now onto 12 x weekly Taxol with Herceptin. (3 weeks in)
It does seem a long road and I have had many a wobble, but once you are onto the weekly it goes quite quickly.
The side effects of the weekly are infinitely less than with the EC.
The unknown is indeed scary... I had a huge panic before starting the weekly but it wasn't that bad. Just keep focused on one day at a time and that there is an end goal.
Good luck xx
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