Evening everyone,
Hi Paula, gosh so many people in your family had/have breast cancer. With so many people It must be highly likely that you all carry the gene. Are you all being tested for it, is it just a swab and how long will you have to wait before finding out the results? It must be reasuring that you daughters are being checked so quickly. Good luck with the results x
Hi Lorraine, what a lovely weekend away and holiday you have planned. I wish i had your energy, you always seem to be doing something. Now i'm feeling alittle better i must plan more things. Its good to have days to look forward to. As i knew i'd be having loads of treatments this year i haven't arranged much, think that needs to change :-). My fingers are crossed your bloods are good for you to get away, god knows you deserve it.
The last time i went away and left my eldest boy he had a car accident (teenagers!!) and we had to come home early!! Thankfully it was nothing serious and he wasn't injured ...but his pride was!! Oh yes and the car was a right off!!!
Hi Stef, i think most oncologists reveal as little information as possible, maybe they don't want to scare us. At my first appointment to discuss and arrange treatment, i was told that my cancer was hormone and her 2 positive and i'd need to have Tamoxifen (as it was hormone fed), chemo, radiotherapy, herceptin (as Lorraine said for the Her2, it was protein fed as well as hormone), and my ovaries blocked to reduce hormone activity. Basically my cancer was a right little so and so, being fed by everything and growing fast, so i need to have practically all treatments to stop it!! I agree with Lorraine you sound like you're hormone + and it's supposed to be the best breast cancer to have (easy to treat and the highest success rate). I'm going on Tamoxifen after chemo. How did you find it while you were taking it? Hope your tea tasted good...it sounds yummy :-) I'm now reaching for the chocolate and gaining another kilo!! Lol.
Hi Kay, your holiday sounds fab. Just what you need after all your treatment. My in-laws have just got back from there and they said how beautiful it was.
This thread is a busy one, i think we all find it hard to keep up with it!
Chelle x
Evening all,
I reckon it might be the tamoxifen that is giving me the huge appetite or perhaps its the boredom of being off work for so long...Still getting the odd horrid migraine in the day and hot flush during the night but other than that, been on it for a month now. Starting the radiotherapy on 22/7 and have my booking appointment the week before, not looking forward to going every day but am sure it won't be too bad?? anyone having theirs at the moment?
On a positive note, my arm and shoulder are on the mend, probably because the fluid subsiding..
Chelle, your BC is definately having everything thrown at it so am sure you are well rid... fingers crossed and good luck with it all..
Lisa x
Thanks Lisa, all i can do is have everything and hope it doesn't come back. Everythings good at the moment....phew :-).
I'm starting Tamoxifen and radiotherapy Sept/Oct time and i'm not looking forward to gaining more weight.Lol! Its been bad enough on chemo!! Have you been menopausal? My husbands dreading me having mood swings etc and being in the dog house all the time lol!! It's great that your arm and shoulder are improving. Hope radiotherapy goes well for you x
Take care Chelle x
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