I had my review with the rads dept this week, and asked about heart etc, being a leftie. The radiographer showed me my scans with the radiation fields marked up, so I could see the beams are not going anywhere near my heart, but are skimming the edge of one lung. Very interesting. Anyone have David Tennant's email? I need some gardening doing....
Hi Christine, I finished on June 9th as well! I'm taking Tamoxifen and have been since results back in April and am honestly feeling ok with them,I take mine at night and have had no sickness and a very odd flush, I get some pain in an old ankle injury and my legs ache If I've been on my feet a lot but I really wouldn't notice I'm taking them, I also take venlafaxine with them which is an antidepressant my surgeon suggested as it helps with side effects, especially hot flushes so I'm guessing they are doing the trick xx Jo
There's trees at Velindre as well. What'with these trees. I notice you're all taking tablets while doing your rads. I've been told I'll be taking tamoxafin when I finish rads. Joyce X
All depends if your boss has had any experience of cancer treatment directly or through other staff? Some people seem to think this is nothing others know the truth and acknowledge /realise the impacts. Hope your boss is understanding. A friend of mine just called up to wish me good luck and then babbled on for 20 minutes about the dancing summer school she's running for kids. Yes! Very nice but I'm about to get my boob nuked and don't give one! I'm sure you can sort the boss out! Good luck.
Hi Jill, good luck this afternoon - sounds like a bundle of fun! I'm taking my daughter to her friends and then coming back for a hot and steamy date - with the ironing pile! We lead such exciting lives!
Hi Jill, Brad Pitt would do if Poldark is not available ha,ha! I'm feeling really tired today - haven't got the energy to do anything. I really need to think about packing and getting sorted for my holiday, but my mind is elsewhere at the minute! Had a bit of panic last night - felt a slight lump above treated boob and mentioned it this morning, they just said to keep an eye on it and it could just be side effects from my first sessions of radiotherapy. Scar tissue is feeling really hard now as well, I'm lucky my surgeon did a really neat scar just round my nipple and managed to perform the sentinel node biopsy through this too! I just keep thinking will I spend the rest of my life worrying over every lump and bump but I guess we all go through this and over time we will stop worrying so much.
As I lay on the bed so long this morning my mind was going into overdrive thinking what have they seen on the images and why is it taking so long, hope it's not as bad tomorrow - my neck and shoulders are painful now I've just got to tell myself not many more now! Sorry for moaning, been let down by my friend this afternoon so I just needed a little moan on here and I will be fine. I need some of your funny stories to cheer me up!
Welcome Lisa, wish you didn't have to join us but since you do I can confirm what everyone else has said, this islet is a life- saver because you can always find someone to talk to who will understand. As good as relatives and friends can be it is just too much to offload on them all our fears about the treatment and the future. It is a real help to be able to sound off and ask questions here without worrying about dragging others down. Jennifer x
Anyone experienced the holding breath technique for left siders? I have been practicing but because my first session is today and I'm feeling nervous can't hold for more than 20 seconds. Scared stiff my heart is going to get caught in the beam and age 10 years over night ( yes - this is what my oncologist told me could happen!).
Good morning back from second booster session - must say I'm not liking this much! It takes a lot longer - I think I was in the room about 25 minutes today! I got a bit worried at one point as I thought they had forgotten I was lying there! Apparently my clips were being elusive!! I started to count the branches on the picture on the ceiling at one point. Do you all have tree pictures on the ceiling at your hospitals? As I'm having boosters they are all in the same room so I have to look at a cherry blossom tree for the next week and a half - be much nicer if Poldark was there ha,ha! Hope you all have a good day, my nights aren't getting any better - think I'm going to start looking for the meteor showers in the skies this week whilst I'm awake!
Thank you for all your replies , it's so helpful and supportive knowing so many are going through the same process.
I am hoping that then my rad will start in sept ( my surgery was 6th July ) I had good news last wk from my onco dx test score was low so no chemo just rad. My lymph node had some micrometastis in so not sure what they will do with that ???
thank u all , hope yr all staying strong
Morning Christine, My oncologist appointment was good, she was a lovely lady and talked through the process with me and the reasoning behind me having it, I was already feeling very relieved not to have needed chemo so didn't question rads and was happy to have them as an extra precaution, they were a doddle to be honest, completely painless and other than a bit of a hot boob come the end I suffered no ill effects, 2 months on I'm back to normal life, you will get there and it's a great feeling! Best of luck today xx love Jo
Hi Lisa and welcome
Sorry you have been diagnosed with BC but glad you are being treated, hopefully cured! As the girls have said, they have to give the wound time to heal before further treatment. It drags on when all you want to do is get it done and over with but makes sense.
sending love Lorna x
Hi Lisa and welcome. I had my second WLE at the end of May and started rads 7 weeks later. I have now had 15 of 25. When we were discussing start dates the oncologist said i had to start within 3 months of my first surgery which was end of April. Mine was high/intermediate grade DCIS so probably a different pathway and different hospitals seem to have their own guidelines. Good luck with it. Xx
Welcome to the BCC discussion forums where I am sure you will get lots of good, honest support from the many informed users of this site.
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I have just joined the forum this evening after reading so many interesting and helpful comments. I was diagnosed with BC in June , had lumpectomy and sne in July . Have my onc appointment this Thursday . Just wondered what will happen and the likelihood of when radiotheraphy may start ? I realise it's all a process and a waiting game ....
Any help would be more than grateful? X