Welcome to the Christmas Chemo Club - May your Xmas meal taste better than Tin and Cardboard.
Lets hope it's more Ho Ho Ho! rather than Oh Oh Oh!
This thread is for all of you good folks going through chemotherapy to browse through, ask questions, answer questions and be there for each other in a way only you guys know how.
If you want to find this post quickly, you can hit the 'Save In My Favourites' button - See discussion tools box
If you need any extra tips, our Chemo Tips Page is something you may find very helpful, and something that you may find you would like to share with others who are also going through chemo. One top tip, ask about parking at the hospital you are being treated at; for some Cancer patients parking is either free or discounted (big discount!) So it's worth asking about.
If you need to refer back a month here is a link to Novembers Thread which will be being locked to replies soon.
Remember, you're never alone, you have us! And, just try to focus on what your chemotherapy is doing. Its hopefully kicking your cancers butt. I hope all of you are doing as well as you can do while going through this tough part of your journeys.
Don't forget all cancer patients are entitled to a 5 Year Prescription Fee Exemption Card from your GP for meds to help with any side effects. Happy December Everyone, fingers crossed for maximum impact and minimal side effects.
All aboard for the Mystery Tour - Hold Tight; ding! ding!
i had choice of lumpectomy or reduction..... no brainier for me I’m having reduction..... being large busted I’ve got a lot to get rid of and have wanted a reduction for quite a few years if I’m honest. (Having both done!!!)
Fingers crossed you can just have lumpectomy xx
You'll be ok Cheeboe not as bad as your head telling you . No6 EC for me on the 11/12 .
not everyone the same we all react differently I've been one of the luckier ones and have had manageable SE .
Keep a diary of how you feel each day so you can see a pattern emerge of when your good days are then plan a treat .
listen to your body fir food and sleep . Drink at least 2 1/2 > 3 litres a day to rehydrate .
hope all goes well
margaret x
Hi
Well done! I'm not far behind you, no 6/7 tomorrow so will finish on the 27th. I think they will ask me if I want to ring the bell but I haven't decided yet. It will be great to finish the chemo part of the journey but I'll be back 3 weeks later to continue the Herceptin/perjeta until October and I also haven't had my surgery yet!!
Cheeboe good luck tomorrow. It is scary the first time, I had a few tears in the waiting room, I didn't want to have this nasty stuff in me. But it's helping us to beat this so I try to think of it as medicine rather than nasty stuff. My side effects have been mild and I've been able to stay positive. My unit (and I'm sure others are the same) is a very upbeat place, I don't dread going now. The staff are so lovely and the patients are all friendly and we have a good chat. The volunteer ladies who bring the tea & biscuits trolley round are a couple of characters and get everyone laughing.
Agree with the advice - rest when you need to, plenty of fluids.....you probably won't forget that bit, I had a raging thirst for a good couple of weeks after the first one. They say pineapple / pineapple juice is very thirst quenching.
Hope it goes well for you.
xx
Two words for you - "whoop, whoop".
Well done and crappy weeks worth it. The bell is a new one on me and last orders for chemo is definitely good. Love your video, particularly the way that your camera person got the main shot (and really warming to see the hug with nurse, bought a tear to my eye) but also finished on the ever important feet shot and the end comments is also class "press the button...'.
Am also very impressed with your technical ability to put a video on here, I struggle (mainly as I can't be bothered to figure out anything technical that involves mental exertion) with getting the right words in the right order with a modicum of correct spellings.
Really happy for you & good luck for next stage.
Sam X
Thanks, it made me laugh when hubby (videoing) asked how you turn it off...... had to show him how to use HIS phone to do the video to start with lol
Ringing bell was bit emotional but marked the end of that part of my journey and I’d been looking forward to doing it for weeks! Xx
Well done so pleased for you that this stage of your journey is over.
Just like west end girl I also have last EC on 27th (which makes 6 in total) and I got on so well with it I switched back from another drug (which was giving me unacceptable side effects) to EC so to echo Margarets note there are quite a number of people that come through it relatively smoothly, And I hope you're one of our gang in that respect.
You will find , as west end girl mentions, that the wards are such a friendly place, despite being full of strong chemicals and some poor;y people. I really enjoy going to the chemo ward to meet people on the receiving end who I've met before, talking to new people, yacking to the nurses (who are excellent fun - the topic today was the "special place" phrase for anyone who watched the baby program on BBC 2 last night) and spending time with my lucky friends who take it in turn to travel from the motherland to watch me have drain cleaner pumped into my viens (I'm quite spoilt).
I really hope you enjoy (odd I know) it as much as I am/have.
Sam X
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