Thanks Runnerbean - feels a bit daft dreading my grey hair growing back when you've been through all this but it matters
Thanks Karana that’s reassuring and great news about your being discharged xx
Morning ladies....sorry not been on here for a while....been bit busy as gotta be out of pub next tues and there is so much to do so not a lot of free time! Busy weekend ahead as having leaving party and family coming to join in!!
Shocked....there seems to be different advice for hair...some people say you need to wait few months others a year before colouring hair....I’ve got mine booked in for beginning of July and I finished chemo end of Jan....I’m happy for my hairdresser to colour it and she’s just as happy to do it....I’m not sure I cld manage much longer looking as dark and grey as I am!!
Had meeting with Oncologist yesterday...she put my mind at rest about lumpy bumpy boob and said it felt all very normal and just the effects of radiotherapy.....my sucken veins in my arm probably won’t get better so gonna just have to get used to looking like I’ve been bitten by a 🦈😱 ....aches and flushes from Tamoxifen are just something we will get used to but she said the benefits of having it out weighs side effects! After discussing that she then discharged me from treatment so that’s me done....whoop whoop....think I can safely say I won 💪💪🤛💪💪🍾🍾🎉🎉🎉🎉🎉🎉
sending you all big love 💕 💕💕💕💕💕
Hi October ladies, I am from the January thread and hoping some of you can advise. I had my last chemo yesterday YAY and the nurse said I shouldn't colour my hair when it starts growing back for a year:WHOAH: - that is almost as bad as losing it in the first place for me, what advice have you ladies had about colouring?
Hope hubby is paying for it to be fixed 😊 I've just planted my bulbs I had 30 to do so just dug holes randomly and stuck a couple in each one 😕 so hoping they'll grow 🌸
Hello all! Yes lovely weekend here, spent most of it gardening. OH helpfully reminded me at 10pm last night that I hadn't planted the bulbs I'd soaked 😡So I've got to go out there now and do it ☹️Still glorious here today although I think it's due to change tomorrow.
Cassie, hope you're feeling better soon. How's the 🚗?
Funny you should mention Ali Shi, I was only thinking about her this morning and wondering how she was.
What's the Fitbit thing?! xx
Mishy, great info that you were able to give Rachel on the rads thread, I'm sure it will be useful xx
Hi Karebear, yes I have in my fingers and toes. I haven't got pain with it, just numbness and occasionally a bit of pins and needles. I was told at radiotherapy last week that it can take a few months to go (she said it can be as long as 5-6months)I was told it's because they're the furthest away from our hearts they take the longest to get back to normal x
No, she's not on a specific chemo thread, but has started a new one on here titled Triple Negative and in the Rads threads. She has taken my advice and posted on the TN section, but that can be a bit quiet sometimes and perhaps even more so as it's a Saturday and B Hol x
Do all TN's have to have chemo? Until I had my op and cancer was found in 3 lymph nodes, only having rads had been mentioned to me xx
Hope everyone is enjoying themselves in this lovely sunshine! I'm enjoying a day off from having to go to the hospital!
There's a lady called Rachel, who's posted on rads thread and on the chemo monthly, looking for anyone who has TN in Newcastle. She didn't get any replies, so I've replied and told her to go onto the TN thread. I did say if she didn't get any response, to come on here or Nov thread as there are TN ladies who can help her xx
Meesh my boob is still achy 3 years on, 8 weeks is still very early days in terms of finishing rads as the effects go on for a while after, a ladies I keep in touch with has recently had a problem with hers swelling and being uncomfortable several years on but all is ok , everything has us freaking out and your wise to get it checked but I'm sure it's all fine 😊Xx Jo
Thanks Mishy, I've got an appt next Wednesday. I'm just finding it annoying as you think "yay I'm done with treatment I need to start getting myself back on track" then when you do this sort of thing happens and you think "aaarghhhhh when will it end?"
No I don't think I've done anything to aggravate it. Doesn't seem to ache quite as much today but it's still swollen. I'm trying not to be 😳😳😳about it.
Its comforting to hear that some of you also have had some issues, although I'd rather we all didn't if you know what I mean. Just when I start to think I'm getting back to normal too 🙄
Btw, what happened to the forum yesterday?! I kept trying to send a message, but it wouldn't let me! x
Thank you all for your rads good wishes x 3 down, 22 to go! Finding my arms ache as so far I've had to keep them in the same position for about 40mins! (Found it slightly easier today as I took some paracetamol first) Also, having to keep holding my breath is quite tiring. I was better at it today, apparently yesterday I wasn't as good as Monday! I keep thinking it's only for 5 weeks, but at the moment it seems like a long time! xx
Starting radiotherapy at long last tomorrow! Feeling a little apprehensive now though! xx